Back

White Matter Lesion Asymmetry and Carotid Intraplaque Hemorrhage: A Novel Imaging Phenotype for Stroke Risk in Older Men

Simard, N.; Honarvar, F.; Noronha, J.; Gibicar, A.; Tyrrell, P. N.; Moody, A. R.; Rajah, M. N.; Black, S. E.; Jabehdar Maralani, P.; Khademi, A.

2026-01-30 neuroscience
10.64898/2026.01.27.702169 bioRxiv
Show abstract

BackgroundWhile identifying high-risk carotid disease remains a significant clinical challenge, the specific role of carotid intraplaque hemorrhage (IPH) is poorly understood. Although IPH has been linked to white matter lesion (WML) burden, current assessments overlook the directional impact of plaque instability on the brain. This study sought to determine whether IPH is an independent driver of asymmetric WML pathology and evaluate if this phenotype can identify a high-risk demographic for TIA and stroke. MethodsThis multi-center retrospective study analyzed 264 participants (mean age 71.8 years) from the Canadian Atherosclerosis Imaging Network (2010-2015). Participants underwent 3T MRI to assess carotid IPH and WMLs. We quantified WMLs using a deep-learning pipeline to extract three biomarkers: volume (WML-ICV), intensity (WML-Intensity), and intensity ratio (WML-IR). The Asymmetry Index Measure (AIM) defined the inter-hemispheric log-ratio, while the association between IPH and AIM was examined using multivariable linear regression adjusted for age, sex, stenosis, and scanner manufacturer. A secondary composite outcome of TIA/stroke was analyzed via logistic regression to evaluate the interaction between IPH, age, and sex. ResultsWhile whole-brain WML burden did not significantly differ by IPH status (p > 0.60), IPH status was a robust independent predictor of hemispheric asymmetry (WML-ICV: p = 0.01; WML-Intensity, p = 0.01). Post-hoc analysis confirmed WML burden was significantly higher in IPH+ older males ([&ge;] 70 years) compared to younger cohorts (p < 0.04). This older male subgroup also demonstrated 4.57-fold higher adjusted odds of TIA/stroke (p = 0.02) compared to other demographic subgroups (all p > 0.87). ConclusionsCarotid IPH is independently associated with a rightward asymmetric WML phenotype not captured by global metrics. This imaging marker identifies a high-risk demographic of older males with a nearly five-fold increase in clinical events, suggesting that hemispheric-level analysis provides critical prognostic value for stroke risk stratification.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

1
NeuroImage: Clinical
132 papers in training set
Top 0.1%
19.8%
2
Alzheimer's & Dementia
143 papers in training set
Top 0.5%
14.6%
3
Frontiers in Neurology
91 papers in training set
Top 0.5%
10.3%
4
Journal of Cerebral Blood Flow & Metabolism
43 papers in training set
Top 0.1%
6.5%
50% of probability mass above
5
Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring
38 papers in training set
Top 0.3%
4.9%
6
Neurology
44 papers in training set
Top 0.4%
3.6%
7
Human Brain Mapping
295 papers in training set
Top 2%
2.6%
8
Scientific Reports
3102 papers in training set
Top 45%
2.6%
9
Stroke
35 papers in training set
Top 0.4%
2.6%
10
PLOS ONE
4510 papers in training set
Top 50%
1.9%
11
Frontiers in Aging Neuroscience
67 papers in training set
Top 2%
1.7%
12
Alzheimer's Research & Therapy
52 papers in training set
Top 1%
1.7%
13
Neurobiology of Aging
95 papers in training set
Top 2%
1.4%
14
Frontiers in Neuroscience
223 papers in training set
Top 6%
1.0%
15
Experimental Neurology
57 papers in training set
Top 1.0%
1.0%
16
Brain Communications
147 papers in training set
Top 3%
0.9%
17
Imaging Neuroscience
242 papers in training set
Top 3%
0.9%
18
Fluids and Barriers of the CNS
21 papers in training set
Top 0.3%
0.8%
19
Neurobiology of Disease
134 papers in training set
Top 4%
0.8%
20
NeuroImage
813 papers in training set
Top 6%
0.7%
21
Journal of Alzheimer's Disease
43 papers in training set
Top 1%
0.7%
22
Brain Structure and Function
83 papers in training set
Top 0.7%
0.7%
23
Nature Communications
4913 papers in training set
Top 65%
0.7%
24
Annals of Neurology
57 papers in training set
Top 3%
0.5%
25
Atherosclerosis
29 papers in training set
Top 1%
0.5%
26
Brain Research
35 papers in training set
Top 3%
0.5%
27
Journal of Stroke and Cerebrovascular Diseases
12 papers in training set
Top 0.6%
0.5%
28
Journal of Psychiatric Research
28 papers in training set
Top 1.0%
0.5%
29
eneuro
389 papers in training set
Top 11%
0.5%
30
BMC Geriatrics
15 papers in training set
Top 0.6%
0.5%