White matter changes in patients with cognitive impairment

Cerebral white matter changes (WMC), detected with computed tomography (CT) or magnetic resonance imaging (MRI), represent a common condition in elderly people. However, the prognostic, symptomatological and biochemical constituents of WMC are only partially known. The aim of the present study was to evaluate WMC in relation to clinical manifestations in patients with mild cognitive impairment (MCI) and dementia and, by means of cerebrospinal fluid (CSF) analyses, to study different structural biomarkers possibly reflecting the pathophysiological process of WMC in non-disabled patients. In study I, significant associations were found between WMC and age, sex, hypertension, ischaemic heart disease and TIA/minor stroke. Furthermore there were significant associations between WMC and apathy, mental slowness, disinhibition, gait disturbance and focal neurological symptoms, but not with depressed mood. In study II, CSF was analysed for biomarkers known to be related to Alzheimer’s disease [AD; the 1-40 and 1-42 fragments of amyloid-β, αand β-cleaved soluble amyloid precursor proteins (sAPPα, sAPPβ), total tau (T-tau), hyperphosphorylated tau (P-tau)] and vascular dementia [VaD; neurofilament protein light subunit (NFL), sulfatide, and CSF/S-albumin ratio]. NFL and sulfatide but not the AD biomarkers were related to WMC. In study III, low CSF levels of the myelin lipid sulfatide but not biomarker deviations associated with axonal degenration (NFL), or AD were found to be related to progressive WMC. In study IV it was found that WMC were associated with ventricular atrophy which in turn was associated with neuropsychological dysfunction. Furthermore, tissue inhibitor of metalloproteinase 1 (TIMP-1), NFL and sAPPβ were related to both ventricular atrophy as well as WMC. Matrix metalloproteinase 9 (MMP-9) was the only marker representing WMC progression. The results indicate that WMC in patients with cognitive impairment are independently related to a dysexecutive-related behavioural symptom profile, vascular disorders and a nonAD biochemical profile associated with vessel-wall pathology and demyelination. The findings may have implications for definition and nosological knowledge of AD and vascular cognitive disorder.