Takei Takashi, Otsubo Shigeru, Uchida Keiko, Matsugami Keiko, Mimuro Tomoko, Kabaya Takashi, Akiba Takashi, Nitta Kosaku
Department of Medicine, Kidney Center, Tokyo Women's Medical University, Tokyo, Japan.
Nephron Clin Pract. 2008;108(4):c278-83. doi: 10.1159/000127361. Epub 2008 Apr 22.
BACKGROUND/AIM: Vascular calcification is thought to be associated with a high cardiovascular mortality rate in patients with end-stage renal disease. Control of hyperphosphataemia is important for the treatment of the vascular calcification. The aim of the present study was to evaluate the effects of sevelamer hydrochloride on the progression of aortic calcification in haemodialysis (HD) patients.
42 HD patients were studied in this study and divided into two groups (sevelamer vs. calcium). Sevelamer was added and titrated up to achieve serum P control for 6 months. The estimations of aortic calcification index (ACI) by abdominal computed tomography scans were performed twice in each patient. We compared the changes in serum calcium, phosphorus, intact parathyroid hormone, and lipids in two groups.
Serum phosphorus levels decreased significantly from 6.7 +/- 0.7 to 6.2 +/- 0.5 mg/dl with no changes in serum intact parathyroid hormone levels in the sevelamer group (p < 0.01), and increased from 6.5 +/- 1.0 to 6.7 +/- 1.1 mg/dl in the calcium group (p < 0.05). Serum calcium levels did not change in the sevelamer group and calcium group. The serum levels of total cholesterol decreased significantly from 158.5 +/- 20.7 to 146.2 +/- 24.1 mg/dl (p = 0.024) and the low-density lipoprotein cholesterol level from 65.3 +/- 14.4 to 54.7 +/- 11.6 mg/dl (p = 0.014) in the sevelamer group. Serum C-reactive protein decreased significantly from 0.14 +/- 0.13 to 0.08 +/- 0.11 mg/dl in the sevelamer group (p = 0.038) and significantly increased (0.18 +/- 0.09 vs. 0.22 +/- 0.12 mg/dl) in the calcium group (p = 0.042). The mean changes in ACI (DeltaACI) were 3.6 +/- 1.5% in the sevelamer group and 8.2 +/- 3.1% in the calcium group.
Sevelamer allows a better serum phosphorus control compared with calcium-based phosphate binder and suppresses the progression of aortic calcification in HD patients.
背景/目的:血管钙化被认为与终末期肾病患者的高心血管死亡率相关。控制高磷血症对于治疗血管钙化很重要。本研究的目的是评估盐酸司维拉姆对血液透析(HD)患者主动脉钙化进展的影响。
本研究纳入42例HD患者,分为两组(司维拉姆组与钙剂组)。添加司维拉姆并进行滴定,以实现血清磷控制6个月。对每位患者进行两次腹部计算机断层扫描以评估主动脉钙化指数(ACI)。我们比较了两组患者血清钙、磷、完整甲状旁腺激素和血脂的变化。
司维拉姆组血清磷水平从6.7±0.7显著降至6.2±0.5mg/dl,血清完整甲状旁腺激素水平无变化(p<0.01),钙剂组血清磷水平从6.5±1.0升至6.7±1.1mg/dl(p<0.05)。司维拉姆组和钙剂组血清钙水平均无变化。司维拉姆组总胆固醇水平从158.5±20.7显著降至146.2±24.1mg/dl(p=0.024),低密度脂蛋白胆固醇水平从65.3±14.4降至54.7±11.6mg/dl(p=0.014)。司维拉姆组血清C反应蛋白从0.14±0.13显著降至0.08±0.11mg/dl(p=0.038),钙剂组显著升高(0.18±0.09 vs. 0.22±0.12mg/dl,p=0.042)。司维拉姆组ACI的平均变化(ΔACI)为3.6±1.5%;钙剂组为8.2±3.1%。
与含钙磷结合剂相比,司维拉姆能更好地控制血清磷,并抑制HD患者主动脉钙化的进展。