Evidence map›Paper›PMID 39667908›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2025

Telomere length, in vivo Alzheimer's disease pathologies and cognitive decline in older adults.

Joon Hyung Jung, Min Soo Byun, Dahyun Yi, Hyejin Ahn, Jun Ho Lee, Jang-Seok Lee, Hyun-Seob Lee, Jun-Young Lee, Yu Kyeong Kim, Yun-Sang Lee and 4 more

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Article in Journal of neurology, neurosurgery, and psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Joon Hyung JungDepartment of Psychiatry, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
Min Soo ByunDepartment of Psychiatry, Seoul National University College of Medicine, Seoul, Korea (the Republic of) byunms@snu.ac.kr.ORCID http://orcid.org/0000-0003-3159-4510
Dahyun YiInstitute of Human Behavioral Medicine, Seoul National University Medical Research Center, Seoul, Korea (the Republic of).
Hyejin AhnInterdisciplinary Program of Cognitive Neuroscience, Seoul National University College of Humanities, Seoul, Korea (the Republic of).
Jun Ho LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea (the Republic of).
Jang-Seok LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Korea (the Republic of).
Hyun-Seob LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Korea (the Republic of).
Jun-Young LeeDepartment of Psychiatry, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
Yu Kyeong KimDepartment of Nuclear Medicine, Seoul Metropolitan Government-Seoul National University (SMG-SNU) Boramae Medical Center, Seoul, Korea (the Republic of).
Yun-Sang LeeDepartment of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
Koung Mi KangDepartment of Radiology, Seoul National University Hospital, Seoul, Korea (the Republic of).
Chul-Ho SohnDepartment of Radiology, Seoul National University Hospital, Seoul, Korea (the Republic of).
Dong Young LeeDepartment of Psychiatry, Seoul National University College of Medicine, Seoul, Korea (the Republic of).ORCID http://orcid.org/0000-0001-8976-8320
KBASE Research Group

Funding

Research Education ComponentP30AG072976 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI ANDREW J SAYKIN · 2021 to 2026
$24.1M
KBASE2: Korean Brain Aging Study, Longitudinal Endophenotypes and Systems BiologyU01AG072177 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LEE, DONG YOUNG, NHO, KWANGSIK TIMOTHY · 2021 to 2025
$11.2M
Memory Circuitry in MCI and Early Alzheimer’s Disease Prodrome: Molecular DriversR01AG019771 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SAYKIN, ANDREW J · 2001 to 2021
$6.9M
NIA NIH HHS P30 AG072976NIA NIH HHS R01 AG019771NIA NIH HHS U01 AG072177
6 · The paper itself

Abstract

backgroundWhether telomere length (TL), an indicator of biological ageing, reflects Alzheimer's disease (AD)-related neuropathological change remains unclear. We investigated the relationships between TL, in vivo AD pathologies, including cerebral beta-amyloid and tau deposition, and cognitive outcomes in older adults.

methodsA total of 458 older adults were included, encompassing both cognitively normal (CN) individuals and those cognitively impaired (CI), with the CI group consisting of individuals with mild cognitive impairment or AD dementia. All participants underwent clinical and neuropsychological assessments, amyloid positron emission tomography (PET) scan and DNA extraction for measuring TL at baseline. A subset of participants (n=140) underwent tau PET scan. At follow-up, the participants underwent neuropsychological assessments annually for up to 4 years.

resultsOverall, longer TL was associated with greater brain tau deposition (B=0.139, 95% CI 0.040, 0.238) and a faster decline in global cognition (B = - 0.371, 95% CI - 0.720, -0.023). In the subgroup analysis, the association between longer TL and greater in vivo AD pathologies, as well as faster cognitive decline, was observed particularly in the CI group. Mediation analysis suggested that longer TL was associated with cognitive decline through increased tau deposition in the CI group.

conclusionOur finding suggests that older adults with relatively longer TL, particularly in the CI group, may have greater in vivo AD pathologies and experience more rapid cognitive decline, potentially mediated by brain tau deposition. Further studies are necessary to elucidate the biological links underlying these associations.

Indexed as

Alzheimer DiseaseCognitive DysfunctionTelomereAgedAged, 80 and overAmyloid beta-PeptidesBrainFemaleHumansMaleNeuropsychological TestsPositron-Emission Tomographytau ProteinsAmyloid beta-Peptidestau ProteinsALZHEIMER'S DISEASEIMAGE ANALYSISNEUROBIOLOGYNEUROPATHOLOGYPET

Identifiers

PMID39667908
PMCPMC12077995

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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.