• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

5-HTTLPR 多态性对冠心病患者抑郁风险的重要影响:一项荟萃分析。

The important effect of 5-HTTLPR polymorphism on the risk of depression in patients with coronary heart disease: a meta-analysis.

机构信息

Department of Cardiology, Beijing Anzhen Hospital Affiliated to Capital Medical University, No. 2 Anzhen Road, Chaoyang District, Beijing, 100029, China.

Center for Evidence-Based and Translational Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, Hubei, China.

出版信息

BMC Cardiovasc Disord. 2020 Mar 18;20(1):141. doi: 10.1186/s12872-020-01424-1.

DOI:10.1186/s12872-020-01424-1
PMID:32188408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7081537/
Abstract

BACKGROUND

Depression has been recognized as an independent risk factor of coronary heart disease (CHD). Moreover, there is interrelationship of both depression and CHD. However, the potential pathophysiological mechanisms remain unknown. It might be influenced by genetic and environmental factors. According to recent researches, there is potential association between serotonin transporter gene-linked polymorphic region (5-HTTLPR) polymorphism and risk of depression in CHD patients, but the results are still inconclusive. Therefore, we performed this meta-analysis based on unadjusted and adjusted data to ascertain a more precise conclusion.

METHODS

We searched relevant articles through PubMed, Embase, Web of Science, Chinese BioMedical Literature (CBM) and Chinese National Knowledge Infrastructure (CNKI) databases up to August 26, 2019. Study selection and data extraction were accomplished by two authors independently. The strength of the correlation was assessed via odds ratios (ORs) with their 95% confidence intervals (95%CIs).

RESULTS

This meta-analysis enrolled six observational studies. Based on unadjusted data, there was significant relationship between 5-HTTLPR polymorphism and depression risk in CHD patients under all genetic models (S vs. L: OR = 1.31, 95%CI = 1.07-1.60; SS vs. LL: OR = 1.73, 95%CI = 1.12-2.67; LS vs. LL: OR = 1.47, 95%CI = 1.13-1.92; LS + SS vs. LL: OR = 1.62, 95%CI = 1.25-2.09; SS vs. LL + LS: OR = 1.33, 95%CI = 1.02-1.74). The results of adjusted data further strengthened this relationship (SS vs. LL: OR = 1.89, 95%CI = 1.28-2.80; LS vs. LL: OR = 1.69, 95%CI = 1.14-2.51; LS + SS vs. LL: OR = 1.80, 95%CI = 1.25-2.59). Subgroup analyses based on ethnicity and major depressive disorder revealed similar results to that of the overall analysis. No evidence of publication bias was observed.

CONCLUSIONS

Our results suggest that 5-HTTLPR polymorphism may have an important effect on the risk of depression among patients with CHD, and carriers of the S allele of 5-HTTLPR are more vulnerable to depression.

摘要

背景

抑郁症已被认为是冠心病(CHD)的独立危险因素。此外,抑郁症和 CHD 之间存在相互关系。然而,潜在的病理生理机制尚不清楚。它可能受到遗传和环境因素的影响。根据最近的研究,5-羟色胺转运体基因连锁多态性区域(5-HTTLPR)多态性与 CHD 患者患抑郁症的风险之间存在潜在关联,但结果仍不确定。因此,我们基于未调整和调整的数据进行了这项荟萃分析,以得出更准确的结论。

方法

我们通过 PubMed、Embase、Web of Science、中国生物医学文献数据库(CBM)和中国国家知识基础设施(CNKI)数据库检索相关文献,检索时间截至 2019 年 8 月 26 日。两名作者独立进行研究选择和数据提取。相关性强度通过比值比(OR)及其 95%置信区间(95%CI)进行评估。

结果

这项荟萃分析纳入了六项观察性研究。基于未调整数据,在所有遗传模型下,5-HTTLPR 多态性与 CHD 患者的抑郁风险均存在显著相关性(S 与 L:OR=1.31,95%CI=1.07-1.60;SS 与 LL:OR=1.73,95%CI=1.12-2.67;LS 与 LL:OR=1.47,95%CI=1.13-1.92;LS+SS 与 LL:OR=1.62,95%CI=1.25-2.09;SS 与 LL+LS:OR=1.33,95%CI=1.02-1.74)。调整数据的结果进一步加强了这种关系(SS 与 LL:OR=1.89,95%CI=1.28-2.80;LS 与 LL:OR=1.69,95%CI=1.14-2.51;LS+SS 与 LL:OR=1.80,95%CI=1.25-2.59)。基于种族和重度抑郁症的亚组分析得出了与总体分析相似的结果。未发现发表偏倚的证据。

结论

我们的结果表明,5-HTTLPR 多态性可能对 CHD 患者患抑郁症的风险有重要影响,携带 5-HTTLPR S 等位基因的个体更容易患抑郁症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/389281d85c89/12872_2020_1424_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/4e7540126f5d/12872_2020_1424_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/e4c667564180/12872_2020_1424_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/9347b6534b03/12872_2020_1424_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/389281d85c89/12872_2020_1424_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/4e7540126f5d/12872_2020_1424_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/e4c667564180/12872_2020_1424_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/9347b6534b03/12872_2020_1424_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dccc/7081537/389281d85c89/12872_2020_1424_Fig4_HTML.jpg

相似文献

1
The important effect of 5-HTTLPR polymorphism on the risk of depression in patients with coronary heart disease: a meta-analysis.5-HTTLPR 多态性对冠心病患者抑郁风险的重要影响:一项荟萃分析。
BMC Cardiovasc Disord. 2020 Mar 18;20(1):141. doi: 10.1186/s12872-020-01424-1.
2
The effect of single nucleotide polymorphisms on depression in combination with coronary diseases: a systematic review and meta-analysis.单核苷酸多态性对合并冠心病的抑郁症的影响:系统评价和荟萃分析。
Front Endocrinol (Lausanne). 2024 Apr 30;15:1369676. doi: 10.3389/fendo.2024.1369676. eCollection 2024.
3
Meta-analysis of 5-hydroxytryptamine transporter gene promoter region polymorphism and post-stroke depression.5-羟色胺转运体基因启动子区多态性与卒中后抑郁的荟萃分析
J Int Med Res. 2020 Jun;48(6):300060520925943. doi: 10.1177/0300060520925943.
4
Association between the serotonin transporter linked polymorphic region and lifelong premature ejaculation: An updated meta-analysis of case-control studies.5-羟色胺转运体基因连锁多态性区域与终身性早泄之间的关联:病例对照研究的最新荟萃分析
Medicine (Baltimore). 2020 Oct 9;99(41):e22169. doi: 10.1097/MD.0000000000022169.
5
Meta-Analysis of the Association Between 5-Hydroxytryptamine Transporter Gene-Linked Polymorphic Region and Functional Dyspepsia and its Subtypes.5-羟色胺转运体基因多态性区与功能性消化不良及其亚型的关联的荟萃分析。
Genet Test Mol Biomarkers. 2023 Mar;27(3):100-108. doi: 10.1089/gtmb.2022.0151.
6
The serotonin transporter gene polymorphism (5-HTTLPR) and irritable bowel syndrome: a meta-analysis of 25 studies.血清素转运体基因多态性(5-HTTLPR)与肠易激综合征:25项研究的荟萃分析
BMC Gastroenterol. 2014 Feb 10;14:23. doi: 10.1186/1471-230X-14-23.
7
A meta-analysis of the effects of the 5-hydroxytryptamine transporter gene-linked promoter region polymorphism on susceptibility to lifelong premature ejaculation.5-羟色胺转运体基因启动子区多态性与终身性早泄易感性的荟萃分析
PLoS One. 2013;8(1):e54994. doi: 10.1371/journal.pone.0054994. Epub 2013 Jan 30.
8
Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis.血红素加氧酶 1 启动子基因多态性与新生儿高胆红素血症的关系:Meta 分析。
J Matern Fetal Neonatal Med. 2021 Jan;34(1):12-23. doi: 10.1080/14767058.2019.1570115. Epub 2019 Jan 30.
9
Pharmacogenetic association of bi- and triallelic polymorphisms of SLC6A4 with antidepressant response in major depressive disorder.单核苷酸多态性与双等位基因和三等位基因 SLC6A4 与抗抑郁药治疗反应的相关性。
J Affect Disord. 2020 Aug 1;273:254-264. doi: 10.1016/j.jad.2020.04.058. Epub 2020 May 11.
10
Association of a serotonin transporter polymorphism (5-HTTLPR) with depression, perceived stress, and norepinephrine in patients with coronary disease: the Heart and Soul Study.冠心病患者中血清素转运体基因多态性(5-HTTLPR)与抑郁、感知压力及去甲肾上腺素的关联:心灵与心脏研究
Am J Psychiatry. 2007 Sep;164(9):1379-84. doi: 10.1176/appi.ajp.2007.06101617.

引用本文的文献

1
Genetic variants of SLC6A4 and risk of coronary artery disease: insights from North Indian population.SLC6A4基因变异与冠状动脉疾病风险:来自北印度人群的见解
Orphanet J Rare Dis. 2025 May 14;20(1):229. doi: 10.1186/s13023-025-03761-w.
2
The effect of single nucleotide polymorphisms on depression in combination with coronary diseases: a systematic review and meta-analysis.单核苷酸多态性对合并冠心病的抑郁症的影响:系统评价和荟萃分析。
Front Endocrinol (Lausanne). 2024 Apr 30;15:1369676. doi: 10.3389/fendo.2024.1369676. eCollection 2024.
3
Depression and coronary heart disease: mechanisms, interventions, and treatments.

本文引用的文献

1
Stratified meta-analysis by ethnicity revealed that ADRB3 Trp64Arg polymorphism was associated with coronary artery disease in Asians, but not in Caucasians.按种族进行的分层荟萃分析表明,ADRB3基因Trp64Arg多态性与亚洲人的冠状动脉疾病相关,但与白种人无关。
Medicine (Baltimore). 2020 Jan;99(4):e18914. doi: 10.1097/MD.0000000000018914.
2
Changes of Serotonin (5-HT), 5-HT2A Receptor, and 5-HT Transporter in the Sprague-Dawley Rats of Depression, Myocardial Infarction and Myocardial Infarction Co-exist with Depression.抑郁症、心肌梗死及抑郁症合并心肌梗死的斯普拉格-道利大鼠中血清素(5-羟色胺,5-HT)、5-HT2A受体及5-HT转运体的变化
Chin Med J (Engl). 2015 Jul 20;128(14):1905-9. doi: 10.4103/0366-6999.160526.
3
抑郁症与冠心病:机制、干预措施及治疗方法
Front Psychiatry. 2024 Feb 9;15:1328048. doi: 10.3389/fpsyt.2024.1328048. eCollection 2024.
4
The effect of CYP7B1 polymorphisms on the risk of coronary heart disease in Hainan Han population.CYP7B1 多态性对海南汉族人群冠心病发病风险的影响。
BMC Med Genomics. 2021 Sep 7;14(1):220. doi: 10.1186/s12920-021-01067-x.
5
Association of serotonin transporter-linked polymorphic region (5-HTTLPR) with heat pain stimulation and postoperative pain in gastric cancer patients.5-羟色胺转运体基因(5-HTTLPR)多态性与胃癌患者热痛刺激和术后疼痛的关系。
Mol Pain. 2021 Jan-Dec;17:17448069211006606. doi: 10.1177/17448069211006606.
6
Association of DRD4 exon III and 5-HTTLPR VNTR genetic polymorphisms with psychiatric symptoms in hemodialysis patients.DRD4 exon III 和 5-HTTLPR VNTR 基因多态性与血液透析患者精神症状的关联。
PLoS One. 2021 Mar 30;16(3):e0249284. doi: 10.1371/journal.pone.0249284. eCollection 2021.
Serotonergic genes and depressive disorder in acute coronary syndrome: The Korean depression in ACS (K-DEPACS) study.
血清素能基因与急性冠状动脉综合征中的抑郁症:韩国急性冠状动脉综合征抑郁症(K-DEPACS)研究
Eur Neuropsychopharmacol. 2015 Jun;25(6):882-8. doi: 10.1016/j.euroneuro.2015.02.006. Epub 2015 Feb 28.
4
Depression as a risk factor for poor prognosis among patients with acute coronary syndrome: systematic review and recommendations: a scientific statement from the American Heart Association.抑郁症作为急性冠状动脉综合征患者预后不良的危险因素:系统评价和建议:美国心脏协会的科学声明。
Circulation. 2014 Mar 25;129(12):1350-69. doi: 10.1161/CIR.0000000000000019. Epub 2014 Feb 24.
5
Meta-analysis of association between the -1438A/G (rs6311) polymorphism of the serotonin 2A receptor gene and major depressive disorder.血清素2A受体基因-1438A/G(rs6311)多态性与重度抑郁症关联的荟萃分析。
Neurol Res. 2013 Jan;35(1):7-14. doi: 10.1179/1743132812Y.0000000111.
6
The role of the sociotype in managing chronic disease: integrating bio-psycho-sociology with systems biology.社会型在慢性病管理中的作用:将生物-心理-社会学与系统生物学相结合。
Med Hypotheses. 2011 Oct;77(4):610-3. doi: 10.1016/j.mehy.2011.06.046. Epub 2011 Jul 26.
7
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement.系统评价与Meta分析的首选报告项目:PRISMA声明。
Open Med. 2009;3(3):e123-30. Epub 2009 Jul 21.
8
Association between a serotonin transporter gene variant and hopelessness among men in the Heart and Soul Study.与希望感相关的血清素转运体基因多态性与“心脏与心灵研究”中男性人群的关系。
J Gen Intern Med. 2010 Oct;25(10):1030-7. doi: 10.1007/s11606-010-1403-0. Epub 2010 May 28.
9
Coronary artery disease and depression: possible role of brain-derived neurotrophic factor and serotonin transporter gene polymorphisms.冠状动脉疾病与抑郁症:脑源性神经营养因子和 5-羟色胺转运体基因多态性的可能作用。
Int J Mol Med. 2009 Dec;24(6):813-8. doi: 10.3892/ijmm_00000297.
10
Relationship of genetic variability and depressive symptoms to adverse events after coronary artery bypass graft surgery.冠状动脉搭桥手术后基因变异性及抑郁症状与不良事件的关系。
Psychosom Med. 2008 Nov;70(9):953-9. doi: 10.1097/PSY.0b013e318187aee6.