Sitagliptin Versus Placebo to Reduce the Incidence and Severity of Posttransplant Diabetes Mellitus After Kidney Transplantation-A Single-center, Randomized, Double-blind Controlled Trial

Transplantation. 2023 May 1;107(5):1180-1187 doi: 10.1097/TP.0000000000004373.
Abstract
BACKGROUND:

Postkidney transplant diabetes mellitus (PTDM) affects cardiovascular, allograft, and recipient health. We tested whether early intervention with sitagliptin for hyperglycemia (blood glucose >200 mg/dL) within the first week of transplant and discontinued at 3 mo could prevent development of PTDM in patients without preexisting diabetes.

METHODS:

The primary efficacy objective was to improve 2-h oral glucose tolerance test (OGTT) by > 20 mg/dL at 3 mo posttransplant. The secondary efficacy objective was to prevent new onset PTDM, defined as a normal OGTT at 3 mo.

RESULTS:

Sixty-one patients consented, and 50 patients were analyzed. The 3-mo 2-h OGTT (end of treatment) was 141.00 ± 62.44 mg/dL in the sitagliptin arm and 165.22 ± 72.03 mg/dL ( P = 0.218) in the placebo arm. The 6-mo 2-h OGTT (end of follow-up) was 174.38 ± 77.93 mg/dL in the sitagliptin arm and 171.86 ± 83.69 ng/dL ( P = 0.918) in the placebo arm. Mean intrapatient difference between 3- and 6-mo 2-h OGTT in the 3-mo period off study drug was 27.56 + 52.74 mg/dL in the sitagliptin arm and -0.14 + 45.80 mg/dL in the placebo arm ( P = 0.0692). At 3 mo, 61.54% of sitagliptin and 43.48% of placebo patients had a normal 2-h OGTT ( P = 0.2062), with the absolute risk reduction 18.06%. There were no differences in HbA1c at 3 or 6 mo between sitagliptin and placebo groups. Participants tolerated sitagliptin well.

CONCLUSIONS:

Although this study did not show a significant difference between groups, it can inform future studies in the use of sitagliptin in the very early posttransplant period.

CET Conclusion
Reviewer: Mr Keno Mentor, Centre for Evidence in Transplantation, Nuffield Department of Surgical Sciences University of Oxford
Conclusion: This double-blind randomised control trial investigated the efficacy of sitagliptin to prevent and treat PTDM. Although the treatment arm showed improved results for both primary and secondary efficacy endpoints at 3 months, neither reached statistical significance. Furthermore, these differences in outcome were not found at 6 months. Safety outcome data was reassuring, with no differences in the rates of acute rejection or serious adverse events reported. This trial was limited by a small sample size and failed to demonstrate a benefit in the use of sitagliptin in the prevention or treatment of PTDM. The authors suggested that the analysis could be used to guide larger trials.
Methodological quality
Jadad score 4
Allocation concealment YES
Data analysis PER PROTOCOL
Study Details
Aims: This study aimed to examine whether sitagliptin was effective in reducing the incidence and severity of posttransplant diabetes mellitus (PTDM) in kidney transplant recipients without preexisting diabetes.
Interventions: Participants were randomised to either the sitagliptin arm or the placebo arm.
Participants: 61 kidney transplant recipients.
Outcomes: The primary efficacy outcome was the assessment of improvement in 2-h oral glucose tolerance test (OGTT) by >20 mg/dL at 3-months posttransplantation. The secondary efficacy outcome was the prevention of new onset PTDM.
Follow Up: 6 months
Metadata
Funding: Industry funding
Publication type: Randomized Controlled Trial, Randomised Controlled Trial
Trial registration: ClinicalTrials.gov - NCT01928199
Organ: Kidney
Language: English
Author email: delossantos@wustl.edu
MeSH terms: Humans; Sitagliptin Phosphate; Hypoglycemic Agents; Diabetes Mellitus, Type 2; Dipeptidyl-Peptidase IV Inhibitors; Kidney Transplantation; Incidence; Blood Glucose; Double-Blind Method; Treatment Outcome; TS63EW8X6F (Sitagliptin Phosphate); 0 (Hypoglycemic Agents); 0 (Dipeptidyl-Peptidase IV Inhibitors); 0 (Blood Glucose)