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ORIGINAL RESEARCH article

Front. Vet. Sci., 25 July 2025

Sec. Veterinary Imaging

Volume 12 - 2025 | https://doi.org/10.3389/fvets.2025.1598038

Association between radiographic equine distal phalanx characteristics and absence, presence and type of horseshoes

  • 1Department of Companion Animals and Horses, University Clinic for Horses, University of Veterinary Medicine, Vienna, Austria
  • 2Department of Veterinary Clinical Sciences, Large Animal Hospital, Easter Bush Veterinary Centre, Easter Bush, Royal (Dick) School of Veterinary Studies, The University of Edinburgh, Roslin, Midlothian, United Kingdom

Most horses are used with horseshoes additionally supported by either dorsoabaxial or dorsal clips. The effects of such clips on bone density and shape of the distal phalanx are currently unclear. The aim of this study was to identify correlations between density and shape of the distal phalanx, comparing front hooves unshod or shod with standard shoes either with two dorsoabaxial clips or with a single dorsal clip. Researchers analyzed Oxspring radiographs of either the left or right front hoof from warmblood horses (n = 137) and ponies (n = 43) aged 3–28 years. The evaluation focused on distal phalanx density at the margo solearis, particularly at three locations corresponding to the clip positions: dorsomedial, dorsal, and dorsolateral. The study examined horse related variables such as age, breed, use, and shoeing type in relation to density parameters, presence of a crena marginalis solearis, an anatomical variation that is an indentation dorsal on the margo solearis, and the shape of the distal phalanx. Distal phalanges of hooves shod with dorsoabaxial clips showed a significantly (p < 0.001) lower width to length ratio (median 1.31, minimum 0.70, maximum 1.66) compared to those with a single dorsal clip (median 1.40, minimum 0.89, maximum 1.75). The width to length ratio of unshod hooves (median 1.37, minimum 0.80, maximum 1.82) was not significantly different from both groups of shod hooves. The results of this study should be considered when selecting horseshoes for equids.

1 Introduction

Humans first shod horses to protect hooves from excessive wear (1). Later, metal clips, semicircular metal protrusions from the shoe that conform to the dorsal or dorsoabaxial hoof wall, were added for additional support (2). The distal phalanx (P3 or coffin bone) forms the hoof’s structural foundation and is critical for equine locomotion (2). It connects to the horn capsule via the laminar interface, enabling efficient load distribution (3). Since the advent of radiography, hoof and P3 morphology have informed shoeing practices (4). Farriery and trimming significantly alter hoof shape (5), which can change notably within 7 weeks of either shoeing or barefoot management (5). Posture and nutrition also affect hoof horn quality and shape (6), thereby influencing P3 morphology (7). Hoof shape is a key determinant of locomotor function in horses (7).

Throughout the 20th century, various methods were used to study shoeing effects on equine performance. Shoe mass increases distal limb mechanical load (8), and standard shoeing increases stride length and joint flexion compared to unshod horses (9). Also, increased stride duration and stride length in trot was noted (9). Aluminum shoes yield a larger minimum carpal angle and lower maximum hoof height than steel shoes (10). Force plate studies documented limb loading and movement, with shod horses showing greater maximum vertical ground reaction forces (11). Pressure plates demonstrate that shoes with a wider toe increase toe contact area and reduce vertical pressure in the toe region (12).

Clips improve horseshoe stability and reduce nail strain (13), this is especially important if the traction of the shoe is enhanced using studs, pins or borium. Clip configuration varies by discipline: dressage horses are typically shod with one dorsal clip on forelimbs and two dorsoabaxial clips on hindlimbs, while on draft and racehorses often a single dorsal clip is used on all hooves (14). In racehorses, dorsal hind clips prevent backward displacement and protect high-power transmission zones (15).

Shoeing alters hoof biomechanics, shifting the center of pressure medially during early stance (13). Finite element models reveal that dorsoabaxial clips exert maximal pressure on the hoof wall by restricting normal hoof expansion at clip positions during loading (14, 15). These clips limit hoof mechanism (14), potentially affecting growth and condition (16). Dorsoabaxial clips are occasionally used on front hooves despite impairing hoof mechanism (14, 15). These clips lead to narrower hooves and they can shift the breakover point and reduce hoof expansion (1720), though effects on the distal phalanx have not yet been considered. Nail placement also influences mechanics, with heel-proximal nails restricting hoof expansion (21).

Thermography revealed cooler soles and reduced blood flow in shod hooves compared to unshod hooves after 8 weeks (22). As in all bones, the forces sustained also affect the osseous quality of the distal phalanx. Bone is constantly turned over, which involves modeling and remodeling mediated by osteoblasts, osteoclasts, and osteocytes, maintaining bone balance (23). A shift toward resorption results in bone loss (24), and excessive strain may weaken the bone potentially leading to microdamage/stress fractures (25). Pathological changes in the distal phalanx occur with conditions such as laminitis, osteitis, or keratoma-induced pressure (2628), with osteitis characterized by demineralization and vascular channel widening (28).

Despite extensive research on the biomechanical effects of horseshoes on equine limbs and hooves, the impact of routine shoeing on radiographic density and morphological adaptations of the distal phalanx remains poorly characterized. The present study aims to investigate associations between dorsal and dorsoabaxial clips and osseous density and structural geometry of the distal phalanx, comparing these associations to unshod hooves. Specifically, we hypothesize that dorsoabaxial clips are associated with (a) localized reductions in radiographic density at the margo solearis beneath clip positions and (b) a narrower in shape distal phalanx configuration, relative to dorsal clips.

2 Materials and methods

2.1 Selection of radiographs

Radiographic images taken during lameness or pre-purchase examinations at an equine clinic between 2016 and 2023 were retrospectively evaluated. Prior to data collection, the responsible person provided written consent allowing the use of clinical data for research purposes. Radiograph selection was performed using the PACS system with JiveX DICOM software. Inclusion criteria required orthograde Oxspring radiographs of one front foot (either left or right) of Warmblood horses (n = 132) or horse-type ponies (n = 43; height at the withers: 120–148 cm). Most radiographs had been taken with mildly radiopaque mass in the sulci of the frog. In the following, both horses and ponies are referred to collectively as “equids.” Equids ranging in age from 3 to 28 years were included in the study, with a mean age of 14.1 years. The height at the withers was not available for all equids. Radiographs with artifacts or visible pathologies, whether noted on the image or in the radiology report, were excluded. If radiographs of both front limbs of an individual were suitable, the image deemed superior for measurement was selected.

All radiographic images meeting these criteria were anonymized by assigning each one a unique, randomly generated numeric identifier. This randomization was carried out by computer software employing a pseudo random number algorithm, ensuring equal probability of number assignment. Each radiograph was measured twice, on separate days, by a single investigator blinded to the animal’s identity. Only the numeric codes were accessible during measurements. The average of the two independent measurements was used for further analysis. Equids were grouped into unshod (US), shod with dorsal clip (SC1), and shod with two dorsoabaxial clips (SC2), referred to as groups for the remainder of the paper.

Four age categories were defined based on existing literature (29, 30): 3–6 years (juvenile = JUV), 7–14 years (young adult = YAD), 15–21 years (mature adult = MAD), and >21 years (OLD). A total of 97 male and 78 female equids were included. Due to the low number of stallions (n = 2), no distinction based on castration status was made. Based on historical data, the equids were also categorized by use, reflecting increasing workload: leisure equids (LE), dressage equids (DE), and jumping equids (JE). For the remainder of the text, we collectively refer to the parameters age, breed, use, and shoeing type as “horse/pony variables.”

Prior to radiography, horseshoes (if present) had been removed, and the hooves had been trimmed to improve image quality, as is standard practice (31, 32). The person responsible for the equid was asked about the duration of the current shoeing or the barefoot period. Of the 175 equids, 145 had a documented shoeing or barefoot status of at least 1 year prior to the inspection date, while for 30 equids the duration of barefoot or shoeing status was not available. Grouping was done based on the status of the equids presented at the clinic, and the shoeing history was only taken in addition to that, but not as the basis for the grouping of the equids. In order to test the relevance of this additional information, parameters of equids with known 12-month prior history (known history) and equids with unknown 12-month history (unknown history) were compared within each group.

A total of 98 right front and 77 left front Oxspring radiographs (175 equids) were ultimately included. The distribution of equids across groups included 58 in US, 66 in SC1, and 51 SC2. After final selection, each radiograph was assigned a new randomized identification number for analysis.

2.2 Image analysis

Using Image J software, 175 selected Oxspring images were analyzed by the first author. This evaluator was blinded to the groups during the measurements and radiographs were analyzed in a random order.

The relative width of the distal phalanx was measured using a transversal latero-medial line at the widest point of the distal phalanx (Figure 1; Nr.2) and the relative length of the distal phalanx was measured with a sagittal line along the axis of the distal phalanx from the center of the margo solearis to the center of the proximal contour of the extensor process (Figure 1; Nr.3), following previously described methods (3339). Width to length ratio (WL ratio) was calculated and used to objectively document the shape (Figure 1; Nr.7) of the distal phalanx as near to elliptic (ratio values near or below 1) or round (ratio values 1 or more). All measurements are summarized in Table 1.

Figure 1
This picture shows two views of a dorsoproximal-palmarodistal radiographs of the left front distal phalanx of a 4-year-old unshod Warmblood mare. Image 1a on the left shows the native radiograph, 1b on the right is annotated with measurement lines for assessing the middle and distal phalanx dimensions, width to length ratio and grey values of the distal phalanx. The distal phalanx is classified as elliptical with visible crena marginis solearis.

Figure 1. Oxspring radiograph (dorsoproximal-palmarodistal projection) of the left front foot of a 4 year old female leisure Warmblood horse (hoof no. 5), belonging to the unshod (US) group (Diagnostic Imaging, Vetmeduni). Lateral is to the left in both images. (a) Native radiograph. (b) Radiograph annotated with measurement lines. The width of the radiographic depiction of the middle phalanx (1; 96.3 mm), the relative width (2; 135.62%) and relative length (3; 91.90%) of the distal phalanx were measured using transverse and sagittal reference lines. Lateral (4; 33.33%), dorsal (5; 33.33%), and medial (6; 33.33%) lines were positioned across the distal phalanx to measure gray values. The width to length ratio (WL ratio) is derived from lines two and three, offering a quantitative representation of the shape of the distal phalanx. The shape of the distal phalanx was subjectively classified as elliptical (7). A crena marginis solearis of the distal phalanx is visible (8). Minimum and maximum bone densities as gray values were recorded within the outlined rectangular measurement area.

Table 1
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Table 1. Measurements used in the present study for the analysis of the distal phalanx.

The presence or absence of a crena marginis solearis was noted (Figure 1; Nr.8). The bone density of the margo solearis was documented at the locations where dorsal and dorsoabaxial clips had been or would have been positioned. Gray values (GV) were obtained along three straight lines as secant lines starting and ending at the margo solearis but intersecting the curvature of the margo solearis (Figure 1; Nr.4, 5, 6), each measuring a third of the relative width of the middle phalanx (Figure 1; Nr.1). Along these lines, GV were collected and referred to as dorsal (D), dorsolateral (L) and dorsomedial (M) gray value series (GVS). The width of the radiographic depiction of the middle phalanx (WRMP) in the images analyzed was used, as not all radiographs had the metal reference marker fully within the collimation. Length measurements of other features of the radiographs were done as percent of the WRMP and only these percentage values were taken forward.

To compare GV between radiographs and to normalize GV in percent resulting in %GV, highest and lowest GV were analyzed within the largest possible rectangle from the hoof. Metal markings, contamination or remnants of shoe nails were excluded. For each GVS the following values were calculated: mean (mn), standard deviation (sd), quantile10 (Q10), quantile25 (Q25), quantile50 (Q50), quantile75 (Q75) and quantile90 (Q90).

2.3 Statistical analysis

Statistical analysis of the results was performed using IBM SPSS Statistics, Python, and Microsoft Excel. The data was tested for normality using the Shapiro–Wilk test. When the statistical test showed significant group differences, we conducted a post-hoc analysis to compare pairs of groups. For normally distributed data, we used ANOVA with Tukey HSD as a post-hoc analysis. If the data did not follow a normal distribution, we applied the Kruskal–Wallis test followed by Dunn’s post-hoc test. To assess whether age and group were independent, we conducted an ANOVA. We also used Spearman’s rank correlation (one-tailed) to analyze the relationship between horse/pony variables and %GV.

We conducted an exploratory analysis to assess the stability of WRMP across different groups and use of equids. We evaluated normality using Shapiro–Wilk tests and homogeneity of variances using Levene’s tests. Due to non-parametric distributions in some groups, we used Kruskal-Wallis tests for group comparisons. Additionally, we calculated the Pearson correlation coefficient between the width of the middle phalanx and the WL ratio from the distal phalanx to examine their relationship.

Presence of crena, use of equid, breed, age, WL ratio, shape of the distal phalanx, and %GV (standard deviation, mean, and Q10 to Q90 of dorsal, medial, and lateral %GV) were additionally analyzed separately for warmblood horses and ponies. To evaluate the accuracy of the subjectively assessed distal phalanx shape, we compared the WL ratio between the two shape categories (oval = 0, round = 1). Descriptive statistics were calculated, and a Welch’s t-test was performed to test for significant differences between the groups. A Pearson correlation was computed to assess the relationship between WL ratio and shape. We calculated Cohen’s d to quantify the effect size between US, SC1, and SC2 pairs in relation to %GV.

3 Results

Two-way ANOVA revealed a significant main effect of US, SC1 and SC2 on WL ratio (F = 13.21, p < 0.001), while the fact, that known or unknown history showed no significant main effect (F = 0.78, p = 0.379) or interaction with US, SC1 and SC2 (F = 1.02, p = 0.413). Descriptive statistics and Dunn’s post-hoc tests with Bonferroni correction yielded consistent results across equids with known duration of barefoot trimming or shoeing and those without such historical data. This consistency was observed in both the magnitude of effects and patterns of statistical significance. Comparison of mean and standard deviation of WL ratio of distal phalanx among group unshod (US), shod with one dorsal clip (SC1), and shod with two dorsoabaxial clips (SC2), stratified by the presence or absence of a known shoeing or trimming history over the previous 12 months, showed no significant effect of shoeing history on the WL ratio within any group. For unknown: US (mean = 1.35, min = 1.17, max = 1.45), SC1 (mean = 1.39, min = 1.25, max = 1.57), SC2 (mean = 1.30, min = 0.7, max = 1.55). For known history: US (mean = 1.37, min = 0.8, max = 1.82), SC1 (mean = 1.41, min = 0.9, max = 1.75), SC2 (mean = 1.32, min = 0.86, max = 1.66). Significant differences were found between SC1 and SC2 in both subgroups (unknown history: Test Statistic = 3.752; p = 0.00093, known history: Test Statistic = 3.928; p = 0.00074).

There were no significant differences between radiographs of left and right distal phalanges in any of the variables examined, therefore left and right forelimb results are presented together. No significant difference in WL ratio was observed between the groups of Warmbloods and ponies (H-statistic = 2,78, p = 0.25).

We assessed normality (Shapiro–Wilk) and homogeneity of variances (Levene’s) for WRMP (mean = 68.01 mm, sd = 5.05 mm) across groups and use of equid. Due to violations of assumptions, we employed Kruskal-Wallis tests. Results showed significant differences in WRMP for groups (p = 0.0057) and use of equid (p = 0.0331). The Pearson correlation between WRMP and WL ratio was negligible (r = 0.008), indicating their independence.

The WL ratio differed significantly between oval and round hooves, (oval: mean 1.301 sd, round: mean 1.396 sd; t = −3.935, p < 0.001).

A statistical difference between male (predominantly castrated) and female equids was found for relative length of the distal phalanx (means male 91.30%, female 95.43%. T-statistic 2.1285; p = 0.0347) and for medial and lateral GV% distributions (medial means male = 0.2356, female = 0.26228. T-statistic 2.7002; p = 0.007; lateral means male = 0.2279, female = 0.2506. T-statistic 2.4073; p = 0.017) (Figures 2, 3).

Figure 2
Box plot showing the distribution of distal phalanx relative length by sex. The plot compares females and males, using pink and blue boxes respectively. Females have a median around 90% with more variance and outliers above 110%. Males have a similar median, slightly higher, with less variance and a few upper outliers.

Figure 2. Distribution of relative length of the distal phalanx length (%) by sex in equids. This boxplot based comparison highlights potential differences in relative distal phalanx length between male and female subjects. Each box represents the interquartile range (IQR), with the median indicated by a central line and whiskers extending to the full range of data (the circles O represent possible outliers). Pink boxes represent females and blue boxes represent males, offering a clear visual distinction of central tendency, dispersion, and outliers for each sex. One extreme outlier in the male group was ignored for the clarity of the visualization.

Figure 3
Bar chart comparing medial and lateral bone densities by sex. Female data is shown in pink and male data in blue. The horizontal axis lists various bone measurements like medmwd and latquantil90, while the vertical axis shows grey values from 0 to 30 percent. Each category has two bars representing female and male densities, with slight variations between sexes.

Figure 3. Comparison of bone density in male (blue) and female (pink) equids. This figure illustrates variations in as median gray value percentages (indicative of bone density), and the 10th, 25th, 50th, 75th, and 90th Quantile of the medial and lateral distal phalanx density of the distal phalanx. Bars represent the sum of the medial and lateral gray value series (GVS). Sums of GVS were significantly higher in female than in male equids (medial p = 0.007; lateral p = 0.016).

Age and groups US, SC1 and SC2 contribute to the variance in WL ratio independently with a two-way ANOVA (F-value = 18.23; p < 0.00001 for age and F-value = 5.56; p = 0.00456 for the groups, respectively). No significant interaction effect was found between the age and the groups (F-value = 0.94; p = 0.39). In equids, higher GV% were seen medial (SC1 = 0.01806, SC2 = 0.01938) and lateral (SC1 = 0.0174, SC2 = 0.0179) in SC2 compared to SC1, but this was not significant (Medial Mann–Whitney U = 1,478.6; p = 0.257. Lateral Mann–Whitney U = 1,813.0; p = 0.4765). Between SC1 and SC2 differences were found in the medial (SC1 mean = 0.235, sd = 0.056, min = 0.137, max = 0.394; SC2 mean = 0.235, sd = 0.068, min = 0.151, max = 0.422) and lateral (SC1 mean = 0.233, sd = 0.054, min = 0.157, max = 0.381; SC2 mean = 0.242, sd = 0.068, min = 0.138, max = 0.421) GV%. In US equids the medial GV% are higher than in SC1, although not strong enough to be significant (US mean = 0.257, sd = 0.071; SC1 mean = 0.235, sd = 0.0558; SC2 mean = 0.25298, sd = 0.0684).

Table 2 shows the radiographic dimension of the middle phalanx length, the relative distal phalanx width and length and WL ratio. No significant differences were found between the relative width of the distal phalanx of SC1 and SC2 (H = 3.27, p = 0.195). However, significant differences were found in the relative length of the distal phalanx between groups (H = 9.33, p = 0.0094).

Table 2
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Table 2. Width of the radiographic depiction of the middle phalanx (WRMP in mm), relative width of the distal phalanx (% of WRMP), relative length of the distal phalanx (% of WRMP), and the width to length ratio of the distal phalanx among three groups of equids: unshod (US), shod with one dorsal clip (SC1), and shod with two dorsoabaxial clips (SC2).

Group US exhibited an average WL ratio of 1.37 (median = 1.38, min = 0.8, max = 1.82). Group SC1 had a slightly higher mean ratio of 1.40 (median = 1.41, min = 0.9, max = 1.75). In contrast, group SC2 demonstrated a significantly lower mean ratio of 1.31 (median = 1.3, min = 0.7, max = 1.66). Groups were significantly different overall (H (2) = 13.01, p = 0.0015), with group SC2 showing a significantly lower WL ratio compared to SC1 (p = 0.00093), whereas no significant differences were documented comparing US and SC2 (p = 0.159) and comparing US and SC1 (p = 0.284).

The presence of a crena marginalis was independently associated with greater distal phalanx relative width and a higher WL ratio. Equids with a crena exhibited a significantly higher distal phalanx relative width (mean difference = 0.049, 95% CI [0.028, 0.071], p = 0.024), independent of group US, SC1, SC2. The WL ratio was significantly higher in individuals with a crena (mean difference = 0.082, 95% CI [0.059, 0.106], p < 0.001), with group US, SC1 and SC2 showing no independent effect (χ2 = 0.62, p = 0.73). There was no association between the presence of a crena and group US, SC1 and SC2 (Figure 4). Breed differences remained evident: warmbloods were overrepresented among equids with a crena, whereas ponies were more likely to have no crena (χ2 = 9.29, p = 0.0096).

Figure 4
Bar chart showing the distribution of Crena Marginalis Solearis among US, SC1, and SC2. The y-axis represents the number of hooves. Red bars indicate presence, and green bars indicate absence. SC1 has the highest number of hooves with presence.

Figure 4. Distribution of presence (red bars) and absence (green bars) of a crena marginalis solearis in distal phalanges of equids of unshod hooves (US), and of hooves shod with a single dorsal clip (SC1), or with two dorsoabaxial clips (SC2).

These findings indicate that the crena marginalis is a key factor associated with the shape of the distal phalanx, particularly its mediolateral dimension, and that its distribution varies significantly across warmbloods and ponies (see Figure 5).

Figure 5
Box plot comparing distal phalanx relative width percentages across three groups (US, SC1, SC2) by the use of equids (LE, DE, JE). Each group displays variability in measurements with corresponding data points indicated as outliers. Different colors represent equid types: blue for LE, red for DE, and green for JE. Sample sizes and counts are provided below each group.

Figure 5. Variation in relative distal phalanx width (%) across unshod (US), single dorsal clip (SC1), and two dorsoabaxial clips (SC2) groups, further subdivided by use of equids (LE: leisure, DE: dressage, JE: jumping). Each boxplot shows the distribution of relative distal phalanx widths within each category, including median values, interquartile range (IQR), and outliers (O). Text annotations indicate sample sizes (n) and the presence of crena marginalis solearis (c). Notably, individuals with a crena show significantly greater distal phalanx relative width (p = 0.001), independent of US, SC1 and SC2 or use, with warmbloods overrepresented in the group with a crena marginalis solearis. These results highlight the crena as an important determinant of distal phalanx morphology, with potential breed specific effects.

Comparing all age groups WL ratio and age differ significantly (JUV = 1.47197, YAD = 1.3776, MAD = 1.3785, OLD = 1.33446. Kruskal H-value = 19.0998; p = 0.0003), and WL ratio of the youngest group JUV (median = 1.47 min = 1.25, max = 1.82) differs significantly from group YAD (median = 1.38, min = 0.86, max = 1.66. Mann–Whitney U = 1,221.0; p = 0.00011), from group MAD (median = 1.37, min = 0.80, max = 1.58. Mann–Whitney U = 835.0; p = 0.00038) and from group OLD (median: 1.36, min = 0.70, max = 1.59. Mann–Whitney U = 361.0; p = 0.00112) (Figure 6).

Figure 6
Box plot illustrating width to length ratio by age, ranging from three to twenty-eight years. The plot showcases median, quartiles, and outliers for each age group, with variability and trends in ratios visible across ages.

Figure 6. Variation of the distal phalanx width to length ratio (WL ratio, a dimensionless value) with age in equids. This figure presents boxplots of the WL ratio grouped by age, illustrating how hoof proportions change as equids grow older. Each boxplot shows the IQR (Interquartile Range), outliers (O), the range between the first quartile (25th percentile) and the third quartile (75th percentile) of a dataset, with the median value indicated. The results suggest that older equids tend to have a lower WL ratio, and thus a relatively narrower distal phalanx, compared to younger equids.

The age distribution for LE peaks between approximately 15 and 20 years, DE shows a peak in equid use between 10 and 15 years of age. In contrast, the JE exhibits its highest density of equid use at the age of 5–10 years. Leisure equids are older than jumping or dressage equids (Figure 7).

Figure 7
Density plot showing the age distribution by use of equids with three groups: LE (blue), DE (red), and JE (green). The x-axis represents age in years, and the y-axis shows relative frequency. Each group forms overlapping curves, indicating differing age distributions.

Figure 7. Age distribution across different uses of equids (leisure LE, dressage DE, and jumping JE). This figure depicts Kernel Density Estimation (KDE) plots of age for LE (blue), DE (red), JE (green). The shaded areas represent the relative frequency of equids within specific age ranges, facilitating visual comparison of age-related demographics across different categories of use. The data suggest that leisure equids tend to be older than those used for jumping or dressage.

No significant differences in the relative distal phalanx width were found for the use of equids. The mean relative widths were 1.2626 for LE, 1.2688 for DE, and 1.3311 for JE, with the Kruskal–Wallis test showing a non-significant result (H = 1.0224, p = 0.5998) (Figure 5).

The single tailed correlations of the radiographs of the distal phalanx of warmblood horses and the single tailed correlations of the radiographs of the distal phalanx of ponies are shown in Tables 3, 4.

Table 3
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Table 3. Significant correlations of gray values in percentage (based on the gray value range of each individual radiograph) of the dorsal, medial, and lateral lines of the distal phalanx in Warmblood horses (N = 132).

Table 4
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Table 4. Significant correlations of gray values in percentage (based on the gray value range of each individual radiograph) of the dorsal and medial lines of the distal phalanx in ponies (N = 43).

4 Discussion

The present retrospective study investigated the association of dorsoabaxial clips with the radiographic shape of the equine distal phalanx of forelimbs and documented a significantly longer distal phalanx relative length in hooves shod with dorsoabaxial clips compared to hooves shod with one dorsal clip, leading to a lower width to length ratio. The hypothesis that the distal phalanx of equids shod with two dorsoabaxial clips differs significantly in shape compared to equids shod with one dorsal clip is supported, specifically due to increased relative length rather than a narrower width. The hypothesis regarding the reduced density at the clip sites is not supported. To the authors’ knowledge, this is the first study documenting the association of dorsoabaxial clips with the shape of the distal phalanx.

The present study is retrospective and the Oxspring radiographs of the forelimbs selected were originally taken for clinic necessities. The advantage of a retrospective study is that many radiographs of the distal phalanx were available, and the goal of a relatively simple and cost effective method (40) to show the effects of horseshoes with dorsoabaxial clips was achieved. In a previous study an even larger number of lateromedial radiographs of the distal phalanx of forelimbs was used to measure the concavity of the parietal solar surface of the distal phalanx of equids, which was negatively correlated with age (41). The sample size in the present study did not reach the high number reported in the previous study (41), where 175 Oxspring radiographs of equids taken during lameness or prepurchase examinations were analyzed. Similar to the above report on the solear surface of distal phalanges (41), only digital radiographs were used in the present study, as they provide consistent and high quality images that facilitate detailed evaluation of bone structures and gray value analysis for assessing bone density.

In horses, middle phalanx dimensions, distal phalanx dimension and navicular bone dimensions show strong correlations and size ratios were similar in ponies, saddle horses and harness horses (42). Based on this relationship, middle phalanx width measured on digital Oxspring radiographs was used as a reference in the present study, documenting a relationship between dorsoabaxial clips and bone density changes and distal phalanx shape, one of the main areas of interest in the distal phalanges (43). Radiological bone size measurements are usually done in standard radiographs to investigate distal phalanx morphology, for example proximodistal shortening of the distal phalanx in laminitis (43). Similar to our study, relative measurements in radiographs are frequently used, in order to overcome the difference between true length measurements and measurements of the same structures in the radiograph, where magnification of an unknown magnitude is present (44).

Oxspring radiographs highlight the solear margin of the distal phalanx, where bone remodeling or lysis can be seen (45), this is also the anatomical feature that the present study is focusing on. Either left or right Oxspring radiographs of any individual equid were used in the present study for further processing, creating a data set where each individual equid was represented only once. As demonstrated in a previous study, which found no radiographic differences between left and right front distal phalanges (46), we also observed no significant differences in our analysis. Therefore, when radiographs of both front distal phalanges were available, the one more suitable for further processing was selected. The selection criteria for artifact free radiographs in this study align with those of a previous investigation on equine distal phalanges that utilized ImageJ to document arterial channel changes (47). Consistent with previous studies (48, 49), evaluation of radiographs in the present study relies on subjective assessment. The present study shows that trained observers can reliably distinguish between narrow and wide distal phalanges from Oxspring radiographs without precise measurements. The alignment between expert visual assessment and quantitative measurements highlights the importance of experienced radiographic interpretation. The ability to make accurate assessments without time consuming measurements is thus invaluable in day to day veterinary work (50), even though subjective evaluations are about to be overtaken by the use of artificial intelligence (51).

After selection of all radiographs of the present study, radiographs were processed in random order, thus, for all intents and purposes, the evaluator was blinded to patient data, history, examination findings, and radiography report. This randomization process was implemented to minimize bias, a method also employed in a previous study assessing measurement variability in osteophytosis scoring systems (52). To address potential size differences in digital radiographs (52), measurements were normalized to the width of the middle phalanx, as not all radiographs had metal markers within the collimation. Recording hoof dimensions before or exact distances to the plate and the generator during radiographic examination was not done, as these measurements were not compatible with routine clinical practice in live equids or the retrospective nature of the study. Disadvantages of evaluating digital radiographs over 3D depictions such as CT, include magnification, summation, and superimposition of bone and soft tissue (53). Similar to our study, relative measurements in radiographs are frequently used, in order to overcome the difference between true length measurements and measurements of the same structures in the radiograph, where magnification of an unknown magnitude is present (44). To mitigate potential confounding effects arising from variations in radiographic technique and patient positioning, the width of the distal phalanx and all other length measurements in the present study were normalized to the width of the middle phalanx, as internal reference markers were absent. This normalization strategy aligns with the methodology described by a previous study (54), which advocated for the use of vertebral body lengths as a normalizing factor for tracheal height measurements in equine radiographs. It was posited that ratios utilizing adjacent osseous landmarks facilitate more robust intersubject comparisons. The normalization to middle phalanx width in the present study was intended to minimize the impact of inconsistent magnification, mirroring normalization strategies employed in prior studies that assessed skeletal dimensions. A recent study acquired lateromedial radiographs of the front feet of unsedated draft horses and calculated the ratio of dorsal hoof wall thickness to the distal phalanx length, also highlights the importance of proportional measurements in radiographic assessment of the equine digit, demonstrating the utility of the ratio of dorsal hoof wall thickness to the length of the distal phalanx in evaluating dorsal hoof wall thickness (55). Similar ratiometric approaches have been used in other species. For example, an other non equine study used vertebral measurements to normalize cardiac dimensions in radiographic studies of mice (56).

As in previous studies, gray values were used to evaluate bone density, aiming to assess the precision and accuracy of bone mineral density measurements from digitized radiographs (57). To ensure comparability between radiographs, we used relative density ranges (0–100%) within each image, excluding nails and other metal dense structures from the gray value range. This approach eliminated the need for aluminum as a contrast agent, as used in some previous studies (58, 59) and allowed for comparison of radiographs processed with different algorithms, which were repeatedly adapted to improve image quality by the radiographers over the time from which the radiographs were sourced.

In the present study, equids only from the age of 3 years onwards were included, as the majority of growth plates are closed by this time (60). This approach aligns with a previous study on navicular disease, which also excluded young equids (61). As demonstrated in this previous study, certain navicular bone shapes are predisposed to developing navicular disease, highlighting the importance of bone shape in equine health (61). Similarly, our study focuses on the distal phalanx, raising the possibility that its shape also plays a role in disease development.

For the aim of the present study, it was imperative that equids were at an age when shoeing would have been a possibility or had been carried out. The present study focused on equids aged 3 years and older, a pivotal age when equids conventionally initiate both athletic training and hoof management through routine shoeing (62, 63). Similar to the population investigated in the present study, the study population of a previous study using radiographic analysis in equids (29, 30) was identified as juvenile, young adults, mature adults and old equids. Regarding the use of the equids, the study population of the present study was grouped as: leisure, jumping or dressage, representing main types of equestrian disciplines, as seen in previous research how management and training practices influence back mechanics and flexibility of equids (64). Dressage equids showed a 33% larger mean degree of motion at L3 than leisure equids and 19% more than show jumpers, highlighting significant differences in back flexibility among these equestrian group (64). In the present study is seen, that show jumpers and dressage equids were younger than leisure equids. This is represented in other large studies of the equine population (65, 66). Performance of dressage and jumping equids increased linearly until age 10, then plateaued in both disciplines (65) with another study highlighting that jumping equids reach peak performance at younger ages compared to dressage equids (66). The present findings on age distribution among show jumpers, dressage equids, and leisure equids align with previous research (64, 65). Grouping into dressage, jumping and leisure equids in the present study allowed for exploration of differences in athletic management practices between competition equids and leisure equids. Additionally, no differences in distal phalanx morphology, within the different uses of equids are seen. This lack of variation contrasts with the different biomechanical demands of various disciplines reported in a previous study (50), suggesting that distal phalanx morphology may be less influenced by use than previously thought.

To understand the more pronounced effect of dorsoabaxial clips on distal phalanx shape and density in the present study compared to a single dorsal clip, it’s essential to consider equine hoof mechanism. Barefoot trimmers often argue against shoeing due to its interference with hoof biomechanics, as heel widening is limited even with horseshoes without clips (15). Dorsoabaxial clips exert greater pressure on the hoof and distal phalanx (14). During the stance phase of locomotion, the hoof undergoes significant deformation. The distal phalanx’s downward force causes the suspensory apparatus to pull the corresponding hoof wall section downwards up to 1.5 mm, most pronounced at the coronary band and decreasing distally (67), where clips are located. Based on the results of the present study, dorsoabaxial clips, typically positioned between the first and second nail, affect the distal phalanx despite one study suggesting less impact in this area compared to clips palmar to the second nail (2). The hoof narrows proximally and expands distally palmar to the widest transverse distance of the coronet and the distal margin of the hoof wall, resulting in an outward movement of the distal parts of the hoof wall (67). Simultaneously, the distal phalanx pushes the sole and frog into contact with the ground, causing the solar arch to flatten and the weight bearing edge to widen behind the broadest section of the hoof (67). The observed changes in bone density near the clip areas and the shape changes of the distal phalanx in the present study suggest potential biomechanical effects of this shoeing method. These findings are further corroborated when comparing the distal phalanges of shod and unshod equids. The influence of shoeing on distal phalanx shape is more pronounced between different shoeing types rather than between shod and unshod hooves. The shape differences observed in equids shod with two dorsoabaxial clips are likely attributable to the position of the two clips rather than the presence of a shoe itself. Furthermore, distal phalanges from equids shod with one dorsal clip exhibited greater similarity to distal phalanges from unshod equids than equids shod with two dorsoabaxial clips. A single dorsal clip is preferable because it does not interfere with the natural expansion of the heels, allowing for more normal hoof use (68, 69). This observation supports the hypothesis that the position of the clip(s) of horseshoes plays a more significant role in distal phalanx morphology than the presence of shoes. These findings are explained by previous research using finite element analysis, which demonstrated that higher pressure acts on the hoof in the area of dorsoabaxial clips compared to a dorsal clip (14), which may exert force on the distal phalanx during the stance phase.

The observed changes in distal phalanx density and shape can be explained by bone remodeling in response to altered load distribution (70). At birth, specific trabecular bone parameters of bones of Warmblood versus Shetland pony foals show that genetic and intrauterine developments are relevant to prepare them for the specific mechanical loading of getting up and moving very quickly after birth (71). With loading, bone is continuously adapted to its function based on Wolff’s law from the late 19th century. Bone adaptation continues to be a significant area of study in veterinary research (72), particularly in horses, the species most closely associated with locomotion. The changes in distal phalanx density and shape observed in the present study can be explained by bone remodeling in response to altered load distribution (70). Functional adaptation of the osseous tissues of the navicular bone of horses has also been described (73). Bone is a dynamic tissue comprising specialized cells such as osteoclasts and osteoblasts, which engage in complex interactions within basic multicellular units to drive the bone remodeling process (74). The balance between bone formation and resorption can be disturbed by various factors such as increasing age, estrogen deficiency, calcitriol deficiency, glucocorticoids (7577), and also increased pressure on the bone, as observed in our study. Additionally, increased pressure on bone leads to bone remodeling (74). This phenomenon is not limited to equines but is also observed in human medicine, for example when the phalanges in fingers change after prolonged wearing of tight rings creating localized pressure on the bone even though the soft tissues remain less changed (78). In cases of such chronic ring erosion injuries, persistent circumferential pressure leads to notable bone modifications of structure and density, which can be detected through radiographic imaging (78).

The crena marginalis solearis is an anatomical feature at the dorsal border of the solar margin of the distal phalanx, representing a normal anatomical variant with individual and breed-related differences (7981). Consistent with previous studies, we found no association between the presence of a crena and shoeing, especially the use of a dorsal clip (38, 82, 83), indicating that the presence of a crena is no contraindication for dorsal clips.

Our results highlight a significant relationship between the presence of a crena and a wide relative distal phalanx with and high width to length ratio, key parameters of distal phalanx shape variation. This suggests the crena may indicate fundamental anatomical differences, possibly reflecting breed specific or adaptive traits (84). The higher prevalence of the crena in warmbloods compared to ponies aligns with documented differences in the morphology of the distal phalanx (80). While the underlying causes, genetic, developmental, or biomechanical, remain unclear, absence or presence of the crena should be considered in morphometric and clinical distal phalanx assessments. Given its influence on principal shape dimensions, we suggest including the presence of the crena marginalis as a covariate in future studies of equine hoof and distal phalanx morphology.

From the results of the present study no conclusions should be drawn about the effects of clips on the distal phalanx of the hindlimbs. The hind hoof is usually narrower and has a different morphology (85) and is subject to different ground reaction forces, with forelimbs experiencing greater vertical and earlier horizontal loads than hindlimbs (86). These differences likely result in varying degrees of hoof deformation during stance, with less widening in the hindlimbs (87). Consequently, the hindlimbs may never reach the counterpressure from abaxial clips that are observed in the front limbs.

While the present study provides the first evidence of distal phalanx shape deformation associated with dorsoabaxial clips, limitations must be considered. Additional information on body mass, foot shape and quality, cold or hot shoeing, shoe specifications beyond the clips, and work history was not available, even though these factors may play an important role; therefore, they should be considered for future studies. Although there were no statistical differences in the density of the distal phalanx in the area of the dorsoabaxial clips, a trend was observed suggesting higher density in this region compared to equids shod with a dorsal clip. We hypothesize that the pressure exerted by the clips leads to bone remodeling and subsequently to an increase in bone density. This hypothesis is supported by previous research demonstrating that continuously applied pressure and cyclic pressure, such as that exerted by clips, can lead to bone resorption through osteoclastogenesis and osteoclast activity (88, 89) and adjacent bone density increases (90).

The present study did not measure the pressure exerted by dorsoabaxial or dorsal clips on the hoof wall and subsequently on the distal phalanx. However, considering the results of a finite element hoof model from a previous study, it has been shown that horseshoes with two dorsoabaxial clips can exert pressure values of 5.36–6.89 N/mm2 onto the medial and lateral hoof wall where dorsoabaxial clips are located (14). This study tested four different types of horseshoes on a hoof model with a total loading of 3,000 N onto the inside of the hoof wall (14). Dorsoabaxial clips were found to reduce outward displacements of the weight bearing rim of the hoof wall in their position by 25–50 μm compared to 100–275 μm wall displacement observed with horseshoes having no clips or one dorsal clip (14). A previous study confirmed that local pressure induced bone resorption results from mechanical forces like cyclic or continuous pressure, leading to the breakdown of bone (88). Continuous compressive pressure from 0.05 N/mm2 to 0.2 N/mm2 significantly inhibited the differentiation of mouse osteoblast like cells, possibly through prostaglandin E2 mediation, leading to an impact on bone formation and resorption (88). Pressure leading to bone resorption even without direct contact was shown as bone resorption was triggered through cyclically applied fluid pressure in alive rats (89). The tibiae of 50 rats went through maximum 0.1 N/mm2 and plateau levels of 0.05 N/mm2 intermittent fluid pressure and bone volume, bone volume fraction, and bone mineral density were measured using Microcomputer tomography (89). A correlation between maximum fluid pressure and fluid pressure plateau and bone volume fraction was seen. Bone resorption was measured as effect of the local fluid pressure (89). As the previous two studies have shown, relatively low pressures between 0.05 N/mm2 and 0.2 N/mm2 lead to bone density changes.

Findings from finite element analyses help explain the increased bone density in warmblood horses shod with dorsoabaxial clips and the distal phalanx shape changes observed in the present study. Hoof conformation is clearly related to the forces applied to the equine foot (61). It is important to emphasize that a relatively longer distal phalanx with an unchanged width, resulting in a lower width to length ratio, could potentially affect hoof biomechanics and stability, even when subjected to the same forces (91). In Thoroughbred racehorses hoof size, shape and balance are related to musculoskeletal injuries as suspensory apparatus failure and fractures of the third metacarpal bone. Musculoskeletal injuries were 0.62 times lower for a 5 mm increase in ground surface of the hoof (34). Thus, morphological distal phalanx change could potentially predispose equids to other conditions or injuries, a consideration that warrants further investigation.

The consistency of results between equids with known and unknown shoeing and barefoot history durations may indicate that actual durations did not differ largely. It is possible, that shoeing or barefoot status was similar over a much longer time period even in the horses, where a 12-month history was given, as the differences in shape of the distal phalanx documented in the present study are expected to require at least that long to be established, even if rapid changes in hoof biomechanics can be seen immediately after shoeing (11). However, further investigations are necessary to understand the temporal dynamics of distal phalanx morphology exposed to different forces.

The present study revealed notable differences in bone density and shape of the distal phalanges between male and female equids. Analysis of 97 Oxspring radiographs from male equids and 78 Oxspring radiographs from female equids demonstrated that female equids have denser distal phalanges medially and laterally compared to males, while male equids had longer middle phalanges. These findings align with previous research on sex related differences in equine bone density. For instance, a study on Lusitano foals found higher leptin levels in females, which negatively correlated with osteocalcin (92). Leptin has been shown to inhibit osteoclast differentiation in mouse cells and potentially act as a local inhibitor of bone resorption in vivo (93). This could explain the higher local bone densities observed in female equids in the present study, potentially due to reduced bone resorption. Additionally, research on Arabian horses has shown sex related differences in phalangeal measurements, with males having longer proximal, middle, and distal phalanges (94). The finding that distal phalanges in male equids are longer compared to females is also observed in the present study. How sex related density and shape changes affect the distal phalanx and shoeing requires further investigations.

5 Conclusion

The present study provides novel insights into potential effects of dorsoabaxial clips on the equine distal phalanx. The observed shape differences of the distal phalanx and the trend toward increased bone density in the area of dorsoabaxial clips suggest that these shoeing practices may have more profound effects on hoof biomechanics and bone remodeling than previously recognized. These findings also have important implications for equine medicine. The potential long-term effects of distal phalanx deformation on hoof health locomotion stability and overall equine performance warrant further investigation. Future studies may consider longitudinal designs to track changes over time associated with shoeing differences.

Data availability statement

The data that support the findings of this study are available from the corresponding author upon reasonable request. Requests to access these datasets should be directed to Lisa Henrietta Ennsmann, bGlzYS5oZW5yaWV0dGEuZW5uc21hbm5AdmV0bWVkdW5pLmFjLmF0.

Ethics statement

Ethical approval was not required for the studies involving animals in accordance with the local legislation and institutional requirements because this study did not require approval from an Ethics Committee or Institutional Review Board, as it utilized only data from electronic case files (radiographs, and data on the equids and their shoeing) for which owners had provided documented consent upon the equids’ arrival at the clinic. Informed consent was obtained from all animal owners. Written informed consent was obtained from the owners for the participation of their animals in this study.

Author contributions

LE: Investigation, Methodology, Data curation, Conceptualization, Validation, Visualization, Formal analysis, Writing – original draft. TL: Investigation, Supervision, Writing – review & editing, Conceptualization, Visualization, Data curation, Methodology, Validation.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2025.1598038/full#supplementary-material

References

1. O’Grady, SE, and Poupard, DA. Proper physiologic horseshoeing. Vet Clin North Am Equine Pract. (2003) 19:333–51. doi: 10.1016/S0749-0739(03)00020-8

Crossref Full Text | Google Scholar

2. Andrea, E, and Floyd, RAM. Equine podiatry. Bd. Section V: Farriery considerations Philadelphia PA, London: Elsevier Health Sciences (2007).

Google Scholar

3. Pollitt, CC. The anatomy and physiology of the suspensory apparatus of the distal phalanx. Vet Clin North Am Equine Pract. (2010) 26:29–49. doi: 10.1016/j.cveq.2010.01.005

PubMed Abstract | Crossref Full Text | Google Scholar

4. Riedesel, EA. Chapter 23 the equine phalanges In: Textbook of veterinary diagnostic radiology-e-book. Elsevier Health Sciences (2012). 429.

Google Scholar

5. Malone, SR, and Davies, HM. Changes in hoof shape during a seven-week period when horses were shod versus barefoot. Animals. (2019) 9:1017. doi: 10.3390/ani9121017

PubMed Abstract | Crossref Full Text | Google Scholar

6. Lindner, A. Applied equine nutrition. 1st Equine Nutrition Conference (Enuco), London, United Kingdom: Hannover, Germany, (2005).

Google Scholar

7. Back, W, and Clayton, HM. Equine locomotion. London, United Kingdom: Elsevier Health Sciences (2013).

Google Scholar

8. Panagiotopoulou, O, Rankin, JW, Gatesy, SM, and Hutchinson, JR. A preliminary case study of the effect of shoe-wearing on the biomechanics of a horse’s foot. PeerJ. (2016) 4:e2164. doi: 10.7717/peerj.2164

PubMed Abstract | Crossref Full Text | Google Scholar

9. Willemen, M, Savelberg, H, and Barneveld, A. The improvement of the gait quality of sound trotting warmblood horses by normal shoeing and its effect on the load on the lower forelimb. Livest Prod Sci. (1997) 52:145–53. doi: 10.1016/S0301-6226(97)00130-9

Crossref Full Text | Google Scholar

10. Huguet, EE, and Duberstein, KJ. Effects of steel and aluminum shoes on forelimb kinematics in stock-type horses as measured at the trot. J Equine Vet Sci. (2012) 32:262–7. doi: 10.1016/j.jevs.2011.09.069

Crossref Full Text | Google Scholar

11. Roepstorff, L, Johnston, C, and Drevemo, S. The effect of shoeing on kinetics and kinematics during the stance phase. Equine Vet J. (1999) 31:279–85. doi: 10.1111/j.2042-3306.1999.tb05235.x

PubMed Abstract | Crossref Full Text | Google Scholar

12. Oomen, A, Oosterlinck, M, Pille, F, Sonneveld, D, Gasthuys, F, and Back, W. Use of a pressure plate to analyse the toe–heel load redistribution underneath a normal shoe and a shoe with a wide toe in sound warmblood horses at the walk and trot. Res Vet Sci. (2012) 93:1026–31. doi: 10.1016/j.rvsc.2012.01.010

PubMed Abstract | Crossref Full Text | Google Scholar

13. Wilson, A, Seelig, T, Shield, R, and Silverman, B. The effect of foot imbalance on point of force application in the horse. Equine Vet J. (1998) 30:540–5. doi: 10.1111/j.2042-3306.1998.tb04531.x

PubMed Abstract | Crossref Full Text | Google Scholar

14. Hinterhofer, C, Stanek, C, and Haider, H. Finite element analysis (FEA) as a model to predict effects of farriery on the equine hoof. Equine Vet J. (2001) 33:58–62. doi: 10.1111/j.2042-3306.2001.tb05360.x

Crossref Full Text | Google Scholar

15. Hinterhofer, C, Weißbacher, N, Buchner, HH, Peham, C, and Stanek, C. Motion analysis of hoof wall, sole and frog under cyclic load in vitro: deformation of the equine hoof shod with regular horse shoe, straight bar shoe and bare hoof. Pferdeheilkd Equine Med. (2006) 22:314. doi: 10.21836/PEM20060311

Crossref Full Text | Google Scholar

16. Al-Agele, R, Paul, E, Taylor, S, Watson, C, Sturrock, C, Drakopoulos, M, et al. Physics of animal health: on the mechano-biology of hoof growth and form. J R Soc Interface. (2019) 16:20190214. doi: 10.1098/rsif.2019.0214

PubMed Abstract | Crossref Full Text | Google Scholar

17. Van Heel, M, Van Weeren, P, and Back, W. Shoeing sound warmblood horses with a rolled toe optimises hoof-unrollment and lowers peak loading during breakover. Equine Vet J. (2006) 38:258–62. doi: 10.2746/042516406776866471

PubMed Abstract | Crossref Full Text | Google Scholar

18. Turner, T. Shoeing principles for the management of navicular disease in horses. J Am Vet Med Assoc. (1986) 189:298–301. doi: 10.2460/javma.1986.189.03.298

PubMed Abstract | Crossref Full Text | Google Scholar

19. Eliashar, E, McGuigan, M, Rogers, K, and Wilson, A. A comparison of three horseshoeing styles on the kinetics of breakover in sound horses. Equine Vet J. (2002) 34:184–90. doi: 10.2746/042516402776767303

PubMed Abstract | Crossref Full Text | Google Scholar

20. Ruthe, H, Mueller, H, and Reinhard, F. The hoof, a textbook of shoeing. Fischer (1988).

Google Scholar

21. Dahl, VE, Singer, ER, Garcia, TC, Hawkins, DA, and Stover, SM. Hoof expansion, deformation, and surface strains vary with horseshoe nail positions. Animals. (2023) 13:1872. doi: 10.3390/ani13111872

PubMed Abstract | Crossref Full Text | Google Scholar

22. Gunkelman, M, Young, J, and Hammer, C. Influence of trimming and shoeing on hoof temperature and digital cushion thickness in mature horses. J Equine Vet Sci. (2019) 76:92. doi: 10.1016/j.jevs.2019.03.125

Crossref Full Text | Google Scholar

23. Clarke, B. Normal bone anatomy and physiology. Clin J Am Soc Nephrol. (2008) 3:S131–9. doi: 10.2215/CJN.04151206

Crossref Full Text | Google Scholar

24. Pettit, AR, Chang, MK, Hume, DA, and Raggatt, LJ. Osteal macrophages: a new twist on coupling during bone dynamics. Bone. (2008) 43:976–82. doi: 10.1016/j.bone.2008.08.128

PubMed Abstract | Crossref Full Text | Google Scholar

25. Milgrom, C, Finestone, A, Novack, V, Pereg, D, Goldich, Y, Kreiss, Y, et al. The effect of prophylactic treatment with risedronate on stress fracture incidence among infantry recruits. Bone. (2004) 35:418–24. doi: 10.1016/j.bone.2004.04.016

PubMed Abstract | Crossref Full Text | Google Scholar

26. Engiles, JB. Pathology of the distal phalanx in equine laminitis: more than just skin deep. Vet Clin Equine Pract. (2010) 26:155–65. doi: 10.1016/j.cveq.2009.12.001

PubMed Abstract | Crossref Full Text | Google Scholar

27. Dyson, S. Nonseptic osteitis of the distal phalanx and its palmar processes. Equine Vet Educ. (2011) 23:472–85. doi: 10.1111/j.2042-3292.2011.00261.x

Crossref Full Text | Google Scholar

28. Rendano, V. Radiographic interpretation. Pedal osteitis. California Veterinary Medical Association (CalVMA) (1979).

Google Scholar

29. Laverty, S, Stover, S, Belanger, D, O’Brien, T, Pool, R, Pascoe, J, et al. Radiographic, high detail radiographic, microangiographic and histological findings of the distal portion of the tarsus in weanling, young and adult horses. Equine Vet J. (1991) 23:413–21.

Google Scholar

30. Byfield, R, Miller, M, Xie, Y, Crosby, M, Schiltz, P, Johnson, PJ, et al. Equine life stage classification from photoplethysmography data by an explainable echo state network. Social Science Research Network (SSRN). Available at SSRN 4561261. (2023).

Google Scholar

31. Redden, RF. Radiographic imaging of the equine foot. Vet Clin Equine Pract. (2003) 19:379–92, vi. doi: 10.1016/S0749-0739(03)00026-9

PubMed Abstract | Crossref Full Text | Google Scholar

32. Redden, RF. Clinical and radiographic examination of the equine foot. American Association of Equine Practitioners (AAEP) (2003).

Google Scholar

33. Dyson, S. Radiological interpretation of the navicular bone. Equine Vet Educ. (2011) 23:73–87. doi: 10.1111/j.2042-3292.2010.00168.x

Crossref Full Text | Google Scholar

34. Kane, AJ, Stover, SM, Gardner, IA, Bock, KB, Case, JT, Johnson, BJ, et al. Hoof size, shape, and balance as possible risk factors for catastrophic musculoskeletal injury of thoroughbred racehorses. Am J Vet Res. (1998) 59:1545. doi: 10.2460/ajvr.1998.59.12.1545

PubMed Abstract | Crossref Full Text | Google Scholar

35. Dyson, SJ, Tranquille, CA, Collins, SN, Parkin, TDH, and Murray, RC. An investigation of the relationships between angles and shapes of the hoof capsule and the distal phalanx. Equine Vet J. (2011) 43:295–301. doi: 10.1111/j.2042-3306.2010.00162.x

PubMed Abstract | Crossref Full Text | Google Scholar

36. Dorner, C. Relationship between the distal phalanx angle and radiographic changes in the navicular bone of horses: a radiological study. Glob J Med Res. (2017) 17:7–13. doi: 10.17406/GJMRG

Crossref Full Text | Google Scholar

37. Cripps, PJ, and Eustace, RA. Radiological measurements from the feet of normal horses with relevance to laminitis. Equine Vet J. (1999) 31:427–32. doi: 10.1111/j.2042-3306.1999.tb03844.x

PubMed Abstract | Crossref Full Text | Google Scholar

38. Mullard, J, Ireland, J, and Dyson, S. Radiographic assessment of the ratio of the hoof wall distal phalanx distance to palmar length of the distal phalanx in 415 front feet of 279 horses. Equine Vet Educ. (2020) 32:2–10. doi: 10.1111/eve.13004

Crossref Full Text | Google Scholar

39. Aoun, R, Charles, I, DeRouen, A, Takawira, C, and Lopez, MJ. Shoe configuration effects on third phalanx and capsule motion of unaffected and laminitic equine hooves in-situ. PLoS One. (2023) 18:e0285475. doi: 10.1371/journal.pone.0285475

PubMed Abstract | Crossref Full Text | Google Scholar

40. Vassar, M, and Matthew, H. The retrospective chart review: important methodological considerations. J Educ Eval Health Prof. (2013) 10:10. doi: 10.3352/jeehp.2013.10.12

PubMed Abstract | Crossref Full Text | Google Scholar

41. Burd, M, Craig, J, and Craig, M. The palmar metric: a novel radiographic assessment of the equine distal phalanx. Open Vet J. (2014) 4:78–81. doi: 10.5455/OVJ.2014.v4.i2.p78

PubMed Abstract | Crossref Full Text | Google Scholar

42. Komosa, M, Purzyc, H, and Fraackowiak, H. Changes in navicular bone (os sesamoideum distale) shape in horses as a result of pathological alterations. Folia Biol (Krakow). (2013) 61:1–10. doi: 10.3409/fb61_1-2.01

PubMed Abstract | Crossref Full Text | Google Scholar

43. Engiles, J, Galantino-Homer, H, Boston, R, McDonald, D, Dishowitz, M, and Hankenson, K. Osteopathology in the equine distal phalanx associated with the development and progression of laminitis. Vet Pathol. (2015) 52:928–44. doi: 10.1177/0300985815588604

PubMed Abstract | Crossref Full Text | Google Scholar

44. Every, L, Hostnik, E, Hostnik, L, Yardley, J, Shore-Khirallah, A, Thompson, A, et al. Radiographic tracheal lumen to vertebral ratios in the normal American miniature horse. Equine Vet J. (2020) 52:428–34. doi: 10.1111/evj.13189

PubMed Abstract | Crossref Full Text | Google Scholar

45. Herthel, D, and Hood, DM. Clinical presentation, diagnosis, and prognosis of chronic laminitis. Vet Clin North Am Equine Pract. (1999) 15:375–94. doi: 10.1016/S0749-0739(17)30151-7

PubMed Abstract | Crossref Full Text | Google Scholar

46. Linford, RL, O’Brien, TR, and Trout, DR. Qualitative and morphometric radiographic findings in the distal phalanx and digital soft tissues of sound thoroughbred racehorses. Am J Vet Res. (1993) 54:38–51.

Google Scholar

47. Reiser, V, Reiser, A, and Licka, TF. Radiological features of arterial channels in the equine third phalanx measured using a novel customized software represent changes of laminitis. Am J Vet Res. (2024) 85:2–4. doi: 10.2460/ajvr.23.07.0150

PubMed Abstract | Crossref Full Text | Google Scholar

48. Esselman, AM, Johnson, SA, Frisbie, DD, Barrett, MF, Zhou, T, and Contino, EK. Substantial variability exists in the interpretation of survey radiographs among equine veterinarians. Equine Vet J. (2025) 57:169–82. doi: 10.1111/evj.14045

PubMed Abstract | Crossref Full Text | Google Scholar

49. Keppie, NJ, Rosenstein, DS, Holcombe, SJ, and Schott, HC II. Objective radiographic assesment abdominal sand accumulation in horses. Vet Radiol Ultrasound. (2008) 49:122–8. doi: 10.1111/j.1740-8261.2008.00337.x

PubMed Abstract | Crossref Full Text | Google Scholar

50. Zalig, V, Vengust, M, Blagus, R, Berner, D, Sandow, C, Hanna, A, et al. The difference in radiographic findings in the distal limbs of working Lipizzan horses, used for dressage or driving. Frontiers in veterinary. Science. (2024) 11:1393325. doi: 10.3389/fvets.2024.1393325

PubMed Abstract | Crossref Full Text | Google Scholar

51. Hennessey, E, DiFazio, M, Hennessey, R, and Cassel, N. Artificial intelligence in veterinary diagnostic imaging: a literature review. Vet Radiol Ultrasound. (2022) 63:851–70. doi: 10.1111/vru.13163

PubMed Abstract | Crossref Full Text | Google Scholar

52. Lacitignola, L, Imperante, A, Staffieri, F, De Siena, R, Luca, P, Muci, A, et al. Assessment of intra-and inter-observer measurement variability in a radiographic metacarpophalangeal joint osteophytosis scoring system for the horse. Vet Sci. (2020) 7:39. doi: 10.3390/vetsci7020039

PubMed Abstract | Crossref Full Text | Google Scholar

53. Arturo, G, and Schwarz, GS. Magnification of radiographic images in clinical roentgenology and its present-day limit. Radiology. (1952) 59:866–78. doi: 10.1148/59.6.866

PubMed Abstract | Crossref Full Text | Google Scholar

54. Carstens, A, Kirberger, RM, Grimbeek, RJ, Donnellan, CMB, and Saulez, MN. Radiographic quantification of tracheal dimensions of the normal thoroughbred horse. Vet Radiol Ultrasound. (2009) 50:492–501. doi: 10.1111/j.1740-8261.2009.01570.x

Crossref Full Text | Google Scholar

55. Larsen, CD, Wilkinson, TE, Roberts, GD, Guess, SC, Mattoon, JS, and Sanz, MG. Radiographic analysis of the dorsal hoof wall thickness in clinically normal draft horses. Am J Vet Res. (2024) 85:2. doi: 10.2460/ajvr.23.06.0145

Crossref Full Text | Google Scholar

56. Ulum, MF, and Noviana, D. Radiographic measurement of cardiac size in laboratory mice. ARSHI Vet Lett. (2018) 2:19–20. doi: 10.29244/avl.2.1.19-20

Crossref Full Text | Google Scholar

57. Vaccaro, C, Busetto, R, Bernardini, D, Anselmi, C, and Zotti, A. Accuracy and precision of computer-assisted analysis of bone density via conventional and digital radiography in relation to dual-energy x-ray absorptiometry. Am J Vet Res. (2012) 73:381–4. doi: 10.2460/ajvr.73.3.381

PubMed Abstract | Crossref Full Text | Google Scholar

58. Trouerbach, WT, Steen, W, Zwamborn, A, and Schouten, H. A study of the radiographic aluminum equivalent values of the mandible. Oral Surg Oral Med Oral Pathol. (1984) 58:610–6. doi: 10.1016/0030-4220(84)90088-4

PubMed Abstract | Crossref Full Text | Google Scholar

59. Secombe, C, Firth, E, Perkins, N, Bailey, D, and Anderson, B. The quantitative assessment of photodensity of the third carpal bone in the horse. N Z Vet J. (2004) 52:70–5. doi: 10.1080/00480169.2004.36407

PubMed Abstract | Crossref Full Text | Google Scholar

60. Strand, E, Braathen, LC, Hellsten, MC, Huse-Olsen, L, and Bjornsdottir, S. Radiographic closure time of appendicular growth plates in the Icelandic horse. Acta Vet Scand. (2007) 49:1–7. doi: 10.1186/1751-0147-49-19

PubMed Abstract | Crossref Full Text | Google Scholar

61. Dik, K, Avan, B, and Den Broek, J. Relationships of age and shape of the navicular bone to the development of navicular disease: a radiological study. Equine Vet J. (2001) 33:172–5. doi: 10.1111/j.2042-3306.2001.tb00596.x

Crossref Full Text | Google Scholar

62. Logan, AA, and Nielsen, BD. Training young horses: the science behind the benefits. Animals. (2021) 11:463. doi: 10.3390/ani11020463

PubMed Abstract | Crossref Full Text | Google Scholar

63. Clarke, EJ, Gillen, A, Turlo, A, and Peffers, MJ. An evaluation of current preventative measures used in equine practice to maintain distal forelimb functionality: a Mini review. Front Vet Sci. (2021) 8:758970. doi: 10.3389/fvets.2021.758970

PubMed Abstract | Crossref Full Text | Google Scholar

64. Tabor, G, Williams, J, and Elliott, A. A comparison of back flexibility in show jumping, dressage and leisure horses. Guelph, Ontario, Canada: International Society for Equitation Science (2019). 45 p.

Google Scholar

65. Brudňaková, M, Filipčík, R, Kopec, T, and Pešan, V. Analyses of the performance of show jumping and dressage horses on the world level. Social Science Research Network (SSRN) (2023) Available at SSRN 4415565.

Google Scholar

66. Rovere, G, Ducro, B, Van Arendonk, J, Norberg, E, and Madsen, P. Analysis of competition performance in dressage and show jumping of Dutch warmblood horses. J Anim Breed Genet. (2016) 133:503–12. doi: 10.1111/jbg.12221

Crossref Full Text | Google Scholar

67. Burn, J, and Brockington, C. Quantification of hoof deformation using optical motion capture. Equine Vet J. (2001) 33:50–3. doi: 10.1111/j.2042-3306.2001.tb05358.x

PubMed Abstract | Crossref Full Text | Google Scholar

68. Douglas, J, Mittal, C, Thomason, J, and Jofriet, J. The modulus of elasticity of equine hoof wall: implications for the mechanical function of the hoof. J Exp Biol. (1996) 199:1829–36. doi: 10.1242/jeb.199.8.1829

PubMed Abstract | Crossref Full Text | Google Scholar

69. Lancaster, LS, Bowker, RM, and Mauer, WA. Equine hoof wall tubule density and morphology. J Vet Med Sci. (2013) 75:773–8. doi: 10.1292/jvms.12-0399

PubMed Abstract | Crossref Full Text | Google Scholar

70. Price, J, Jackson, B, Eastell, R, Wilson, A, Russell, R, Lanyon, L, et al. The response of the skeleton to physical training: a biochemical study in horses. Bone. (1995) 17:221–7. doi: 10.1016/8756-3282(95)00221-X

PubMed Abstract | Crossref Full Text | Google Scholar

71. Gorissen, BMC, Wolschrijn, CF, van Vilsteren, AAM, van Rietbergen, B, and van Weeren, PR. Trabecular bone of precocials at birth; are they prepared to run for the wolf(f)? J Morphol. (2016) 277:948–56. doi: 10.1002/jmor.20548

PubMed Abstract | Crossref Full Text | Google Scholar

72. Johnson, KA. Wolff’s law continues to inspire orthopaedic research. Vet Comp Orthop Traumatol. (2014) 27:V–VI. doi: 10.3415/VCOT-13-12-0142

PubMed Abstract | Crossref Full Text | Google Scholar

73. Bentley, VA, Sample, SJ, Livesey, MA, Scollay, MC, Radtke, CL, Frank, JD, et al. Morphologic changes associated with functional adaptation of the navicular bone of horses. J Anat. (2007) 211:662–72. doi: 10.1111/j.1469-7580.2007.00800.x

PubMed Abstract | Crossref Full Text | Google Scholar

74. Soysa, NS, and Alles, N. Positive and negative regulators of osteoclast apoptosis. Bone Rep. (2019) 11:100225. doi: 10.1016/j.bonr.2019.100225

PubMed Abstract | Crossref Full Text | Google Scholar

75. Cenci, S, Weitzmann, MN, Roggia, C, Namba, N, Novack, D, Woodring, J, et al. Estrogen deficiency induces bone loss by enhancing T-cell production of TNF-α. J Clin Invest. (2000) 106:1229–37. doi: 10.1172/JCI11066

PubMed Abstract | Crossref Full Text | Google Scholar

76. Robling, AG, and Turner, CH. Mechanical signaling for bone modeling and remodeling. Crit Rev Eukaryot Gene Expr. (2009) 19:319–338. doi: 10.1615/critreveukargeneexpr.v19.i4.50

PubMed Abstract | Crossref Full Text | Google Scholar

77. Sims, NA, and Martin, TJ. Coupling the activities of bone formation and resorption: a multitude of signals within the basic multicellular unit. BoneKEy Rep. (2014) 3:3. doi: 10.1038/bonekey.2013.215

PubMed Abstract | Crossref Full Text | Google Scholar

78. Matcuk, GR, Learch, TJ, and Keesara, SR. Chronic circumferential periostitis of proximal phalanges related to tight fitting rings. Emerg Radiol. (2006) 13:89–93. doi: 10.1007/s10140-006-0511-y

PubMed Abstract | Crossref Full Text | Google Scholar

79. Singh, B, and Dyce, KM. Dyce, sack, and Wensing’s textbook of veterinary anatomy. Fifth ed. St. Louis, Missouri: Saunders (2018) Textbook of veterinary anatomy.

Google Scholar

80. Budras, KD. Anatomy of the horse. 5th ed. Hannover: Schlütersche (2009).

Google Scholar

81. Sisson, S, Getty, R, and Grossman, JD In: R Getty, editor. Sisson and Grossman’s the anatomy of the domestic animals. 5th ed. Philadelphia: Saunders (1975) Anatomy of the domestic animals

Google Scholar

82. Ross, M, and Dyson, S. Diagnosis and management of lameness in the horse. Elsevier Saunders (2011).

Google Scholar

83. O’Grady, SE, and Poupard, DA. Physiological horseshoeing: an overview. Equine Vet Educ. (2001) 13:330–4. doi: 10.1111/j.2042-3292.2001.tb00123.x

Crossref Full Text | Google Scholar

84. Fretz, P. The equine distal limb: an atlas of clinical anatomy and comparative imaging. Can Vet J. The Canadian veterinary journal (2002) 43.

Google Scholar

85. Stachurska, A, Kolstrung, R, Pieta, M, Silmanowicz, P, and Klimorowska, A. Differentiation between fore and hind hoof dimensions in the horse (Equus caballus). Arch Anim Breed. (2008) 51:531–40. doi: 10.5194/aab-51-531-2008

Crossref Full Text | Google Scholar

86. Dutto, DJ, Hoyt, DF, Cogger, EA, and Wickler, SJ. Ground reaction forces in horses trotting up an incline and on the level over a range of speeds. J Exp Biol. (2004) 207:3507–14. doi: 10.1242/jeb.01171

PubMed Abstract | Crossref Full Text | Google Scholar

87. Back, W, Schamhardt, HC, Hartman, W, and Barneveld, A. Kinematic differences between the distal portions of the forelimbs and hind limbs of horses at the trot. Am J Vet Res. (1995) 56:1522–8. doi: 10.2460/ajvr.1995.56.11.1522

PubMed Abstract | Crossref Full Text | Google Scholar

88. Imamura, K, Ozawa, H, Hiraide, T, Shibasaki, Y, Fukuhara, T, Takahashi, N, et al. Continuously applied compressive pressure induces bone resorption by a mechanism involving prostaglandin E2 synthesis. J Cell Physiol. (1990) 144:222–8. doi: 10.1002/jcp.1041440207

PubMed Abstract | Crossref Full Text | Google Scholar

89. Fahlgren, A, Bostrom, MP, Yang, X, Johansson, L, Edlund, U, Agholme, F, et al. Fluid pressure and flow as a cause of bone resorption. Acta Orthop. (2010) 81:508–16. doi: 10.3109/17453674.2010.504610

PubMed Abstract | Crossref Full Text | Google Scholar

90. Firth, EC. The response of bone, articular cartilage and tendon to exercise in the horse. J Anat. (2006) 208:513–26. doi: 10.1111/j.1469-7580.2006.00547.x

PubMed Abstract | Crossref Full Text | Google Scholar

91. Balch, OK, Butler, D, White, KL, and Metcalf, SL. Hoof balance and lameness: improper toe length, hoof angle, and mediolateral balance. Compend Contin Educ Vet. (1995) 17:1275–1283.

Google Scholar

92. Fradinho, MJ, Mateus, L, Bernardes, N, Bessa, RJ, Caldeira, RM, and Ferreira-Dias, G. Growth patterns, metabolic indicators and osteoarticular status in the Lusitano horse: a longitudinal study. PLoS One. (2019) 14:e0219900. doi: 10.1371/journal.pone.0219900

PubMed Abstract | Crossref Full Text | Google Scholar

93. Holloway, WR, Collier, FM, Aitken, CJ, Myers, DE, Hodge, JM, Malakellis, M, et al. Leptin inhibits osteoclast generation. J Bone Miner Res. (2002) 17:200–9. doi: 10.1359/jbmr.2002.17.2.200

PubMed Abstract | Crossref Full Text | Google Scholar

94. Gündemir, O, Szara, T, Pazvant, G, Erdikmen, DO, Duro, S, and Perez, W. Radiogrametric analysis of the thoracic limb phalanges in Arabian horses and thoroughbred horses. Animals. (2021) 11:2205. doi: 10.3390/ani11082205

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: horse, distal phalanx, radiology, horseshoe, clips

Citation: Ennsmann LH and Licka TF (2025) Association between radiographic equine distal phalanx characteristics and absence, presence and type of horseshoes. Front. Vet. Sci. 12:1598038. doi: 10.3389/fvets.2025.1598038

Received: 24 March 2025; Accepted: 02 July 2025;
Published: 25 July 2025.

Edited by:

Sarah Jane Hobbs, University of Central Lancashire, United Kingdom

Reviewed by:

Mustajab Hussain Mirza, Louisiana State University, United States
Sokol Duro, Agricultural University of Tirana, Albania
Irene Nocera, University of Pisa, Italy
Simon Curtis, University of Central Lancashire, United Kingdom

Copyright © 2025 Ennsmann and Licka. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lisa Henrietta Ennsmann, bGlzYS5oZW5yaWV0dGEuZW5uc21hbm5AdmV0bWVkdW5pLmFjLmF0; Theresia Franziska Licka, dGhlcmVzaWEubGlja2FAdmV0bWVkdW5pLmFjLmF0

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