Key result
Women with preeclampsia had lower concentrations of PlGF (p<0.0001) and higher concentrations of s-Eng (p=0.001) than healthy pregnant women, with no differences in ox-LDL or s-FLT1.
Why the study?
Are levels of angiogenic factors and oxidized LDL altered in women with preeclampsia from a developing country compared to healthy pregnant women?
Case-Control (n=286)
Yes
Are levels of angiogenic factors and oxidized LDL altered in women with preeclampsia from a developing country compared to healthy pregnant women?
p-value: p=<0.0001
Women with preeclampsia in a developing country exhibit significant angiogenic imbalance and lipid alterations, particularly in severe or early-onset cases.
Angiogenic imbalance linked to preeclampsia in developing countries; hypothesis-generating and requires prospective validation before clinical use.
BACKGROUND: An imbalance between anti-angiogenic factors (e.g. soluble vascular endothelial growth factor receptor-1 (s-FLT1) and soluble endoglin (s-Eng)) and pro-angiogenic factors (e.g. placental growth factor (PlGF)) as well as increased oxidized low-density lipoprotein (ox-LDL) concentrations have been associated with preeclampsia (PE). Risk factors associated with the development of PE, however, are known to be different between developed and developing countries. The aim of the study was to determine the levels of s-FLT1, s-Eng, PIGF, and ox-LDL in women with PE from a developing country. METHODS: A multi-center case-control study was conducted. One hundred and forty three women with PE were matched by age and parity with 143 healthy pregnant women without cardiovascular or endocrine diseases. Before delivery, blood samples were taken and serum was stored until analysis. RESULTS: Women with PE had lower concentrations of PIGF (p<0.0001) and higher concentrations of s-Eng (p=0.001) than healthy pregnant women. There were no differences between the groups regarding ox-LDL or s-FLT1. Women with early onset PE had higher s-FLT1 concentrations (p=0.0004) and lower PIGF concentrations (p<0.0001) than their healthy pregnant controls. Women with late onset PE had higher concentrations of s-Eng (p=0.005). Women with severe PE had higher concentrations of s-Eng (p=0.0008) and ox-LDL (p=0.01), and lower concentrations of PIGF (p<0.0001). CONCLUSIONS: Women with PE from a developing country demonstrated an angiogenic imbalance and an increased rate of LDL oxidation. Findings from this study support the theory that PE is a multifactorial disease, and understanding differences in these subpopulations may provide a better target to approach future therapies.
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Reyes et al. (2012) conducted a case-control in Preeclampsia (n=286). Preeclampsia vs. Healthy pregnant women was evaluated on Levels of s-FLT1, s-Eng, PIGF, and ox-LDL (p=<0.0001). Women with preeclampsia had lower concentrations of PlGF (p<0.0001) and higher concentrations of s-Eng (p=0.001) than healthy pregnant women, with no differences in ox-LDL or s-FLT1.
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