机构地区:[1]海南省三亚市人民医院肾内科,海南三亚572000 [2]海南省人民医院营养科,海南海口570311
出 处:《现代生物医学进展》2020年第18期3572-3576,3562,共6页Progress in Modern Biomedicine
基 金:海南省卫生计生行业科研项目(160132027A2121)。
摘 要:目的:探讨不同剂量百令胶囊联合非布司他对慢性肾功能不全(CRF)伴高尿酸血症(HU)肾功能及血脂水平的影响。方法:选取2017年7月至2018年8月三亚市人民医院收治的CRF伴HU患者167例为研究对象,按照数表法随机分为大剂量联合组(n=42)、中剂量联合组(n=42)、小剂量联合组(n=42)和非布司他单用组(n=41),所有研究对象均给予非布司他(40 mg/次,1次/日)治疗,大、中、小剂量联合组再分别给予百令胶囊3g/次、2g/次、1g/次,均3次/日。比较治疗后的临床疗效、治疗前后肾功能指标[血肌酐(Scr)、血尿素氮(BUN)、血尿酸(UA)、血β_2微球蛋白(血β_2-MG)、尿β_2-MG、24 h尿蛋白定量]、血脂指标[甘油三酯(TG)、总胆固醇(TC)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)]水平以及不良反应。结果:治疗后,大剂量联合组肾功能及高尿酸血症的临床总有效率最优(P<0.05),其次为中剂量联合组,小剂量联合组和非布司他单用组比较差异无统计学意义(P>0.05);各组患者治疗后BUN、Scr、UA、血β_2-MG、尿β_2-MG、24h尿蛋白定量水平均有不同程度的下降,其中大剂量联合组降低最显著(P<0.05),小剂量联合组和非布司他单用组比较差异无统计学意义(P>0.05);大、中、小剂量联合组患者治疗后TG、TC、LDL均有下降,HDL上升,其中大剂量联合组TG、TC、LDL降低最显著(P<0.05),HDL升高最显著(P<0.05);各组患者不良反应发生率比较无统计学差异(P>0.05)。结论:大剂量百令胶囊联合非布司他治疗CRF伴HU能改善患者的肾功能和血脂指标,其不良反应发生率较低,但是稍高于其他剂量组,建议临床医师根据患者病情选择合适的剂量。Objective:To investigate the effects of different doses of Bailing capsule combined with febuxostat on renal function and blood lipid levels in patients with chronic renal insufficiency(CRF)with hyperuricemia(HU).Methods:167 patients with CRF with HU who were admitted to Sanya People’s Hospital from July 2017 to August 2018 were selected as the study subjects,they were randomly divided into high-dose combination group(n=42),medium-dose combination group(n=42),low-dose combination group(n=42)and febuxostat alone group(n=41)according to the number table method.All subjects were treated with febuxostat(40 mg/time,1time/day),the high,medium and low dose groups were given Bailing capsule 3 g/time,2 g/time and 1 g/time respectively,3times/day.The clinical efficacy of patients after treatment,renal function indicators before and after treatment[serum creatinine(Scr),blood urea nitrogen(BUN),serum uric acid(UA),urine protein index urineβ2microglobulin(urineβ2-MG),bloodβ2microglobulin(bloodβ2-MG),24 h urine protein quantitation],blood lipid indicators[triglyceride(TG),total cholesterol(TC),high density lipoprotein(HDL)and low density lipoprotein(LDL)]levels and adverse reactions were compared.Results:After treatment,the high-dose combination group had the best improvement in renal function and hyperuricemia,followed by the medium-dose group(P<0.05).There was no significant difference between the low-dose combination group and the febuxostat alone group(P>0.05).The levels of BUN,Scr,UA,urinaryβ2-MG,bloodβ2-MG,and 24 h urinary protein were decreased in different groups,and the high-dose combination group was significantly lower(P<0.05).There was no significant difference between the low-dose group and the febuxostat alone group(P>0.05).After treatment,TG,TC and LDL decreased in high,medium and low dose groups,and HDL increased.Among them,TG,TC and LDL in the high-dose combination group decreased most significantly(P<0.05),and HDL increased most significantly(P<0.05).There was no significant difference in the inciden
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