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Resumen

White matter hyperintensities (WMH) are an MRI-based biomarker associated with aging, Alzheimer’s disease, and vascular dementia. Although the volume of WMH typically increases over time (growth) for individuals, WMH volume in some cases can also decrease (regress). This suggests the presence of active brain injury recovery mechanisms. Whether WMH regression reflects a true biological phenomenon or results from imaging artifacts or measurement errors, however, remains controversial. Here, we review published reports, following PRISMA search guidelines, describing or referring to WMH regression, the methods used to detect and quantitate regression, and proposed underlying mechanisms. Of 174 reviewed articles, 31 (26 original research studies and five case reports) were identified as directly related to WMH regression. Technical factors such as differences in longitudinal scan parameters, motion artifacts, and the interval between baseline and follow-up scans can affect WMH volume measurements. These factors may lead to inaccurate conclusions if appropriate controls are not employed. Although the use of standardized and systematic measurement protocols is essential, there is strong evidence indicating that WMH regression is a robust and biologically important phenomenon that may be influenced by clinical interventions. Further studies are needed to investigate WMH regression in relation to cerebrovascular risk mitigation and other therapeutic strategies.

Idioma originalEnglish
Número de artículoPMID 8100437
Páginas (desde-hasta)33-46
Número de páginas14
PublicaciónNeurobiology of Aging
Volumen159
DOI
EstadoPublished - mar 2026

Nota bibliográfica

Publisher Copyright:
© 2025 Elsevier Inc.

Financiación

We are grateful to the colleagues and research participants who made this study possible. This work was partially supported by the National Institute on Aging (P30AG072946, P01AG078116) and the National Institute of Neurological Disorder and Stroke (UF1NS125488). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute on AgingP01AG078116, P30AG072946
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilUF1NS125488

    ASJC Scopus subject areas

    • General Neuroscience
    • Aging
    • Developmental Biology
    • Clinical Neurology
    • Geriatrics and Gerontology

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