# Associations of serum creatinine and blood urea nitrogen with depressive symptoms among community-dwelling older adults in Guangzhou, China: a cross-sectional study

**Authors:** Jinping Huang, Yuanzheng Fu, Yushui Fu, Yangjian Pan, Yurong Hu, Jinquan Zhang, Wanwei Guo, Xiaoyan Du

PMC · DOI: 10.3389/fpsyt.2026.1746646 · Frontiers in Psychiatry · 2026-02-09

## TL;DR

This study found that higher levels of serum creatinine and blood urea nitrogen are linked to increased odds of depressive symptoms in older adults in China.

## Contribution

The study provides new evidence on the association between renal biomarkers and depressive symptoms in community-dwelling older adults in China.

## Key findings

- Higher serum creatinine and blood urea nitrogen levels were independently associated with increased odds of depressive symptoms.
- The association of serum creatinine with depression was stronger in older individuals, those with higher BMI, and those with hypertension.
- Estimated glomerular filtration rate was inversely associated with depressive symptoms.

## Abstract

Depression is a common and serious mental health concern among older adults, with depressive symptoms highly prevalent in elderly populations across China. Although several studies have examined the associations between renal biomarkers—such as serum creatinine (Scr) and blood urea nitrogen (BUN)—and depressive symptoms, evidence remains limited, particularly in community-dwelling older adults. This study aimed to investigate the associations of renal biomarkers (Scr, BUN, and their ratio) with depressive symptoms in a community-based cohort of older adults in Guangzhou, China.

This cross-sectional study included 1, 994 adults aged ≥ 65 years from community-based health screenings in Guangzhou. Depressive symptoms were assessed using the Patient Health Questionnaire-9 (PHQ-9). Renal function was evaluated using Scr, BUN, and the BUN/Scr ratio. Multivariable logistic regression models were used to assess the association between these renal biomarkers and depressive symptoms, adjusting for potential confounders including age, sex, body mass index (BMI), and chronic disease history. To ensure robustness, we conducted sensitivity analyses by substituting Scr with estimated glomerular filtration rate (eGFR). Restricted cubic splines were used to evaluate dose-response shapes. Subgroup analyses tested for effect modification by sex, age group, BMI category, and histories of hypertension, diabetes, and dyslipidemia.

Among the 1, 994 participants (median age: 71 years), 158 (7.9%) exhibited depressive symptoms. After full adjustment, higher Scr (adjusted OR per 1 μmol/L = 1.002, 95% CI 1.000–1.004) and BUN (adjusted OR per 1 mmol/L = 1.064, 95% CI 1.007–1.123) were independently associated with higher odds of depressive symptoms, whereas the BUN/Scr ratio showed no significant association. In sensitivity analyses, eGFR was inversely associated with depressive symptoms (OR = 0.992, 95% CI 0.985–0.999). Restricted cubic spline analyses revealed an approximately linear dose–response for BUN (P for nonlinearity = 0.407). Subgroup analyses indicated significant effect modification for Scr, with stronger associations observed among participants aged ≥70 years, those with overweight/obesity (BMI ≥24 kg/m²), and those with hypertension (all P for interaction< 0.05).

Higher Scr and BUN levels were independently associated with increased odds of depressive symptoms among community-dwelling older adults. The association of Scr with depression was particularly pronounced in older individuals, those with higher BMI, and those with hypertension.

## Linked entities

- **Diseases:** depression (MONDO:0002050), diabetes (MONDO:0005015), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, CST3 (cystatin C) [NCBI Gene 1471] {aka ADLDWA, ARMD11, HEL-S-2}
- **Diseases:** COVID-19 (MESH:D000086382), Uremic neurotoxicity (MESH:D006463), microvascular injury (MESH:D017566), nutritional deficiency (MESH:D044342), hypertension (MESH:D006973), kidney impairment (MESH:D007674), Depression (MESH:D003866), underweight (MESH:D013851), type 2 diabetes (MESH:D003924), diabetes (MESH:D003920), neuroinflammation (MESH:D000090862), CKD (MESH:D051436), cerebral dysfunction (MESH:D002547), inflammation (MESH:D007249), muscle (MESH:D019042), dyslipidemia (MESH:D050171), kidney function (MESH:D007680), muscle mass (MESH:C536030), obese (MESH:D009765), affective disturbances (MESH:D019964), overweight (MESH:D050177)
- **Chemicals:** urea (MESH:D014508), Scr (-), alcohol (MESH:D000438), creatinine (MESH:D003404), urea nitrogen (MESH:C530477)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926125/full.md

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Source: https://tomesphere.com/paper/PMC12926125