Suppr超能文献

H3Africa撒哈拉以南非洲2型糖尿病患病率及环境与遗传决定因素的多中心研究:研究方案

H3Africa multi-centre study of the prevalence and environmental and genetic determinants of type 2 diabetes in sub-Saharan Africa: study protocol.

作者信息

Ekoru K, Young E H, Adebamowo C, Balde N, Hennig B J, Kaleebu P, Kapiga S, Levitt N S, Mayige M, Mbanya J C, McCarthy M I, Nyan O, Nyirenda M, Oli J, Ramaiya K, Smeeth L, Sobngwi E, Rotimi C N, Sandhu M S, Motala A A

机构信息

Department of Medicine, University of Cambridge, Cambridge, UK.

Genetic Epidemiology Group, Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.

出版信息

Glob Health Epidemiol Genom. 2016 Mar 8;1:e5. doi: 10.1017/gheg.2015.6. eCollection 2016.

Abstract

The burden and aetiology of type 2 diabetes (T2D) and its microvascular complications may be influenced by varying behavioural and lifestyle environments as well as by genetic susceptibility. These aspects of the epidemiology of T2D have not been reliably clarified in sub-Saharan Africa (SSA), highlighting the need for context-specific epidemiological studies with the statistical resolution to inform potential preventative and therapeutic strategies. Therefore, as part of the Human Heredity and Health in Africa (H3Africa) initiative, we designed a multi-site study comprising case collections and population-based surveys at 11 sites in eight countries across SSA. The goal is to recruit up to 6000 T2D participants and 6000 control participants. We will collect questionnaire data, biophysical measurements and biological samples for chronic disease traits, risk factors and genetic data on all study participants. Through integrating epidemiological and genomic techniques, the study provides a framework for assessing the burden, spectrum and environmental and genetic risk factors for T2D and its complications across SSA. With established mechanisms for fieldwork, data and sample collection and management, data-sharing and consent for re-approaching participants, the study will be a resource for future research studies, including longitudinal studies, prospective case ascertainment of incident disease and interventional studies.

摘要

2型糖尿病(T2D)及其微血管并发症的负担和病因可能受到不同行为和生活方式环境以及遗传易感性的影响。在撒哈拉以南非洲(SSA),T2D流行病学的这些方面尚未得到可靠的阐明,这凸显了开展针对特定背景的流行病学研究的必要性,这类研究需具备统计学分辨率,以为潜在的预防和治疗策略提供依据。因此,作为非洲人类遗传与健康(H3Africa)倡议的一部分,我们设计了一项多中心研究,在SSA八个国家的11个地点进行病例收集和基于人群的调查。目标是招募多达6000名T2D参与者和6000名对照参与者。我们将收集所有研究参与者的问卷数据、生物物理测量数据以及用于慢性病特征、风险因素和基因数据的生物样本。通过整合流行病学和基因组技术,该研究为评估整个SSA地区T2D及其并发症的负担、范围以及环境和遗传风险因素提供了一个框架。凭借既定的实地调查、数据和样本收集与管理、数据共享以及再次联系参与者的同意机制,该研究将成为未来研究的资源,包括纵向研究、新发疾病的前瞻性病例确定以及干预性研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3116/5870428/87b2d2fa3b82/S2054420015000068_fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验