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

IF 1.1 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Global Health Epidemiology and Genomics Pub Date : 2016-03-08 eCollection Date: 2016-01-01 DOI:10.1017/gheg.2015.6
K Ekoru, E H Young, C Adebamowo, N Balde, B J Hennig, P Kaleebu, S Kapiga, N S Levitt, M Mayige, J C Mbanya, M I McCarthy, O Nyan, M Nyirenda, J Oli, K Ramaiya, L Smeeth, E Sobngwi, C N Rotimi, M S Sandhu, A A Motala
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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.

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H3Africa 撒哈拉以南非洲 2 型糖尿病发病率及环境和遗传决定因素多中心研究:研究方案。
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。撒哈拉以南非洲地区(SSA)尚未可靠地阐明 T2D 流行病学的这些方面,这凸显出需要针对具体情况进行具有统计分辨率的流行病学研究,以便为潜在的预防和治疗策略提供信息。因此,作为非洲人类遗传与健康(H3Africa)计划的一部分,我们设计了一项多地点研究,包括在撒哈拉以南非洲 8 个国家的 11 个地点进行病例收集和人群调查。目标是招募多达 6000 名 T2D 患者和 6000 名对照组患者。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慢性病特征、风险因素和遗传数据的生物样本。通过整合流行病学和基因组学技术,该研究为评估整个撒哈拉以南非洲地区 T2D 及其并发症的负担、发病范围、环境和遗传风险因素提供了一个框架。由于建立了实地调查、数据和样本收集与管理、数据共享和重新接触参与者的同意机制,该研究将成为未来研究的资源,包括纵向研究、前瞻性发病病例确定和干预研究。
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来源期刊
Global Health Epidemiology and Genomics
Global Health Epidemiology and Genomics PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.40
自引率
0.00%
发文量
10
审稿时长
20 weeks
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