Like many neurodegenerative diseases, Parkinson’s disease (PD) is a thief that hacks into human operating systems and corrupts their cognitive hard drives until they can no longer control their movements or perform activities of daily living. Often, in its later stages, Parkinson’s disease steals data too, leading to memory loss, confusion and dementia.
Both the cause and cure of Parkinson’s disease remain elusive, but research has helped afflicted individuals manage their symptoms and lead healthier post-diagnosis lives. Individuals diagnosed with Parkinson’s disease tend to have higher education than the general population and are often in their prime earning years, and the reasons for these two quirks are not well understood.
A recent study led by an MUSC neuropsychologist will help researchers in the field better evaluate whether their clinical trials are producing valuable outcomes in reducing the symptoms of individuals with PD.
Along with a team of collaborators, Travis Turner, PhD, assistant professor and director of the Neuropsychology Division at MUSC, dug deep into an existing trove of data to clarify the cognitive impact of the early stages of PD. What he found initially seemed counter-intuitive and challenges the notion of cognitive deficits in individuals experiencing PD for less than five years.
Turner and his colleagues determined that the disease generally does not reduce cognitive function during the first five years of the disease, at least not as measured by standardized tests on patients. This finding applies as well to those who were already experiencing mild cognitive impairment.
Specifically, Turner’s team examined cognitive test results from the Parkinson’s Progression Markers Initiative (PPMI) on nearly 400 individuals, including 253 newly diagnosed PD patients and 134 healthy controls. Within the cohort, 84 of the individuals were identified as having pre-existing mild cognitive impairment. PPMI conducted a battery of tests on memory, visuospatial functions, processing speed, working memory and verbal fluency.
Parkinson’s disease patients performed normally on all but two tests, a measure of working memory and a processing speed test. Further examination of the results determined that the latter difference was entirely a function of motor decline: PD patients could not physically respond as quickly because of motor symptoms like tremor and rigidity. Employing a test to account for that variable eliminated the difference between PD patients and the control group.
For the memory test, individuals with PD experienced a mild dip, perhaps the source of what some who are diagnosed describe as brain fog. “Mild means some degree of subjective decline with more complicated tasks: doing bills, taxes, personal scheduling, non-routine work,” said Turner. The difference, he says, would not generally be noticeable by anyone but the individual.
The results were contrary to the team’s expectations, particularly with regard to PD patients who were already experiencing mild impairment, Turner said. The data suggested that even those already affected suffered little-to-no further cognitive decline during the first five years after diagnosis.
Another surprise: that no other researchers had mined the repository of information and analyzed the results previously.
“Early cognitive decline is commonly reported by PD patients. There have been a lot of neuro-protective trials that look at non-motor symptoms like anxiety, depression and cognition, but no one had looked at this robust data set before,” he said.
Previous tests on Parkinson’s disease patients have produced a variety of results, some even somewhat contradictory according to Turner, but they lacked the controls or the sample size that his study included.
