Neuroanatomical localisation and clinical correlates of white matter lesions in the elderly. Issue 9 (16th August 2004)

• Record Type: Journal Article
• Authors: Artero, S; Tiemeier, H; Prins, N D; Sabatier, R; Breteler, M M B; Ritchie, K
• Is Part Of: Journal of neurology, neurosurgery and psychiatry. Volume 75:Issue 9(2004)
• Page Start: 1304
• Page End: 1308
• Publication Date: 2004-08-16
• Subjects: CESD, Center of Epidemiologic Studies depression scale -- MCA, multiple correspondence analysis -- MMSE, mini-mental state examination -- WML, white matter lesion; depression -- elderly -- white matter lesion; Neurology -- Periodicals; Nervous system -- Surgery -- Periodicals; Psychiatry -- Periodicals; 616.8
• DOI: 10.1136/jnnp.2003.023713
• Languages: English
• ISSNs: 0022-3050

Abstract

Abstract : Background: White matter lesions (WML) in elderly people co-occur with hypertension, depression, and cognitive impairment. Little is known about the density and distribution of WML in normal elderly people, whether they occur randomly in the aging brain or tend to cluster in certain areas, or whether patterns of WML aggregation are linked to clinical symptoms. Objectives: To describe patterns of WML distribution in a large representative population of elderly people using non-inferential cluster analysis; and to determine the extent to which such patterns are associated with clinical symptomatology. Method: A population sample of 1077 elderly people was recruited. Multiple analysis of correspondence followed by automatic classification methods was used to explore overall patterns of WML distribution. Correspondence was then sought between these patterns and a range of cerebrovascular, psychiatric, and neurological symptoms. Results: Three distinct patterns of spatial localisation within the brain were observed, corresponding to distinct clusters of clinical symptoms. In particular WML aggregation in temporal and occipital areas was associated with greater age, hypertension, late onset depressive disorder, poor global cognitive function, and overall WML frequency. Conclusions: WML localisation is not random in the aging brain, and their distribution is associated with age and the presence of clinical symptoms. Age differences suggest there may be patterns of progression across time; however, this requires confirmation from longitudinal imaging studies.