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HSPA8 Single-Nucleotide Polymorphism Is Associated with Serum HSC70 Concentration and Carotid Artery Atherosclerosis in Nonalcoholic Fatty Liver Disease

Authors :
Wenli Zhao
Hitoe Mori
Yuki Tomiga
Kenichi Tanaka
Rasheda Perveen
Keiichiro Mine
Chika Inadomi
Wataru Yoshioka
Yoshihito Kubotsu
Hiroshi Isoda
Takuya Kuwashiro
Satoshi Oeda
Takumi Akiyama
Ye Zhao
Iwata Ozaki
Seiho Nagafuchi
Atsushi Kawaguchi
Shinichi Aishima
Keizo Anzai
Hirokazu Takahashi
Source :
Genes, Vol 13, Iss 7, p 1265 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

There is an association between nonalcoholic fatty liver disease (NAFLD) and atherosclerosis, but the genetic risk of atherosclerosis in NAFLD remains unclear. Here, a single-nucleotide polymorphism (SNP) of the heat shock 70 kDa protein 8 (HSPA8) gene was analyzed in 123 NAFLD patients who had been diagnosed using a liver biopsy, and the NAFLD phenotype including the maximum intima–media thickness (Max-IMT) of the carotid artery was investigated. Patients with the minor allele (A/G or G/G) of rs2236659 showed a lower serum heat shock cognate 71 kDa protein concentration than those with the major A/A allele. Compared with the patients with the major allele, those with the minor allele showed a higher prevalence of hypertension and higher Max-IMT in men. No significant associations between the HSPA8 genotype and hepatic pathological findings were identified. In decision-tree analysis, age, sex, liver fibrosis, and HSPA8 genotype were individually associated with severe carotid artery atherosclerosis (Max-IMT ≥ 1.5 mm). Noncirrhotic men aged ≥ 65 years were most significantly affected by the minor allele of HSPA8. To predict the risk of atherosclerosis and cardiovascular disease, HSPA8 SNP genotyping might be useful, particularly for older male NAFLD patients.

Details

Language :
English
ISSN :
20734425
Volume :
13
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Genes
Publication Type :
Academic Journal
Accession number :
edsdoj.90f7bf5313f84c0eb2cace14b7aa69c9
Document Type :
article
Full Text :
https://doi.org/10.3390/genes13071265