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The function of adipsin and C9 protein in the complement system in HIV-associated preeclampsia
Mikyle David1, Jagidesa Moodley2, Thajasvarie Naicker3
1Optics and Imaging Centre, Nelson R. Mandela School of Medicine, Dorris Duke Medical Research InstituteCollege of Health Sciences, University of KwaZulu-NatalKwaZulu-Natal, Durban, South Africa. mikyledavid101@gmail.com.
Insights
Adipsin levels are elevated in preeclampsia, regardless of HIV status, suggesting it could be a diagnostic biomarker for this condition. C9 levels did not show significant differences in preeclampsia.
Area of Science:
- Immunology
- Obstetrics & Gynecology
- Infectious Diseases
Background:
- Preeclampsia involves increased complement activation and complement component expression.
- Investigating specific complement components like adipsin and C9 in HIV-associated preeclampsia is crucial.
Purpose of the Study:
- To investigate the concentrations of adipsin and C9 in HIV-associated preeclampsia.
- To determine if adipsin or C9 can serve as biomarkers for preeclampsia in HIV-positive and HIV-negative individuals.
Main Methods:
- Serum samples from 76 participants were analyzed.
- Participants were stratified by pregnancy status (normotensive pregnant, preeclampsia) and HIV status.
- Adipsin and C9 concentrations were measured using a Bioplex immunoassay.
Main Results:
- Adipsin concentration was significantly higher in preeclampsia groups compared to normotensive groups, irrespective of HIV status.
- Significant differences in adipsin were observed between HIV-negative normotensive and HIV-negative preeclampsia groups, and between HIV-negative preeclampsia and HIV-positive preeclampsia groups.
- No statistically significant differences in C9 protein expression were found between normotensive and preeclampsia groups, or between HIV-positive and HIV-negative groups.
Conclusions:
- Adipsin up-regulation strongly correlates with preeclampsia.
- Adipsin shows promise as a diagnostic biomarker for preeclampsia.
- C9 does not appear to be a reliable biomarker for preeclampsia in this study population.
Objective:
In preeclampsia, there are excessive complement components expressed due to increased complement activation; therefore, this study investigated the concentration of adipsin and C9 in HIV-associated preeclampsia.
Method:
The study population (n = 76) was stratified by pregnancy type (normotensive pregnant and preeclampsia) and by HIV status. Serum was assayed for the concentration of adipsin and C9 using a Bioplex immunoassay procedure.
Results:
Maternal weight did not differ (p = 0.1196) across the study groups. The concentration of adipsin was statistically different between the PE vs normotensive pregnant groups, irrespective of HIV status (p = 0.0439). There was no significant difference in adipsin concentration between HIV-negative vs HIV-positive groups, irrespective of pregnancy type (p = 0.6290). Additionally, there was a significant difference in adipsin concentration between HIV-negative normotensive vs HIV-negative preeclampsia (p < 0.05), as well as a difference between HIV-negative preeclampsia vs HIV-positive preeclampsia (p < 0.05). C9 protein expression was not statistically different between the normotensive and PE groups, regardless of HIV status (p = 0.5365). No statistical significance in C9 expression was found between HIV-positive vs HIV-negative groups, regardless of pregnancy type (p = 0.3166). Similarly, no statistical significance was noted across all study groups (p = 0.0774).
Conclusion:
This study demonstrates that there is a strong correlation between the up-regulation of adipsin and PE and that adipsin is a promising biomarker to use as a diagnostic tool for PE.
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