Key result
Low PAPP-A in early pregnancy shows no significant association with serum urotensin-II levels.
Why the study?
The relationship between urotensin II levels and pregnancy-associated plasma protein-A in early pregnancy and their potential role in placental processes and pregnancy complications is not well understood.
Case-Control (n=84)
No
Mean Difference: -111.1 (95% CI -301.33–79.13)
Absolute Event Rate: 334.37% vs 445.47%
p-value: p=0.25
No association in this review tempers biomarker expectations; leaves open urotensin-II's role in pregnancy cardiovascular risk.
Urotensin II (UT II) is an important factor of cellular homeostasis. This regulatory peptide is involved in the pathophysiology of many disorders. For example, it plays an important role in the pathogenesis of acute and chronic diseases, stressful and adaptive reactions of the body, in the development of cardiovascular pathologies, metabolic syndrome, inflammation, liver cirrhosis, renal failure, diabetic nephropathy, reproductive dysfunction, progression of psychosomatic, psychoendocrinal and psychiatric disorders. In this concern, the involvement of UT II in the pathophysiology of many processes determines the perspectives for the development of blockers of urotensin receptors for the treatment of the aforementioned diseases. It is important that even today this kind of perspective is feasible due to the synthesis of a series of GPR14 blockers. The objective of this review is to discuss current molecular mechanisms of biological activity, regulatory functions of UT II, its role in the pathogenesis of different nosologies, as well as analysis of the possible routes of exposure to GPR14 as potential therapeutic targets.
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Svistunov et al. (2017) conducted a case-control in Pregnancy (first-trimester) (n=84). Low PAPP-A (≤0.5 MoM) vs. Normal PAPP-A (>0.5 MoM) was evaluated on Serum urotensin-II concentration (ng/mL) (MD -111.10, 95% CI -301.33 to 79.13, p=0.25).
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