Front Horm Res. 2019;52:49-60. doi: 10.1159/000493237. Epub 2019 Jan 15.
Chronic hyponatremia may not cause overt symptoms, and therefore frequently remains untreated. More recently, growing evidence indicate that this condition is not benign, and can lead to unsteady gait, deterioration of bone mass and strength, increased fragility, and increased all-cause mortality. We provided the first evidence for hyponatremia-induced osteoporosis based on markedly reduced bone mineral density and bone structural changes in hyponatremic rats, which is an experimental model of the syndrome of inappropriate antidiuresis (SIAD). These animal data were supported by results of the analysis of the National Health and Nutrition Examination Survey III dataset showing a 2.5-fold increased OR of osteoporosis in participants with serum sodium concentration [Na+] below 135 mmol/L. A subsequent cross-sectional study from Michigan analyzed data from 25,000 patients and found a strong association between the odds of osteoporosis by bone density and hyponatremia. This study pointed out that age-dependent decline in bone density may mask hyponatremia-induced bone loss. Multiple independent retrospective studies, epidemiological studies, and prospective clinical studies have since confirmed and extended our findings, reporting evidence for increased bone fractures and increased mortality in patients with hyponatremia. Cell culture studies have elucidated some of the adaptive mechanisms by which low extracellular fluid [Na+] increases osteoclast formation and bone resorbing activity, thereby liberating stored sodium from the bone matrix. Studies on older SIAD rats indicated that the damage may not be restricted to bone alone, but may involve other organs, including the heart, testis, kidney, and the brain. Finally, compelling open questions and future research directions about the effect of hyponatremia on bone are outlined.
慢性低钠血症可能不会引起明显的症状,因此经常得不到治疗。最近,越来越多的证据表明,这种情况并非良性,它可导致步态不稳、骨量和骨强度下降、脆性增加以及全因死亡率增加。我们提供了第一个低钠血症性骨质疏松的证据,即低钠血症大鼠的骨密度明显降低和骨结构改变,这是抗利尿激素分泌不当综合征(SIAD)的实验模型。这些动物数据得到了 National Health and Nutrition Examination Survey III 数据集分析结果的支持,该结果显示血清钠浓度 [Na+]低于 135mmol/L 的参与者骨质疏松的 OR 值增加了 2.5 倍。随后,密歇根州的一项横断面研究分析了 25000 名患者的数据,发现骨密度和低钠血症导致骨质疏松的几率之间存在很强的相关性。这项研究指出,年龄相关的骨密度下降可能掩盖了低钠血症引起的骨丢失。此后,多项独立的回顾性研究、流行病学研究和前瞻性临床研究证实并扩展了我们的研究结果,报告称低钠血症患者的骨折风险增加和死亡率增加。细胞培养研究阐明了一些适应机制,即低细胞外液 [Na+]增加破骨细胞形成和骨吸收活性,从而将储存的钠从骨基质中释放出来。对老年 SIAD 大鼠的研究表明,这种损伤可能不仅限于骨骼,还可能涉及其他器官,包括心脏、睾丸、肾脏和大脑。最后,概述了关于低钠血症对骨骼影响的一些引人关注的开放性问题和未来的研究方向。