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Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis

HSPA8 is involved in many stroke-associated cellular processes, playing a pivotal role in the protein quality control system. Here we report the results of the pilot study aimed at determining whether HSPA8 SNPs are linked to the risk of ischemic stroke (IS). DNA samples from 2139 Russians (888 IS p...

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Autores principales: Kobzeva, Ksenia A., Soldatova, Maria O., Stetskaya, Tatiana A., Soldatov, Vladislav O., Deykin, Alexey V., Freidin, Maxim B., Bykanova, Marina A., Churnosov, Mikhail I., Polonikov, Alexey V., Bushueva, Olga Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298525/
https://www.ncbi.nlm.nih.gov/pubmed/37372351
http://dx.doi.org/10.3390/genes14061171
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author Kobzeva, Ksenia A.
Soldatova, Maria O.
Stetskaya, Tatiana A.
Soldatov, Vladislav O.
Deykin, Alexey V.
Freidin, Maxim B.
Bykanova, Marina A.
Churnosov, Mikhail I.
Polonikov, Alexey V.
Bushueva, Olga Y.
author_facet Kobzeva, Ksenia A.
Soldatova, Maria O.
Stetskaya, Tatiana A.
Soldatov, Vladislav O.
Deykin, Alexey V.
Freidin, Maxim B.
Bykanova, Marina A.
Churnosov, Mikhail I.
Polonikov, Alexey V.
Bushueva, Olga Y.
author_sort Kobzeva, Ksenia A.
collection PubMed
description HSPA8 is involved in many stroke-associated cellular processes, playing a pivotal role in the protein quality control system. Here we report the results of the pilot study aimed at determining whether HSPA8 SNPs are linked to the risk of ischemic stroke (IS). DNA samples from 2139 Russians (888 IS patients and 1251 healthy controls) were genotyped for tagSNPs (rs1461496, rs10892958, and rs1136141) in the HSPA8 gene using probe-based PCR. SNP rs10892958 of HSPA8 was associated with an increased risk (risk allele G) of IS in smokers (OR = 1.37; 95% CI = 1.07–1.77; p = 0.01) and patients with low fruit and vegetable consumption (OR = 1.36; 95% CI = 1.14–1.63; p = 0.002). SNP rs1136141 of HSPA8 was also associated with an increased risk of IS (risk allele A) exclusively in smokers (OR = 1.68; 95% CI = 1.23–2.28; p = 0.0007) and in patients with a low fruit and vegetable intake (OR = 1.29; 95% CI = 1.05–1.60; p = 0.04). Sex-stratified analysis revealed an association of rs10892958 HSPA8 with an increased risk of IS in males (risk allele G; OR = 1.30; 95% CI = 1.05–1.61; p = 0.01). Thus, SNPs rs10892958 and rs1136141 in the HSPA8 gene represent novel genetic markers of IS.
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spelling pubmed-102985252023-06-28 Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis Kobzeva, Ksenia A. Soldatova, Maria O. Stetskaya, Tatiana A. Soldatov, Vladislav O. Deykin, Alexey V. Freidin, Maxim B. Bykanova, Marina A. Churnosov, Mikhail I. Polonikov, Alexey V. Bushueva, Olga Y. Genes (Basel) Article HSPA8 is involved in many stroke-associated cellular processes, playing a pivotal role in the protein quality control system. Here we report the results of the pilot study aimed at determining whether HSPA8 SNPs are linked to the risk of ischemic stroke (IS). DNA samples from 2139 Russians (888 IS patients and 1251 healthy controls) were genotyped for tagSNPs (rs1461496, rs10892958, and rs1136141) in the HSPA8 gene using probe-based PCR. SNP rs10892958 of HSPA8 was associated with an increased risk (risk allele G) of IS in smokers (OR = 1.37; 95% CI = 1.07–1.77; p = 0.01) and patients with low fruit and vegetable consumption (OR = 1.36; 95% CI = 1.14–1.63; p = 0.002). SNP rs1136141 of HSPA8 was also associated with an increased risk of IS (risk allele A) exclusively in smokers (OR = 1.68; 95% CI = 1.23–2.28; p = 0.0007) and in patients with a low fruit and vegetable intake (OR = 1.29; 95% CI = 1.05–1.60; p = 0.04). Sex-stratified analysis revealed an association of rs10892958 HSPA8 with an increased risk of IS in males (risk allele G; OR = 1.30; 95% CI = 1.05–1.61; p = 0.01). Thus, SNPs rs10892958 and rs1136141 in the HSPA8 gene represent novel genetic markers of IS. MDPI 2023-05-27 /pmc/articles/PMC10298525/ /pubmed/37372351 http://dx.doi.org/10.3390/genes14061171 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kobzeva, Ksenia A.
Soldatova, Maria O.
Stetskaya, Tatiana A.
Soldatov, Vladislav O.
Deykin, Alexey V.
Freidin, Maxim B.
Bykanova, Marina A.
Churnosov, Mikhail I.
Polonikov, Alexey V.
Bushueva, Olga Y.
Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title_full Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title_fullStr Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title_full_unstemmed Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title_short Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis
title_sort association between hspa8 gene variants and ischemic stroke: a pilot study providing additional evidence for the role of heat shock proteins in disease pathogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298525/
https://www.ncbi.nlm.nih.gov/pubmed/37372351
http://dx.doi.org/10.3390/genes14061171
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