Shinya Nakada, Joey Ward, Rona J Strawbridge, Paul Welsh, Carlos Celis-Morales, Frederick K Ho, Jill P Pell
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Cox proportional hazard models were used to examine associations between anxiety disorder and depression and CAD.</p><p><strong>Results: </strong>Both anxiety disorder (HR 2.31, 95% CI 1.92-2.78) and depression (HR 2.15, 95% CI 1.90-2.24) were associated with CAD after adjusting for sociodemographic confounders. There was an addictive interaction between depression and PRS<sub>CAD</sub> (RERI 0.97, 95% CI 0.12-1.81) such that the association between depression and CAD was strongest among those with a high PRS<sub>CAD</sub> whilst there was no such evidence for anxiety disorder. Anxiety disorder only (HR 1.68, 95% 1.16-2.44), depression only (HR 2.13, 95% CI 1.72-2.64), and concomitant anxiety disorder and depression (HR 3.85, 95% CI 2.48-5.98) were associated with CAD even among people with a low PRS<sub>CAD</sub>. Adjusting for potential mediators attenuated all these associations across PRS categories.</p><p><strong>Conclusions: </strong>CAD genetic susceptibility might partly contribute to the clustering of depression and CAD but does not provide a full explanation, nor does it explain the association between anxiety disorder and CAD. Therefore, other mechanisms should be explored.</p>","PeriodicalId":9188,"journal":{"name":"BMC Medicine","volume":"23 1","pages":"73"},"PeriodicalIF":8.3000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11804096/pdf/","citationCount":"0","resultStr":"{\"title\":\"Anxiety disorder, depression and coronary artery disease: associations and modification by genetic susceptibility.\",\"authors\":\"Shinya Nakada, Joey Ward, Rona J Strawbridge, Paul Welsh, Carlos Celis-Morales, Frederick K Ho, Jill P Pell\",\"doi\":\"10.1186/s12916-025-03915-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Associations of anxiety disorder and depression with coronary artery disease (CAD) are heterogeneous between populations. This study investigated how genetic susceptibility to CAD alters these associations with incident CAD, comparing and combining anxiety disorder and depression.</p><p><strong>Methods: </strong>This is a prospective cohort study using UK Biobank. Diagnoses of anxiety disorder and depression were ascertained through linked hospital admission data. Incident CAD was ascertained through hospital admission and death certificate data after baseline. CAD polygenic risk score (PRS<sub>CAD</sub>) was obtained from CARDIoGRAMplus4 and categorised into low, intermediate, and high. Cox proportional hazard models were used to examine associations between anxiety disorder and depression and CAD.</p><p><strong>Results: </strong>Both anxiety disorder (HR 2.31, 95% CI 1.92-2.78) and depression (HR 2.15, 95% CI 1.90-2.24) were associated with CAD after adjusting for sociodemographic confounders. There was an addictive interaction between depression and PRS<sub>CAD</sub> (RERI 0.97, 95% CI 0.12-1.81) such that the association between depression and CAD was strongest among those with a high PRS<sub>CAD</sub> whilst there was no such evidence for anxiety disorder. Anxiety disorder only (HR 1.68, 95% 1.16-2.44), depression only (HR 2.13, 95% CI 1.72-2.64), and concomitant anxiety disorder and depression (HR 3.85, 95% CI 2.48-5.98) were associated with CAD even among people with a low PRS<sub>CAD</sub>. Adjusting for potential mediators attenuated all these associations across PRS categories.</p><p><strong>Conclusions: </strong>CAD genetic susceptibility might partly contribute to the clustering of depression and CAD but does not provide a full explanation, nor does it explain the association between anxiety disorder and CAD. 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引用次数: 0
摘要
背景:焦虑障碍和抑郁与冠状动脉疾病(CAD)的关联在人群中是异质的。本研究调查了CAD的遗传易感性如何改变这些与冠心病的关联,比较并结合了焦虑障碍和抑郁症。方法:这是一项使用英国生物银行的前瞻性队列研究。通过相关的住院数据确定焦虑障碍和抑郁的诊断。通过基线后的住院和死亡证明数据确定冠心病事件。从CARDIoGRAMplus4中获得CAD多基因风险评分(PRSCAD),分为低、中、高三个等级。Cox比例风险模型用于检查焦虑障碍、抑郁和CAD之间的关系。结果:在调整社会人口混杂因素后,焦虑障碍(HR 2.31, 95% CI 1.92-2.78)和抑郁(HR 2.15, 95% CI 1.90-2.24)都与CAD相关。抑郁和PRSCAD之间存在成瘾性的相互作用(rei 0.97, 95% CI 0.12-1.81),因此在PRSCAD高的人群中,抑郁和CAD之间的关联最强,而焦虑障碍则没有这样的证据。即使在PRSCAD较低的人群中,仅焦虑障碍(HR 1.68, 95% 1.16-2.44)、仅抑郁(HR 2.13, 95% CI 1.72-2.64)和伴发焦虑障碍和抑郁(HR 3.85, 95% CI 2.48-5.98)也与CAD相关。对潜在介质的调整减弱了PRS类别之间的所有这些关联。结论:CAD遗传易感性可能部分促成了抑郁和CAD的聚集,但不能提供一个完整的解释,也不能解释焦虑障碍和CAD之间的关联。因此,应该探索其他机制。
Anxiety disorder, depression and coronary artery disease: associations and modification by genetic susceptibility.
Background: Associations of anxiety disorder and depression with coronary artery disease (CAD) are heterogeneous between populations. This study investigated how genetic susceptibility to CAD alters these associations with incident CAD, comparing and combining anxiety disorder and depression.
Methods: This is a prospective cohort study using UK Biobank. Diagnoses of anxiety disorder and depression were ascertained through linked hospital admission data. Incident CAD was ascertained through hospital admission and death certificate data after baseline. CAD polygenic risk score (PRSCAD) was obtained from CARDIoGRAMplus4 and categorised into low, intermediate, and high. Cox proportional hazard models were used to examine associations between anxiety disorder and depression and CAD.
Results: Both anxiety disorder (HR 2.31, 95% CI 1.92-2.78) and depression (HR 2.15, 95% CI 1.90-2.24) were associated with CAD after adjusting for sociodemographic confounders. There was an addictive interaction between depression and PRSCAD (RERI 0.97, 95% CI 0.12-1.81) such that the association between depression and CAD was strongest among those with a high PRSCAD whilst there was no such evidence for anxiety disorder. Anxiety disorder only (HR 1.68, 95% 1.16-2.44), depression only (HR 2.13, 95% CI 1.72-2.64), and concomitant anxiety disorder and depression (HR 3.85, 95% CI 2.48-5.98) were associated with CAD even among people with a low PRSCAD. Adjusting for potential mediators attenuated all these associations across PRS categories.
Conclusions: CAD genetic susceptibility might partly contribute to the clustering of depression and CAD but does not provide a full explanation, nor does it explain the association between anxiety disorder and CAD. Therefore, other mechanisms should be explored.
期刊介绍:
BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.