L-carnitine as a novel approach for pain and inflammation relief in rheumatoid arthritis

Abdallah A Eldisouky1, Sahar K Hegazy2, Salwa Elmorsy Abd Elghany3

  • 1Department of Clinical Pharmacy, Faculty of Pharmacy, Tanta University, Tanta, 315272, Egypt. abdallahaboelazm605@gmail.com.

Inflammopharmacology
|October 2, 2025
PubMed

Insights

L-carnitine supplementation improved rheumatoid arthritis (RA) symptoms and reduced inflammation markers in patients. Further research is needed to clarify its effects on specific molecular pathways like STAT3 and TGF-β1.

Area of Science:

  • Immunology
  • Rheumatology
  • Pharmacology

Background:

  • Rheumatoid arthritis (RA) is a chronic autoimmune disease causing joint inflammation.
  • The Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway and transforming growth factor-beta1 (TGF-β1) are implicated in RA pathogenesis.
  • L-carnitine's potential as an adjunct therapy targeting these pathways in RA requires investigation.

Purpose of the Study:

  • To evaluate the efficacy and safety of L-carnitine as an add-on therapy for rheumatoid arthritis.
  • To assess L-carnitine's impact on clinical symptoms, disease activity, and inflammatory markers.
  • To explore potential modulation of the JAK/STAT pathway and TGF-β1 by L-carnitine in RA patients.

Main Methods:

  • A 12-week randomized controlled trial involving 46 active RA patients.
  • Patients received either standard disease-modifying antirheumatic drugs (DMARDs) or DMARDs plus L-carnitine (1000 mg/day).
  • Evaluations included clinical assessments (TJC, SJC, VAS, morning stiffness, DAS28, MHAQ) and laboratory markers (CRP, STAT3, TGF-β1) at baseline and 12 weeks.

Main Results:

  • The L-carnitine group demonstrated significant improvements in morning stiffness, pain (VAS), joint counts (TJC, SJC), CRP, DAS28, and MHAQ compared to baseline.
  • While STAT3 levels increased in the control group, no significant changes were observed in STAT3 or TGF-β1 within the L-carnitine group.
  • No significant within-group changes in STAT3 or TGF-β1 were noted for the L-carnitine group.

Conclusions:

  • L-carnitine as an adjunct to DMARDs may improve clinical outcomes and reduce systemic inflammation in RA patients.
  • The precise mechanisms by which L-carnitine affects RA, particularly its influence on STAT3 and TGF-β1, require further elucidation.
  • L-carnitine shows promise as a supportive therapy for managing rheumatoid arthritis symptoms.