2015
DOI: 10.1111/joim.12334
|View full text |Cite
|
Sign up to set email alerts
|

Involvement of the −420C>G RETN polymorphism in myocardial fibrosis in patients with hypertrophic cardiomyopathy

Abstract: Aims Hypertrophic cardiomyopathy (HCM) is characterized by left ventricular hypertrophy and fibrosis. HCM is an autosomal‐dominant disease caused by more than 400 mutations in sarcomeric genes. Changes in nonsarcomeric genes contribute to its phenotypic heterogeneity. Cardiac fibrosis can be studied using late gadolinium enhancement (LGE) cardiac magnetic resonance imaging. We evaluated the potential role of two polymorphisms in nonsarcomeric genes on interstitial fibrosis in HCM. Materials and methods Two pol… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2015
2015
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 34 publications
0
3
0
Order By: Relevance
“…Hypertrophic cardiomyopathy (HCM) is a genetic disorder of the myocardium due to genetic mutations in sarcomere protein genes and is associated with hypertrophy, heart failure, arrhythmias, and sudden cardiac death . Myocardial fibrosis occurs as a maladaptive reaction against impaired cardiac relaxation .…”
Section: Introductionmentioning
confidence: 99%
“…Hypertrophic cardiomyopathy (HCM) is a genetic disorder of the myocardium due to genetic mutations in sarcomere protein genes and is associated with hypertrophy, heart failure, arrhythmias, and sudden cardiac death . Myocardial fibrosis occurs as a maladaptive reaction against impaired cardiac relaxation .…”
Section: Introductionmentioning
confidence: 99%
“…To date, resistin levels or the role of this SNP have been studied and associated with different conditions, such as cardiovascular diseases, insulin resistance, type 2 diabetes, periodontal inflammation and serious infections among others [5,7,[9][10][11][12][13]18,[20][21][22]. In these studies, the G allele and/or the GG genotype were associated with higher circulating resistin levels.…”
Section: Discussionmentioning
confidence: 99%
“…Resistin-420 Cytosine/Guanine (C/G) polymorphism, located in the promoter region of the resistin gene, was reported to be associated with the regulation of resistin gene expression and serum resistin level (11). In addition, an association has been shown between the Resistin-420 C/G variant and diabetes, obesity, and cardiovascular disease in several studies (12)(13)(14). The peroxisome proliferator-activated receptor-gamma (PPAR-γ), localized on chromosome 3p25, is another related gene that is mainly expressed in adipose tissue, the colon, and macrophages.…”
Section: Introductionmentioning
confidence: 99%