Etanercept Treatment in Children With New-Onset Type 1 Diabetes: Pilot Randomized, Placebo-Controlled, Double-Blind Study
Year: 2009
Type: article
Study designs: Randomized Controlled Trial, Clinical Trial
Abstract: OBJECTIVE — To gather preliminary data on the feasibility and efficacy of etanercept therapy to prolong endogenous insulin production in pediatric patients with newly diagnosed type 1 diabetes. RESEARCH DESIGN AND METHODS — This was a 24-week double-blind, randomized, placebo-controlled study conducted at the Diabetes Center, Women and Children’s Hospital of Buffalo. Eighteen subjects (11 male and 7 female, aged 7.8–18.2 years) were randomly assigned to receive either placebo or etanercept. Inclusion criteria included age 3–18 years, GAD-65 and/or islet cell antibody positivity, A1C �6%, three insulin injections per day, white blood cell count 3,000–10,000, platelets �100,000, and normal liver and renal function. Intention-to-treat analysis was used. RESULTS — A1C at week 24 was lower in the etanercept group (5.91 � 0.5%) compared with that in the placebo group (6.98 � 1.2%; P � 0.05) with a higher percent decrease from baseline than in the placebo group (etanercept 0.41 � 0.1 vs. placebo 0.18 � 0.21; P � 0.01). The percent change in C-peptide area under the curve from baseline to week 24 showed a 39% increase in the etanercept group and a 20 % decrease in the placebo group (P � 0.05). From
Source: Diabetes Care
DOI: 10.2337/dc09-1571
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: hybrid
Funder: Amgen
OpenAlex ID: W2126942673
