Addressing the Ethnicity Gap in Catechol O-Methyl Transferase Inhibitor Trials in Parkinson’s Disease: A Review of Available Global Data

Author:

Poplawska-Domaszewicz Karolina12,Limbachiya Naomi23ORCID,Qamar Mubasher23,Batzu Lucia23,Jones Shelley3,Sauerbier Anna24,Rota Silvia23ORCID,Lau Yue Hui5ORCID,Chaudhuri K. Ray23ORCID

Affiliation:

1. Department of Neurology, Poznan University of Medical Sciences, 60-355 Poznan, Poland

2. Basic and Clinical Neuroscience Department, The Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, 5 Cutcombe Road, London SE5 9RX, UK

3. Parkinson’s Foundation Centre of Excellence, King’s College Hospital, Denmark Hill, London SE5 9RS, UK

4. Department of Neurology, University Hospital Cologne, Faculty of Medicine, 50937 Cologne, Germany

5. Division of Neurology, Medical Department, Tengku Ampuan Rahimah Hospital, Klang 41200, Malaysia

Abstract

Catechol-O-methyltransferase inhibitors (COMT-Is) have significantly improved the quality of life and symptom management for those at advanced stages of Parkinson’s Disease (PD). Given that PD is one of the fastest-growing neurodegenerative diseases worldwide, there is a need to establish a clear framework for the systematic distribution of COMT-Is, considering inter-individual and intra-individual variations in patient response. One major barrier to this is the underrepresentation of ethnic minority participants in clinical trials investigating COMT-Is. To investigate this, we performed a narrative review. We searched PubMed for clinical trials investigating COMT-Is in patients with PD and examined the ethnic diversity of cohorts. A total of 63 articles were identified, with 34 trials found to match our inclusion criteria. Among the 34 trials meeting our inclusion criteria, only 8 reported participants’ ethnic backgrounds. Our findings reveal a consistent underrepresentation of ethnic minority groups in trials investigating COMT-Is in PD cohorts—a trend that reflects broader concerns across clinical research. In this review, we explore potential reasons for the underrepresentation of ethnic minorities in clinical trials and propose strategies to address this issue.

Publisher

MDPI AG

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