Evidence map›Paper›PMID 40499086›Full record

ArticleNeurology2025

Association of Leucocyte Telomere Length With Stroke, Dementia, and Late-Life Depression: The Role of Modifiable Risk Factors.

Tamara N Kimball, Savvina Prapiadou, Reinier W P Tack, Benjamin Yong-Qiang Tan, Jasper R Senff, Christina Kourkoulis, Sanjula Singh, Jonathan Rosand, Christopher D Anderson

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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4 · The record

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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

9 authors.

Tamara N KimballBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0002-1107-0771
Savvina PrapiadouBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0001-7415-2566
Reinier W P TackBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0003-3204-0309
Benjamin Yong-Qiang TanBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0003-1824-9077
Jasper R SenffBrain Care Labs, Mass General Brigham, Boston.ORCID 0009-0002-6540-480X
Christina KourkoulisBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0001-6330-9169
Sanjula SinghBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0001-9304-8107
Jonathan RosandBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0002-1014-9138
Christopher D AndersonBrain Care Labs, Mass General Brigham, Boston.ORCID 0000-0002-0053-2002

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesStroke, dementia, and late-life depression (LLD) are age-related brain diseases that pose significant public health challenges and costs. Leucocyte telomere length (LTL) is a biological aging marker influenced by both genetic and lifestyle factors. The aim of our study was to determine the association between LTL and these diseases. We further investigated whether modifying risk factors of age-related brain disease, as measured using the Brain Care Score (BCS), mitigates LTL associations.

methodsWe analyzed participants from the UK Biobank with available LTL and risk factor information. We examined LTL's associations with stroke, dementia, and LLD, individually and as a composite outcome, using continuous measures and tertile stratification. Disease risks were evaluated through cumulative incidence curves, incidence rates per 1,000 person-years, and adjusted Cox models. Risk comparisons across LTL tertiles were stratified by risk factor profiles, with high BCS (≥15) indicating healthier lifestyle choices and low BCS (≤10) reflecting less optimal lifestyle choices. Mendelian randomization (MR) was used to test causal associations.

resultsThe study included 356,173 participants (median age 56 years; 53.69% female). Shorter LTL was consistently associated with higher incidence rates across all outcomes. Participants in the shortest LTL tertile had elevated risks of the composite outcome (hazard ratio [HR] 1.11; 95% CI 1.08-1.15), stroke (HR 1.08; 95% CI 1.02-1.15), dementia (HR 1.19; 95% CI 1.12-1.26), and LLD (HR 1.14; 95% CI 1.09-1.18). Individuals with both shorter LTL and lower BCS faced significantly increased risks of age-related brain diseases (HR 1.11; 95% CI 1.07-1.16) and individually for stroke (HR 1.10; 95% CI 1.02-1.19), dementia (HR 1.17; 95% CI 1.08-1.28), and LLD (HR 1.13; 95% CI 1.07-1.19). Conversely, individuals with higher BCS within the shortest LTL group did not show a significant increase in risk of any age-related brain diseases. MR analyses did not identify causal relationships between LTL and these outcomes. DISCUSSION: Individuals with shorter LTL are at increased risk of stroke, dementia, and LLD. Improved modifiable risk factor profiles seem to mitigate the impact of LTL on these diseases. Future research should explore the effectiveness of lifestyle interventions in mitigating adverse biological aging effects on brain health.

Indexed as

DementiaDepressionLeukocytesStrokeTelomereAgedFemaleHumansIncidenceMaleMendelian Randomization AnalysisMiddle AgedRisk FactorsUnited Kingdom

Identifiers

PMID40499086
PMCPMC12165286

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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.