Related Subjects:
| Osteoporosis
β οΈ Important: Use strontium ranelate only under specialist supervision.
There are significant cardiovascular and thrombotic risks β prescribe only when other osteoporosis treatments (e.g. bisphosphonates, denosumab, teriparatide) are contraindicated or not tolerated.
π§ About
- Strontium ranelate is a unique agent with dual action on bone: it both increases bone formation and decreases bone resorption.
- Its use in the UK is now highly restricted following MHRA and EMA safety warnings (2013β2014) due to increased cardiovascular risk.
- Therapy should be initiated only by a physician experienced in managing osteoporosis and with regular review of cardiovascular status (every 6β12 months).
- Should be used as part of a comprehensive plan that includes lifestyle measures, calcium, and vitamin D supplementation.
βοΈ Mode of Action
- Strontium (atomic number 38) is chemically similar to calcium and can be incorporated into the bone matrix.
- Stimulates osteoblast replication and collagen synthesis while simultaneously reducing osteoclast differentiation and activity.
- This βrebalancingβ effect leads to an increase in bone formation markers and bone mineral density.
- Unlike bisphosphonates, it does not inhibit the mevalonate pathway; instead, it exerts effects via calcium-sensing receptors and osteoprotegerin modulation.
π― Indications
- Treatment of severe postmenopausal osteoporosis in women and osteoporosis in men at high risk of fracture β only when other approved treatments are unsuitable.
- Prescribers must:
- Assess cardiovascular risk before starting.
- Monitor blood pressure and cardiovascular health every 6β12 months.
- Discontinue immediately if the patient develops ischaemic heart disease, peripheral arterial disease, cerebrovascular disease, or uncontrolled hypertension.
π Dose
| Name |
Starting Dose |
Frequency |
Route |
| Strontium ranelate |
2 g sachet dissolved in water |
Once daily at bedtime (nocte) |
Oral |
β οΈ Administration Advice
- Take at bedtime, preferably at least 2 hours after food or milk.
- Food, milk, and calcium supplements markedly reduce absorption β separate dosing by β₯2 hours.
- Do not take with aluminium or magnesium antacids; if needed, wait 2 hours after taking strontium.
- Ensure adequate vitamin D and calcium intake during treatment.
π« Contraindications
- Current or previous venous thromboembolism (VTE) β including DVT or pulmonary embolism.
- History of ischaemic heart disease, peripheral arterial disease, or cerebrovascular disease.
- Uncontrolled hypertension.
- Temporary or permanent immobilisation (e.g. post-surgery, prolonged bed rest).
- Hypersensitivity to strontium or excipients.
β οΈ Cautions
- Perform a baseline cardiovascular assessment before treatment.
- Reassess benefitβrisk balance at each follow-up visit.
- Advise patient to report chest pain, dyspnoea, or leg swelling immediately (possible VTE or cardiac event).
- Use caution in renal impairment; avoid if eGFR < 30 mL/min.
- Monitor for dermatological reactions such as rash or eczema.
π₯ Side Effects
- Common: Nausea, diarrhoea, headache, dermatitis, eczema, peripheral oedema.
- Cardiovascular: Increased risk of venous thromboembolism and myocardial infarction.
- Allergic reactions: DRESS (Drug Reaction with Eosinophilia and Systemic Symptoms) β rare but potentially life-threatening.
- Gastrointestinal: Reflux, abdominal pain, dyspepsia, vomiting, flatulence, constipation, stomatitis.
- Haematological: Rare bone marrow suppression or cytopenias.
π‘ Teaching Tip
- Strontium ranelate represents a βdual-action bone agentβ β both anabolic and antiresorptive β but its clinical value is now overshadowed by safety concerns.
- Explain to learners that while it increases BMD, strontium atoms are heavier than calcium, potentially artificially inflating DEXA readings.
- Mnemonic: βSTRONG but STRONtium risksβ β effective for bones, risky for the heart.
π References
- BNF: Strontium Ranelate
- MHRA Drug Safety Update (2014): Cardiovascular risk with strontium ranelate (Protelos/Osseor)
- European Medicines Agency: PRAC recommendations, 2014
- NICE NG226: Osteoporosis: assessment and management (2023)