# White Matter Hyperintensity Burden and Decline in Driving Performance Among Older Adults

**Authors:** Madhur Parihar, Yasheng Chen, Byron Xu, Semere Bekena, Ramkrishna K. Singh, Yiqi Zhu, Jean-Francois Trani, Jin-Moo Lee, David B. Carr, Chia-Ling Phuah, Ganesh M. Babulal

PMC · DOI: 10.1001/jamanetworkopen.2025.54501 · JAMA Network Open · 2026-01-29

## TL;DR

Higher white matter hyperintensity (WMH) in the brain, especially in the posterior regions, is linked to worse driving performance and increased risk in older adults, particularly those who later develop cognitive issues.

## Contribution

The study identifies posterior WMH burden as a potential biomarker for driving risk in aging populations.

## Key findings

- Greater baseline and progressive WMH burden is associated with reduced driving frequency, complexity, and safety.
- Posterior WMH growth is strongly linked to increased crash risk in those developing cognitive impairment.
- Antihypertensive therapy, especially ACE inhibitors, initially attenuates WMH-related risky driving but not after adjustment.

## Abstract

How is total or regional white matter hyperintensity (WMH) burden associated with longitudinal changes in naturalistic driving performance among older adults?

In this cohort study of 220 cognitively normal older adults followed up longitudinally, greater baseline and progressive WMH burden, particularly in posterior regions, was associated with reduced driving frequency, complexity, and safety, especially among participants who later developed cognitive impairment. In the unadjusted model, antihypertensive therapy was associated with reduced WMH-related adverse driving behaviors; however, there was no association after adjustment.

This study suggests that posterior WMH burden may serve as a biomarker of increased driving risk in older adults.

White matter hyperintensity (WMH) burden is associated with cognitive decline, but its association with driving performance among older adults and the associations of modifiable risk factors remain unclear.

To evaluate the association of total and regional WMH burden with longitudinal naturalistic driving performance in cognitively normal older adults and evaluate moderating associations of cognitive decline and antihypertensive therapy.

This prospective longitudinal cohort study enrolled community-dwelling older adults (≥65 years) in the Driving Real-World In-Vehicle Evaluation System Project. Baseline 3-T brain magnetic resonance imaging (MRI) scans and data from continuous in-vehicle driving monitoring were collected from January 1, 2015, to December 31, 2024 (mean [SD] follow-up, 5.6 [1.8] years), with annual cognitive and clinical assessments.

Total and regional WMH volumes, cognitive status change, and antihypertensive medication use.

Monthly driving trip frequency, trip distance, unique destinations, driving entropy, and safety events. Longitudinal associations were evaluated using linear mixed-effects models adjusted for demographic characteristics, socioeconomic status, and vascular risk.

Among 220 participants (mean [SD] age, 72.9 [5.0] years; 119 men [54%]) with low vascular risk (mean [SD] Framingham Stroke Risk Profile, 6.4% [1.3%]), greater baseline WMH burden was correlated with lower driving frequency (β = −0.16; 95% CI, −0.27 to −0.06; P = .002), reduced driving entropy (β = −0.17; 95% CI, −0.27 to −0.06; P = .002), and fewer unique destinations (β = −0.17; 95% CI, −0.27 to −0.07; P = .001). Longitudinally, higher WMH was associated with faster declines in driving frequency (β = −0.08; 95% CI, −0.13 to −0.04; P < .001), entropy (β = −0.11; 95% CI, −0.17 to −0.06; P < .001), and unique destinations (β = −0.09; 95% CI, −0.14 to −0.04; P < .001). Growth in posterior WMH burden showed the strongest association with increased crash risk (β = 1.71; 95% CI, 1.17-2.24; P < .001) among those developing cognitive impairment (38 [17%]). Among participants, 135 used antihypertensive therapy and 113 underwent follow-up MRI. Antihypertensive therapy, particularly angiotensin-converting enzyme inhibitors, was associated with attenuated WMH-related risky driving before adjustment, but not after adjustment (β = −0.17; 95% CI, −0.37 to 0.03; unadjusted P = .02; false discovery rate–adjusted P = .08). Sensitivity analyses confirmed associations were independent of Alzheimer dementia pathology.

In this cohort study of older drivers, higher WMH burden, especially in posterior regions, was associated with progressive driving self-regulation and increased errors in those developing cognitive impairment. Antihypertensive use attenuated WMH-associated unsafe driving. Posterior WMH may represent a biomarker for identifying older drivers at risk and may inform mobility-preserving interventions in aging populations.

This cohort study evaluates how white matter hyperintensity (WMH) burden is associated with longitudinal changes in naturalistic driving performance among cognitively normal older adults

## Full-text entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** atrial fibrillation (MESH:D001281), amyloid (MESH:C000718787), diabetes (MESH:D003920), Alzheimer (MESH:D000544), depression (MESH:D003866), death (MESH:D003643), Cognitive impairment (MESH:D003072), vascular dementia (MESH:D015140), myocardial infarction (MESH:D009203), leukoaraiosis (MESH:D049292), inflammatory (MESH:D007249), functional decline (MESH:D060825), Stroke (MESH:D020521), HTN (MESH:D006973), Matter Hyperintensity (MESH:D056784), ID (MESH:C537985), Dementia (MESH:D003704), neural (MESH:D015441), cerebral small vessel disease (MESH:D059345)
- **Chemicals:** Pittsburgh compound B (MESH:C475519), 18F-flortaucipir (MESH:C000591008), carbon 11- (MESH:C000615233), 18F-florbetapir (MESH:C545186)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12856682/full.md

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Source: https://tomesphere.com/paper/PMC12856682