Polymorphism (-499C/G) in DDAH2 promoter may act as a protective factor for metabolic syndrome: A case-control study in Azar-Cohort population

Globally developing metabolic syndrome (MetS) prevalence as a major health problem can be related to multiple factors of genetic and environmental. Dimethylaminohydrolase 2 (DDAH2) is the main enzyme implicated in the cardiovascular system, which regulates the nitric oxide pathway. This study invest...

Full description

Saved in:
Bibliographic Details
Published in:Archives of Endocrinology and Metabolism Vol. 65; no. 4; pp. 443 - 449
Main Authors: Faramarzi, Elnaz, Aftabi, Younes, Ansarin, Khalil, Somi, Mohammad Hossein, Gilani, Neda, Seyedrezazadeh, Ensiyeh
Format: Journal Article
Language:English
Published: Brazil Sociedade Brasileira de Endocrinologia e Metabologia 03-11-2021
Brazilian Society of Endocrinology and Metabolism
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Globally developing metabolic syndrome (MetS) prevalence as a major health problem can be related to multiple factors of genetic and environmental. Dimethylaminohydrolase 2 (DDAH2) is the main enzyme implicated in the cardiovascular system, which regulates the nitric oxide pathway. This study investigated the association of polymorphism -499C/G (rs805305) with the risk of MetS among the Azar-Cohort population. The occurrence of SNP rs805305 in the gene was tested using the PCR-RFLP method in 332 MetS cases and 294 healthy controls. Afterward, the association of the allele and genotypes with the risk of MetS and its components were examined. The G allele and GC genotype were significantly associated with a reduced risk of MetS ( ≤ 0.001). Also, the dominant genetic model (GG+GC) significantly decreased the risk of MetS ( = 0.001), however, in sex subtypes MetS risk was significantly reduced in males before and in females after adjustment for age ( ≤ 0.02). The -499C/G polymorphism of may play a protective role and reduce MetS risk among the Azar-Cohort population.
Bibliography:Disclosure: no potential conflict of interest relevant to this article was reported.
Author contribution: the contributions of the authors for this study were done as follow: Conceptualization: Ensiyeh Seyedrezazadeh and Younes Aftabi; Formal analysis Software: Elnaz Faramarzi, Neda Gilani; the investigation, methodology, and project administration: Mohammad Hossein Somi; Khalil Ansarin; Supervision; Elnaz Faramarzi, Ensiyeh Seyedrezazadeh; Roles/Writing - original draft; Writing – review &editing: Elnaz Faramarzi, Ensiyeh Seyedrezazadeh, Younes Aftabi.
ISSN:2359-3997
2359-4292
DOI:10.20945/2359-3997000000391