BDNF val66met polymorphism and depressive disorders in patients with acute coronary syndrome

被引:15
作者
Kang, Hee-Ju [1 ]
Bae, Kyung-Yeol [1 ]
Kim, Sung-Wan [1 ]
Shin, Il-Seon [1 ]
Hong, Young Joon [2 ]
Ahn, Youngkeun [2 ]
Jeong, Myung Ho [2 ]
Yoon, Jin-Sang [1 ]
Kim, Jae-Min [1 ]
机构
[1] Chonnam Natl Univ, Sch Med, Dept Psychiat, 160 Baekseoro, Gwangju 501746, South Korea
[2] Chonnam Natl Univ, Sch Med, Dept Cardiol, Gwangju, South Korea
基金
新加坡国家研究基金会;
关键词
Depression; BDNF; Polymorphism; Acute coronary syndrome; Escitalopram; ACUTE MYOCARDIAL-INFARCTION; NEUROTROPHIC-FACTOR; ARTERY-DISEASE; SEROTONIN TRANSPORTER; K-DEPACS; GENE POLYMORPHISMS; MAJOR DEPRESSION; HEART-DISEASE; ESCITALOPRAM TREATMENT; MOOD DISORDERS;
D O I
10.1016/j.jad.2016.01.033
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Brain-derived neurotrophic factor (BDNF) may be the key to understanding the development of depression in patients with acute coronary syndrome (ACS), as it is associated with both conditions. Because the expression of BDNF is influenced by genetic polymorphisms, in this study we investigated the association between the BDNF polymorphism val66met and both the risk of depression in ACS and the treatment response. Methods: Among the 969 patients with recent ACS at baseline, 711 were re-evaluated after 1 year of follow-up. Depressive disorder status was assessed according to the DSM-IV criteria both at baseline and at follow-up. Baseline prevalence, follow-up incidence, and the persistence of depression were also determined. Of the 378 patients diagnosed with depression at baseline, 255 were randomized to a 24 week double-blind placebo-controlled trial of escitalopram; the remaining 123 received the usual care. Associations between the BDNF val66met polymorphism and both depression status and treatment response were investigated using logistic regression models. Results: The prevalence and persistence, but not the incidence of depressive disorders were significantly associated with BDNF met alleles. Patients in the escitalopram group who carried the met allele had a significantly higher rate of remission than those who did not. Depressive disorders tended to persist at 1 year in patients managed with placebo or medical treatment only, and particularly those patients positive for BDNF met alleles, although the difference was not statistically significant. Limitations: The generalizability should be considered since this study conducted in a single center. Conclusions: ACS patients positive for BDNF met alleles are vulnerable to depressive disorders at baseline and to its persistence. Antidepressant treatment may be effective in this subgroup of patients and may prevent the persistence of depression. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 60 条
[1]   2012 ACCF/AHA Focused Update Incorporated Into the ACCF/AHA 2007 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction [J].
Anderson, Jeffrey L. ;
Adams, Cynthia D. ;
Antman, Elliott M. ;
Bridges, Charles R. ;
Califf, Robert M. ;
Casey, Donald E., Jr. ;
Chavey, William E., II ;
Fesmire, Francis M. ;
Hochman, Judith S. ;
Levin, Thomas N. ;
Lincoff, A. Michael ;
Peterson, Eric D. ;
Theroux, Pierre ;
Wenger, Nanette K. ;
Wright, R. Scott ;
Jneid, Hani ;
Anderson, Jeffrey L. ;
Wright, R. Scott ;
Adams, Cynthia D. ;
Bridges, Charles R. ;
Casey, Donald E., Jr. ;
Ettinger, Steven M. ;
Fesmire, Francis M. ;
Ganiats, Theodore G. ;
Lincoff, A. Michael ;
Peterson, Eric D. ;
Philippides, George J. ;
Theroux, Pierre ;
Wenger, Nanette K. ;
Anderson, Jeffrey L. ;
Jacobs, Alice K. ;
Halperin, Jonathan L. ;
Albert, Nancy M. ;
Creager, Mark A. ;
DeMets, David ;
Ettinger, Steven M. ;
Guyton, Robert A. ;
Hochman, Judith S. ;
Kushner, Frederick G. ;
Ohman, E. Magnus ;
Stevenson, William ;
Yancy, Clyde W. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 61 (23) :E179-E347
[2]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[3]   Coronary artery disease and depression: Possible role of brain-derived neurotrophic factor and serotonin transporter gene polymorphisms [J].
Bozzini, Sara ;
Gambelli, Patrick ;
Boiocchi, Chiara ;
Schirinzi, Sandra ;
Falcone, Rossana ;
Buzzi, Paola ;
Storti, Cesare ;
Falcone, Colomba .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2009, 24 (06) :813-818
[4]   A systematic review and meta-analysis of clinical studies on major depression and BDNF levels: implications for the role of neuroplasticity in depression [J].
Brunoni, Andre Russowsky ;
Lopes, Mariana ;
Fregni, Felipe .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2008, 11 (08) :1169-1180
[5]   Depression, the autonomic nervous system, and coronary heart disease [J].
Carney, RM ;
Freedland, KE ;
Veith, RC .
PSYCHOSOMATIC MEDICINE, 2005, 67 :S29-S33
[6]   Genetic Sensitivity to the Environment: The Case of the Serotonin Transporter Gene and Its Implications for Studying Complex Diseases and Traits [J].
Caspi, Avshalom ;
Hariri, Ahmad R. ;
Holmes, Andrew ;
Uher, Rudolf ;
Moffitt, Terrie E. .
AMERICAN JOURNAL OF PSYCHIATRY, 2010, 167 (05) :509-527
[7]   BDNF/TRKB/P75NTR polymorphisms and their consequences on antidepressant efficacy in depressed patients [J].
Colle, Romain ;
Deflesselle, Eric ;
Martin, Severine ;
David, Denis J. ;
Hardy, Patrick ;
Taranu, Adela ;
Falissard, Bruno ;
Verstuyft, Celine ;
Corruble, Emmanuelle .
PHARMACOGENOMICS, 2015, 16 (09) :997-1013
[8]  
Daimon M., 2004, Patent No. [JP -2004-059065, 2004059065, JP-2004-059065]
[9]  
Daimon M., 2004, Patent No. [PCT/JP05/03500, 0503500]
[10]  
Daimon M., 2004, Patent No. [US 2008/ 0146498 Al, 20080146498A1]