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Associations of gender inequality with child malnutrition and mortality across 96 countries. 性别不平等与96个国家儿童营养不良和死亡率的关系。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-03-23 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2016.1
A A Marphatia, T J Cole, C Grijalva-Eternod, J C K Wells

National efforts to reduce low birth weight (LBW) and child malnutrition and mortality prioritise economic growth. However, this may be ineffective, while rising gross domestic product (GDP) also imposes health costs, such as obesity and non-communicable disease. There is a need to identify other potential routes for improving child health. We investigated associations of the Gender Inequality Index (GII), a national marker of women's disadvantages in reproductive health, empowerment and labour market participation, with the prevalence of LBW, child malnutrition (stunting and wasting) and mortality under 5 years in 96 countries, adjusting for national GDP. The GII displaced GDP as a predictor of LBW, explaining 36% of the variance. Independent of GDP, the GII explained 10% of the variance in wasting and stunting and 41% of the variance in child mortality. Simulations indicated that reducing GII could lead to major reductions in LBW, child malnutrition and mortality in low- and middle-income countries. Independent of national wealth, reducing women's disempowerment relative to men may reduce LBW and promote child nutritional status and survival. Longitudinal studies are now needed to evaluate the impact of efforts to reduce societal gender inequality.

减少低出生体重、儿童营养不良和死亡率的国家努力优先考虑经济增长。然而,这可能是无效的,而不断增长的国内生产总值(GDP)也增加了健康成本,如肥胖和非传染性疾病。有必要确定改善儿童健康的其他可能途径。我们调查了性别不平等指数(GII)与96个国家的低体重、儿童营养不良(发育迟缓和消瘦)和5岁以下儿童死亡率之间的关系,该指数是妇女在生殖健康、赋权和劳动力市场参与方面处于劣势的国家标志。GII取代了GDP,成为LBW的预测指标,解释了36%的差异。独立于GDP之外,全球创新指数解释了10%的消瘦和发育迟缓差异以及41%的儿童死亡率差异。模拟结果表明,减少全球免疫指数可能导致低收入和中等收入国家的低体重、儿童营养不良和死亡率大幅下降。与国家财富无关,减少妇女相对于男子的权力剥夺可能会减少低体重,促进儿童营养状况和生存。现在需要进行纵向研究,以评估减少社会性别不平等的努力的影响。
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引用次数: 62
The development of a localised HIV epidemic and the associated excess mortality burden in a rural area of South Africa. 南非农村地区局部艾滋病毒流行的发展及其相关的过高死亡率负担。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-03-23 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2016.3
P Mee, K Kahn, C W Kabudula, R G Wagner, F X Gómez-Olivé, S Madhavan, Mark A Collinson, S M Tollman, P Byass

The human immunodeficiency virus (HIV) epidemic in South Africa rapidly developed into a major pandemic. Here we analyse the development of the epidemic in a rural area of the country. The data used were collected between 1992 and 2013 in a longitudinal population survey, the Agincourt Health and Demographic Surveillance Study, in the northeast of the country. Throughout the period of study mortality rates were similar in all villages, suggesting that there were multiple index cases evenly spread geographically. These were likely to have been returning migrant workers. For those aged below 39 years the HIV mortality rate was higher for women, above this age it was higher for men. This indicates the protective effect of greater access to HIV testing and treatment among older women. The recent convergence of mortality rates for Mozambicans and South Africans indicates that the former refugee population are being assimilated into the host community. More than 60% of the deaths occurring in this community between 1992 and 2013 could be attributed directly or indirectly to HIV. Recently there has been an increasing level of non-HIV mortality which has important implications for local healthcare provision. This study demonstrates how evidence from longitudinal analyses can support healthcare planning.

人类免疫缺陷病毒(HIV)在南非的流行迅速发展成为一场大流行病。我们在此分析该流行病在该国农村地区的发展情况。所使用的数据是在1992年至2013年期间在该国东北部的纵向人口调查——阿金库尔健康和人口监测研究中收集的。在整个研究期间,所有村庄的死亡率相似,这表明有多个指示病例在地理上均匀分布。这些人很可能是返乡的移民工人。39岁以下妇女的艾滋病毒死亡率较高,39岁以上男子的艾滋病毒死亡率较高。这表明老年妇女获得更多艾滋病毒检测和治疗的保护作用。莫桑比克人和南非人的死亡率最近趋于一致,这表明以前的难民人口正在被收容社区同化。1992年至2013年期间,该社区60%以上的死亡可直接或间接归因于艾滋病毒。最近,非艾滋病毒死亡率不断上升,这对当地的保健服务产生了重要影响。本研究展示了纵向分析的证据如何支持医疗保健计划。
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引用次数: 8
H3Africa multi-centre study of the prevalence and environmental and genetic determinants of type 2 diabetes in sub-Saharan Africa: study protocol. 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。
IF 1.1 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH 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

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.

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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引用次数: 0
Regulatory developments in the conduct of clinical trials in India. 在印度进行临床试验的监管发展。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-02-23 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2015.5
R Roy Chaudhury, D Mehta

There has been a drop in clinical research in India following stringent conditions put in place by the Indian Supreme Court in 2013. The Court's orders came in the wake of irregularities highlighted in the conduct of clinical trials in the country. This paper highlights the steps taken by the Indian regulator, the Central Drugs Standard Control Organisation to comply with these directions. These are of three kinds: strengthening regulatory institutions, protecting participant safety and creating regulatory certainty for sponsors and investigators. Examples include the large-scale training of Ethics Committees, framing detailed guidelines on compensation and audiovisual recording of the informed consent process, as well as reducing the time taken to process applications. It is expected that these measures will inspire confidence for the much-needed resumption of clinical research.

在印度最高法院于2013年制定了严格的条件后,印度的临床研究有所下降。法院的命令是在该国临床试验中突出的违规行为之后发出的。本文重点介绍了印度监管机构中央药物标准控制组织为遵守这些指示所采取的步骤。这些措施有三种:加强监管机构、保护参与者安全、为发起人和调查人员创造监管确定性。例子包括对伦理委员会进行大规模培训,制定关于补偿和知情同意过程的视听记录的详细准则,以及缩短处理申请所需的时间。预计这些措施将激发人们对恢复急需的临床研究的信心。
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引用次数: 5
A forum for global population health, technological advances and implementation science. 全球人口健康、技术进步和执行科学论坛。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-02-05 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2015.2
M S Sandhu
Welcome to Global Health, Epidemiology & Genomics (GHEG), a new Open Access journal committed to providing a forum for communicating research and views on interdisciplinary global health. GHEG welcomes research contributions that address and increase our understanding of human population diversity, health and disease, with a special emphasis on those that describe advances in technologies [1] and implementation science [2] relevant to global health and disadvantaged populations. In the face of emerging epidemics, neglected diseases, drug resistance and complex epidemiological transitions, we need to improve access to and delivery of healthcare on a global scale, including integrated healthcare systems for both communicable and non-communicable diseases and co-morbidities at a cost that can be borne by nations with limited resourcing and within the most challenging environments [3]. To facilitate the integration of research findings and evidence into healthcare policy and practice, we will also need to assimilate discovery science and technological advances, including new drugs, vaccines, and methods for disease surveillance and diagnosis. Such advances have the potential to save millions of lives, globally. In these contexts, GHEG will disseminate a broad range of research and views on global health. We aim to promote research that spans genetic disease susceptibility and genomic medicine [4], pathogen surveillance and disease transmission, to the integration of e-health resources, mobile technologies, point-of-care testing for diseases [1], healthcare systems and delivery, and pragmatic community or therapeutic interventions to improve global human health. The breadth of this journal will be its strength. As an Open Access and on-line journal, we encourage readers to access articles outside the immediate scope of their own work and thereby increase and strengthen knowledge beyond their individual specialties. We believe that by building an interactive, open and welcoming community of global health research and implementation professionals we can increase the level of interest, understanding and commitment to work in the global health arena. To that end, alongside the journal, we have developed an active website featuring interviews, blog articles and social media comments. We encourage our readership to actively contribute in this area. For ease of navigation, we have categorised contributions to GHEG by subject matter covering a comprehensive range of relevant areas including epidemiology, genetics, observational epidemiological studies, community interventions, clinical trials, health systems and services, and population demography and history. Given that many articles will have multidisciplinary themes, we will link articles across research themes, disciplines and by geographic region. These future developments will help identify knowledge gaps and research needs. We also plan to publish themed collections of the journal to allow for detailed
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引用次数: 8
Study profile: the Durban Diabetes Study (DDS): a platform for chronic disease research. 研究简介:德班糖尿病研究(DDS):一个慢性疾病研究平台。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-02-05 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2015.3
T R Hird, E H Young, F J Pirie, J Riha, T M Esterhuizen, B O'Leary, M I McCarthy, M S Sandhu, A A Motala

The Durban Diabetes Study (DDS) is a population-based cross-sectional survey of an urban black population in the eThekwini Municipality (city of Durban) in South Africa. The survey combines health, lifestyle and socioeconomic questionnaire data with standardised biophysical measurements, biomarkers for non-communicable and infectious diseases, and genetic data. Data collection for the study is currently underway and the target sample size is 10 000 participants. The DDS has an established infrastructure for survey fieldwork, data collection and management, sample processing and storage, managed data sharing and consent for re-approaching participants, which can be utilised for further research studies. As such, the DDS represents a rich platform for investigating the distribution, interrelation and aetiology of chronic diseases and their risk factors, which is critical for developing health care policies for disease management and prevention. For data access enquiries please contact the African Partnership for Chronic Disease Research (APCDR) at data@apcdr.org or the corresponding author.

德班糖尿病研究(DDS)是一项以南非德班市(eThekwini)城市黑人人口为基础的横断面调查。这项调查将健康、生活方式和社会经济问卷数据与标准化的生物物理测量、非传染性疾病和传染病的生物标志物以及遗传数据结合起来。该研究的数据收集目前正在进行中,目标样本量为10,000名参与者。DDS有一个既定的基础设施,用于调查现场工作、数据收集和管理、样本处理和存储、管理数据共享和同意重新接近参与者,这可以用于进一步的研究。因此,DDS为调查慢性病的分布、相互关系和病因及其危险因素提供了一个丰富的平台,这对制定疾病管理和预防的卫生保健政策至关重要。有关数据访问查询,请通过data@apcdr.org与非洲慢性病研究伙伴关系(APCDR)或通讯作者联系。
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引用次数: 17
Capitalizing on natural experiments in low- to middle-income countries to explore epigenetic contributions to disease risk in migrant populations. 利用中低收入国家的自然实验,探索表观遗传因素对移徙人口疾病风险的影响。
IF 1.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2016-02-05 eCollection Date: 2016-01-01 DOI: 10.1017/gheg.2015.4
J Jaime Miranda, Caren Weinhouse, Rodrigo M Carrillo-Larco, Lijing L Yan
Migration poses a significant and worsening public health problem. As the world becomes increasingly interdependent and the global population continues to expand, rates of bothwithincountry and international migration are rising. Migrants tend to experience differential risks for chronic disease, including cardiovascular and metabolic diseases [1–7]. Differential health outcomes in international migrants are not limited to migrants fromdeveloping todevelopedcountries;migrants fromonedeveloped country to anotherwith regional differences in chronic disease risk may be impacted, as well [8]. Lifestyle factors do not fully explain increased disease risk in some migrant populations. Prior studies have suggested that increases in body mass and blood pressure in migrant populations are related to stress-induced dietary or physical activity changes. These increased risk factors may subsequently influence disease risk [3]. However, individuals that migrated from a subsistence lifestyle on Pacific atoll Tokelau to an urbanized Western lifestyle in New Zealand showed increased blood pressure in men that cannot be fully explained by concomitant dietary changes and weight gain [4]. Migrants often display cardiovascular disease (CVD) risk intermediate to that of non-migrants in their country of origin and to host population natives [5, 9]. These outcomes suggest that setting of origin, together with initial exposures to such settings, plays a role in acquired disease even in the presence of host population lifestyle factors [5, 9]. Although lifetime risks in migrant groups may approach those of the host population over time, there is evidence for differential health outcomes in migrant populations as compared with non-migrants in studies with relatively long follow-up periods. For example, the Finnish Twins Cohort study reported CVD risk intermediate to that of the migrants’ country of origin and of the host population after a 23-year follow-up [5]. Further, in cases in which lifetime risks of migrants do approach the host population over time, the intervening period of differential health is of strong public health interest. Genetic differences do not fully explain differential disease risk, either. Genetic heterogeneity within a country may contribute to differences in health outcomes between migrants and non-migrants if migration is non-random for genetic markers [8]. However, twins that migrated from Finland to Sweden displayed a higher CVD risk than low-risk native Swedes, but a lower risk than their co-twins in highrisk Finland. These data suggest that differential health by the migration status is strongly influenced by environmental factors [5]. In addition, cardiovascular risk factors in * Address for correspondence: J. Jaime Miranda, MD, PhD, CRONICAS Centro de Excelencia en Enfermedades Cronicas, Universidad Peruana Cayetano Heredia, Av. Armendariz 497, Miraflores, Lima 18, Peru. (Email: jaime.miranda@upch.pe)
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引用次数: 0
期刊
Global Health Epidemiology and Genomics
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