Cited by 151Parkinson's Disease Mechanisms and TreatmentsInflammatory Bowel DiseaseGut microbiota and health

Inflammatory bowel disease and Parkinson’s disease: common pathophysiological links

Open access
Lee, Ho-Su, Lobbestael, Evy, Vermeire, Séverine, Sabino, João, Cleynen, Isabelle·2021·Gut

Abstract

Inflammatory bowel disease and Parkinson’s disease are chronic progressive disorders that mainly affect different organs: the gut and brain, respectively. Accumulating evidence has suggested a bidirectional link between gastrointestinal inflammation and neurodegeneration, in accordance with the concept of the ‘gut–brain axis’. Moreover, recent population-based studies have shown that inflammatory bowel disease might increase the risk of Parkinson's disease. Although the precise mechanisms underlying gut–brain interactions remain elusive, some of the latest findings have begun to explain the link. Several genetic loci are shared between both disorders with a similar direction of effect on the risk of both diseases. The most interesting example is LRRK2 (leucine-rich repeat kinase 2), initially identified as a causal gene in Parkinson's disease, and recently also implicated in Crohn’s disease. In this review, we highlight recent findings on the link between these seemingly unrelated diseases with shared genetic susceptibility. We discuss supporting and conflicting data obtained from epidemiological and genetic studies along with remaining questions and concerns. In addition, we discuss possible biological links including the gut–brain axis, microbiota, autoimmunity, mitochondrial function and autophagy.

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Crossref · 10.1136/gutjnl-2020-322429

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  • Anti-tumor necrosis factor treatments that decrease gastrointestinal inflammation and improve intestinal permeability dysfunction can reduce the risk of developing PD.

    “while anti-tumor necrosis factor treatments that decrease gastrointestinal inflammation and improve intestinal permeability dysfunction can reduce the risk of developing PD [27].”

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References 100 · Cited by 151

Authors
Lee, H.-S., Lobbestael, E., Vermeire, S., Sabino, J., & Cleynen, I.
Affiliations
  • University of Ulsan (KR)
  • KU Leuven (BE)
  • Universitair Ziekenhuis Leuven (BE)
Corresponding author
Cleynen, Isabelle
Venue
Gut
Publisher
BMJ
Published
2020-10-16
Volume
70
Issue
2
Pages
408-417
ISSN
  • 0017-5749 (ISSN-L)
  • 1468-3288
OpenAlex
W3093257229
Cited by
151
References
100
Citations by year
2026: 10 · 2025: 25 · 2024: 24 · 2023: 32 · 2022: 38 · 2021: 20 · 2020: 1
FWCI
2.55
Type
journal article
Language
en
Open access
Licence
other-oa
Locations
  • Gut (publishedVersion)
  • PubMed (publishedVersion)
  • Lirias (submittedVersion, other-oa)
Funders
  • Michael J. Fox Foundation for Parkinson's Research (17194)
  • National Research Foundation of Korea (NRF) MRC grant funded by the Korean government (2018R1A5A2020732)
  • Research Foundation Flanders (G0E1917N)
Topics
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Keywords
inflammatory bowel disease, Parkinson's disease, gut-brain axis, Crohn's disease, LRRK2, shared genetic risk, microbiota, autoimmunity, mitochondrial function, autophagy, neurodegeneration, gastrointestinal inflammation, disease risk
MeSH terms
Gastrointestinal Microbiome, Humans, Parkinson Disease, Risk Factors, Inflammatory Bowel Diseases, Genetic Predisposition to Disease

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