UGENE project_DATABASE_All participants.xlsx

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 com...

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Hauptverfasser: Vliora, Maria, Dinas, Petros C., Nintou, Eleni, Pravednikova, Anna E., Sakellariou, Paraskevi, Witkowicz, Agata, Kachaev, Zaur M., Kerchev, Victor V., Larina, Svetlana N., Cotton, James, Kowalska, Anna, Gkiata, Paraskevi, Bargiota, Alexandra, Khachatryan, Zaruhi A., Hovhannisyan, Anahit A., Antonosyan, Mariya A., Margaryan, Sona, Partyka, Anna, Bogdanski, Pawel, Szulinska, Monika, Kregielska-Narozna, Matylda, Czepczyński, Rafał, Ruchała, Marek, Tomkiewicz, Anna, Yepiskoposyan, Levon, Karabon, Lidia, Shidlovskii, Yulii, Metsios, George, Flouris, Andreas
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Sprache:eng
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Zusammenfassung: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 common CMP and their risk factors across Armenia, Greece, Poland, Russia and United Kingdom. This case-control study included genotyping of these SNPs, from 2,283 Caucasians. Results were extended via systematic review and meta-analysis. In Armenia, GA genotype and A allele of Ala64Thr displayed ~2-fold higher risk for CMP compared to GG genotype and G allele, respectively (p
DOI:10.6084/m9.figshare.17206709