Dean of the Medical Faculty, Semmelweis University
(STIA-OTKA-2021)
(PD 113022) Támogató: OTKA
(FK129206)
There is no early - first trimester- risk estimation available to predict later (gestational
week 24-28) gestational diabetes mellitus (GDM) - however it would be beneficial to
start an early treatment to prevent the development of complications.We aimed to identify
early, first trimester prediction markers for GDM.The present case-control study is
based on the study cohort of a Hungarian biobank containing the biological samples
and follow-up data from 2545 pregnant women. Oxidative-nitrative stress-related parameters,
steroid hormone, and metabolite levels were measured in the serum/plasma samples collected
at the end of the first trimester from 55-55 randomly selected control and later GDM
women.Pregnant women, who developed GDM later during the pregnancy were older and
had higher body mass indexes (BMI). The following parameters showed higher concentration
in their serum/plasma samples: fructosamine, total antioxidant capacity (TAC), testosterone,
cortisone, 21-deoxycortisol; while soluble urokinase plasminogen activator receptor
(SuPAR), dehydroepiandrosterone sulfate (DHEAS), dihydrotestosterone (DHT), cortisol
and 11-deoxycorticosterone levels were lower. Analyzing these variables using a forward
stepwise multivariate logistic regression model we established a GDM prediction model
with a specificity of 96.6% and sensitivity of 97.5% (included variables: fructosamine,
cortisol, cortisone, 11-deoxycorticosterone, SuPAR).Based on these measurements we
accurately predict the development of later onset GDM (24th-28th weeks of pregnancy).
Early risk estimation provides the opportunity for targeted prevention and the timely
treatment of GDM. Prevention and slowing the progression of GDM result in a lower
lifelong metabolic risk for both mother and offspring.