GALUŠKA, David, Lucie DLOUHÁ, Jaroslav HUBÁČEK and Kateřina KAŇKOVÁ. Genetics of T2DM and Its Chronic Complications: Are We Any Closer to the Individual Prediction of Genetic Risk? FOLIA BIOLOGICA. PRAGUE: CHARLES UNIV PRAGUE, FIRST FACULTY MEDICINE, 2022, vol. 68, 5-6, p. 159-179. ISSN 0015-5500. Available from: https://dx.doi.org/10.14712/fb2022068050159.
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Basic information
Original name Genetics of T2DM and Its Chronic Complications: Are We Any Closer to the Individual Prediction of Genetic Risk?
Authors GALUŠKA, David (203 Czech Republic, belonging to the institution), Lucie DLOUHÁ (203 Czech Republic, guarantor), Jaroslav HUBÁČEK (203 Czech Republic) and Kateřina KAŇKOVÁ (203 Czech Republic, belonging to the institution).
Edition FOLIA BIOLOGICA, PRAGUE, CHARLES UNIV PRAGUE, FIRST FACULTY MEDICINE, 2022, 0015-5500.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30101 Human genetics
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 0.600
RIV identification code RIV/00216224:14110/22:00134644
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.14712/fb2022068050159
UT WoS 001010557100001
Keywords in English diabetes mellitus; diabetes complication; polymorphism; Central European population; genetic; GWAS; diabetic neuropathy; diabetic kidney disease; diabetic retinopathy; cardiovascular disease
Tags 14110518, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 9/8/2023 12:06.
Abstract
Type 2 diabetes mellitus (T2DM) is a com-plex disease that has risen in global prevalence over recent decades, resulting in concomitant and enor-mous socio-economic impacts. In addition to the well-documented risk factors of obesity, poor dietary habits and sedentary lifestyles, genetic background plays a key role in the aetiopathogenesis of diabetes and the development of associated micro-and macro -vascular complications. Recent advances in genomic research, notably next-generation sequencing and ge-nome-wide association studies, have greatly improved the efficiency with which genetic backgrounds to com-plex diseases are analysed. To date, several hundred single-nucleotide polymorphisms have been associ-ated with T2DM or its complications. Given the poly -genic background to T2DM (and numerous other complex diseases), the degree of genetic predisposi-tion can be treated as a "continuous trait" quantified by a genetic risk score. Focusing mainly on the Central European population, this review summa-rizes recent state-of-the-art methods that have en-abled us to better determine the genetic architecture of T2DM and the utility of genetic risk scores in dis-ease prediction.
Links
NV18-01-00046, research and development projectName: Genetické skóre v predikci rizika diabetu a jeho komplikací
Investor: Ministry of Health of the CR
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