在代表性不足的非洲人群中的帕金森遗传学研究:现状和未来前景。

Wael Mohamed
{"title":"在代表性不足的非洲人群中的帕金森遗传学研究:现状和未来前景。","authors":"Wael Mohamed","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Parkinson's disease (PD), the most common motoric neurodegenerative illness, has been extensively researched to better understand its complex pathophysiology. Nearly 80% of genome-wide association studies have been conducted on persons of European ancestry, indicating a lack of diversity in human genetics. Disparate representation may result in disparities that impede the equitable adoption of personalized medicine and may also limit our knowledge of illness etiology. Even though Parkinson's disease (PD) is a global affliction, the AfrAbia population remains understudied. We conducted a dynamic and longitudinal bibliometric analysis to investigate existing studies on Parkinson's disease genetics in the AfrAbia area and identify data gaps and possible new research avenues. All PD papers concentrating on PD genetics were found using the search terms \"Parkinson's Disease\", \"Genetics\", and \"Africa\" in the PubMed/MEDLINE database. Only English publications published between 1992 and 2023 were chosen using filters. Original English-language research publications disclosing genetic results on Parkinson's disease in non-European Africans were examined for inclusion. Two sets of independent reviewers discovered and extracted pertinent data. The bibliometric study was carried out using the R software packages Bibliometrix and Biblioshiny. The narrowed search yielded 43 publications, all published between 2006 and 2022. Yet, after applying filters and considering the inclusion requirements, the search results comprise just 16 original articles out of 43 articles. There were 27 articles eliminated. This study puts emphasis on the critical need for more diverse participant demographics in Parkinson's disease investigations. AfrAbia-PD-Genetic Consortium (AAPDGC) is GP2 initiative that helps to represent AfrAbia PD genetics.</p>","PeriodicalId":72170,"journal":{"name":"American journal of neurodegenerative disease","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195393/pdf/ajnd0012-0023.pdf","citationCount":"0","resultStr":"{\"title\":\"Parkinson's genetics research on underrepresented AfrAbia populations: current state and future prospects.\",\"authors\":\"Wael Mohamed\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Parkinson's disease (PD), the most common motoric neurodegenerative illness, has been extensively researched to better understand its complex pathophysiology. Nearly 80% of genome-wide association studies have been conducted on persons of European ancestry, indicating a lack of diversity in human genetics. Disparate representation may result in disparities that impede the equitable adoption of personalized medicine and may also limit our knowledge of illness etiology. Even though Parkinson's disease (PD) is a global affliction, the AfrAbia population remains understudied. We conducted a dynamic and longitudinal bibliometric analysis to investigate existing studies on Parkinson's disease genetics in the AfrAbia area and identify data gaps and possible new research avenues. All PD papers concentrating on PD genetics were found using the search terms \\\"Parkinson's Disease\\\", \\\"Genetics\\\", and \\\"Africa\\\" in the PubMed/MEDLINE database. Only English publications published between 1992 and 2023 were chosen using filters. Original English-language research publications disclosing genetic results on Parkinson's disease in non-European Africans were examined for inclusion. Two sets of independent reviewers discovered and extracted pertinent data. The bibliometric study was carried out using the R software packages Bibliometrix and Biblioshiny. The narrowed search yielded 43 publications, all published between 2006 and 2022. Yet, after applying filters and considering the inclusion requirements, the search results comprise just 16 original articles out of 43 articles. There were 27 articles eliminated. This study puts emphasis on the critical need for more diverse participant demographics in Parkinson's disease investigations. AfrAbia-PD-Genetic Consortium (AAPDGC) is GP2 initiative that helps to represent AfrAbia PD genetics.</p>\",\"PeriodicalId\":72170,\"journal\":{\"name\":\"American journal of neurodegenerative disease\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195393/pdf/ajnd0012-0023.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of neurodegenerative disease\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of neurodegenerative disease","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

帕金森病(PD)是最常见的运动神经退行性疾病,为了更好地了解其复杂的病理生理,人们对其进行了广泛的研究。近80%的全基因组关联研究都是在欧洲血统的人身上进行的,这表明人类遗传学缺乏多样性。不同的代表可能导致阻碍公平采用个性化医疗的差异,也可能限制我们对疾病病因的了解。尽管帕金森氏症(PD)是一种全球性的疾病,但对非洲人群的研究仍然不足。我们进行了一项动态和纵向文献计量分析,以调查非洲地区帕金森病遗传学的现有研究,并确定数据缺口和可能的新研究途径。在PubMed/MEDLINE数据库中使用搜索词“帕金森病”、“遗传学”和“非洲”可以找到所有关于帕金森病遗传学的论文。只有1992年至2023年间出版的英文出版物被使用过滤器筛选。研究人员检查了披露非欧洲非洲人帕金森病遗传结果的原始英语研究出版物。两组独立的审查人员发现并提取了相关数据。文献计量学研究采用R软件包Bibliometrix和Biblioshiny进行。缩小范围的搜索结果产生了43篇论文,全部发表于2006年至2022年之间。然而,在使用过滤器并考虑纳入要求后,搜索结果中只有43篇原创文章中的16篇。有27篇文章被淘汰。这项研究强调了帕金森病调查中更多样化的参与者人口统计的迫切需要。AfrAbia-PD- genetic Consortium (AAPDGC)是GP2的倡议,帮助代表非洲PD遗传学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Parkinson's genetics research on underrepresented AfrAbia populations: current state and future prospects.

Parkinson's disease (PD), the most common motoric neurodegenerative illness, has been extensively researched to better understand its complex pathophysiology. Nearly 80% of genome-wide association studies have been conducted on persons of European ancestry, indicating a lack of diversity in human genetics. Disparate representation may result in disparities that impede the equitable adoption of personalized medicine and may also limit our knowledge of illness etiology. Even though Parkinson's disease (PD) is a global affliction, the AfrAbia population remains understudied. We conducted a dynamic and longitudinal bibliometric analysis to investigate existing studies on Parkinson's disease genetics in the AfrAbia area and identify data gaps and possible new research avenues. All PD papers concentrating on PD genetics were found using the search terms "Parkinson's Disease", "Genetics", and "Africa" in the PubMed/MEDLINE database. Only English publications published between 1992 and 2023 were chosen using filters. Original English-language research publications disclosing genetic results on Parkinson's disease in non-European Africans were examined for inclusion. Two sets of independent reviewers discovered and extracted pertinent data. The bibliometric study was carried out using the R software packages Bibliometrix and Biblioshiny. The narrowed search yielded 43 publications, all published between 2006 and 2022. Yet, after applying filters and considering the inclusion requirements, the search results comprise just 16 original articles out of 43 articles. There were 27 articles eliminated. This study puts emphasis on the critical need for more diverse participant demographics in Parkinson's disease investigations. AfrAbia-PD-Genetic Consortium (AAPDGC) is GP2 initiative that helps to represent AfrAbia PD genetics.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Exceptionally giant neglected sacral chordoma in a post-poliotic residual paralysis patient - a rare case scenario. Evaluation of willingness to obtain of Covid 19 vaccine in patients with multiple sclerosis. Short segment posterior fixation of unstable thoracolumbar vertebral fractures with fractured vertebra augmentation with intermediate pedicle screw - a clinicoradiological analysis. Single-cell RNA sequencing analysis and Alzheimer's disease: a bibliometric analysis. Leveraging genetic diversity to understand monogenic Parkinson's disease's landscape in AfrAbia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1