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Faster-acting insulin aspart versus insulin aspart in the treatment of type 1 or type 2 diabetes during pregnancy and post-delivery (CopenFast): an open-label, single-centre, randomised controlled trial

医学 门冬氨酸胰岛素 打开标签 2型糖尿病 1型糖尿病 随机对照试验 内科学 怀孕 胰岛素 糖尿病 内分泌学 生物 遗传学
作者
Sidse Kjærhus Nørgaard,Julie Carstens Søholm,Elisabeth R. Mathiesen,Kirsten Nørgaard,Tine D. Clausen,Pernille Holmager,Nicoline Callesen,Peter Damm,Lene Ringholm
出处
期刊:The Lancet Diabetes & Endocrinology [Elsevier BV]
卷期号:11 (11): 811-821 被引量:11
标识
DOI:10.1016/s2213-8587(23)00236-x
摘要

Background Faster-acting insulin aspart (faster aspart) is considered safe for use during pregnancy and breastfeeding but has not been evaluated in this population. We aimed to evaluate the effect of faster aspart versus insulin aspart on fetal growth, in women with type 1 or type 2 diabetes during pregnancy and post-delivery. Methods This open-label, single-centre, superiority trial was conducted at Rigshospitalet, Copenhagen, Denmark. Participants aged 18 years or older with type 1 or type 2 diabetes were stratified by diabetes type and insulin treatment modality (multiple daily injections or insulin pump), randomly assigned 1:1 to faster aspart or insulin aspart, from 8 weeks and 0 days (8+0) of gestation to 13+6 weeks of gestation, and followed up until 3 months post-delivery. Primary outcome was infant birthweight SD score. Secondary outcomes included HbA1c as well as maternal and fetal outcomes in all participants during the trial. This trial is registered with ClinicalTrials.gov, NCT03770767. Findings Between Nov 11, 2019 and May 10, 2022, 109 participants were included in the faster aspart group and 107 in the insulin aspart group. Primary outcome data were available in 203 (94%) of 216 participants, and no participants discontinued treatment during the trial. Mean birthweight SD score was 1·0 (SD 1·4) in the faster aspart group versus 1·2 (1·3) in the insulin aspart group; estimated treatment difference –0·22 [–0·58 to 0·14]; p=0·23. At 33 weeks of gestation, mean HbA1c was 42 mmol/mol (SD 6 mmol/mol; 6·0% [SD 0·9%]) versus 43 mmol/mol (SD 7 mmol/mol; 6·1% [SD 1·2%]); estimated treatment difference –1·01 (–2·86 to 0·83), p=0·28. No additional safety issues were observed with faster aspart compared with insulin aspart. Interpretation Treatment with faster aspart resulted in similar fetal growth and HbA1c, relative to insulin aspart, in women with type 1 or type 2 diabetes. Faster aspart can be used in women with type 1 or type 2 diabetes during pregnancy and post-delivery with no additional safety issues. Funding Novo Nordisk. Translation For the Danish translation of the abstract see Supplementary Materials section.
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