• 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

心脏代谢危险因素遗传研究的基本原理与设计:德黑兰心脏代谢遗传研究(TCGS)方案

Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS).

作者信息

Daneshpour Maryam S, Fallah Mohammad-Sadegh, Sedaghati-Khayat Bahareh, Guity Kamran, Khalili Davood, Hedayati Mehdi, Ebrahimi Ahmad, Hajsheikholeslami Farhad, Mirmiran Parvin, Ramezani Tehrani Fahimeh, Momenan Amir-Abbas, Ghanbarian Arash, Amouzegar Atieh, Amiri Parisa, Azizi Fereidoun

机构信息

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Islamic Republic Of Iran.

Prevention Of Metabolic Disorders Research Center, Research Institute For Endocrine Sciences, Shahid Beheshti University Of Medical Sciences, Tehran, Islamic Republic Of Iran.

出版信息

JMIR Res Protoc. 2017 Feb 23;6(2):e28. doi: 10.2196/resprot.6050.

DOI:10.2196/resprot.6050
PMID:28232301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5344981/
Abstract

BACKGROUND

Cardiometabolic risk factors comprise cardiovascular diseases and/or diabetes, and need to be evaluated in different fields.

OBJECTIVE

The primary aim of the Tehran Cardiometabolic Genetic Study (TCGS) is to create a comprehensive genome-wide database of at least 16,000 Tehranians, who are participants of the ongoing Tehran Lipid and Glucose Study (TLGS) cohort.

METHODS

TCGS was designed in collaboration with the Research Institute for Endocrine Sciences and the genetic company deCODE. Participants had already been followed for over a 20-year period for major cardiometabolic-related health events including myocardial infarction, stroke, diabetes mellitus, hypertension, obesity, hyperlipidemia, and familial hypercholesterolemia.

RESULTS

The TCGS cohort described here comprises 17,186 (86.3%) of the 19,905 TLGS participants who provided a baseline blood sample that was adequate for plasma and deoxyribonucleic acid analysis. This study is comprised of 849 individuals and 3109 families with at least one member having genotype information. Finally, 5977 males and 7422 females with the total genotyping rate of 0.9854 were genotyped with HumanOmniExpress-24-v1-0 bead chips (containing 649,932 single-nucleotide polymorphism loci with an average mean distance of 4 kilobases).

CONCLUSIONS

Investigations conducted within the TCGS will seek to identify relevant patterns of genetic polymorphisms that could be related to cardiometabolic risk factors in participants from Tehran. By linking genome-wide data to the existing databank of TLGS participants, which includes comprehensive behavioral, biochemical, and clinical data on each participant since cohort inception in 1999, the TCGS will also allow exploration of gene-gene and gene-environment interactions as they relate to disease status.

摘要

背景

心脏代谢危险因素包括心血管疾病和/或糖尿病,需要在不同领域进行评估。

目的

德黑兰心脏代谢基因研究(TCGS)的主要目的是创建一个至少包含16000名德黑兰人的全基因组数据库,这些人是正在进行的德黑兰脂质与葡萄糖研究(TLGS)队列的参与者。

方法

TCGS是与内分泌科学研究所和基因公司deCODE合作设计的。参与者已经被跟踪了20多年,以观察主要的心脏代谢相关健康事件,包括心肌梗死、中风、糖尿病、高血压、肥胖、高脂血症和家族性高胆固醇血症。

结果

这里描述的TCGS队列包括19905名TLGS参与者中的17186名(86.3%),他们提供了足以进行血浆和脱氧核糖核酸分析的基线血样。本研究由849名个体和3109个家庭组成,其中至少有一名成员具有基因型信息。最后,使用HumanOmniExpress-24-v1-0珠芯片(包含649932个单核苷酸多态性位点,平均间距为4千碱基)对5977名男性和7422名女性进行基因分型,总基因分型率为0.9854。

结论

在TCGS内进行的研究将试图识别可能与德黑兰参与者心脏代谢危险因素相关的遗传多态性相关模式。通过将全基因组数据与TLGS参与者的现有数据库相链接,该数据库包括自1999年队列开始以来每个参与者的全面行为、生化和临床数据,TCGS还将允许探索与疾病状态相关的基因-基因和基因-环境相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c42e/5344981/5925039306f9/resprot_v6i2e28_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c42e/5344981/5925039306f9/resprot_v6i2e28_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c42e/5344981/5925039306f9/resprot_v6i2e28_fig1.jpg

相似文献

1
Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS).心脏代谢危险因素遗传研究的基本原理与设计:德黑兰心脏代谢遗传研究(TCGS)方案
JMIR Res Protoc. 2017 Feb 23;6(2):e28. doi: 10.2196/resprot.6050.
2
Cohort profile update: Tehran cardiometabolic genetic study.队列资料更新:德黑兰心脏代谢遗传学研究。
Eur J Epidemiol. 2023 Jun;38(6):699-711. doi: 10.1007/s10654-023-01008-1. Epub 2023 May 12.
3
Outcomes of a Longitudinal Population-based Cohort Study and Pragmatic Community Trial: Findings from 20 Years of the Tehran Lipid and Glucose Study.一项基于人群的纵向队列研究和实用社区试验的结果:德黑兰脂质与血糖研究20年的发现。
Int J Endocrinol Metab. 2018 Oct 13;16(4 Suppl):e84748. doi: 10.5812/ijem.84748. eCollection 2018 Oct.
4
Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women.女性基因组健康研究的基本原理、设计与方法:一项针对超过25000名初始健康的美国女性的全基因组关联研究。
Clin Chem. 2008 Feb;54(2):249-55. doi: 10.1373/clinchem.2007.099366. Epub 2007 Dec 10.
5
Sex, age, and ethnic dependency of lipoprotein variants as the risk factors of ischemic heart disease: a detailed study on the different age-classes and genders in Tehran Cardiometabolic Genetic Study (TCGS).脂蛋白变异作为缺血性心脏病危险因素的性别、年龄和种族依赖性:德黑兰心脏代谢遗传研究(TCGS)中不同年龄和性别的详细研究。
Biol Sex Differ. 2022 Jan 28;13(1):4. doi: 10.1186/s13293-022-00413-7.
6
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS).通过伊朗家系的联合连锁和连锁不平衡分析发现RPGRIP1L基因中rs13334070与肥胖因素的新型关联:德黑兰心脏代谢遗传学研究(TCGS)
Genet Epidemiol. 2019 Apr;43(3):342-351. doi: 10.1002/gepi.22179. Epub 2018 Dec 30.
7
Rationale and design of the LURIC study--a resource for functional genomics, pharmacogenomics and long-term prognosis of cardiovascular disease.LURIC研究的基本原理与设计——心血管疾病功能基因组学、药物基因组学及长期预后的资源
Pharmacogenomics. 2001 Feb;2(1 Suppl 1):S1-73. doi: 10.1517/14622416.2.1.S1.
8
Sex-specific association of FABP2 polymorphisms with the risk of obesity in the Tehran Cardio-Metabolic Genetic Study (TCGS).FABP2 多态性与德黑兰心脏代谢遗传研究 (TCGS) 中肥胖风险的性别特异性关联。
Gene. 2023 Aug 5;876:147519. doi: 10.1016/j.gene.2023.147519. Epub 2023 May 30.
9
[Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers].[心肌梗死中的遗传因素——β受体阻滞剂候选基因与全基因组研究结果]
Herz. 2002 Nov;27(7):649-61. doi: 10.1007/s00059-002-2432-1.
10
Parental Transmission Plays the Major Role in High Aggregation of Type 2 Diabetes in Iranian Families: Tehran Lipid and Glucose Study.父母遗传在 2 型糖尿病的家族高度聚集中起主要作用:德黑兰血脂和血糖研究。
Can J Diabetes. 2022 Feb;46(1):60-68. doi: 10.1016/j.jcjd.2021.05.009. Epub 2021 Jun 1.

引用本文的文献

1
Tracking the correlation of mineral intakes among family pairs over nine years: a longitudinal study.追踪九年期间家庭配对成员间矿物质摄入量的相关性:一项纵向研究。
BMC Nutr. 2025 Jan 20;11(1):15. doi: 10.1186/s40795-025-00995-6.
2
The trend of correlation changes of macronutrient intakes among different familial pairs: a prospective study among participants of Tehran Lipid and Glucose Study.不同家庭配对中宏量营养素摄入量相关性变化的趋势:德黑兰血脂和血糖研究参与者的前瞻性研究。
BMC Public Health. 2024 Oct 16;24(1):2854. doi: 10.1186/s12889-024-20362-7.
3
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes.

本文引用的文献

1
Genetics: Implications for Prevention and Management of Coronary Artery Disease.遗传学:对冠状动脉疾病的预防和管理的启示。
J Am Coll Cardiol. 2016 Dec 27;68(25):2797-2818. doi: 10.1016/j.jacc.2016.10.039.
2
Web-Based Interventions Targeting Cardiovascular Risk Factors in Middle-Aged and Older People: A Systematic Review and Meta-Analysis.针对中老年人心血管危险因素的基于网络的干预措施:系统评价与荟萃分析
J Med Internet Res. 2016 Mar 11;18(3):e55. doi: 10.2196/jmir.5218.
3
GWAS as a Driver of Gene Discovery in Cardiometabolic Diseases.
家庭结构对 2 型糖尿病遗传仍缺失率和基因组预测准确性的影响。
Hum Genomics. 2024 Sep 11;18(1):98. doi: 10.1186/s40246-024-00669-7.
4
Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran.探讨伊朗青少年起病的成年型糖尿病(MODY)的临床和遗传谱。
Sci Rep. 2024 Aug 27;14(1):19860. doi: 10.1038/s41598-024-70864-y.
5
Bibliometric overview of the Tehran Lipid and Glucose Study (TLGS) publications from 2000 to 2022.2000年至2022年德黑兰脂质与葡萄糖研究(TLGS)出版物的文献计量学概述。
J Diabetes Metab Disord. 2024 Feb 13;23(1):343-351. doi: 10.1007/s40200-024-01392-9. eCollection 2024 Jun.
6
Three candidate SNPs show associations with thyroid-stimulating hormone in euthyroid subjects: Tehran thyroid study.三个候选单核苷酸多态性与甲状腺功能正常受试者的促甲状腺激素存在关联:德黑兰甲状腺研究。
J Diabetes Metab Disord. 2024 Jan 23;23(1):1047-1055. doi: 10.1007/s40200-023-01383-2. eCollection 2024 Jun.
7
The Tehran longitudinal family-based cardiometabolic cohort study sheds new light on dyslipidemia transmission patterns.德黑兰基于家系的心血管代谢纵向队列研究为血脂异常的传播模式提供了新的视角。
Sci Rep. 2024 Feb 27;14(1):4739. doi: 10.1038/s41598-024-53504-3.
8
An optimized method for PCR-based genotyping to detect human APOE polymorphisms.一种基于聚合酶链反应(PCR)基因分型检测人类载脂蛋白E(APOE)多态性的优化方法。
Heliyon. 2023 Oct 19;9(11):e21102. doi: 10.1016/j.heliyon.2023.e21102. eCollection 2023 Nov.
9
Association of rs2282679 polymorphism in vitamin D binding protein gene (GC) with the risk of vitamin D deficiency in an iranian population: season-specific vitamin D status.维生素 D 结合蛋白基因(GC)rs2282679 多态性与伊朗人群维生素 D 缺乏风险的关联:特定季节的维生素 D 状态。
BMC Endocr Disord. 2023 Oct 10;23(1):217. doi: 10.1186/s12902-023-01463-7.
10
Familial resemblance and family-based heritability of nutrients intake in Iranian population: Tehran cardiometabolic genetic study.伊朗人群营养素摄入的家族相似性和基于家庭的遗传性:德黑兰心血管代谢遗传学研究。
BMC Public Health. 2023 Sep 14;23(1):1789. doi: 10.1186/s12889-023-16708-2.
GWAS 作为心脏代谢疾病基因发现的驱动力。
Trends Endocrinol Metab. 2015 Dec;26(12):722-732. doi: 10.1016/j.tem.2015.10.004. Epub 2015 Nov 18.
4
Mitigation of non-communicable diseases in developing countries with community health workers.利用社区卫生工作者减轻发展中国家的非传染性疾病负担
Global Health. 2015 Nov 10;11:43. doi: 10.1186/s12992-015-0129-5.
5
Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors.识别冠状动脉疾病中的新型基因变异以及与多种心血管危险因素相关的共享基因。
Circ Res. 2016 Jan 8;118(1):83-94. doi: 10.1161/CIRCRESAHA.115.306629. Epub 2015 Oct 20.
6
Using genome-wide associations to identify metabolic pathways involved in maize aflatoxin accumulation resistance.利用全基因组关联分析来鉴定参与玉米黄曲霉毒素积累抗性的代谢途径。
BMC Genomics. 2015 Sep 3;16(1):673. doi: 10.1186/s12864-015-1874-9.
7
The CardioMetabolic Health Alliance: Working Toward a New Care Model for the Metabolic Syndrome.心血管代谢健康联盟:致力于代谢综合征的新型护理模式。
J Am Coll Cardiol. 2015 Sep 1;66(9):1050-67. doi: 10.1016/j.jacc.2015.06.1328.
8
Update on Prevention of Cardiovascular Disease in Adults With Type 2 Diabetes Mellitus in Light of Recent Evidence: A Scientific Statement From the American Heart Association and the American Diabetes Association.基于最新证据的2型糖尿病成年患者心血管疾病预防最新进展:美国心脏协会和美国糖尿病协会的科学声明
Circulation. 2015 Aug 25;132(8):691-718. doi: 10.1161/CIR.0000000000000230. Epub 2015 Aug 5.
9
Effect of a Web-Based Behavior Change Program on Weight Loss and Cardiovascular Risk Factors in Overweight and Obese Adults at High Risk of Developing Cardiovascular Disease: Randomized Controlled Trial.基于网络的行为改变计划对有心血管疾病高风险的超重和肥胖成年人减肥及心血管危险因素的影响:随机对照试验。
J Med Internet Res. 2015 Jul 16;17(7):e177. doi: 10.2196/jmir.3828.
10
Genetically determined height and coronary artery disease.基因决定的身高与冠状动脉疾病。
N Engl J Med. 2015 Apr 23;372(17):1608-18. doi: 10.1056/NEJMoa1404881. Epub 2015 Apr 8.