Clinical Trials on Diabetic Nephropathy: A Cross-Sectional Analysis

被引:4
作者
Modafferi, Sergio [1 ,2 ]
Ries, Markus [1 ]
Calabrese, Vittorio [2 ]
Schmitt, Claus. P. [1 ]
Nawroth, Peter [3 ,4 ,5 ]
Kopf, Stefan [3 ,4 ]
Peters, Verena [1 ]
机构
[1] Heidelberg Univ, Ctr Pediat & Adolescent Med, Heidelberg, Germany
[2] Univ Catania, Dept Biomed & Biotechnol Sci, Sch Med, Catania, Italy
[3] Heidelberg Univ, Dept Endocrinol Diabetol & Clin Chem, Univ Heidelberg Hosp, Heidelberg, Germany
[4] Deutsch Zentrum Diabetesforsch eV DZD, Neuherberg, Germany
[5] Helmholtz Zentrum, Joint Heidelberg IDC Translat Diabet Program, Inst Diabet & Canc, Neuherberg, Germany
关键词
ACE inhibitors; Angiotensin-II receptors; ClinicalTrials; gov; Diabetes mellitus; Diabetic nephropathy; Dipeptidyl-peptidase-4-inhibitors; Phase III clinical trials; SEVERE RENAL IMPAIRMENT; CHRONIC KIDNEY-DISEASE; LONG-TERM EFFICACY; DOUBLE-BLIND; MICROVASCULAR OUTCOMES; OXIDATIVE STRESS; TYPE-2; MICROALBUMINURIA; PROGRESSION; MELLITUS;
D O I
10.1007/s13300-018-0551-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionTreatment options and decisions are often based on the results of clinical trials. We have evaluated the public availability of results from completed, registered phase III clinical trials on diabetic nephropathy and current treatment options.MethodsThis was a cross-sectional analysis in which STrengthening the Reporting of OBservational studies in Epidemiology criteria were applied for design and analysis. In June 2017, 34 completed phase III clinical trials on diabetic nephropathy in the ClinicalTrials. gov registry were identified and matched to publications in the ClinicalTrials.gov registry and to those in the PubMed and Google Scholar databases. If no publication was identified, the principal investigator was contacted. The ratio of published and non-published studies was calculated. Various parameters, including study design, drugs, and comparators provided, were analyzed.ResultsDrugs/supplements belonged to 26 different categories of medications, with the main ones being angiotensin-converting enzyme inhibitors, angiotensin-II receptors blockers, and dipeptidyl-peptidase-4-inhibitors. Among the trials completed before 2016 (n=32), 22 (69%) were published, and ten (31%) remained unpublished. Thus, data on 11 different interventions and more than 1000 patients remained undisclosed. Mean time to publication was 26.5months, which is longer than the time constrictions imposed by the U.S. Food and Drug Administration Amendments Act. Most trials only showed weak effects on micro- and macroalbuminuria, with an absolute risk reduction of 1.0 and 0.3%, respectively, and the number needed to treat varied between 91 and 333, without any relevant effect on end-stage-renal disease by intensive glucose-lowering treatment. Comparison of the results, however, was difficult since study design, interventions, and the renal outcome parameters vary greatly between the studies.ConclusionDespite the financial and human resources involved and the relevance for therapeutic guidelines and clinical decisions, about one-third of phase III clinical trials on diabetic nephropathy remain unpublished. Interventions used in published trials showed a low efficacy on renal outcome.FundingDeutsche Forschungsgemeinschaft (DFG): SFB 1118.
引用
收藏
页码:229 / 243
页数:15
相关论文
共 48 条
[1]   Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables [J].
Ahlqvist, Emma ;
Storm, Petter ;
Karajamaki, Annemari ;
Martinell, Mats ;
Dorkhan, Mozhgan ;
Carlsson, Annelie ;
Vikman, Petter ;
Prasad, Rashmi B. ;
Aly, Dina Mansour ;
Almgren, Peter ;
Wessman, Ylva ;
Shaat, Nael ;
Spegel, Peter ;
Mulder, Hindrik ;
Lindholm, Eero ;
Melander, Olle ;
Hansson, Ola ;
Malmqvist, Ulf ;
Lernmark, Ake ;
Lahti, Kaj ;
Forsen, Tom ;
Tuomi, Tiinamaija ;
Rosengren, Anders H. ;
Groop, Leif .
LANCET DIABETES & ENDOCRINOLOGY, 2018, 6 (05) :361-369
[2]  
Anantharaman R, 2011, Indian J Med Res, V134, P658, DOI 10.4103/0971-5916.90991
[3]   Angiotensin-receptor blockade versus converting-enzyme inhibition in type 2 diabetes and nephropathy [J].
Barnett, AH ;
Bain, SC ;
Bouter, P ;
Karlberg, B ;
Madsbad, S ;
Jervell, J ;
Mustonen, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (19) :1952-1961
[4]   Publication status of completed registered studies in paediatric appendicitis: a cross-sectional analysis [J].
Breil, Thomas ;
Boettcher, Michael ;
Hoffmann, Georg F. ;
Ries, Markus .
BMJ OPEN, 2018, 8 (07)
[5]   Diabetic nephropathy: landmark clinical trials and tribulations [J].
Chan, Gary C. W. ;
Tang, Sydney C. W. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 (03) :359-368
[6]   The effect of sodium glucose cotransporter 2 inhibition with empagliflozin on microalbuminuria and macroalbuminuria in patients with type 2 diabetes [J].
Cherney, David ;
Lund, Soren S. ;
Perkins, Bruce A. ;
Groop, Per-Henrik ;
Cooper, Mark E. ;
Kaspers, Stefan ;
Pfarr, Egon ;
Woerle, Hans J. ;
von Eynatten, Maximilian .
DIABETOLOGIA, 2016, 59 (09) :1860-1870
[7]   Effects of pulsatile intravenous insulin therapy on the progression of diabetic nephropathy [J].
Dailey, GE ;
Boden, GH ;
Creech, RH ;
Johnson, DG ;
Gleason, RE ;
Kennedy, FP ;
Weinrauch, LA ;
Weir, M ;
D'Elia, JA .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (11) :1491-1495
[8]   Intensive Diabetes Therapy and Glomerular Filtration Rate in Type 1 Diabetes [J].
de Boer, Ian H. ;
Sun, Wanjie ;
Cleary, Patricia A. ;
Lachin, John M. ;
Molitch, Mark E. ;
Steffes, Michael W. ;
Zinman, Bernard .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (25) :2366-2376
[9]   Temporal Trends in the Prevalence of Diabetic Kidney Disease in the United States [J].
de Boer, Ian H. ;
Rue, Tessa C. ;
Hall, Yoshio N. ;
Heagerty, Patrick J. ;
Weiss, Noel S. ;
Himmelfarb, Jonathan .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2011, 305 (24) :2532-2539
[10]   FACTORS INFLUENCING PUBLICATION OF RESEARCH RESULTS - FOLLOW-UP OF APPLICATIONS SUBMITTED TO 2 INSTITUTIONAL REVIEW BOARDS [J].
DICKERSIN, K ;
MIN, YI ;
MEINERT, CL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 267 (03) :374-378