IF 1.6 4区 医学 Q3 CLINICAL NEUROLOGY
Felipe Duarte-Zambrano, David Felipe Alfonso-Cedeño, Jorge A Barrero, Luis Alejandro Rodríguez-Vanegas, Valentina Moreno-Cárdenas, Anamaría Olarte-Díaz, Gonzalo Arboleda, Humberto Arboleda
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引用次数: 0

摘要

特发性帕金森病(PD)是一种受遗传、环境和生活方式等因素影响的复杂性状,其遗传率估计接近 30%。然而,与帕金森病相关的遗传变异中仍有很大一部分不确定,部分原因是祖先的偏见。扩大对西班牙裔人群的研究有助于填补这一空白。回顾拉丁美洲与特发性帕金森病相关的遗传变异证据。我们在MEDLINE、EMBASE和LILACS上进行了符合PRISMA标准的系统性综述,汇编了截至2025年2月7日发表的研究。共纳入 19 项病例对照研究。两项无假设研究分别通过 XWAS 和 GWAS 将 H2BW1 附近的 rs525496 确定为保护因素,将 SNCA 中的 rs356182 确定为风险因素。十七项假设驱动研究检测了三百多个变体,确定了十九个遗传标记;风险因素包括 NR4A2 中的一个 INDEL,PRKN、SNCA 和 PLA2G6 中的 CNV 负担,以及 GBA、APOEε4、MTHFR、LRRK2 和 SNCA 等六个位点中的十四个变体。PICALM、ALDH1A1和APOE-ε3位点中的三个SNP被确定为保护因素。此外,六个 SNCA 变异单倍型似乎会增加 PD 风险,而两个 NR4A2 INDELs 单倍型则表现出混合效应。本综述总结了拉丁美洲人群中与特发性帕金森病相关的遗传位点,证明这些位点与欧洲的研究结果有重叠之处,同时还发现了一些新的位点,但尚待复制和验证。这些观察结果有助于人们了解该疾病的遗传结构,并强调有必要在代表性不足的群体中开展进一步的基因组研究,包括在混血队列中进行当地祖先分析,以指导开发个性化治疗方法和针对特定人群的干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variants associated with idiopathic Parkinson's disease in Latin America: A systematic review.

Idiopathic Parkinson's disease (PD) constitutes a complex trait influenced by genetic, environmental, and lifestyle factors, with an estimated heritability of nearly 30%. However, a large proportion of the heritable variation linked to PD remains uncertain, partly due to ancestral bias. Expanding research into Hispanic populations can contribute to address this gap. To review the evidence of genetic variants associated with idiopathic PD in Latin America. A PRISMA-compliant systematic review was conducted in MEDLINE, EMBASE and LILACS, compiling studies published up to February 7, 2025. Nineteen case-control studies were included. Two hypothesis-free studies identified rs525496 near H2BW1 as a protective factor and rs356182 in SNCA as a risk factor through XWAS and GWAS, respectively. Seventeen hypothesis-driven studies examined over three hundred variants, identifying nineteen genetic markers; risk factors included one INDEL in NR4A2, CNV burdens in PRKN, SNCA, and PLA2G6, along with fourteen variants in six loci including GBA, APOEε4, MTHFR, LRRK2, and SNCA. Three SNPs in the PICALM, ALDH1A1, and APOE-ε3 loci were identified as protective factors. Additionally, six SNCA variant haplotypes appear to increase PD risk, while two NR4A2 INDELs haplotypes showed mixed effects. This review summarized genetic loci associated with idiopathic PD in Latin American populations evidencing an overlap with European findings as well as novel loci, although awaiting replication and validation. These observations contribute to the understanding of genetic configuration of the disease and highlight the need for further genomic research in underrepresented groups that include local ancestry analysis within admixed cohorts to guide development of personalized treatments and population-specific interventions.

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来源期刊
Neurogenetics
Neurogenetics 医学-临床神经学
CiteScore
3.90
自引率
0.00%
发文量
24
审稿时长
6 months
期刊介绍: Neurogenetics publishes findings that contribute to a better understanding of the genetic basis of normal and abnormal function of the nervous system. Neurogenetic disorders are the main focus of the journal. Neurogenetics therefore includes findings in humans and other organisms that help understand neurological disease mechanisms and publishes papers from many different fields such as biophysics, cell biology, human genetics, neuroanatomy, neurochemistry, neurology, neuropathology, neurosurgery and psychiatry. All papers submitted to Neurogenetics should be of sufficient immediate importance to justify urgent publication. They should present new scientific results. Data merely confirming previously published findings are not acceptable.
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