AbstractsPsychology

Neurodegenerative diseases are a heterogeneous group of disorders that are characterized by the progressive degeneration of structure and function of the nervous system. They include diseases such as Alzheimer’s disease (AD), multiple sclerosis (MS) and others. The main aims of this thesis were to study functional and/or structural brain changes in AD and MS using novel magnetic resonance imaging (MRI) techniques. The concentration of β-amyloid1-42 (Aβ42), total tau (T-tau) and tau phosphorylated at position threonine 181 (P-tau181p) in cerebrospinal fluid (CSF) may reflect brain pathophysiological processes in AD. We found a positive correlation between functional connectivity within the default mode network (DMN) and the ratio of Aβ42/P-tau181p in sporadic AD (Paper I). Furthermore, there were correlations between AD CSF biomarkers and changes of gray matter volume, fractional anisotropy (FA) and mean diffusivity (MD). The majority of brain regions with statistically significant correlation with biomarkers of AD overlapped with the DMN (Paper II). These findings implicate that the brain functional connectivity and structure are affected by pathological changes at an early stage in AD. We also found a significantly increased MD in pre-symptomatic mutation carriers (pre-MCs) of AD compared with non-carriers (NCs), and increased MD associated with AD CSF biomarkers (Paper III). Similar results were observed both in sporadic and familial AD, which suggests that MD may reflect pathology of early stage AD. Although the exact causes of these changes are difficult to identify, the increased MD may be explained by myelin loss. In MS, myelin loss is one of the characteristic events of the pathological process. By combining susceptibility-weighted MRI with analysis of the