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Diabetes mellitus, hypertension and medial temporal lobe atrophy: the LADIS study
Author(s) -
Korf E. S. C.,
Van Straaten E. C. W.,
De Leeuw F.E.,
Van Der Flier W. M.,
Barkhof F.,
Pantoni L.,
Basile A. M.,
Inzitari D.,
Erkinjuntti T.,
Wahlund L.O.,
Rostrup E.,
Schmidt R.,
Fazekas F.,
Scheltens P.
Publication year - 2007
Publication title -
diabetic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 145
eISSN - 1464-5491
pISSN - 0742-3071
DOI - 10.1111/j.1464-5491.2007.02049.x
Subject(s) - medicine , diabetes mellitus , leukoaraiosis , hyperintensity , blood pressure , cardiology , atrophy , vascular disease , endocrinology , disease , magnetic resonance imaging , dementia , radiology
Hypothesis  Based on recent findings on the association between vascular risk factors and hippocampal atrophy, we hypothesized that hypertension and diabetes mellitus (DM) are associated with medial temporal lobe atrophy (MTA) in subjects without disability, independent of the severity of white matter hyperintensities. Methods  In the Leukoaraiosis And DISability in the elderly (LADIS) study, we investigated the relationships between DM, hypertension, blood pressure and MTA in 582 subjects, stratified by white matter hyperintensity severity, using multinomial logistic regression. MTA was visually scored for the left and right medial temporal lobe (score 0–4), and meaned. Results  Mean age was 73.5 years ( sd  5.1), 54% was female. Of the subjects, 15% had DM, and 70% had a history of hypertension. The likelihood of having MTA score 3 was significantly higher in subjects with DM (OR 2.9; 95% CI: 1.1–7.8) compared with an MTA score of 0 (no atrophy). The odds ratio for MTA score 2 was not significantly increased (OR 1.8; CI: 0.9–4). Systolic and diastolic blood pressure and a history of hypertension were not associated with MTA. There was no interaction between DM and hypertension. Stratification on white matter hyperintensities (WMH) did not alter the associations. Conclusion Our study strengthens the observation that MTA is associated with DM, independently of the amount of small vessel disease as reflected by WMH.

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