PTPN22 gene functional polymorphism (rs2476601) in older adults with frailty syndrome
Language English Country Netherlands Media print-electronic
Document type Journal Article
Grant support
ProSNI 2018
Universidad de Guadalajara
PubMed
33611779
DOI
10.1007/s11033-021-06212-4
PII: 10.1007/s11033-021-06212-4
Knihovny.cz E-resources
- Keywords
- Frailty syndrome, Lymphoid tyrosine phosphatase locus (LYP/PTPN22), Multivariate analysis, Older adults, PTPN22 gene polymorphism, SNP rs2476601,
- MeSH
- Alleles MeSH
- Phenotype MeSH
- Genetic Predisposition to Disease * MeSH
- Genetic Association Studies * MeSH
- Genotype MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Cohort Studies MeSH
- Frailty genetics physiopathology MeSH
- Frail Elderly MeSH
- Quality of Life MeSH
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Protein Tyrosine Phosphatase, Non-Receptor Type 22 genetics MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Mexico epidemiology MeSH
- Names of Substances
- PTPN22 protein, human MeSH Browser
- Protein Tyrosine Phosphatase, Non-Receptor Type 22 MeSH
The frailty syndrome is a common clinical marker of vulnerability in older adults conducive to an overall decline in inflammatory stress responsiveness; yet little is known about the genetic risk factors for frailty in elderly. Our aim was to investigate the association between the rs2476601 polymorphism in PTPN22 gene and susceptibility to frailty in Mexican older adults. Data included 630 subjects 70 and older from The Coyoacán cohort, classified as frail, pre-frail, and non-frail following Fried's criteria. Sociodemographic and clinical characteristics were compared between groups at baseline and after a multivariate analysis. The rs2476601 polymorphism was genotyped by TaqMan genotyping assay using real-time PCR and genotype frequencies were determined for each frailty phenotype in all participants and subsets by age range. Genetic association was examined using stratified and interaction analyses adjusting for age, sex and variables selected in the multivariate analysis. Disability for day-life activities, depression and cognitive impairment were associated with the risk of pre-frailty and frailty at baseline and after adjustment. Carrying the T allele increased significantly the risk of frailty in patients 76 and older (OR 5.64, 95% CI 4.112-7.165) and decreased the risk of pre-frailty under no clinical signs of depression (OR 0.53; 95% CI 0.17-1.71). The PTPN22 polymorphism, rs2476601, could be a genetic risk factor for frailty as subject to quality of life. This is the first study analyzing such relationship in Mexican older adults. Confirming these findings requires additional association studies on wider age ranges in populations of older adults with frailty syndrome.
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