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This page is alzhub.org's plain-English summary of a published study, not the paper itself. It is generated from the record we hold for this study, sourced and linked below — check the original for the full text and methods.

✓ Peer-reviewed alzhub usefulness score 47 out of 100. Risk factors

Topic: Amyloid, tau and blood-test diagnosis

Our study included 74,275 weeks of driving data (2015-2024, average follow-up 6.1 years). Increased WMH burden correlated with decreased trip frequency (p = 0.0005), fewer near-home trips (p = 0.0004), reduced unique destinations (p = 0.0003), and lower driving entropy (p = 0.001) over time. Decrease in driving complexity was primarily driven by posteriorly-located WMH lesions, especially in parietal and occipital regions (β=-0.09, p = 0.002 and β=-0.10, p = 0.0009, respectively) involved in visual processing, motion detection and spatial awareness. WMH impact on driving behavior intensified over time in participants developing cognitive impairment (n = 36), manifesting as increased hard breaking and impact events. WMH in OA significantly impacts driving behavior, leading to latent self-regulation and reduced driving complexity. Cognitive impairment with WMH increases risky driving. Posterior WMH influence suggests a dominant role of AD pathology in driving performance decline. WMH shows potential as a biomarker for identifying individuals at higher risk of unsafe driving and premature driving cessation, highlighting its value in early screening and intervention strategies for road safety among aging populations, particularly those at risk for AD.

Key findings

Why it matters

This study found that more white matter hyperintensities were linked to simpler driving patterns over time, and that in people developing cognitive impairment, risky driving events increased. It suggests these brain changes may help identify people at risk of unsafe driving, but it does not test a treatment, cure, or prevention.

Study details

How this study scored 47/100
How this study's score is builtJournal tier 7 of 10; Journal's citation record 2 of 4; Study design 7 of 12; Strength of evidence 3 of 5; Peer-review validation 10 of 10; How recent 4 of 5; Sample size 1 of 4; Effect reported 0 of 3; Studied in people 3 of 3; Randomised / blinded 0 of 2; Times cited 0 of 7; Citations per year 0 of 5; Impact for its field and year 0 of 6; Cited by studies here 0 of 6; Still being cited 0 of 4; Senior author's track record 2 of 4; Institution's track record 2 of 3; Multi-centre collaboration 2 of 3; Indexed in PubMed 2 of 2; Free to read 2 of 2. Total 47 of 100.47 of 100 points earned53 not earned

Published in a peer-reviewed journal, and it is a longitudinal study following the same people over time. Scored zero for effect reported and randomised / blinded because the record does not state it.

ComponentPointsWhy
Journal tier 7 / 10 Tier 3 — peer-reviewed journal (Alzheimer s & Dementia)
Journal's citation record 2 / 4 Alzheimer s & Dementia: journal h-index 228 (OpenAlex, 2026-10-29)
Study design 7 / 12 A longitudinal study following the same people over time
Strength of evidence 3 / 5 Rated “moderate” in our summary
Peer-review validation 10 / 10 Peer-reviewed. Published as an article in a named peer-reviewed journal.
How recent 4 / 5 2025 — within 3 year(s) of the newest study here
Sample size 1 / 4 36 participants
Effect reported 0 / 3 No effect size reported — scores zero (not stated in the record — scored 0)
Studied in people 3 / 3 Studied in people (participant count stated)
Randomised / blinded 0 / 2 No randomisation or blinding stated — scores zero (not stated in the record — scored 0)
Times cited 0 / 7 Cited 0 times (OpenAlex, 2026-10-10)
Citations per year 0 / 5 0.0 citations a year over 3 year(s) since 2025
Impact for its field and year 0 / 6 Cited 0.0× the average for papers of its field and year (OpenAlex FWCI)
Cited by studies here 0 / 6 No other study in this library cites it
Still being cited 0 / 4 Cited 0 times in 2024–2026 (2026 still in progress; OpenAlex)
Senior author's track record 2 / 4 Last-listed author Ganesh Muneshwar Babulal: h-index 31 (OpenAlex, whole career)
Institution's track record 2 / 3 Washington University in St. Louis: institution h-index 1,962 (OpenAlex)
Multi-centre collaboration 2 / 3 OpenAlex lists 4 institution(s) in 2 countries
Indexed in PubMed 2 / 2 Indexed in PubMed (PMID 41433463)
Free to read 2 / 2 Free to read
Total 47 / 100 —

What each of these 20 components measures, and what this score is not →

Read the original

Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).

Cite this study APA, Vancouver, BibTeX · download .bib or .ris

Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.

APA 7th

Phuah, C., Parihar, M., Chen, Y., Carr, D. B., Lee, J., & Babulal, G. M. (2025). White Matter Hyperintensities Predict Driving Behavior Changes in Preclinical Alzheimer’s Disease. Alzheimer s & Dementia. https://doi.org/10.1002/alz70862_110306

Vancouver

Phuah C, Parihar M, Chen Y, Carr DB, Lee J, Babulal GM. White Matter Hyperintensities Predict Driving Behavior Changes in Preclinical Alzheimer’s Disease. Alzheimer s & Dementia. 2025. doi:10.1002/alz70862_110306. PMID: 41433463.

BibTeX

@article{phuah2025-41433463,
  author  = {Phuah, Chia‐Ling and Parihar, Madhur and Chen, Yasheng and Carr, David B. and Lee, Jin‐Moo and Babulal, Ganesh Muneshwar},
  title   = {{White Matter Hyperintensities Predict Driving Behavior Changes in Preclinical Alzheimer’s Disease}},
  journal = {Alzheimer s \& Dementia},
  year    = {2025},
  doi     = {10.1002/alz70862_110306},
  pmid    = {41433463},
  url     = {https://doi.org/10.1002/alz70862_110306}
}

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