Suppr超能文献

听力障碍的公共卫生负担与基因组学和环境研究的前景:以非洲加纳为例。

Public Health Burden of Hearing Impairment and the Promise of Genomics and Environmental Research: A Case Study in Ghana, Africa.

机构信息

1 West African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana , Accra, Ghana .

2 ENT Unit, Audiology Section Korle-Bu Teaching Hospital , Accra, Ghana .

出版信息

OMICS. 2017 Nov;21(11):638-646. doi: 10.1089/omi.2017.0145.

Abstract

Hearing impairment (HI) is one of the most disabling conditions of major global health burden that contributes adversely to the social and economic development of a country, if not managed properly. A proper assessment of the nationwide burden and etiology of HI is instrumental in the prevention, treatment, and management of the condition. This article sought to perform an expert review of HI in Ghana to determine the present knowledge of its burden and possible causes of the condition. A literature search was conducted in PubMed using the following keywords: "hearing loss" OR "hearing impairment" OR "deafness" AND "Ghana." The literature was scanned until July 20, 2017, with specific inclusion of targeted landmark and background articles on HI. From the search, 18 of out 5869 articles were selected and considered for the review. The results of the search indicated that there were no extensive studies to determine the national burden of HI in Ghana. However, the few studies assessed suggested that the disease is either acquired or inherited. The burden of acquired HI was higher in adults than children, women than men, and people working in a noisy environment. Regarding the genetic cause, specific founder mutations in GJB2 gene (R143W, L79P, V178A, R184Q, A197S, I203K, and L214P) was the only identified genetic cause of HI in Ghana, but the other HI genes were not investigated. There has been some modest effort to study HI in Ghana, but comprehensive studies on the genetic and environmental etiologies (using the "multi-OMICS" approaches), classification, and burden of HI on Ghana are needed.

摘要

听力障碍(HI)是全球主要健康负担中最具致残性的疾病之一,如果管理不当,会对国家的社会和经济发展产生不利影响。对全国 HI 负担和病因进行适当评估,有助于预防、治疗和管理该病。本文旨在对加纳的 HI 进行专家审查,以确定其目前的疾病负担和可能病因的相关知识。在 PubMed 中使用以下关键字进行文献检索:“听力损失”或“听力障碍”或“耳聋”和“加纳”。文献检索截至 2017 年 7 月 20 日,具体包括针对 HI 的重点标志性和背景文章。从检索中,共选出 5869 篇文章中的 18 篇进行综述。检索结果表明,加纳没有广泛的研究来确定 HI 的全国负担。然而,评估的少数研究表明,这种疾病要么是后天获得的,要么是遗传的。后天 HI 的负担在成人中高于儿童,女性高于男性,在嘈杂环境中工作的人高于其他人。至于遗传原因,在 GJB2 基因(R143W、L79P、V178A、R184Q、A197S、I203K 和 L214P)中发现的特定的致病变异是加纳 HI 的唯一遗传病因,但其他 HI 基因并未被研究。加纳对 HI 进行了一些适度的研究,但仍需要对 HI 的遗传和环境病因(采用“多组学”方法)、分类以及对加纳的疾病负担进行更全面的研究。

相似文献

5
and Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.加纳非综合征性儿童听力损失中的突变
Front Genet. 2019 Sep 18;10:841. doi: 10.3389/fgene.2019.00841. eCollection 2019.

本文引用的文献

1
Global hearing health care: new findings and perspectives.全球听力保健:新发现和新视角。
Lancet. 2017 Dec 2;390(10111):2503-2515. doi: 10.1016/S0140-6736(17)31073-5. Epub 2017 Jul 10.
4
Precision medicine, genomics and drug discovery.精准医学、基因组学与药物研发。
Hum Mol Genet. 2016 Oct 1;25(R2):R166-R172. doi: 10.1093/hmg/ddw246. Epub 2016 Aug 18.
9
Otoacoustic emission testing in Ghanaian children with sickle-cell disease.加纳镰状细胞病患儿的耳声发射测试
Trop Med Int Health. 2015 Sep;20(9):1209-1212. doi: 10.1111/tmi.12533. Epub 2015 May 21.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验