ApoE Polymorphism Analysis in Health and Disease of South Asian Populations: A Systematic Review and Meta-Analysis.

IF 2.3 3区 医学 Q2 GENETICS & HEREDITY
Prayash Paudel, Asutosh Sah, Poonam Paudel
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Abstract

This systematic review and meta-analysis assesses the distribution and health implications of apolipoprotein E (ApoE) ε2, ε3, and ε4 alleles, which play crucial roles in lipoprotein metabolism, in South Asian populations, with a focus on neurodegenerative diseases, movement disorders, traumatic brain injury, mental health disorders, cardiovascular disorders, metabolic disorders, and trauma-related disorders. A total of 53 studies identified through comprehensive searches in PubMed, Embase, and Google Scholar up to July 31, 2024, were included on the basis of predefined eligibility criteria after Risk of Bias Assessment via the New York Ottawa Scale. ε3/ε3 was found to be the most prevalent genotype, followed by ε3/ε4 and ε2/ε3. ε4-containing genotypes were associated with susceptibility to Alzheimer's disease, coronary artery disease, vascular dementia, and obesity, though high heterogeneity in some associations necessitates cautious interpretation, whereas the ε2/ε3 and ε2 alleles showed protective effects in some conditions. These studies had several limitations, including data gaps for specific health conditions, underrepresentation of some South Asian countries, and heterogeneity in outcomes. Despite gaps in the data for some countries and specific health conditions, this review reveals distinct South Asian patterns in ApoE polymorphism-disease associations, highlighting the need for targeted genetic research and tailored public health strategies to advance personalized medicine and healthcare policies in this region. There was no specific funding for this study. The study was registered in PROSPERO (registration number CRD42024575197).

南亚人群健康和疾病中的载脂蛋白e多态性分析:系统回顾和荟萃分析
本系统综述和荟萃分析评估了载脂蛋白E (ApoE) ε2、ε3和ε4等位基因在南亚人群中的分布和健康意义,这些等位基因在脂蛋白代谢中起着至关重要的作用,重点关注神经退行性疾病、运动障碍、创伤性脑损伤、精神健康障碍、心血管疾病、代谢疾病和创伤相关疾病。截至2024年7月31日,在PubMed、Embase和谷歌Scholar中通过综合检索确定了53项研究,并通过纽约渥太华量表进行偏倚风险评估,根据预先确定的资格标准纳入。以ε3/ε3基因型最为普遍,其次为ε3/ε4和ε2/ε3。含有ε4的基因型与阿尔茨海默病、冠状动脉疾病、血管性痴呆和肥胖的易感性相关,但某些关联的高异质性需要谨慎解释,而ε2/ε3和ε2等位基因在某些情况下显示出保护作用。这些研究存在一些局限性,包括特定健康状况的数据缺口,一些南亚国家代表性不足,以及结果的异质性。尽管一些国家和特定健康状况的数据存在差距,但本综述揭示了载脂蛋白e多态性与南亚疾病关联的独特模式,强调了有针对性的遗传研究和量身定制的公共卫生战略的必要性,以推进该地区的个性化医疗和卫生保健政策。这项研究没有专门的资金支持。该研究已在PROSPERO注册(注册号CRD42024575197)。
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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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