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Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study

BACKGROUND: Preeclampsia (PE) is a multisystemic metabolic disease with an undetermined etiology. PE is a worldwide cause of maternal and perinatal morbidity, subdivided into early (EoPE) and late-onset (LoPE) according to 34 wk of gestation as a divider. Many researchers investigated biomarkers for...

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Autores principales: Amer Ali, Eham, Nori, Wassan, Salman, Alea Farhan, Al-Rawi, Taghreed S Saeed, Hameed, Ban H, Al-Ani, Raid M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303616/
https://www.ncbi.nlm.nih.gov/pubmed/37388778
http://dx.doi.org/10.12998/wjcc.v11.i17.3993
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author Amer Ali, Eham
Nori, Wassan
Salman, Alea Farhan
Al-Rawi, Taghreed S Saeed
Hameed, Ban H
Al-Ani, Raid M
author_facet Amer Ali, Eham
Nori, Wassan
Salman, Alea Farhan
Al-Rawi, Taghreed S Saeed
Hameed, Ban H
Al-Ani, Raid M
author_sort Amer Ali, Eham
collection PubMed
description BACKGROUND: Preeclampsia (PE) is a multisystemic metabolic disease with an undetermined etiology. PE is a worldwide cause of maternal and perinatal morbidity, subdivided into early (EoPE) and late-onset (LoPE) according to 34 wk of gestation as a divider. Many researchers investigated biomarkers for predicting PE to halt its consequences on the feto-maternal outcome. Elabela (Ela) is a newly discovered peptide hormone that was implicated in PE pathogenesis. Earlier rodent studies discussed Ela’s role in controlling blood pressure. Moreover, Ela deficiency was associated with PE development. AIM: To test whether plasma Ela could serve as a reliable marker for predicting PE based on the time of onset (EoPE vs LoPE) compared to age and body mass matched healthy controls since no definitive treatment exists for PE but to terminate a pregnancy. METHODS: This case-control study recruited (n = 90) pregnant who fulfilled inclusion criteria; they were allocated into three groups: EoPE (30/90) (< 34 wk of gestation); LoPE (30/90) (≥ 34 wk of gestation); and healthy pregnant (30/90). Demographic criteria; biochemical, hematological, and maternal plasma Ela levels were recorded for comparison. RESULTS: Serum Ela was significantly reduced in EoPE compared to LoPE and healthy controls (P = 0.0023). The correlation confirmed a strong inverse relationship with mean atrial blood pressure (r = -0.7, P < 0.001), while gestational age and platelets count showed a moderate correlation with (r = 0.4 with P < 0.0001). No correlation was confirmed between the body mass index (BMI) and urine albumin. The predictive ability of 25 centile serum Ela had an Odds ratio of 5.21, 95% confidence interval (1.28, 21.24), P = 0.02 for predicting EoPE. The receiver operator characteristic curve defined the Ela cutoff value at > 9.156 with 96.7% and 93.3% sensitivity and specificity, P < 0.0001 in predicting EoPE. CONCLUSION: A strong correlation of serum Ela with PE parameters with excellent sensitivity and specificity in distinguishing EoPE independent of the BMI, age, and blood pressure which makes Ela a recommendable marker in screening. Further research is warranted to explore prognostic and therapeutic applications for Ela in PE.
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spelling pubmed-103036162023-06-29 Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study Amer Ali, Eham Nori, Wassan Salman, Alea Farhan Al-Rawi, Taghreed S Saeed Hameed, Ban H Al-Ani, Raid M World J Clin Cases Case Control Study BACKGROUND: Preeclampsia (PE) is a multisystemic metabolic disease with an undetermined etiology. PE is a worldwide cause of maternal and perinatal morbidity, subdivided into early (EoPE) and late-onset (LoPE) according to 34 wk of gestation as a divider. Many researchers investigated biomarkers for predicting PE to halt its consequences on the feto-maternal outcome. Elabela (Ela) is a newly discovered peptide hormone that was implicated in PE pathogenesis. Earlier rodent studies discussed Ela’s role in controlling blood pressure. Moreover, Ela deficiency was associated with PE development. AIM: To test whether plasma Ela could serve as a reliable marker for predicting PE based on the time of onset (EoPE vs LoPE) compared to age and body mass matched healthy controls since no definitive treatment exists for PE but to terminate a pregnancy. METHODS: This case-control study recruited (n = 90) pregnant who fulfilled inclusion criteria; they were allocated into three groups: EoPE (30/90) (< 34 wk of gestation); LoPE (30/90) (≥ 34 wk of gestation); and healthy pregnant (30/90). Demographic criteria; biochemical, hematological, and maternal plasma Ela levels were recorded for comparison. RESULTS: Serum Ela was significantly reduced in EoPE compared to LoPE and healthy controls (P = 0.0023). The correlation confirmed a strong inverse relationship with mean atrial blood pressure (r = -0.7, P < 0.001), while gestational age and platelets count showed a moderate correlation with (r = 0.4 with P < 0.0001). No correlation was confirmed between the body mass index (BMI) and urine albumin. The predictive ability of 25 centile serum Ela had an Odds ratio of 5.21, 95% confidence interval (1.28, 21.24), P = 0.02 for predicting EoPE. The receiver operator characteristic curve defined the Ela cutoff value at > 9.156 with 96.7% and 93.3% sensitivity and specificity, P < 0.0001 in predicting EoPE. CONCLUSION: A strong correlation of serum Ela with PE parameters with excellent sensitivity and specificity in distinguishing EoPE independent of the BMI, age, and blood pressure which makes Ela a recommendable marker in screening. Further research is warranted to explore prognostic and therapeutic applications for Ela in PE. Baishideng Publishing Group Inc 2023-06-16 2023-06-16 /pmc/articles/PMC10303616/ /pubmed/37388778 http://dx.doi.org/10.12998/wjcc.v11.i17.3993 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Control Study
Amer Ali, Eham
Nori, Wassan
Salman, Alea Farhan
Al-Rawi, Taghreed S Saeed
Hameed, Ban H
Al-Ani, Raid M
Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title_full Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title_fullStr Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title_full_unstemmed Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title_short Elabela is a reliable biomarker for predicting early onset preeclampsia: A comparative study
title_sort elabela is a reliable biomarker for predicting early onset preeclampsia: a comparative study
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303616/
https://www.ncbi.nlm.nih.gov/pubmed/37388778
http://dx.doi.org/10.12998/wjcc.v11.i17.3993
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