Evidence map›Paper›PMID 39044293›Full record

ArticleAlzheimer's research & therapy2024

Moderation of thyroid hormones for the relationship between amyloid and tau pathology.

Jeong Hyeon Byeon, Min Soo Byun, Dahyun Yi, Joon Hyung Jung, Bo Kyung Sohn, Yoon Young Chang, Nayeong Kong, Gijung Jung, Hyejin Ahn, Jun-Young Lee and 4 more

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Article in Alzheimer's research & therapy, 2024. 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

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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

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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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5 · Who and what money

Authors and funding

14 authors.

Jeong Hyeon ByeonDepartment of Neuropsychiatry, Seoul National University Hospital, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Republic of Korea.
Min Soo ByunDepartment of Neuropsychiatry, Seoul National University Hospital, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Republic of Korea.
Dahyun YiInstitute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Joon Hyung JungDepartment of Psychiatry, Chungbuk National University Hospital, Cheongju, Republic of Korea.
Bo Kyung SohnDepartment of Psychiatry, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea.
Yoon Young ChangDepartment of Psychiatry, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea.
Nayeong KongDepartment of Psychiatry, Keimyung University Hospital, Daegu, Republic of Korea.
Gijung JungInstitute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Hyejin AhnInterdisciplinary Program of Cognitive Science, Seoul National University, Seoul, Republic of Korea.
Jun-Young LeeDepartment of Psychiatry, Seoul National University College of Medicine, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Republic of Korea.
Yun-Sang LeeDepartment of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yu Kyeong KimDepartment of Nuclear Medicine, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea.
Dong Young LeeDepartment of Neuropsychiatry, Seoul National University Hospital, 101 Daehak-Ro, Jongno-Gu, Seoul, 03080, Republic of Korea. selfpsy@snu.ac.kr.
KBASE Research Group

Funding

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
Ministry of Health & Welfare, Republic of Korea HI18C0630 & HI19C0149Ministry of Science and ICT, Republic of Korea NRF-2014M3C7A1046042National Institute of Aging, United States of America U01AG072177NIA NIH HHS U01 AG072177Seoul National University Hospital, Republic of Korea No. 3020200030
6 · The paper itself

Abstract

backgroundAltered thyroid hormone levels have been associated with increased risk of Alzheimer's disease (AD) dementia and related cognitive decline. However, the neuropathological substrates underlying the link between thyroid hormones and AD dementia are not yet fully understood. We first investigated the association between serum thyroid hormone levels and in vivo AD pathologies including both beta-amyloid (Aβ) and tau deposition measured by positron emission tomography (PET). Given the well-known relationship between Aβ and tau pathology in AD, we additionally examined the moderating effects of thyroid hormone levels on the association between Aβ and tau deposition.

methodsThis cross-sectional study was conducted as part of the Korean Brain Aging Study for Early Diagnosis and Prediction of Alzheimer's Disease (KBASE) cohort. This study included a total of 291 cognitively normal adults aged 55 to 90. All participants received comprehensive clinical assessments, measurements for serum total triiodothyronine (T3), free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH), and brain imaging evaluations including [

resultsNo associations were found between either thyroid hormones or TSH and Aβ and tau deposition on PET. However, fT4 (p = 0.002) and fT3 (p = 0.001) exhibited significant interactions with Aβ on tau deposition: The sensitivity analyses conducted after the removal of an outlier showed that the interaction effect between fT4 and Aβ deposition was not significant, whereas the interaction between fT3 and Aβ deposition remained significant. However, further subgroup analyses demonstrated a more pronounced positive relationship between Aβ and tau in both the higher fT4 and fT3 groups compared to the lower group, irrespective of outlier removal. Meanwhile, neither T3 nor TSH had any interaction with Aβ on tau deposition.

conclusionOur findings suggest that serum thyroid hormones may moderate the relationship between cerebral Aβ and tau pathology. Higher levels of serum thyroid hormones could potentially accelerate the Aβ-dependent tau deposition in the brain. Further replication studies in independent samples are needed to verify the current results.

Indexed as

Amyloid beta-PeptidesPositron-Emission Tomographytau ProteinsThyroid HormonesAgedAged, 80 and overAlzheimer DiseaseBrainCohort StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedThyrotropinThyroxineAmyloid beta-Peptidestau ProteinsThyroid HormonesThyrotropinThyroxineAlzheimer’s diseaseAmyloid betaPositron emission tomographyTauThyroid hormoneThyroid-stimulating hormone

Identifiers

PMID39044293
PMCPMC11264392

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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.