Structural, functional and circulatory placental changes associated with impaired glucose metabolism

Eur J Obstet Gynecol Reprod Biol. 2002 Nov 15;105(2):136-42. doi: 10.1016/s0301-2115(02)00161-6.

Abstract

Objective: To investigate associations between structural, functional and circulatory placental changes in pregnancies complicated by impaired glucose metabolism.

Design: Umbilical artery (UA) blood flow resistance was measured by Doppler velocimetry in 21 gravidae with diabetes/impaired glucose tolerance (IGT) and 10 healthy gravidae. Umbilical and placental vessel segments were incubated for determination of prostacyclin and thromboxane synthesis, and tissues histologically examined. Non-parametric statistical tests at a two-tailed P<0.05 were used.

Results: Placental lesions were more common in diabetes/IGT and, although not being an uniform finding, in general associated with a higher vascular synthesis of thromboxane and/or lower prostacyclin/thromboxane synthesis ratio. As an exception, ischemic villitis was associated with a higher ratio and higher UA flow resistance.

Conclusions: Placental lesions are associated with an altered vascular prostanoid synthesis in diabetes/IGT, but not until structural signs of ischemia develop is a rise of UA blood flow resistance detected.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / biosynthesis
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Diabetes, Gestational / pathology
  • Diabetes, Gestational / physiopathology*
  • Female
  • Glucose Intolerance / pathology
  • Glucose Intolerance / physiopathology*
  • Humans
  • Infarction
  • Ischemia / pathology
  • Ischemia / physiopathology
  • Placenta / blood supply*
  • Placenta Diseases / pathology
  • Placenta Diseases / physiopathology*
  • Pregnancy
  • Pregnancy in Diabetics / pathology
  • Pregnancy in Diabetics / physiopathology*
  • Thrombosis / physiopathology
  • Thromboxane B2 / biosynthesis
  • Umbilical Arteries / physiopathology
  • Vascular Resistance

Substances

  • Thromboxane B2
  • 6-Ketoprostaglandin F1 alpha