A Mendelian randomization study of the effect of mental disorders on cardiovascular disease

被引:1
作者
Yu, Yunfeng [1 ,2 ]
Yang, Xinyu [1 ]
Wu, Jingyi [3 ]
Hu, Gang [2 ]
Bai, Siyang [1 ]
Yu, Rong [1 ,2 ]
机构
[1] Hunan Univ Chinese Med, Sch Tradit Chinese Med, Changsha, Hunan, Peoples R China
[2] Hunan Univ Chinese Med, Hosp 1, Changsha, Hunan, Peoples R China
[3] Zhejiang Chinese Med Univ, Sch Clin Med 3, Hangzhou, Zhejiang, Peoples R China
来源
FRONTIERS IN CARDIOVASCULAR MEDICINE | 2024年 / 11卷
基金
中国国家自然科学基金;
关键词
mental disorders; cardiovascular disease; risk factor; Mendelian randomization; depression; anxiety disorder; autism spectrum disorder; ANXIETY DISORDER; GLOBAL BURDEN; RISK; DEPRESSION; CHILDREN; HEART; STRESS; EPIDEMIOLOGY; HOMOCYSTEINE; INFLAMMATION;
D O I
10.3389/fcvm.2024.1329463
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective The effect of mental disorders (MD) on cardiovascular disease (CVD) remains controversial, and this study aims to analyze the causal relationship between eight MD and CVD by Mendelian randomization (MR). Methods Single nucleotide polymorphisms of attention-deficit/hyperactivity disorder (ADHD), anorexia nervosa (AN), anxiety disorder (ANX), autism spectrum disorder (ASD), bipolar disorder (BD), depression, obsessive-compulsive disorder (OCD), schizophrenia (SCZ), and CVD were obtained from UK Biobank and FinnGen. Exposure-outcome causality was tested using inverse variance weighted (IVW), MR-Egger, and weighted median. Horizontal pleiotropy and heterogeneity were assessed by MR-Egger intercept and Cochran's Q, respectively, while stability of results was assessed by leave-one-out sensitivity analysis. Results MR analysis showed that ANX (IVW [odds ratio (OR) 1.11, 95% confidence intervals (CI) 1.07-1.15, p < 0.001]; MR-Egger [OR 1.03, 95% CI 0.92-1.14, p = 0.652]; weighted median [OR 1.09, 95% CI 1.03-1.14, p = 0.001]), ASD (IVW [OR 1.05, 95% CI 1.00-1.09, p = 0.039]; MR-Egger [OR 0.95, 95% CI 0.84-1.07, p = 0.411]; weighted median [OR 1.01, 95% CI 0.96-1.06, p = 0.805]), depression (IVW [OR 1.15, 95% CI 1.10-1.19, p < 0.001]; MR-Egger [OR 1.10, 95% CI 0.96-1.26, p = 0.169]; weighted median [OR 1.13, 95% CI 1.08-1.19, p < 0.001]) were significantly associated with increased risk of CVD, whereas ADHD, AN, BD, OCD, and SCZ were not significantly associated with CVD (p > 0.05). Intercept analysis showed no horizontal pleiotropy (p > 0.05). Cochran's Q showed no heterogeneity except for BD (p = 0.035). Sensitivity analysis suggested that these results were robust. Conclusions ANX, ASD, and depression are associated with an increased risk of CVD, whereas AN, ADHD, BD, OCD, and SCZ are not causally associated with CVD. Active prevention and treatment of ANX, ASD, and depression may help reduce the risk of CVD.
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页数:9
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共 68 条
[1]   A global reference for human genetic variation [J].
Altshuler, David M. ;
Durbin, Richard M. ;
Abecasis, Goncalo R. ;
Bentley, David R. ;
Chakravarti, Aravinda ;
Clark, Andrew G. ;
Donnelly, Peter ;
Eichler, Evan E. ;
Flicek, Paul ;
Gabriel, Stacey B. ;
Gibbs, Richard A. ;
Green, Eric D. ;
Hurles, Matthew E. ;
Knoppers, Bartha M. ;
Korbel, Jan O. ;
Lander, Eric S. ;
Lee, Charles ;
Lehrach, Hans ;
Mardis, Elaine R. ;
Marth, Gabor T. ;
McVean, Gil A. ;
Nickerson, Deborah A. ;
Wang, Jun ;
Wilson, Richard K. ;
Boerwinkle, Eric ;
Doddapaneni, Harsha ;
Han, Yi ;
Korchina, Viktoriya ;
Kovar, Christie ;
Lee, Sandra ;
Muzny, Donna ;
Reid, Jeffrey G. ;
Zhu, Yiming ;
Chang, Yuqi ;
Feng, Qiang ;
Fang, Xiaodong ;
Guo, Xiaosen ;
Jian, Min ;
Jiang, Hui ;
Jin, Xin ;
Lan, Tianming ;
Li, Guoqing ;
Li, Jingxiang ;
Li, Yingrui ;
Liu, Shengmao ;
Liu, Xiao ;
Lu, Yao ;
Ma, Xuedi ;
Tang, Meifang ;
Wang, Bo .
NATURE, 2015, 526 (7571) :68-+
[2]   The Levels of Vitamin D, Vitamin D Receptor, Homocysteine and Complex B Vitamin in Children with Autism Spectrum Disorders [J].
Altun, Hatice ;
Kurutas, Ergul Beige ;
Sahin, Nilfer ;
Gungor, Olcay ;
Findikli, Ebru .
CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2018, 16 (04) :383-390
[3]   Rodent models for psychiatric disorders: problems and promises [J].
Baker, Matthew ;
Hong, Sa-Ik ;
Kang, Seungwoo ;
Choi, Doo-Sup .
LABORATORY ANIMAL RESEARCH, 2020, 36 (01)
[4]   Prevalence and prevention of cardiovascular disease and diabetes mellitus [J].
Balakumar, Pitchai ;
Maung-U, Khin ;
Jagadeesh, Gowraganahalli .
PHARMACOLOGICAL RESEARCH, 2016, 113 :600-609
[5]   Anxiety and new onset of cardiovascular disease: critical review and meta-analysis [J].
Batelaan, Neeltje M. ;
Seldenrijk, Adrie ;
Bot, Mariska ;
van Balkom, Anton J. L. M. ;
Penninx, Brenda W. J. H. .
BRITISH JOURNAL OF PSYCHIATRY, 2016, 208 (03) :223-+
[6]   Dysregulated phosphate metabolism in autism spectrum disorder: associations and insights for future research [J].
Brown, Ronald B. .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2023, 25
[7]   Autonomic Neural Circuit and Intervention for Comorbidity Anxiety and Cardiovascular Disease [J].
Chen, Xuanzhao ;
Xu, Li ;
Li, Zeyan .
FRONTIERS IN PHYSIOLOGY, 2022, 13
[8]   State of the Art Review: Depression, Stress, Anxiety, and Cardiovascular Disease [J].
Cohen, Beth E. ;
Edmondson, Donald ;
Kronish, Ian M. .
AMERICAN JOURNAL OF HYPERTENSION, 2015, 28 (11) :1295-1302
[9]   Chronic stress, glucocorticoid receptor resistance, inflammation, and disease risk [J].
Cohen, Sheldon ;
Janicki-Deverts, Denise ;
Doyle, William J. ;
Miller, Gregory E. ;
Frank, Ellen ;
Rabin, Bruce S. ;
Turner, Ronald B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (16) :5995-5999
[10]   Controlled direct effect of psychiatric disorders on cardiovascular disease: evidence from a large Kurdish cohort [J].
Darabi, Zahra ;
Najafi, Farid ;
Safari-Faramani, Roya ;
Salimi, Yahya .
BMC CARDIOVASCULAR DISORDERS, 2020, 20 (01)