• December 12, 2011
  • More Widespread Brain Atrophy Detected in Parkinson's Disease with Newly Developed Structural Pattern

  • Hippocampal Atrophy Seen with Early Cognitive Decline in Parkinson's Disease

PHILADELPHIA – Atrophy in the hippocampus, the region of the brain known for memory formation and storage, is evident in Parkinson’s disease (PD) patients with cognitive impairment, including early decline known as mild cognitive impairment (MCI), according to a study by researchers in the Perelman School of Medicine at the University of Pennsylvania. 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.

The research team included Dr. Weintraub, Jimit Doshi, MS, Deepthi Koka, MS, Christos Davatzikos, PhD, Andrew Siderowf, MD, MSCE, John Duda, MD, David Wolk, MD, Paul Moberg, PhD, Sharon Xie, PhD, and Christopher Clark, MD, representing the Penn Udall Center for Parkinson’s Research and the Perelman School of Medicine’s departments of Psychiatry, Neurology, Radiology, Biostatistics and Epidemiology. Dr. Weintraub and Dr. Duda are also with Philadelphia Veterans Affairs Medical Center. Dr. Clark is with Avid Radiopharmaceuticals.

The study was funded by grants from the National Institutes of Health’s National Institute of Neurological Disorders and Strokes and National Institute of Aging, as well as a grant awarded by Department of Health of the Commonwealth of Pennsylvania from the Tobacco Master Settlement Agreement.

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Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $4.3 billion enterprise.

The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 17 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $392 million awarded in the 2013 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania -- recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report; Penn Presbyterian Medical Center; Chester County Hospital; Penn Wissahickon Hospice; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Chestnut Hill Hospital and Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2013, Penn Medicine provided $814 million to benefit our community.

 

 

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