Pattern of brain atrophy rates in autopsy-confirmed dementia with Lewy bodies

. 2015 Jan ; 36 (1) : 452-61. [epub] 20140715

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid25128280

Grantová podpora
U01 AG032438 NIA NIH HHS - United States
R21 NS066147 NINDS NIH HHS - United States
R01AG040042 NIA NIH HHS - United States
U01 AG024904 NIA NIH HHS - United States
R01 AG040042 NIA NIH HHS - United States
R01-AG11378 NIA NIH HHS - United States
P01 AG017216 NIA NIH HHS - United States
P50 AG016574 NIA NIH HHS - United States
U01 HL096917 NHLBI NIH HHS - United States
R01 AG015866 NIA NIH HHS - United States
R01 AG011378 NIA NIH HHS - United States
R01 AG037551 NIA NIH HHS - United States
P50-AG16574 NIA NIH HHS - United States
UL1 TR000135 NCATS NIH HHS - United States
U24 AG026395 NIA NIH HHS - United States
P50-AG16574/P1 NIA NIH HHS - United States
P50 NS072187 NINDS NIH HHS - United States
P50 AG044170 NIA NIH HHS - United States
R00 AG037573 NIA NIH HHS - United States
U01 AG006786 NIA NIH HHS - United States
AG015866 NIA NIH HHS - United States

Dementia with Lewy bodies (DLB) is characterized by preserved whole brain and medial temporal lobe volumes compared with Alzheimer's disease dementia (AD) on magnetic resonance imaging. However, frequently coexistent AD-type pathology may influence the pattern of regional brain atrophy rates in DLB patients. We investigated the pattern and magnitude of the atrophy rates from 2 serial MRIs in autopsy-confirmed DLB patients (n = 20) and mixed DLB/AD patients (n = 22), compared with AD (n = 30) and elderly nondemented control subjects (n = 15), followed antemortem. DLB patients without significant AD-type pathology were characterized by lower global and regional rates of atrophy, similar to control subjects. The mixed DLB/AD patients displayed greater atrophy rates in the whole brain, temporoparietal cortices, hippocampus and amygdala, and ventricle expansion, similar to AD patients. In the DLB and DLB/AD patients, the atrophy rates correlated with Braak neurofibrillary tangle stage, cognitive decline, and progression of motor symptoms. Global and regional atrophy rates are associated with AD-type pathology in DLB, and these rates can be used as biomarkers of AD progression in patients with LB pathology.

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