Evidence map›Paper›PMID 27861536›Full record

ArticlePloS one2016

Muscle-Related Polymorphisms (MSTN rs1805086 and ACTN3 rs1815739) Are Not Associated with Exceptional Longevity in Japanese Centenarians.

Noriyuki Fuku, Rafael Alis, Thomas Yvert, Hirofumi Zempo, Hisashi Naito, Yukiko Abe, Yasumichi Arai, Haruka Murakami, Motohiko Miyachi, Helios Pareja-Galeano and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Frontiers in genetics · 2018
    Review
  7. 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

13 authors at 6 institutions in 3 countries.

Noriyuki FukuGraduate School of Health and Sports Science, Juntendo University, Chiba, Japan.
Rafael AlisSchool of Medicine and Research Institute "Dr. Viña Giner", Molecular and Mitochondrial Medicine, Catholic University of Valencia San Vicente Mártir, Valencia, Spain.
Thomas YvertSchool of Doctorate Studies and Research, Universidad Europea de Madrid, Madrid, Spain.
Hirofumi ZempoGraduate School of Health and Sports Science, Juntendo University, Chiba, Japan.
Hisashi NaitoGraduate School of Health and Sports Science, Juntendo University, Chiba, Japan.
Yukiko AbeCenter for Supercentenarian Study, Keio University School of Medicine, Tokyo, Japan.
Yasumichi AraiCenter for Supercentenarian Study, Keio University School of Medicine, Tokyo, Japan.
Haruka MurakamiDepartment of Health Promotion and Exercise, National Institute of Health Nutrition, Tokyo, Japan.
Motohiko MiyachiDepartment of Health Promotion and Exercise, National Institute of Health Nutrition, Tokyo, Japan.
Helios Pareja-GaleanoEuropean University of Madrid, Madrid, Spain.
Enzo Emanuele2E Science, Robbio, Pavia, Italy.
Nobuyoshi HiroseCenter for Supercentenarian Study, Keio University School of Medicine, Tokyo, Japan.
Alejandro LuciaEuropean University of Madrid, Madrid, Spain.
Juntendo University · JPKeio University · JPUniversidad Europea de Madrid · ESNational Institute of Health Sciences · JPHospital Universitari i Politècnic La Fe · ESPavia nel Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myostatin (MSTN) and α-actinin-3 (ACTN3) genes are potentially associated with preservation of muscle mass and oxidative capacity, respectively. To explore the possible role of these genes in exceptional longevity (EL), the allele/genotype frequency distribution of two polymorphisms in MSTN (rs1805086, K153R) and ACTN3 (rs1815739, R577X) was studied in Japanese centenarians of both sexes (n = 742) and healthy controls (n = 814). The rs1805086 R-allele (theoretically associated with muscle mass preservation at the expense of oxidative capacity) was virtually absent in the two groups, where genotype distributions were virtually identical. Likewise, no differences in allele (p = 0.838 (women); p = 0.193 (men); p = 0.587 (both sexes)) or genotype distribution were found between groups for ACTN3 rs1815739 (p = 0.975 (women), p = 0.136 (men), p = 0.752 (both sexes)). Of note, however, the frequency of the rs1805086 R-allele observed here is the lowest been reported to date whereas that of the 'highly oxidative/efficient' rs1815739 XX genotype in Japanese male centenarians (33.3%) or supercentenarians of both sexes (≥110 years) are the highest (32.6%), for a non-American population. No definite conclusions can be inferred in relation to EL owing to its lack of association with both rs1815739 and rs1805086. However, it cannot be excluded that these gene variants could eventually be related to a "healthy" metabolic phenotype in the Japanese population. Further research might determine if such metabolic profile is among the factors that can potentially predispose these individuals to live longer than Caucasians and what genetic variants might be actually involved.

Indexed as

Genetic Association StudiesPolymorphism, GeneticPopulation SurveillanceActininAllelesAsian PeopleFemaleGene FrequencyGenotypeHumansJapanLongevityMaleMyostatinActininACTN3 protein, humanMSTN protein, humanMyostatin

Identifiers

PMID27861536
PMCPMC5115755
OpenAlexW2554214081

What OpenQuestion holds

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LicenceCC BY
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.