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ORIGINAL RESEARCH article

Front. Public Health, 23 December 2021
Sec. Environmental health and Exposome

Factors Affecting the Aluminum, Arsenic, Cadmium and Lead Concentrations in the Knee Joint Structures

\nGuoyong LiGuoyong Li1Chunfeng XiongChunfeng Xiong2Wenhua XuWenhua Xu3Runhong MeiRunhong Mei1Tao Cheng
Tao Cheng4*Xuefeng Yu
Xuefeng Yu1*
  • 1Department of Orthopaedics, The Fourth Affiliated Hospital of Nanchang University, Nanchang, China
  • 2Department of Urology, Jiangxi Children's Hospital Affiliated to Nanchang University, Nanchang, China
  • 3Department of Orthopaedics, Yichun People's Hospital, Yichun, China
  • 4Department of Orthopaedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China

Background: Toxic elements, such as aluminum (Al), arsenic (As), cadmium (Cd), and lead (Pb), are persistent environmental pollutants that can cause adverse effects on the health of exposed individuals. Bone is one of the primary target organs of accumulation and potential damage from toxic elements.

Objectives: This study was performed to determine the Al, As, Cd, and Pb concentrations in the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage, tibial cancellous bone and infrapatellar fat pad. Furthermore, the aim of this study was to explore the relationships between toxic element concentrations and related factors such as gender, age, place of residence, hypertension and diabetes, and to determine the correlations among these toxic elements in knee joint structures.

Methods: The samples used this study were collected from 51 patients following total knee arthroplasty. The Al, As, Cd, and Pb concentrations were determined using inductively coupled plasma optic emission spectrometry.

Results: Significant differences were found in the Al, As, Cd, and Pb concentrations among the knee joint structures. Cd concentration in the tibial cancellous bone in women was significantly higher than in men. Pb concentration in the infrapatellar fat pad of urban patients was significantly higher as compared to rural patients. Al concentrations in the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus and tibial cartilage were significantly higher in patients living in urban areas than in rural areas. As concentration in the tibial cancellous bone of diabetic patients was significantly higher compared to non-diabetic patients. In addition, significant Spearman's positive correlations were found between Al and Pb in the knee joint structures.

Conclusion: The obtained results of the investigated toxic elements may serve as a basis for establishing the reference values of Al, As, Cd, and Pb in the knee joint structures. The results reported in the study provides novel data regarding the relationships between the toxic element concentrations and gender, age, place of residence, hypertension and diabetes in the studied structures of knee joint. Furthermore, new interactions among these toxic elements were noted.

Introduction

Toxic elements are worldwide environmental pollutants with various ill-health effects (1). Environmental and occupational exposure to toxic elements has become a major public health concern. Human beings are exposed to toxic elements from multiple sources, such as contaminated food, air, drinking water and soil, as well as occupational exposure, which are usually absorbed into the body through inhalation, dermal and ingestion routes (2, 3). These toxic elements interfere with homeostasis in the organism and pose serious threats to human health (4). We are challenged by an increasing necessity of monitoring not only environmental pollution but also the toxic element concentrations in human tissues (5). Due to the characteristics and long-term remodeling of bone, it may reflect chronic exposure to the toxic elements and serve as a basis for the indirect assessment on the degree of environmental pollution (58).

Al is integrated into the bone matrix with a half-life of 10–20 years (9, 10). Al deposition in bone inhibits bone mineralization by reducing the calcium, magnesium, and phosphorus levels (11). In addition, Al can decrease collagen synthesis, reduce bone formation and damage bone remodeling (12), which can lead to bone diseases, such as renal osteodystrophy (13) and osteomalacia (14). As has been related to the decreased osteoblast proliferation and increased osteoclasts multiplication (15), possibly due to the As-induced reduction in transcription factor expression such as bone morphogenetic protein-2 and osteocalcin. Such results lead to alterations of cortical and trabecular bone microarchitecture (16, 17) and reduce bone mineral density and trabecular bone volume (18). Clinical epidemiological trials have demonstrated the correlation between As poisoning and Paget's disease (19). Bone is one of the primary target organs of Cd toxicity in the body (20). The reduction of bone mineral density is closely associated with Cd pollution in the environment (21). Cd can directly affect bone-related cell activity, which accelerates bone resorption, inhibits bone formation, destroys bone microstructure, and eventually causes bone injury (20, 22). Long-term exposure to Cd can lead to bone metabolic diseases, such as itai-itai disease (23) and osteoporosis (20). Pb exhibits the high affinity for bone due to its ability to replace other divalent cations, such as calcium and magnesium ions in the body (24). Studies have demonstrated that Pb exposure is associated with decreased bone density, bone growth retardation, osteoporosis and osteoarthritis (25, 26). Oxidative stress is considered as one of the main factors in Pb-induced bone damages because of the production of reactive oxygen species induced by Pb exposure (27). In addition, Pb inhibits osteoblast activity and induces osteoblast apoptosis by controlling the Wnt signaling pathway (28).

To our knowledge, there is limited data on the As concentration in the knee joint and the available information concerning the Al, Cd, and Pb concentrations is insufficient (Table 1). Studies focusing on the Al, As, Cd, and Pb concentrations in joints were performed mainly in the Polish population (Table 1). The distributions of toxic elements in the environment differ across regions (42). Hence, this study was performed to determine the Al, As, Cd, and Pb concentrations in the knee joint in Chinese population. The aim of this study was to explore the relationships between the toxic element concentrations and biological factors, environmental factors and health status, and to examine the correlations among these toxic elements in the studied structures of knee joint.

TABLE 1
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Table 1. Mean concentrations of Al, As, Cd, and Pb in the cartilage, cancellous bone, anterior cruciate ligament, meniscus and infrapatellar fat pad in patients from various countries, based on literature data.

Materials and Methods

Subject Selection

This study was conducted with the approval of Ethics Committee of Shanghai Sixth People's Hospital No. 2021-KY-022(k). A total of 51 participants aged 54–81 years were involved in this study. Thirty-five cases were women aged 54–81 years and the remaining 16 cases were men aged 56–79 years. The indication of total knee arthroplasty was the knee degenerative disease with severe dysfunction and chronic pain. The patients signed the written consent form to participate in this study and were surveyed regarding their demographics and health status, with special emphasis on factors that possibly affected the toxic element concentrations in the knee joint. Participants were grouped according to age, gender, place of residence, hypertension and diabetes. All samples, including 51 samples of femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage, tibial cancellous bone and infrapatellar fat pad, were obtained from 51 patients following total knee arthroplasty. The samples were marked with codes and stored in modified polyethylene containers in a refrigerator at a temperature of −22°C.

Mineralization and ICP-OES Analysis

The knee samples were prepared according to the study of Kuo et al. (37) with some modifications. The research materials were immersed into acetone for 1 h to remove the lipid and were cleaned by ultrapure water (Integral V, milliQ, USA). Subsequently, the sample was dried in an incubator at 105°C until no further weight reduction occurred. Tissue samples with a known mass (0.2 g) were mineralized using 5 ml of concentrated 65% nitric acid (Suprapure Merck, Darmstadt, Germany) and 1 ml of 30% hydrogen peroxide (Baker Analyzed, Phillipsburg, NJ, USA) in a microwave digestion system (ETHOS One, Milestone, Italy). Mineralization was a two-stage procedure. The first stage lasted 10 min at 140°C, whereas the second stage was 30 min at 180°C. The post-mineralization solution was diluted to the milliliter mark with ultrapure water.

The determination of Al, As, Cd, and Pb concentrations in mineralized samples were performed adopting inductively coupled plasma optic emission spectrometry (ICP-OES, Agilent 5100, USA) (43). The operating parameters were as follows: RF power, 1.0 kW; plasma flow, 12 L/min; auxiliary flow, 1.0 L/min; pump rate, 12 rpm; emission lines of Al: λ = 396.152 nm, As: λ = 188.980 nm, Cd: λ = 226.502 nm, Pb: λ = 220.353 nm. The calibration curve method was adopted. The standard solutions of 0.1 mg/ml (Inorganic Ventures, USA) as well as ultrapure water were applied. The results correspond to the average concentrations obtained for all analytical lines of the toxic elements, with standard deviation of not higher than 1.5%. The National Institute of Standards and Technology-Standard Reference Material (NIST-SRM) 1486 bone meal was used to validate the accuracy of the analytical procedure. The concentration values of standard reference materials were provided by the manufacturers and our measured values were presented in Table 2.

TABLE 2
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Table 2. Analysis of NIST-SRM 1486 (National Institute of Standards and Technology-Standard Reference Material) bone meal (mg/kg dry weight).

Statistical Analysis

The statistical analysis was performed with IBM SPSS Statistics, version 26.0 (IBM Corp., Armonk, NY). The normal distribution of data was not confirmed after applying the Shapiro-Wilk test. Statistical analysis utilized non-parametric tests. Intergroup comparisons were performed using the Mann-Whitney U test. The Kruskal-Wallis test was used for the comparisons of multiple groups. Moreover, the Spearman's rank correlations between these toxic elements occurring in the knee joint structures were determined. The differences were considered statistically significant at p < 0.05.

Results

The concentrations of the toxic elements in almost all of the analyzed structures of knee joint were in descending order as follows: Al>As>Pb>Cd (Table 3). Al concentration was the highest in the infrapatellar fat pad. As concentration in the meniscus was by far higher than in the femoral cancellous bone (Table 3). Significant differences were observed in the concentrations of Al, As, Cd, and Pb among the knee joint structures (Table 3).

TABLE 3
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Table 3. Analysis of the Al, As, Cd, and Pb concentrations among the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage, tibial cancellous bone and infrapatellar fat pad.

Gender and Age

As for the gender, only Cd concentration in the tibial cancellous bone, approximately 60% higher in women than in men, was statistically significantly different. As concentrations in the knee joint structures were higher in men than in women, whereas Pb concentrations were reverse. Despite the noticeable differences in the concentrations of Al, As, and Pb in the studied samples, they were not statistically significant (Table 4). No significant differences were found in the Al, As, Cd, and Pb concentrations between the group up to 65 years and over 65 years.

TABLE 4
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Table 4. Analysis of the Al, As, Cd, and Pb concentrations in the structures of knee joint in men and in women.

Place of Residence

When comparing these toxic element concentrations in the knee joint structures between patients living in town and in village, Al concentrations in the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage in patients living in town were statistically significantly higher than in village at 37.41 vs. 24.93, 37.55 vs. 25.17, 36.34 vs. 24.80, 22.44 vs. 13.60, and 37.95 vs. 25.78 mg/kg dw, respectively (Figure 1). Pb concentration in the infrapatellar fat pad in patients living in town was statistically significantly higher compared to those residing in village at 0.79 vs. 0.47 mg/kg dw, respectively (Figure 1). Cd concentrations in the knee joint structures were higher in patients living in village than in town. Though the observable differences in Cd concentrations in the studied samples, they were not statistically significant (Figure 1).

FIGURE 1
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Figure 1. The comparison of the aluminum, arsenic, cadmium, and lead concentrations with residents living in town and village. FCB, femoral cancellous bone; FC, femoral cartilage; ACL, anterior cruciate ligament; M, meniscus; TC, tibial cartilage; TCB, tibial cancellous bone; IFP, infrapatellar fat pad; mg/kg dw, mg/kg dry weight; *p < 0.05; **p <0.01. (A) Comparison of aluminum concentration between urban and rural patients. Al concentrations in the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage in patients living in town were statistically significantly higher than in village at 37.41 vs. 24.93, 37.55 vs. 25.17, 36.34 vs. 24.80, 22.44 vs. 13.60, and 37.95 vs. 25.78 mg/kg dw, respectively. (B) Comparison of arsenic concentration between urban and rural patients. (C) Comparison of cadmium concentration between urban and rural patients. (D) Comparison of lead concentration between urban and rural patients. Pb concentration in the infrapatellar fat pad in patients living in town was statistically significantly higher compared to those residing in village at 0.79 vs. 0.47 mg/kg dw, respectively.

Hypertension and Diabetes

The comparisons of these toxic element concentrations in the knee joint structures indicated no significant differences between patients with hypertension (n = 20) and with normal blood pressure (n = 31). Al and Cd concentrations were higher in normotensive participants than in hypertensive subjects. Taking into consideration diabetes, only As concentration in the tibial cancellous bone had statistically significant difference (U = 372, p = 0.035), approximately 41% higher in diabetics than in non-diabetics at 4.27 and 3.03 mg/kg dw, respectively. No significant differences in the concentrations of Al, Cd, and Pb in the knee joint structures between diabetic patients and non-diabetic patients were found.

Spearman's Correlation Coefficient

Statistically significant Spearman's positive correlation coefficients were observed between Al and Pb in the knee joint structures (Table 5).

TABLE 5
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Table 5. Spearman's correlation coefficients between Al and Pb in the analyzed structures of knee joint.

Discussion

The accumulation and retention of toxic elements may have adverse effects on the health by replacing other elements necessary for normal metabolism and interfering with homeostasis in the organism (8). Joint damage caused by the toxic elements may occur after many years of exposure or may be sudden. It is becoming increasingly urgent to assess the risk of joint tissue exposed to toxic elements from environmental pollution (31). Due to slow remodeling and low metabolic rate, knee joint structures, including meniscus and anterior cruciate ligament, can serve as good biomarkers for long-term toxic element accumulation resulting from environmental or occupational exposure (7, 44).

In this study, these toxic element concentrations in almost all of the knee joint structures can be arranged in the following ascending series: Cd <Pb <As <Al (Table 3). Al concentration was the highest in the south part of Poland (35) and the lowest in Kaluga Region, Russia (7). Some authors reported that Cd concentration in the cancellous bone usually varied from 0.014 mg/kg dw to 0.94 mg/kg dw (Table 1). Cd concentration in this study was lower or higher than their results (3, 5, 7, 29, 31, 34, 36, 38, 39). The highest Cd concentration was observed in patients inhabiting in urban areas of the Upper Silesian Industrial Zone, Poland (29), while the lowest was noted in the Kragujevac region, Serbian (3). Various outcomes were found in the studies about the residents from the different counties, demonstrating that the levels of toxic elements were related to the geographic areas. When compared with the concentrations of ribs, Al, Cd, and Pb concentrations in the tibial cancellous bone are higher in this study (7). According to the study by Stojsavljević et al. (3), the femoral head shows higher As concentration and lower concentrations of Cd and Pb as compared to this study. These findings indicate that the bone sites may differ in the content of toxic elements.

Interactions between toxic elements can disturb the homeostasis in the organisms, which can cause their toxic effects (33). Lanocha-Arendarczyk et al. (38) found significant positive correlation between Pb and Cd in the tibial plateau, which was consistent with the study conducted by Brodziak-Dopierala et al. (44). This study also observed the positive correlations between Cd and Pb in the knee joint structures without significant difference. Based on the conducted studies, significant positive correlation between Pb and Al in the knee joint structures was found. Positive quantitative correlations between Pb and Cd, as well as Pb and Al in the knee joint structures probably arise from a common environmental origin of the elements (45).

Some studies have indicated that the toxic element concentrations in the joint are influenced by gender (8, 38). Babuśka-Roczniak et al. (35) indicated that women had more Al concentrations in the tibial cancellous bone and meniscus than men. Nevertheless, our study found higher Al concentrations in the tibial cancellous bone and meniscus of men compared to women. Roczniak et al. (39) noticed that Cd concentration in the tibial cancellous bone in women was lower than in men (0.015 vs. 0.019 mg/kg dw), which was similar to the study by Lanocha-Arendarczyk et al. (38). However, we observed significantly higher Cd concentration in tibial cancellous bone of women as compared to men. The tendency of a greater Cd accumulation in women was often cited in the literature (29, 46), which can be due to the promotion of gastrointestinal absorption of Cd under low Fe stores (47). This finding may be the primary reason why itai-itai disease mainly influences women (44). Kosik-Bogacka et al. (33) noticed that Pb concentrations in the anterior cruciate ligament, meniscus and cartilage were higher in men than in women, while significant difference of Pb concentration between men and women only existed in meniscus. Roczniak et al. (40) noted significantly higher Pb concentrations in the femur, tibia and meniscus of men (3.22, 3.99, and 0.53 mg/kg dw, respectively) compared to women (2.41, 2.16, and 0.24 mg/kg dw, respectively). However, this study found higher Pb concentrations in the knee joint structures of women as compared to men. This finding may be because the toxic element concentrations in the female body are affected by hormonal changes occurring during menstruation, pregnancy or menopause (33, 48). Low Fe concentration in women will promote the Cd absorption in the gastrointestinal tract (47), and a synergistic correlation between Cd and Pb is observed (45). Hence, the concentrations of Cd and Pb in the body are generally higher in women than in men (39).

Age is associated with the occurrence and deposition of toxic elements in bone (35). Some toxic elements may increase with age in bone (7, 37). Zaichick et al. (7) demonstrated that the concentrations of Al, Pb, and Cd in the ribs in the group over 35 years old were higher than in the group up to 35 years old, but no significant differences between the two age groups were found. Taking into account Cd, Chang et al. (49) indicated that Cd concentration in bone increased with age. Nevertheless, Cd concentration between the two age groups was nearly at the same level in this study, thereby confirming the result of Roczniak et al. (39). It is suggested that Cd storage in the human body is constantly exchanged and no long-term accumulation is present (39). Kosik-Bogacka et al. (33) noted that Pb concentration in the cartilage was positively correlated with increasing age, which was similar to the studies by Jurkiewicz et al. (32) and Brodziak-Dopierała et al. (30). Zaneta et al. (41) observed no significant difference in Pb concentration in the infrapatellar fat pad between the groups aged 56–74 and 75–87 years. We also found no significant difference in Pb concentration in the knee joint structures between the group up to 65 years and over 65 years. These findings mean that Pb concentration in bone remains at a stable level after adulthood, which is of great significance to bone metabolism and human health (49).

The differences in the toxic element concentrations between urban and rural residents can reflect the degree of environmental pollution (50). Based on our conducted studies, Pb concentration in the infrapatellar fat pad in town was significantly higher compared to village. However, Zaneta et al. (41) indicated that Pb concentration in the infrapatellar fat pad was higher in rural areas than in urban areas without significant difference. The differences between the obtained values might result from the size and diversity of the studied samples. Pb isotope compositions show that Pb pollution is caused by incinerator ash, gasoline Pb and building materials, indicating that the atmospheric deposition is the main source. Pb pollution may be more serious in urban areas than in rural areas (51). This finding is similar to the results of this study.

Toxic elements are considered as risk factors for cardiovascular disease (52, 53). Zhang et al. (52) indicated that Al could induce hypertension, which may be caused by the dysfunction of erythrocyte membrane after acute or chronic Al exposure. Schmidt et al. (54) found the positive association between circulating plasma Al levels and hypertension. Abhyankar et al. (55) noticed that As resulted in hypertension through oxidative stress and nitric oxide inhibition. Hall et al. (56) observed a significant positive correlation between As concentration in the blood and the prevalence of hypertension. Da Cunha Martins et al. (57) demonstrated that Cd could increase the risk of hypertension through sodium retention and volume overload due to the renal tubules injuries caused by Cd. Miao et al. (58) found a positive correlation between blood Pb level and hypertension. Nevertheless, no significant differences in the effect of hypertension on the concentrations of Al, As, Pb, and Cd were observed in this study. Kosik-Bogacka et al. (33) also found no significant impact of hypertension on Pb concentration in the knee joint.

Strengths of the Study

To the best of our knowledge, this study is the first comprehensive determination of the Al, As, Cd, and Pd concentrations in the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage, tibial cancellous bone and infrapatellar fat pad simultaneously, which can provide a basis for the establishment of reference values of toxic elements in the knee joint structures and is helpful to the assessment of environmental pollution caused by toxic elements. Additionally, the relationships between relevant factors such as gender, age, place of residence, hypertension, diabetes and the toxic elements, which have guiding significance for the prevention and control of adverse health caused by toxic elements, have been demonstrated in this study, thereby improving public health.

Limitations of the Study

This study has several limitations. First, 51 patients participated in this study. Such an insufficient sample size can preliminarily explore the relationships between the toxic element concentrations and age, gender, place of residence, hypertension and diabetes, and support the conclusion of this study in the knee joint structures. In the follow-up research, we will collect more samples to investigate the influence of relevant factors on the toxic element concentrations in the knee joint structures, thereby resulting in more significant meaningful conclusions. Second, occupational exposure is one of the sources of toxic element accumulation. The utilization of these toxic elements in various industries, such as color pigments and alloys, will lead to occupational exposure (59). However, no qualified samples were collected in this study because of the limited number of patients with occupational exposure to toxic elements. Hence, this study does not involve occupational exposure. In the future, we will continue to collect samples of patients with a history of occupational exposure to toxic elements. Finally, this study explored the relationships between Al, As, Cd, and Pb concentrations and relevant factors such as age, gender, place of residence, hypertension and diabetes. However, other factors also affect the accumulation of toxic elements. Thus, the relationships between these toxic element accumulation and related factors such as food, drinking water, air, alcohol and tobacco should further establish, and the pollution data in the studied regions must be mastered to find more influencing factors in the follow-up studies.

Conclusion

The obtained results of the investigated toxic elements may serve as a basis for establishing reference values of Al, As, Cd, and Pb for the femoral cancellous bone, femoral cartilage, anterior cruciate ligament, meniscus, tibial cartilage, tibial cancellous bone and infrapatellar fat pad of patients with knee degenerative diseases. Analysis of the relationships between relevant factors and the toxic elements in the knee joint demonstrated the effect of gender, age, place of residence, hypertension and diabetes. Furthermore, the correlations between Al and Pb were found. These findings have guiding significance for the prevention and control of adverse health caused by toxic elements, thereby improving public health.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by the Ethics Committee of the Sixth People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, China. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author Contributions

XY, TC, and GL designed the research and conducted the experiments. CX, RM, and WX analyzed the data and drafted the manuscript. All authors contributed to the article and approved the submitted version.

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.

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.

References

1. Briggs D. Environmental pollution and the global burden of disease. Br Med Bull. (2003) 68:1–24. doi: 10.1093/bmb/ldg019

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Järup L. Hazards of heavy metal contamination. Br Med Bull. (2003) 68:167–82. doi: 10.1093/bmb/ldg032

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Stojsavljević A, Škrivanj S, Trifković J, Djoković N, Trifunović SR, Borković-Mitić S, et al. The content of toxic and essential elements in trabecular and cortical femoral neck: a correlation with whole blood samples. Environ Sci Pollut Res Int. (2019) 26:16577–87. doi: 10.1007/s11356-019-04796-w

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Zioła-Frankowska A, Kubaszewski Ł, Dabrowski M, Kowalski A, Rogala P, Strzyzewski W, et al. The content of the 14 metals in cancellous and cortical bone of the hip joint affected by osteoarthritis. BioMed research international. (2015) 2015:815648. doi: 10.1155/2015/815648

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Lanocha N, Kalisińska E, Kosik-Bogacka D, Budis H, Sokołowski S, Bohatyrewicz A. Comparison of concentrations of lead and cadmium in various parts of the femur head in patients after arthroplasty of the hip joint in Northwest Poland. BES. (2012) 25:577–82. doi: 10.3967/0895-3988.2012.05.012

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Kot K, Kosik-Bogacka D, Zietek P, Karaczun M, Ciosek Z, Łanocha-Arendarczyk N. Impact of varied factors on iron, nickel, molybdenum and vanadium concentrations in the knee joint. Int J Environ Res Public Health. (2020) 17:813. doi: 10.3390/ijerph17030813

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Zaichick S, Zaichick V, Karandashev VK, Moskvina IR. The effect of age and gender on 59 trace-element contents in human rib bone investigated by inductively coupled plasma mass spectrometry. Biol Trace Elem Res. (2011) 143:41–57. doi: 10.1007/s12011-010-8837-4

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Kosik-Bogacka DI, Lanocha-Arendarczyk N, Kot K, Ciosek Z, Zietek P, Karaczun M, et al. Effects of biological factors and health condition on mercury and selenium concentrations in the cartilage, meniscus and anterior cruciate ligament. J Trace Elem Med Biol. (2017) 44:201–8. doi: 10.1016/j.jtemb.2017.08.008

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Chappard D, Mabilleau G, Moukoko D, Henric N, Steiger V, Le Nay P, et al. Aluminum and iron can be deposited in the calcified matrix of bone exostoses. J Inorg Biochem. (2015) 152:174–9. doi: 10.1016/j.jinorgbio.2015.09.008

PubMed Abstract | CrossRef Full Text | Google Scholar

10. VanDuyn N, Settivari R, LeVora J, Zhou S, Unrine J, Nass R. The metal transporter SMF-3/DMT-1 mediates aluminum-induced dopamine neuron degeneration. J Neurochem. (2013) 124:147–57. doi: 10.1111/jnc.12072

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Li X, Hu C, Zhu Y, Sun H, Li Y, Zhang Z. Effects of aluminum exposure on bone mineral density, mineral, and trace elements in rats. Biol Trace Elem Res. (2011) 143:378–85. doi: 10.1007/s12011-010-8861-4

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Sun X, Wang H, Huang W, Yu H, Shen T, Song M, et al. Inhibition of bone formation in rats by aluminum exposure via Wnt/β-catenin pathway. Chemosphere. (2017) 176:1–7. doi: 10.1016/j.chemosphere.2017.02.086

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Crisponi G, Fanni D, Gerosa C, Nemolato S, Nurchi VM, Crespo-Alonso M, et al. The meaning of aluminium exposure on human health and aluminium-related diseases. Biomol Concepts. (2013) 4:77–87. doi: 10.1515/bmc-2012-0045

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Chappard D, Bizot P, Mabilleau G, Hubert L. Aluminum and bone: review of new clinical circumstances associated with Al(3+) deposition in the calcified matrix of bone. Morphologie. (2016) 100:95–105. doi: 10.1016/j.morpho.2015.12.001

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Gaffney-Stomberg E. The impact of trace minerals on bone metabolism. Biol Trace Elem Res. (2019) 188:26–34. doi: 10.1007/s12011-018-1583-8

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Wu CT, Lu TY, Chan DC, Tsai KS, Yang RS, Liu SH. Effects of arsenic on osteoblast differentiation in vitro and on bone mineral density and microstructure in rats. Environ Health Perspect. (2014) 122:559–65. doi: 10.1289/ehp.1307832

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Galvez-Fernandez M, Grau-Perez M, Garcia-Barrera T, Ramirez-Acosta S, Gomez-Ariza JL, Perez-Gomez B, et al. Arsenic, cadmium, and selenium exposures and bone mineral density-related endpoints: the HORTEGA study. Free Radic Biol Med. (2021) 162:392–400. doi: 10.1016/j.freeradbiomed.2020.10.318

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Hu YC, Cheng HL, Hsieh BS, Huang LW, Huang TC, Chang KL. Arsenic trioxide affects bone remodeling by effects on osteoblast differentiation and function. Bone. (2012) 50:1406–15. doi: 10.1016/j.bone.2012.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Lever JH. Paget's disease of bone in Lancashire and arsenic pesticide in cotton mill wastewater: a speculative hypothesis. Bone. (2002) 31:434–6. doi: 10.1016/S8756-3282(02)00833-5

PubMed Abstract | CrossRef Full Text | Google Scholar

20. He S, Zhuo L, Cao Y, Liu G, Zhao H, Song R, et al. Effect of cadmium on osteoclast differentiation during bone injury in female mice. Environ Toxicol. (2020) 35:487–94. doi: 10.1002/tox.22884

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Xie D, Sheng Z. Low-Level Cadmium Exposure and Bone Health. J Bone Miner Res. (2017) 32:419. doi: 10.1002/jbmr.3049

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Wallin M, Barregard L, Sallsten G, Lundh T, Sundh D, Lorentzon M, et al. Low-level cadmium exposure is associated with decreased cortical thickness, cortical area and trabecular bone volume fraction in elderly men: the MrOS Sweden study. Bone. (2021) 143:115768. doi: 10.1016/j.bone.2020.115768

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Bhattacharyya MH. Cadmium osteotoxicity in experimental animals: mechanisms and relationship to human exposures. Toxicol Appl Pharmacol. (2009) 238:258–65. doi: 10.1016/j.taap.2009.05.015

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Millán J, Mateo R, Taggart MA, López-Bao JV, Viota M, Monsalve L, et al. Levels of heavy metals and metalloids in critically endangered Iberian lynx and other wild carnivores from Southern Spain. Sci Total Environ. (2008) 399:193–201. doi: 10.1016/j.scitotenv.2008.03.038

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Sheng Z, Wang S, Zhang X, Li X, Li B, Zhang Z. Long-term exposure to low-dose lead induced deterioration in bone microstructure of male mice. Biol Trace Elem Res. (2020) 195:491–8. doi: 10.1007/s12011-019-01864-7

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Potula V, Henderson A, Kaye W. Calcitropic hormones, bone turnover, and lead exposure among female smelter workers. Arch Environ Occup Health. (2005) 60:195–204. doi: 10.3200/AEOH.60.4.195-204

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Abdelhamid FM, Mahgoub HA, Ateya AI. Ameliorative effect of curcumin against lead acetate-induced hemato-biochemical alterations, hepatotoxicity, and testicular oxidative damage in rats. Environ Sci Pollut Res Int. (2020) 27:10950–65. doi: 10.1007/s11356-020-07718-3

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Ma Y, Fu D, Liu Z. Effect of lead on apoptosis in cultured rat primary osteoblasts. Toxicol Ind Health. (2012) 28:136–46. doi: 10.1177/0748233711407956

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Brodziak-Dopierała B, Kwapuliński J, Sobczyk K, Wiechuła D. Analysis of the content of cadmium and zinc in parts of the human hip joint. Biol Trace Elem Res. (2015) 163:73–80. doi: 10.1007/s12011-014-0168-4

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Brodziak-Dopierała B, Kowol J, Kwapuliński J, Kusz D, Cieliński Ł. Lead and calcium content in the human hip joint. Biol Trace Elem Res. (2011) 144:6–16. doi: 10.1007/s12011-011-9014-0

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Brodziak-Dopierala B, Kwapulinski J, Gajda Z, Toborek J, Bogunia M. Changes of heavy metal concentrations in cross-sections of human femur head. Biol Trace Elem Res. (2006) 114:107–14. doi: 10.1385/BTER:114:1:107

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Jurkiewicz A, Wiechuła D, Nowak R, Loska K. Lead content in the femoral heads of inhabitants of Silesia (Poland). J Trace Elem Med Biol. (2005) 19:165–70. doi: 10.1016/j.jtemb.2005.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Kosik-Bogacka DI, Lanocha-Arendarczyk N, Kot K, Zietek P, Karaczun M, Prokopowicz A, et al. Calcium, magnesium, zinc and lead concentrations in the structures forming knee joint in patients with osteoarthritis? J Trace Elem Med Biol. (2018) 50:409–14. doi: 10.1016/j.jtemb.2018.08.007

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Lanocha N, Kalisinska E, Kosik-Bogacka DI, Budis H, Sokolowski S, Bohatyrewicz A, et al. The effect of environmental factors on concentration of trace elements in hip joint bones of patients after hip replacement surgery. Ann Agric Environ Med. (2013) 20:487–93. doi: 10.1016/j.jtemb.2011.11.006

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Babuśka-Roczniak M, Brodziak-Dopierała B, Mitko K, Cipora E, Roczniak W. Concentration of selected elements in the tissues of the knee joint. Biomed Environ Sci. (2020) 33:807–11. doi: 10.5772/intechopen.95418

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Jurkiewicz A, Wiechuła D, Nowak R, Gazdzik T, Loska K. Metal content in femoral head spongious bone of people living in regions of different degrees of environmental pollution in Southern and Middle Poland. Ecotoxicol Environ Saf. (2004) 59:95–101. doi: 10.1016/j.ecoenv.2004.01.002

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Kuo HW, Kuo SM, Chou CH, Lee TC. Determination of 14 elements in Taiwanese bones. Sci Total Environ. (2000) 255:45–54. doi: 10.1016/S0048-9697(00)00448-4

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Lanocha-Arendarczyk N, Kosik-Bogacka DI, Prokopowicz A, Kalisinska E, Sokolowski S, Karaczun M, et al. The effect of risk factors on the levels of chemical elements in the Tibial Plateau of patients with osteoarthritis following knee surgery. Biomed Res Int. (2015) 2015:650282. doi: 10.1155/2015/650282

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Roczniak W, Brodziak-Dopierała B, Cipora E, Jakóbik-Kolon A, Kluczka J, Babuśka-Roczniak M. Factors that affect the content of cadmium, nickel, copper and zinc in tissues of the knee joint. Biol Trace Elem Res. (2017) 178:201–9. doi: 10.1007/s12011-016-0927-5

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Roczniak W, Brodziak-Dopierała B, Cipora E, Mitko K, Jakóbik-Kolon A, Konieczny M, et al. The content of structural and trace elements in the knee joint tissues. Int J Environ Res Public Health. (2017) 14. doi: 10.3390/ijerph14121441

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Żaneta C, Danuta KB, Natalia Ł A, Karolina K, Maciej K, Paweł Z, et al. Concentration of selected elements in the infrapatellar fat pad of patients with a history of total knee arthroplasty. Int J Environ Res Public Health. (2019) 16. doi: 10.3390/ijerph16040525

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Rembert N, He K, Judd SE, McClure LA. The geographic distribution of trace elements in the environment: the REGARDS study. Environ Monit Assess. (2017) 189:84. doi: 10.1007/s10661-016-5733-1

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Donati GL, Amais RS, Williams CB. Recent advances in inductively coupled plasma optical emission spectrometry. J Anal At Spectrom. (2017) 32:1283–96. doi: 10.1039/C7JA00103G

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Brodziak-Dopierala B, Kwapulinski J, Kusz D, Gajda Z, Sobczyk K. Interactions between concentrations of chemical elements in human femoral heads. Arch Environ Contam Toxicol. (2009) 57:203–10. doi: 10.1007/s00244-008-9228-0

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Długaszek M. Studies on relationships between essential and toxic elements in selected body fluids, cells and tissues. Chem Biol Interact. (2019) 297:57–66. doi: 10.1016/j.cbi.2018.10.011

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Zaichick V, Zaichick S, Karandashev V, Nosenko S. The effect of age and gender on Al, B, Ba, Ca, Cu, Fe, K, Li, Mg, Mn, Na, P, S, Sr, V, and Zn contents in rib bone of healthy humans. Biol Trace Elem Res. (2009) 129:107–15. doi: 10.1007/s12011-008-8302-9

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Ohta H, Ohba K. Involvement of metal transporters in the intestinal uptake of cadmium. J Toxicol Sci. (2020) 45:539–48. doi: 10.2131/jts.45.539

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Vahter M, Berglund M, Akesson A, Lidén C. Metals and women's health. Environ Res. (2002) 88:145–55. doi: 10.1006/enrs.2002.4338

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Chang L, Shen S, Zhang Z, Song X, Jiang Q. Study on the relationship between age and the concentrations of heavy metal elements in human bone. Ann Transl Med. (2018) 6:320. doi: 10.21037/atm.2018.08.09

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Dabrowski M, Zioła-Frankowska A, Kubaszewski Ł, Rogala P, Frankowski M. Urban and rural area differences in the interaction between oxidative process elements in human femoral bone. Environ Sci Pollut Res Int. (2018) 25:30475–87. doi: 10.1007/s11356-018-3053-4

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Walraven N, Bakker M, van Os B, Klaver G, Middelburg JJ, Davies G. Pollution and oral bioaccessibility of Pb in soils of villages and cities with a long habitation history. Int J Environ Res Public Health. (2016) 13:221. doi: 10.3390/ijerph13020221

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Zhang Q, Cao Z, Sun X, Zuang C, Huang W, Li Y. Aluminum trichloride induces hypertension and disturbs the function of erythrocyte membrane in male rats. Biol Trace Elem Res. (2016) 171:116–23. doi: 10.1007/s12011-015-0504-3

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Shi P, Jing H, Xi S. Urinary metal/metalloid levels in relation to hypertension among occupationally exposed workers. Chemosphere. (2019) 234:640–7. doi: 10.1016/j.chemosphere.2019.06.099

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Schmidt PM, Escobar AG, Torres JG, Martinez CS, Rizzetti DA, Kunz SN, et al. Aluminum exposure for one hour decreases vascular reactivity in conductance and resistance arteries in rats. Toxicol Appl Pharmacol. (2016) 313:109–18. doi: 10.1016/j.taap.2016.10.023

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Abhyankar LN, Jones MR, Guallar E, Navas-Acien A. Arsenic exposure and hypertension: a systematic review. Environ Health Perspect. (2012) 120:494–500. doi: 10.1289/ehp.1103988

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Hall EM, Acevedo J, López FG, Cortés S, Ferreccio C, Smith AH, et al. Hypertension among adults exposed to drinking water arsenic in Northern Chile. Environ Res. (2017) 153:99–105. doi: 10.1016/j.envres.2016.11.016

PubMed Abstract | CrossRef Full Text | Google Scholar

57. da Cunha Martins A Jr, Carneiro MFH, Grotto D, Adeyemi JA, Barbosa F Jr. Arsenic, cadmium, and mercury-induced hypertension: mechanisms and epidemiological findings. J Toxicol Environ Health B Crit Rev. (2018) 21:61–82. doi: 10.1080/10937404.2018.1432025

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Miao H, Liu Y, Tsai TC, Schwartz J, Ji JS. Association between blood lead level and uncontrolled hypertension in the US Population (NHANES 1999-2016). J Am Heart Assoc. (2020) 9:e015533. doi: 10.1161/JAHA.119.015533

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Rehman K, Fatima F, Waheed I, Akash MSH. Prevalence of exposure of heavy metals and their impact on health consequences. J Cell Biochem. (2018) 119:157–84. doi: 10.1002/jcb.26234

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: aluminum, arsenic, cadmium, lead, knee joint, structures, factors

Citation: Li G, Xiong C, Xu W, Mei R, Cheng T and Yu X (2021) Factors Affecting the Aluminum, Arsenic, Cadmium and Lead Concentrations in the Knee Joint Structures. Front. Public Health 9:758074. doi: 10.3389/fpubh.2021.758074

Received: 13 August 2021; Accepted: 02 December 2021;
Published: 23 December 2021.

Edited by:

Mejdi Snoussi, University of Hail, Saudi Arabia

Reviewed by:

Khadhraoui Moncef, University of Sfax, Tunisia
Riadh Badraoui, Tunis El Manar University, Tunisia

Copyright © 2021 Li, Xiong, Xu, Mei, Cheng and Yu. 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: Tao Cheng, dr_tao.cheng@hotmail.com; Xuefeng Yu, yxf_1958@sina.com

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