FNDC5 (irisin) gene and exceptional longevity: a functional replication study with rs16835198 and rs726344 SNPs

Fabian Sanchis-Gomar1, Nuria Garatachea2,3, Zi-hong He4, Helios Pareja-Galeano1, Noriyuki Fuku5, Ye Tian4, Yasumichi Arai6, Yukiko Abe6, Haruka Murakami7, Motohiko Miyachi7, Thomas Yvert8, Catalina Santiago8, Letizia Venturini9, Carmen Fiuza-Luces10,8, Alejandro Santos-Lozano10,11, Gabriel Rodríguez-Romo12, Giovanni Ricevuti9, Nobuyoshi Hirose6, Enzo Emanuele9, Alejandro Lucia8,10
1Department of Physiology, University of Valencia and Fundación para la Investigación del Hospital Clínico Universitario (INCLIVA), Valencia, Spain
2Faculty of Health and Sport Science, University of Zaragoza, Huesca, Spain
3Research Institute of Hospital 12 de Octubre (‘i+12’), Madrid, Spain
4Biology Centre, China Institute of Sport Science, Beijing, China
5Graduate School of Health and Sports Science, Juntendo University, Inzai-city, Japan
6Center for Supercentenarian Study, Keio University School of Medicine, Shinjuku-ku, Japan
7Department of Health Promotion and Exercise, National Institute of Health and Nutrition, Shinjuku-ku, Japan
8European University of Madrid, Madrid, Spain
9Department of Health Sciences, University of Pavia, Pavia, Italy
10Hospital Universitario 12 de Octubre, Research Institute (i+12), Madrid, Spain
11Department of Biomedical Science, University of León, León, Spain
12INEF, Universidad Politécnica de Madrid, Madrid, Spain

Tóm tắt

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.

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