Inflammatory Bowel Disease Appears to Impact Risk of Parkinson's Disease

14 November 2019

Patients with inflammatory bowel disease are more likely to get Parkinson's disease, reports JPD, however, the risk is very small

Amsterdam, NL – Relatively new research findings indicating that the earliest stages of Parkinson's disease (PD) may occur in the gut have been gaining traction in recent years. In a review published in the Journal of Parkinson's Disease, Tomasz Brudek, PhD, evaluates evidence for the association between inflammatory bowel disease (IBD) and PD and proposes directions for future research.

"Parkinsonism is probably not just a brain disorder, but a group of diseases that may have their onset in the periphery, particularly in the gastrointestinal tract," explained Dr. Brudek, of the Research Laboratory for Stereology and Neuroscience, and Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg, and Frederiksberg Hospital, Copenhagen, Denmark. “Taken together, all data, including human, animal, and microbiome studies, suggest quite strongly that individuals with an increased tendency for peripheral inflammation have a higher risk to acquire PD. Given the potentially critical role of gut pathology in the pathogenesis of PD, there is reason to suspect that IBD may impact PD risk."

This review explores and discusses the latest knowledge about links between IBD and PD and presents evidence from animal studies that peripheral immune system alterations may play a role in PD, which has the potential for new therapeutic strategies. It shows how our understanding and appreciation of the importance of the so-called gut-brain axis, the connection between gut and the brain in PD, has grown rapidly in recent years. It also provides important new insights into ways in which the immune system and inflammation can play a role in PD.

The inflammatory processes that occur in some patients with PD have naturally led to discussion of an association between IBD and PD since the two share some basic characteristics. IBD is currently considered an inappropriate immune response to the microbiota in the intestines, characterized by chronic pro-inflammatory immune activity, a trait now also suggested to be a fundamental element of neurodegenerative disorders. Highlighting the relevance of the immune system, large genome-wide association studies (GWAS) and pathway analyses based on 138,511 individuals of European ancestry identified 17 shared loci between PD and seven autoimmune diseases including celiac disease, rheumatoid arthritis, type 1 diabetes, multiple sclerosis, psoriasis, ulcerative colitis and Crohn's disease.

Many epidemiological and genetic studies have found that there seems to be an increased risk of developing PD among people with IBD. The association between IBD and PD may simply be that IBD is just one type of intestinal inflammation, so it is not IBD specifically that increases the PD risk but perhaps intestinal or peripheral inflammation in a broader sense.

"Inflammation of the gut is only one of many symptoms on the list of changes in the gut and is associated with neural structures in PD patients. Thus, IBD might be just one of many sources of intestinal inflammation," said Dr. Brudek, who is quick to point out that, "while IBD patients are more likely to get PD, the risk is still very small. For a given IBD patient, the probability of not getting the diagnosis is 95%–97%."

Looking forward, Dr Brudek noted that:

• Identification of risk factors associated with prodromal phases of PD may allow for early intervention studies that could modify or slow down disease progress.
• More biomarker and observational studies are needed to identify patients at risk to develop PD in order to start early therapy interventions.
• Future pharmacological therapies aiming at slowing or stopping PD progression should not only target patients well into the course of the disease, but also be administered to patients in the very early phases of the disease or at risk for developing PD.
• Clinicians should be aware of early Parkinsonian symptoms in IBD patients but also in patients with chronic inflammatory disorders.

"We should direct our focus on the immune system in all Parkinsonian disorders, and further investigate the role of systemic inflammation and the immune system as such in these neurological diseases. A clear knowledge of the mechanisms implicated in gut/immune/nervous communication could help improve the prognostic and therapeutic tools leading to better quality of life for patients, reducing the exacerbation of PD symptoms, and delaying the progression of the disease," he concluded.

PD is a slowly progressive disorder that affects movement, muscle control and balance. It is the second most common age-related neurodegenerative disorder affecting about 3% of the population by the age of 65 and up to 5% of individuals over 85 years of age. During the 20th century, PD was thought to be primarily a brain disorder, however, research has shown that it may actually begin in the enteric nervous system, the part of the autonomic nervous system that controls the gastrointestinal organs.


Full open access study: "Inflammatory Bowel Diseases and Parkinson's Disease" by Tomasz Brudek, PhD (DOI: 10.3233/JPD-191729). The article is published in the Journal of Parkinson's Disease, Volume 9, Supplement 2 entitled "The Gut-Brain Axis in Parkinson's Disease Revisited," Guest Editor Teus van Laar, MD, PhD, Director, Parkinson Expertise Center Groningen, Department of Neurology, University Medical Center Groningen, University of Groningen, The Netherlands. It is openly available at:

The paper was supported by The Parkinson Association Denmark (Parkinsonforeningen), Aage og Johanne Louis-Hansens Foundation, The MSA Coalition Research Grant, Landsforeningen Multipel System Atrofi, Bjarne Saxofs Foundation, Toyota-Fonden, Civilingeniør Frode V. Nyegaard og Hustru's Fond, Grosserer L. F. Foghts Fond, and Tømmerhandler Vilhelm Bangs Fond.

For additional information and requests for interviews, contact Diana Murray, IOS Press (+1 718 640-5678 or To reach the authors, contact Tomasz Brudek (+45 3863 5600 or

About this Supplement to JPD: The Gut-Brain Axis in Parkinson's Disease
This special supplement to the Journal of Parkinson's Disease reveals the enormous complexity of the gut-brain axis and demonstrates that there are still unanswered questions. Does PD start in the gut in all patients, or is this potential trigger site relevant only in a small subgroup of patients? What is the role of constipation, and what distinguishes those patients who are not constipated in terms of underlying disease mechanisms? What is the effect of constipation on the microbiome? Does constipation lead to a different subtype of PD? The supplement explores a variety of topics and hopefully will contribute to an improved understanding of the role of the gut in PD, and ultimately stimulate the development of new therapies that improve the lives of patients with PD. This supplement to is openly available at or via the short link

About Journal of Parkinson's Disease
Launched in 2011, the Journal of Parkinson's Disease (JPD) is dedicated to providing an open forum for original research in basic science, translational research and clinical medicine that will expedite our fundamental understanding and improve treatment of Parkinson’s disease. The journal is international and multidisciplinary and aims to promote progress in the epidemiology, etiology, genetics, molecular correlates, pathogenesis, pharmacology, psychology, diagnosis and treatment of Parkinson's disease. JPD publishes research reports, reviews, short communications, and letters-to-the-editor and offers very rapid publication and an affordable open access option.

About IOS Press
IOS Press is headquartered in Amsterdam with satellite offices in the USA, Germany, India and China and serves the information needs of scientific and medical communities worldwide. IOS Press now publishes more than 80 international journals and about 75 book titles each year on subjects ranging from computer science, artificial intelligence, and engineering to medicine, neuroscience, and cancer research.