Evidence map›Paper›PMID 35879401›Full record

Observational studyMolecular psychiatry2022

Alcohol consumption and telomere length: Mendelian randomization clarifies alcohol's effects.

A Topiwala, B Taschler, K P Ebmeier, S Smith, H Zhou, D F Levey, V Codd, N J Samani, J Gelernter, T E Nichols and 1 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Molecular psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

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  19. Prolonged exposure to leisure screen time notably accelerates biological aging: Evidence from observational studies and genetic associations.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Observational
  20. 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

11 authors at 5 institutions in 3 countries.

A TopiwalaNuffield Department Population Health, Big Data Institute, University of Oxford, Oxford, OX3 7LF, UK. anya.topiwala@bdi.ox.ac.uk.ORCID http://orcid.org/0000-0002-8408-0372
B TaschlerWellcome Centre for Integrative Neuroimaging (WIN FMRIB), Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, OX3 9DU, UK.ORCID http://orcid.org/0000-0001-6574-4789
K P EbmeierDepartment of Psychiatry, University of Oxford, Warneford Hospital, Oxford, OX3 7JX, UK.ORCID http://orcid.org/0000-0002-5190-7038
S SmithWellcome Centre for Integrative Neuroimaging (WIN FMRIB), Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, OX3 9DU, UK.
H ZhouDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-7694-6391
D F LeveyDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-8431-9569
V CoddDepartment of Cardiovascular Sciences, University of Leicester, Leicester, UK.
N J SamaniDepartment of Cardiovascular Sciences, University of Leicester, Leicester, UK.
J GelernterDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-4067-1859
T E NicholsNuffield Department Population Health, Big Data Institute, University of Oxford, Oxford, OX3 7LF, UK.ORCID http://orcid.org/0000-0002-4516-5103
S BurgessMRC Biostatistics Unit, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SR, UK.ORCID http://orcid.org/0000-0001-5365-8760
University of Oxford · GBYale University · USUniversity of Leicester · GBUniversity of Cambridge · GBWarneford Hospital · GB

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Spatial inference methods for image analysisR01EB026859 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHWARTZMAN, ARMIN · 2019 to 2022
$1.7M
Genetic Causality of Alcohol Intake and Alcohol Use Disorder on Cancer RiskR21CA252916 · NCI · YALE UNIVERSITY · PI ZHOU, HANG · 2021 to 2022
$334k
British Heart Foundation CH/12/2/29428British Heart Foundation RG/13/13/30194British Heart Foundation RG/18/13/33946CSRD VA I01 CX001849Department of Health BRC-1215-20010Department of Health BRC-1215-20014Medical Research Council G1001354Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00002/7Medical Research Council MR/K013351/1Medical Research Council MR/M012816/1NCATS NIH HHS UL1 TR001863NCI NIH HHS R21 CA252916NIBIB NIH HHS R01 EB026859Wellcome TrustWellcome Trust 100309/Z/12/ZWellcome Trust 204623/Z/16/ZWellcome Trust 216462/Z/19/Z
6 · The paper itself

Abstract

Alcohol's impact on telomere length, a proposed marker of biological aging, is unclear. We performed the largest observational study to date (in n = 245,354 UK Biobank participants) and compared findings with Mendelian randomization (MR) estimates. Two-sample MR used data from 472,174 participants in a recent genome-wide association study (GWAS) of telomere length. Genetic variants were selected on the basis of associations with alcohol consumption (n = 941,280) and alcohol use disorder (AUD) (n = 57,564 cases). Non-linear MR employed UK Biobank individual data. MR analyses suggested a causal relationship between alcohol traits, more strongly for AUD, and telomere length. Higher genetically-predicted AUD (inverse variance-weighted (IVW) β = -0.06, 95% confidence interval (CI): -0.10 to -0.02, p = 0.001) was associated with shorter telomere length. There was a weaker association with genetically-predicted alcoholic drinks weekly (IVW β = -0.07, CI: -0.14 to -0.01, p = 0.03). Results were consistent across methods and independent from smoking. Non-linear analyses indicated a potential threshold relationship between alcohol and telomere length. Our findings indicate that alcohol consumption may shorten telomere length. There are implications for age-related diseases.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisAlcohol DrinkingEthanolHumansPolymorphism, Single NucleotideTelomereEthanol

Identifiers

PMID35879401
PMCPMC9718662
OpenAlexW4287831571

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.