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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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 |
format | Article |
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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&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.
DIABETES</description><subject>Adult</subject><subject>Antigens</subject><subject>Biological and medical sciences</subject><subject>Bipolar disorder</subject><subject>C-Reactive Protein - genetics</subject><subject>C-Reactive Protein - metabolism</subject><subject>Child</subject><subject>Cluster Analysis</subject><subject>Cytokines - blood</subject><subject>Cytokines - genetics</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Type 1 - blood</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diagnosis</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling - methods</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Monocytes - metabolism</subject><subject>Pathogenesis</subject><subject>Pathophysiology</subject><subject>Research design</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Serum Amyloid P-Component - genetics</subject><subject>Serum Amyloid P-Component - metabolism</subject><subject>Tumor necrosis factor-TNF</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkV1rFDEUhgdR7Fq98A_IICgIjuZj8nUjLNtahUq9UPAuZDJndlNmkm0yo-2_N9MdWvVGcpHAeXjJed6ieI7RO0KpeN82SFaoVvxBscKKqooS8eNhsUIIkwoLJY6KJyldIoR4Po-LIyyZUgyrVbE-cWl03o7ll-CDvRmhPAMP1en1PkJKLvjyawyd6yGVzpfraQxuGCYP5YkzDYyQnhaPOtMneLbcx8X3j6ffNp-q84uzz5v1eWUZ5WPFhIS6MbThDQJaY6QkA6taghS2uKO15UggIinitKHCdEh0rbGdrA0zCgg9Lj4ccvdTM0BrwY_R9Hof3WDijQ7G6b8n3u30NvzUhDHMpcwBr5eAGK4mSKMeXLLQ98ZDmJLmKtuh9P8gwURQxmfw5T_gZZiizxYyw2tJyW1adYC2pgedVQc_wvVoQ9_DFnR2tLnQaywlZgpjmvk3B97GkFKE7m5FjPRct57r1nPdmX3xp5N7cuk3A68WwCRr-i4ab12640hWLhSeg94euJ3b7n65CLpd6r1_MHH7A5EX_w1WrcA1</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>PADMOS, Roos C</creator><creator>SCHLOOT, Nanette C</creator><creator>DREXHAGE, Roos C</creator><creator>MENART, Barbara</creator><creator>LESLIE, R. David</creator><creator>DREXHAGE, Hemmo A</creator><creator>BEYAN, Huriya</creator><creator>RUWHOF, Cindy</creator><creator>STAAL, Frank J. T</creator><creator>DE RIDDER, Dick</creator><creator>AANSTOOT, Henk-Jan</creator><creator>LAM-TSE, Wai Kwan</creator><creator>DE WIT, Harm</creator><creator>DE HERDER, Christian</creator><general>American Diabetes Association</general><scope>IQODW</scope><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081001</creationdate><title>Distinct Monocyte Gene-Expression Profiles in Autoimmune Diabetes</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-578e4ba3b6b0e3410985ec9d2091c1f34c6070283063b37af07fdacf84a5a9e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Antigens</topic><topic>Biological and medical sciences</topic><topic>Bipolar disorder</topic><topic>C-Reactive Protein - genetics</topic><topic>C-Reactive Protein - metabolism</topic><topic>Child</topic><topic>Cluster Analysis</topic><topic>Cytokines - blood</topic><topic>Cytokines - genetics</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Type 1 - blood</topic><topic>Diabetes Mellitus, Type 1 - genetics</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diagnosis</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Monocytes - metabolism</topic><topic>Pathogenesis</topic><topic>Pathophysiology</topic><topic>Research design</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Serum Amyloid P-Component - genetics</topic><topic>Serum Amyloid P-Component - metabolism</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PADMOS, Roos C</au><au>SCHLOOT, Nanette C</au><au>DREXHAGE, Roos C</au><au>MENART, Barbara</au><au>LESLIE, R. 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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