Early pregnancy metabolites predict gestational diabetes mellitus: implications for fetal programming

被引:27
作者
Koos, Brian J. [1 ]
Gornbein, Jeffrey A. [2 ,3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Computat Core, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Stat Core, Dept Med, Los Angeles, CA 90095 USA
关键词
diabetes; epigenetics; fetal programming; metabolomics; pregnancy; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; RISK; WOMEN; PATHOPHYSIOLOGY; METABOLOMICS; BIOMARKERS; STRESS; IMPACT;
D O I
10.1016/j.ajog.2020.07.050
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Aberrant fetal programming in gestational diabetes mellitus seems to increase the risk of obesity, type 2 diabetes, and cardiovascular disease. The inability to accurately identify gestational diabetes mellitus in the first trimester of pregnancy has thwarted ascertaining whether early therapeutic interventions reduce the predisposition to these prevalent medical disorders. OBJECTIVE: A metabolomics study was conducted to determine whether advanced analytical methods could identify accurate predictors of gestational diabetes mellitus in early pregnancy. STUDY DESIGN: This nested observational case-control study was composed of 92 gravidas (46 in the gestational diabetes mellitus group and 46 in the control group) in early pregnancy, who were matched by maternal age, body mass index, and gestational age at urine collection. Gestational diabetes mellitus was diagnosed according to community standards. A comprehensive metabolomics platform measured 626 endogenous metabolites in randomly collected urine. Consensus multivariate criteria or the most important by 1 method identified low-molecular weight metabolites independently associated with gestational diabetes mellitus, and a classification tree selected a subset most predictive of gestational diabetes mellitus. RESULTS: Urine for both groups was collected at a mean gestational age of 12 weeks (range, 6-19 weeks' gestation). Consensus multivariate analysis identified 11 metabolites independently linked to gestational diabetes mellitus. Classification tree analysis selected a 7-metabolite subset that predicted gestational diabetes mellitus with an accuracy of 96.7%, independent of maternal age, body mass index, and time of urine collection. CONCLUSION: Validation of this high-accuracy model by a larger study is now needed to support future studies to determine whether therapeutic interventions in the first trimester of pregnancy for gestational diabetes mellitus reduce shortand long-term morbidity.
引用
收藏
页码:215.e1 / 215.e7
页数:7
相关论文
共 40 条
[1]   Fetal Programming and Cardiovascular Pathology [J].
Alexander, Barbara T. ;
Dasinger, John Henry ;
Intapad, Suttira .
COMPREHENSIVE PHYSIOLOGY, 2015, 5 (02) :997-1025
[2]   Classification and Diagnosis of Diabetes [J].
不详 .
DIABETES CARE, 2015, 38 :S8-S16
[3]  
[Anonymous], 2018, Obstet Gynecol, V131, pe49, DOI 10.1097/AOG.0000000000002501
[4]   Assessment of Cardiac Function in Fetuses of Gestational Diabetic Mothers During the Second Trimester [J].
Atiq, Mehnaz ;
Ikram, Anum ;
Hussain, Batool M. ;
Saleem, Bakhtawar .
PEDIATRIC CARDIOLOGY, 2017, 38 (05) :941-945
[5]   Potential prognostic biomarkers of cardiovascular disease in fetal macrosomia: the impact of gestational diabetes [J].
Briana, Despina D. ;
Germanou, Kleopatra ;
Boutsikou, Maria ;
Boutsikou, Theodora ;
Athanasopoulos, Nikolaos ;
Marmarinos, Antonios ;
Gourgiotis, Dimitrios ;
Malamitsi-Puchner, Ariadne .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2018, 31 (07) :895-900
[6]   Higher Maternal Gestational Glucose Concentration Is Associated with Lower Offspring Insulin Sensitivity and Altered β-Cell Function [J].
Bush, Nikki C. ;
Chandler-Laney, Paula C. ;
Rouse, Dwight J. ;
Granger, Wesley M. ;
Oster, Robert A. ;
Gower, Barbara A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (05) :E803-E809
[7]   LONGITUDINAL CHANGES IN INSULIN RELEASE AND INSULIN RESISTANCE IN NONOBESE PREGNANT-WOMEN [J].
CATALANO, PM ;
TYZBIR, ED ;
ROMAN, NM ;
AMINI, SB ;
SIMS, EAH .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1991, 165 (06) :1667-1672
[8]   CARBOHYDRATE-METABOLISM DURING PREGNANCY IN CONTROL SUBJECTS AND WOMEN WITH GESTATIONAL DIABETES [J].
CATALANO, PM ;
TYZBIR, ED ;
WOLFE, RR ;
CALLES, J ;
ROMAN, NM ;
AMINI, SB ;
SIMS, EAH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (01) :E60-E67
[9]   Human fetoplacental arterial and venous endothelial cells are differentially programmed by gestational diabetes mellitus, resulting in cell-specific barrier function changes [J].
Cvitic, Silvija ;
Novakovic, Boris ;
Gordon, Lavinia ;
Ulz, Christine M. ;
Muehlberger, Magdalena ;
Diaz-Perez, Francisca I. ;
Joo, Jihoon E. ;
Svendova, Vendula ;
Schimek, Michael G. ;
Trajanoski, Slave ;
Saffery, Richard ;
Desoye, Gernot ;
Hiden, Ursula .
DIABETOLOGIA, 2018, 61 (11) :2398-2411
[10]   Epigenetics and gestational diabetes: a review of epigenetic epidemiology studies and their use to explore epigenetic mediation and improve prediction [J].
Elliott, Hannah R. ;
Sharp, Gemma C. ;
Relton, Caroline L. ;
Lawlor, Deborah A. .
DIABETOLOGIA, 2019, 62 (12) :2171-2178