Bridges and boundaries in dementia with lewy bodies: Heterogeneity of clinical and neuroimaging features

BACKGROUND: White matter hyperintensity (WMH), which is considered a sign of vascular lesions, is often found in patients with DLB, but its association with vascular lesions has not been proven. We assessed WMH in patients with DLB and markers of vascular damage and vascular risk factors. METHOD: We examined 78 patients that fulfilled clinical criteria of DLB. The clinical assessment included MoCA, MMSE, ACE‐R, IQCODE, NPI‐4, UM‐PDHQ, UPDRS‐III, RBD1Q, orthostatic hypotension test. All patients underwent 1,5 T brain MRI. WMH was evaluated with Fazekas score and ARWMC. Patients were performed ultrasound assessment of flow‐mediated vasodilation. Laboratory investigation included Willebrand factor, lipid profile, microalbumin/creatinine ratio. RESULT: MRI revealed with moderate to severe WMH in 43 participants. There were no significant differences in vascular risk factors, vessel reactivity, laboratory results between patients with or without WMH. These findings were associated more likely with hyppocampal atrophy and disease duration than vascular risk factors. CONCLUSION: WMH in DLB may be associated with neurodegenerative pathology. Further investigations with diffusion MRI techniques and prospective studies can be helpful in interpretation of neuroimaging findings and understanding of its contribution to the course of the disease.

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Publication Details

Journal
PubMed Central
Published
2025-01-09
DOI
https://doi.org/10.1002/alz.095103
Primary Topic
Legal and Regulatory Analysis
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article
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article

Bridges and boundaries in dementia with lewy bodies: Heterogeneity of clinical and neuroimaging features

PubMed Central
Legal and Regulatory Analysis
article

Bridges and boundaries in dementia with lewy bodies: Heterogeneity of clinical and neuroimaging features

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Abstract

BACKGROUND: White matter hyperintensity (WMH), which is considered a sign of vascular lesions, is often found in patients with DLB, but its association with vascular lesions has not been proven. We assessed WMH in patients with DLB and markers of vascular damage and vascular risk factors. METHOD: We examined 78 patients that fulfilled clinical criteria of DLB. The clinical assessment included MoCA, MMSE, ACE‐R, IQCODE, NPI‐4, UM‐PDHQ, UPDRS‐III, RBD1Q, orthostatic hypotension test. All patients underwent 1,5 T brain MRI. WMH was evaluated with Fazekas score and ARWMC. Patients were performed ultrasound assessment of flow‐mediated vasodilation. Laboratory investigation included Willebrand factor, lipid profile, microalbumin/creatinine ratio. RESULT: MRI revealed with moderate to severe WMH in 43 participants. There were no significant differences in vascular risk factors, vessel reactivity, laboratory results between patients with or without WMH. These findings were associated more likely with hyppocampal atrophy and disease duration than vascular risk factors. CONCLUSION: WMH in DLB may be associated with neurodegenerative pathology. Further investigations with diffusion MRI techniques and prospective studies can be helpful in interpretation of neuroimaging findings and understanding of its contribution to the course of the disease.

PubMed Central
Russian Medical Academy of Continuous Professional Education (RU)
Good health and well-being
Openalex Percentile: Top 48%
Legal and Regulatory Analysis
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Bridges and boundaries in dementia with lewy bodies: Heterogeneity of clinical and neuroimaging features · PubMed Central (2025) | TGRS Research Map | TGRS