Kidney disease end points in a pooled analysis of individual patient-level data from a large clinical trials program of the dipeptidyl peptidase 4 inhibitor linagliptin in type 2 diabetes

Mark E. Cooper, Vlado Perkovic, Janet B. McGill, Per-Henrik Groop, Christoph Wanner, Julio Rosenstock, Uwe Hehnke, Hans Juergen Woerle, Maximilian Von Eynatten

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Abstract

Background: Although assessment of cardiovascular safety is mandated by regulatory agencies for the development of new drugs to treat type 2 diabetes, evaluation of their renal safety has been relatively neglected. Study Design: Individual patient-level data pooled analysis of 13 phase 2 or 3 randomized, double-blind, placebo-controlled, clinical trials of the dipeptidyl peptidase 4 inhibitor linagliptin. Setting & Participants: Participants who participated in any of 13 randomized clinical trials and fulfilled predefined inclusion/exclusion criteria, such as being drug-naive (hemoglobin A1c, 7.0%-11.0% [53-97 mmol/mol]) or being on background glucose-lowering therapy (hemoglobin A1c, 6.5%-10.5% [48-91 mmol/mol]). Intervention: Of 5,466 consenting individuals with inadequately controlled type 2 diabetes, 3,505 received linagliptin, 5 mg/d, and 1,961 received placebo. Outcomes: The primary kidney disease outcome was defined as first occurrence during the study of 6 predefined safety end points: new onset of moderate elevation of albuminuria (urinary albumin-creatinine ratio [ACR] >30 mg/g with baseline values & 30 mg/g), new onset of severe elevation of albuminuria (ACR > 300 mg/g with baseline values 300 mg/g), reduction in kidney function (serum creatinine increase to 250 μmol/L from a baseline value < 250 μmol/L), halving of estimated glomerular filtration rate (loss of baseline eGFR > 50%), acute renal failure (ascertained from diagnostic codes), or death from any cause. Measurements: Albuminuria was assessed using ACR. GFR was estimated using the CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) equation. Results: Cumulative exposure (person-years) was 1,751 for linagliptin and 1,055 for placebo. The primary composite outcome occurred in 448 (12.8%) and 306 (15.6%) participants in the linagliptin and placebo groups, respectively. Linagliptin treatment significantly reduced the hazard of kidney disease events by 16% compared with placebo (HR, 0.84; 95% CI, 0.72-0.97; P = 0.02). Limitations Retrospective and hypothesis-generating study involving short- to midterm clinical trials. Conclusions: Linagliptin was not associated with increased kidney disease risk in patients with type 2 diabetes. The potential of this drug to improve kidney disease outcomes warrants further investigation.

Original languageEnglish
Pages (from-to)441-449
Number of pages9
JournalAmerican Journal of Kidney Diseases
Volume66
Issue number3
DOIs
Publication statusPublished - Sep 2015
Externally publishedYes

Keywords

  • albuminuria
  • glucose control
  • glucose-lowering therapy
  • hyperglycemia
  • Index Words Dipeptidyl peptidase 4 (DPP-4) inhibition
  • kidney disease end points
  • linagliptin
  • pooled analysis
  • renal function
  • renal risk
  • type 2 diabetes mellitus (T2DM)

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