Early pregnancy prediction of gestational diabetes mellitus risk using prenatal screening biomarkers in nulliparous women

Autor: Laura L. Jelliffe-Pawlowski, Scott P. Oltman, Wei Bao, Brittney M. Snyder, Rebecca J. Baer, Knute D. Carter, Andrea L. Greiner, Jennifer G. Robinson, Audrey F. Saftlas, Larry Rand, Kelli K. Ryckman, Patrick Breheny
Rok vydání: 2020
Předmět:
Inhibin a
Endocrinology
Diabetes and Metabolism

Early pregnancy factor
Reproductive health and childbirth
Gestational diabetes mellitus
Cohort Studies
0302 clinical medicine
Endocrinology
Pregnancy
Prenatal Diagnosis
Medicine
Psychology
030212 general & internal medicine
Pediatric
education.field_of_study
screening and diagnosis
biology
Obstetrics
Diabetes
General Medicine
Gestational diabetes
Detection
Prenatal screening
Gestational
Public Health and Health Services
Female
Cohort study
4.2 Evaluation of markers and technologies
Adult
medicine.medical_specialty
Population
Clinical Sciences
030209 endocrinology & metabolism
Article
03 medical and health sciences
Endocrinology & Metabolism
Prediction model
Clinical Research
Diabetes mellitus
Internal Medicine
Humans
Conditions Affecting the Embryonic and Fetal Periods
education
Receiver operating characteristic
business.industry
Prevention
Perinatal Period - Conditions Originating in Perinatal Period
medicine.disease
Clinical utility
4.1 Discovery and preclinical testing of markers and technologies
Diabetes
Gestational

Risk management
biology.protein
business
Biomarkers
Zdroj: Diabetes Res Clin Pract
Popis: Aims To evaluate the clinical utility of first and second trimester prenatal screening biomarkers for early pregnancy prediction of gestational diabetes mellitus (GDM) risk in nulliparous women. Methods We conducted a population-based cohort study of nulliparous women participating in the California Prenatal Screening Program from 2009 to 2011 (n = 105,379). GDM was ascertained from hospital discharge records or birth certificates. Models including maternal characteristics and prenatal screening biomarkers were developed and validated. Risk stratification and reclassification were performed to assess clinical utility of the biomarkers. Results Decreased levels of first trimester pregnancy-associated plasma protein A (PAPP-A) and increased levels of second trimester unconjugated estriol (uE3) and dimeric inhibin A (INH) were associated with GDM. The addition of PAPP-A only and PAPP-A, uE3, and INH to maternal characteristics resulted in small, yet significant, increases in area under the receiver operating characteristic curve (AUC) (maternal characteristics only: AUC 0.714 (95% CI 0.703–0.724), maternal characteristics + PAPP-A: AUC 0.718 (95% CI 0.707–0.728), maternal characteristics + PAPP-A, uE3, and INH: AUC 0.722 (0.712–0.733)); however, no net improvement in classification was observed. Conclusions PAPP-A, uE3, and INH have limited clinical utility for prediction of GDM risk in nulliparous women. Utility of other readily accessible clinical biomarkers in predicting GDM risk warrants further investigation.
Databáze: OpenAIRE