1.上海中医药大学附属曙光医院肾病科,上海中医药大学中医肾病研究所,上海市中医临床重点实验室,肝肾疾病病证教育部重点实验室(上海 201203)
杨婧,女,博士,主治医师,主要从事中医药防治慢性肾脏病的临床研究工作
王琛,博士,主任医师;E-mail:chenwang42@163.com
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杨婧, 邹赟, 吴琪琪, 等. 肾衰Ⅱ号方对慢性肾脏病3-4期轻中度蛋白尿患者影响的临床研究[J]. 上海中医药杂志, 2021,55(2):71-75.
Jing YANG, Yun ZOU, Qiqi WU, et al. Clinical study on the effect of Shenshuai Ⅱ Decoction on chronic kidney diseases 3-4 stages patients with mild-to-moderate proteinuria[J]. Shanghai Journal of Traditional Chinese Medicine, 2021,55(2):71-75.
杨婧, 邹赟, 吴琪琪, 等. 肾衰Ⅱ号方对慢性肾脏病3-4期轻中度蛋白尿患者影响的临床研究[J]. 上海中医药杂志, 2021,55(2):71-75. DOI: 10.16305/j.1007-1334.2021.2009106.
Jing YANG, Yun ZOU, Qiqi WU, et al. Clinical study on the effect of Shenshuai Ⅱ Decoction on chronic kidney diseases 3-4 stages patients with mild-to-moderate proteinuria[J]. Shanghai Journal of Traditional Chinese Medicine, 2021,55(2):71-75. DOI: 10.16305/j.1007-1334.2021.2009106.
目的,2,观察肾衰Ⅱ号方对慢性肾脏病(CKD)3-4期轻中度蛋白尿患者的影响。,方法,2,将88例CKD3-4期轻中度蛋白尿患者,随机分为治疗组和对照组,每组44例。两组均予基础治疗,对照组加用尿毒清颗粒,治疗组加用肾衰Ⅱ号方。两组疗程均为6个月,观察临床疗效,比较两组中医症状积分、血肌酐(Scr)、尿素氮(BUN)、肾小球滤过率(eGFR)、24h尿蛋白定量(24hUpro)、尿视黄醇结合蛋白(RBP)、尿α1微球蛋白(α1-MG)、尿β2-微球蛋白(β2-MG)的变化情况。,结果,2,①治疗组、对照组临床总有效率分别为86.36%、61.36%;组间临床疗效比较,治疗组优于对照组(,P,<,0.05)。②治疗前后组内比较,治疗组中医症状各分项积分及总分均较治疗前明显下降(,P,<,0.05),对照组除面色晦暗、恶心呕吐外,其余症状各分项积分及总分明显下降(,P,<,0.05);组间治疗后比较,除口干口苦外,治疗组症状各分项积分及总分均低于对照组(,P,<,0.05)。③治疗前后组内比较,治疗组Scr、BUN明显下降(,P,<,0.05),eGFR明显上升(,P,<,0.05),对照组Scr明显下降(,P,<,0.05);组间治疗后比较,治疗组BUN较对照组明显下降(,P,<,0.05)。④治疗前后组内比较,治疗组24hUpro、尿β2-MG、尿α1-MG、尿RBP均明显下降(,P,<,0.05),对照组24hUpro、尿α1-MG明显下降(,P,<,0.05);组间治疗后比较,治疗组尿β2-MG、尿α1-MG、尿RBP明显低于对照组(,P,<,0.05)。,结论,2,肾衰Ⅱ号方治疗CKD3-4期轻中度蛋白尿的临床疗效优于尿毒清颗粒,能显著改善患者的中医症状、肾功能及肾小管性尿蛋白水平,延缓慢性肾脏病的进展。
Objective,2,To observe the effect of Shenshuai Ⅱ Decoction on chronic kidney diseases (CKD) 3-4 patients with mild-to-moderate proteinuria.,Methods,2,A total of 88 patients of CKD3-4 stages with mild-to-moderate proteinuria were randomly divided into control group (44 cases) and treatment group (44 cases). On the basic treatment, the treatment group was treated with Shenshuai Ⅱ Decoction, and the control group was treated with Niaoduqing Granule. The course of treatment in both groups was 6 months. The clinical efficacy and TCM symptom score, renal function (Scr, BUN, eGFR), urine protein (24hUpro, URBP, Uα1-MG, Uβ2-MG)were observed., Results,2,①The total effective rate was 86.36% in the treatment group and 61.36% in the control group, and the clinical efficacy in the treatment group was better than that in the control group(,P,<,0.05). ②After treatment, the single scores and the total scores of TCM symptoms in the treatment group were significantly decreased (,P,<,0.05), while those in the control group were significantly decreased except dark complexion, nausea and vomiting (,P,<,0.05). Except dry mouth and bitter mouth, the single scores and the total scores of TCM symptoms in the treatment group were lower than those in the control group (,P,<,0.05).③After treatment, the levels of Scr and BUN were significantly decreased, and the eGFR level was significantly increased in the treatment group (,P,<,0.05). In the control group, the level of Scr was significantly decreased (,P,<,0.05). The level of BUN was lower in the treatment group than that in the control group (,P,<,0.05). ④After treatment, the levels of 24hUpro, Uβ 2-MG, Uα 1-MG and URBP significantly decreased in the treatment group (,P,<,0.05), while 24hUpro and Uα1-MG decreased significantly in the control group (,P,<,0.05). The levels of Uβ 2-MG, Uα 1-MG and URBP were lower in the treatment group than those in the control group(,P,<,0.05).,Conclusion,2,Shenshuai Ⅱ Decoction has better clinical efficacy than Niaoduqing Granule in the treatment of CKD3-4 patients with mild-to-moderate proteinuria, which significantly improves TCM symptoms and renal function, reduces the level of tubular proteinuria, and delays the progression of CKD.
慢性肾脏病肾衰Ⅱ号方蛋白尿肾功能临床试验
chronic kidney diseaseShenshuai Ⅱ Decoctionproteinuriarenal functionclinic trial
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