Figures
Abstract
Background
Depression is a common global mood disorder problem and one of the major disabling factors. The Clínica Universidad de Navarra-Body Adiposity Estimator (CUN-BAE) index is an important composite indicator for measuring fat content in the body. Our goal is to find out the relationship between the CUN-BAE index and depression, as well as the mediating effect of the Systemic Inflammatory Response Index (SIRI) between the two.
Methods
All participants aged ≥ 20 from the 2005–2020 cycles of the NHANES in the US were included in the research. To assess the relationships between CUN-BAE and SIRI and depression, we used weighted multivariable logistic regression models. Potential nonlinearity was examined using restricted cubic splines (RCS) regression models. We performed mediation analysis with 1000 bootstrap replicates to evaluate the mediating function of SIRI in the relationship of CUN-BAE and depression.
Results
31,592 participants were examined for the statistical analysis, of whom 28,825 were classified into the non-depression group and 2,767 were identified as belonging to depression group. Individuals in the depression group were more probable to be female and to have diabetes and hypertension, and higher SIRI and CUN-BAE levels. An incremental rise of one unit in CUN-BAE was connected to a 2% elevation in the odds of developing depression (OR = 1.02; 95% CI: 1.01–1.03; P < 0.001). The regression analysis revealed a statistically significant non-linear positive relationship between CUN-BAE levels and depressive status (P for non-linearity = 0.005), alongside a J-shaped curve characterizing the association between log-transformed SIRI and depression (P for non-linearity = 0.007). The AUC of CUN-BAE for predicting depression was 0.60(0.59,0.61). With a 3% mediating effect, SIRI functioned as a partial mediator in the pathway linking CUN-BAE levels to depression.
Citation: Li M, Qi Y, Cao M, Lou H, Teng W, Wang L (2025) The association between the CUN-BAE index and depression mediated by SIRI: A large cross-sectional study. PLoS One 20(10): e0334655. https://doi.org/10.1371/journal.pone.0334655
Editor: Zhenhua Li, Henan Polytechnic University, CHINA
Received: August 1, 2025; Accepted: September 30, 2025; Published: October 31, 2025
Copyright: © 2025 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The dataset provided at https://wwwn.cdc.gov/nchs/nhanes/Default.aspx supports the results of this study.
Funding: This work was funded by the National Natural Science Foundation of China (NO. 81303044), the Natural Science Foundation of Heilongjiang Province Project (NO. LH2022H082) and the Project of the Administration of Traditional Chinese Medicine of Heilongjiang Province (NO. ZHY2020-120). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: AUC, Area Under Curve; BMI, body mass index; CRP, C-reactive protein; CUN-BAE, Clínica Universidad de Navarra-Body Adiposity Estimator; DE, direct effect; IE, indirect effect; IL, interleukin; TNF-α, tumor necrosis factor-alpha; NHANES, National Health and Nutrition Examination Survey; PHQ-9, Patient Health Questionnaire-9; PIR, poverty income ratio; ROC, Receiver Operating Characteristic; SIRI, Systemic Inflammatory Response Index; TE, total effect.
1. Introduction
Due to the accelerated pace of life and changes in the social environment, psychological problems have gradually received extensive attention from society [1]. Depression is a common global mood disorder problem and one of the major disabling factors, with persistent low mood, absence of passion, and delayed thinking as the main clinical features, as well as low recognition, low consultation, and low treatment rate [2]. With the intensification of social competition and the acceleration of urbanization, the prevalence of depression has been rising globally. The prevalence of depression in kids and teenagers has been reported to be as high as 21.3% worldwide, with a constant trend as mentioned above [3]. And 13.3% of older adults suffer from severe depression [4]. Beyond its detrimental impact on individual quality of life, depression imposes considerable burdens on familial dynamics and broader societal functioning. In Austria, the annual direct cost of refractory depression in 2021 is reported to be estimated at €345 million, and the indirect cost is estimated at €684.7 million [5]. However, currently, the treatment of depression is based on oral antidepressants combined with psychotherapy. Antidepressants commonly used in clinical practice usually have a slow onset of action, need to be taken for a long period of time, and have varying degrees of adverse effects, such as nausea, diarrhea, headache, and dry mouth [6,7]. Therefore, the discovery of risk factors for depression and early intervention are of great significance in delaying disease progression and improving patients’ quality of life.
An expanding body of evidence supports a significant relationship between excessive obesity and an increased susceptibility to depression [8], and there are multiple common biological mechanisms between the two, including genetic factors, immune-inflammation, energy metabolism, and gut microbial imbalance [9,10]. Obesity can increase the risk of depression through the interplay of multiple mechanisms, including chronic low-grade inflammation, hypothalamic–pituitary–adrenal (HPA) axis dysregulation, and disturbances in energy metabolism. These processes disrupt the synthesis, release, and metabolism of central neurotransmitters such as serotonin and dopamine, thereby significantly contributing to the development of depression [11,12]. Currently, body mass index (BMI), visceral adiposity index, and other metrics are frequently employed to measure obesity. Although the above indicators can measure the degree of obesity to a certain extent, they are unable to assess the body fat accumulation. The Clínica Universidad de Navarra-Body Adiposity Estimator (CUN-BAE) index, a composite indicator created by Gómez-Ambrosi [13] and others, is comprised of age, gender, and BMI, which can serve as a reliable alternative indicator for measuring body fat percentage. Meanwhile, previous studies have shown that it is more effective in predicting cardiometabolic risk factors with higher correlation than BMI and waist circumference [13]. Therefore, we hypothesize that CUN-BAE may also serve as a potential risk factor for depression; however, this remains to be confirmed by further studies.
Obesity is widely recognized not only as a metabolic disturbance but also as a state characterized by persistent low-grade inflammation. Adipose tissue, especially visceral fat, can release a variety of pro-inflammatory factors, such as interleukin-1β, interleukin-6, monocyte chemotactic protein-1, and so on. In an obese state, this condition stimulates the innate immune system, culminating in a generalized pro-inflammatory state throughout the organism. And depressed patients are often accompanied by increased concentrations of inflammatory signs, such as C-reactive protein and tumor necrosis factor-α. Inflammatory factors can induce or exacerbate depression by interfering with central nervous system function through mechanisms such as affecting neurotransmitter metabolism, down-regulating the level of brain-derived neurotrophic factor, and contributes to the activation of the hypothalamic–pituitary–adrenal axis. The Systemic Inflammatory Response Index (SIRI) is a reliable marker for assessing inflammatory status. Li et al. [14] further demonstrated a significant positive association between SIRI and depression (OR = 1.06, 95% CI = 1.01–1.10, P = 0.016). Based on these findings, we hypothesize that SIRI may serve as a potential mediator in the association between CUN-BAE and depression.
Grounded in the aforementioned theoretical framework, this investigation was aiming at elucidating the dose-response relationship between the CUN-BAE index and depression, and to assess the potential mediating effect of the Systemic Inflammatory Response Index (SIRI) in this relationship. The findings are expected to provide a scientific basis for improving earlier detection and preventive strategies for depression.
2. Materials and methods
2.1. Study design and participants
This study includes NHANES participants aged ≥ 20 from the 2005–2020 cycles in the U.S. Other researchers introduced the characteristics of the NHANES database [15]. Fig 1 presents the participant selection process. Out of 76,496 initial respondents, those were excluded if they were younger than 20 years of age, pregnant, or lacked appropriate survey weights (n = 35,745); or lack information from Patient Health Questionnaire-9 (PHQ-9) (n = 4,210); were missing essential variables for calculating CUN-BAE (n = 380) or SIRI (n = 1,404); or lacked critical covariate information, including age, sex, or racial classification (n = 3,165). Finally, the statistical analysis included 31,592 participants in totality. The protocols of the NHANES survey have got ethical clearance from the National Center for Health Statistics’ Research Ethics Review Board. Everyone who participated signed an informed consent document before starting their involvement.
2.2. Definition of depression
Within the context of the present analysis, the PHQ-9 was used to examine the existence of depression. This tool, constructed by Kroenke et al., was applied to quantify the intensity of depressive symptomatology within the last two weeks [16]. The PHQ-9 comprises nine items, each item is rated on a 4-point Likert scale ranging from 0 (“not at all”) to 3 (“nearly every day”), yielding a cumulative score between 0 and 27. Referring to earlier research, depression is described as a total score of PHQ-9 ≥ 10 points [17].
2.3. Two indexes and laboratory measurement
All participants underwent interviews at their homes and physical exams at a mobile examination center (MEC). Height and weight data were measured by trained health technicians using standardized protocols at the MEC. The history of diabetes and hypertension was obtained at home through self-reported, collected by trained interviewers using the computer-assisted personal interview system. All participants were instructed to fast for at least nine hours prior to blood collection. The Beckman Coulter DxH 800 instrument was used to perform complete blood count on blood specimens and provide a distribution of blood cells for all participants [18].
The assessment indexes were computed using the following formulas [19,20]:
It is worth emphasizing that both depression and the two indices (CUN-BAE and SIRI) were assessed at the same cross-sectional time point.
2.4. Covariates
Covariates including age, gender, race, education level, poverty income ratio (PIR), and marital status were taken from the baseline household questionnaires. Additionally, histories of diabetes and hypertension, drinking and smoking, and other behaviors were gathered. The NHANES website provided the public with further information about the aforementioned covariates.
2.5. Statistical analysis
The analysis of the entire study was carried out by R 4.4.1, with two-tailed P < 0.05 interpreted as significant. Considering the usage characteristics of the NHANES database, we incorporated MEC examination weights to ensure nationally representative estimates [21]. Baseline variables were contrasted between participants with and without depression. Continuous data were expressed as weighted means with standard deviations and analyzed using weighted t-tests for normally distributed metrics or weighted Wilcoxon rank-sum tests for non-normally distributed parameters. Categorical variables, presented as frequencies and corresponding weighted proportions, were assessed utilizing weighted chi-square tests [22]. Due to the right-skewed distribution of SIRI, SIRI was Ln-transformed prior to analysis [23].
To evaluate the relationship of CUN-BAE and SIRI with depression, weighted multivariable logistic regression models were implemented: Model 1 didn’t include any covariate adjustments, whereas Model 2 was adjusted for demographic variables, including age, sex, race/ethnicity, educational attainment, PIR, and marital status, and Model 3 adjusted for all potential covariates. CUN-BAE and SIRI were both used in continuous analyses and categorical analyses and P for trend was calculated. Potential nonlinearity was examined using restricted cubic splines (RCS) regression models [24]. If there is a significant non-monotonic correlation, two-piecewise linear regression based on threshold analysis was employed [25]. Subsequently, subgroup analyses were used to evaluate possible effects of interactions between CUN-BAE and covariates on the risk of depression. The discriminative capacity of CUN-BAE in identifying individuals with depression was evaluated via receiver operating characteristic (ROC) curve analysis [26]. The larger the area under the curve (AUC) value, the higher the predictive performance of CUN-BAE. To assess the intermediary function of SIRI in the relationship between CUN-BAE and depressive outcomes, a mediation analysis was conducted employing 1,000 bootstrap iterations. Mediation analysis included the total effect (TE), direct effect (DE), as well as indirect effect (IE) between variables [27].
3. Results
3.1. Characteristics of study participants
The research included 31,592 participants, of whom 28,825 were in the non-depression group and 2,767 were in the depression group. Participants in the depression group tended to be female, aged 40–59 years, with lower education levels, lower PIR, current smokers, current moderate drinkers, and had a greater prevalence of diabetes and hypertension than the non-depression group. Importantly, the depression group had significantly higher SIRI and CUN-BAE levels (Table 1).
3.2. Association between CUN-BAE, SIRI and depression
Table 2 showed the association between CUN-BAE, SIRI, and depression in weighted logistic regression models. In Model 1, the risk of depression increased by 3% for every unit rise in CUN-BAE (95% CI: 1.03, 1.04, P < 0.001). In Model 2, the risk of depression increased by 3% for every unit rise in CUN-BAE (OR: 1.03, 95% CI: 1.02, 1.03, P < 0.001). In Model 3, the risk of depression increased by 2% for every unit rise in CUN-BAE (OR: 1.02, 95% CI: 1.01, 1.03, P < 0.001). Stratified analysis by CUN-BAE quartiles in Model 3 revealed a statistically significant upward trend in depression risk corresponding to elevated CUN-BAE levels (P for trend < 0.001). In contrast to the Q1 group, the Q4 group had a 56% higher risk of depression (OR: 1.56, 95% CI: 1.26, 1.93, P < 0.001).
In Model 1, a one-unit increase in log-transformed SIRI (Ln-SIRI) was related to a 21% elevation in depression risk (OR = 1.21, 95% CI: 1.10–1.33, P < 0.001). Model 2 indicated a 26% higher likelihood of depression per unit increase in CUN-BAE (OR = 1.14, 95% CI: 1.03–1.39, P < 0.001). In the fully adjusted Model 3, each unit increment in Ln-SIRI corresponded to a 14% rise in depression risk (OR = 1.14, 95% CI: 1.02–1.26, P < 0.001). Additionally, quartile-based analysis of SIRI showed a significant trend of increasing depression risk with higher SIRI levels in Model 3 (P for trend = 0.048).
3.3. Dose-response relationships between CUN-BAE, Ln-SIRI and depression
RCS regression was applied to examine the relationships between CUN-BAE, Ln-SIRI, and depression (Fig 2). The model demonstrated a non-linear positive relationship between CUN-BAE and depression (P for non-linear = 0.005) and a J-shaped correlation between Ln-SIRI and depression (P for non-linear = 0.007).
Models were adjusted for age, gender, race, education, PIR, marital status, smoking status, drinking status, diabetes and hypertension.
Therefore, we further established threshold analysis to investigate the J-shaped correlation between SIRI and depression (Table 3). Threshold effect analysis identified a turning point at Ln-SIRI = −0.364. The log-likelihood ratio test confirmed a significant threshold at Ln-SIRI = 0.364 (P = 0.002). When Ln-SIRI was > −0.364, a 22.4% increase in the incidence of depression was linked to every unit rise in Ln-SIRI (OR: 1.224, 95% CI: 1.116, 1.342, P < 0.001).
3.4. Subgroup analysis and ROC curve of the predicted performance of CUN-BAE
Stratified analyses across subgroups were conducted to examine the association between CUN-BAE levels and depression (Table 4). The positive correlation between CUN-BAE and depression was consistent in most subgroups. We found that gender, race, marital status, and diabetes regulated associations between CUN-BAE and the risk of depression (P for interaction < 0.05). The impact of CUN-BAE on depression is stronger in female, other Hispanic, married/living with partner, and diabetes groups.
ROC analysis was utilized to examine the predictive validity of CUN-BAE for identifying individuals with depression (Fig 3). CUN-BAE predicted the AUC (95% CI) of 0.60 (0.59, 0.61), and the cutoff value is 50. CUN-BAE had a better predictive performance in identifying depression patients.
3.5. The mediating role of SIRI
Mediation modeling was conducted to evaluate the intermediary role of SIRI in the pathway linking CUN-BAE to depression (Fig 4). The TE of CUN-BAE on depression was 8.56 × 10 ⁻4 (95% CI: 7.55 × 10 ⁻4, 9.19 × 10 ⁻4, P < 0.001). The IE through SIRI was 2.56 × 10 ⁻5 (95% CI: 4.38 × 10 ⁻6, 5.16 × 10 ⁻5, P = 0.024), accounting for 3.0% of the total effect. The DE was 8.30 × 10⁻4 (95% CI: 7.20 × 10 ⁻4, 9.00 × 10 ⁻4, P < 0.001).
Model was adjusted for age, gender, race, education, PIR, marital status, smoking status, drinking status, diabetes and hypertension.
4. Discussion
Drawing on data from a large-scale cross-sectional cohort, our analysis identified a statistically significant positive relationship between CUN-BAE and depression. The application of the RCS regression model revealed a non-linear yet positive correlation between CUN-BAE and the presence of depression. The AUC value of the CUN-BAE index for diagnosis of depression was 0.60 (0.59, 0.61). The result of mediation effect illustrated that SIRI partially mediated the relationship between CUN-BAE and depression. Our research illustrated that higher levels of CUN-BAE are an independent risk factor for depression, and improving lipid metabolic status and inflammatory response might lessen the chance of developing depression.
Obesity and lipid deposition have been implicated as key contributors to depression. We constructed a large-scale cross-sectional investigation to systematically characterize the dose–response correlation between the CUN-BAE index and depression. We found that CUN-BAE was significantly and favorably correlated with depression, which is comparable to the results of earlier research. The Metabolic Score for Visceral Fat (METS-VF) is an important surrogate for exploring the level of visceral fat, and Liu et al. [28] suggested that the level of METS-VF was related to depression in individuals who were overweight or obese. Nong et al. [29] discovered a nonlinear correlation between depression and BMI. The CUN-BAE, as a comprehensive assessment of body fat that integrates age, gender, and BMI, is known as a more accurate evaluation of the body’s adiposity and distribution than BMI alone and is considered to be a more reliable marker for measuring obesity-related health risks [30,31]. On the one hand, elevated adiposity is linked to a chronic low-grade inflammatory state, which could lead to increased production of inflammatory substances, for example TNF-α, IL-1β, and CRP [32]. The latter, in turn, can trigger adrenocorticotropic hormone secretion, hypothalamus-adrenocorticotropic hormone axis activation, and cortisolism cascade response, which ultimately leads to neuronal apoptosis, dendritic atrophy, and reactive gliosis, which thus raises the chance of developing depression [33]. On the other hand, excessive body fat levels may trigger negative body imagery, social stigmatization, and decreased self-esteem, especially more pronounced in women. These psychosocial stressors may promote or exacerbate depression through pathways such as increased life stress and decreased social participation and support [34]. The above mechanisms may, in part, explain the significant positive link between CUN-BAE and the risk of depression.
In addition, the mediating effect results indicated that SIRI mediated the link between CUN-BAE and the risk of depression. The SIRI index, which is composed of neutrophil, monocyte, and lymphocyte counts, is acknowledged as a reliable indicator for assessing the state of inflammation in the organism. A substantial body of prior literature has highlighted the critical involvement of chronic low-grade inflammation in the pathogenesis of both obesity and depressive disorders [35–39]. We found that the SIRI index exhibited a significant mediating effect between CUN-BAE and the risk of depression, illustrating that systemic inflammation might be an important physiological mechanism linking body fat levels and the risk of depression. Excessive obesity can activate the immune system, which causes the release of pro-inflammatory mediators by immune cells [40], a process often associated with elevated SIRI values; and the sustained effects of inflammatory factors may interfere with neurotransmitter synthesis and metabolism, impacting mood regulation and brain function, raising the likelihood of depression [41]. However, it is worth emphasizing that although we observed a mediating effect of SIRI in the association between CUN-BAE and depression, the proportion of mediation is relatively small, indicating that SIRI represents only one of multiple potential mediating factors and cannot fully account for the relationship between CUN-BAE and depression.
There are some advantages to this study. First, we investigated the link between CUN-BAE and depression based on a comprehensive cross-sectional dataset with broad population representation. Second, we explored the mediating effect of the inflammatory index SIRI between CUN-BAE and depression, which provides new evidence to support the correlation between obesity and depression. The research does have a few limitations, though. First, we were unable to establish a causal correlation between the CUN-BAE index and depression because of the cross-sectional study design. Second, this study included a population from the United States only, and additional investigation is required to ascertain whether the results are transferable to other demographics and geographical areas. Third, although our findings suggest that SIRI may play a mediating role in the association between CUN-BAE and depression, the complex interrelationships among depression, inflammation, and adiposity mean that reverse or bidirectional associations among these three variables cannot be ruled out. Future longitudinal and mechanistic studies are warranted to further clarify their underlying relationships. Finally, although we adjusted for several covariates, we were unable to account for all potential factors, such as dietary supplement use, due to data limitations and complexity.
5. Conclusion
In conclusion, we illustrated that the CUN-BAE index was significantly and positively linked to the risk of depression, and SIRI had a mediating role between the two. This suggests that the level of CUN-BAE could be a potential indicator for assessing an individual’s risk of developing depression. Monitoring body fat and inflammation levels might be useful for early recognition of individuals potentially at risk for depression.
References
- 1. Baryshnikov I, Isometsä E. Psychological pain and suicidal behavior: A review. Front Psychiatry. 2022;13:981353. pmid:36203837
- 2. Monroe SM, Harkness KL. Major Depression and Its Recurrences: Life Course Matters. Annu Rev Clin Psychol. 2022;18:329–57. pmid:35216520
- 3. Lu B, Lin L, Su X. Global burden of depression or depressive symptoms in children and adolescents: A systematic review and meta-analysis. J Affect Disord. 2024;354:553–62. pmid:38490591
- 4. Abdoli N, Salari N, Darvishi N, Jafarpour S, Solaymani M, Mohammadi M, et al. The global prevalence of major depressive disorder (MDD) among the elderly: A systematic review and meta-analysis. Neurosci Biobehav Rev. 2022;132:1067–73. pmid:34742925
- 5. Walter E, Traunfellner M, Gleitsmann M, Zalesak M, Helmenstein C. The cost-of-illness and burden-of-disease of treatment-resistant depression in Austria. J Med Econ. 2023;26(1):1432–44. pmid:37768864
- 6. Cuijpers P, Quero S, Dowrick C, Arroll B. Psychological Treatment of Depression in Primary Care: Recent Developments. Curr Psychiatry Rep. 2019;21(12):129. pmid:31760505
- 7. Dubovsky SL, Ghosh BM, Serotte JC, Cranwell V. Psychotic Depression: Diagnosis, Differential Diagnosis, and Treatment. Psychother Psychosom. 2021;90(3):160–77. pmid:33166960
- 8. Fulton S, Décarie-Spain L, Fioramonti X, Guiard B, Nakajima S. The menace of obesity to depression and anxiety prevalence. Trends Endocrinol Metab. 2022;33(1):18–35. pmid:34750064
- 9. Milaneschi Y, Simmons WK, van Rossum EFC, Penninx BW. Depression and obesity: evidence of shared biological mechanisms. Mol Psychiatry. 2019;24(1):18–33. pmid:29453413
- 10. Gerardo G, Peterson N, Goodpaster K, Heinberg L. Depression and Obesity. Curr Obes Rep. 2025;14(1):5. pmid:39752052
- 11. Steptoe A, Frank P. Obesity and psychological distress. Philos Trans R Soc Lond B Biol Sci. 2023;378(1888):20220225. pmid:37661745
- 12. Kurhe Y, Mahesh R. Mechanisms linking depression co-morbid with obesity: An approach for serotonergic type 3 receptor antagonist as novel therapeutic intervention. Asian J Psychiatr. 2015;17:3–9. pmid:26243683
- 13. Gómez-Ambrosi J, Silva C, Catalán V, Rodríguez A, Galofré JC, Escalada J, et al. Clinical usefulness of a new equation for estimating body fat. Diabetes Care. 2012;35(2):383–8. pmid:22179957
- 14. Li X, Huan J, Lin L, Hu Y. Association of systemic inflammatory biomarkers with depression risk: Results from National Health and Nutrition Examination Survey 2005-2018 analyses. Front Psychiatry. 2023;14:1097196. pmid:36846218
- 15. Wolffenbuttel BHR, Heiner-Fokkema MR, Green R, Gans ROB. Relationship between serum B12 concentrations and mortality: experience in NHANES. BMC Med. 2020;18(1):307. pmid:33032595
- 16. Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001;16(9):606–13. pmid:11556941
- 17. Ba DM, Gao X, Al-Shaar L, Muscat JE, Chinchilli VM, Beelman RB, et al. Mushroom intake and depression: A population-based study using data from the US National Health and Nutrition Examination Survey (NHANES), 2005-2016. J Affect Disord. 2021;294:686–92.
- 18. Kuznik A, Mardekian J. Trends in utilization of lipid- and blood pressure-lowering agents and goal attainment among the U.S. diabetic population, 1999-2008. Cardiovasc Diabetol. 2011;10:31.
- 19. Peng Q, Feng Z, Cai Z, Liu D, Zhong J, Zhao H, et al. The relationship between the CUN-BAE body fatness index and incident diabetes: a longitudinal retrospective study. Lipids Health Dis. 2023;22(1):21. pmid:36747216
- 20. Lu Y, Lu C, Luo Z, Chen P, Xiong H, Li W. Association between the systemic inflammatory response index and mortality in patients with sarcopenia. PLoS One. 2024;19(11):e0312383. pmid:39556533
- 21. Shi L, Zhang L, Zhang D, Chen Z. Association between systemic immune-inflammation index and low muscle mass in US adults: a cross-sectional study. BMC Public Health. 2023;23(1):1416. pmid:37488531
- 22. Xu L, Lin X, Zhou T, Liu Y, Ge S. High cotinine levels as an associated factor with frailty status in older adults: evidence from the NHANES study. BMC Geriatr. 2024;24(1):894. pmid:39478478
- 23. Liu B, Wang J, Li Y-Y, Li K-P, Zhang Q. The association between systemic immune-inflammation index and rheumatoid arthritis: evidence from NHANES 1999-2018. Arthritis Res Ther. 2023;25(1):34. pmid:36871051
- 24. Ni J, Lv L, Wu P, Xu C. Associations between the platelet/high-density lipoprotein cholesterol ratio and likelihood of nephrolithiasis: a cross-sectional analysis in United States adults. Front Endocrinol (Lausanne). 2024;15:1289553. pmid:38449847
- 25. Xie R, Xiao M, Li L, Ma N, Liu M, Huang X, et al. Association between SII and hepatic steatosis and liver fibrosis: A population-based study. Front Immunol. 2022;13:925690. pmid:36189280
- 26. Ren Z, Xue Y, Zhang H, Zhang T, Wang M, Guo T, et al. Association between probiotic consumption and periodontitis: Evidence from NHANES 2009-2014. J Clin Periodontol. 2023;50(11):1476–86. pmid:37596796
- 27. Wang J, Wang Y, Li S, Wu B, Feng Q, Qiu W, et al. Waist-to-weight index and cognitive impairment: Understanding the link through depression mediation in the NHANES. J Affect Disord. 2024;365:313–20. pmid:39147151
- 28. Liu H, Dong H, Zhou Y, Jin M, Hao H, Yuan Y, et al. The association between Metabolic Score for Visceral Fat and depression in overweight or obese individuals: evidence from NHANES. Front Endocrinol (Lausanne). 2024;15:1482003. pmid:39391878
- 29. Nong Y, Wu G, Lu J, Wei X, Yu D. The mediating role of obesity in the development of depression in individuals with diabetes: A population-based study from NHANES 2005-2014. J Affect Disord. 2024;351:977–82. pmid:38355056
- 30. Vinknes KJ, Nurk E, Tell GS, Sulo G, Refsum H, Elshorbagy AK. The relation of CUN-BAE index and BMI with body fat, cardiovascular events and diabetes during a 6-year follow-up: the Hordaland Health Study. Clin Epidemiol. 2017;9:555–66. pmid:29184445
- 31. Martín V, Dávila-Batista V, Castilla J, Godoy P, Delgado-Rodríguez M, Soldevila N, et al. Comparison of body mass index (BMI) with the CUN-BAE body adiposity estimator in the prediction of hypertension and type 2 diabetes. BMC Public Health. 2016;16:82. pmid:26817835
- 32. Esser N, L’homme L, De Roover A, Kohnen L, Scheen AJ, Moutschen M, et al. Obesity phenotype is related to NLRP3 inflammasome activity and immunological profile of visceral adipose tissue. Diabetologia. 2013;56(11):2487–97. pmid:24013717
- 33. Ruiz NAL, Del Ángel DS, Olguín HJ, Silva ML. Neuroprogression: the hidden mechanism of depression. Neuropsychiatr Dis Treat. 2018;14:2837–45. pmid:30464468
- 34. Thorup L, Zulfikari M, Sørensen CLB, Biering K. Body image and depressive symptoms in Danish adolescents: A cross-sectional national study. J Affect Disord. 2024;365:65–72. pmid:39153549
- 35. Kawai T, Autieri MV, Scalia R. Adipose tissue inflammation and metabolic dysfunction in obesity. Am J Physiol Cell Physiol. 2021;320(3):C375–91. pmid:33356944
- 36. Schleh MW, Caslin HL, Garcia JN, Mashayekhi M, Srivastava G, Bradley AB, et al. Metaflammation in obesity and its therapeutic targeting. Sci Transl Med. 2023;15(723):eadf9382. pmid:37992150
- 37. Beurel E, Toups M, Nemeroff CB. The Bidirectional Relationship of Depression and Inflammation: Double Trouble. Neuron. 2020;107(2):234–56. pmid:32553197
- 38. Calagua-Bedoya EA, Rajasekaran V, De Witte L, Perez-Rodriguez MM. The Role of Inflammation in Depression and Beyond: A Primer for Clinicians. Curr Psychiatry Rep. 2024;26(10):514–29. pmid:39187612
- 39. Ly M, Yu GZ, Mian A, Cramer A, Meysami S, Merrill DA, et al. Neuroinflammation: A Modifiable Pathway Linking Obesity, Alzheimer’s disease, and Depression. Am J Geriatr Psychiatry. 2023;31(10):853–66. pmid:37365110
- 40. Taylor EB. The complex role of adipokines in obesity, inflammation, and autoimmunity. Clin Sci (Lond). 2021;135(6):731–52. pmid:33729498
- 41. Leonard BE. Impact of inflammation on neurotransmitter changes in major depression: an insight into the action of antidepressants. Prog Neuropsychopharmacol Biol Psychiatry. 2014;48:261–7. pmid:24189118