Tariq Fatima, Ahmad Mehjabeen, Subhan Muhammad, Zaid Alvi Syed Muhammad, Tariq Muhammad Umar, Ullah Sami, Khalid Asma, Bibi Ruqiya, Shafique Ur Rehman Muaz, Abbas Ayesha
Internal Medicine, University of Health Sciences, Lahore, PAK.
Internal Medicine, Nishtar Medical University and Hospital, Multan, PAK.
Cureus. 2024 Nov 17;16(11):e73882. doi: 10.7759/cureus.73882. eCollection 2024 Nov.
Chronic kidney disease (CKD) has shown a growing association with osteoporosis, comprising part of the broader CKD-mineral and bone disorder (CKD-MBD). CKD-MBD is marked by alterations in calcium, phosphorus, parathyroid hormone (PTH), and vitamin D metabolism, significantly elevating fracture risk. While traditional osteoporosis treatments such as bisphosphonates, denosumab, and teriparatide have been adapted for CKD patients, recent innovations have introduced agents aimed at enhancing bone mass and reducing fracture incidence. This study aims to evaluate the pathophysiology, diagnostic methods, and tailored management strategies for osteoporosis in CKD patients. A detailed review of the literature was conducted, involving an in-depth search of PubMed, Medical Literature Analysis and Retrieval System Online (MEDLINE), and the Cochrane Library databases for studies published between 2017 and 2024. Studies were selected based on inclusion criteria focusing on CKD-related osteoporosis, diagnostic criteria, and treatment outcomes. Data extraction and quality assessment were independently performed by multiple reviewers to ensure thoroughness and reduce bias. Findings highlight that conventional treatments, such as bisphosphonates, denosumab, and teriparatide, when tailored to CKD stages, demonstrate variable effectiveness in lowering fracture risk. Additionally, emerging pharmacologic agents hold promise in improving bone density, though evidence on these newer therapies remains limited. Osteoporosis management in CKD patients necessitates a personalized approach guided by the disease's stage and individual profile. This review underscores the potential of emerging therapies and emphasizes the need for further research to refine treatment protocols, aiming to enhance patient outcomes in this complex population.
慢性肾脏病(CKD)与骨质疏松症的关联日益增加,是更广泛的慢性肾脏病-矿物质和骨异常(CKD-MBD)的一部分。CKD-MBD的特征是钙、磷、甲状旁腺激素(PTH)和维生素D代谢改变,显著增加骨折风险。虽然双膦酸盐、地诺单抗和特立帕肽等传统骨质疏松症治疗方法已适用于CKD患者,但最近的创新引入了旨在增加骨量和降低骨折发生率的药物。本研究旨在评估CKD患者骨质疏松症的病理生理学、诊断方法和针对性管理策略。对文献进行了详细综述,深入检索了PubMed、医学文献分析和联机检索系统(MEDLINE)以及Cochrane图书馆数据库,以查找2017年至2024年发表的研究。根据纳入标准选择研究,重点关注与CKD相关的骨质疏松症、诊断标准和治疗结果。由多名评审员独立进行数据提取和质量评估,以确保全面性并减少偏差。研究结果表明,双膦酸盐、地诺单抗和特立帕肽等传统治疗方法,根据CKD分期进行调整后,在降低骨折风险方面显示出不同的效果。此外,新兴药物有望改善骨密度,尽管关于这些新疗法的证据仍然有限。CKD患者的骨质疏松症管理需要根据疾病阶段和个体情况采取个性化方法。本综述强调了新兴疗法的潜力,并强调需要进一步研究以完善治疗方案,旨在改善这一复杂人群的患者预后。