» Articles » PMID: 39296937

First-trimester Predictive Models for Adverse Pregnancy Outcomes-a Base for Implementation of Strategies to Prevent Cardiovascular Disease Development

Overview
Specialty Cell Biology
Date 2024 Sep 19
PMID 39296937
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: This study aimed to establish efficient, cost-effective, and early predictive models for adverse pregnancy outcomes based on the combinations of a minimum number of miRNA biomarkers, whose altered expression was observed in specific pregnancy-related complications and selected maternal clinical characteristics.

Methods: This retrospective study included singleton pregnancies with gestational hypertension (GH, n = 83), preeclampsia (PE, n = 66), HELLP syndrome (n = 14), fetal growth restriction (FGR, n = 82), small for gestational age (SGA, n = 37), gestational diabetes mellitus (GDM, n = 121), preterm birth in the absence of other complications (n = 106), late miscarriage (n = 34), stillbirth (n = 24), and 80 normal term pregnancies. MiRNA gene expression profiling was performed on the whole peripheral venous blood samples collected between 10 and 13 weeks of gestation using real-time reverse transcription polymerase chain reaction RT-PCR).

Results: Most pregnancies with adverse outcomes were identified using the proposed approach (the combinations of selected miRNAs and appropriate maternal clinical characteristics) (GH, 69.88%; PE, 83.33%; HELLP, 92.86%; FGR, 73.17%; SGA, 81.08%; GDM on therapy, 89.47%; and late miscarriage, 84.85%). In the case of stillbirth, no addition of maternal clinical characteristics to the predictive model was necessary because a high detection rate was achieved by a combination of miRNA biomarkers only [91.67% cases at 10.0% false positive rate (FPR)].

Conclusion: The proposed models based on the combinations of selected cardiovascular disease-associated miRNAs and maternal clinical variables have a high predictive potential for identifying women at increased risk of adverse pregnancy outcomes; this can be incorporated into routine first-trimester screening programs. Preventive programs can be initiated based on these models to lower cardiovascular risk and prevent the development of metabolic/cardiovascular/cerebrovascular diseases because timely implementation of beneficial lifestyle strategies may reverse the dysregulation of miRNAs maintaining and controlling the cardiovascular system.

Citing Articles

Abnormal microRNA expression profile at early stages of gestation in pregnancies destined to develop placenta previa.

Hromadnikova I, Kotlabova K, Krofta L Front Med (Lausanne). 2024; 11:1469855.

PMID: 39691371 PMC: 11650449. DOI: 10.3389/fmed.2024.1469855.

References
1.
Libby G, Murphy D, McEwan N, Greene S, Forsyth J, Chien P . Pre-eclampsia and the later development of type 2 diabetes in mothers and their children: an intergenerational study from the Walker cohort. Diabetologia. 2006; 50(3):523-30. DOI: 10.1007/s00125-006-0558-z. View

2.
Hromadnikova I, Kotlabova K, Krofta L . Novel First-Trimester Prediction Model for Any Type of Preterm Birth Occurring before 37 Gestational Weeks in the Absence of Other Pregnancy-Related Complications Based on Cardiovascular Disease-Associated MicroRNAs and Basic Maternal Clinical.... Biomedicines. 2022; 10(10). PMC: 9599357. DOI: 10.3390/biomedicines10102591. View

3.
Berks D, Hoedjes M, Raat H, Duvekot J, Steegers E, Habbema J . Risk of cardiovascular disease after pre-eclampsia and the effect of lifestyle interventions: a literature-based study. BJOG. 2013; 120(8):924-31. DOI: 10.1111/1471-0528.12191. View

4.
Audibert F, FRIEDMAN S, Frangieh A, Sibai B . Clinical utility of strict diagnostic criteria for the HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome. Am J Obstet Gynecol. 1996; 175(2):460-4. DOI: 10.1016/s0002-9378(96)70162-x. View

5.
Hromadnikova I, Kotlabova K, Krofta L . First trimester prediction models for small-for- gestational age and fetal growth restricted fetuses without the presence of preeclampsia. Mol Cell Probes. 2023; 72:101941. DOI: 10.1016/j.mcp.2023.101941. View