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. 2025 Aug 16;25:2793. doi: 10.1186/s12889-025-24096-y

Associations of indoor musty odors with depression and anxiety symptoms in Chinese older adults: a nationwide study

Xue Wang 1, Zhihua Yin 2, Qian Gao 3, Yunfeng Song 4, Hanchen Xu 1, Shuang Zang 1,
PMCID: PMC12357380  PMID: 40819072

Abstract

Background

Indoor air pollution has been recognized as a risk factor for mental health, particularly depression and anxiety symptoms. Indoor musty odors are considered a component of indoor air pollution. However, evidence on the associations between indoor musty odors and mental health among older adults is limited.

Methods

The current study utilized data from the Chinese Longitudinal Healthy Longevity Survey (CLHLS). We employed self-reported data to ascertain indoor musty odors. Depression symptoms were evaluated utilizing the Center for Epidemiologic Studies Depression Scale-10 (CES-D-10), and anxiety symptoms were measured using the Generalized Anxiety Disorder Scale-7 (GAD-7). This study implemented logistic regression and linear regression to examine the associations of indoor musty odors with depression and anxiety symptoms.

Results

A total of 11,950 older adults (mean age = 83.11 ± 11.12 years) were included in this study. The study indicated that indoor musty odors were significantly associated with depression symptoms (adjusted odds ratio (OR) 1.83, 95% CI 1.58, 2.11) and anxiety symptoms (adjusted OR 2.12, 95% CI 1.78, 2.53).

Conclusions

These findings provide valuable insights of indoor musty odors into the potential health risks associated with older adults’ depression and anxiety symptoms.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12889-025-24096-y.

Keywords: Musty odors, Depression symptoms, Anxiety symptoms, Older adults

Introduction

Healthy aging is a critical issue that has garnered significant attention globally due to the demographic challenges posed by the aging population [1]. China is the country with the largest aging population, which has also raised concerns about the health of older adults [2]. Mental health has been consistently recognized as a crucial concern among the various health issues encountered by the age population, with depression and anxiety being pervasive and commonly encountered problems [3].

According to global statistics, the prevalence of depression and anxiety in older adults is approximately 7.0% and 3.8%, respectively [4]. However, this prevalence in China is higher than the global average. Specifically, evidence has revealed that this prevalence among older adults in China was 23.6% and 24.6%, respectively [5, 6]. Depression and anxiety issues among older adults in China deserve special attention. Numerous studies have indicated that depression and anxiety are associated with a range of negative physical outcomes in older adults, including insomnia [7], malnutrition [8], decreased immune function [9], cognitive decline [10], and exacerbation of cardiovascular diseases [11]. These disorders can also weaken older adults’ self-esteem [12], self-efficacy [13], and social support [14], leading to feelings of loneliness [15] and social isolation [16]. Furthermore, they can adversely affect older adults’ overall sense of well-being [17] and quality of life [18]. Given the high prevalence of depression and anxiety and their significant burdens on older adults, it is imperative to comprehend the factors associated with these mental health disorders to prevent their occurrence.

The mental disorders of depression and anxiety are complex and associated with multiple factors, such as sociodemographic factors [19], socioeconomic status [20], lifestyle behaviors [21], health status [22], and social support [23]. In addition, multiple studies have confirmed that depression and anxiety are also associated with environmental factors, including exposure to outdoor and indoor air pollution [2426]. Musty odors are a common problem in indoor environments and are caused by the presence of mold and dampness [27].

Mold exposure has been associated with physical symptoms such as allergic reactions [28], respiratory problems [29], and neurological symptoms [30], but these studies have primarily focused on physical health outcomes, and research on the impact of mold or musty odors on the mental health of older adults remains limited. Existing evidence suggests that exposure to indoor musty odors constitutes a chronic psychological stressor, potentially contributing to the onset and worsening of mental health problems [31]. Several studies have indicated that indoor mold exposure may lead to mood disturbances [32] and attention deficits [33].

However, there is a notable scarcity of research investigating the associations between indoor musty odors and depression or anxiety, especially among older adults who spend substantial time indoors and are particularly vulnerable to adverse health effects from indoor environmental toxins. Importantly, most previous research has been conducted in specific regions outside China [34, 35], with limited generalizability to the Chinese context. Given China’s large aging population and unique environmental and cultural factors influencing indoor living conditions [36, 37], nationally representative data are essential to understand these associations within this context.

Therefore, the present study seeks to address this gap by examining the relationships between indoor musty odors and depression and anxiety symptoms in a large, nationally representative sample of Chinese older adults, providing valuable insights for targeted public health interventions.

Methods

Study population

The Chinese Longitudinal Healthy Longevity Survey (CLHLS) is a countrywide community-based, longitudinal investigation intended to study the health condition and determinants impacting longevity in the older population in China. The CLHLS initiated its baseline survey in 1998 and subsequently conducted follow-up surveys biennially or triennially. The CLHLS was carried out in a randomly selected half of the counties and cities within 23 out of the 31 provinces/municipalities in China, spanning over 85% of the Chinese population. The CLHLS used a multistage stratified cluster sampling design to select its sample. The first stage involved selecting counties/districts within each province/municipality based on their economic development level and geographic location. The second stage involved selecting communities within each county/district using probability proportional to size sampling. The third stage involved selecting households within each community using a combination of random and systematic sampling methods. Finally, all eligible individuals within selected households were asked to participate in the survey. The survey utilized a face-to-face interview method to collect data from participants, and interviews were conducted by trained survey staff who visited participants in their homes. The CLHLS employed rigorous quality control procedures to ensure the validity and reliability of the gathered data. These procedures included pretesting of survey instruments, training of survey staff, and regular monitoring of data quality [38].

This study utilized data from the 2018 wave of the CLHLS, which collected information from 15,874 participants through face-to-face interviews. We excluded those younger than 60 years old (n = 12), and those with missing data on indoor musty odors (n = 706), depressive symptoms (n = 3,136), or anxiety symptoms (n = 70). Only participants with complete and matched information on both exposure (indoor musty odors) and outcomes (depressive and anxiety symptoms) were retained, resulting in a final analytical sample of 11,950 individuals (Fig. 1). All data were collected within the same wave and survey interview session, ensuring consistency and alignment across variables.

Fig. 1.

Fig. 1

Flow chart of inclusion of participants from the Chinese Longitudinal Healthy Longevity Survey

The CLHLS received ethical approval from the Biomedical Ethics Committee of Peking University (IRB00001052-13074). All participants provided written informed consent before completing the survey. Our study was conducted in accordance with the WMA Declaration of Helsinki–Ethical Principles for Medical Research Involving Human Subjects.

Indoor musty odors

Indoor musty odors were evaluated utilizing the question, “Do you frequently smell musty odors within your indoor environment?” Response to indoor musty odors was categorized as no or yes.

Outcomes

The Center for Epidemiologic Studies Depression Scale-10 (CES-D-10) is used to evaluate participants’ depression symptoms [39]. Each item is scored on a 4-point scale of 0–3, ranging from “less than 1 day” to “5–7 days”. Summed scores on the CES-D-10 range from 0 to 30, with higher scores representing greater severity of the depression symptom. Following prior studies [40, 41], depression symptoms are defined with a cut-off score of 10 and above on the CES-D-10. The Cronbach’s α for the CES-D-10 of this study was 0.736.

The Generalized Anxiety Disorder Scale-7 (GAD-7) is used to measure participants’ anxiety symptoms [42]. Each item is scored on a 4-point scale of 0–3, ranging from “never” to “almost every day”. Summed scores on the GAD-7 range from 0 to 21, with higher scores indicating greater severity of the anxiety symptom. Following prior studies [43, 44], anxiety symptoms are defined with a cut-off score of 5 and above on the GAD-7. The Cronbach’s α for the GAD-7 of this study was 0.919.

Covariates

Based on previous studies [45, 46], we considered multiple potential confounding variables, including age (continuous variable), gender (male vs. female), urban‒rural distribution (urban vs. rural), education level (illiterate, primary school, and high school and above), having a spouse (no vs. yes), smoking status (no vs. yes), drinking alcohol (no vs. yes), living alone (no vs. yes), having chronic diseases (no vs. yes), regular exercise (no vs. yes), body mass index (continuous variable), fuel choice (clean fuel vs. solid fuel), indoor ventilation (no vs. yes), using air purification devices (no vs. yes), distance to the major roadway (≤ 100 m, 101–300 m, and > 300 m), annual household income (< 10,000 yuan, 10,000–50,000 yuan, and > 50,000 yuan), and cognitive impairment (absence vs. presence).

The Chinese Mini-Mental State Examination (CMMSE) is used to assess participants’ cognitive function [47]. The CMMSE consists of 24 items covering 7 cognitive domains: orientation, registration, naming foods, attention and calculation, copying a figure, recalling, and language. Summed scores on the CMMSE range from 0 to 30, with higher scores indicating better cognitive function. Following prior studies [48, 49], cognitive impairment is defined with a cut-off score of less than 18 on the CMMSE. The Cronbach’s α for the MMSE of this study was 0.865.

Statistical analysis

First, the Kolmogorov‒Smirnov test was applied to assess the normality of continuous variables. The continuous variables were approximately normally distributed based on the visual examination of Q-Q plots. The descriptive statistics for continuous variables were reported as the mean and standard deviation (SD), while categorical variables were presented as numbers and percentages. The chi-squared test was conducted to compare the categorical variables, while variance analysis was employed to compare the continuous variables. Second, we utilized multivariable logistic regression models to examine the potential associations between indoor musty odors and depression and anxiety symptoms. We also employed multiple linear models to assess the associations of indoor musty odors with depression and anxiety symptom scores. In each analysis, three models were employed: Model 1 without covariate adjustment, Model 2 adjusting for age and gender, and Model 3 adjusting for all covariates. Third, we performed stratified and interaction analyses based on categorical variables to evaluate potential effect modifications.

We also performed three sensitivity analyses. First, we conducted multiple imputations via chained equations to account for missing data. Second, we excluded participants with cognitive impairment (n = 1,220), as they may have been subject to substantial recall bias when reporting information. Third, we calculated E-values to assess the likelihood that unmeasured confounders could explain our results [50].

A two-tailed P value < 0.05 indicated statistical significance. All statistical analyses in this study were conducted using Stata version 16.0 (StataCorp, College Station, TX, USA).

Results

Characteristics of participants

Among the participants, 10,355 participants reported that their indoors had no musty odors, and the remaining 1595 participants reported that their indoors had musty odors. The participants had a mean age of 83.11 years. Participants who reported indoor musty odors had higher mean scores for depression and anxiety symptoms than those who reported the absence of indoor musty odors. Participants reporting indoor musty odors tended to have a lower education level, live in rural areas, exercise irregularly, and be without indoor ventilation than those not reporting indoor musty odors (Table 1).

Table 1.

Characteristics of the study population

Characteristic Total Indoor had no musty odors Indoor had musty odors P value
N 11,950 10,355 1595
CES-D-10 scores, mean (SD) 7.33 (4.42) 7.07 (4.25) 9.08 (5.12) < 0.001
Depression symptoms, n (%) < 0.001
 Absence 8738 (73.12) 7795 (75.28) 943 (59.12)
 Presence 3212 (26.88) 2560 (24.72) 652 (40.88)
GAD-7 scores, mean (SD) 1.39 (2.73) 1.24 (2.54) 2.33 (3.56) < 0.001
Anxiety symptoms, n (%) < 0.001
 Absence 10,548 (88.27) 9289 (89.71) 1259 (78.93)
 Presence 1402 (11.73) 1066 (10.29) 336 (21.07)
Age (years), mean (SD) 83.11 (11.12) 83.16 (11.15) 82.78 (10.91) 0.249
Gender, n (%) 0.777
 Male 5591 (46.79) 4850 (46.84) 741 (46.46)
 Female 6359 (53.21) 5505 (53.16) 854 (53.54)
Urban–rural distribution, n (%) 0.009
 Urban 6617 (55.37) 5782 (55.84) 835 (52.35)
 Rural 5333 (44.63) 4573 (44.16) 760 (47.65)
Education level, n (%) < 0.001
 Illiterate 4536 (44.40) 3825 (43.23) 711 (51.90)
 Primary school 3516 (34.41) 3066 (34.66) 450 (32.85)
 High school and above 2165 (21.19) 1956 (22.11) 209 (15.26)
Had a spouse, n (%) 0.760
 No 6160 (52.07) 5343 (52.12) 817 (51.71)
 Yes 5671 (47.93) 4908 (47.88) 763 (48.29)
Smoking status, n (%) 0.013
 No 9880 (83.49) 8596 (83.82) 1284 (81.32)
 Yes 1954 (16.51) 1659 (16.18) 295 (18.68)
Drinking alcohol, n (%) 0.830
 No 9912 (84.30) 8588 (84.33) 1324 (84.12)
 Yes 1846 (15.70) 1596 (15.67) 250 (15.88)
Lived alone, n (%) < 0.001
 No 9753 (82.79) 8545 (83.77) 1208 (76.41)
 Yes 2028 (17.21) 1655 (16.23) 373 (23.59)
Chronic diseases, n (%) < 0.001
 No 3558 (29.77) 3142 (30.34) 416 (26.08)
 Yes 8392 (70.23) 7213 (69.66) 1179 (73.92)
Regular exercise, n (%) < 0.001
 No 7721 (65.53) 6613 (64.81) 1108 (70.22)
 Yes 4061 (34.47) 3591 (35.19) 470 (29.78)
Body mass index (kg/m2), mean (SD) 22.53 (3.87) 22.58 (3.86) 22.22 (3.92) < 0.001
Fuel choice, n (%) < 0.001
 Clean fuel 8600 (73.29) 7654 (75.19) 946 (60.84)
 Solid fuel 3135 (26.71) 2526 (24.81) 609 (39.16)
Indoor ventilation, n (%) < 0.001
 No 1061 (8.93) 747 (7.26) 314 (19.82)
 Yes 10,815 (91.07) 9545 (92.74) 1270 (80.18)
Used air purification devices, n (%) 0.019
 No 10,918 (91.83) 9435 (91.59) 1483 (93.33)
 Yes 972 (8.17) 866 (8.41) 106 (6.67)
Distance to the major roadway (meters), n (%) 0.192
 ≤ 100 3796 (34.14) 3304 (34.23) 492 (33.56)
 101–300 2227 (20.03) 1954 (20.24) 273 (18.62)
 > 300 5095 (45.83) 4394 (45.52) 701 (47.82)
Annual household income (yuan), n (%) < 0.001
 < 10,000 5086 (46.38) 4184 (43.94) 902 (62.38)
 10,000–50,000 2273 (20.73) 2037 (21.39) 236 (16.32)
 > 50,000 3608 (32.90) 3300 (34.66) 308 (21.30)
Cognitive impairment, n (%) 0.001
 Absence 10,730 (89.79) 9334 (90.14) 1396 (87.52)
 Presence 1220 (10.21) 1021 (9.86) 199 (12.48)

Total percentages within categories may not equal 100% due to rounding. Continuous variables are presented as mean (standard deviation); categorical variables are presented as counts (percentages). Group comparisons were conducted using independent t-tests for continuous variables and chi-square tests for categorical variables

Association of indoor musty odors with depression symptoms

In unadjusted logistic regression analysis, there was a significant association between indoor musty odors and depression symptoms (odds ratio (OR): 2.11, 95% confidence interval (CI): 1.89, 2.35). After adjusting for the covariates of age and gender in the logistic regression analysis, the association remained consistent in terms of direction but was enhanced in terms of magnitude (OR: 2.14, 95% CI: 1.92, 2.39). This association was attenuated but persisted with statistical significance in the fully adjusted logistic regression analysis (OR: 1.83, 95% CI: 1.58, 2.11). The results of the unadjusted linear regression analysis indicated a significant association between indoor musty odors and depression symptom scores compared to no indoor musty odors (coefficient (β): 2.01, 95% CI: 1.78, 2.24). After adjusting for the covariates of age and gender in the linear regression analysis, the association remained consistent in terms of direction but was enhanced in terms of magnitude (β: 2.02, 95% CI: 1.79, 2.25). This association was attenuated but persisted with statistical significance in the fully adjusted linear regression analysis (β: 1.67, 95% CI: 1.39, 1.94) (Table 2).

Table 2.

Association of indoor musty odors with depression symptoms

Model Indoor had no musty odors Indoor had musty odors P value
Logistic regression, odds ratio of depression symptoms (95% CI)
Model 1 Reference 2.11 (1.89, 2.35) < 0.001
Model 2 Reference 2.14 (1.92, 2.39) < 0.001
Model 3 Reference 1.83 (1.58, 2.11) < 0.001
Linear regression, coefficient for depression symptom scores (95% CI)
Model 1 Reference 2.01 (1.78, 2.24) < 0.001
Model 2 Reference 2.02 (1.79, 2.25) < 0.001
Model 3 Reference 1.67 (1.39, 1.94) < 0.001

Model 1 was unadjusted

Model 2 was adjusted for age and gender

Model 3 was adjusted for age, gender, urban–rural distribution, education level, whether having a spouse, smoking status, drinking alcohol, whether living alone, whether having chronic diseases, regular exercise, body mass index, fuel choice, indoor ventilation, whether using air purification devices, distance to the major roadway, annual household income, and cognitive impairment

Association of indoor musty odors with anxiety symptoms

The unadjusted logistic regression analysis showed a significant association between indoor musty odors and anxiety symptoms, with an OR of 2.33 (95% CI: 2.03, 2.66). Adjusting for age and gender in the logistic regression analysis strengthened the association between indoor musty odors and anxiety symptoms in terms of magnitude while maintaining its direction (OR: 2.34, 95% CI: 2.04, 2.68). After controlling for all potential confounders, the association remained significant (OR: 2.12, 95% CI: 1.78, 2.53). The unadjusted linear regression analysis showed a significant association between indoor musty odors and anxiety symptom scores (β: 1.09, 95% CI: 0.95, 1.23). After adjustment for age and gender, the magnitude and direction of this association remained consistent (β: 1.09, 95% CI: 0.94, 1.23). This association was attenuated but remained statistically significant in the fully adjusted linear regression analysis (β: 0.92, 95% CI: 0.74, 1.09) (Table 3).

Table 3.

Association of indoor musty odors with anxiety symptoms

Model Indoor had no musty odors Indoor had musty odors P value
Logistic regression, odds ratio of anxiety symptoms (95% CI)
Model 1 Reference 2.33 (2.03, 2.66) < 0.001
Model 2 Reference 2.34 (2.04, 2.68) < 0.001
Model 3 Reference 2.12 (1.78, 2.53) < 0.001
Linear regression, coefficient for anxiety symptom scores (95% CI)
Model 1 Reference 1.09 (0.95, 1.23) < 0.001
Model 2 Reference 1.09 (0.94, 1.23) < 0.001
Model 3 Reference 0.92 (0.74, 1.09) < 0.001

Model 1 was unadjusted

Model 2 was adjusted for age and gender

Model 3 was adjusted for age, gender, urban–rural distribution, education level, whether having a spouse, smoking status, drinking alcohol, whether living alone, whether having chronic diseases, regular exercise, body mass index, fuel choice, indoor ventilation, whether using air purification devices, distance to the major roadway, annual household income, and cognitive impairment

Stratified and interaction analyses

The results of stratified analyses by categorical variables (gender, urban‒rural distribution, education level, having a spouse, smoking status, drinking alcohol, living alone, having chronic diseases, regular exercise, fuel choice, indoor ventilation, using air purification devices, distance to the major roadway, annual household income, and cognitive impairment) are shown in Supplementary Table 1 (dependent variables are categorical variables) and 2 (dependent variables are continuous variables). The associations of indoor musty odors with depression and anxiety symptoms were generally persistent in these subgroups. The interaction results showed that the distance to the major roadway and annual household income had significant interactions with indoor musty odors on depression symptoms or depression symptom scores (P interaction < 0.05). Using air purification devices had significant interactions with indoor musty odors on anxiety symptoms or anxiety symptom scores (P interaction < 0.05).

Sensitivity analyses

In the first sensitivity analysis, we imputed the key covariates that participants were missing. The results remained consistent (all P < 0.05) (Supplementary Tables 3 and 4). In the second sensitivity analysis, we assessed the impact of excluding participants with cognitive impairment. For all analyses, the exclusion of participants with cognitive impairment did not change the statistical significance of the associations (all P < 0.05) (Supplementary Tables 5 and 6). In the third sensitivity analysis, we generated the E-values to assess the sensitivity to unmeasured confounding factors. The E-values of this study were 3.06, 2.92, 3.66, and 3.06 for depression symptoms, depression symptom scores, anxiety symptoms, and anxiety symptom scores, respectively. Based on the E-values, unmeasured confounding is unlikely to fully explain our results.

Discussion

To our knowledge, this population-based study is the first to explore the associations of indoor musty odors with depression and anxiety symptoms among older adults in China. The results revealed a significant association of indoor musty odors with depression and anxiety symptoms among older adults.

Our findings support earlier studies that have found an association between indoor mold and depression symptoms. A study by Shenassa et al. [51] demonstrated an association of mold with depression symptoms, independent of demographic or housing-related variables. Two studies employing a combination of subjective and objective measures to evaluate mold and dampness observed significant associations with depression and self-reported emotional distress [52, 53]. Hopton et al. have identified independent associations between inhabiting damp and mold-infested housing and mental distress [54]. In addition, a study from England also found that mold and dampness were associated with depression symptoms [34]. As visible mold is not exactly equal to musty smell. Our findings contribute to the extant evidence demonstrating the association of indoor mold with depression symptoms from the perspective of smell.

Our findings showed an association of indoor musty odors with anxiety symptoms among older adults in China. This result was consistent with the findings of prior studies that had shown an association of exposure to indoor molds with mental health, including anxiety-like behavior [35]. Several studies have also shown an association between spending time in moldy buildings and self-reported anxiety symptoms [55, 56]. The findings of this study add to the growing body of evidence highlighting the importance of indoor air quality and its potential association with mental health, particularly among older adults. The negative association between indoor musty odors and anxiety symptoms suggests that exposure to indoor molds may have significant implications for the mental health of older adults. The results of the interaction also showed that distance to the major road and using air purification devices had interactions with indoor musty odors on depression or anxiety symptoms. Residential properties located near main roads are typically exposed to higher levels of pollution resulting from traffic, which can impede the airflow inside buildings and reduce indoor ventilation [57]. Additionally, the noise pollution caused by traffic may lead residents to close their windows or install sealed windows and doors to mitigate noise disturbances, further limiting indoor air circulation [58]. Considering these findings, it is important to prioritize interventions aimed at improving indoor air quality, particularly in settings where older adults tend to allocate substantial portions of their time, such as long-term care facilities and residential homes. Such interventions may include the use of air purifiers, improved ventilation systems, and regular maintenance and cleaning to prevent the growth of indoor molds and other pollutants.

Several biological mechanisms have been postulated to elucidate the underlying reasons and mechanisms through which exposure to indoor musty odors may be associated with the development of depression and anxiety symptoms. One potential mechanism is the impact of indoor air pollutants on the immune system. Exposure to mold and other indoor air pollutants may induce an inflammatory response in the body, leading to the production of cytokines that have been linked to the development of depression and anxiety symptoms [59, 60]. In addition, indoor musty odors may also affect the neuroendocrine system, leading to alterations in the levels of stress hormones such as cortisol and norepinephrine. Elevated levels of these hormones have been associated with the development of anxiety and depression [61, 62]. Furthermore, exposure to indoor air pollutants may lead to oxidative stress, which has also been implicated in the pathophysiology of depression and anxiety [63, 64]. Another possible mechanism is the impact of indoor air quality on the respiratory system. Exposure to indoor musty odors and other pollutants may exacerbate respiratory symptoms and allergies, which have been associated with the development of depression and anxiety symptoms [65, 66]. Additionally, poor indoor air quality may contribute to sleep disturbances, which have also been linked to the development of mood disorders [67, 68]. It is noteworthy that the biological mechanisms underlying the association between indoor musty odors and depression and anxiety symptoms are likely multifaceted and complex. Future research is warranted to enhance comprehension of the specific pathways through which indoor air pollutants may be associated with mental health outcomes and to identify effective interventions to reduce exposure to indoor pollutants and promote healthy aging.

Prior studies have found that unpleasant odors may be associated with depression and anxiety symptoms [69, 70], which further supports our findings. Neuroscientific research has indicated that there is a close association between the olfactory system and emotional regulation [71]. Unpleasant odors can activate the emotional center, inducing negative emotional reactions such as sadness and anxiety [72]. Additionally, there is a strong connection between the olfactory system and memory [73], and unpleasant odors may trigger unpleasant memories, thereby increasing emotional burden [74]. Therefore, when individuals are exposed to an unpleasant odor environment, it may induce depressive and anxious emotional reactions. These findings underscore the necessity of more closely attending to the influence of unpleasant odors on human mental health and shed light on the need to better manage our living environments to avoid exposure to unpleasant odors, which can further help maintain individual mental health.

Several limitations of this study require acknowledgement. First, the cross-sectional design limits causal inference. Although indoor musty odor exposure and both depression and anxiety symptoms were assessed concurrently in the 2018 CLHLS, the only wave that included anxiety assessment, this limits our ability to examine temporal or cumulative exposure effects. Prior research has demonstrated that environmental exposures, including ambient air pollution, may exert delayed or cumulative effects on health outcomes across extended timeframes [75]. Future research with multi-wave exposure and outcome assessments is warranted to clarify causal relationships and better capture potential long-term impacts. Second, this study used depression and anxiety screening tools (i.e., the CES-D-10 and GAD-7 scales) to assess symptoms instead of employing clinical diagnostic interviews. Third, exposure to indoor musty odors was assessed through self-reported data, which may be subject to multiple sources of bias. Specifically, the perception of musty odors may be influenced by participants’ individual olfactory sensitivity and cognitive function, particularly among older adults. Although we adjusted for age and cognitive impairment in our models and conducted a sensitivity analysis excluding individuals with cognitive impairment, residual bias cannot be fully excluded. Fourth, unlike pollutants such as PM2.5 or NO₂, indoor musty odors are difficult to quantify objectively, and our dataset lacked information on important exposure-related variables such as the duration of musty odor exposure and length of residence. As a result, we were unable to assess potential dose-response relationships or cumulative exposure. This limitation underscores the need for future studies to incorporate objective environmental monitoring and more detailed exposure assessments. Finally, although E-value analysis suggested that unmeasured confounding was unlikely to fully account for our findings, the possibility of residual bias cannot be entirely ruled out.

Conclusions

The results of this study demonstrate associations of indoor musty odors with elevated risks of experiencing symptoms of depression and anxiety. These findings supplement the expanding corpus of evidence highlighting the importance of indoor environmental quality in maintaining mental health, specifically emphasizing the need to safeguard older adults from experiencing symptoms of depression and anxiety arising from exposure to indoor air pollution. This study provides support for the national blueprint of ecological civilization and strategic preparations for an aging society.

Supplementary Information

Supplementary Material 1 (30.4KB, docx)

Acknowledgements

Not applicable.

Authors’ contributions

X.W. and S.Z. designed the study. X.W. controlled the quality of the data and performed statistical analysis. X.W., Z.Y., Q.G., Y.S., and S.Z. managed and checked all the data. X.W. wrote the main manuscript text. X.W. prepared figure 1. X.W., Z.Y., Q.G., Y.S., H.X., and S.Z. contributed to manuscript review. X.W., Z.Y., Q.G., Y.S., H.X., and S.Z. read, checked, and approved the final manuscript.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

Data availability

Publicly available datasets were analyzed in this study. This data can be found here: https://opendata.pku.edu.cn/dataverse/CHADS.

Declarations

Ethics approval and consent to participate

The CLHLS received ethical approval from the Biomedical Ethics Committee of Peking University (IRB00001052-13074). All participants provided written informed consent before completing the survey. Our study was conducted in accordance with the WMA Declaration of Helsinki–Ethical Principles for Medical Research Involving Human Subjects.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Gerland P, Hertog S, Wheldon M, et al. World Population Prospects 2022. Summary of Results; 2022. [Google Scholar]
  • 2.Chen X, Giles J, Yao Y, et al. The path to healthy ageing in China: a Peking University-Lancet commission. Lancet. 2022;400(10367):1967–2006. 10.1016/s0140-6736(22)01546-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Zhou M, Wang H, Zeng X, et al. Mortality, morbidity, and risk factors in China and its provinces, 1990–2017: a systematic analysis for the global burden of disease study 2017. Lancet. 2019;394(10204):1145–58. 10.1016/s0140-6736(19)30427-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Sorel E. The who world mental health surveys: global perspectives on the epidemiology of mental disorders. Am J Psychiatry. 2010;167:354–5. 10.1176/appi.ajp.2009.09081218. [Google Scholar]
  • 5.Li D, Zhang D-J, Shao J, et al. A meta-analysis of the prevalence of depressive symptoms in Chinese older adults. Arch Gerontol Geriatr. 2013;58. 10.1016/j.archger.2013.07.016. [DOI] [PubMed]
  • 6.Zhang X, Norton J, Carrière I, et al. Generalized anxiety in community-dwelling elderly: prevalence and clinical characteristics. J Affect Disord. 2015;172:24–9. 10.1016/j.jad.2014.09.036. [DOI] [PubMed] [Google Scholar]
  • 7.Brenes GA, Miller ME, Stanley MA, et al. Insomnia in older adults with generalized anxiety disorder. Am J Geriatr Psychiatry. 2009;17(6):465–72. 10.1097/jgp.0b013e3181987747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.O’Keeffe M, Kelly M, O’Herlihy E, et al. Potentially modifiable determinants of malnutrition in older adults: A systematic review. Clin Nutr. 2019;38(6):2477–98. 10.1016/j.clnu.2018.12.007. [DOI] [PubMed] [Google Scholar]
  • 9.Mwangala PN, Nasambu C, Wagner RG, et al. Prevalence and factors associated with mild depressive and anxiety symptoms in older adults living with HIV from the Kenyan Coast. J Int AIDS Soc. 2022;25(Suppl 4):e25977. 10.1002/jia2.25977. [DOI] [PMC free article] [PubMed]
  • 10.Johansson M, Stomrud E, Johansson PM, et al. Development of apathy, anxiety, and depression in cognitively unimpaired older adults: effects of Alzheimer’s disease pathology and cognitive decline. Biol Psychiatry. 2022;92(1):34–43. 10.1016/j.biopsych.2022.01.012. [DOI] [PubMed] [Google Scholar]
  • 11.Wu M, Zhu Y, Lv J, et al. Association of anxiety with cardiovascular disease in a Chinese cohort of 0.5 million adults. J Affect Disord. 2022;315:291–6. 10.1016/j.jad.2022.08.008. [DOI] [PubMed] [Google Scholar]
  • 12.van Tuijl LA, Bennik EC, Penninx B, et al. Predictive value of implicit and explicit Self-Esteem for the recurrence of depression and anxiety disorders: A 3-Year Follow-up study. J Abnorm Psychol. 2020;129(8):788–98. 10.1037/abn0000634. [DOI] [PubMed] [Google Scholar]
  • 13.Stanley MA, Novy DM, Hopko DR, et al. Measures of self-efficacy and optimism in older adults with generalized anxiety. Assessment. 2002;9(1):70–81. 10.1177/1073191102009001009. [DOI] [PubMed] [Google Scholar]
  • 14.Al-Dwaikat TN, Rababa M, Alaloul F. Relationship of stigmatization and social support with depression and anxiety among cognitively intact older adults. Heliyon. 2022;8(9):e10722. 10.1016/j.heliyon.2022.e10722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Steiner JF, Ross C, Stiefel M, et al. Association between changes in loneliness identified through screening and changes in depression or anxiety in older adults. J Am Geriatr Soc. 2022;70(12):3458–68. 10.1111/jgs.18012. [DOI] [PubMed] [Google Scholar]
  • 16.Robb CE, de Jager CA, Ahmadi-Abhari S, et al. Associations of social isolation with anxiety and depression during the early Covid-19 pandemic: A survey of older adults in london, Uk. Front Psychiatry. 2020;11:591120. 10.3389/fpsyt.2020.591120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Malone C, Wachholtz A. The relationship of anxiety and depression to subjective well-being in a mainland Chinese sample. J Relig Health. 2018;57(1):266–78. 10.1007/s10943-017-0447-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Ribeiro O, Teixeira L, Araújo L, et al. Anxiety, depression and quality of life in older adults: trajectories of influence across age. Int J Environ Res Public Health. 2020. 10.3390/ijerph17239039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Benke C, Autenrieth LK, Asselmann E, et al. Lockdown, quarantine measures, and social distancing: associations with depression, anxiety and distress at the beginning of the Covid-19 pandemic among adults from Germany. Psychiatry Res. 2020;293: 113462. 10.1016/j.psychres.2020.113462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Azizabadi Z, Aminisani N, Emamian MH. Socioeconomic inequality in depression and anxiety and its determinants in Iranian older adults. BMC Psychiatry. 2022;22(1):761. 10.1186/s12888-022-04433-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.De Boni RB, Balanzá-Martínez V, Mota JC, et al. Depression, anxiety, and lifestyle among essential workers: A web survey from Brazil and Spain during the Covid-19 pandemic. J Med Internet Res. 2020;22(10):e22835. 10.2196/22835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Samadoulougou S, Idzerda L, Letarte L, et al. Self-perceived health status among adults with obesity in Quebec: a cluster analysis. Ann Epidemiol. 2022;67:43–9. 10.1016/j.annepidem.2021.11.008. [DOI] [PubMed] [Google Scholar]
  • 23.Hutten E, Jongen EMM, Vos A, et al. Loneliness and mental health: the mediating effect of perceived social support. Int J Environ Res Public Health. 2021. 10.3390/ijerph182211963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Vert C, Sánchez-Benavides G, Martínez D, et al. Effect of long-term exposure to air pollution on anxiety and depression in adults: a cross-sectional study. Int J Hyg Environ Health. 2017;220(6):1074–80. 10.1016/j.ijheh.2017.06.009. [DOI] [PubMed] [Google Scholar]
  • 25.Pun VC, Manjourides J, Suh H. Association of ambient air pollution with depressive and anxiety symptoms in older adults: results from the Nshap study. Environ Health Perspect. 2017;125(3):342–8. 10.1289/ehp494. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Smith L, Veronese N, López Sánchez GF, et al. The association of cooking fuels with depression and anxiety symptoms among adults aged ≥ 65 years from low- and middle-income countries. J Affect Disord. 2022;311:494–9. 10.1016/j.jad.2022.05.103. [DOI] [PubMed] [Google Scholar]
  • 27.Crawford JA, Rosenbaum PF, Anagnost SE, et al. Indicators of airborne fungal concentrations in urban homes: understanding the conditions that affect indoor fungal exposures. Sci Total Environ. 2015;517:113–24. 10.1016/j.scitotenv.2015.02.060. [DOI] [PubMed] [Google Scholar]
  • 28.Sharpe RA, Thornton CR, Tyrrell J, et al. Variable risk of atopic disease due to indoor fungal exposure in NHANES 2005–2006. Clin Exp Allergy. 2015;45(10):1566–78. 10.1111/cea.12549. [DOI] [PubMed] [Google Scholar]
  • 29.Sharpe RA, Thornton CR, Nikolaou V, et al. Higher energy efficient homes are associated with increased risk of doctor diagnosed asthma in a UK subpopulation. Environ Int. 2015;75:234–44. 10.1016/j.envint.2014.11.017. [DOI] [PubMed] [Google Scholar]
  • 30.Zhang X, Norbäck D, Fan Q, et al. Dampness and mold in homes across china: associations with rhinitis, ocular, throat and dermal symptoms, headache and fatigue among adults. Indoor Air. 2019;29(1):30–42. 10.1111/ina.12517. [DOI] [PubMed] [Google Scholar]
  • 31.Azuma K, Ikeda K, Kagi N, et al. Effects of water-damaged homes after flooding: health status of the residents and the environmental risk factors. Int J Environ Health Res. 2014;24(2):158–75. 10.1080/09603123.2013.800964. [DOI] [PubMed] [Google Scholar]
  • 32.Ratnaseelan AM, Tsilioni I, Theoharides TC. Effects of mycotoxins on neuropsychiatric symptoms and immune processes. Clin Ther. 2018;40(6):903–17. 10.1016/j.clinthera.2018.05.004. [DOI] [PubMed] [Google Scholar]
  • 33.Casas L, Tiesler C, Thiering E, et al. Indoor factors and behavioural problems in children: the Giniplus and Lisaplus birth cohort studies. Int J Hyg Environ Health. 2013;216(2):146–54. 10.1016/j.ijheh.2012.03.006. [DOI] [PubMed] [Google Scholar]
  • 34.Packer CN, Stewart-Brown S, Fowle SE. Damp housing and adult health: results from a lifestyle study in Worcester, England. J Epidemiol Community Health. 1994;48(6):555–9. 10.1136/jech.48.6.555. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Harding CF, Pytte CL, Page KG, et al. Mold inhalation causes innate immune activation, neural, cognitive and emotional dysfunction. Brain Behav Immun. 2020;87:218–28. 10.1016/j.bbi.2019.11.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Zhao L. China’s aging population: a review of living arrangement, intergenerational support, and wellbeing. Health Care Science. 2023;2(5):317–27. 10.1002/hcs2.64. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Wang S, Cheng C, Tan S. Housing determinants of health in urban china: A structural equation modeling analysis. Soc Indic Res. 2019;143:1245–70. [Google Scholar]
  • 38.Zeng Y, Feng Q, Hesketh T, et al. Survival, disabilities in activities of daily living, and physical and cognitive functioning among the oldest-old in China: a cohort study. Lancet. 2017;389(10079):1619–29. 10.1016/s0140-6736(17)30548-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Björgvinsson T, Kertz SJ, Bigda-Peyton JS, et al. Psychometric properties of the CES-D-10 in a psychiatric sample. Assessment. 2013;20(4):429–36. 10.1177/1073191113481998. [DOI] [PubMed] [Google Scholar]
  • 40.Andresen EM, Malmgren J, Carter WB, et al. Screening for depression in well older adults: evaluation of a short form of the Ces-D (Center for epidemiologic studies depression scale. Am J Prev Med. 1993;10:77–84. [PubMed] [Google Scholar]
  • 41.Boey K. Cross-validation of a short form of the CES-D in Chinese elderly. Int J Geriatr Psychiatry. 1999;14(8):608–17. [DOI] [PubMed] [Google Scholar]
  • 42.Rutter LA, Brown TA. Psychometric properties of the generalized anxiety disorder Scale-7 (GAD -7) in outpatients with anxiety and mood disorders. J Psychopathol Behav Assess. 2017;39(1):140–6. 10.1007/s10862-016-9571-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Tong X, An D, Park S-P, et al. Validation of the generalized anxiety Disorder-7 (GAD -7) among Chinese people with epilepsy. Epilepsy Res. 2015;120. 10.1016/j.eplepsyres.2015.11.019. [DOI] [PubMed]
  • 44.Plummer F, Manea L, Trepel D, et al. Screening for anxiety disorders with the GAD-7 and GAD-2: a systematic review and diagnostic metaanalysis. Gen Hosp Psychiatry. 2016;39:24–31. 10.1016/j.genhosppsych.2015.11.005. [DOI] [PubMed] [Google Scholar]
  • 45.Hao Z, Ruggiano N, Li Q, et al. Disparities in depression among Chinese older adults with neurodegenerative diseases. Aging Ment Health. 2022;26(3):632–8. 10.1080/13607863.2021.1871879. [DOI] [PubMed] [Google Scholar]
  • 46.Deng Y, Zhao H, Liu Y, et al. Association of using biomass fuel for cooking with depression and anxiety symptoms in older Chinese adults. Sci Total Environ. 2022;811: 152256. 10.1016/j.scitotenv.2021.152256. [DOI] [PubMed] [Google Scholar]
  • 47.Folstein MF, Folstein SE, McHugh PR. Mini-Mental state. A practical method for grading the cognitive state.of patients for the clinician. J Psychiatr Res. 1975;12(3):189–98. 10.1016/0022-3956(75)90026-6. [DOI] [PubMed] [Google Scholar]
  • 48.Jin X, He W, Zhang Y, et al. Association of Apoe Ε4 genotype and lifestyle with cognitive function among Chinese adults aged 80 years and older: A Cross-Sectional study. PLoS Med. 2021;18(6):e1003597. 10.1371/journal.pmed.1003597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Zhang Q, Wu Y, Han T, et al. Changes in cognitive function and risk factors for cognitive impairment of the elderly in China: 2005–2014. Int J Environ Res Public Health. 2019. 10.3390/ijerph16162847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Haneuse S, VanderWeele TJ, Arterburn D. Using the E-value to assess the potential effect of unmeasured confounding in observational studies. JAMA. 2019;321(6):602–3. 10.1001/jama.2018.21554. [DOI] [PubMed] [Google Scholar]
  • 51.Shenassa ED, Daskalakis C, Liebhaber A, et al. Dampness and mold in the home and depression: an examination of mold-Related illness and perceived control of one’s home as possible depression pathways. Am J Public Health. 2007;97(10):1893–9. 10.2105/ajph.2006.093773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Hyndman SJ. Housing dampness and health amongst British Bengalis in East London. Soc Sci Med. 1990;30(1):131–41. 10.1016/0277-9536(90)90336-q. [DOI] [PubMed] [Google Scholar]
  • 53.Martin CJ, Platt SD, Hunt SM. Housing conditions and ill health. Br Med J (Clin Res Ed). 1987;294(6580):1125–7. 10.1136/bmj.294.6580.1125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Hopton JL, Hunt SM. Housing conditions and mental health in a disadvantaged area in Scotland. J Epidemiol Community Health. 1996;50(1):56–61. 10.1136/jech.50.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Harding C, Liao D, Persaud R, et al. Differential effects of exposure to toxic or nontoxic mold spores on brain inflammation and Morris water maze performance. Behav Brain Res. 2023;442: 114294. 10.1016/j.bbr.2023.114294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Harding C, Pytte C, Page K et al. Environmental Mold, Brain Inflammation, Cognitive Deficits, and Increased Anxiety and Fear, vol. 40; 2013.
  • 57.Francisco PW, Jacobs DE, Targos L, et al. Ventilation, indoor air quality, and health in homes undergoing weatherization. Indoor Air. 2017;27(2):463–77. 10.1111/ina.12325. [DOI] [PubMed] [Google Scholar]
  • 58.Oldham DJ, de Salis MH, Sharples S. Reducing the ingress of urban noise through natural ventilation openings. Indoor Air 14 Suppl. 2004;8:118–26. 10.1111/j.1600-0668.2004.00294.x. [DOI] [PubMed] [Google Scholar]
  • 59.Holme JA, Øya E, Afanou AKJ, et al. Characterization and pro-inflammatory potential of indoor mold particles. Indoor Air. 2020;30(4):662–81. 10.1111/ina.12656. [DOI] [PubMed] [Google Scholar]
  • 60.Slavich GM, Irwin MR. From stress to inflammation and major depressive disorder: a social signal transduction theory of depression. Psychol Bull. 2014;140(3):774–815. 10.1037/a0035302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Kiecolt-Glaser JK, Graham JE, Malarkey WB, et al. Olfactory influences on mood and autonomic, endocrine, and immune function. Psychoneuroendocrinology. 2008;33(3):328–39. 10.1016/j.psyneuen.2007.11.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Southwick SM, Vythilingam M, Charney DS. The psychobiology of depression and resilience to stress: implications for prevention and treatment. Annu Rev Clin Psychol. 2005;1:255–91. 10.1146/annurev.clinpsy.1.102803.143948. [DOI] [PubMed] [Google Scholar]
  • 63.Rabha R, Ghosh S, Padhy PK. Indoor air pollution in rural North-East India: elemental compositions, changes in haematological indices, oxidative stress and health risks. Ecotoxicol Environ Saf. 2018;165:393–403. 10.1016/j.ecoenv.2018.09.014. [DOI] [PubMed] [Google Scholar]
  • 64.Zhang YJ, Huang C, Lv YS, et al. Polycyclic aromatic hydrocarbon exposure, oxidative potential in dust, and their relationships to oxidative stress in human body: a case study in the indoor environment of Guangzhou, South China. Environ Int. 2021;149: 106405. 10.1016/j.envint.2021.106405. [DOI] [PubMed] [Google Scholar]
  • 65.Grimsley LF, Chulada PC, Kennedy S, et al. Indoor environmental exposures for children with asthma enrolled in the heal study, Post-Katrina new Orleans. Environ Health Perspect. 2012;120(11):1600–6. 10.1289/ehp.1104840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Hurtado-Ruzza R, Iglesias Ó, Dacal-Quintas R, et al. Asthma, much more than a respiratory disease: Influence of depression and anxiety. Rev Assoc Med Bras. 2021;67(4):571–6. 10.1590/1806-9282.20201066. [DOI] [PubMed] [Google Scholar]
  • 67.Liu J, Wu T, Liu Q, et al. Air pollution exposure and adverse sleep health across the life course: a systematic review. Environ Pollut. 2020;262: 114263. 10.1016/j.envpol.2020.114263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Baglioni C, Nanovska S, Regen W, et al. Sleep and mental disorders: a meta-analysis of polysomnographic research. Psychol Bull. 2016;142(9):969–90. 10.1037/bul0000053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Sookoian S, Burgueño A, Gianotti TF, et al. Odor perception between heterosexual partners: its association with depression, anxiety, and genetic variation in odorant receptor Or7d4. Biol Psychol. 2011;86(3):153–7. 10.1016/j.biopsycho.2010.11.003. [DOI] [PubMed] [Google Scholar]
  • 70.Peng M, Potterton H, Chu JTW, et al. Olfactory shifts linked to postpartum depression. Sci Rep. 2021;11(1):14947. 10.1038/s41598-021-94556-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Krusemark EA, Novak LR, Gitelman DR, et al. When the sense of smell meets emotion: anxiety-state-dependent olfactory processing and neural circuitry adaptation. J Neurosci. 2013;33(39):15324–32. 10.1523/jneurosci.1835-13.2013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Satoh S, Morita N, Matsuzaki I, et al. Relationship between odor perception and depression in the Japanese elderly. Psychiatry Clin Neurosci. 1996;50(5):271–5. 10.1111/j.1440-1819.1996.tb00563.x. [DOI] [PubMed] [Google Scholar]
  • 73.Gheusi G, Lledo PM. Adult neurogenesis in the olfactory system shapes odor memory and perception. Prog Brain Res. 2014;208:157–75. 10.1016/b978-0-444-63350-7.00006-1. [DOI] [PubMed] [Google Scholar]
  • 74.Ehrlichman H, Halpern JN. Affect and memory: effects of pleasant and unpleasant odors on retrieval of happy and unhappy memories. J Pers Soc Psychol. 1988;55(5):769–79. 10.1037/0022-3514.55.5.769. [DOI] [PubMed] [Google Scholar]
  • 75.Cao Z, Yuan Y, White AJ, et al. Air pollutants and risk of parkinson’s disease among women in the sister study. Environ Health Perspect. 2024;132(1):17001. 10.1289/ehp13009. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Material 1 (30.4KB, docx)

Data Availability Statement

Publicly available datasets were analyzed in this study. This data can be found here: https://opendata.pku.edu.cn/dataverse/CHADS.


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