TY - JOUR
T1 - UCP3 polymorphisms, hand grip performance and survival at old age: Association analysis in two Danish middle aged and elderly cohorts
AU - Dato, Serena
AU - Soerensen, Mette
AU - Montesanto, Alberto
AU - Lagani, Vincenzo
AU - Passarino, Giuseppe
AU - Christensen, Kaare
AU - Christiansen, Lene
N1 - Generated from Scopus record by KAUST IRTS on 2023-09-23
PY - 2012/8/1
Y1 - 2012/8/1
N2 - An efficient uncoupling process is generally considered to have a protective effect on the aging muscle by slowing down its age-related decay. Genetic polymorphisms in the Uncoupling Protein 3 (UCP3) gene, whose product is mainly expressed in skeletal muscle, were suggested to be associated with hand grip (HG) performances in elderly populations. Considering the population specificity of the quality of aging, we aimed to add further support to this evidence by analyzing the association between four SNPs in the UCP3 gene and relative haplotypes in two large cohorts of middle aged (N= 708) and oldest old Danes (N= 908). We found that the variability at rs1685354 and rs11235972 was associated with HG levels both at single and haplotypic level in both cohorts. Furthermore, taking advantage of large cohort and period survival data of the oldest cohort, we tested the association of each SNP with survival at 10. years from the baseline visit. Interestingly, we found that allele A at rs11235972, associated in this cohort with lowest HG scores, influences also the survival patterns, with people carrying this allele showing higher mortality rates. On the whole, our work supports the role of UCP3 gene in functional status and survival at old age. © 2012 Elsevier Ireland Ltd.
AB - An efficient uncoupling process is generally considered to have a protective effect on the aging muscle by slowing down its age-related decay. Genetic polymorphisms in the Uncoupling Protein 3 (UCP3) gene, whose product is mainly expressed in skeletal muscle, were suggested to be associated with hand grip (HG) performances in elderly populations. Considering the population specificity of the quality of aging, we aimed to add further support to this evidence by analyzing the association between four SNPs in the UCP3 gene and relative haplotypes in two large cohorts of middle aged (N= 708) and oldest old Danes (N= 908). We found that the variability at rs1685354 and rs11235972 was associated with HG levels both at single and haplotypic level in both cohorts. Furthermore, taking advantage of large cohort and period survival data of the oldest cohort, we tested the association of each SNP with survival at 10. years from the baseline visit. Interestingly, we found that allele A at rs11235972, associated in this cohort with lowest HG scores, influences also the survival patterns, with people carrying this allele showing higher mortality rates. On the whole, our work supports the role of UCP3 gene in functional status and survival at old age. © 2012 Elsevier Ireland Ltd.
UR - https://linkinghub.elsevier.com/retrieve/pii/S0047637412001054
UR - http://www.scopus.com/inward/record.url?scp=84865361929&partnerID=8YFLogxK
U2 - 10.1016/j.mad.2012.06.004
DO - 10.1016/j.mad.2012.06.004
M3 - Article
SN - 0047-6374
VL - 133
SP - 530
EP - 537
JO - Mechanisms of Ageing and Development
JF - Mechanisms of Ageing and Development
IS - 8
ER -