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A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients

BACKGROUND: Evident adolescent idiopathic scoliosis (AIS) incurs high treatment costs, low quality of life, and many complications. Early screening of AIS is essential to avoid progressing to an evident stage. However, there is no valid serum biomarker for AIS for early screening. METHODS: Antibody-...

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Autores principales: Shao, Zhenxuan, Zhang, Zengjie, Tu, Yiting, Huang, Chongan, Chen, Liang, Sun, Anna, Sheng, Sunren, Zhang, Xiaolei, Wu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478410/
https://www.ncbi.nlm.nih.gov/pubmed/37667193
http://dx.doi.org/10.1186/s12864-023-09624-7
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author Shao, Zhenxuan
Zhang, Zengjie
Tu, Yiting
Huang, Chongan
Chen, Liang
Sun, Anna
Sheng, Sunren
Zhang, Xiaolei
Wu, Yan
author_facet Shao, Zhenxuan
Zhang, Zengjie
Tu, Yiting
Huang, Chongan
Chen, Liang
Sun, Anna
Sheng, Sunren
Zhang, Xiaolei
Wu, Yan
author_sort Shao, Zhenxuan
collection PubMed
description BACKGROUND: Evident adolescent idiopathic scoliosis (AIS) incurs high treatment costs, low quality of life, and many complications. Early screening of AIS is essential to avoid progressing to an evident stage. However, there is no valid serum biomarker for AIS for early screening. METHODS: Antibody-based array is a large-scale study of proteins, which is expected to reveal a serum protein signature as biomarker for AIS. There are two segments of the research, including biomarkers screening and validation. In the biomarkers screening group, a total of 16 volunteers participated in this study, and we carried out differentially expressed proteins screening via protein array assay between No-AIS group and the AIS group, through which GeneSet enrichment analysis was performed. In the validation group with a total of 62 volunteers, the differentially expressed proteins from screening group were verified by Enzyme-Linked immunosorbent assay (ELISA), and then multiple regression analysis. RESULTS: In our study, there were twenty-nine differentially expressed proteins in AIS, through Protein array assay and GeneSet enrichment analysis in the biomarkers screening group. Then the expression of FAP, CD23 and B2M decreased as the degree of AIS increased via ELISA in validation group (FAP, p < 0.0001; CD23, p = 0.0002; B2M, p < 0.0001). Further, the results of multiple regression analysis showed that FAP, CD23 are linked to Cobb angle, whereas B2M were excluded because of multicollinearity. CONCLUSIONS: Altogether, we found that serum protein FAP and CD23 are intimately related to AIS, suggesting FAP and CD23 are expected to serve as the serum biomarkers, which significantly facilitate frequent longitudinal monitoring as to keep track of disease progression and tailor treatment accordingly. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09624-7.
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spelling pubmed-104784102023-09-06 A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients Shao, Zhenxuan Zhang, Zengjie Tu, Yiting Huang, Chongan Chen, Liang Sun, Anna Sheng, Sunren Zhang, Xiaolei Wu, Yan BMC Genomics Research BACKGROUND: Evident adolescent idiopathic scoliosis (AIS) incurs high treatment costs, low quality of life, and many complications. Early screening of AIS is essential to avoid progressing to an evident stage. However, there is no valid serum biomarker for AIS for early screening. METHODS: Antibody-based array is a large-scale study of proteins, which is expected to reveal a serum protein signature as biomarker for AIS. There are two segments of the research, including biomarkers screening and validation. In the biomarkers screening group, a total of 16 volunteers participated in this study, and we carried out differentially expressed proteins screening via protein array assay between No-AIS group and the AIS group, through which GeneSet enrichment analysis was performed. In the validation group with a total of 62 volunteers, the differentially expressed proteins from screening group were verified by Enzyme-Linked immunosorbent assay (ELISA), and then multiple regression analysis. RESULTS: In our study, there were twenty-nine differentially expressed proteins in AIS, through Protein array assay and GeneSet enrichment analysis in the biomarkers screening group. Then the expression of FAP, CD23 and B2M decreased as the degree of AIS increased via ELISA in validation group (FAP, p < 0.0001; CD23, p = 0.0002; B2M, p < 0.0001). Further, the results of multiple regression analysis showed that FAP, CD23 are linked to Cobb angle, whereas B2M were excluded because of multicollinearity. CONCLUSIONS: Altogether, we found that serum protein FAP and CD23 are intimately related to AIS, suggesting FAP and CD23 are expected to serve as the serum biomarkers, which significantly facilitate frequent longitudinal monitoring as to keep track of disease progression and tailor treatment accordingly. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09624-7. BioMed Central 2023-09-04 /pmc/articles/PMC10478410/ /pubmed/37667193 http://dx.doi.org/10.1186/s12864-023-09624-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shao, Zhenxuan
Zhang, Zengjie
Tu, Yiting
Huang, Chongan
Chen, Liang
Sun, Anna
Sheng, Sunren
Zhang, Xiaolei
Wu, Yan
A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title_full A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title_fullStr A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title_full_unstemmed A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title_short A targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
title_sort targeted antibody-based array reveals a serum protein signature as biomarker for adolescent idiopathic scoliosis patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478410/
https://www.ncbi.nlm.nih.gov/pubmed/37667193
http://dx.doi.org/10.1186/s12864-023-09624-7
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