Department of Paediatric Nephrology, Gazi University Faculty of Medicine, Ankara, Turkey.
Department of Paediatric Nephrology, Rheumatology and Dermatology, University Children's Hospital, Lyon, France.
Nephrol Dial Transplant. 2021 Feb 20;36(3):413-425. doi: 10.1093/ndt/gfaa210.
Mineral and bone disorder (MBD) is widely prevalent in children with chronic kidney disease (CKD) and is associated with significant morbidity. CKD may cause disturbances in bone remodelling/modelling, which are more pronounced in the growing skeleton, manifesting as short stature, bone pain and deformities, fractures, slipped epiphyses and ectopic calcifications. Although assessment of bone health is a key element in the clinical care of children with CKD, it remains a major challenge for physicians. On the one hand, bone biopsy with histomorphometry is the gold standard for assessing bone health, but it is expensive, invasive and requires expertise in the interpretation of bone histology. On the other hand, currently available non-invasive measures, including dual-energy X-ray absorptiometry and biomarkers of bone formation/resorption, are affected by growth and pubertal status and have limited sensitivity and specificity in predicting changes in bone turnover and mineralization. In the absence of high-quality evidence, there are wide variations in clinical practice in the diagnosis and management of CKD-MBD in childhood. We present clinical practice points (CPPs) on the assessment of bone disease in children with CKD Stages 2-5 and on dialysis based on the best available evidence and consensus of experts from the CKD-MBD and Dialysis working groups of the European Society for Paediatric Nephrology and the CKD-MBD working group of the European Renal Association-European Dialysis and Transplant Association. These CPPs should be carefully considered by treating physicians and adapted to individual patients' needs as appropriate. Further areas for research are suggested.
矿物质和骨代谢紊乱(MBD)在慢性肾脏病(CKD)患儿中普遍存在,与较高的发病率相关。CKD 可引起骨重塑/改建紊乱,在生长中的骨骼中更为明显,表现为身材矮小、骨痛和畸形、骨折、骨骺滑脱和异位钙化。尽管评估骨骼健康是 CKD 患儿临床治疗的关键要素,但这对医生来说仍是一项重大挑战。一方面,骨活检和组织形态计量学是评估骨骼健康的金标准,但它昂贵、有创,需要骨组织学解读方面的专业知识。另一方面,目前可用的非侵入性措施,包括双能 X 射线吸收法和骨形成/吸收的生物标志物,受到生长和青春期状态的影响,在预测骨转换和矿化变化方面的敏感性和特异性有限。由于缺乏高质量证据,儿童 CKD-MBD 的诊断和管理在临床实践中存在广泛差异。我们根据来自 CKD-MBD 和透析工作组的最佳现有证据和专家共识,提出了用于评估 CKD 2-5 期和透析患儿骨骼疾病的临床实践要点(CPP)。这些 CPP 应由治疗医生仔细考虑,并根据患者的个体需求进行适当调整。建议进一步研究其他领域。