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Dulaglutide as an Effective Replacement for Prandial Insulin in Kidney Transplant Recipients with Type 2 Diabetes Mellitus: A Retrospective Review.

Diabetes Metab J · 2021

Last updated 2026-05-28

In a study of 37 kidney transplant recipients with type 2 diabetes, switching from multiple daily insulin injections to a combination of basal insulin and once-weekly dulaglutide maintained similar blood sugar control (HbA1c of 7.1% vs. 7.0%) over 6 months. The change also led to a small reduction in fasting blood sugar by 9.7 mg/dL, a weight loss of 4.9 kg, and a decrease in basal insulin dose by 9.52 units.

AI summary of the abstract below.

JournalDiabetes Metab J, 2021
Citations17
Relative citation ratio1.06
NIH percentile52
Molecules dulaglutide
Conditions studied Type 2 Diabetes, Chronic Kidney Disease

Abstract

Dulaglutide, a weekly injectable glucagon-like peptide-1 receptor agonist, has demonstrated effectiveness when combined with basal insulin. We examined whether the efficacy of dulaglutide is comparable to that of prandial insulin in kidney transplant (KT) recipients with type 2 diabetes mellitus (T2DM) undergoing multiple daily insulin injection (MDI) therapy. Thirty-seven patients, who switched from MDI therapy to basal insulin and dulaglutide, were retrospectively analyzed. Changes in glycosylated hemoglobin (HbA1c) and fasting plasma glucose (FPG) levels, body weight, and basal insulin dose were evaluated over 6 months. Dulaglutide was comparable to three injections of prandial insulin in terms of glycemic control (HbA1c 7.1% vs. 7.0%; 95% confidence interval [CI], -0.53 to 0.28; P=0.53). The basal insulin and dulaglutide combination resulted in a reduction in FPG levels by 9.7 mg/dL (95% CI, 2.09 to 41.54; P=0.03), in body weight by 4.9 kg (95% CI, 2.87 to 6.98; P<0.001), and in basal insulin dose by 9.52 IU (95% CI, 5.80 to 3.23; P<0.001). Once-weekly dulaglutide may be an effective alternative for thrice-daily prandial insulin in KT recipients with T2DM currently receiving MDI therapy.

Verbatim abstract via PubMed 33535737 ↗

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