Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia

Background Preeclampsia (PE) is a serious pregnancy complication, resulting in potentially life-threatening conditions for both mother and foetus. It is worth noting that early-onset PE has become a great challenge for clinicians due to its complex manifestation, rapid progression and serious compli...

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Main Authors: Qinghong Ji, Shulin Zhang, Wen Jiang, Jue Wang, Yun Luan, Qian Xin
Format: Article
Language:English
Published: Taylor & Francis Group 2023-12-01
Series:Journal of Obstetrics and Gynaecology
Subjects:
Online Access:http://dx.doi.org/10.1080/01443615.2023.2259982
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author Qinghong Ji
Shulin Zhang
Wen Jiang
Jue Wang
Yun Luan
Qian Xin
author_facet Qinghong Ji
Shulin Zhang
Wen Jiang
Jue Wang
Yun Luan
Qian Xin
author_sort Qinghong Ji
collection DOAJ
description Background Preeclampsia (PE) is a serious pregnancy complication, resulting in potentially life-threatening conditions for both mother and foetus. It is worth noting that early-onset PE has become a great challenge for clinicians due to its complex manifestation, rapid progression and serious complications. This study aims to investigate differential serum proteome profiles in patients with early-onset PE. Methods Each serum sample was separated using a nanoliter flow rate Easy-nLC chromatography system. Then the samples were analysed by mass spectrometry. Bioinformatics analyses were conducted to analyse the functional categories or signal transduction pathways for differentially abundant proteins. Key proteins identified by mass spectrometry were verified by ELISA. Results We found 30 and 34 proteins were upregulated and downregulated in early-onset PE patients (n = 3) vs controls (n = 3), respectively. Functional enrichment analysis revealed differentially expressed proteins related to the immune response and regulation of peptidase activity. ELISA confirmed that there were lower CSH1 levels and higher LPA concentrations in the serum samples of early-onset PE patients (n = 22) than in healthy controls (n = 19) (p < 0.05 for CSH1 and p < 0.001 for LPA). Conclusions This study revealed the critical features of serum proteins in early-onset PE patients. LPA and CSH1 may serve as biomarkers for early-onset PE diagnosis and therapy.
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spelling doaj.art-38f67c44e67c4766af884927eb731b362023-11-02T13:56:29ZengTaylor & Francis GroupJournal of Obstetrics and Gynaecology0144-36151364-68932023-12-0143210.1080/01443615.2023.22599822259982Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsiaQinghong Ji0Shulin Zhang1Wen Jiang2Jue Wang3Yun Luan4Qian Xin5Department of Obstetrics, The Second Hospital of Shandong UniversityDepartment of Digestive Disease, The Second Hospital of Shandong UniversityCentral Laboratory, Institute of Medical Science, The Second Hospital of Shandong UniversityCentral Laboratory, Institute of Medical Science, The Second Hospital of Shandong UniversityCentral Laboratory, Institute of Medical Science, The Second Hospital of Shandong UniversityCentral Laboratory, Institute of Medical Science, The Second Hospital of Shandong UniversityBackground Preeclampsia (PE) is a serious pregnancy complication, resulting in potentially life-threatening conditions for both mother and foetus. It is worth noting that early-onset PE has become a great challenge for clinicians due to its complex manifestation, rapid progression and serious complications. This study aims to investigate differential serum proteome profiles in patients with early-onset PE. Methods Each serum sample was separated using a nanoliter flow rate Easy-nLC chromatography system. Then the samples were analysed by mass spectrometry. Bioinformatics analyses were conducted to analyse the functional categories or signal transduction pathways for differentially abundant proteins. Key proteins identified by mass spectrometry were verified by ELISA. Results We found 30 and 34 proteins were upregulated and downregulated in early-onset PE patients (n = 3) vs controls (n = 3), respectively. Functional enrichment analysis revealed differentially expressed proteins related to the immune response and regulation of peptidase activity. ELISA confirmed that there were lower CSH1 levels and higher LPA concentrations in the serum samples of early-onset PE patients (n = 22) than in healthy controls (n = 19) (p < 0.05 for CSH1 and p < 0.001 for LPA). Conclusions This study revealed the critical features of serum proteins in early-onset PE patients. LPA and CSH1 may serve as biomarkers for early-onset PE diagnosis and therapy.http://dx.doi.org/10.1080/01443615.2023.2259982early-onset preeclampsialabel-free quantitative proteomicsbiomarkerschorionic somatomammotropin hormone 1lysophosphatidic acid
spellingShingle Qinghong Ji
Shulin Zhang
Wen Jiang
Jue Wang
Yun Luan
Qian Xin
Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
Journal of Obstetrics and Gynaecology
early-onset preeclampsia
label-free quantitative proteomics
biomarkers
chorionic somatomammotropin hormone 1
lysophosphatidic acid
title Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
title_full Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
title_fullStr Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
title_full_unstemmed Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
title_short Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia
title_sort serum protein profile analysis via label free quantitation proteomics in patients with early onset preeclampsia
topic early-onset preeclampsia
label-free quantitative proteomics
biomarkers
chorionic somatomammotropin hormone 1
lysophosphatidic acid
url http://dx.doi.org/10.1080/01443615.2023.2259982
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