Nephrology Division, Department of Medicine, Universidade Federal de São Paulo, Rua Botucatu 740 - Vila Clementino, São Paulo, 04023-900, Brazil.
Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, USA.
Curr Osteoporos Rep. 2024 Dec;22(6):576-589. doi: 10.1007/s11914-024-00888-w. Epub 2024 Oct 2.
The impact of nephrolithiasis on skeletal growth and bone health across the life span of kidney stone formers is reviewed.
Bone disease is an early event among kidney stone formers (SF), with distinct phenotypes according to each age, sex, menopausal status, dietary, hormonal and genetic factors. Nephrolithiasis-associated bone disorder is characterized by reduced bone mineral density (BMD) and histologically discloses low bone formation, high bone resorption and abnormal mineralization. Although hypercalciuria has been presumed to be pathogenic for bone loss in SF, the association of BMD with urinary calcium is not uniform in all studies. Hypocitraturia, metabolic disturbances, cytokines and receptors, growth factors and acid-base status may all influence skeletal outcomes. The potential link of bone disease with vascular calcification and cardiovascular disease among SF is discussed. The unique vulnerability of the younger skeleton to the effects of nephrolithiasis on attainment of peak bone mass and strength is highlighted and the association of bone loss with kidney stone formation early in life indicate the opportunity for intervention to reduce the risk of future bone fractures.
肾结石形成者(SF)一生中肾结石对骨骼生长和骨骼健康的影响。
骨骼疾病是 SF 的早期事件,根据每个年龄、性别、绝经状态、饮食、激素和遗传因素,具有不同的表型。肾结石相关的骨骼疾病的特征是骨密度(BMD)降低,组织学上表现为低骨形成、高骨吸收和异常矿化。尽管高钙尿症被认为是 SF 骨丢失的致病因素,但 BMD 与尿钙的关系在所有研究中并不一致。低柠檬酸尿症、代谢紊乱、细胞因子和受体、生长因子以及酸碱状态都可能影响骨骼结局。SF 中骨骼疾病与血管钙化和心血管疾病之间的潜在联系也进行了讨论。年轻骨骼对肾结石对获得峰值骨量和强度的影响更为脆弱,以及年轻时骨丢失与肾结石形成的关联表明有机会进行干预,以降低未来骨折的风险。