Individual participant data meta-analysis of metabolomics on sustained knee pain in primary osteoarthritis patients

Author:

Costello Christie A1ORCID,Rockel Jason S23,Liu Ming1,Gandhi Rajiv23,Perruccio Anthony V2345,Rampersaud Y Raja23,Mahomed Nizar N23,Rahman Proton6,Randell Edward W7,Furey Andrew89,Kapoor Mohit2310,Zhai Guangju1

Affiliation:

1. Division of Biomedical Sciences (Genetics), Faculty of Medicine, Memorial University of Newfoundland , St John’s, NL, Canada

2. Osteoarthritis Research Program, Division of Orthopedics, Schroeder Arthritis Institute, University, Health Network , Toronto, ON, Canada

3. Krembil Research Institute, University Health Network , Toronto, ON, Canada

4. Institute for Health Policy, Management & Evaluation, Dalla Lana School of Public Health, University of Toronto , Toronto, ON, Canada

5. Department of Surgery, Faculty of Medicine, University of Toronto , Toronto, ON, Canada

6. Discipline of Medicine, Faculty of Medicine, Memorial University of Newfoundland , St. John’s, NL, Canada

7. Discipline of Laboratory Medicine, Faculty of Medicine, Memorial University of Newfoundland , St. John’s, NL, Canada

8. Division of Orthopaedics, Faculty of Medicine, Memorial University of Newfoundland , St John’s, NL, Canada

9. Office of the Premier, Province of Newfoundland & Labrador , St. John’s, NL, Canada

10. Department of Laboratory Medicine and Pathobiology, University of Toronto , Toronto, ON, Canada

Abstract

Abstract Objectives Knee pain is the major driver for OA patients to seek healthcare, but after pursuing both conservative and surgical pain interventions, ∼20% of patients continue to report long-term pain following total knee arthroplasty (TKA). This study aimed to identify a metabolomic signature for sustained knee pain after TKA to elucidate possible underlying mechanisms. Methods Two independent cohorts from St John’s, NL, Canada (n = 430), and Toronto, ON, Canada (n = 495) were included in the study. Sustained knee pain was assessed using the WOMAC pain subscale (five questions) at least 1 year after TKA for primary OA. Those reporting any pain on all five questions were considered to have sustained knee pain. Metabolomic profiling was performed on fasted pre-operative plasma samples using the Biocrates Absolute IDQ p180 kit. Associations between metabolites and pair-wise metabolite ratios with sustained knee pain in each individual cohort were assessed using logistic regression with adjustment for age, sex and BMI. Random-effects meta-analysis using inverse variance as weights was performed on summary statistics from both cohorts. Results One metabolite, phosphatidylcholine (PC) diacyl (aa) C28:1 (odds ratio = 0.66, P = 0.00026), and three metabolite ratios, PC aa C32:0 to PC aa C28:1, PC aa C28:1 to PC aa C32:0, and tetradecadienylcarnitine (C14:2) to sphingomyelin C20:2 (odds ratios = 1.59, 0.60 and 1.59, respectively; all P < 2 × 10−5), were significantly associated with sustained knee pain. Conclusions Though further investigations are needed, our results provide potential predictive biomarkers and drug targets that could serve as a marker for poor response and be modified pre-operatively to improve knee pain and surgical response to TKA.

Funder

Canadian Institutes of Health Research

The Research and Development Corporation of Newfoundland and Labrador

The Memorial University of Newfoundland Medical Research Fund

Tony and Shari Fell Platinum Chair in Arthritis Research

Canada Research Chairs

Schroeder Arthritis Institute

University Health Network

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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