Efficacy of the cardiac glycoside digoxin as an adjunct to csDMARDs in rheumatoid arthritis patients: a randomized, double-blind, placebo-controlled trial

BackgroundInflammation and angiogenesis are two main mechanisms that act as mutual pathways in rheumatoid arthritis (RA). This work aimed to study the efficacy of digoxin as an adjunct therapy to conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) in active RA patients.MethodsIn...

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Main Authors: Nageh A. El-Mahdy (Author), Mariam G. Tadros (Author), Thanaa A. El-Masry (Author), Ammena Y. Binsaleh (Author), Nawal Alsubaie (Author), Amani Alrossies (Author), Medhat I. Abd Elhamid (Author), Enas Y. Osman (Author), Hadeel M. Shalaby (Author), Dalia S. Saif (Author)
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Published: Frontiers Media S.A., 2024-10-01T00:00:00Z.
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100 1 0 |a Nageh A. El-Mahdy  |e author 
700 1 0 |a Mariam G. Tadros  |e author 
700 1 0 |a Thanaa A. El-Masry  |e author 
700 1 0 |a Ammena Y. Binsaleh  |e author 
700 1 0 |a Nawal Alsubaie  |e author 
700 1 0 |a Amani Alrossies  |e author 
700 1 0 |a Medhat I. Abd Elhamid  |e author 
700 1 0 |a Enas Y. Osman  |e author 
700 1 0 |a Hadeel M. Shalaby  |e author 
700 1 0 |a Dalia S. Saif  |e author 
245 0 0 |a Efficacy of the cardiac glycoside digoxin as an adjunct to csDMARDs in rheumatoid arthritis patients: a randomized, double-blind, placebo-controlled trial 
260 |b Frontiers Media S.A.,   |c 2024-10-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2024.1445708 
520 |a BackgroundInflammation and angiogenesis are two main mechanisms that act as mutual pathways in rheumatoid arthritis (RA). This work aimed to study the efficacy of digoxin as an adjunct therapy to conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) in active RA patients.MethodsIn a randomized, double-blinded, placebo-controlled study, 60 adult patients with active RA received a placebo or digoxin (0.25 mg every other day) combined with csDMARDs for 6 months. The American College of Rheumatology (ACR) 20, ACR50, and ACR70 response rates and the disease activity score (DAS28) were assessed for patients. Flow cytometric analysis of Th17 cells and serum concentrations of IL-17A, IL-23, HIF-1α, and VEGF were evaluated before and after three and 6 months of therapy.ResultsFollowing three and 6 months of digoxin therapy combined with csDMARDs, significant differences were detected in laboratory and clinical parameters relative to the control group. After 6 months, 83.3% of patients in the digoxin group, compared to 56.7% in the control group, achieved an ACR20 response (p = 0.024). The digoxin group had a significantly higher percentage of patients who achieved DAS28 remission after 6 months (p = 0.024). Notable improvements in the Health Assessment Questionnaire Disability Index, ACR50, and ACR70 were detected in the digoxin group.ConclusionDigoxin was well tolerated and exerted profound immunomodulatory and anti-inflammatory effects in RA patients, and may also exhibit anti-angiogenic properties, indicating that it might be an effective adjunct to csDMARDs in treating RA.Clinical Trial Registrationclinicaltrials.gov, identifier NCT04834557. 
546 |a EN 
690 |a rheumatoid arthritis 
690 |a digoxin 
690 |a inflammatory markers 
690 |a angiogenesis 
690 |a ACR 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 15 (2024) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2024.1445708/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/1ec5a91c2c8f4c4ab7cd9d7630ee5eb7  |z Connect to this object online.