Plasma-glycated CD59 as an early biomarker for gestational diabetes mellitus: prospective cohort study protocol.
Plasma-glycated CD59 as an early biomarker for gestational diabetes mellitus: prospective cohort study protocol.
复制标题
血浆糖化CD59作为妊娠期糖尿病早期生物标志物:前瞻性队列研究方案。
DOI:
10.1136/bmjopen-2021-054773
复制
发表时间:
2022-04-20
期刊:
影响因子:
2.9
通讯作者:
Halperin, Jose
中科院分区:
文献类型:
--
作者:
Andrews, Chloe;Toth-Castillo, Michelle;Aktas, Huseyin;Fernandez, Miguel-Angel Luque;Wong, Steven Koon;Sen, Sarbattama;Halperin, Jose
The significant maternal and neonatal outcomes of gestational diabetes mellitus (GDM) make it a major public health concern. Mothers with GDM are at greater risk of pregnancy complications and their offspring are at higher risk of diabetes and obesity. Currently, GDM is diagnosed with glucose load methods which are time-consuming and inconvenient to administer more than once during pregnancy; for this reason, there is a recognised need for a more accurate and simpler test for GDM. Previous studies indicate that plasma-glycated CD59 (pGCD59) is a novel biomarker for GDM. We present here the protocol of a prospective cohort study designed to (1) determine the accuracy of pGCD59 as an early, first trimester predictor of GDM and gestational impaired glucose tolerance and (2) assess the associations between pGCD59 levels and adverse maternal and neonatal outcomes. We will obtain discarded plasma samples from pregnant women at two time points: first prenatal visit (usually <14 weeks gestation) and gestational weeks 24–28. A study-specific medical record abstraction tool will be used to obtain relevant maternal and neonatal clinical data from the EPIC clinical database. The prevalence of GDM will be determined using standard of care glucose load test results. We will determine the sensitivity and specificity of pGCD59 to predict the diagnosis of GDM and gestational impaired glucose tolerance, as well as the associations between levels of pGCD59 and the prevalence of maternal and neonatal outcomes. This study has been approved by the Mass General Brigham Institutional Review Board (protocol 2011P002254). The results of this study will be presented at international meetings and disseminated in peer-reviewed journals.
登录
查看更多内容
影响因子:
81.5
作者:
McIntyre, H. David;Catalano, Patrick;Damm, Peter
通讯作者:
Damm, Peter
影响因子:
3.1
作者:
Jelsma JG;van Poppel MN;Galjaard S;Desoye G;Corcoy R;Devlieger R;van Assche A;Timmerman D;Jans G;Harreiter J;Kautzky-Willer A;Damm P;Mathiesen ER;Jensen DM;Andersen L;Dunne F;Lapolla A;Di Cianni G;Bertolotto A;Wender-Oegowska E;Zawiejska A;Blumska K;Hill D;Rebollo P;Snoek FJ;Simmons D
通讯作者:
Simmons D
DOI:
10.1016/s0002-9378(87)80045-5
发表时间:
1987-09-01
影响因子:
9.8
作者:
LANGER, O;BRUSTMAN, L;MAZZE, R
通讯作者:
MAZZE, R
影响因子:
9.8
作者:
Jensen, DM;Damm, P;Beck-Nielsen, H
通讯作者:
Beck-Nielsen, H
影响因子:
16.2
作者:
CEFALU, WT;PRATHER, KL;PERNOLL, ML
通讯作者:
PERNOLL, ML