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Alteration of heat shock protein 20 expression in preeclamptic patients and its effect in vascular and coagulation
Fanfan Li1, Mengzhou He1, Meitao Yang1
1Department of Gynecology and Obstetrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Insights
Decreased levels of Heat Shock Protein 20 (HSP20) in preeclampsia (PE) may contribute to the disorder. Reduced HSP20 impacts vascular function and blood clotting, suggesting a role in PE pathogenesis.
Area of Science:
- Obstetrics
- Cardiovascular Biology
- Hematology
Background:
- Preeclampsia (PE) is a major cause of maternal and perinatal mortality globally.
- PE is characterized by excessive vasoconstriction and impaired coagulation.
- The role of Heat Shock Protein 20 (HSP20) in PE pathogenesis is not well understood.
Purpose of the Study:
- To investigate the levels and function of HSP20 in women with and without PE.
- To explore the association between HSP20 and vascular/coagulation abnormalities in PE.
Main Methods:
- Collected chorionic plate resistance arteries (CPAs) and serum from healthy pregnant women and those with PE.
- Measured HSP20 and phosphorylated HSP20 levels.
- Assessed CPA vasodilative function and analyzed coagulation parameters.
Main Results:
- HSP20 and phosphorylated HSP20 were downregulated in CPAs from women with PE.
- Preeclamptic vessels showed impaired relaxation responses.
- Serum HSP20 was reduced in PE, alongside decreased platelet volume and increased clotting times.
Conclusions:
- Decreased HSP20 levels in PE may contribute to impaired vasodilation and dysregulated coagulation.
- HSP20's role in vasorelaxation and coagulation suggests its involvement in PE pathogenesis.
Abstract:
Preeclampsia (PE) is a pregnancy-specific, multi-system disorder and the leading cause of maternal and perinatal morbidity and mortality in obstetrics worldwide. Excessive vasoconstriction and dysregulated coagulation function are closely associated with PE. Heat shock protein 20 (HSP20) is ubiquitously expressed under normal physiological conditions and has important roles in vascular dilatation and suppression of platelet aggregation. However, the role of HSP20 in the pathogenesis of PE remains unclear. In this study, we collected chorionic plate resistance arteries (CPAs) and serum from 118 healthy pregnant women and 80 women with PE and detected the levels of HSP20 and its phosphorylated form. Both HSP20 and phosphorylated HSP20 were downregulated in CPAs from women with PE. Comparison of the vasodilative ability of CPAs from the two groups showed impaired relaxation responses to acetyl choline in preeclamptic vessels. In addition to the reduced HSP20 in serum from women with PE, the platelet distribution width and mean platelet volume were also decreased, and the activated partial thromboplastin time and thromboplastin time were elevated.With regard to the vital roles of HSP20 in mediating vasorelaxation and coagulation function, the decreased HSP20 might contribute to the pathogenesis of PE.
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