» Articles » PMID: 29971183

Visfatin As a Predictor for Growth of Fetus and Infant

Overview
Date 2018 Jul 5
PMID 29971183
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Visfatin is an adipocytokine that functions as an enzyme and a growth factor to investigate the relationship between serum visfatin and the fetus's anthropometric markers up to a year after birth.

Materials And Methods: Forty-one eligible pregnant women in their first trimester were divided and matched in terms of body mass index (BMI) before pregnancy into normal and higher than normal BMI groups, A and B. Serum visfatin levels were measured during 6-12 and 15-20 weeks of gestation using ELISA.

Results: The infants were followed up for a mean duration of 10.19±2.83 months. In group A, there was a strong positive relationship between birth head circumference and the first (p=0.054, r=0.580) and second trimester visfatin levels (p=0.051, r=0.530). In group B, second trimester visfatin levels correlated negatively with birth length (p=0.015, r=-0.523) and infant's head circumference (p=0.050, r=-0.392). In a separate study on group B, visfatin levels in the first and second trimesters showed a significant negative correlation with infant's weight. A significant correlation was observed between the first and second trimesters visfatin level with infant's height in both groups, such that this relationship was positive in group A and negative in group B. Linear regression analysis revealed that first and second trimester visfatin levels were significant independent predictors of infant's weight in group B and infant's height in both groups. Second trimester visfatin level was a significant predictor of birth height in group B.

Conclusion: Maternal serum visfatin level shows a relationship with fetal and infant anthropometric indicators, with different effects in the two groups, suggesting visfatin dysfunction in the overweight group before pregnancy.

Citing Articles

Impact of Gestational Diabetes Mellitus on Fetal Growth and Nutritional Status in Newborns.

Karcz K, Krolak-Olejnik B Nutrients. 2024; 16(23).

PMID: 39683486 PMC: 11643953. DOI: 10.3390/nu16234093.


Novel Biomolecules in the Pathogenesis of Gestational Diabetes Mellitus.

Ruszala M, Niebrzydowska M, Pilszyk A, Kimber-Trojnar Z, Trojnar M, Leszczynska-Gorzelak B Int J Mol Sci. 2021; 22(21).

PMID: 34769010 PMC: 8584125. DOI: 10.3390/ijms222111578.


The Role of the Adipokines in the Most Common Gestational Complications.

Gutaj P, Sibiak R, Jankowski M, Awdi K, Bryl R, Mozdziak P Int J Mol Sci. 2020; 21(24).

PMID: 33321877 PMC: 7762997. DOI: 10.3390/ijms21249408.

References
1.
Ma Y, Cheng Y, Wang J, Cheng H, Zhou S, Li X . The changes of visfatin in serum and its expression in fat and placental tissue in pregnant women with gestational diabetes. Diabetes Res Clin Pract. 2010; 90(1):60-5. DOI: 10.1016/j.diabres.2010.06.010. View

2.
Dietrich M, Antunes C, Geliang G, Liu Z, Borok E, Nie Y . Agrp neurons mediate Sirt1's action on the melanocortin system and energy balance: roles for Sirt1 in neuronal firing and synaptic plasticity. J Neurosci. 2010; 30(35):11815-25. PMC: 2965459. DOI: 10.1523/JNEUROSCI.2234-10.2010. View

3.
He X, He J, Shi Y, Pi C, Yang Y, Sun Y . Nicotinamide phosphoribosyltransferase (Nampt) may serve as the marker for osteoblast differentiation of bone marrow-derived mesenchymal stem cells. Exp Cell Res. 2017; 352(1):45-52. DOI: 10.1016/j.yexcr.2017.01.021. View

4.
Zhang T, Kraus W . SIRT1-dependent regulation of chromatin and transcription: linking NAD(+) metabolism and signaling to the control of cellular functions. Biochim Biophys Acta. 2009; 1804(8):1666-75. PMC: 2886162. DOI: 10.1016/j.bbapap.2009.10.022. View

5.
Haider D, Schaller G, Kapiotis S, Maier C, Luger A, Wolzt M . The release of the adipocytokine visfatin is regulated by glucose and insulin. Diabetologia. 2006; 49(8):1909-14. DOI: 10.1007/s00125-006-0303-7. View