Literature DB >> 32613553

SNP rs2043211 (p.C10X) in CARD8 Is Associated with Large-Artery Atherosclerosis Stroke in a Chinese Population.

Jinyu Gu1, Chong Shen2, Mengmeng Gu3, Mengmeng Wang4, Zhizhong Zhang1,4, Xinfeng Liu5,6.   

Abstract

SNP rs2043211 in CARD8 was found to have significant association with ischemic stroke. This study aimed to explore the possible association between rs2043211 and large-artery atherosclerosis stroke in Chinese and explain the possible mechanism. In total, 716 large-artery atherosclerosis stroke patients and 1088 controls were included in the study. Co-dominant, dominant, and recessive genetic models were constructed to evaluate the relationship between rs2043211 and large-artery atherosclerosis stroke risk by odds ratios with 95% confidence intervals. Stratified and interaction analyses were also done. We selected another 111 large-artery atherosclerosis stroke patients and measured the CARD8 levels in their plasma samples by enzyme-linked immunosorbent assay. Participants who carry T/T genotype have a higher risk of large-artery atherosclerosis stroke compared with those carry A/T or A/A genotypes (odds ratio = 1.35, 95% confidence intervals 1.03-1.77, P = 0.029). The higher risk for the T/T genotype is still notable in female, people with hypertension, and people without diabetes. In the interaction analysis, compared to the non-hypertensive participants with the wild homozygote type A/A, the hypertensive participants with the A/T+T/T homozygote had 3.27-fold increased risk (odds ratio = 3.27, 95% confidence intervals 2.33-4.60). The A/A group had lower CARD8 levels in plasma than the A/T and T/T group (P < 0.001). Further bioinformatics prediction indicated that the rs2043211 could significantly influence the mRNA secondary structure and protein expression of CARD8 (eQTL P = 9.8 × 10-198). The rs2043211 is probably a novel biomarker for large-artery atherosclerosis stroke in Chinese.

Entities:  

Keywords:  CARD8; Polymorphism; Rs2043211; Stroke

Year:  2020        PMID: 32613553     DOI: 10.1007/s12031-020-01647-z

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  1 in total

1.  Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus.

Authors:  Fotis Tsetsos; Athanasios Roumeliotis; Xanthippi Tsekmekidou; Sophia Alexouda; Stefanos Roumeliotis; Marios Theodoridis; Elias Thodis; Stylianos Panagoutsos; Nikolaos Papanas; Dimitrios Papazoglou; Kalliopi Kotsa; John G Yovos; Efstratios Maltezos; Ploumis Passadakis; Peristera Paschou; Marianthi Georgitsi
Journal:  Diab Vasc Dis Res       Date:  2020 Nov-Dec       Impact factor: 3.291

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.