Fracture Risk in Chronic Kidney Disease: Addressing an Overlooked Complication.

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metabolites Pub Date : 2025-07-07 DOI:10.3390/metabo15070460
Guido Gembillo, Concetto Sessa, Walter Morale, Luca Zanoli, Antonino Catalano, Salvatore Silipigni, Luca Soraci, Andrea Corsonello, Maria Princiotto, Carlo Lomonte, Domenico Santoro
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引用次数: 0

Abstract

Fracture risk is a serious yet underrecognized complication among patients with chronic kidney disease (CKD), especially in those with stages G3-G5D. The overlap between CKD-Mineral and Bone Disorder (CKD-MBD) and osteoporosis leads to complex bone changes that increase the likelihood of fragility fractures. Studies show that 18% to 32% of CKD patients also have osteoporosis, and these individuals are more than 2.5 times as likely to suffer from fractures compared to those without CKD. In the advanced stages of the disease, fracture risk is up to four times higher than in the general population, with the femur, forearm, and humerus being the most commonly affected sites. Hip fractures are of particular concern as they are linked to longer hospital stays and higher rates of morbidity and mortality. Furthermore, dialysis patients who experience hip fractures have a mortality rate 2.4 times higher than those in the general population with similar fractures. This increased risk underscores the need for proactive bone health maintenance in CKD patients to prevent fractures and related complications. This review explores the underlying pathophysiological mechanisms, diagnostic challenges, and treatment options related to bone fragility in CKD. Diagnostic tools, such as bone mineral density (BMD) assessments, the trabecular bone score (TBS), and biochemical markers, remain underused, especially in advanced CKD stages. Recent treatment strategies emphasize a multidisciplinary, stage-specific approach, incorporating calcium and vitamin D supplements, anti-resorptive agents like denosumab, and anabolic therapies such as teriparatide and romosozumab. Effective management needs to be tailored to the patient's bone turnover status and stage of CKD. Despite progress in understanding bone fragility in CKD, significant gaps remain in both diagnosis and treatment. Personalized care, guided by updated KDIGO recommendations and based on an interdisciplinary approach, is essential to reduce fracture risk and improve outcomes in this vulnerable population. Further research is needed to validate risk assessment tools and refine therapeutic protocols.

慢性肾脏疾病的骨折风险:解决一个被忽视的并发症。
骨折风险是慢性肾脏疾病(CKD)患者中一种严重但未被充分认识的并发症,特别是在G3-G5D期患者中。ckd -矿物质和骨骼疾病(CKD-MBD)和骨质疏松症之间的重叠导致复杂的骨骼变化,增加脆性骨折的可能性。研究表明,18%至32%的CKD患者同时患有骨质疏松症,这些患者发生骨折的可能性是无CKD患者的2.5倍以上。在疾病的晚期,骨折的风险是一般人群的四倍,股骨、前臂和肱骨是最常见的受累部位。髋部骨折尤其令人担忧,因为它与更长的住院时间和更高的发病率和死亡率有关。此外,经历髋部骨折的透析患者的死亡率比患有类似骨折的普通人群高2.4倍。这种增加的风险强调了CKD患者需要积极的骨骼健康维护,以防止骨折和相关并发症。这篇综述探讨了CKD中与骨脆性相关的潜在病理生理机制、诊断挑战和治疗选择。诊断工具,如骨矿物质密度(BMD)评估,骨小梁评分(TBS)和生化标志物,仍然没有得到充分利用,特别是在晚期CKD阶段。最近的治疗策略强调多学科,阶段特异性的方法,结合钙和维生素D补充剂,抗再吸收药物如denosumab,以及合成代谢治疗如teriparatide和romosozumab。有效的管理需要根据患者的骨转换状态和CKD的分期进行调整。尽管在了解CKD的骨脆性方面取得了进展,但在诊断和治疗方面仍存在重大差距。在最新的KDIGO建议的指导下,基于跨学科方法的个性化护理对于降低这一弱势群体的骨折风险和改善预后至关重要。需要进一步的研究来验证风险评估工具和完善治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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