Corcoran Siobhan M, Achamallah Natalie, Loughlin John O', Stafford Philip, Dicker Pat, Malone Fergal D, Breathnach Fionnuala
RCSI Department of Obstetrics and Gynaecology, Ireland.
RCSI Department of Obstetrics and Gynaecology, Ireland.
Eur J Obstet Gynecol Reprod Biol. 2018 Mar;222:7-12. doi: 10.1016/j.ejogrb.2017.12.051. Epub 2018 Jan 1.
Screening and diagnosis of gestational diabetes (GDM) has been a source of controversy. The prevalence has increased in line with an obesity epidemic and a trend towards delayed child-bearing. Treatment of even modest glycaemic impairment in pregnancy has been shown to be beneficial in preventing its clinical sequalae. However the cumbersome nature and timing of the oral glucose tolerance test coupled with debate around universal versus risk factor based screening have been problematic. This group aimed to investigate a panel of biomarkers which have shown promise in the literature to predict GDM from the first trimester in a group of high risk women.
Serum samples were drawn on 248 women deemed at risk of GDM before 15 weeks' gestation to measure C-reactive protein, sex hormone binding globulin, adiponectin and 1,5 anhydroglucitol. Patients underwent an oral glucose tolerance test as per IADPSG criteria at 28 weeks' gestation. Multiple logistic regression was used to examine the link between incidence of GDM and early pregnancy serum biomarkers.
Adiponectin levels in the first trimester are independently linked to the risk of GDM. Serum adiponectin <8.9 μg/ml gives an odds ratio of 3.3 for GDM.Mean 1,5 AG levels are significantly lower in those that go on to develop GDM. SHBG levels measured in the first trimester were linked to the risk of GDM. However, this was no longer statistically significant once BMI, ethnicity and family history were taken into consideration. First trimester measurement of CRP is not a useful indicator of GDM risk.
First trimester measurement of Adiponectin and 1,5 Anhydroglucitol are potential early biomarkers for the later onset of GDM. Risk stratification using these biomarkers may facilitate early diagnosis and management of GDM to mitigate against its complications.
妊娠期糖尿病(GDM)的筛查与诊断一直存在争议。其患病率随着肥胖流行以及生育推迟趋势而上升。已表明孕期即使是轻度血糖受损的治疗对于预防其临床后遗症是有益的。然而,口服葡萄糖耐量试验操作繁琐且时机难以把握,同时围绕普遍筛查与基于风险因素的筛查的争论也存在问题。该团队旨在研究一组生物标志物,这些生物标志物在文献中已显示出在一组高危女性中从孕早期预测GDM的前景。
在妊娠15周前抽取248名被认为有GDM风险的女性的血清样本,以测量C反应蛋白、性激素结合球蛋白、脂联素和1,5 -脱水葡萄糖醇。患者在妊娠28周时按照国际糖尿病与妊娠研究组(IADPSG)标准进行口服葡萄糖耐量试验。采用多元逻辑回归分析来检验GDM发病率与孕早期血清生物标志物之间的联系。
孕早期脂联素水平与GDM风险独立相关。血清脂联素<8.9μg/ml时,GDM的比值比为3.3。最终发展为GDM的患者中平均1,5 -脱水葡萄糖醇水平显著较低。孕早期测量的性激素结合球蛋白水平与GDM风险相关。然而,一旦考虑到体重指数、种族和家族史,这种相关性就不再具有统计学意义。孕早期C反应蛋白的测量不是GDM风险的有用指标。
孕早期测量脂联素和1,5 -脱水葡萄糖醇是GDM后期发病的潜在早期生物标志物。使用这些生物标志物进行风险分层可能有助于GDM的早期诊断和管理,以减轻其并发症。