Impact of obesity on angiogenic and inflammatory markers in the Finnish Genetics of Pre-eclampsia Consortium (FINNPEC) cohort

Int J Obes (Lond). 2019 May;43(5):1070-1081. doi: 10.1038/s41366-018-0217-8. Epub 2018 Sep 25.

Abstract

Background: While several studies have demonstrated that obesity increases the risk of pre-eclampsia (PE), the mechanisms have yet to be elucidated. We assessed the association between maternal/paternal obesity and PE and hypothesized that maternal body mass index (BMI) would be associated with an adverse inflammatory and angiogenic profile. High-sensitivity C-reactive protein (hs-CRP) and following serum angiogenic markers were determined: soluble endoglin (sEng), soluble fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF).

Methods: Data on BMI were available from 1450 pregnant women with PE and 1065 without PE. Serum concentrations of hs-CRP and angiogenic markers were available from a subset at first and third trimesters.

Results: Prepregnancy BMI was higher in the PE group than in controls (mean ± SD) 25.3 ± 5.2 vs. 24.1 ± 4,4, p < 0.001, adjusted for parity, mother's age, and smoking status before pregnancy. Increased hs-CRP concentrations were observed in both PE and non-PE women similarly according to BMI category. In women with PE, a higher BMI was associated with lower sFlt-1 and sEng concentrations throughout the pregnancy (p = 0.004, p = 0.008, respectively). There were no differences in PlGF in PE women according to BMI.

Conclusions: We confirmed increased pre-pregnancy BMI in women with PE. Enhanced inflammatory state was confirmed in all women with overweight/obesity. Partly paradoxically we observed that PE women with obesity had less disturbed levels of angiogenic markers than normal weight women with PE. This should be taken into account when angiogenic markers are used in PE prediction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Body Mass Index
  • Cohort Studies
  • Endoglin / metabolism
  • Female
  • Finland / epidemiology
  • Humans
  • Inflammation / etiology
  • Inflammation / physiopathology*
  • Obesity / complications
  • Obesity / metabolism
  • Obesity / physiopathology*
  • Placenta Growth Factor / metabolism
  • Pre-Eclampsia / etiology
  • Pre-Eclampsia / genetics*
  • Pre-Eclampsia / metabolism
  • Pre-Eclampsia / physiopathology*
  • Predictive Value of Tests
  • Pregnancy
  • Pregnancy Complications / metabolism
  • Pregnancy Complications / physiopathology*
  • Pregnancy Trimester, First
  • Pregnancy Trimester, Third
  • Receptors, Immunologic / metabolism

Substances

  • Biomarkers
  • CRP protein, human
  • Endoglin
  • PGF protein, human
  • Receptors, Immunologic
  • Placenta Growth Factor