Rademaker Doortje, de Wit Leon, van der Wel Anne, van den Akker Eline, Braams-Lisman Babette, Dullemond Remke, Evers Inge, Galjaard Sander, Hermsen Brenda, van Hoorn Marion, Huisjes Anjoke, Kaandorp Joepe, Lub Annemiek, Lunshof Simone, van der Made Flip, Nijman Remco, van Laar Judith, Vollebregt Karlijn, Velzel Joost, Vlemmix Floortje, Westerhuis Michelle, Wijnberger Lia, Wouters Maurice, Zwart Joost, Bosmans Judith, Bossuyt Patrick, Duijnhoven Ruben, Lopriore Enrico, de Miranda Esteriek, Verhoeven Corine, Mol Ben Willem, Franx Arie, DeVries J Hans, van Rijn Bas, Painter Rebecca
Department of Obstetrics and Gynecology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
BMC Pregnancy Childbirth. 2025 Feb 17;25(1):173. doi: 10.1186/s12884-025-07230-x.
Gestational diabetes mellitus (GDM), or hyperglycemia first diagnosed in pregnancy, affects 7-10% of all pregnancies worldwide. Perinatal risk rises with increasing glycemia at oral glucose tolerance test (OGTT). The new (2013) WHO criteria recommend a lower fasting, and a higher post-load threshold for GDM diagnosis in comparison to the old (1999) WHO criteria. To date, however, outcomes of GDM treatment for those affected by the altered diagnostic criteria, has not been well investigated. We hypothesized that intensive GDM treatment according to the new (2013) GDM criteria would result in a reduction in infants with birth weight > 90th centile (large for gestational age, LGA), in comparison to treatment according to the old criteria (1999).
The TANGO-DM trial is an open label, multicenter randomized controlled trial. Participants are pregnant with a gestational age between 16 + 0 and 32 + 0 weeks, who underwent a 1-step venous 2- or 3-point 75-gram oral OGTT, were eligible if they had glucose concentrations discordant between the old (1999) and the new (2013) criteria. After informed consent, women are randomized to either intensive GDM treatment, consisting of dietary advice and glucose monitoring and, if euglycemia is not reached, antihyperglycemic agents, or normal obstetric care without GDM treatment. The primary outcome is large-for-gestational-age infants (birth weight > 90th percentile). Secondary outcome measures include maternal complications, obstetric complications, neonatal complications, obstetric interventions, quality of life, and healthcare and societal costs. Outcomes will be analyzed according to the intention-to-treat principle. The study is powered to detect a reduction in LGA from 16% in the untreated to 10% in the treated group, which requires 1032 participants (516 per arm; alpha-error 5% for 80% power).
The TANGO-DM trial will provide high-level evidence to support or refute the use of the new 2013 WHO diagnostic criteria in terms of their ability to lower the number of large for gestational age infants and/or improve maternal and perinatal outcomes and/or costs in women with gestational diabetes.
Central Committee on Research Involving Human Subjects (CCMO) (NL63013.018.18). Registered on 22 September 2018.
妊娠期糖尿病(GDM),即首次在孕期诊断出的高血糖症,影响着全球7% - 10%的妊娠。口服葡萄糖耐量试验(OGTT)时血糖水平越高,围产期风险越高。与旧的(1999年)世界卫生组织标准相比,新的(2013年)世界卫生组织标准推荐更低的空腹血糖值和更高的负荷后血糖阈值用于GDM诊断。然而,迄今为止,对于受诊断标准改变影响的GDM患者的治疗结果尚未得到充分研究。我们假设,与按照旧标准(1999年)治疗相比,根据新的(2013年)GDM标准进行强化GDM治疗将使出生体重>第90百分位数(大于胎龄儿,LGA)的婴儿数量减少。
TANGO - DM试验是一项开放标签、多中心随机对照试验。参与者孕周在16 + 0至32 + 0周之间,接受了一步静脉2点或3点75克口服OGTT,如果其血糖浓度在旧的(1999年)和新的(2013年)标准之间不一致则符合条件。在获得知情同意后,女性被随机分为两组,一组接受强化GDM治疗,包括饮食建议和血糖监测,如果未达到血糖正常,则使用降糖药物;另一组接受不进行GDM治疗的常规产科护理。主要结局是大于胎龄儿(出生体重>第90百分位数)。次要结局指标包括母体并发症、产科并发症、新生儿并发症、产科干预、生活质量以及医疗保健和社会成本。结局将根据意向性分析原则进行分析。该研究旨在检测LGA发生率从未治疗组的16%降至治疗组的10%,这需要1032名参与者(每组516名;80%检验效能下α错误为5%)。
TANGO - DM试验将提供高级别证据,以支持或反驳2013年世界卫生组织新诊断标准在降低妊娠期糖尿病女性中大于胎龄儿数量和/或改善母婴结局和/或成本方面的应用。
涉及人类受试者研究中央委员会(CCMO)(NL63013.018.18)。于2018年9月22日注册。