Semi-individualised Chinese medicine treatment as an adjuvant management for diabetic nephropathy: a pilot add-on, randomised, controlled, multicentre, open-label pragmatic clinical trial

被引:9
作者
Chan, Kam Wa [1 ]
Ip, Tai Pang [2 ]
Kwong, Alfred Siu Kei [3 ]
Lui, Sing Leung [2 ]
Chan, Gary Chi Wang [4 ]
Cowling, Benjamin John [5 ]
Yiu, Wai Han [1 ]
Wong, Dickson Wai Leong [1 ]
Liu, Yang [1 ]
Feng, Yibin [6 ]
Tan, Kathryn Choon Beng [7 ]
Chan, Loretta Yuk Yee [1 ]
Leung, Joseph Chi Kam [1 ]
Lai, Kar Neng [1 ]
Tang, Sydney Chi Wai [1 ]
机构
[1] Univ Hong Kong, Div Nephrol, Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Tung Wah Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
[3] Queen Mary Hosp, Dept Family Med & Primary Healthcare, Hong Kong, Hong Kong, Peoples R China
[4] Queen Mary Hosp, Div Nephrol, Dept Med, Hong Kong, Hong Kong, Peoples R China
[5] Univ Hong Kong, Sch Publ Hlth, Div Epidemiol & Biostat, Hong Kong, Hong Kong, Peoples R China
[6] Univ Hong Kong, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[7] Univ Hong Kong, Div Endocrinol, Dept Med, Hong Kong, Hong Kong, Peoples R China
来源
BMJ OPEN | 2016年 / 6卷 / 08期
关键词
CHRONIC KIDNEY-DISEASE; SAMPLE-SIZE; FIBROSIS; RATS; EXPRESSION; INJURY;
D O I
10.1136/bmjopen-2015-010741
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Diabetes mellitus and diabetic nephropathy (DN) are prevalent and costly to manage. DN is the leading cause of end-stage kidney disease. Conventional therapy blocking the renin-angiotensin system has only achieved limited effect in preserving renal function. Recent observational data show that the use of Chinese medicine (CM), a major form of traditional medicine used extensively in Asia, could reduce the risk of end-stage kidney disease. However, existing clinical practice guidelines are weakly evidence-based and the effect of CM remains unclear. This trial explores the effect of an existing integrative Chinese-Western medicine protocol for the management of DN. Objective: To optimise parameters and assess the feasibility for a subsequent phase III randomised controlled trial through preliminary evaluation on the effect of an adjuvant semi-individualised CM treatment protocol on patients with type 2 diabetes with stages 2-3 chronic kidney disease and macroalbuminuria. Methods and analysis: This is an assessor-blind, add-on, randomised, controlled, parallel, multicentre, open-label pilot pragmatic clinical trial. 148 patients diagnosed with DN will be recruited and randomised 1:1 to a 48-week additional semi-individualised CM treatment programme or standard medical care. Primary end points are the changes in estimated glomerular filtration rate and spot urine albumin-to-creatinine ratio between baseline and treatment end point. Secondary end points include fasting blood glucose, glycated haemoglobin, brain natriuretic peptide, fasting insulin, C peptide, fibroblast growth factor 23, urinary monocyte chemotactic protein-1, cystatin C, nephrin, transforming growth factor-beta 1 and vascular endothelial growth factor. Adverse events are monitored through self-completed questionnaire and clinical visits. Outcomes will be analysed by regression models. Enrolment started in July 2015. Ethics and registration: This protocol is approved by the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster (reference number UW 14-301).
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页数:8
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共 32 条
  • [1] [Anonymous], 2014, IDF DIAB ATL
  • [2] Ban CR, 2008, VASC HEALTH RISK MAN, V4, P575
  • [3] Census and Statistics Department, 2010, 45 DEP CAS
  • [4] Diabetic nephropathy: landmark clinical trials and tribulations
    Chan, Gary C. W.
    Tang, Sydney C. W.
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 (03) : 359 - 368
  • [5] Astragaloside IV improves high glucose-induced podocyte adhesion dysfunction via α3β1 integrin upregulation and integrin-linked kinase inhibition
    Chen, Jianguo
    Gui, Dingkun
    Chen, Yifang
    Mou, Lijun
    Liu, Yi
    Huang, Jianhua
    [J]. BIOCHEMICAL PHARMACOLOGY, 2008, 76 (06) : 796 - 804
  • [6] Astragaloside IV ameliorates diabetic nephropathy involving protection of podocytes in streptozotocin induced diabetic rats
    Chen, Jianguo
    Chen, Yifang
    Luo, Yunling
    Gui, Dingkun
    Huang, Jianhua
    He, Dongyuan
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2014, 736 : 86 - 94
  • [7] Views on traditional Chinese medicine amongst Chinese population: a systematic review of qualitative and quantitative studies
    Chung, Vincent C. H.
    Ma, Polly H. X.
    Lau, Chun Hong
    Wong, Samuel Y. S.
    Yeoh, Eng Kiong
    Griffiths, Sian M.
    [J]. HEALTH EXPECTATIONS, 2014, 17 (05) : 622 - 636
  • [8] ERA-EDTA Registry, 2015, ERA EDTA REG ANN REP, P1
  • [9] Astragaloside IV ameliorates renal injury in streptozotocin-induced diabetic rats through inhibiting NF-κB-mediated inflammatory genes expression
    Gui, Dingkun
    Huang, Jianhua
    Guo, Yongping
    Chen, Jianguo
    Chen, Yifang
    Xiao, Wenzhen
    Liu, Xusheng
    Wang, Niansong
    [J]. CYTOKINE, 2013, 61 (03) : 970 - 977
  • [10] Astragaloside IV, a Novel Antioxidant, Prevents Glucose-Induced Podocyte Apoptosis In Vitro and In Vivo
    Gui, Dingkun
    Guo, Yongping
    Wang, Feng
    Liu, Wei
    Chen, Jianguo
    Chen, Yifang
    Huang, Jianhua
    Wang, Niansong
    [J]. PLOS ONE, 2012, 7 (06):