Key result
First-trimester lathosterol levels are ~58% higher in high-risk women who develop late-onset preeclampsia.
Why the study?
Although preeclampsia is linked to dyslipidemia, the accurate molecular mechanisms of lipid profile parameters in its pathology have not been fully decoded.
Does cholesterol metabolic profiling differ between pregnant women who develop late-onset preeclampsia and those who remain high-risk?
Observational (n=90)
No
Does cholesterol metabolic profiling differ between pregnant women who develop late-onset preeclampsia and those who remain high-risk?
Absolute Event Rate: 15% vs 9.49%
p-value: p=0.02
Late-onset preeclampsia is associated with altered cholesterol homeostasis, specifically increased lathosterol levels detectable in the first trimester.
Elevated first-trimester lathosterol may flag late-onset preeclampsia risk in high-risk women; hypothesis-generating and needs prospective validation.
INTRODUCTION: The link between preeclampsia and dyslipidemia has been established. Even though lipid profile parameters have been intensively investigated in the pathology of preeclampsia, their accurate molecular mechanisms of action have not been fully decoded. OBJECTIVES: We aimed to identify the specifics of cholesterol metabolism in women affected by late-onset preeclampsia and single out potential biomarkers associated with late-onset syndrome. PATIENTS AND METHODS: A total of 90 pregnant women with a priori risk for preeclampsia were monitored at 4 time points during gestation and, based on the outcome of pregnancy, they were classified into the high-risk group (70 women) and the preeclampsia group (20 women). Cholesterol metabolic profiling was done using liquid chromatography-tandem mass spectrometry. RESULTS: The only significant change in the preeclampsia group was an increase in the lathosterol level (P = 0.001). The first-trimester lathosterol level was higher in the preeclampsia group compared with the high-risk group (P = 0.02). Further, in the preeclampsia group, positive correlations were found between desmosterol and β-sitosterol (ρ = 0.474; P = 0.03) in the third trimester, desmosterol and campesterol changes between the second and the first (ρ = 0.546; P = 0.02), and the third and first trimesters (ρ = 0.754; P <0.001), as well as between the desmosterol and β-sitosterol differences between the third and first trimesters (ρ = 0.568; P = 0.01). No similar correlations were found in the high-risk group. CONCLUSIONS: Late-onset preeclampsia could be associated with an altered lipid profile. By studying the quantitative metabolic signatures of cholesterol, we might assume that both cholesterol synthesis and absorption are increased, that is, there is an imbalance in the cholesterol homeostasis regulation in women affected by the disease.
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Antonić et al. (2021) conducted an observational in Preeclampsia (n=90). Late-onset preeclampsia vs. High-risk pregnancy without preeclampsia was evaluated on First-trimester lathosterol level (µmol/l) (p=0.02). Women who developed late-onset preeclampsia had significantly higher first-trimester lathosterol levels compared to high-risk women who did not develop the condition.
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