Atrophy in the hippocampus - brain region known for memory formation is evident in Parkinson's disease patients with cognitive impairment, reveals study conducted by Perelman School of Medicine at the University of Pennsylvania researchers. The study is published in the December issue of the Archives of Neurology, one of the JAMA/Archives journals.
First, using traditional imaging analyses, researchers found that Parkinson's patients with MCI had more atrophy in the hippocampus, basal ganglia, amygdala, and insula compared with Parkinson's patients with normal cognition, whereas Parkinson's patients with normal cognition showed no significant loss of brain volume compared with healthy controls. For Parkinson's patients with full-blown dementia, atrophy was present not only in the hippocampus but also the surrounding medial temporal lobe, also crucial to memory and other cognitive abilities.
Then researchers generated the first structural pattern of classifying brain atrophy associated with dementia in Parkinson's disease by analyzing the scans of PD with either dementia or normal cognition.
"When we layer different information gathered from structural MRIs and generate a structural pattern that weighs different brain regions on their ability to distinguish PD with dementia from those with normal cognition, we can see a pattern of diffuse gray matter and white matter atrophy in the brains of Parkinson's patients with cognitive decline," explains the study's lead author, Daniel Weintraub, MD, associate professor of Geriatric Psychiatry with Penn's Perelman School of Medicine and the Philadelphia Veterans Affairs Medical Center. "This complex analysis of brain imaging data suggests that it is possible to detect a wide range of brain atrophy at the initial stages of cognitive decline in patients with Parkinson's disease, which has not been reported previously."
As Parkinson's-related mild cognitive impairment (PD-MCI) is increasingly recognized as an important clinical syndrome of possible precursor of Parkinson's dementia, biomarkers with good screening or diagnostic validity can help categorize levels of cognitive impairment, may predict future cognitive decline, and may ultimately help inform treatment decisions.
The neurodegeneration that contributes to cognitive decline seen in Parkinson's, particularly in regions of the brain known to play a role in Alzheimer's disease, such as the hippocampus, is likely due to a "complex interaction of different disease pathologies," the researchers said. Approximately 80 percent of Parkinson's disease patients ultimately develop dementia.
Parkinson's patients with normal cognition showed no atrophy and had similar brain volumes to healthy controls without Parkinson's or cognitive impairment. Therefore, researchers believe that significant brain atrophy in areas subserving cognition does not occur in Parkinson's disease without a comorbid cognitive impairment.
Eighty-four Parkinson's patients from the Penn Parkinson's Disease and Movement Disorders Center and 23 healthy controls received MRIs of the brain. Of the 84 Parkinson's patients, 61 had normal cognition, 12 were classified as having mild cognitive impairment, and 11 were diagnosed with Parkinson's disease dementia.