Diagnostic value of lobar microbleeds in individuals without intracerebral hemorrhage

Sergi Martinez-Ramirez, Jose Rafael Romero, Ashkan Shoamanesh, Ann C. McKee, Ellis Van Etten, Octavio Pontes-Neto, Eric A. Macklin, Alison Ayres, Eitan Auriel, Jayandra J. Himali, Alexa S. Beiser, Charles Decarli, Thor D. Stein, Victor E. Alvarez, Matthew P. Frosch, Jonathan Rosand, Steven M. Greenberg, M. Edip Gurol, Sudha Seshadri, Anand Viswanathan

Producción científica: Articlerevisión exhaustiva

115 Citas (Scopus)

Resumen

Introduction The Boston criteria are the basis for a noninvasive diagnosis of cerebral amyloid angiopathy (CAA) in the setting of lobar intracerebral hemorrhage (ICH). We assessed the accuracy of these criteria in individuals with lobar microbleeds (MBs) without ICH. Methods We identified individuals aged >55 years having brain magnetic resonance imaging (MRI) and pathological assessment of CAA in a single academic hospital and a community-based population (Framingham Heart Study [FHS]). We determined the positive predictive value (PPV) of the Boston criteria for CAA in both cohorts, using lobar MBs as the only hemorrhagic lesion to fulfill the criteria. Results We included 102 individuals: 55 from the hospital-based cohort and 47 from FHS (mean age at MRI 74.7 ± 8.5 and 83.4 ± 10.9 years; CAA prevalence 60% and 46.8%; cases with any lobar MB 49% and 21.3%; and cases with ≥2 strictly lobar MBs 29.1% and 8.5%, respectively). PPV of "probable CAA" (≥2 strictly lobar MBs) was 87.5% (95% confidence interval [CI], 60.4-97.8) and 25% (95% CI, 13.2-78) in hospital and general populations, respectively. Discussion Strictly lobar MBs strongly predict CAA in non-ICH individuals when found in a hospital context. However, their diagnostic accuracy in the general population appears limited.

Idioma originalEnglish (US)
Páginas (desde-hasta)1480-1488
Número de páginas9
PublicaciónAlzheimer's and Dementia
Volumen11
N.º12
DOI
EstadoPublished - dic 1 2015
Publicado de forma externa

ASJC Scopus subject areas

  • Epidemiology
  • Health Policy
  • Developmental Neuroscience
  • Clinical Neurology
  • Geriatrics and Gerontology
  • Cellular and Molecular Neuroscience
  • Psychiatry and Mental health

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