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胰岛素原在妊娠期糖尿病的识别和危险分层中的作用:一项前瞻性、纵向队列研究的研究方案。

Proinsulin in the identification and risk stratification of gestational diabetes mellitus: study protocol for a prospective, longitudinal cohort study.

机构信息

Diabetes Research Group, Swansea University, Swansea, UK.

出版信息

BMJ Open. 2018 Aug 29;8(8):e022571. doi: 10.1136/bmjopen-2018-022571.

Abstract

INTRODUCTION

Gestational diabetes mellitus (GDM) is a common metabolic disorder occurring in up to 10% of pregnancies in the western world. Most women with GDM are asymptomatic; therefore, it is important to screen, diagnose and manage the condition as it is associated with an increased risk of maternal and perinatal complications. Diagnosis of GDM is made in the late second trimester or early third trimester because accurate diagnosis or risk stratification in the first trimester is still lacking. An increase in serum proinsulin may be seen earlier in pregnancy and before a change in glycaemic control can be identified. This study will aim to establish if fasting proinsulin concentrations at 16-18 weeks gestation will help to identify or risk stratify high-risk pregnant women with GDM.

METHODS AND ANALYSIS

This is a prospective, longitudinal cohort study. Two oral glucose tolerance tests will be carried out at 16-18 and 24-28 weeks gestation in 200 pregnant women with at least one risk factor for GDM (body mass index>30 kg/m, previous macrosomic baby (>4.5 kg), previous gestational diabetes, first degree relative with type 2 diabetes mellitus) recruited from antenatal clinics. Blood samples will be taken fasting and at 30 min, 1 and 2 hours following the 75 g glucose load. In addition, a fasting blood sample will be taken 6-weeks post delivery. All samples will be analysed for glucose, insulin, C peptide and proinsulin. Recruitment began in November 2017. Optimal cut-off points for proinsulin to diagnose gestational diabetes according to National Institute for Health and Care Excellence (2015) criteria will be established by the receiver operating characteristic plot and sensitivity and specificity will be calculated to assess the diagnostic accuracy of proinsulin at 16-18 weeks gestation.

ETHICS AND DISSEMINATION

This study received ethical approval from the Wales Research Ethics Committee (Panel 6) (Ref. 17/WA/0194). Data will be presented at international conferences and published in peer-reviewed journals.

TRIAL REGISTRATION NUMBER

ISRCTN16416602; Pre-results.

摘要

简介

妊娠糖尿病(GDM)是一种常见的代谢紊乱疾病,在西方世界高达 10%的妊娠中出现。大多数患有 GDM 的女性无症状;因此,筛查、诊断和管理这种疾病非常重要,因为它与母婴围产期并发症的风险增加有关。GDM 的诊断是在妊娠晚期或妊娠早期进行的,因为在妊娠早期仍然缺乏准确的诊断或风险分层。在血糖控制发生变化之前,血清前胰岛素可能会更早升高。本研究旨在确定妊娠 16-18 周时空腹前胰岛素浓度是否有助于识别或对 GDM 高危孕妇进行风险分层。

方法和分析

这是一项前瞻性、纵向队列研究。将在 200 名至少有一个 GDM 危险因素(BMI>30kg/m2、既往巨大儿(>4.5kg)、既往妊娠糖尿病、2 型糖尿病一级亲属)的孕妇中进行两次口服葡萄糖耐量试验,在妊娠 16-18 周和 24-28 周时进行。在服用 75g 葡萄糖负荷后 30 分钟、1 小时和 2 小时采集空腹和 30 分钟、1 小时和 2 小时的血样。此外,还将在分娩后 6 周采集空腹血样。所有样本均分析血糖、胰岛素、C 肽和前胰岛素。招募工作于 2017 年 11 月开始。根据国家卫生与保健卓越研究所(2015 年)标准,通过接受者操作特征图确定前胰岛素诊断妊娠糖尿病的最佳截断点,并计算敏感性和特异性,以评估妊娠 16-18 周时前胰岛素的诊断准确性。

伦理和传播

本研究获得了威尔士研究伦理委员会(第 6 小组)的伦理批准(参考号 17/WA/0194)。数据将在国际会议上展示,并发表在同行评议的期刊上。

试验注册号

ISRCTN6416602;预结果。

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