慢性肾脏病成人患者的继发性甲状旁腺功能亢进与不良健康结局

Secondary hyperparathyroidism and adverse health outcomes in adults with chronic kidney disease.

作者信息

Xu Yang, Evans Marie, Soro Marco, Barany Peter, Carrero Juan Jesus

机构信息

Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Global HEOR, GPMA, Vifor Pharma, Opfikon, Switzerland.

出版信息

Clin Kidney J. 2021 Jan 20;14(10):2213-2220. doi: 10.1093/ckj/sfab006. eCollection 2021 Oct.

Abstract

BACKGROUND

Secondary hyperparathyroidism (sHPT) develops frequently in patients with chronic kidney disease (CKD). However, the burden and long-term impact of sHPT on the risk of adverse health outcomes are not well studied.

METHODS

We evaluated all adults receiving nephrologist care in Stockholm during 2006-11 who were not undergoing kidney replacement therapy and had not developed sHPT. Incident sHPT was identified by using clinical diagnoses, initiated medications or two consecutive parathyroid hormone (PTH) measurements ≥130 pg/mL. We characterized sHPT incidence by estimated glomerular filtration rate (eGFR) strata, evaluated clinical predictors and quantified the association between incident sHPT (time-varying exposure) and the risk of fractures, CKD progression, major adverse cardiovascular events (MACEs) and death.

RESULTS

We identified 2556 adults with CKD Stages 1-5 (mean age 66 years, 38% women), of whom 784 developed sHPT during follow-up. The incidence of sHPT increased with advancing CKD: from 57 cases/1000 person-years in CKD Stage G3 to 230 cases/1000 person-years in Stage G5. In multivariable analyses, low eGFR was the strongest sHPT predictor, followed by young age, male sex and diabetes. Incident sHPT was associated with a 1.3-fold (95% confidence interval 1.1-1.8) increased risk of death, a 2.2-fold (1.42-3.28) higher risk of MACEs, a 5.0-fold (3.5-7.2) higher risk of CKD progression and a 1.3-fold (1.5-2.2) higher risk of fractures. Results were consistent in stratified analyses and after excluding early events.

CONCLUSIONS

Our findings illustrate the burden of sHPT in advanced CKD and highlight the susceptibility for adverse outcomes of patients developing sHPT. This may inform clinical decisions regarding pre-sHPT risk stratification, PTH monitoring and risk-prevention strategies post-sHPT development.

摘要

背景

继发性甲状旁腺功能亢进(sHPT)在慢性肾脏病(CKD)患者中频繁发生。然而,sHPT对不良健康结局风险的负担及长期影响尚未得到充分研究。

方法

我们评估了2006年至2011年期间在斯德哥尔摩接受肾脏病专家治疗、未接受肾脏替代治疗且未发生sHPT的所有成年人。通过临床诊断、开始使用的药物或连续两次甲状旁腺激素(PTH)测量值≥130 pg/mL来确定新发sHPT。我们按估计肾小球滤过率(eGFR)分层来描述sHPT的发病率,评估临床预测因素,并量化新发sHPT(随时间变化的暴露因素)与骨折、CKD进展、主要不良心血管事件(MACE)及死亡风险之间的关联。

结果

我们确定了2556例CKD 1-5期的成年人(平均年龄66岁,38%为女性),其中784例在随访期间发生了sHPT。sHPT的发病率随CKD进展而增加:从CKD G3期的57例/1000人年增加到G5期的230例/1000人年。在多变量分析中,低eGFR是最强的sHPT预测因素,其次是年轻、男性和糖尿病。新发sHPT与死亡风险增加1.3倍(95%置信区间1.1-1.8)、MACE风险增加2.2倍(1.42-3.28)、CKD进展风险增加5.0倍(3.5-7.2)以及骨折风险增加1.3倍(1.5-2.2)相关。分层分析及排除早期事件后的结果一致。

结论

我们的研究结果说明了晚期CKD中sHPT的负担,并突出了发生sHPT患者出现不良结局的易感性。这可能为sHPT发生前的风险分层、PTH监测及sHPT发生后的风险预防策略等临床决策提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56f7/8483675/7716eb0c448f/sfab006f1.jpg

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