Evidence map›Paper›PMID 25427998›Full record

ArticleAge (Dordrecht, Netherlands)2014

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

Fabian Sanchis-Gomar, Nuria Garatachea, Zi-hong He, Helios Pareja-Galeano, Noriyuki Fuku, Ye Tian, Yasumichi Arai, Yukiko Abe, Haruka Murakami, Motohiko Miyachi and 10 more

Open access · bronzeAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Age (Dordrecht, Netherlands), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Risk Polymorphisms ofInternational journal of molecular sciences · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 11 institutions in 4 countries.

Fabian Sanchis-GomarDepartment of Physiology, University of Valencia and Fundación para la Investigación del Hospital Clínico Universitario (INCLIVA), Av. Blasco Ibañez, 15, Valencia, 46010, Spain, fabian.sanchis@uv.es.
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
Keio University Hospital · JPUniversidad Europea de Madrid · ESUniversity of Pavia · ITChina Institute of Sport Science · CNHospital Universitario 12 De Octubre · ESNational Institute of Infectious Diseases · JPINCLIVA Health Research Institute · ESJuntendo University · JPUniversidad de Zaragoza · ESUniversidad Politécnica de Madrid · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Gene FrequencyPolymorphism, Single NucleotideAdultAgedAged, 80 and overAgingCohort StudiesConfidence IntervalsFemaleFibronectinsGenotypeHumansItalyJapanLogistic ModelsLongevityFibronectinsFNDC5 protein, human

Identifiers

PMID25427998
PMCPMC4245403
OpenAlexW1976632317

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.