BARC (Barts Research Centre for Women's Health), Institute of Population Health Sciences, Queen Mary University of London Barts and The London School of Medicine and Dentistry, London, UK.
Department of Statistics and Operational Research, Complutense University of Madrid, Madrid, Spain.
BMJ Open. 2022 Mar 11;12(3):e050110. doi: 10.1136/bmjopen-2021-050110.
To determine the feasibility and acceptability of conducting a randomised trial on the effects of myo-inositol in preventing gestational diabetes in high-risk pregnant women.
A multicentre, double-blind, placebo-controlled, pilot randomised trial with nested qualitative evaluation.
Five inner city UK National Health Service hospitals PARTICIPANTS: Multiethnic pregnant women at 12 and 15 weeks' gestation with risk factors for gestational diabetes.
2 g of myo-inositol or placebo, both included 200 µg folic acid, twice daily until delivery.
Rates of recruitment, randomisation, adherence and follow-up.
Glycaemic indices (including homoeostatic model assessment-insulin resistance HOMA-IR), gestational diabetes (diagnosed using oral glucose tolerance test at 28 weeks and by delivery), maternal, perinatal outcomes, acceptability of intervention and costs.
Of the 1326 women screened, 58% (773/1326) were potentially eligible, and 27% (205/773) were recruited. We randomised 97% (198/205) of all recruited women (99 each in intervention and placebo arms) and ascertained outcomes in 90% of women (178/198) by delivery. The mean adherence was 52% (SD 44) at 28 weeks' and 34% (SD 41) at 36 weeks' gestation. HOMA-IR and serum insulin levels were lower in the myo-inositol vs placebo arm (mean difference -0.6, 95% CI -1.2 to 0.0 and -2.69, 95% CI -5.26 to -0.18, respectively). The study procedures were acceptable to women and healthcare professionals. Women who perceived themselves at high risk of gestational diabetes were more likely to participate and adhere to the intervention. The powder form of myo-inositol and placebo, along with nausea in pregnancy were key barriers to adherence.
A future trial on myo-inositol versus placebo to prevent gestational diabetes is feasible. The intervention will need to be delivered in a non-powder form to improve adherence. There is a signal for efficacy in reducing insulin resistance in pregnancy with myo-inositol.
ISRCTN48872100.
确定肌醇预防高危孕妇妊娠期糖尿病的效果进行随机试验的可行性和可接受性。
多中心、双盲、安慰剂对照、嵌套定性评价的试点随机试验。
英国五家内城国家卫生服务医院。
12 周和 15 周妊娠、有妊娠期糖尿病风险因素的多民族孕妇。
每天两次服用 2g 肌醇或安慰剂,均含有 200μg 叶酸,直至分娩。
招募率、随机化、依从性和随访率。
血糖指数(包括稳态模型评估-胰岛素抵抗 HOMA-IR)、妊娠期糖尿病(28 周时通过口服葡萄糖耐量试验和分娩时诊断)、母婴、围产结局、干预措施的可接受性和成本。
在筛查的 1326 名女性中,58%(773/1326)有潜在资格,27%(205/773)被招募。我们对所有招募的女性(205 名)进行了 97%(198/205)的随机分组(干预组和安慰剂组各 99 名),并通过分娩确定了 90%(178/198)的结局。28 周时的平均依从率为 52%(SD 44),36 周时为 34%(SD 41)。与安慰剂组相比,肌醇组的 HOMA-IR 和血清胰岛素水平较低(平均差异-0.6,95%CI-1.2 至 0.0 和-2.69,95%CI-5.26 至-0.18)。研究程序得到了女性和医疗保健专业人员的认可。认为自己有患妊娠期糖尿病高风险的女性更有可能参与并坚持干预措施。肌醇和安慰剂的粉末形式以及妊娠期间的恶心是影响依从性的关键障碍。
肌醇预防妊娠期糖尿病的未来试验是可行的。该干预措施需要以非粉末形式提供,以提高依从性。肌醇在降低妊娠期间胰岛素抵抗方面有一定的疗效信号。
ISRCTN48872100。