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国际妊娠糖尿病协会标准用于妊娠期糖尿病筛查和诊断的影响。

The impact of adoption of the international association of diabetes in pregnancy study group criteria for the screening and diagnosis of gestational diabetes.

机构信息

Department of Obstetrics and Gynecology, St Michael's Hospital, University of Toronto Faculty of Medicine, Toronto, ON, Canada.

Department of Laboratory Medicine, St Michael's Hospital, University of Toronto Faculty of Medicine, Toronto, ON, Canada.

出版信息

Am J Obstet Gynecol. 2015 Feb;212(2):224.e1-9. doi: 10.1016/j.ajog.2014.08.027. Epub 2014 Aug 27.

Abstract

OBJECTIVE

The objective of the study was to compare the International Association of Diabetes in Pregnancy Study Group (IADPSG) and the Canadian Diabetes Association (CDA) criteria for the diagnosis of gestational diabetes mellitus (GDM).

STUDY DESIGN

This was a retrospective cohort study involving all pregnant women who underwent screening for GDM at a tertiary medical center between 2008 and 2011. Diagnosis of GDM during the study period was based on the CDA 2008 recommendations of universal screening with a 50 g oral glucose challenge test (GCT; threshold 140 mg/dL [7.8 mmol/L]) and a diagnostic test using a fasting 2 hour, 75 g oral glucose tolerance test (OGTT). Diagnosis of GDM required the presence of 2 or more abnormal values, whereas a single abnormal value was diagnostic of impaired glucose intolerance. Because the OGTT thresholds based on the IADPSG criteria are lower than the CDA 2008 thresholds (92 mg/dL [5.1 mmol], 180 mg/dL [10.0 mmol/L], and 153 mg/dL [8.5 mmol/L]), we identified a group of women who would have been diagnosed as GDM based on the IADPSG criteria but not the CDA 2008 criteria (OGTT-IADPSG group). The pregnancy outcome of that group as well as that of women with a positive OGTT according to the CDA 2008 criteria (OGTT-CDA group) and women with a negative OGTT (OGTT-NEGATIVE group) was compared with that of a control group consisting of women with a negative GCT (GCT-NEGATIVE group).

RESULTS

Overall, 5429 women were eligible for the study, of which 4183 were included in the GCT-NEGATIVE group, 526 in the OGTT-NEGATIVE group, 155 in the OGTT-IADPSG group, and 385 in the OGTT-CDA group. Applying the IADPSG criteria to the study population would increase the rate of GDM from 3.2% (7.3% when including impaired glucose intolerance) to 10.3%. The majority of the increase in the rate of GDM was attributed to the use of a single abnormal value to define GDM (5.3% increase) rather than the use of lower threshold values (1.8% increase). Of the 3 threshold values, the lower 1 hour threshold was the most significant contributor to the higher GDM rate. A positive OGTT in both the OGTT-IADPSG group and the OGTT-CDA group was independently associated with a higher rate of the composite adverse outcome (odds ratio, 1.4; 95% confidence interval, 1.1-1.9).

CONCLUSION

The use of the IADPSG criteria instead of the CDA criteria would result in a considerable increase in the rate of GDM, but this also appears to identify additional women at similar risk of adverse pregnancy outcome. Further studies are needed to determine whether this observation persists after controlling for confounders such as body mass index as well as whether treatment in these cases would improve perinatal outcome.

摘要

目的

本研究旨在比较国际妊娠糖尿病研究组(IADPSG)和加拿大糖尿病协会(CDA)的诊断标准,以评估妊娠糖尿病(GDM)的诊断。

研究设计

这是一项回顾性队列研究,纳入了 2008 年至 2011 年期间在一家三级医疗中心接受 GDM 筛查的所有孕妇。研究期间 GDM 的诊断基于 CDA 2008 年的建议,即采用 50g 口服葡萄糖耐量试验(GCT;阈值 140mg/dL[7.8mmol/L])进行普遍筛查,并采用禁食 2 小时、75g 口服葡萄糖耐量试验(OGTT)进行诊断性检测。GDM 的诊断需要 2 项或更多异常值,而单次异常值则提示糖耐量受损。由于基于 IADPSG 标准的 OGTT 阈值低于 CDA 2008 年的阈值(92mg/dL[5.1mmol/L]、180mg/dL[10.0mmol/L]和 153mg/dL[8.5mmol/L]),我们确定了一组根据 IADPSG 标准但不符合 CDA 2008 年标准(OGTT-IADPSG 组)诊断为 GDM 的女性。该组的妊娠结局以及根据 CDA 2008 年标准(OGTT-CDA 组)呈阳性 OGTT 和 OGTT 阴性(OGTT-NEGATIVE 组)的女性的妊娠结局与阴性 GCT(GCT-NEGATIVE 组)的对照组进行了比较。

结果

总体而言,共有 5429 名女性符合研究条件,其中 4183 名女性纳入 GCT-NEGATIVE 组,526 名女性纳入 OGTT-NEGATIVE 组,155 名女性纳入 OGTT-IADPSG 组,385 名女性纳入 OGTT-CDA 组。在研究人群中应用 IADPSG 标准将 GDM 的发生率从 3.2%(包括糖耐量受损时为 7.3%)提高到 10.3%。GDM 发生率的增加主要归因于使用单一异常值来定义 GDM(增加 5.3%),而不是使用较低的阈值(增加 1.8%)。在这 3 个阈值中,较低的 1 小时阈值是导致 GDM 发生率升高的最主要因素。OGTT-IADPSG 组和 OGTT-CDA 组的阳性 OGTT 与复合不良结局的发生率较高独立相关(比值比,1.4;95%置信区间,1.1-1.9)。

结论

与 CDA 标准相比,使用 IADPSG 标准会导致 GDM 发生率显著增加,但这似乎也能识别出具有相似不良妊娠结局风险的额外女性。需要进一步的研究来确定这种观察结果在控制了肥胖指数等混杂因素后是否仍然存在,以及在这些情况下进行治疗是否能改善围产期结局。

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