Department of Medical Biochemistry, Faculty of Pharmacy, University of Belgrade, Belgrade, Serbia.
Department for High-risk Pregnancy, Gynecology and Obstetrics Clinic Narodni Front, Belgrade, Serbia
Pol Arch Intern Med. 2021 Dec 22;131(12). doi: 10.20452/pamw.16144. Epub 2021 Nov 26.
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.
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.
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.
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.
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.
子痫前期与血脂异常之间存在关联。尽管脂代谢参数已在子痫前期病理中得到深入研究,但它们的确切分子作用机制尚未完全解码。
我们旨在确定受晚发型子痫前期影响的女性的胆固醇代谢特征,并确定与晚发型综合征相关的潜在生物标志物。
总共监测了 90 名有子痫前期风险的孕妇,在妊娠的 4 个时间点进行监测,并根据妊娠结局将其分为高危组(70 名孕妇)和子痫前期组(20 名孕妇)。使用液相色谱-串联质谱法进行胆固醇代谢谱分析。
子痫前期组仅出现羊毛固醇水平的显著升高(P = 0.001)。与高危组相比,子痫前期组在孕早期的羊毛固醇水平更高(P = 0.02)。此外,在子痫前期组中,在孕晚期,发现-desmosterol 和 β-谷甾醇之间存在正相关(ρ = 0.474;P = 0.03),在孕中期和孕早期之间,desmosterol 和胆固醇变化之间存在正相关(ρ = 0.546;P = 0.02),以及孕晚期和孕早期之间(ρ = 0.754;P < 0.001),以及在孕晚期和孕早期之间的-desmosterol 和 β-谷甾醇差异之间也存在正相关(ρ = 0.568;P = 0.01)。在高危组中未发现类似的相关性。
晚发型子痫前期可能与脂质谱异常有关。通过研究胆固醇的定量代谢特征,我们可以假设胆固醇的合成和吸收都增加了,即疾病影响的女性的胆固醇稳态调节失衡。