TY - JOUR
T1 - Global brain atrophy but not hippocampal atrophy is related to type 2 diabetes
AU - Wisse, Laura E. M.
AU - de Bresser, Jeroen
AU - Geerlings, Mirjam I.
AU - Reijmer, Yael D.
AU - Portegies, Marileen L. P.
AU - Brundel, Manon
AU - Kappelle, L. Jaap
AU - van der Graaf, Yolanda
AU - Biessels, Geert Jan
AU - Utrecht Diabetic Encephalopathy Study Group
AU - de Haan, E.
N1 - Copyright © 2014 Elsevier B.V. All rights reserved.
PY - 2014/9/15
Y1 - 2014/9/15
N2 - Aims It has been suggested that in patients with type 2 diabetes mellitus (T2DM), brain atrophy is most pronounced in the hippocampus, but this has not been investigated systematically. The present pooled analysis of three studies examined if hippocampal atrophy is more prominent than global brain atrophy in patients with T2DM relative to controls. Methods Data were derived from a cohort study of patients with vascular disease (SMART-Medea (T2DM = 120; no T2DM = 502)), and from two case-control studies (UDES1 (T2DM = 61; controls = 30) and UDES2 (T2DM = 54; controls = 53)). In SMART-Medea and UDES1, hippocampal volume was obtained by manual tracing on 1.5 Tesla (T) MRI scans. Total brain and intracranial volume (ICV) were determined by an automated segmentation method. In UDES2, hippocampal and total brain volume were determined by FreeSurfer and ICV by manual segmentation on 3 T MRI scans. Results The pooled analyses, adjusted for age and sex, showed a significant negative relation between T2DM and total brain-to-ICV ratio (standardized mean difference = - 1.24%, 95% CI: - 1.63; - 0.86), but not between T2DM and hippocampal-to-ICV ratio (0.00%, 95% CI: - 0.01; 0.00) or between T2DM and hippocampal-to-total brain volume ratio (0.01%, 95% CI: - 0.01; 0.02). In patients with T2DM no associations were found between brain volume measures and HbA1c or memory. Conclusion Patients with T2DM had greater brain atrophy but not hippocampal atrophy, compared to controls. These findings do not support specific vulnerability of the hippocampus in patients with T2DM. © 2014 Elsevier B.V.
AB - Aims It has been suggested that in patients with type 2 diabetes mellitus (T2DM), brain atrophy is most pronounced in the hippocampus, but this has not been investigated systematically. The present pooled analysis of three studies examined if hippocampal atrophy is more prominent than global brain atrophy in patients with T2DM relative to controls. Methods Data were derived from a cohort study of patients with vascular disease (SMART-Medea (T2DM = 120; no T2DM = 502)), and from two case-control studies (UDES1 (T2DM = 61; controls = 30) and UDES2 (T2DM = 54; controls = 53)). In SMART-Medea and UDES1, hippocampal volume was obtained by manual tracing on 1.5 Tesla (T) MRI scans. Total brain and intracranial volume (ICV) were determined by an automated segmentation method. In UDES2, hippocampal and total brain volume were determined by FreeSurfer and ICV by manual segmentation on 3 T MRI scans. Results The pooled analyses, adjusted for age and sex, showed a significant negative relation between T2DM and total brain-to-ICV ratio (standardized mean difference = - 1.24%, 95% CI: - 1.63; - 0.86), but not between T2DM and hippocampal-to-ICV ratio (0.00%, 95% CI: - 0.01; 0.00) or between T2DM and hippocampal-to-total brain volume ratio (0.01%, 95% CI: - 0.01; 0.02). In patients with T2DM no associations were found between brain volume measures and HbA1c or memory. Conclusion Patients with T2DM had greater brain atrophy but not hippocampal atrophy, compared to controls. These findings do not support specific vulnerability of the hippocampus in patients with T2DM. © 2014 Elsevier B.V.
KW - Aged
KW - Atrophy/etiology
KW - Brain/pathology
KW - Case-Control Studies
KW - Cognition Disorders/etiology
KW - Diabetes Mellitus, Type 2/complications
KW - Female
KW - Hippocampus/pathology
KW - Humans
KW - Linear Models
KW - Magnetic Resonance Imaging
KW - Male
KW - Memory Disorders/etiology
KW - Middle Aged
KW - Neuropsychological Tests
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84906794839&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/24958596
U2 - https://doi.org/10.1016/j.jns.2014.06.008
DO - https://doi.org/10.1016/j.jns.2014.06.008
M3 - Article
C2 - 24958596
SN - 0022-510X
VL - 344
SP - 32
EP - 36
JO - Journal of the neurological sciences
JF - Journal of the neurological sciences
IS - 1-2
ER -