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FNDC5 (irisin) gene and exceptional longevity: a functional replication study with rs16835198 and rs726344 SNPs
Authors:Fabian Sanchis-Gomar  Nuria Garatachea  Zi-hong He  Helios Pareja-Galeano  Noriyuki Fuku  Ye Tian  Yasumichi Arai  Yukiko Abe  Haruka Murakami  Motohiko Miyachi  Thomas Yvert  Catalina Santiago  Letizia Venturini  Carmen Fiuza-Luces  Alejandro Santos-Lozano  Gabriel Rodríguez-Romo  Giovanni Ricevuti  Nobuyoshi Hirose  Enzo Emanuele  Alejandro Lucia
Affiliation:1.Department of Physiology,University of Valencia and Fundación para la Investigación del Hospital Clínico Universitario (INCLIVA),Valencia,Spain;2.Faculty of Health and Sport Science,University of Zaragoza,Huesca,Spain;3.Research Institute of Hospital 12 de Octubre (“i+12”),Madrid,Spain;4.Biology Centre,China Institute of Sport Science,Beijing,China;5.Graduate School of Health and Sports Science,Juntendo University,Inzai-city,Japan;6.Center for Supercentenarian Study,Keio University School of Medicine,Shinjuku-ku,Japan;7.Department of Health Promotion and Exercise,National Institute of Health and Nutrition,Shinjuku-ku,Japan;8.European University of Madrid,Madrid,Spain;9.Department of Health Sciences,University of Pavia,Pavia,Italy;10.Hospital Universitario 12 de Octubre,Research Institute (i+12),Madrid,Spain;11.Department of Biomedical Science,University of León,León,Spain;12.INEF, Universidad Politécnica de Madrid,Madrid,Spain
Abstract:Irisin might play an important role in reducing the risk of obesity, insulin resistance, or several related diseases, and high irisin levels may contribute to successful aging. Thus, the irisin precursor (FNDC5) gene is a candidate to influence exceptional longevity (EL), i.e., being a centenarian. It has been recently shown that two single-nucleotide polymorphisms (SNPs) in the FNDC5 gene, rs16835198 and rs726344, are associated with in vivo insulin sensitivity in adults. We determined luciferase gene reporter activity in the two above-mentioned SNPs and studied genotype distributions among centenarians (n = 175, 144 women) and healthy controls (n = 347, 142 women) from Spain. We also studied an Italian [79 healthy centenarians (40 women) and 316 healthy controls (156 women)] and a Japanese cohort [742 centenarians (623 women) and 499 healthy controls (356 women)]. The rs726344 SNP had functional significance, as shown by differences in luciferase activity between the constructs of this SNP (all P ≤ 0.05), with the variant A-allele having higher luciferase activity compared with the G-allele (P = 0.04). For the rs16835198 SNP, the variant T-allele tended to show higher luciferase activity compared with the G-allele (P = 0.07). However, we found no differences between genotype/allele frequencies of the two SNPs in centenarians versus controls in any cohort, and no significant association (using logistic regression adjusted by sex) between the two SNPs and EL. Further research is needed with different cohorts as well as with additional variants in the FNDC5 gene or in other genes involved in irisin signaling.
Keywords:Myokines   Cardiometabolic   Disorders   Allele   Longevity   Centenarians
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