Difference in white matter microstructure in differential diagnosis of normal pressure hydrocephalus and Alzheimer's disease

. 2016 Jan ; 140 () : 52-9. [epub] 20151119

Jazyk angličtina Země Nizozemsko Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26646649
Odkazy

PubMed 26646649
DOI 10.1016/j.clineuro.2015.11.010
PII: S0303-8467(15)30076-7
Knihovny.cz E-zdroje

OBJECTIVES: Alzheimer's disease (AD) and normal pressure hydrocephalus (NPH) are both associated with cognitive decline and ventriculomegaly. While promising approach in differentiating between the two diseases, only a few diffusion tensor imaging (DTI) studies compared directly NPH and AD patients. The current study compares global whitematter (WM) alterations in AD and NPH addressing some of the methodological issues of previous studies. PATIENTS AND METHODS: Diffusion tensor images were obtained from 17 patients with NPH, 14 with AD, and 17 healthy controls. White matter integrity was quantified by fractional anisotropy (FA), mean (MD), axial (λ1) and radial diffusivity (RD). The diffusion parameters were compared between the groups in 'skeletonised' tracts representing the core of the fibre bundles. RESULTS: Reduced FA was found in NPH patients throughout the corpus callosum, particularly in the splenium, along with increased RD. On the other hand, FA, MD and RD were higher in NPH in the cortico-fugal fibres arising from the frontal and parietal cortex. While no FA changes were detected in AD patients compared to controls, widespread increased RD was observed. When comparing NPH and AD patients, higher FA, MD and RD was observed in the corona radiata in the periventricular fibres arising from the frontal and parietal cortex in NPH patients. The ventricular volumes were correlated with diffusivity parameters in the tracts next to the ventricles in AD and NPH patients. CONCLUSION: Our analysis identified a pattern of WM diffusion alterations that can differentiate NPH patients from controls and AD patients.

Department of Neurology Faculty of General Medicine University of Szeged Szeged Hungary

Department of Neurosurgery 1st Faculty of Medicine Charles University and University Central Military Hospital Prague Czech Republic

Department of Neurosurgery University Hospital of Marburg Germany

Department of Radiodiagnostics University Central Military Hospital Prague Czech Republic

Department of Radiology 2nd Faculty of Medicine Charles University and University Hospital Motol Prague Czech Republic

Department of Radiology Mayo Clinic Rochester MN USA

International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic

International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic; Department of Neurology Faculty of General Medicine University of Szeged Szeged Hungary

International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic; Department of Neurosurgery 1st Faculty of Medicine Charles University and University Central Military Hospital Prague Czech Republic

International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic; Department of Radiology 2nd Faculty of Medicine Charles University and University Hospital Motol Prague Czech Republic

International Clinical Research Center St Anne's University Hospital Brno Brno Czech Republic; Memory Disorders Clinic Department of Neurology 2nd Faculty of Medicine Charles University Prague and Motol University Hospital Czech Republic

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