Medical Research Unit Kidney Disease, Specialty Hospital, CMNO, Guadalajara, Mexico.
Arch Med Res. 2013 Nov;44(8):633-7. doi: 10.1016/j.arcmed.2013.10.016. Epub 2013 Nov 8.
Inflammation is highly prevalent in patients on dialysis. Statins have anti-inflammatory actions but their use has been scarcely studied in continuous ambulatory peritoneal dialysis (CAPD). We undertook this study to compare the effect of pravastatin vs. placebo on the serum concentrations of C-reactive protein (CRP) in patients on CAPD.
In a double-blind, controlled and crossover clinical trial, 76 CAPD patients were randomized to either pravastatin or placebo for 2 months. After this first period of treatment, patients had a 1-month wash-out period and, finally, they were crossed-over to receive the other drug (or placebo) for 2 more months. Measurement of clinical and biochemical variables and CRP was performed at the beginning and at the end of each treatment period.
Median CRP was only significantly decreased in the pravastatin group in both periods of treatment: first period (baseline vs. final, mg/L): pravastatin 7.4 (2-21) vs. 2.6 (1-6), p <0.05; placebo 3.9 (2-10) vs. 6.8 (3-12), pNS; second period: pravastatin 4.3 (2-15) vs. 1.9 (1-7), p <0.05; placebo 4.9 (2-17) vs. 6.8 (2-19), p <0.05. Results were significantly different (p <0.05) between groups only at the end of each treatment period. Additionally, total and LDL-cholesterol significantly decreased in the pravastatin group.
Pravastatin significantly reduced serum levels of CRP and total and LDL-cholesterol compared to placebo. This treatment may be of great help to decrease the inflammatory status and probably the cardiovascular disease of CAPD patients.
炎症在透析患者中普遍存在。他汀类药物具有抗炎作用,但在持续不卧床腹膜透析(CAPD)中,其应用研究甚少。我们进行这项研究是为了比较普伐他汀与安慰剂对 CAPD 患者血清 C 反应蛋白(CRP)浓度的影响。
在一项双盲、对照、交叉临床试验中,76 例 CAPD 患者被随机分为普伐他汀组或安慰剂组,分别接受为期 2 个月的治疗。在第一个治疗期后,患者有 1 个月的洗脱期,最后交叉接受另一种药物(或安慰剂)治疗 2 个月。在每个治疗期开始和结束时,测量临床和生化变量及 CRP。
只有普伐他汀组的 CRP 在两个治疗期均显著降低:第一期(基线 vs. 终末,mg/L):普伐他汀 7.4(2-21)vs. 2.6(1-6),p<0.05;安慰剂 3.9(2-10)vs. 6.8(3-12),pNS;第二期:普伐他汀 4.3(2-15)vs. 1.9(1-7),p<0.05;安慰剂 4.9(2-17)vs. 6.8(2-19),p<0.05。仅在每个治疗期末,两组之间的结果才有显著差异(p<0.05)。此外,普伐他汀组总胆固醇和 LDL 胆固醇显著降低。
与安慰剂相比,普伐他汀显著降低了 CRP 以及总胆固醇和 LDL 胆固醇的血清水平。这种治疗可能有助于降低 CAPD 患者的炎症状态和心血管疾病风险。