This study investigated neuropsychological dysfunction and gray matter atrophy in mild cognitive impairment (MCI) depending on the age at onset. MCI refers to a preclinical stage of Alzheimer's disease (AD). AD can be divided into early onset and late...
This study investigated neuropsychological dysfunction and gray matter atrophy in mild cognitive impairment (MCI) depending on the age at onset. MCI refers to a preclinical stage of Alzheimer's disease (AD). AD can be divided into early onset and late onset. Early onset AD (EOAD) and late
onset AD (LOAD) differ in neuropsychological, neuroimaging characteristics, and clinical course. MCI, like AD, can be divided into early onset MCI (EOMCI) and late onset MCI (LOMCI). We enrolled 101 patients with amnestic MCI (40 EOMCI, 61 LOMCI) and 2 age-matched control groups. The LOMCI patients obtained significantly lower scores in language function than the EOMCI patients. The EOMCI group, campared to the young controls, demonstrated more atrophy in parietal areas. The LOMCI group demonstrated more atrophy in temporal areas than old controls. Our study suggests that LOMCI differs from EOMCI in neuropsychological function and neuroimaging character. In addition, current neuropsychological assessment can detect early feature of LOMCI, but not search out neuropsychological feature associated with parietal areas in EOMCI. Therefore, cognitive function of young patients with MCI symptoms should be carefully evaluated through various methods.