Neridronate
Neridronate is a bisphosphonate used in the treatment of various bone diseases, including Paget's disease of bone, osteogenesis imperfecta, and bone pain associated with metastatic bone disease. It works by inhibiting osteoclast-mediated bone resorption, leading to an overall increase in bone density and a reduction in bone pain and fractures.
Mechanism of Action[edit | edit source]
Neridronate binds to hydroxyapatite crystals in the bone and inhibits the activity of osteoclasts, the cells responsible for bone resorption. By reducing the resorption of bone, neridronate helps to rebalance bone turnover in favor of bone formation, leading to an increase in bone mineral density and a reduction in the risk of fractures.
Indications[edit | edit source]
Neridronate is indicated for the treatment of:
- Paget's disease of bone, a condition characterized by the abnormal breakdown and formation of bone tissue.
- Osteogenesis imperfecta, a genetic bone disorder known for causing bones to break easily.
- Bone pain associated with metastatic bone disease.
Administration[edit | edit source]
Neridronate can be administered both intravenously and orally, depending on the specific needs and conditions of the patient. The dosage and frequency of administration vary based on the indication and the patient's response to treatment.
Side Effects[edit | edit source]
Common side effects of neridronate include:
- Flu-like symptoms, such as fever, chills, and muscle aches.
- Gastrointestinal disturbances, including nausea and abdominal pain.
- Hypocalcemia, a condition characterized by low levels of calcium in the blood.
Patients are advised to ensure adequate calcium and vitamin D intake during treatment with neridronate to mitigate the risk of hypocalcemia.
Contraindications[edit | edit source]
Neridronate is contraindicated in patients with:
- Hypersensitivity to neridronate or any component of the formulation.
- Severe renal impairment, due to the risk of accumulation and potential toxicity.
Pharmacokinetics[edit | edit source]
Neridronate is well absorbed when administered intravenously, with a bioavailability that decreases with oral administration. It has a strong affinity for bone tissue and a long half-life, reflecting its prolonged action in inhibiting bone resorption.
Clinical Trials[edit | edit source]
Clinical trials have demonstrated the efficacy of neridronate in increasing bone mineral density and reducing bone pain in patients with Paget's disease of bone, osteogenesis imperfecta, and metastatic bone disease. Ongoing research continues to explore the potential applications of neridronate in other bone-related conditions.
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Contributors: Prab R. Tumpati, MD