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夜间血液透析对钙磷代谢及骨矿物质密度的影响

Calcium phosphate metabolism and bone mineral density with nocturnal hemodialysis.

作者信息

Toussaint Nigel, Boddington Janeane, Simmonds Rosemary, Waldron Claire, Somerville Christine, Agar John

机构信息

Department of Renal Medicine, The Geelong Hospital, Barwon Health, Geelong, Vic., Australia.

出版信息

Hemodial Int. 2006 Jul;10(3):280-6. doi: 10.1111/j.1542-4758.2006.00109.x.

Abstract

An elevated calcium x phosphate product (Ca x P) is an independent risk factor for vascular calcification and cardiovascular death in dialysis patients. More physiological dialysis in patients undergoing nocturnal hemodialysis (NHD) has been shown to produce biochemical advantages compared with conventional hemodialysis (CHD) including superior phosphate (P) control. Benefits of dialysate with greater calcium (Ca) concentration are also reported in NHD to prevent Ca depletion and subsequent hyperparathyroidism, but there are concerns that a higher dialysate Ca concentration may contribute to raised serum Ca levels and greater Ca x P and vascular disease. The NHD program at our unit has been established for 4 years, and we retrospectively analyzed Ca and P metabolism in patients undergoing NHD (8-9 h/night, 6 nights/week). Our cohort consists of 11 patients, mean age 49.3 years, who had been on NHD for a minimum of 12 months, mean 34.3 months. Commencement was with low-flux (LF) NHD and 1.5 mmol/L Ca dialysate concentration, with conversion to high-flux (HF) dialyzers after a period (mean duration 18.7 months). We compared predialysis serum albumin, intact parathyroid hormone, P, total corrected Ca, and Ca x P at baseline on CHD, after conversion to LF NHD and during HF NHD. We also prospectively measured bone mineral density (BMD) on all patients entering the NHD program. Bone densitometry (DEXA) scans were performed at baseline (on CHD) and yearly after commencement of NHD. With the introduction of HF dialyzers, the Ca dialysate concentration was concurrently raised to 1.75 mmol/L after demonstration on DEXA scans of worsening osteopenia. Analysis of BMD, for all parameters, revealed a decrease over the first 12 to 24 months (N = 11). When the dialysate Ca bath was increased, the median T and Z scores subsequently increased (data at 3 years, N = 6). The mean predialysis P levels were significantly lower on LF NHD vs. CHD (1.51 vs. 1.77 mmol/L, p = 0.014), while on HF NHD P was lower again (1.33 mmol/L, p = 0.001 vs. CHD). Predialysis Ca levels decreased with conversion from CHD to LF NHD (2.58 vs. 2.47 mmol/L, p = 0.018) using a 1.5 mmol/L dialysate Ca concentration. The mean Ca x P on CHD was 4.56 compared with a significant reduction of 3.74 on LF NHD (p = 0.006) and 3.28 on HF NHD (p = 0.001 vs. CHD), despite the higher dialysate Ca in the latter. We conclude that an elevated dialysate Ca concentration is required to prevent osteopenia. With concerns that prolonged higher Ca levels contribute to increased cardiovascular mortality, the optimal Ca dialysate bath is still unknown. Better P control on NHD, however, reduces the overall Ca x P, despite the increased Ca concentration, therefore reducing the risk of vascular calcification.

摘要

钙磷乘积(Ca×P)升高是透析患者血管钙化和心血管死亡的独立危险因素。与传统血液透析(CHD)相比,夜间血液透析(NHD)患者采用更符合生理状态的透析方式已显示出一些生化优势,包括更好地控制磷(P)。在NHD中,也有报道称采用钙(Ca)浓度更高的透析液可预防Ca缺乏及随后的甲状旁腺功能亢进,但有人担心较高的透析液Ca浓度可能导致血清Ca水平升高、Ca×P升高及血管疾病。我们单位的NHD项目已开展4年,我们对接受NHD(每晚8 - 9小时,每周6晚)的患者的Ca和P代谢进行了回顾性分析。我们的队列包括11名患者,平均年龄49.3岁,他们接受NHD至少12个月,平均34.3个月。开始时采用低通量(LF)NHD和1.5 mmol/L的透析液Ca浓度,一段时间后(平均持续18.7个月)转换为高通量(HF)透析器。我们比较了在CHD时、转换为LF NHD后及HF NHD期间基线时的透析前血清白蛋白、完整甲状旁腺激素、P、总校正Ca和Ca×P。我们还对所有进入NHD项目的患者进行了前瞻性骨密度(BMD)测量。在基线(CHD时)及NHD开始后每年进行骨密度测定(DEXA)扫描。随着HF透析器的引入,在DEXA扫描显示骨质减少恶化后,透析液Ca浓度同时提高到1.75 mmol/L。对所有参数的BMD分析显示,在最初的12至24个月内(N = 11)有所下降。当透析液Ca浓度提高后,T和Z评分中位数随后升高(3年时的数据,N = 6)。与CHD相比,LF NHD时的平均透析前P水平显著更低(1.51 vs. 1.77 mmol/L,p = 0.014),而在HF NHD时P水平再次降低(1.33 mmol/L,与CHD相比p = 0.001)。采用1.5 mmol/L的透析液Ca浓度时,从CHD转换为LF NHD后透析前Ca水平降低(2.58 vs. 2.47 mmol/L,p = 0.018)。CHD时的平均Ca×P为4.56,而LF NHD时显著降低至3.74(p = 0.006),HF NHD时为3.28(与CHD相比p = 0.001),尽管后者的透析液Ca浓度更高。我们得出结论,需要提高透析液Ca浓度以预防骨质减少。鉴于担心长期较高的Ca水平会导致心血管死亡率增加,最佳的透析液Ca浓度仍不清楚。然而,NHD中更好地控制P可降低总体Ca×P,尽管Ca浓度增加,从而降低血管钙化风险。

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