Division of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
Human Health Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
PLoS One. 2024 Aug 29;19(8):e0309657. doi: 10.1371/journal.pone.0309657. eCollection 2024.
Patients undergoing hemodialysis are at an elevated risk of fractures; however, substantial evidence for osteoporosis treatment in this population is lacking. We explored the efficacy of denosumab, an anti-IgG2 antibody that targets the receptor activator of nuclear factor-kappa B ligand, in reducing fracture incidence and all-cause mortality in patients undergoing hemodialysis.
This retrospective cohort study-conducted from December 2013 to December 2022-evaluated the effects of denosumab on fracture incidence and all-cause mortality. Patients who initiated denosumab treatment during the study period were defined as the denosumab group, while those without a history of denosumab administration were defined as the non-denosumab group. Kaplan-Meier curves and log-rank tests were used to assess survival and fracture/mortality risks, respectively. Cox proportional hazards models were used to analyze both fractures and all-cause mortality.
Among 214 patients undergoing hemodialysis, 52 (24.3%) received denosumab. The median age was 73.0 ± 11.5 years, with 92 (43.0%) females, and the median dialysis duration was 59 months (interquartile range, 6-126). During the study, thirty-seven non-denosumab-treated patients had fractures compared to eight in the denosumab group. No significant differences were observed in the unadjusted model (HR, 0.53; 95% confidence interval (CI), 0.24-1.14). Adjusting for competing mortality and clinical factors, the HR remained at 0.64 (95% CI, 0.27-1.51). Regarding all-cause mortality, we found a statistically significant difference in the unadjusted model (HR, 0.61 [95% CI, 0.38-0.98]). A significant reduction in mortality was observed in the adjusted model (HR, 0.46 [95% CI, 0.26-0.80]). Notably, the denosumab group showed a significant decrease in mortality, particularly in cardiovascular disease-related cases (HR, 0.33 [95% CI, 0.14-0.78]).
Denosumab may reduce all-cause mortality in patients undergoing hemodialysis, particularly in those with cardiovascular complications. This finding offers a promising direction for osteoporosis treatment in patients undergoing hemodialysis.
接受血液透析的患者骨折风险升高;然而,针对该人群骨质疏松症治疗的大量证据仍存在不足。我们探索了地舒单抗(一种靶向核因子 κB 配体受体激活剂的 IgG2 抗体)在降低血液透析患者骨折发生率和全因死亡率方面的疗效。
这项回顾性队列研究于 2013 年 12 月至 2022 年 12 月进行,评估了地舒单抗对骨折发生率和全因死亡率的影响。在研究期间开始接受地舒单抗治疗的患者被定义为地舒单抗组,而未接受地舒单抗治疗的患者被定义为非地舒单抗组。Kaplan-Meier 曲线和对数秩检验分别用于评估生存和骨折/死亡率风险。Cox 比例风险模型用于分析骨折和全因死亡率。
在 214 名接受血液透析的患者中,52 名(24.3%)接受了地舒单抗治疗。中位年龄为 73.0±11.5 岁,92 名(43.0%)为女性,中位透析时间为 59 个月(四分位距,6-126)。在研究期间,37 名非地舒单抗治疗的患者发生了骨折,而地舒单抗组有 8 名患者发生了骨折。未校正模型中未见显著差异(HR,0.53;95%置信区间(CI),0.24-1.14)。调整竞争死亡率和临床因素后,HR 仍为 0.64(95%CI,0.27-1.51)。关于全因死亡率,我们在未校正模型中发现了统计学显著差异(HR,0.61[95%CI,0.38-0.98])。校正模型中观察到死亡率显著降低(HR,0.46[95%CI,0.26-0.80])。值得注意的是,地舒单抗组死亡率显著降低,尤其是心血管疾病相关病例(HR,0.33[95%CI,0.14-0.78])。
地舒单抗可能降低血液透析患者的全因死亡率,特别是在伴有心血管并发症的患者中。这一发现为血液透析患者骨质疏松症治疗提供了一个有前途的方向。