Serum Protein Profiling of Adults and Children With Crohn Disease

ABSTRACT Objectives: Crohn disease (CD) and ulcerative colitis (UC), known collectively as inflammatory bowel diseases (IBDs), are chronic immunoinflammatory pathologies of unknown aetiology. Despite the frequent use of biomarkers in medical practice, there is a relative lack of information regardin...

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Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 2015-01, Vol.60 (1), p.42-47
Hauptverfasser: Vaiopoulou, Anna, Gazouli, Maria, Papadopoulou, Aggeliki, Anagnostopoulos, Athanassios K., Karamanolis, George, Theodoropoulos, George E., M'Koma, Amosy, Tsangaris, George T.
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container_issue 1
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container_title Journal of pediatric gastroenterology and nutrition
container_volume 60
creator Vaiopoulou, Anna
Gazouli, Maria
Papadopoulou, Aggeliki
Anagnostopoulos, Athanassios K.
Karamanolis, George
Theodoropoulos, George E.
M'Koma, Amosy
Tsangaris, George T.
description ABSTRACT Objectives: Crohn disease (CD) and ulcerative colitis (UC), known collectively as inflammatory bowel diseases (IBDs), are chronic immunoinflammatory pathologies of unknown aetiology. Despite the frequent use of biomarkers in medical practice, there is a relative lack of information regarding validated paediatric biomarkers for IBD. Furthermore, biomarkers proved to be efficacious in adults are frequently extrapolated to the paediatric clinical setting without considering that the pathogenesis of many diseases is distinctly different in children. In the present study, proteomics technology was used to monitor differences in protein expression among adult and young patients with CD, identify a panel of candidate protein biomarkers that may be used to improve prognostic–diagnostic accuracy, and advance paediatric medical care. Methods: Male and female serum samples from 12 adults and 12 children with active CD were subjected to 2‐dimensional gel electrophoresis. Following the relative quantitation of protein spots exhibiting a differential expression between the 2 groups by densitometry, the spots were further characterized by matrix‐assisted laser desorption tandem time‐of‐flight mass spectrometer. The results were confirmed by Western blot analysis. Results: Clusterin was found to be significantly overexpressed in adults with CD, whereas ceruloplasmin and apolipoprotein B‐100 were found to be significantly overexpressed in children, indicating that the expression of these proteins may be implicated in the onset or progression of CD in these 2 subgroups of patients. Conclusions: Interestingly, we found a differential expression of several proteins in adults versus paediatric patients with CD. Undoubtedly, future experiments using a larger cohort of patients with CD are needed to evaluate the relevance of our preliminary findings.
doi_str_mv 10.1097/MPG.0000000000000579
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Despite the frequent use of biomarkers in medical practice, there is a relative lack of information regarding validated paediatric biomarkers for IBD. Furthermore, biomarkers proved to be efficacious in adults are frequently extrapolated to the paediatric clinical setting without considering that the pathogenesis of many diseases is distinctly different in children. In the present study, proteomics technology was used to monitor differences in protein expression among adult and young patients with CD, identify a panel of candidate protein biomarkers that may be used to improve prognostic–diagnostic accuracy, and advance paediatric medical care. Methods: Male and female serum samples from 12 adults and 12 children with active CD were subjected to 2‐dimensional gel electrophoresis. Following the relative quantitation of protein spots exhibiting a differential expression between the 2 groups by densitometry, the spots were further characterized by matrix‐assisted laser desorption tandem time‐of‐flight mass spectrometer. The results were confirmed by Western blot analysis. Results: Clusterin was found to be significantly overexpressed in adults with CD, whereas ceruloplasmin and apolipoprotein B‐100 were found to be significantly overexpressed in children, indicating that the expression of these proteins may be implicated in the onset or progression of CD in these 2 subgroups of patients. Conclusions: Interestingly, we found a differential expression of several proteins in adults versus paediatric patients with CD. 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Despite the frequent use of biomarkers in medical practice, there is a relative lack of information regarding validated paediatric biomarkers for IBD. Furthermore, biomarkers proved to be efficacious in adults are frequently extrapolated to the paediatric clinical setting without considering that the pathogenesis of many diseases is distinctly different in children. In the present study, proteomics technology was used to monitor differences in protein expression among adult and young patients with CD, identify a panel of candidate protein biomarkers that may be used to improve prognostic–diagnostic accuracy, and advance paediatric medical care. Methods: Male and female serum samples from 12 adults and 12 children with active CD were subjected to 2‐dimensional gel electrophoresis. Following the relative quantitation of protein spots exhibiting a differential expression between the 2 groups by densitometry, the spots were further characterized by matrix‐assisted laser desorption tandem time‐of‐flight mass spectrometer. The results were confirmed by Western blot analysis. Results: Clusterin was found to be significantly overexpressed in adults with CD, whereas ceruloplasmin and apolipoprotein B‐100 were found to be significantly overexpressed in children, indicating that the expression of these proteins may be implicated in the onset or progression of CD in these 2 subgroups of patients. Conclusions: Interestingly, we found a differential expression of several proteins in adults versus paediatric patients with CD. 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Despite the frequent use of biomarkers in medical practice, there is a relative lack of information regarding validated paediatric biomarkers for IBD. Furthermore, biomarkers proved to be efficacious in adults are frequently extrapolated to the paediatric clinical setting without considering that the pathogenesis of many diseases is distinctly different in children. In the present study, proteomics technology was used to monitor differences in protein expression among adult and young patients with CD, identify a panel of candidate protein biomarkers that may be used to improve prognostic–diagnostic accuracy, and advance paediatric medical care. Methods: Male and female serum samples from 12 adults and 12 children with active CD were subjected to 2‐dimensional gel electrophoresis. Following the relative quantitation of protein spots exhibiting a differential expression between the 2 groups by densitometry, the spots were further characterized by matrix‐assisted laser desorption tandem time‐of‐flight mass spectrometer. The results were confirmed by Western blot analysis. Results: Clusterin was found to be significantly overexpressed in adults with CD, whereas ceruloplasmin and apolipoprotein B‐100 were found to be significantly overexpressed in children, indicating that the expression of these proteins may be implicated in the onset or progression of CD in these 2 subgroups of patients. Conclusions: Interestingly, we found a differential expression of several proteins in adults versus paediatric patients with CD. Undoubtedly, future experiments using a larger cohort of patients with CD are needed to evaluate the relevance of our preliminary findings.</abstract><cop>United States</cop><pub>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</pub><pmid>25250685</pmid><doi>10.1097/MPG.0000000000000579</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Age of Onset
Apolipoprotein B-100 - blood
Apolipoprotein B-100 - chemistry
Apolipoprotein B-100 - metabolism
Biomarkers - blood
Biomarkers - chemistry
Biomarkers - metabolism
Blood Proteins - analysis
Blood Proteins - chemistry
Blood Proteins - metabolism
Blotting, Western
Ceruloplasmin - analysis
Ceruloplasmin - chemistry
Ceruloplasmin - metabolism
Child
Clusterin - blood
Clusterin - chemistry
Clusterin - metabolism
Crohn disease
Crohn Disease - blood
Crohn Disease - epidemiology
Crohn Disease - physiopathology
Female
Greece - epidemiology
Humans
inflammatory bowel disease
Male
paediatric
Peptide Mapping
proteomics
Proteomics - methods
Severity of Illness Index
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Two-Dimensional Difference Gel Electrophoresis
ulcerative colitis
title Serum Protein Profiling of Adults and Children With Crohn Disease
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