Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes

Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes Roos C. Padmos 1 , Nanette C. Schloot 2 , Huriya Beyan 3 , Cindy Ruwhof 1 , Frank J.T. Staal 1 , Dick de Ridder 4 , Henk-Jan Aanstoot 1 , Wai Kwan Lam-Tse 1 , Harm de Wit 1 , Christian de Herder 2 , Roos C. Drexhage 1 , Barbara Menart...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2008-10, Vol.57 (10), p.2768-2773
Hauptverfasser: PADMOS, Roos C, SCHLOOT, Nanette C, DREXHAGE, Roos C, MENART, Barbara, LESLIE, R. David, DREXHAGE, Hemmo A, BEYAN, Huriya, RUWHOF, Cindy, STAAL, Frank J. T, DE RIDDER, Dick, AANSTOOT, Henk-Jan, LAM-TSE, Wai Kwan, DE WIT, Harm, DE HERDER, Christian
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container_end_page 2773
container_issue 10
container_start_page 2768
container_title Diabetes (New York, N.Y.)
container_volume 57
creator PADMOS, Roos C
SCHLOOT, Nanette C
DREXHAGE, Roos C
MENART, Barbara
LESLIE, R. David
DREXHAGE, Hemmo A
BEYAN, Huriya
RUWHOF, Cindy
STAAL, Frank J. T
DE RIDDER, Dick
AANSTOOT, Henk-Jan
LAM-TSE, Wai Kwan
DE WIT, Harm
DE HERDER, Christian
description Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes Roos C. Padmos 1 , Nanette C. Schloot 2 , Huriya Beyan 3 , Cindy Ruwhof 1 , Frank J.T. Staal 1 , Dick de Ridder 4 , Henk-Jan Aanstoot 1 , Wai Kwan Lam-Tse 1 , Harm de Wit 1 , Christian de Herder 2 , Roos C. Drexhage 1 , Barbara Menart 2 , R. David Leslie 3 , Hemmo A. Drexhage 1 and the LADA Consortium * 1 Department of Immunology, Erasmus MC, Rotterdam, the Netherlands 2 German Diabetes Center, Düsseldorf, Germany 3 St. Bartholomew's Hospital, London, U.K 4 Delft University of Technology, Delft, the Netherlands Corresponding author: Hemmo A. Drexhage, h.drexhage{at}erasmusmc.nl Abstract OBJECTIVE— There is evidence that monocytes of patients with type 1 diabetes show proinflammatory activation and disturbed migration/adhesion, but the evidence is inconsistent. Our hypothesis is that monocytes are distinctly activated/disturbed in different subforms of autoimmune diabetes. RESEARCH DESIGN AND METHODS— We studied patterns of inflammatory gene expression in monocytes of patients with type 1 diabetes (juvenile onset, n = 30; adult onset, n = 30) and latent autoimmune diabetes of the adult (LADA) ( n = 30) (controls subjects, n = 49; type 2 diabetic patients, n = 30) using quantitative PCR. We tested 25 selected genes: 12 genes detected in a prestudy via whole-genome analyses plus an additional 13 genes identified as part of a monocyte inflammatory signature previously reported. RESULTS— We identified two distinct monocyte gene expression clusters in autoimmune diabetes. One cluster (comprising 12 proinflammatory cytokine/compound genes with a putative key gene PDE4B ) was detected in 60% of LADA and 28% of adult-onset type 1 diabetic patients but in only 10% of juvenile-onset type 1 diabetic patients. A second cluster (comprising 10 chemotaxis, adhesion, motility, and metabolism genes) was detected in 43% of juvenile-onset type 1 diabetic and 33% of LADA patients but in only 9% of adult-onset type 1 diabetic patients. CONCLUSIONS— Subgroups of type 1 diabetic patients show an abnormal monocyte gene expression with two profiles, supporting a concept of heterogeneity in the pathogenesis of autoimmune diabetes only partly overlapping with the presently known diagnostic categories. Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 3 July 2008. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not
doi_str_mv 10.2337/db08-0496
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David ; DREXHAGE, Hemmo A ; BEYAN, Huriya ; RUWHOF, Cindy ; STAAL, Frank J. T ; DE RIDDER, Dick ; AANSTOOT, Henk-Jan ; LAM-TSE, Wai Kwan ; DE WIT, Harm ; DE HERDER, Christian</creator><creatorcontrib>PADMOS, Roos C ; SCHLOOT, Nanette C ; DREXHAGE, Roos C ; MENART, Barbara ; LESLIE, R. David ; DREXHAGE, Hemmo A ; BEYAN, Huriya ; RUWHOF, Cindy ; STAAL, Frank J. T ; DE RIDDER, Dick ; AANSTOOT, Henk-Jan ; LAM-TSE, Wai Kwan ; DE WIT, Harm ; DE HERDER, Christian ; LADA Consortium ; the LADA Consortium</creatorcontrib><description>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes Roos C. Padmos 1 , Nanette C. Schloot 2 , Huriya Beyan 3 , Cindy Ruwhof 1 , Frank J.T. Staal 1 , Dick de Ridder 4 , Henk-Jan Aanstoot 1 , Wai Kwan Lam-Tse 1 , Harm de Wit 1 , Christian de Herder 2 , Roos C. Drexhage 1 , Barbara Menart 2 , R. David Leslie 3 , Hemmo A. Drexhage 1 and the LADA Consortium * 1 Department of Immunology, Erasmus MC, Rotterdam, the Netherlands 2 German Diabetes Center, Düsseldorf, Germany 3 St. Bartholomew's Hospital, London, U.K 4 Delft University of Technology, Delft, the Netherlands Corresponding author: Hemmo A. Drexhage, h.drexhage{at}erasmusmc.nl Abstract OBJECTIVE— There is evidence that monocytes of patients with type 1 diabetes show proinflammatory activation and disturbed migration/adhesion, but the evidence is inconsistent. Our hypothesis is that monocytes are distinctly activated/disturbed in different subforms of autoimmune diabetes. RESEARCH DESIGN AND METHODS— We studied patterns of inflammatory gene expression in monocytes of patients with type 1 diabetes (juvenile onset, n = 30; adult onset, n = 30) and latent autoimmune diabetes of the adult (LADA) ( n = 30) (controls subjects, n = 49; type 2 diabetic patients, n = 30) using quantitative PCR. We tested 25 selected genes: 12 genes detected in a prestudy via whole-genome analyses plus an additional 13 genes identified as part of a monocyte inflammatory signature previously reported. RESULTS— We identified two distinct monocyte gene expression clusters in autoimmune diabetes. One cluster (comprising 12 proinflammatory cytokine/compound genes with a putative key gene PDE4B ) was detected in 60% of LADA and 28% of adult-onset type 1 diabetic patients but in only 10% of juvenile-onset type 1 diabetic patients. A second cluster (comprising 10 chemotaxis, adhesion, motility, and metabolism genes) was detected in 43% of juvenile-onset type 1 diabetic and 33% of LADA patients but in only 9% of adult-onset type 1 diabetic patients. CONCLUSIONS— Subgroups of type 1 diabetic patients show an abnormal monocyte gene expression with two profiles, supporting a concept of heterogeneity in the pathogenesis of autoimmune diabetes only partly overlapping with the presently known diagnostic categories. Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 3 July 2008. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. * * Members of the LADA Consortium can be found in the appendix . Accepted June 21, 2008. Received April 11, 2008. DIABETES</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/db08-0496</identifier><identifier>PMID: 18599519</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Adult ; Antigens ; Biological and medical sciences ; Bipolar disorder ; C-Reactive Protein - genetics ; C-Reactive Protein - metabolism ; Child ; Cluster Analysis ; Cytokines - blood ; Cytokines - genetics ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Type 1 - blood ; Diabetes Mellitus, Type 1 - genetics ; Diabetes. Impaired glucose tolerance ; Diagnosis ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Gene expression ; Gene Expression Profiling - methods ; Genetic aspects ; Genomes ; Health aspects ; Humans ; Hypotheses ; Male ; Medical sciences ; Monocytes - metabolism ; Pathogenesis ; Pathophysiology ; Research design ; Reverse Transcriptase Polymerase Chain Reaction ; Serum Amyloid P-Component - genetics ; Serum Amyloid P-Component - metabolism ; Tumor necrosis factor-TNF</subject><ispartof>Diabetes (New York, N.Y.), 2008-10, Vol.57 (10), p.2768-2773</ispartof><rights>2008 INIST-CNRS</rights><rights>COPYRIGHT 2008 American Diabetes Association</rights><rights>Copyright American Diabetes Association Oct 2008</rights><rights>Copyright © 2008, American Diabetes Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-578e4ba3b6b0e3410985ec9d2091c1f34c6070283063b37af07fdacf84a5a9e23</citedby><cites>FETCH-LOGICAL-c536t-578e4ba3b6b0e3410985ec9d2091c1f34c6070283063b37af07fdacf84a5a9e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2551688/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2551688/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20707916$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18599519$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PADMOS, Roos C</creatorcontrib><creatorcontrib>SCHLOOT, Nanette C</creatorcontrib><creatorcontrib>DREXHAGE, Roos C</creatorcontrib><creatorcontrib>MENART, Barbara</creatorcontrib><creatorcontrib>LESLIE, R. David</creatorcontrib><creatorcontrib>DREXHAGE, Hemmo A</creatorcontrib><creatorcontrib>BEYAN, Huriya</creatorcontrib><creatorcontrib>RUWHOF, Cindy</creatorcontrib><creatorcontrib>STAAL, Frank J. T</creatorcontrib><creatorcontrib>DE RIDDER, Dick</creatorcontrib><creatorcontrib>AANSTOOT, Henk-Jan</creatorcontrib><creatorcontrib>LAM-TSE, Wai Kwan</creatorcontrib><creatorcontrib>DE WIT, Harm</creatorcontrib><creatorcontrib>DE HERDER, Christian</creatorcontrib><creatorcontrib>LADA Consortium</creatorcontrib><creatorcontrib>the LADA Consortium</creatorcontrib><title>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes Roos C. Padmos 1 , Nanette C. Schloot 2 , Huriya Beyan 3 , Cindy Ruwhof 1 , Frank J.T. Staal 1 , Dick de Ridder 4 , Henk-Jan Aanstoot 1 , Wai Kwan Lam-Tse 1 , Harm de Wit 1 , Christian de Herder 2 , Roos C. Drexhage 1 , Barbara Menart 2 , R. David Leslie 3 , Hemmo A. Drexhage 1 and the LADA Consortium * 1 Department of Immunology, Erasmus MC, Rotterdam, the Netherlands 2 German Diabetes Center, Düsseldorf, Germany 3 St. Bartholomew's Hospital, London, U.K 4 Delft University of Technology, Delft, the Netherlands Corresponding author: Hemmo A. Drexhage, h.drexhage{at}erasmusmc.nl Abstract OBJECTIVE— There is evidence that monocytes of patients with type 1 diabetes show proinflammatory activation and disturbed migration/adhesion, but the evidence is inconsistent. Our hypothesis is that monocytes are distinctly activated/disturbed in different subforms of autoimmune diabetes. RESEARCH DESIGN AND METHODS— We studied patterns of inflammatory gene expression in monocytes of patients with type 1 diabetes (juvenile onset, n = 30; adult onset, n = 30) and latent autoimmune diabetes of the adult (LADA) ( n = 30) (controls subjects, n = 49; type 2 diabetic patients, n = 30) using quantitative PCR. We tested 25 selected genes: 12 genes detected in a prestudy via whole-genome analyses plus an additional 13 genes identified as part of a monocyte inflammatory signature previously reported. RESULTS— We identified two distinct monocyte gene expression clusters in autoimmune diabetes. One cluster (comprising 12 proinflammatory cytokine/compound genes with a putative key gene PDE4B ) was detected in 60% of LADA and 28% of adult-onset type 1 diabetic patients but in only 10% of juvenile-onset type 1 diabetic patients. A second cluster (comprising 10 chemotaxis, adhesion, motility, and metabolism genes) was detected in 43% of juvenile-onset type 1 diabetic and 33% of LADA patients but in only 9% of adult-onset type 1 diabetic patients. CONCLUSIONS— Subgroups of type 1 diabetic patients show an abnormal monocyte gene expression with two profiles, supporting a concept of heterogeneity in the pathogenesis of autoimmune diabetes only partly overlapping with the presently known diagnostic categories. Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 3 July 2008. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. * * Members of the LADA Consortium can be found in the appendix . Accepted June 21, 2008. Received April 11, 2008. 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David</creatorcontrib><creatorcontrib>DREXHAGE, Hemmo A</creatorcontrib><creatorcontrib>BEYAN, Huriya</creatorcontrib><creatorcontrib>RUWHOF, Cindy</creatorcontrib><creatorcontrib>STAAL, Frank J. 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David</au><au>DREXHAGE, Hemmo A</au><au>BEYAN, Huriya</au><au>RUWHOF, Cindy</au><au>STAAL, Frank J. T</au><au>DE RIDDER, Dick</au><au>AANSTOOT, Henk-Jan</au><au>LAM-TSE, Wai Kwan</au><au>DE WIT, Harm</au><au>DE HERDER, Christian</au><aucorp>LADA Consortium</aucorp><aucorp>the LADA Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>57</volume><issue>10</issue><spage>2768</spage><epage>2773</epage><pages>2768-2773</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes Roos C. Padmos 1 , Nanette C. Schloot 2 , Huriya Beyan 3 , Cindy Ruwhof 1 , Frank J.T. Staal 1 , Dick de Ridder 4 , Henk-Jan Aanstoot 1 , Wai Kwan Lam-Tse 1 , Harm de Wit 1 , Christian de Herder 2 , Roos C. Drexhage 1 , Barbara Menart 2 , R. David Leslie 3 , Hemmo A. Drexhage 1 and the LADA Consortium * 1 Department of Immunology, Erasmus MC, Rotterdam, the Netherlands 2 German Diabetes Center, Düsseldorf, Germany 3 St. Bartholomew's Hospital, London, U.K 4 Delft University of Technology, Delft, the Netherlands Corresponding author: Hemmo A. Drexhage, h.drexhage{at}erasmusmc.nl Abstract OBJECTIVE— There is evidence that monocytes of patients with type 1 diabetes show proinflammatory activation and disturbed migration/adhesion, but the evidence is inconsistent. Our hypothesis is that monocytes are distinctly activated/disturbed in different subforms of autoimmune diabetes. RESEARCH DESIGN AND METHODS— We studied patterns of inflammatory gene expression in monocytes of patients with type 1 diabetes (juvenile onset, n = 30; adult onset, n = 30) and latent autoimmune diabetes of the adult (LADA) ( n = 30) (controls subjects, n = 49; type 2 diabetic patients, n = 30) using quantitative PCR. We tested 25 selected genes: 12 genes detected in a prestudy via whole-genome analyses plus an additional 13 genes identified as part of a monocyte inflammatory signature previously reported. RESULTS— We identified two distinct monocyte gene expression clusters in autoimmune diabetes. One cluster (comprising 12 proinflammatory cytokine/compound genes with a putative key gene PDE4B ) was detected in 60% of LADA and 28% of adult-onset type 1 diabetic patients but in only 10% of juvenile-onset type 1 diabetic patients. A second cluster (comprising 10 chemotaxis, adhesion, motility, and metabolism genes) was detected in 43% of juvenile-onset type 1 diabetic and 33% of LADA patients but in only 9% of adult-onset type 1 diabetic patients. CONCLUSIONS— Subgroups of type 1 diabetic patients show an abnormal monocyte gene expression with two profiles, supporting a concept of heterogeneity in the pathogenesis of autoimmune diabetes only partly overlapping with the presently known diagnostic categories. Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 3 July 2008. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. * * Members of the LADA Consortium can be found in the appendix . Accepted June 21, 2008. Received April 11, 2008. DIABETES</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>18599519</pmid><doi>10.2337/db08-0496</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Antigens
Biological and medical sciences
Bipolar disorder
C-Reactive Protein - genetics
C-Reactive Protein - metabolism
Child
Cluster Analysis
Cytokines - blood
Cytokines - genetics
Diabetes
Diabetes mellitus
Diabetes Mellitus, Type 1 - blood
Diabetes Mellitus, Type 1 - genetics
Diabetes. Impaired glucose tolerance
Diagnosis
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Gene expression
Gene Expression Profiling - methods
Genetic aspects
Genomes
Health aspects
Humans
Hypotheses
Male
Medical sciences
Monocytes - metabolism
Pathogenesis
Pathophysiology
Research design
Reverse Transcriptase Polymerase Chain Reaction
Serum Amyloid P-Component - genetics
Serum Amyloid P-Component - metabolism
Tumor necrosis factor-TNF
title Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes
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