Major depressive disorder increased the risk of hypertension: A Mendelian randomization study

被引:2
作者
Zhang, Xu [1 ]
Li, Cheng [2 ]
机构
[1] Second Hosp Jilin Univ, Dept Cardiovasc Surg, Changchun, Jilin, Peoples R China
[2] First Hosp Jilin Univ, Dept Cardiovasc Ctr, Changchun, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Hypertension; Major depressive disorder; Mendelian randomization; Psychiatric disorders; METAANALYSIS; PREVALENCE; HEALTH; LIFE;
D O I
10.1016/j.jad.2024.03.144
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Despite the high prevalence of comorbid hypertension in patients with major depressive disorder (MDD), the relationship between the two diseases has received little attention. Previous observational studies have descripted the association between MDD and hypertension, the causality from MDD on hypertension remained unknown. The present Mendelian randomization (MR) study aimed to assess the causal effect of MDD on hypertension. Methods: A set of genetics instrument was used for analysis, derived from publicly available genetic meta -analysis data. A total of 44 single -nucleotide polymorphisms (SNPs) associated with MDD. The largest genome-wide association study (GWAS) for hypertension (54,358 cases and 408,652 controls) was used to assess the effect of MDD on hypertension. Inverse variance weighted method (IVW), weighted median method (WM), and MREgger regression were used for MR analyses. The MR-Egger_intercept test and Cochran 's Q statistic were used to determine the pleiotropy and the heterogeneity, respectively. Results: A total of 28 independent and effective MDD genetic instrumental variables were extracted from the hypertension GWAS summary statistics. Pleiotropy analysis suggested no significant pleiotropic variant among the 28 selected MDD genetic instrument variants in hypertension GWAS datasets. As MDD based on genetic changes increased, the risk of hypertension increased using MR -Egger (OR = 1.004436, 95%CI 0.9884666 -1.020663, P = 0.5932928), WM (OR =1.000499, 95%CI 1.0000188 -1.000980, P = 0.0416871), and IVW (OR = 1.000573, 95%CI 1.0000732 -1.001074, P = 0.0246392). Our results were robust, with no obvious bias based on investigating the single MDD SNP on hypertension. Conclusions: Our result suggested a causal associated between genetically increased MDD and increased hypertension risk in European population.
引用
收藏
页码:184 / 189
页数:6
相关论文
共 36 条
[1]   Depression and risk of heart failure among older persons with isolated systolic hypertension [J].
Abramson, J ;
Berger, A ;
Krumholz, HM ;
Vaccarino, V .
ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (14) :1725-1730
[2]  
Adamis D, 2000, INT J GERIATR PSYCH, V15, P248, DOI 10.1002/(SICI)1099-1166(200003)15:3<248::AID-GPS102>3.0.CO
[3]  
2-L
[4]  
Barquera S, 2010, SALUD PUBLICA MEXICO, V52, pS63
[5]   Pharmacological treatment of unipolar depressive disorders: summary of WFSBP guidelines [J].
Bauer, Michael ;
Severus, Emanuel ;
Moller, Hans-Jurgen ;
Young, Allan H. .
INTERNATIONAL JOURNAL OF PSYCHIATRY IN CLINICAL PRACTICE, 2017, 21 (03) :166-176
[6]   Meta-analysis and Mendelian randomization: A review [J].
Bowden, Jack ;
Holmes, Michael, V .
RESEARCH SYNTHESIS METHODS, 2019, 10 (04) :486-496
[7]   Bidirectional associations between mental disorders, antidepressants and cardiovascular disease [J].
Cao, Hongbao ;
Baranova, Ancha ;
Zhao, Qian ;
Zhang, Fuquan .
BMJ MENTAL HEALTH, 2024, 27 (01)
[8]   Psychosocial Risk Factors for Hypertension: an Update of the Literature [J].
Cuffee, Yendelela ;
Ogedegbe, Chinwe ;
Williams, Natasha J. ;
Ogedegbe, Gbenga ;
Schoenthaler, Antoinette .
CURRENT HYPERTENSION REPORTS, 2014, 16 (10)
[9]   Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015 [J].
Forouzanfar, Mohammad H. ;
Afshin, Ashkan ;
Alexander, Lily T. ;
Anderson, H. Ross ;
Bhutta, Zulficiar A. ;
Biryukov, Stan ;
Brauer, Michael ;
Burnett, Richard ;
Cercy, Kelly ;
Charlson, Fiona J. ;
Cohen, Aaron J. ;
Dandona, Lalit ;
Estep, Kara ;
Ferrari, Alize J. ;
Frostad, Joseph J. ;
Fullman, Nancy ;
Gething, Peter W. ;
Godwin, William W. ;
Griswold, Max ;
Kinfu, Yohannes ;
Kyu, Hmwe H. ;
Larson, Heidi J. ;
Liang, Xiaofeng ;
Lim, Stephen S. ;
Liu, Patrick Y. ;
Lopez, Alan D. ;
Lozano, Rafael ;
Marczak, Laurie ;
Mensah, George A. ;
Mokdad, Ali H. ;
Moradi-Lakeh, Maziar ;
Naghavi, Mohsen ;
Neal, Bruce ;
Reitsma, Marissa B. ;
Roth, Gregory A. ;
Salomon, Joshua A. ;
Sur, Patrick J. ;
Vos, Theo ;
Wagner, Joseph A. ;
Wang, Haidong ;
Zhao, Yi ;
Zhou, Maigeng ;
Aasvang, Gunn Marit ;
Abajobir, Amanuel Alemu ;
Abate, Kalkidan Hassen ;
Abbafati, Cristiana ;
Abbas, Kaja M. ;
Abd-Allah, Foad ;
Abdulle, Abdishakur M. ;
Abera, Semaw Ferede .
LANCET, 2016, 388 (10053) :1659-1724
[10]   Effects of Selenium on Chronic Kidney Disease: A Mendelian Randomization Study [J].
Fu, Shaojie ;
Zhang, Li ;
Ma, Fuzhe ;
Xue, Shuai ;
Sun, Tao ;
Xu, Zhonggao .
NUTRIENTS, 2022, 14 (21)