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Nicotinic acid and related compounds: A meta-analysis of their use for hyperphosphatemia in dialysis patients

机译:烟酸和相关的化合物:透析患者中​​使用过高磷血症的META分析

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Background: Studies indicate that nicotinic acid and related compounds may decrease phosphorus concentrations effectively by reducing the absorption in the gastrointestinal tract. However, the efficacy and safety of oral niacin treatments have only been investigated in a limited number of small-scale studies. Methods: We performed this meta-analysis by pooling 12 qualified relevant preclinical and clinical trials to evaluate the association of nicotinic acid (and its related compounds) treatment and hyperphosphatemia among dialysis patients . Baseline and after treatment data were collected from the studies to evaluate drug efficacy, effect on lipid profile, and drug safety. To evaluate drug efficacy, subgroups were created based on different exposure time (i.e., 4 wks, 8 wks, 12 wks, and 24 wks) and each subgroup was compared against baseline data. In the assessment of lipid profile and drug safety, results of 8-week treatment were compared against baseline data. Results: Our study showed that in the efficacy assessment of drug treatment, serum phosphorus concentration was only significantly reduced in the 4-week (SMD, 0.68; 95% CI, 0.40 to 0.97; P = .000; n = 8), and 8-week (SMD, 1.05; 95% CI, 0.68 to 1.42; P = .000; n = 10) treatment groups. The calcium × phosphorus product showed significantly reduced concentration in all the drug exposure time settings, and no rebound was detected (4-wk treatment: SMD, 0.61; 95% CI, 0.18 to 1.04; P = .005; n = 5; 8-wk treatment: SMD, 0.76; 95% CI, 0.32 to 1.18, P = .001; n = 8; and 12-wks treatment: SMD, 0.28, 95% CI, ?0.06 to 0.61; P = .103; n = 3). Lipid profile monitoring showed that high-density lipoprotein (HDL) and triglycerides (TG) significantly changed after 8 weeks of treatment (HDL: SMD, ?0.63; 95% CI, ?1.03 to 0.24; P = .002; n = 5) and TG: SMD, 0.25; 95% CI, 0.02 to 0.49; P = .033; n = 5). Assessment of drug safety detected significant association for incidence of diarrhea (8% incidence rate; 95% CI, 4% to 12%; P = .001) and total adverse event (41% incidence rate, 95% CI: 12% to 69%, P = .001). Conclusion: Our study concludes that nicotinic acid and related compounds can significantly reduce serum phosphorus concentration with additive antilipemic effects. We also recommend that the safety of this drug be further studied, as our results suggest significant incidence of adverse events.
机译:背景:研究表明,通过减少胃肠道中的吸收,烟酸和相关化合物可以减少磷浓度。然而,仅在有限数量的小规模研究中研究了口腔烟酸处理的疗效和安全性。方法:通过汇集12个合格的相关的临床前和临床试验,进行该荟萃分析,以评估尼古丁酸(及其相关化合物)治疗和透析患者的高磷血症的关联。从研究中收集基线和治疗数据以评估药物疗效,对脂质型材的影响和药物安全性。为了评估药物功效,基于不同的暴露时间(即,4个WK,8个WK,12个WK和24个WKS)产生亚组,并将每个子组与基线数据进行比较。在评估脂质型材和药物安全性中,将8周处理的结果与基线数据进行比较。结果表明,我们的研究表明,在药物治疗的功效评估中,血清磷浓度在4周(SMD,0.68; 95%CI,0.40至0.97; p = .000; n = 8)显着降低。 8周(SMD,1.05; 95%CI,0.68至1.42; p = .000; n = 10)治疗组。钙×磷产品在所有药物暴露时间设置中显示出显着降低的浓度,并且没有检测到反弹(4-WK处理:SMD,0.61; 95%CI,0.18至1.04; P = .005; n = 5; 8 -WK治疗:SMD,0.76; 95%CI,0.32至1.18,p = .001; n = 8;和12 WKS治疗:SMD,0.28,95%CI,Δ06至0.61; p = .103; n = 3)。脂质剖面监测显示,在治疗8周后,高密度脂蛋白(HDL)和甘油三酯(TG)显着改变(HDL:SMD,α0.65%CI,Δ1.03至0.24; p = .002; n = 5)和TG:SMD,0.25; 95%CI,0.02至0.49; p = .033; n = 5)。药物安全评估检测了腹泻发生率的重大关联(8%发生率; 95%CI,4%至12%; P = .001)和总不良事件(41%发生率,95%CI:12%至69 %,p = .001)。结论:我们的研究得出结论,烟酸和相关化合物可以显着降低血清磷浓度与添加剂抗癫痫作用。我们还建议进一步研究该药物的安全性,因为我们的结果表明不良事件的显着发生率。

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