Association of polymorphisms within the Renin-Angiotensin System with metabolic syndrome in a cohort of Chilean subjects
datacite.alternateIdentifier.citation | ARCHIVES OF ENDOCRINOLOGY METABOLISM,Vol.60,190-198,2016 | |
datacite.alternateIdentifier.doi | 10.1590/2359-3997000000134 | |
datacite.creator | Herrera, Christian L. | |
datacite.creator | Castillo, Wilma | |
datacite.creator | Estrada, Patricia | |
datacite.creator | Mancilla, Barbara | |
datacite.creator | Reyes, Gerardo | |
datacite.creator | Saavedra, Nicolas | |
datacite.creator | Guzman Oyarzo, Neftali | |
datacite.creator | Seron, Pamela | |
datacite.creator | Lanas, Fernando | |
datacite.creator | Salazar, Luis A. | |
datacite.date | 2016 | |
datacite.subject.english | Metabolic syndrome | |
datacite.subject.english | gender | |
datacite.subject.english | polymorphisms | |
datacite.subject.english | renin-angiotensin system | |
datacite.title | Association of polymorphisms within the Renin-Angiotensin System with metabolic syndrome in a cohort of Chilean subjects | |
dc.date.accessioned | 2021-04-30T16:40:40Z | |
dc.date.available | 2021-04-30T16:40:40Z | |
dc.description.abstract | Objective: Metabolic syndrome (MetS) is associated with hypertension, obesity and dyslipidemia. Thus, genetic variants related with these conditions may modulate its development. We evaluated the effect of polymorphisms in the renin-angiotensin system (RAS) on metabolic syndrome risk in a cohort of Chilean subjects. Subjects and methods: A total of 152 subjects, 83 with MetS (51.2 +/- 9.6 years) and 69 without MetS (49.5 +/- 9.3 years) of both genders were included, according to the ATP III update criteria. The rs4340 Insertion/Deletion (I/D), rs699 (T>C) and rs5186 (A>C) of the ACE, AGT and AGTR1 genes, respectively, were genotyped. Results: After adjusting for age and gender, we observed the DD genotype of rs4340 associated with MetS (p = 0.02). Specifically, the DD genotype was associated with MetS risk in women (OR = 4.62, 95% CI, 1.41 - 15.04; p < 0.01). In males, the AA genotype for rs5186 variant was associated with an increased risk for developing MetS when compared with women carrying the same genotype (OR = 3.2; 95% CI, 1.03 - 9.89; p = 0.04). In subjects without MetS, DD genotype was associated with increased waist circumference (p = 0.023) while subjects with MetS carrying the rs5186 TT genotype showed higher levels of HDL-cholesterol (p = 0.031). Conclusion: The present study contributes data highlighting the role for RAS polymorphisms in predisposing to metabolic syndrome in Chilean subjects. | |
dc.identifier.uri | http://repositoriodigital.uct.cl/handle/10925/3256 | |
dc.language.iso | en | |
dc.publisher | SBEM-SOC BRASIL ENDOCRINOLOGIA & METABOLOGIA | |
dc.source | ARCHIVES OF ENDOCRINOLOGY METABOLISM | |
oaire.resourceType | Article | |
uct.catalogador | WOS | |
uct.indizacion | SCI |