Evidence map›Paper›PMID 34893828›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2022

No Evidence That Genetic Variation at the Klotho Locus Is Associated With Longevity in Caucasians from the Newcastle 85+ Study and the UK Biobank.

Hasnat A Amin, Heather J Cordell, Carmen Martin-Ruiz, Louise Robinson, Tom Kirkwood, Alexandra I Blakemore, Fotios Drenos

Open access · hybridAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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 at 5 institutions in 1 country.

Hasnat A AminDepartment of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, UK.ORCID 0000-0002-3054-838X
Heather J CordellPopulation Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, UK.
Carmen Martin-RuizBioScreening Core Facility, Biosciences Institute, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, UK.
Louise RobinsonPopulation Health Sciences Institute, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, UK.
Tom KirkwoodAgeing Research Laboratories, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, UK.
Alexandra I BlakemoreDepartment of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, UK.
Fotios DrenosDepartment of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, UK.
Brunel University of London · GBNewcastle University · GBCentre for Life · GBImperial College London · GBNewcastle Hospitals - Campus for Ageing and Vitality · GB

Funding

Biotechnology and Biological Sciences Research CouncilBritish Heart Foundation PG/08/026/24712Department of Health NIHR SPCR 303Medical Research Council G0500997Medical Research Council G0601333Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/J50001X/1NIH HHSThe Dunhill Medical Trust R124/0509
6 · The paper itself

Abstract

The demographics of Western populations are changing, with an increase in the proportion of older adults. There is evidence to suggest that genetic factors may influence the aging process: studying these may lead to interventions to help individuals live a longer and healthier life. Evidence from several groups indicates that Klotho (KL), a gene encoding a single-pass transmembrane protein that acts as an FGF23 co-receptor, may be associated with longevity and healthy aging. We aimed to explore this area further by comparing the genotype counts in 642 long-lived individuals from the Newcastle 85+ Study with 18 295 middle-aged Newcastle-based controls from the UK Biobank to test whether variants at the KL gene locus are over- or under-represented in older individuals. If KL is associated with longevity, then we would expect the genotype counts to differ between the 2 cohorts. We found that the rs2283368 CC genotype and the rs9536338 C allele, but not the KL-VS haplotype, were associated with reaching very old age. However, these associations did not replicate in the remainder of the UK Biobank cohort. Thus, our results do not reliably support the role of KL as a longevity factor.

Indexed as

Biological Specimen BanksLongevityAgedGenetic VariationGlucuronidaseHumansKlotho ProteinsMiddle AgedUnited KingdomGlucuronidaseKlotho ProteinsHuman geneticsLongevityQuantitative genetics

Identifiers

PMID34893828
PMCPMC8893196
OpenAlexW4200128454

What OpenQuestion holds

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Registered trials

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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.