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dc.contributor.authorHawani Sasmaya, Prameswari-
dc.contributor.authorAchmad Fitrah, Khalid-
dc.contributor.authorDewi, Anggraeni-
dc.contributor.authorSetyorini, Irianti-
dc.contributor.authorMohammad Rizki, Akbar-
dc.date.accessioned2022-08-06T09:12:29Z-
dc.date.available2022-08-06T09:12:29Z-
dc.date.issued2022-01-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2040-
dc.description.abstractDifferences in maternal soluble ST2 levels in the third trimester of normal pregnancy versus preeclampsia Prameswari Hawani Sasmayaa,⁎, Khalid Achmad Fitraha, Anggraeni Dewia, Irianti Setyorinib, Akbar Mohammad Rizkia a Department of Cardiology, Hasan Sadikin General Hospital, Universitas Padjadjaran, Bandung, West Java, Indonesia b Department of Obsetrics and Gynecology, Hasan Sadikin General Hospital, Universitas Padjadjaran, Bandung, West Java, Indonesia article info Article history: Received 17 June 2021 Received in revised form 27 September 2021 Accepted 4 December 2021 Available online 7 December 2021 Keywords: soluble ST2 biomarkers pregnancy preeclampsia abstract Background: Preeclampsia is associated with intense inflammatory response in pregnancy, and soluble ST2 (sST2) is pathologically increased in this condition. No data exist regarding maternal sST2 levels in normal pregnancy versus preeclampsia in areas of southeast Asia with an ethnic Malay predominance. Materials and Methods: Patients were sorted into normal pregnancy or preeclampsia. Patients with a history of allergic, inflammatory, or malignant disease were excluded. One sample was taken per patient; all samples were taken during the third trimester of pregnancy. Thirty samples from each group were enrolled in the study, totaling 60 samples. Soluble ST2 levels in maternal plasma were measured using the Presage® ST2 Assay according to manufacturer instructions, and data was analyzed using SPSS 23. Results: Patients in the preeclampsia group were significantly older than those in the normal pregnancy group (p = 0.01). Most patients with preeclampsia presented as early-onset (n = 23). Both systolic blood pressure (SBP) and diastolic blood pressure (DBP) were significantly higher (p < 0.001) in the preeclampsia group. Mean sST2 level in the preeclampsia group (85.89 ng/ml) was significantly higher than the normal pregnancy group mean (38.3 ng/ml) during the third trimester (p < 0.001). This study also found a cor relation between sST2 and preeclampsia (p < 0.001, r = 0.480), SBP (p < 0.001, r = 0.407), and DBP (p = 0.007, r = 0.342), while preeclampsia was found to be the best explanatory variable of sST2 levels (r = 0.468, p < 0.001). sST2 level > 63.66 ng/ml has sensitivity 50% and specificity 93.3%, with AUC of 0.78 [95% CI 0.66 – 0.90], p < 0.001. The sST2 > 63.66 ng/ml has an OR of 14.0 [95% CI 2.82 – 69.6], p < 0.001 for preeclampsia. The dose-response relationship between sST2 level and preeclampsia was linear. Conclusion: Soluble ST2 levels were increased in both normal pregnancy and preeclampsia but were nificantly higher in patients with preeclampsia. Preeclampsia was also found to be the best explanatory variable for the increase of sST2 levels in ethnic Malay predominance.en_US
dc.subjectsoluble ST2 biomarkers pregnancy preeclampsiaen_US
dc.titleDifferences in maternal soluble ST2 levels in the third trimester of normal pregnancy versus preeclampsiaen_US
dc.typeArticleen_US
Appears in Collections:1. European Journal of Obstetrics & Gynecology and Reproductive Biology

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