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慢性肾脏病相关代谢并发症的发病时间。

Timing of onset of CKD-related metabolic complications.

作者信息

Moranne Olivier, Froissart Marc, Rossert Jerome, Gauci Cedric, Boffa Jean-Jacques, Haymann Jean Philippe, M'rad Mona Ben, Jacquot Christian, Houillier Pascal, Stengel Benedicte, Fouqueray Bruno

机构信息

INSERM Unit 780, 16, avenue Paul Vaillant-Couturier, 94807 Villejuif Cedex, France.

出版信息

J Am Soc Nephrol. 2009 Jan;20(1):164-71. doi: 10.1681/ASN.2008020159. Epub 2008 Nov 12.

Abstract

Chronic kidney disease (CKD) guidelines recommend evaluating patients with GFR <60 ml/min per 1.73 m(2) for complications, but little evidence supports the use of a single GFR threshold for all metabolic disorders. We used data from the NephroTest cohort, including 1038 adult patients who had stages 2 through 5 CKD and were not on dialysis, to study the occurrence of metabolic complications. GFR was measured using renal clearance of (51)Cr-EDTA (mGFR) and estimated using two equations derived from the Modification of Diet in Renal Disease study. As mGFR decreased from 60 to 90 to <20 ml/min per 1.73 m(2), the prevalence of hyperparathyroidism increased from 17 to 85%, anemia from 8 to 41%, hyperphosphatemia from 1 to 30%, metabolic acidosis from 2 to 39%, and hyperkalemia from 2 to 42%. Factors most strongly associated with metabolic complications, independent of mGFR, were younger age for acidosis and hyperphosphatemia, presence of diabetes for acidosis, diabetic kidney disease for anemia, and both male gender and the use of inhibitors of the renin-angiotensin system for hyperkalemia. mGFR thresholds for detecting complications with 90% sensitivity were 50, 44, 40, 39, and 37 ml/min per 1.73 m(2) for hyperparathyroidism, anemia, acidosis, hyperkalemia, and hyperphosphatemia, respectively. Analysis using estimated GFR produced similar results. In summary, this study describes the onset of CKD-related complications at different levels of GFR; anemia and hyperparathyroidism occur earlier than acidosis, hyperkalemia, and hyperphosphatemia.

摘要

慢性肾脏病(CKD)指南建议,对于估算肾小球滤过率(GFR)<60ml/(min·1.73m²)的患者评估其并发症情况,但几乎没有证据支持对所有代谢紊乱都采用单一的GFR阈值。我们使用了NephroTest队列研究的数据,该队列包括1038例2至5期CKD且未接受透析的成年患者,以研究代谢并发症的发生情况。GFR通过(51)Cr-EDTA肾清除率(mGFR)进行测量,并使用源自肾脏疾病饮食改良研究的两个公式进行估算。随着mGFR从60降至90再降至<20ml/(min·1.73m²),甲状旁腺功能亢进的患病率从17%增至85%,贫血从8%增至41%,高磷血症从1%增至30%,代谢性酸中毒从2%增至39%,高钾血症从2%增至42%。与代谢并发症最密切相关的因素,独立于mGFR之外,酸中毒和高磷血症为年龄较轻,酸中毒为患有糖尿病,贫血为患有糖尿病肾病,高钾血症为男性以及使用肾素-血管紧张素系统抑制剂。检测并发症敏感度达90%时的mGFR阈值,甲状旁腺功能亢进、贫血、酸中毒、高钾血症和高磷血症分别为50、44、40、39和37ml/(min·1.73m²)。使用估算GFR进行分析得出了相似结果。总之,本研究描述了不同GFR水平下CKD相关并发症的发生情况;贫血和甲状旁腺功能亢进比酸中毒、高钾血症和高磷血症出现得更早。

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