{"title":"Monogenic Diabetes Reported in South Asians: A Systematic Review","authors":"Venkatesan Radha, Sekar Kanthimathi, Anandakumar Amutha, Balaji Bhavadharini, Ranjit Mohan Anjana, Ranjit Unnikrishnan, Viswanathan Mohan","doi":"10.1007/s41745-023-00399-0","DOIUrl":null,"url":null,"abstract":"<div><p>Monogenic diabetes refers to a group of single gene disorders of insulin secretion impairment resulting in diabetes. We selected two of the commonest forms of monogenic diabetes namely, maturity onset of diabetes of the young (MODY) and neonatal diabetes mellitus (NDM), and looked for studies that reported these two conditions in South Asians (SA). The primary aim was to identify the number of monogenic diabetes cases reported so far in SA. We searched major databases from 1990 to 2022 to identify articles published on monogenic diabetes in SA countries and SAs. Original articles that showed the prevalence or reported cases of monogenic diabetes through genetic analysis, on children, adolescents and adults, published in the English Language were included. Following an initial screening by title and abstract by three reviewers, the full texts retrieved were independently screened by two reviewers. A total of 3176 studies on monogenic diabetes were obtained and 2525 abstracts were selected for the title and abstract screening, subsequently were excluded. The remaining 235 abstracts underwent full-text analysis. Finally, 46 studies (MODY, <i>n</i> = 18 and NDM, <i>n</i> = 28) were included in this paper. A total of 89 variants in MODY and 139 variants in NDM were recorded. Among the documented variants, 38 were causal for MODY and 116 were causal for NDM. This review provides the list of causal variants of MODY and NDM in SA. This could be helpful in the clinical setting for planning the treatment of MODY and NDM individuals in SA.</p><p><b>Systematic Review registration</b> https://www.crd.york.ac.uk/prospero/#myprospero (ID: CRD42022296268).</p></div>","PeriodicalId":675,"journal":{"name":"Journal of the Indian Institute of Science","volume":"103 1","pages":"309 - 334"},"PeriodicalIF":1.8000,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Indian Institute of Science","FirstCategoryId":"103","ListUrlMain":"https://link.springer.com/article/10.1007/s41745-023-00399-0","RegionNum":4,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Monogenic diabetes refers to a group of single gene disorders of insulin secretion impairment resulting in diabetes. We selected two of the commonest forms of monogenic diabetes namely, maturity onset of diabetes of the young (MODY) and neonatal diabetes mellitus (NDM), and looked for studies that reported these two conditions in South Asians (SA). The primary aim was to identify the number of monogenic diabetes cases reported so far in SA. We searched major databases from 1990 to 2022 to identify articles published on monogenic diabetes in SA countries and SAs. Original articles that showed the prevalence or reported cases of monogenic diabetes through genetic analysis, on children, adolescents and adults, published in the English Language were included. Following an initial screening by title and abstract by three reviewers, the full texts retrieved were independently screened by two reviewers. A total of 3176 studies on monogenic diabetes were obtained and 2525 abstracts were selected for the title and abstract screening, subsequently were excluded. The remaining 235 abstracts underwent full-text analysis. Finally, 46 studies (MODY, n = 18 and NDM, n = 28) were included in this paper. A total of 89 variants in MODY and 139 variants in NDM were recorded. Among the documented variants, 38 were causal for MODY and 116 were causal for NDM. This review provides the list of causal variants of MODY and NDM in SA. This could be helpful in the clinical setting for planning the treatment of MODY and NDM individuals in SA.
单基因糖尿病是指由胰岛素分泌障碍引起的一组单基因疾病。我们选择了两种最常见的单基因糖尿病,即年轻期糖尿病(MODY)和新生儿糖尿病(NDM),并寻找在南亚(SA)报道这两种情况的研究。主要目的是确定迄今为止在南非报道的单基因糖尿病病例的数量。我们检索了1990年至2022年的主要数据库,以确定SA国家和SA中发表的关于单基因糖尿病的文章。通过对儿童、青少年和成人进行基因分析,显示单基因糖尿病患病率或报告病例的原创文章被纳入其中。在三位审稿人对标题和摘要进行初步筛选之后,检索到的全文由两位审稿人独立筛选。共获得3176篇关于单基因糖尿病的研究,选取2525篇摘要进行标题和摘要筛选,随后排除。对其余235篇摘要进行全文分析。最终纳入46项研究(MODY, n = 18, NDM, n = 28)。MODY共记录89个变异,NDM共记录139个变异。在记录的变异中,38个与MODY相关,116个与NDM相关。这篇综述提供了SA中MODY和NDM的因果变异列表。这可能有助于制定SA中MODY和NDM个体的临床治疗计划。系统评论注册https://www.crd.york.ac.uk/prospero/#myprospero (ID: CRD42022296268)。
期刊介绍:
Started in 1914 as the second scientific journal to be published from India, the Journal of the Indian Institute of Science became a multidisciplinary reviews journal covering all disciplines of science, engineering and technology in 2007. Since then each issue is devoted to a specific topic of contemporary research interest and guest-edited by eminent researchers. Authors selected by the Guest Editor(s) and/or the Editorial Board are invited to submit their review articles; each issue is expected to serve as a state-of-the-art review of a topic from multiple viewpoints.