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骨矿物质参数变化与血液透析患者死亡率的关系:ARO 队列的研究结果。

Association of changes in bone mineral parameters with mortality in haemodialysis patients: insights from the ARO cohort.

机构信息

Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Medical University of Innsbruck, Innsbruck, Austria.

Department of Renal Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden.

出版信息

Nephrol Dial Transplant. 2020 Mar 1;35(3):478-487. doi: 10.1093/ndt/gfz060.

Abstract

BACKGROUND

There is little information in haemodialysis (HD) patients on whether temporal changes in serum calcium, phosphate or intact parathyroid hormone (iPTH) are associated with mortality.

METHODS

We analysed associations of phosphate, total calcium and iPTH with all-cause and cardiovascular mortality in 8817 incident HD patients from the European second Analyzing Data, Recognizing Excellence and Optimizing Outcomes (AROii) cohort enrolled in 2007-09, which were prospectively followed for a median of 3 years, using time-dependent Cox proportional hazards models. We evaluated changes in risk over time depending on changes in phosphate, calcium or iPTH.

RESULTS

The association of phosphate and iPTH with all-cause mortality was U-shaped, with the lowest risk ranges between 1.20 and 1.89 mmol/L for phosphate and between 239 and 710 ng/L for iPTH. For total calcium, the associations were J-shaped, with an increased risk for all-cause mortality at levels >2.36 mmol/L. Lowest risk ranges for cardiovascular mortality did not change markedly for all three parameters. If iPTH was below the lowest risk range at baseline (iPTH <239 ng/L), a subsequent increase in levels was associated with improved survival. For phosphate, an increase or decrease out of the lowest risk range was associated with increased mortality risk. For calcium, this was only the case when the values increased above the lowest risk range.

CONCLUSION

In the AROii cohort, the ranges of bone mineral biomarkers associated with the lowest mortality ranges were largely consistent with the current Kidney Disease: Improving Global Outcomes chronic kidney disease-mineral and bone disorder guideline recommendations. Allowing a suppressed iPTH to increase was associated with a lower mortality, whereas shifts of phosphate or calcium outside the lowest risk range increased mortality.

摘要

背景

关于血清钙、磷或全段甲状旁腺激素(iPTH)的时间变化是否与死亡率相关,在血液透析(HD)患者中信息较少。

方法

我们分析了 2007-09 年欧洲第二分析数据、识别卓越和优化结果(AROii)队列中 8817 例新进入 HD 的患者中磷、总钙和 iPTH 与全因和心血管死亡率的相关性,这些患者前瞻性随访中位数为 3 年,使用时间依赖性 Cox 比例风险模型。我们评估了随着时间的推移,风险变化取决于磷、钙或 iPTH 的变化。

结果

磷和 iPTH 与全因死亡率呈 U 形相关,磷的最低风险范围在 1.20-1.89mmol/L 之间,iPTH 的最低风险范围在 239-710ng/L 之间。对于总钙,相关性呈 J 形,所有全因死亡率风险增加的水平>2.36mmol/L。对于所有三个参数,心血管死亡率的最低风险范围没有明显变化。如果基线时 iPTH 低于最低风险范围(iPTH<239ng/L),随后 iPTH 水平升高与生存率提高相关。对于磷,在最低风险范围之外升高或降低与死亡率增加相关。对于钙,只有当值升高超过最低风险范围时才会出现这种情况。

结论

在 AROii 队列中,与最低死亡率范围相关的骨矿物质生物标志物的范围在很大程度上与当前的肾脏病:改善全球肾脏病预后倡议慢性肾脏病矿物质和骨异常指南建议一致。允许抑制的 iPTH 增加与较低的死亡率相关,而磷或钙的变化超出最低风险范围则会增加死亡率。

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