慢性肾病患者血清钾浓度的决定因素。

IF 1.1 4区 医学 Q3 UROLOGY & NEPHROLOGY Clinical nephrology Pub Date : 2024-10-30 DOI:10.5414/CN111490
Yinna Wang, Kenneth R Phelps, Darren E Gemoets, Elvira O Gosmanova
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引用次数: 0

摘要

背景:如果 Ccr 是肌酐清除率(肾小球滤过率 (GFR) 的替代指标),那么血清钾浓度 (Ks) 就是 EK/Ccr 和 TRK/Ccr 的总和,即每滤液体积排出和(净)重吸收的钾量(Ks = EK/Ccr + TRK/Ccr)。我们研究了 EK/Ccr、TRK/Ccr 和 Ks 在慢性肾脏病(CKD)不同阶段的变化:我们对 452 名 CKD G1 - 5 期患者进行了回顾性研究。通过同时测量血清和尿液中的钾和肌酐浓度(Ks、Ku、crs 和 cru),计算出 1,007 个 EK/Ccr 和 TRK/Ccr 值,分别为 Ku×crs/cru 和 Ks - EK/Ccr。EK/Ccr 和 TRK/Ccr 的平均值按 CKD G1 - 5 期确定。在每个分期中,还确定了高钾血症(Ks > 5.1 mmol/L)、正常血钾(Ks 3.8 - 5.1 mmol/L)和低钾血症(Ks < 3.8 mmol/L)子群的比率平均值:与 CKD G1 - 2 期的数值相比,EK/Ccr 在每一个更高的阶段都会上升,而 TRK/Ccr 则会下降。在 G3a 和 G3b 阶段,TRK/Ccr 的下降与 EK/Ccr 的上升相等,而 Ks 保持稳定。在 G4 - 5 阶段,EK/Ccr 的上升超过了 TRK/Ccr 的下降,Ks 也相应上升。在每个慢性肾脏病分期中,EK/Ccr 在三个肾小球贫血亚组中都非常相似;因此,TRK/Ccr 的差异是 Ks 差异的唯一来源:结论:在 CKD 的各个阶段,EK/Ccr 会上升,TRK/Ccr 会下降。在 G3a - 3b 阶段,Ks 保持稳定,而 EK/Ccr 和 TRK/Ccr 的变化相同且相反。在 G4 - 5 期,由于 EK/Ccr 的上升幅度大于 TRK/Ccr 的下降幅度,Ks 逐渐增加。在每个 CKD 阶段中,TRK/Ccr 的差异完全解释了高钾、正常和低钾血症亚群之间 Ks 的差异。TRK/Ccr 变异的原因需要进一步研究。
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Determinants of the serum potassium concentration in chronic kidney disease.

Background: If Ccr is creatinine clearance, a surrogate for glomerular filtration rate (GFR), the serum potassium concentration (Ks) is the sum of EK/Ccr and TRK/Ccr, which are amounts of potassium excreted and (net) reabsorbed per volume of filtrate (Ks = EK/Ccr + TRK/Ccr). We investigated changes in EK/Ccr, TRK/Ccr, and Ks through the stages of chronic kidney disease (CKD).

Materials and methods: We performed a retrospective study of 452 patients with CKD stages G1 - 5. Simultaneous measurements of serum and urine potassium and creatinine concentrations (Ks, Ku, crs, and cru) were used to calculate 1,007 individual values of EK/Ccr and TRK/Ccr as Ku×crs/cru and Ks - EK/Ccr, respectively. Mean values of EK/Ccr and TRK/Ccr were determined in CKD stages G1 - 5. Within each stage, means of the ratios were also ascertained in subsets with hyperkalemia (Ks > 5.1 mmol/L), normokalemia (Ks 3.8 - 5.1 mmol/L), and hypokalemia (Ks < 3.8 mmol/L).

Results: In comparison to values in CKD stages G1 - 2, EK/Ccr rose and TRK/Ccr fell in each higher stage. Decrements in TRK/Ccr equaled increments in EK/Ccr in G3a and G3b, and Ks remained stable. In G4 - 5, the ascent of EK/Ccr exceeded the decline in TRK/Ccr, and Ks rose accordingly. Within each CKD stage, EK/Ccr was remarkably similar in the three kalemic subsets; consequently, differences in TRK/Ccr were the sole source of differences in Ks.

Conclusion: EK/Ccr rises and TRK/Ccr falls through the stages of CKD. Ks remains stable in stages G3a - 3b in association with equal and opposite changes in EK/Ccr and TRK/Ccr. In stages G4 - 5, Ks increases progressively because EK/Ccr rises more than TRK/Ccr falls. Within each CKD stage, differences in TRK/Ccr account entirely for differences in Ks among hyper-, normo-, and hypokalemic subsets. Causes of variability of TRK/Ccr require additional investigation.

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来源期刊
Clinical nephrology
Clinical nephrology 医学-泌尿学与肾脏学
CiteScore
2.10
自引率
9.10%
发文量
138
审稿时长
4-8 weeks
期刊介绍: Clinical Nephrology appears monthly and publishes manuscripts containing original material with emphasis on the following topics: prophylaxis, pathophysiology, immunology, diagnosis, therapy, experimental approaches and dialysis and transplantation.
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