Evidence map›Paper›PMID 38947089›Full record

ArticleResearch square2024

Sex-Specific Risk Factors and Clinical Dementia Outcomes for White Matter Hyperintensities in a large South Korean Cohort.

Noah Schweitzer, Sang Joon Son, Rebecca C Thurston, Jinghang Li, Chang-Le Chen, Howard Aizenstein, Shaolin Yang, Bistra Iordanova, Chang Hyung Hong, Hyun Woong Roh and 13 more

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In one paragraph

Article in Research square, 2024. 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Noah SchweitzerUniversity of Pittsburgh.
Sang Joon SonAjou University School of Medicine.
Rebecca C ThurstonUniversity of Pittsburgh School of Medicine.
Jinghang LiUniversity of Pittsburgh.
Chang-Le ChenUniversity of Pittsburgh.
Howard AizensteinUniversity of Pittsburgh.
Shaolin YangUniversity of Pittsburgh.
Bistra IordanovaUniversity of Pittsburgh.
Chang Hyung HongAjou University School of Medicine.
Hyun Woong RohAjou University School of Medicine.
Yong Hyuk ChoAjou University School of Medicine.
Sunhwa HongAjou University School of Medicine.
You Jin NamAjou University School of Medicine.
Dong Yun LeeAjou University School of Medicine.
Bumhee ParkAjou University School of Medicine.
Na-Rae KimAjou University School of Medicine.
Jin Wook ChoiAjou University School of Medicine.
Jaeyoun CheongAjou University School of Medicine.
Sang Woon SeoSamsung Medical Centre, Sungkyunkwan University School of Medicine.
Young-Sil AnAjou University School of Medicine.
So Young MoonAjou University School of Medicine.
Seung Jin HanAjou University School of Medicine.
Minjie WuUniversity of Pittsburgh School of Medicine.

Funding

A Cerebrovascular Basis for Sex Differences in Alzheimer's Disease RiskR01AG067018 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WU, MINJIE · 2020 to 2023
$1.7M
NIA NIH HHS R01 AG067018
6 · The paper itself

Abstract

Objective: White matter hyperintensities (WMH) on brain MRI images are the most common feature of cerebral small vessel disease (CSVD). Studies have yielded divergent findings on the modifiable risk factors for WMH and WMH's impact on cognitive decline. Mounting evidence suggests sex differences in WMH burden and subsequent effects on cognition. Thus, we aimed to identify sex-specific modifiable risk factors for WMH. We then explored whether there were sex-specific associations of WMH to longitudinal clinical dementia outcomes. Methods: Participants aged 49-89 years were recruited at memory clinics and underwent a T2-weighted fluid-attenuated inversion recovery (FLAIR) 3T MRI scan to measure WMH volume. Participants were then recruited for two additional follow-up visits, 1-2 years apart, where clinical dementia rating sum of boxes (CDR-SB) scores were measured. We first explored which known modifiable risk factors for WMH were significant when tested for a sex-interaction effect. We additionally tested which risk factors were significant when stratified by sex. We then tested to see whether WMH is longitudinally associated with clinical dementia that is sex-specific. Results: The study utilized data from 713 participants (241 males, 472 females) with a mean age of 72.3 years and 72.8 years for males and females, respectively. 57.3% and 59.5% of participants were diagnosed with mild cognitive impairment (MCI) for males and females, respectively. 40.7% and 39.4% were diagnosed with dementia for males and females, respectively. Of the 713 participants, 181 participants had CDR-SB scores available for three longitudinal time points. Compared to males, females showed stronger association of age to WMH volume. Type 2 Diabetes was associated with greater WMH burden in females but not males. Finally, baseline WMH burden was associated with worse clinical dementia outcomes longitudinally in females but not in males. Discussion: Elderly females have an accelerated increase in cerebrovascular burden as they age, and subsequently are more vulnerable to clinical dementia decline due to CSVD. Additionally, females are more susceptible to the cerebrovascular consequences of diabetes. These findings emphasize the importance of considering sex when examining the consequences of CSVD. Future research should explore the underlying mechanisms driving these sex differences and personalized prevention and treatment strategies. Clinical trial registration: The BICWALZS is registered in the Korean National Clinical Trial Registry (Clinical Research Information Service; identifier, KCT0003391). Registration Date 2018/12/14.

Identifiers

PMID38947089
PMCPMC11213210

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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.