Annual average exposure to ambient air pollution, polygenic risk, and incidence of major chronic diseases: a large-scale prospective cohort study.

IF 3.4 2区 生物学 Q2 GENETICS & HEREDITY
Jing Tian, Sicong Wang, Xinyi Chang, Yi Han
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引用次数: 0

Abstract

Ambient air pollution is a major environmental risk factor for chronic diseases, yet its independent effects, as well as its joint associations and interactions with genetic susceptibility, on multiple chronic conditions remain understudied. This study aims to investigate the association between annual average exposure to multiple air pollutants and five major chronic diseases, while quantifying the role of polygenic risk in these relationships. We included 313,534 participants from the UK Biobank. Land use regression models were used to estimate annual average air pollution concentrations at residential addresses. Chronic diseases (cardiovascular, respiratory, neurodegenerative, hypertension, and diabetes) were identified using ICD-9 and ICD-10 codes. Weighted polygenic risk scores (PRS) were constructed for each disease. Cox proportional hazards models were used to assess associations, and additive interactions were evaluated using RERI and AP. Annual average exposure to PM2.5, PM10, NO2, and NOx was significantly associated with increased chronic disease risk. PM2.5 showed the strongest association (HR = 1.22 per 5 µg/m³, 95% CI: 1.19-1.26). High genetic risk was independently associated with disease incidence (e.g., diabetes: HR = 1.77 per SD increase in PRS). Significant additive interactions were observed between high genetic risk and high PM2.5 exposure for neurodegenerative disease (RERI = 0.14) and diabetes (RERI = 0.21). Participants with both high genetic risk and high pollution exposure had the highest disease burden. Annual average exposure to air pollutants is associated with increased risks of multiple chronic diseases, with effect modification by genetic susceptibility.

年平均暴露于环境空气污染、多基因风险和主要慢性病发病率:一项大规模前瞻性队列研究
环境空气污染是慢性疾病的一个主要环境风险因素,但其对多种慢性疾病的独立影响以及与遗传易感性的联合关联和相互作用仍未得到充分研究。本研究旨在探讨年平均暴露于多种空气污染物与五种主要慢性疾病之间的关系,同时量化多基因风险在这些关系中的作用。我们纳入了来自英国生物银行的313534名参与者。土地利用回归模型用于估算居住地址的年平均空气污染浓度。慢性疾病(心血管、呼吸、神经退行性、高血压和糖尿病)使用ICD-9和ICD-10代码进行鉴定。为每种疾病构建加权多基因风险评分(PRS)。使用Cox比例风险模型评估相关性,并使用rei和AP评估加性相互作用。PM2.5、PM10、NO2和NOx的年平均暴露与慢性疾病风险增加显著相关。PM2.5的相关性最强(HR = 1.22 / 5µg/m³,95% CI: 1.19-1.26)。高遗传风险与疾病发病率独立相关(例如,糖尿病:每SD PRS增加的HR = 1.77)。神经退行性疾病(rei = 0.14)和糖尿病(rei = 0.21)的高遗传风险与高PM2.5暴露之间存在显著的加性相互作用。高遗传风险和高污染暴露的参与者的疾病负担最高。年平均暴露于空气污染物与多种慢性疾病的风险增加有关,其影响因遗传易感性而改变。
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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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