4.6 Article

Association of White Matter Lesions and Lacunar Infarcts With Executive Functioning The SMART-MR Study

Journal

AMERICAN JOURNAL OF EPIDEMIOLOGY
Volume 170, Issue 9, Pages 1147-1155

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/aje/kwp256

Keywords

brain infarction; cognition; leukoaraiosis; magnetic resonance imaging

Funding

  1. Netherlands Organization for Scientific Research-Medical Sciences [904-65-095]
  2. Netherlands Organization for Scientific Research [917-66-311]

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The authors investigated the association of white matter lesions and lacunar infarcts with cognitive performance and whether brain atrophy mediates these associations. Within the Second Manifestations of Arterial Disease-Magnetic Resonance study (2001-2005, the Netherlands), cross-sectional analyses of 522 patients were performed (mean age, 57 years (standard deviation, 10); 76% male). Brain segmentation was used to quantify volumes of brain tissue, cerebrospinal fluid, and white matter lesions. Infarcts were rated visually. Brain volume, ventricular volume, and gray matter volume were divided by intracranial volume to obtain indicators of brain atrophy. Neuropsychological tests assessing executive functioning and memory were performed, and scores were transformed into z scores. The authors used linear regression analyses, adjusted for age, sex, education, intelligence, and vascular risk factors, to investigate the association of white matter lesions and number of lacunar infarcts with cognitive performance. A 1-standard-deviation higher volume of white matter lesions (beta = -0.12, 95% confidence interval: -0.20, -0.04) and the presence of >= 2 lacunar infarcts (beta = -0.48, 95% confidence interval: -0.87, -0.09) were associated with worse executive functioning. These associations remained after adjusting for brain atrophy. Both were not associated with worse memory. Results suggest that subcortical ischemic vascular lesions are associated with decreased executive functioning, but not with memory functioning, independent of brain atrophy.

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