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ORIGINAL RESEARCH article

Front. Psychol., 11 August 2025

Sec. Psychology of Aging

Volume 16 - 2025 | https://doi.org/10.3389/fpsyg.2025.1628719

Predictive features analysis and nomogram construction for predicting depression in elderly patients

    WL

    Wei Lin 1

    ZZ

    Zijun Zhao 2

    YY

    Yingshan Yu 1

    HC

    Hongbin Chen 2*

  • 1. Department of Geriatrics, Fuzhou First General Hospital Affiliated with Fujian Medical University, Fuzhou, Fujian, China

  • 2. Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, Fujian, China

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Abstract

Introduction:

In elderly populations, depression is highly prevalent among those with chronic diseases and cognitive impairment, leading to distress, disability, and poor medical outcomes. With the aging of the population, the prevalence of geriatric depression is rising rapidly. The Comprehensive Geriatric Assessment (CGA), a multidimensional approach, evaluates medical, psychological, and functional capacities to identify highrisk individuals and may be correlated with depression in the elderly.

Methods:

From 2021 to 2023, a total of 219 geriatric patients were recruited. These patients were divided into two groups: a modeling group of 153 patients and a validation group of 66 patients. We collected patients’ basic information and CGA results and analyzed them using univariate and multivariate regression. Independent variables influencing depression were identified.

Results:

Multivariate regression analyses revealed that several factors had an impact on depression in these patients, including social support level (SSRS), Pain, Anxiety, Basic Activities of Daily Living (BADL) and Gender. By integrating these factors into the nomogram, we found good predictive performance in the training set (AUC 0.867, 95% CI: 0.799–0.936) and in the test set (AUC 0.724, 95%CI:0.5919–0.894). The calibration and discrimination accuracy of the nomograms for predicting depression risk in the elderly were satisfactory, and the decision curve analysis demonstrated significant clinical utility.

Discussion:

The model demonstrated robust performance in our study and may constitute a valuable tool for clinical screening.

1 Introduction

Depression is a common and serious mental disorder. It has a high prevalence among the older population and profoundly impacts their lives. Global epidemiological data show that the prevalence of depression among community-dwelling older persons is approximately 10–15% (Gundersen and Bensadon, 2023). This prevalence can be as high as 30–40% among older persons with chronic illnesses or those in need of long-term care (Borges et al., 2021; Li et al., 2022). The disease not only impairs patients’ emotional wellbeing and quality of life, but also significantly increases the likelihood of cognitive decline, physical illness worsening, suicide risk, and premature death (Wang et al., 2025; Dai et al., 2024). As the global population ages, the prevalence of depression in the elderly is expected to rise further. It constitutes a growing public health burden due to increased functional dependence, dramatic increases in healthcare resource consumption, and heavy caregiver burden (Loyal et al., 2025; Dafsari et al., 2023). With the acceleration of global aging, exploring effective strategies for early identification and accurate prediction of geriatric depression has become a key breakthrough for improving health outcomes and optimizing healthcare resource allocation in older adults (Schutz et al., 2022).

Geriatric depression is a complex disorder characterized by multiple biological, psychological, and social factors. Studies have shown that reduced levels of brain-derived neurotrophic factor (BDNF) are associated with depressive symptoms. Additionally, some inflammatory factors, such as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α), may be associated with depression and cognitive decline (Borges et al., 2022; Xue et al., 2025). Furthermore, studies have shown that depression in the elderly results from the dynamic interaction of multiple factors such as quality of life, emotional health, social engagement, and physical health. These factors form a complex ‘biopsychosocial’ etiological network (Han et al., 2023; Wang et al., 2020).

Studies have shown that active and healthy lifestyle factors can significantly buffer the risk of depression (Linnan et al., 2020): a strong social network provides emotional support and a sense of belonging; regular social activities and physical exercise play an antidepressant role by enhancing neuroplasticity and self-worth (Gao et al., 2024); and maintaining Activities of Daily Living (ADL) and Instrumental Activities of Daily Living (IADL) helps reduce depression risk and lowers the likelihood of developing depression (Cole et al., 2023). Leisure activities enhance social support, emotional wellbeing, and overall life satisfaction (Parra-Rizo et al., 2022). Maintaining these functions is the basis for dignity and social participation. These factors are not only indicators of health status, but also provide precise targets for preventive interventions (e.g., social promotion programs, exercise prescription) (Kris-Etherton et al., 2021).

Geriatric depression has a complex etiology and diverse manifestations. The Comprehensive Geriatric Assessment (CGA) is a multidimensional approach that assesses medical, psychological, and functional abilities (Schutz et al., 2022). It has been shown to be uniquely valuable for systematically identifying predictive features and individuals at high risk of geriatric depression. Multiple studies confirm that CGA dimensions such as functional dependence, cognitive impairment, polypharmacy, and social isolation significantly predict depression development in the elderly (Dafsari et al., 2023). Its strength lies in its ability to go beyond a single biological perspective and to capture the complex biopsychosocial interactions behind geriatric depression (Zhang et al., 2024).

Although CGA offers a rich database for identifying geriatric depression risks and multidimensional risk and protective factors are well recognized, there is no user-friendly, visual predictive tool based on CGA data. This gap limits CGA’s full potential for prospective prediction and personalized prevention. This gap limits the full potential of the CGA for prospective risk prediction and personalized prevention. To address this critical need, this study aims to construct an integrated depression screening model using the core components of the CGA. We hypothesized that lower levels of social support, greater functional impairment, and higher anxiety or pain scores—as measured by the CGA—would be significantly associated with depressive symptoms in elderly patients.

2 Methods

2.1 Study population, general characteristics, and chronic diseases

A cross-sectional design was selected to explore associations between CGA parameters and depressive symptoms in a defined hospital-based elderly population. The determination of the study sample size followed the rule that the number of events must be at least 10 times the number of variables in the model (Steyerberg, 2016). From June 2021 to June 2023, we conducted a cross-sectional study of 219 elderly patients from the Geriatrics Department of Fuzhou First General Hospital Affiliated with Fujian Medical University. All elderly patients aged ≥65 years with complete comprehensive geriatric assessment data who agreed to participate in the study were included. Patients unable to walk due to neuromusculoskeletal disorders, such as severe cerebrovascular disease, Parkinson’s disease, knee or hip osteoarthritis, and lumbar spinal stenosis, as well as participants with severe cognitive impairment, autoimmune dis-eases, severe liver and kidney dysfunction, or malignant tumors, were excluded from the study. The study was conducted in accordance with the Declaration of Helsinki and approved by The Ethics Committee of The Fuzhou First General Hospital Affiliated with Fujian Medical University (Approval Number: 20230304). A structured and pre-tested questionnaire was administered by trained clinicians to collect baseline sociodemographic and clinical data. Patient name, sex, age, BMI, hospitalization number, and chronic diseases (diabetes, cardiovascular disease, peptic ulcer disease) were evaluated using a custom-designed face-to-face interview questionnaire. Comorbidity data were initially collected from patient interviews and subsequently verified using electronic medical records, covering all records from 1 year before admission to 6 months after the first diagnosis. The medical record system used ICD-10 and ICD-9-CM codes to identify the comorbid conditions. Patients were randomly assigned using a computer-generated sequence in a 7: 3 ratio to either the training (n = 153) or validation (n = 66) cohort.

2.2 Comprehensive geriatric assessment

A comprehensive geriatric assessment (CGA) was performed by trained clinicians on the first day of admission for patients who met the inclusion criteria. The assessment mainly included the following: The 15-item Geriatric Depression Scale (GDS-15), which was culturally validated for Chinese populations (Zhang et al., 2020), is a short form of the GDS and is used to screen, diagnose, and evaluate depression in elderly individuals. Patients with a GDS-15 score ≥5 were considered to have clinically significant depressive symptoms, as per established thresholds in prior validation studies (Shin et al., 2019). When the critical score is <5 points indicates no depressive status, and ≥5 points indicates depressive status, the higher the score is, the more obvious the depression tendency. The Self-Assessment Scale for Anxiety (SAS) contains 20 items reflecting subjective feelings of anxiety, and each item is rated on a four-point scale according to the frequency of symptoms (Yue et al., 2020). The SAS was developed to assess anxiety: <50 points for no anxiety symptoms, 50–59 points for mild anxiety, 60–69 points for moderate anxiety and ≥69 points for severe anxiety. The Mini Nutritional Assessment (MNA) can be used to rapidly and effortlessly evaluate the nutritional status of geriatric patients in a reliable and noninvasive manner (Mastronuzzi and Grattagliano, 2019). The MNA score ranged from ≥24 points for good nutrition, 17–23.5 points for potentially poor nutrition and 0–17 points for poor nutrition. The SSRS (Social Support Rating Scale) was originally developed by Xiao Shuiyuan in 1986 for the Chinese population (Mcmahon et al., 2017). It has already been widely used in various studies in different Chinese communities and has been shown to have good validity and reliability, with scores ranging from 0 to 19 points for less social support, with scores ranging from 20 to 30 points for general social support and >30 points for satisfactory social support. The insomnia assessment included the use of the AIS scale: 0–3 points for no insomnia disorder, 4–6 points for suspected insomnia, and 7–24 points for insomnia. BADL (Basic Activity of Daily Living) were evaluated through six subscales: Bathing, Dressing, Toileting, Indoor mobility, Continence of defecation, and Eating (Zhang et al., 2021). A total of 100 points indicated normal daily life function, 61–99 points indicated mild functional impairment, 41–60 points indicated moderate functional impairment, and ≤40 points indicated severe functional impairment. The insomnia assessment included the use of the AIS (Athens Insomnia Scale): 0–3 points for no insomnia disorder, 4–6 points for suspected insomnia, and 7–24 points for insomnia. The visual analog method was used for pain assessment, with scores ranging from 0 for no pain, 1–3 for mild pain, 4–6 for moderate pain and 7–10 for severe pain.

2.3 Statistical analysis process

SPSS 25.0 was used for the analysis of the data. Categorical data are presented as frequencies and proportions, and the variables were compared using either the chi-square test or Fisher’s exact test in univariate analysis. Continuous data are expressed as medians and interquartile ranges, and the Mann–Whitney U test was used for comparisons of these variables. To obtain the most accurate results, variables with a p value less than 0.10 (Chen et al., 2024) in the univariate analysis were subjected to stepwise backward multivariate logistic regression analysis. A two-tailed p value of less than 0.05 was considered to indicate statistical significance (p < 0.05). The adjusted odds ratios (aORs) and 95% confidence intervals (CIs) for the predictive features were obtained by means of multivariate-adjusted binary logistic regression. R version 3.6.11 and the “rms” and “ggplot2” packages were used to construct a nomogram. The significant predictive features identified in the multivariate analysis were selected for inclusion in the prediction nomogram. In the nomogram, each variable is assigned a distinct predicted score, and the total score is obtained by summing all the scores. The total predicted scores are then converted into predicted probabilities. The receiver operating characteristic (ROC) curve and the area under the curve (AUC) were calculated to evaluate the accuracy of the nomogram. Based on the cutoff points, the sensitivity and specificity were calculated. Internal validation was performed using 1,000 bootstrap resamples and Hosmer–Lemeshow test were performed to test the internal validation and stability of fit. In addition, calibration plots were generated, and decision curve analysis (DCA) was performed to quantify the performance ability and clinical utility of the model.

3 Results

3.1 Participant characteristics and predictive features

Table 1 presents the general characteristics of the 219 patients, including 61.2% women and 38.8% men. Many subjects were assessed for various factors, including Album, Mini Nutritional Assessment (MNA), Mini-Mental State Examination (MMSE), Anxiety, Cardiovascular Disease (CVD), Peptic Ulcer Disease (PUD), Diabetes, Pain, Insomnia, Constipation, Basic Activity of Daily Living (BADL), and Age.

Table 1

Variable ALL N = 219 No depression, N% Depression, N% p. overall
Gender: 0.923
Female 85 (38.81%) 66 (39.29%) 19 (37.25%)
Male 134 (61.19%) 102 (60.71%) 32 (62.75%)
Age 87.00 [78.00; 91.00] 86.50 [78.00; 91.00] 88.00 [79.50; 92.00] 0.361
Alb 38.20 [35.25; 41.00] 38.55 [35.10; 41.10] 37.80 [35.65; 40.45] 0.782
BADL: <0.001
No 59 (26.94%) 50 (29.76%) 9 (17.65%)
Mild 118 (53.88%) 102 (60.71%) 16 (31.37%)
Moderate 33 (15.07%) 13 (7.74%) 20 (39.22%)
Severe 9 (4.11%) 3 (1.79%) 6 (11.76%)
MNA 22.00 [19.00; 25.00] 23.00 [19.00; 26.00] 20.00 [16.00; 22.75] <0.001
MMSE 24.00 [20.00; 27.00] 24.00 [20.00; 27.00] 24.00 [20.00; 26.00] 0.714
Anxiety: 0.001
No 132 (60.27%) 110 (65.48%) 22 (43.14%)
Mild 55 (25.11%) 42 (25.00%) 13 (25.49%)
Moderate 23 (10.50%) 13 (7.74%) 10 (19.61%)
Severe 9 (4.11%) 3 (1.79%) 6 (11.76%)
Pain: 0.014
No 149 (68.04%) 122 (72.62%) 27 (52.94%)
Yes 70 (31.96%) 46 (27.38%) 24 (47.06%)
CVD: 0.106
No 114 (52.05%) 93 (55.36%) 21 (41.18%)
Yes 105 (47.95%) 75 (44.64%) 30 (58.82%)
Diabetes: 0.788
No 143 (65.30%) 111 (66.07%) 32 (62.75%)
Yes 76 (34.70%) 57 (33.93%) 19 (37.25%)
PUD: 0.195
No 190 (86.76%) 149 (88.69%) 41 (80.39%)
Yes 29 (13.24%) 19 (11.31%) 10 (19.61%)
Insomnia 2.00 [0.00; 10.00] 1.50 [0.00; 7.25] 6.00 [0.00; 11.50] 0.024
SSRS 27.00 [21.00; 32.50] 28.00 [23.00; 34.00] 21.00 [15.50; 27.50] <0.001
Constipation: 0.490
No 123 (56.16%) 97 (57.74%) 26 (50.98%)
Yes 96 (43.84%) 71 (42.26%) 25 (49.02%)

Characteristics of the subjects according to the prevalence of depression, N (%).

As shown in Table 2, univariate and multivariate logistic regression analyses using the AIC-based backward procedure identified several independent factors influencing the onset of depression in elderly patients. These factors included SSRS (OR = 0.909; CI: 0.852–0.964, p = 0.002), Pain (OR = 3.092; CI: 1.128–8.924, p = 0.031), Anxiety (OR = 2.061; CI: 1.228–3.562, p = 0.007), BADL (OR = 5.060; CI: 2.471–11.82, p = 0), and Gender (OR = 3.034; CI: 1.073–9.498, p = 0.044).

Table 2

Variable Univariate analysis Multivariate analysis
OR 95% CI p value OR 95% CI p value
Constipation 1.006 1.006 (0.471–2.117) 0.988
SSRS 0.915 0.915 (0.868–0.959) 0 0.91 0.909 (0.852–0.964) 0.002
Insomnia 1.034 1.034 (0.977–1.093) 0.24
PUD 1.677 1.677 (0.546–4.704) 0.338
Diabetes 1.069 1.069 (0.482–2.302) 0.866
CVD 1.997 1.997 (0.948–4.278) 0.07 2.002 2.002 (0.746–5.579) 0.172
Pain 2.05 2.05 (0.954–4.396) 0.064 3.092 3.092 (1.128–8.924) 0.031
Anxiety 2.104 2.104 (1.398–3.242) 0 2.061 2.061 (1.228–3.562) 0.007
MMSE 0.996 0.996 (0.924–1.08) 0.925
MNA 0.886 0.886 (0.812–0.964) 0.006 0.941 0.941 (0.831–1.063) 0.331
BADL 4.431 4.431 (2.475–8.652) 0 5.06 5.060 (2.471–11.82) 0
Alb 0.995 0.995 (0.917–1.081) 0.905
Age 1.023 1.023 (0.981–1.068) 0.299
Gender 1.988 1.988 (0.917–4.545) 0.09 3.034 3.034 (1.073–9.498) 0.044

Independent predictors of depression in elderly patients.

3.2 Nomogram construction and validation

Utilizing these distinct variables, we created a nomogram to predict the risk of depression among senior patients, as illustrated in Figure 1. The location of each point is determined by the intersection of the respective variable with the vertical line of the point axis. By aggregating the points associated with each variable, we obtain the total risk score. The likelihood of depression can then be ascertained from the total score axis.

Figure 1

Nomogram chart depicting points associated with variables: SSRS, Pain, Anxiety, BADL, and Gender. The chart helps calculate total points, which correlate with diagnostic possibilities, ranging from zero to two hundred twenty total points and zero to one in diagnostic probability.

The nomogram model for the prediction of depression in elderly patients.

We validated this nomogram. Collectively, these results indicate that the nomogram is a reliable tool for predicting depression in patients older than 65 years. The Hosmer–Lemeshow test for the training set was 0.172 (p > 0.05), suggesting good calibration. At the optimal cutoff value of 0.273 determined by maximizing Youden’s index, the model demonstrated a sensitivity of 0.862 and specificity of 0.757 in the training set (Figure 2A), and sensitivity of 0.615 and specificity of 0.857 in the test set (Figure 2B). The AUCs of the nomograms were 0.867 (95% CI: 0.799–0.936) in the training set (Figure 2C) and 0.724 (95% CI: 0.5919–0.894) in the test set, indicating robust discriminative ability in the training cohort and moderate generalizability in external validation.

Figure 2

Graphs A and B show Receiver Operating Characteristic (ROC) curves with red lines. Graph A has an AUC of 0.867 and a sensitivity marker at 0.273 (0.862, 0.757). Graph B has an AUC of 0.742 with a marker at 0.130 (0.615, 0.857). Graphs C and D display ROC curves with light blue confidence bands. Graph C shows an AUC of 0.867 with a ninety-five percent confidence interval from 0.799 to 0.936. Graph D has an AUC of 0.742 with a ninety-five percent confidence interval from 0.591 to 0.894.

The ROC curve for assessing the predictive accuracy of the nomogram model (A,C: training set; B,D: test set).

Figure 3 presents the calibrated curve that was generated using the bootstrap method. This approach was iteratively employed 1,000 times to shape the curves, and the results revealed that both the bias-adjusted and visible curves closely mirrored the reference line, signifying a robust correlation between the estimated and actual risks of depression. A subsequent Hosmer–Lemeshow test of model adequacy yielded a chi-squared statistic of 5.265 with a p value of 0.729 reinforcing the adequacy of the model’s fit. Furthermore, to evaluate the clinical significance of our nomogram, we constructed a decision curve analysis (DCA) plot. The DCA curve findings indicated that the model provides a substantial net benefit across a substantial threshold range, ranging from approximately 5–80%, thereby underlining its practicality in guiding decision-making in clinical contexts (Figure 4).

Figure 3

Calibration plot showing actual probability versus predicted probability. The plot includes three lines: ideal (diagonal), logistic calibration (solid), and nonparametric (dotted). Statistics such as Dxy, C (ROC), and R2 are listed to the left with respective values. Vertical lines indicate data distribution along the axes.

The calibration curve of the nomogram model.

Figure 4

Decision curve analysis graph showing net benefit versus threshold probability and cost-benefit ratio. The red line represents "Nomo," indicating a decreasing net benefit as threshold probability increases. Lines for "All" and "None" are shown for comparison.

The DCA curve of the nomogram model.

4 Discussion

This study represents a novel approach for constructing a depression screening model of depression risk in elderly patients. The incorporation of CGA parameters represents a significant advance in the field. The findings of this study indicate that a number of indicators are strongly associated with depression. In particular, the results indicate that anxiety level, pain, level of social support (SSRS), ability to perform activities of daily living (BADL) and gender are associated with depression in elderly patients. The calibration curves of the modeling and verification groups demonstrated that the model exhibited favorable discrimination and fit. Depression is characterized by a low mood or feeling sad and a loss of interest or pleasure in daily activities.

In the relationship between depression and anxiety, previous studies have suggested that anxiety and depression are causative of each other, with similarities in biological basis and causative factors, and that they can produce pathological shaping of the patient’s personality, which is reversible but irreversible to the physiological functions of the organism (Frances et al., 1992). Although anxiety and depression are considered two distinct entities according to the diagnostic criteria, anxious depression is a relatively common syndrome (Choi et al., 2020). Research indicates that a broad range of depressive and anxiety symptoms are linked to a heightened risk of disability in the later stages of life (Dong et al., 2020).

A study revealed that among Chinese senior citizens, those experiencing difficulties in basic and instrumental activities of daily living (BADL/IADL), particularly BADL, had a significant correlation with depressive symptoms (Liu et al., 2023). The dynamics of this relationship are complex. Seniors often face initial issues with instrumental activities of daily living (IADL), progressing to issues with basic activities of daily living (BADL). These issues lead to decreased purposeful actions, negative affect, and emotional impacts from physical decline. Impairments can disrupt routines and social interaction and can trigger depression (Bacon et al., 2016; Bruce, 2001; Luo et al., 2017). Moreover, these impairments can curtail daily routines and diminish social interaction, contributing to the onset of depression (Bacon et al., 2016; Bruce, 2001).

Chronic pain demonstrates significant predictive value for depression onset and progression in elderly populations, with pain-related functional interference emerging as the strongest independent predictor (Landi et al., 2005). This suggests that chronic pain may not only directly affect mood through biological pathways involving cytokines and neuroinflammation, but also indirectly by impairing physical function and reducing quality of life. Prospective investigations reveal a dose–response relationship, evidenced by a Hong Kong cohort study (N = 318) where baseline pain severity predicted depressive symptom exacerbation at 12-month follow-up (β = 0.32, p < 0.01) after adjusting for confounding factors (Chou and Chi, 2005). This temporal association is further substantiated by large-scale data (N = 5,372) showing daily pain exposure correlates with 44% higher depression scores (3.6 vs. 2.5 points) and 1.5–2.3 fold increased risks of core depressive symptoms compared to pain-free individuals (Landi et al., 2005).

Gender serves as a significant predictor of depression in elderly patients, with robust evidence highlighting sex-specific disparities in prevalence and clinical manifestations. These findings suggest not only biological (e.g., hormonal) but also psychosocial determinants—such as caregiving roles, social expectations, and access to care—may explain gender disparities in late-life depression. Population-based studies reveal that elderly women exhibit higher rates of depressive symptoms compared to men, with community-dwelling women showing a 15% prevalence of depressive symptoms versus 1–3% for major depressive disorder in men (Heo et al., 2023). This disparity persists in disease-specific cohorts: women with heart failure demonstrated nearly double the prevalence of clinically significant depressive symptoms (CES-D ≥ 16: 39% vs. 21%, p < 0.001) (Heo et al., 2023), and those with chronic vestibular dysfunction showed stronger associations between female sex and depressive symptom severity (β = 1.32, p < 0.05) (Gazzola et al., 2009). Metabolic syndromestudies further revealed sex-dimorphic patterns, where male patients with optic neuritis exhibited a significantly higher risk of developing depressive disorders compared to female patients, with an adjusted hazard ratio (HR) of 1.450 (95% CI: 1.338–1.571) (Kim et al., 2025). These findings underscore sex-related biological vulnerabilities sociocultural factors as key mediators of depression risk stratification by gender in aging populations (Targum et al., 1992).

More importantly, however, we found a significant association between depression and the Mini Nutritional Assessment score, which has previously been shown to reflect nutritional levels in elderly hospitalized patients. Malnutrition may contribute to depression through mechanisms involving reduced tryptophan availability, impaired neurotransmitter synthesis, and inflammation. As the world’s population continues to age, researchers in a variety of fields are becoming increasingly concerned about the intersection of nutrition and depression in elderly people. A pertinent study published in the last year’s issue of nutrition highlighted a profound link between nutritional status and depression (Mcfarland et al., 2020). Similar research has also shown that elderly patients suffering from depression tend to score significantly lower on the Mini Nutritional Assessment than those without depression, suggesting a possible link between depression and malnutrition (German et al., 2008).

Our study revealed that higher levels of social support, which refers to the unpaid help that vulnerable groups in society receive from outside sources, such as moral and material assistance and services, significantly reduced the risk of depression in older patients. It is plausible that social support mitigates the psychological burden of functional limitations and chronic pain, thereby attenuating the depressive response. Consistent with our study, our research revealed that social support can affect an individual’s cognitive functioning and behavior and has a greater impact on the mental health of older people (Muhammad and Maurya, 2022). In particular, during the COVID-19 pandemic in recent years, social isolation has had a serious impact on the physical and mental health of older people, including mental illnesses such as anxiety and depression (Sepúlveda-Loyola et al., 2020). Another study showed that with strong social support, depressive symptoms were significantly reduced, and even chronic pain was reduced with increased levels of support (Sepúlveda-Loyola et al., 2020; Hung et al., 2017). Family support, which focuses on emotional wellbeing, such as respect and under-standing, aids in reducing depression among elderly people. However, the importance of social support from friends is equally crucial and is becoming a growing area of focus (Taylor et al., 2018).

The present study has the following limitations. First, this model identifies variables statistically associated with depression status but cannot infer causality due to the cross-sectional design. Features such as anxiety may be consequences rather than causes of depression. Future longitudinal studies are required to establish causal roles. Second, the samples included were all elderly hospitalized patients aged 65 years and above, which cannot represent the entire elderly population. Since participants were all hospitalized, they may exhibit higher baseline functional impairment and comorbidity burden, which may overestimate the prevalence of depressive symptoms compared to community-dwelling older adults. In addition, the integrity and credibility of the comprehensive geriatric assessment are compromised by differences in medical standards between healthcare institutions and in patients’ understanding of their own past health, which affects the assessment results. Although our comprehensive geriatric assessment comprehensively assesses the overall condition of elderly people, some scales related to nutritional status and frailty, such as gait speed, grip strength, and leg circumference, were not included in this experiment. Future research on older people will continue to improve this topic.

This model has shown potential in aiding healthcare professionals with the early detection of patients at high risk and the formulation of tailored intervention strategies. Considering that machine learning methods can capture complex nonlinear relationships and interactions, future studies will further investigate the application of methods such as Random Forests, Gradient Boosting Machines (XGBoost, LightGBM), Support Vector Machines (SVM), and Neural Networks (Du et al., 2025a; Du et al., 2025b). To confirm its extensive applicability, especially in light of the constraints imposed by a single-center data source and a moderate sample size, it is essential to perform external validation across multicenter cohorts and assess its predictive accuracy over time.

5 Conclusion

Geriatric depression is closely related to a variety of predictive features (i.e., multiple geriatric syndromes); thus, healthcare professionals should not only focus on the surface of geriatric depression but also intervene in geriatric syndromes. Second, the depression probability estimator constructed in this study is also effective, and early screening of predictive features will help healthcare professionals provide timely guidance to patients to prevent the occurrence of geriatric depression. Second, the model demonstrated robust performance in our study and may constitute a valuable tool for clinical screening, contingent upon external validation.

Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors without undue reservation.

Ethics statement

The studies involving humans were approved by Ethics Committee of Fuzhou First General Hospital Affiliated with Fujian Medical University. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements.

Author contributions

WL: Writing – original draft, Investigation, Data curation, Formal analysis, Conceptualization, Visualization. ZZ: Validation, Software, Resources, Writing – original draft, Formal analysis. YY: Resources, Writing – original draft, Validation, Investigation, Data curation. HC: Supervision, Project administration, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the Project of Fujian Medical University Union Hospital (No. 2022XH026).

Acknowledgments

The authors would like to thank the Geriatric Department of Fuzhou First General Hospital Affiliated with Fujian Medical University. We sincerely thank Director Lixin Zhang of the Geriatrics Department at Fuzhou First General Hospital Affiliated with Fujian Medical University for his organizational and coordination efforts in this study. Additionally, we wish to acknowledge all participants of this project and the investigators for collecting the data.

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.

Abbreviations

CVD, Cardiovascular Disease; PUD, peptic ulcer disease; GDS, Geriatric Depression Scale; SAS, The Self-Assessment Scale for Anxiety; MNA, Mini Nutritional Assessment; SSRS, Social Support Rating Scale; AIS, Athens Insomnia Scale; BADL, Basic Activity of Daily Living; ROC, Receiver Operating Characteristic Curve; AUC, Area Under the Curve; DCA, Decision Curve Analysis.

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Summary

Keywords

depression, predictive features, nomogram, elderly patients, depression screening model

Citation

Lin W, Zhao Z, Yu Y and Chen H (2025) Predictive features analysis and nomogram construction for predicting depression in elderly patients. Front. Psychol. 16:1628719. doi: 10.3389/fpsyg.2025.1628719

Received

14 May 2025

Accepted

29 July 2025

Published

11 August 2025

Volume

16 - 2025

Edited by

Taolin Chen, Sichuan University, China

Reviewed by

María Antonia Parra Rizo, Miguel Hernández University of Elche, Spain

Du Jinsong, Zaozhuang University, China

Updates

Copyright

*Correspondence: Hongbin Chen,

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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.

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