Summary: Study finds evidence of inflammation in the blood of patients during the early stages of Parkinson’s disease. The findings support the theory that inflammation is a driver of the neurodegenerative disorder. The effect was most noticeable in women with Parkinson’s.
New research shows evidence of inflammation in the blood of Parkinson’s disease patients during the earliest stages of the disease, lending support to theories that inflammation is a major driver of PD.
The findings, from researchers at the Alabama Udall Center at the University of Alabama at Birmingham, were published April 13 in npj Parkinson’s Disease, part of the Nature Partner Journal series in partnership with the Parkinson’s Foundation.
UAB is one of six National Institutes of Health-funded Morris K. Udall Centers of Excellence in Parkinson’s Disease Research.
“There is a growing body of evidence suggesting that inflammation plays a major role in the development and progression of Parkinson’s disease,” said David Standaert, M.D., Ph.D., chair of the UAB Department of Neurology in the School of Medicine and senior author of the study. “This is one of the first studies to pinpoint inflammation in the blood in patients with early PD, supporting the idea that systemic immune system activation is present early in PD.”
Standaert also says the study revealed interesting differences in the inflammation signature in women compared to men. While PD is much more common in men, there is increasing evidence that there are also other differences between the sexes in the symptoms and course of the disease. The findings bolster the idea that different approaches to treatment are needed based on the sex of the patient.
The study enrolled 34 patients, 21 males and 13 females. Eighteen had early Parkinson’s disease and 16 were healthy age-matched controls. Those with PD were within two years of symptom onset and had not begun taking anti-Parkinsonian medications.
“The majority of studies into the role of inflammation in PD have been conducted in patients with long-standing disease and wide variations in disease severity. Most had also received a number of different treatments for the disease,” said first author Samantha Carlisle, Ph.D., with the UAB Center for Clinical and Translational Science.
“We looked at newly diagnosed patients to improve our understanding of whether inflammation is present early on, or develops as the disease progresses.”
The study examined blood monocytes, cells that are derived from bone marrow, which have been linked to the development of PD. They appear to have a central role in immune signaling through engulfing, processing and presenting foreign antigens for recognition by the adaptive arm of the immune system, thus turning on the immune system in the presence of PD.
The research team used molecular approaches to examine the state of activation of peripheral blood monocytes in human PD. They found evidence of inflammation in blood monocytes, with an unexpectedly strong effect in women.
“We found that there was a striking effect of sex on monocyte gene expression, with increased inflammatory activation of monocytes in females with PD,” said Hongwei Qin, Ph.D., associate professor in the UAB Department of Cell, Integrated and Developmental Biology.
“In males, the activation patterns were more diverse. This indicates the importance of systemic monocyte activation in PD, and the importance of studies which examine how men and women respond in different ways to the disease.”
The Parkinson’s Foundation estimates there are nearly one million people living with Parkinson’s disease in the United States and more than 10 million worldwide. Men are 1.5 times more likely to have PD than women.
“In addition to the greater frequency of PD in men, there are other differences between men and women, in frequency of tremor and imbalance, response to medications and cognitive features,” Standaert said.
“Identification of an inflammatory signature in the blood of PD patients opens the door to novel approaches to both biomarkers and treatment as well as an increased understanding that therapies for PD need to be tailored to the patient.”
Standaert says the study of inflammation in Parkinson’s disease is a major focus of the Alabama Udall Center.
Additional co-authors are R. Curtis Hendrickson, Richard E. Kennedy, Ph.D., Zhaoqi Yan, Talene A. Yacoubian, M.D., Etty N. Benveniste, Ph.D., and Ashley Harms, Ph.D., Alabama Udall Center: Jordana E. Muwanguzi, and Elliot J. Lefkowitz,, Ph.D., UAB CCTS; Andrew B. West, Ph.D., Duke University.
Funding: Supported by the Alabama Morris K. Udall Center of Excellence in Parkinson Disease Research (P50NS108675), NIH grant P20NS092530, and by the UAB Center for Clinical and Translational Science Grant Number UL1TR003096 from the National Center for Advancing Translational Sciences.
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Source: UAB Contact: Bob Shepard – UAB Image: The image is credited to UAB
Sex-based differences in the activation of peripheral blood monocytes in early Parkinson disease
Increasing evidence supports the role of brain and systemic inflammation in the etiology of Parkinson disease (PD). We used gene expression profiling to examine the activation state of peripheral blood monocytes in 18 patients with early, untreated PD and 16 healthy control (HC) subjects.
Monocytes were isolated by negative selection, and gene expression studied by RNA-seq and gene set enrichment analysis.
A computational model that incorporated case/control status, sex, and the interaction between case/control status and sex was utilized.
We found that there was a striking effect of sex on monocyte gene expression. There was inflammatory activation of monocytes in females with PD, with enrichment of gene sets associated with interferon gamma stimulation. In males, the activation patterns were more heterogeneous.
These data point to the importance of systemic monocyte activation in PD, and the importance of studies which examine the differential effects of sex on pathophysiology of the disease.