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...
Gespeichert in:
Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 2015-01, Vol.60 (1), p.42-47 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 47 |
---|---|
container_issue | 1 |
container_start_page | 42 |
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1640480356</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1640480356</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4569-68d0bc4aee3ddeb48ab4f2a173919e5cab095cd55650a841dda9f1e60bf2bbf3</originalsourceid><addsrcrecordid>eNqNkDFPwzAQhS0EoqXwDxDKyJJiJ7aTDAyl0AIqUIlKjJYTX4jBSYqdqOq_J1ULQixwy1u-9-7uIXRK8JDgJLp4mE-H-OewKNlDfcJC7tMYk33Ux0EU-QEhvIeOnHvrmIgyfIh6AQsY5jHro9Ez2Lb05rZuQFcbzbXR1atX595ItaZxnqyUNy60URYq70U3hTe2dVF519qBdHCMDnJpHJzsdIAWk5vF-NafPU3vxqOZn1HGE5_HCqcZlQChUpDSWKY0DySJwoQkwDKZ4oRlijHOsIwpUUomOQGO0zxI0zwcoPNt7NLWHy24RpTaZWCMrKBunSCc4u7tkPEOpVs0s7VzFnKxtLqUdi0IFpvuRNed-N1dZzvbbWjTEtS36ausDoi3wKo2DVj3btoVWFGANE3xV_blzqoNrP91j7ifP4ZXExwREoafqsCL3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1640480356</pqid></control><display><type>article</type><title>Serum Protein Profiling of Adults and Children With Crohn Disease</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Wiley Online Library All Journals</source><creator>Vaiopoulou, Anna ; Gazouli, Maria ; Papadopoulou, Aggeliki ; Anagnostopoulos, Athanassios K. ; Karamanolis, George ; Theodoropoulos, George E. ; M'Koma, Amosy ; Tsangaris, George T.</creator><creatorcontrib>Vaiopoulou, Anna ; Gazouli, Maria ; Papadopoulou, Aggeliki ; Anagnostopoulos, Athanassios K. ; Karamanolis, George ; Theodoropoulos, George E. ; M'Koma, Amosy ; Tsangaris, George T.</creatorcontrib><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.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/MPG.0000000000000579</identifier><identifier>PMID: 25250685</identifier><language>eng</language><publisher>United States: by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</publisher><subject>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</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2015-01, Vol.60 (1), p.42-47</ispartof><rights>2015 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>2015 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4569-68d0bc4aee3ddeb48ab4f2a173919e5cab095cd55650a841dda9f1e60bf2bbf3</citedby><cites>FETCH-LOGICAL-c4569-68d0bc4aee3ddeb48ab4f2a173919e5cab095cd55650a841dda9f1e60bf2bbf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2FMPG.0000000000000579$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2FMPG.0000000000000579$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25250685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vaiopoulou, Anna</creatorcontrib><creatorcontrib>Gazouli, Maria</creatorcontrib><creatorcontrib>Papadopoulou, Aggeliki</creatorcontrib><creatorcontrib>Anagnostopoulos, Athanassios K.</creatorcontrib><creatorcontrib>Karamanolis, George</creatorcontrib><creatorcontrib>Theodoropoulos, George E.</creatorcontrib><creatorcontrib>M'Koma, Amosy</creatorcontrib><creatorcontrib>Tsangaris, George T.</creatorcontrib><title>Serum Protein Profiling of Adults and Children With Crohn Disease</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><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.</description><subject>Adult</subject><subject>Age of Onset</subject><subject>Apolipoprotein B-100 - blood</subject><subject>Apolipoprotein B-100 - chemistry</subject><subject>Apolipoprotein B-100 - metabolism</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - chemistry</subject><subject>Biomarkers - metabolism</subject><subject>Blood Proteins - analysis</subject><subject>Blood Proteins - chemistry</subject><subject>Blood Proteins - metabolism</subject><subject>Blotting, Western</subject><subject>Ceruloplasmin - analysis</subject><subject>Ceruloplasmin - chemistry</subject><subject>Ceruloplasmin - metabolism</subject><subject>Child</subject><subject>Clusterin - blood</subject><subject>Clusterin - chemistry</subject><subject>Clusterin - metabolism</subject><subject>Crohn disease</subject><subject>Crohn Disease - blood</subject><subject>Crohn Disease - epidemiology</subject><subject>Crohn Disease - physiopathology</subject><subject>Female</subject><subject>Greece - epidemiology</subject><subject>Humans</subject><subject>inflammatory bowel disease</subject><subject>Male</subject><subject>paediatric</subject><subject>Peptide Mapping</subject><subject>proteomics</subject><subject>Proteomics - methods</subject><subject>Severity of Illness Index</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Two-Dimensional Difference Gel Electrophoresis</subject><subject>ulcerative colitis</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkDFPwzAQhS0EoqXwDxDKyJJiJ7aTDAyl0AIqUIlKjJYTX4jBSYqdqOq_J1ULQixwy1u-9-7uIXRK8JDgJLp4mE-H-OewKNlDfcJC7tMYk33Ux0EU-QEhvIeOnHvrmIgyfIh6AQsY5jHro9Ez2Lb05rZuQFcbzbXR1atX595ItaZxnqyUNy60URYq70U3hTe2dVF519qBdHCMDnJpHJzsdIAWk5vF-NafPU3vxqOZn1HGE5_HCqcZlQChUpDSWKY0DySJwoQkwDKZ4oRlijHOsIwpUUomOQGO0zxI0zwcoPNt7NLWHy24RpTaZWCMrKBunSCc4u7tkPEOpVs0s7VzFnKxtLqUdi0IFpvuRNed-N1dZzvbbWjTEtS36ausDoi3wKo2DVj3btoVWFGANE3xV_blzqoNrP91j7ifP4ZXExwREoafqsCL3w</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Vaiopoulou, Anna</creator><creator>Gazouli, Maria</creator><creator>Papadopoulou, Aggeliki</creator><creator>Anagnostopoulos, Athanassios K.</creator><creator>Karamanolis, George</creator><creator>Theodoropoulos, George E.</creator><creator>M'Koma, Amosy</creator><creator>Tsangaris, George T.</creator><general>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201501</creationdate><title>Serum Protein Profiling of Adults and Children With Crohn Disease</title><author>Vaiopoulou, Anna ; Gazouli, Maria ; Papadopoulou, Aggeliki ; Anagnostopoulos, Athanassios K. ; Karamanolis, George ; Theodoropoulos, George E. ; M'Koma, Amosy ; Tsangaris, George T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4569-68d0bc4aee3ddeb48ab4f2a173919e5cab095cd55650a841dda9f1e60bf2bbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Age of Onset</topic><topic>Apolipoprotein B-100 - blood</topic><topic>Apolipoprotein B-100 - chemistry</topic><topic>Apolipoprotein B-100 - metabolism</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - chemistry</topic><topic>Biomarkers - metabolism</topic><topic>Blood Proteins - analysis</topic><topic>Blood Proteins - chemistry</topic><topic>Blood Proteins - metabolism</topic><topic>Blotting, Western</topic><topic>Ceruloplasmin - analysis</topic><topic>Ceruloplasmin - chemistry</topic><topic>Ceruloplasmin - metabolism</topic><topic>Child</topic><topic>Clusterin - blood</topic><topic>Clusterin - chemistry</topic><topic>Clusterin - metabolism</topic><topic>Crohn disease</topic><topic>Crohn Disease - blood</topic><topic>Crohn Disease - epidemiology</topic><topic>Crohn Disease - physiopathology</topic><topic>Female</topic><topic>Greece - epidemiology</topic><topic>Humans</topic><topic>inflammatory bowel disease</topic><topic>Male</topic><topic>paediatric</topic><topic>Peptide Mapping</topic><topic>proteomics</topic><topic>Proteomics - methods</topic><topic>Severity of Illness Index</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Two-Dimensional Difference Gel Electrophoresis</topic><topic>ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vaiopoulou, Anna</creatorcontrib><creatorcontrib>Gazouli, Maria</creatorcontrib><creatorcontrib>Papadopoulou, Aggeliki</creatorcontrib><creatorcontrib>Anagnostopoulos, Athanassios K.</creatorcontrib><creatorcontrib>Karamanolis, George</creatorcontrib><creatorcontrib>Theodoropoulos, George E.</creatorcontrib><creatorcontrib>M'Koma, Amosy</creatorcontrib><creatorcontrib>Tsangaris, George T.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vaiopoulou, Anna</au><au>Gazouli, Maria</au><au>Papadopoulou, Aggeliki</au><au>Anagnostopoulos, Athanassios K.</au><au>Karamanolis, George</au><au>Theodoropoulos, George E.</au><au>M'Koma, Amosy</au><au>Tsangaris, George T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum Protein Profiling of Adults and Children With Crohn Disease</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2015-01</date><risdate>2015</risdate><volume>60</volume><issue>1</issue><spage>42</spage><epage>47</epage><pages>42-47</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0277-2116 |
ispartof | Journal of pediatric gastroenterology and nutrition, 2015-01, Vol.60 (1), p.42-47 |
issn | 0277-2116 1536-4801 |
language | eng |
recordid | cdi_proquest_miscellaneous_1640480356 |
source | MEDLINE; Journals@Ovid Complete; Wiley Online Library All Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T19%3A31%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Serum%20Protein%20Profiling%20of%20Adults%20and%20Children%20With%20Crohn%20Disease&rft.jtitle=Journal%20of%20pediatric%20gastroenterology%20and%20nutrition&rft.au=Vaiopoulou,%20Anna&rft.date=2015-01&rft.volume=60&rft.issue=1&rft.spage=42&rft.epage=47&rft.pages=42-47&rft.issn=0277-2116&rft.eissn=1536-4801&rft_id=info:doi/10.1097/MPG.0000000000000579&rft_dat=%3Cproquest_cross%3E1640480356%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1640480356&rft_id=info:pmid/25250685&rfr_iscdi=true |