Related Experiment Video
Updated: Mar 8, 2026

Author Spotlight: Fu's Subcutaneous Needling for Knee Osteoarthritis Pain
Published on: March 24, 2023
Strontium ranelate, a promising disease modifying osteoarthritis drug
Weiyu Han1,2,3, Shicai Fan1,2, Xiaochun Bai1,2
1a Department of Orthopaedics , 3rd Affiliated Hospital of Southern Medical University , Guangzhou , China.
Introduction:
The articular cartilage and subchondral bone may have potential crosstalk in the development and progression of osteoarthritis (OA). Strontium ranelate (SrR) has the ability to dissociate the bone remodeling process and to change the balance between bone resorption and bone formation. Its effect on subchondral bone makes it a potential disease- modifying osteoarthritis drug (DMOAD) in the treatment of OA. The aim of the current review is to summarize up-to-date pharmacological and clinical data of SrR for OA treatment. Areas covered: A literature search was performed on PubMed and European Medicines Agency (EMA) website for all publications and documents related to SrR and OA. References of related studies were searched by hand. Treatment with SrR, especially at the dosage of 2 g/day, was associated with reduced radiographic knee OA progression, and with meaningful clinical improvement. It was also significantly associated with decreased MRI-assessed cartilage volume loss (CVL) and bone marrow lesions (BMLs). Expert opinion: SrR could be a promising DMOAD particularly for OA patients with bone phenotypes. The clinical efficacy and side effects of SrR for OA treatment need to be further investigated in future clinical trials before clinical application.
Insights
Strontium ranelate (SrR) shows promise as a disease-modifying osteoarthritis drug (DMOAD), reducing knee osteoarthritis progression and improving clinical symptoms. Further trials are needed to confirm its efficacy and safety for OA patients.
Area of Science:
- Pharmacology
- Orthopedics
- Rheumatology
Background:
- Osteoarthritis (OA) involves crosstalk between articular cartilage and subchondral bone.
- Strontium ranelate (SrR) modulates bone remodeling, potentially impacting OA.
- SrR's effect on subchondral bone suggests it as a candidate disease-modifying osteoarthritis drug (DMOAD).
Purpose of the Study:
- To review current pharmacological and clinical data on Strontium ranelate (SrR) for osteoarthritis (OA) treatment.
- To evaluate SrR's potential as a DMOAD.
Main Methods:
- Literature search of PubMed and European Medicines Agency (EMA) databases.
- Hand-searching references of relevant studies.
- Review of pharmacological and clinical trial data.
Main Results:
- SrR treatment (2 g/day) associated with reduced radiographic knee OA progression.
- Meaningful clinical improvement observed with SrR treatment.
- Significant reduction in MRI-assessed cartilage volume loss (CVL) and bone marrow lesions (BMLs).
Conclusions:
- SrR demonstrates potential as a DMOAD, especially for OA patients with bone phenotypes.
- Further clinical trials are necessary to validate SrR's efficacy and safety for OA treatment before widespread application.
More Related Videos
08:53Drug Treatment and In Vivo Imaging of Osteoblast-Osteoclast Interactions in a Medaka Fish Osteoporosis Model
Published on: January 1, 2017
14:49Clinical Protocol of Producing Adipose Tissue-Derived Stromal Vascular Fraction for Potential Cartilage Regeneration
Published on: September 29, 2018
Related Concept Videos
Rheumatic Heart Disease III: Medical Management
Rheumatic Heart Disease IV: Nursing Management
Restless Leg Syndrome and Night Terrors
The exact cause of RLS is not fully understood, but it is believed to involve dopamine, a neurotransmitter that helps regulate muscle movement. Imbalances in dopamine levels...
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Cardiomyopathy IV: Restrictive Cardiomyopathy
Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin
The binding of dantrolene to the RYR1...