Fetal growth regulation via insulin-like growth factor axis in normal and diabetic pregnancy

J Perinat Med. 2022 Apr 4;50(7):947-960. doi: 10.1515/jpm-2021-0510. Print 2022 Sep 27.

Abstract

Objectives: Diabetes mellitus (DM) in pregnancy and gestational diabetes remain a considerable cause of pregnancy complications, and fetal macrosomia is among them. Insulin, insulin-like growth factors (IGFs), and components of their signal-transduction axes belong to the predominant growth regulators and are implicated in glucose homeostasis. This study aimed to evaluate the available evidence on the association between the IGF axis and fetal anthropometric parameters in human diabetic pregnancy.

Methods: PubMed, Medline, Web of Science, and CNKI databases (1981-2021) were searched.

Results: Maternal and cord serum IGF-I levels are suggested to be positively associated with weight and length of neonates born to mothers with type 1 DM. The results concerning IGF-II and IGFBPs in type 1 DM or any of the IGF axis components in type 2 DM remain controversial. The alterations of maternal serum IGFs concentrations throughout diabetic and non-diabetic pregnancy do not appear to be the same. Maternal 1st trimester IGF-I level is positively associated with fetal birth weight in DM.

Conclusions: Research on the IGF axis should take gestational age of sampling, presence of DM, and insulin administration into account. Maternal 1st trimester IGF-I level might become a predictor for macrosomia development in diabetic pregnancy.

Keywords: IGF; birth weight; diabetes mellitus; fetal growth; insulin-like growth factor; macrosomia.

MeSH terms

  • Birth Weight
  • Diabetes Mellitus, Type 1* / complications
  • Diabetes Mellitus, Type 1* / metabolism
  • Female
  • Fetal Blood / metabolism
  • Fetal Macrosomia / etiology
  • Fetal Macrosomia / metabolism
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Insulin
  • Insulin-Like Growth Factor I / metabolism
  • Pregnancy
  • Pregnancy in Diabetics* / metabolism

Substances

  • Insulin
  • Insulin-Like Growth Factor I