Prevalence of uncoupling protein one genetic polymorphisms and their relationship with cardiovascular and metabolic health
Petros C. DinasiD, Eleni NintouiD, Maria VlioraiD, Paraskevi Sakellariou, Anna E. PravednikovaiD, Agata WitkowicziD, Zaur M. KachaeviD, Victor V. KercheviD, Ларина Светлана НиколаевнаiD, James M. CottoniD, Anna KowalskaiD, Paraskevi GkiataiD, Αlexandra BargiotaiD, Zaruhi KhachatryaniD, Anahit HovhannisyaniD, Mariya AntonosyaniD, Sona Margaryan, Anna PartykaiD, Paweł BogdańskiiD, Monika SzulińskaiD, Matylda Kręgielska-NarożnaiD, Rafał CzepczyńskiiD, Marek RuchałaiD, Anna TomkiewicziD, Levon YepiskoposyaniD, , Andreas D. FlourisiD
Abstract
The contribution of UCP1 single nucleotide polymorphisms (SNPs) to susceptibility for cardiometabolic pathologies (CMP) and their involvement in specific risk factors for these conditions varies across populations. We tested whether UCP1 SNPs A-3826G, A-1766G, Ala64Thr and A-112C are associated with the most common CMP (cardiovascular disease, hypertension, metabolic syndrome, and type-2 diabetes) and CMP risk factors. This case-control study included blood sample collection from 2,283 Caucasians (1,139 healthy; 1,144 CMP) across Armenia, Greece, Poland, Russia and United Kingdom for genotyping of the above-mentioned SNPs. We extended the results via a systematic review and meta-analysis, covering PubMed, Embase, and Cochrane Library databases. In Armenia the GA genotype and A allele of Ala64Thr were associated with [~]2-fold higher risk for CMP compared to the GG genotype or G allele, respectively (p0.05). Thus, we conclude that the studied SNPs could be associated with the most common CMP and their risk factors in some populations.
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