Evidence map›Paper›PMID 41249831›Full record

ArticleScientific reports2025

The association of the SIRT6 rs117385980 variant with frailty and longevity: an exploratory study.

E Sheikholmolouki, F Sharifi, Z Nickhah, A Vahidi, R Lajevardi, V Haghpanah, M M Amoli

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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

7 authors.

E SheikholmoloukiMetabolic Disorders Research Centre, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
F SharifiElderly Health Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran. farshad.sharifi@gmail.com.
Z NickhahEndocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
A VahidiMetabolic Disorders Research Centre, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
R LajevardiMetabolic Disorders Research Centre, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
V HaghpanahEndocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
M M AmoliMetabolic Disorders Research Centre, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran. amolimm@tums.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Frailty, a common geriatric syndrome, is characterized by diminished physiological reserves and heightens the risk of adverse health events, including falls, hospitalizations, and mortality. Prevalence of frailty is increasing in populations by age. Sirtuin 6 (SIRT6) plays a pivotal role in energy metabolism, inflammation, DNA repair, oxidative stress, and fibrosis. Despite numerous studies investigating the functions of SIRT6, the role of its genetic variations in frailty remains poorly understood. The aim of this study was to investigate the association between SIRT6 SNP rs117385980 (C > T) and frailty syndrome. This study included samples from a cohort of older adults in Birjand, Iran, comprising 227 subjects, aged 60-90 years divided according to frailty status. Allele and genotype frequencies of the SIRT6 rs117385980 variant were analyzed in all participants. Results of the study indicated the increased presence of non-frail and pre-frail individuals compared to the frail group. Among individuals aged 60-69, 70-79, and 80-90 years, the frequency of the heterozygous CT genotype demonstrated a declining trend with advancing age (p = 0.07). Our findings suggest that the presence of rs117385980 T allele was decreased in older subjects but increased with robustness suggesting a diverse effect. Further studies with larger sample sizes and Dates of death data are warranted to confirm these preliminary findings.

Indexed as

FrailtyLongevityPolymorphism, Single NucleotideSirtuinsAgedAged, 80 and overAllelesFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansIranMaleMiddle AgedSIRT6 protein, humanSirtuinsAgingFrailLifespanPolymorphismSirtuin 6SNP

Identifiers

PMID41249831
PMCPMC12624115

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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.