Related Experiment Video
Updated: Aug 9, 2026

Evaluation of the Cognitive Performance of Hypertensive Patients with Silent Cerebrovascular Lesions
Published on: April 23, 2021
Lesion probability maps of white matter hyperintensities in elderly individuals: results of the Austrian stroke
Christian Enzinger1, Stephen Smith, Franz Fazekas
1Department of Neurology, Medical University Graz, Auenbruggerplatz 22, 8036 Graz, Austria. chris.enzinger@meduni-graz.at
Objective:
White matter hyperintensities (WMH) are common on brain MRI of the elderly. Their size ranges from punctate to early confluent to confluent lesions. While this increase in extension is frequently seen as evidence for a continuum of changes, histological data and clinical follow-up suggest differences in underlying pathology and their progression.
Methods:
We tested this hypothesis by exploring the distributions of punctuate and confluent lesions using lesion probability maps (LPM) generated from MRI scans of 189 participants (mean age 60.8+/-6.2 years) in the Austrian Stroke Prevention Study. We dichotomised WMH according to the classification by Fazekas et al. [punctate (n=143) vs. early confluent and confluent (n=33)] to run voxel-based t-tests using permutation-based nonparametric inference. To test alternative hypotheses, we created similar LPM for age and arterial hypertension.
Results:
We observed significant differences in the spatial distribution of lesions for the two WMH groups (p<0.01). Punctate lesions were more diffusely distributed throughout the cerebral white matter (peak probability approximately 5%) relative to confluent lesions (peak probability 45%). Confluent lesions had greatest likelihood of being found in perfusion "watershed" regions. These differences in distribution could not be explained by differences in age or hypertension only, as both greater age and the diagnosis of hypertension were associated with WMH abutting the occipital horns.
Conclusions:
Punctate and early confluent to confluent WMH show distinguishable differences in their spatial distribution within a normal elderly population. The pattern of punctate WMH is probably a consequence of mixed etiologies. Preferential localization of the more confluent WMH with arterial watershed areas implies a stronger ischemic component in their development.
Insights
Punctate and confluent white matter hyperintensities (WMH) show distinct spatial distributions in elderly brains. Confluent WMH are more common in watershed areas, suggesting a stronger ischemic cause.
Area of Science:
- Neurology
- Radiology
- Neuroimaging
Background:
- White matter hyperintensities (WMH) are common in the elderly and appear in varying degrees of severity.
- Existing understanding often views WMH progression as a continuum, but histological and clinical data suggest differing pathologies.
Purpose of the Study:
- To investigate whether punctate and confluent WMH have distinct spatial distributions in the brain.
- To explore potential differences in underlying pathology and progression based on lesion distribution.
Main Methods:
- Utilized lesion probability maps (LPM) from MRI scans of 189 participants.
- Dichotomized WMH into punctate versus early confluent/confluent groups using Fazekas classification.
- Performed voxel-based t-tests with permutation-based nonparametric inference, creating LPM for age and hypertension as controls.
Main Results:
- Significant differences in spatial distribution were found between punctate and confluent WMH (p<0.01).
- Punctate lesions were diffusely distributed (peak ~5%), while confluent lesions were concentrated (peak ~45%), particularly in perfusion "watershed" regions.
- Age and hypertension were associated with WMH near occipital horns, but did not fully explain the distribution differences observed between WMH types.
Conclusions:
- Punctate and confluent WMH exhibit distinguishable spatial patterns in the elderly brain.
- The diffuse pattern of punctate WMH likely results from mixed etiologies.
- The localization of confluent WMH in watershed areas suggests a more significant ischemic component in their development.

