White matter integrity in dementia with Lewy bodies: a voxel-based analysis of diffusion tensor imaging

. 2015 Jun ; 36 (6) : 2010-7. [epub] 20150314

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/pmid25863527

Grantová podpora
P50 AG16574 NIA NIH HHS - United States
U19 AG10483 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
U01-HL096917 NHLBI NIH HHS - United States
U01 AG010483 NIA NIH HHS - United States
R01-AG15866 NIA NIH HHS - United States
U01 AG006786 NIA NIH HHS - United States
R01-AG037551 NIA NIH HHS - United States
U01 AG032438 NIA NIH HHS - United States
C06 RR018898 NCRR NIH HHS - United States
R01AG040042 NIA NIH HHS - United States
U01-AG032438 NIA NIH HHS - United States
R01 AG11378 NIA NIH HHS - United States
P50 AG016574 NIA NIH HHS - United States
U01 HL096917 NHLBI NIH HHS - United States
U01 AG024904 NIA NIH HHS - United States
U19 AG010483 NIA NIH HHS - United States
U01-24904 PHS HHS - United States
P50 AG44170 NIA 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
U24-AG26395 NIA NIH HHS - United States
U01 AG06786 NIA NIH HHS - United States
P50 AG044170 NIA NIH HHS - United States
R01-AG011378 NIA NIH HHS - United States
U01-AG06786 NIA NIH HHS - United States
AG-16574 NIA NIH HHS - United States
1-P50-AG16574/P1 NIA NIH HHS - United States
U01 AG042791 NIA NIH HHS - United States

Many patients with dementia with Lewy bodies (DLB) have overlapping Alzheimer's disease (AD)-related pathology, which may contribute to white matter (WM) diffusivity alterations on diffusion tensor imaging (DTI). Consecutive patients with DLB (n = 30), age- and sex-matched AD patients (n = 30), and cognitively normal controls (n = 60) were recruited. All subjects underwent DTI, 18F 2-fluoro-deoxy-d-glucose, and (11)C Pittsburgh compound B positron emission tomography scans. DLB patients had reduced fractional anisotropy (FA) in the parietooccipital WM but not elsewhere compared with cognitively normal controls, and elevated FA in parahippocampal WM compared with AD patients, which persisted after controlling for β-amyloid load in DLB. The pattern of WM FA alterations on DTI was consistent with the more diffuse posterior parietal and occipital glucose hypometabolism of 2-fluoro-deoxy-d-glucose positron emission tomography in the cortex. DLB is characterized by a loss of parietooccipital WM integrity, independent of concomitant AD-related β-amyloid load. Cortical glucose hypometabolism accompanies WM FA alterations with a concordant pattern of gray and WM involvement in the parietooccipital lobes in DLB.

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