Skip Navigation



European Heart Journal Advance Access published online on August 17, 2009

European Heart Journal, doi:10.1093/eurheartj/ehp308
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Rogacev, K. S.
Right arrow Articles by Heine, G. H.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rogacev, K. S.
Right arrow Articles by Heine, G. H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org

Monocyte heterogeneity in obesity and subclinical atherosclerosis

Kyrill S. Rogacev1,{dagger}, Christof Ulrich1,{dagger}, Lutz Blömer1, Florian Hornof1, Katrin Oster1, Maren Ziegelin1, Bodo Cremers2, Yvonne Grenner3, Jürgen Geisel4, Axel Schlitt5, Hans Köhler1, Danilo Fliser1, Matthias Girndt1 and Gunnar H. Heine1,*

1 Department of Internal Medicine IV, Saarland University Hospital, Homburg 66421, Germany
2 Department of Internal Medicine III, Saarland University Hospital, Homburg, Germany
3 Department of Internal Medicine II, Saarland University Hospital, Homburg, Germany
4 Central Clinical Chemistry Laboratory, Saarland University Hospital, Homburg, Germany
5 Department of Internal Medicine III, Martin-Luther-University, Halle/Saale, Germany

Received 22 September 2008; revised 14 June 2009; accepted 15 July 2009 * Corresponding author. Tel: +49 6841 162 3527, Fax: +49 6841 1623545, Email: gunnar.heine{at}uks.eu

Aims: Monocytes and monocyte-derived macrophages have been recognised as the cellular hallmark of atherosclerosis decades ago. Recently, they have also been shown to play a pivotal role in obesity. Monocytes display immunophenotypic heterogeneity with functionally distinct subpopulations. We initiated the I LIKE HOMe study to examine monocyte heterogeneity in obesity and subclinical atherosclerosis.

Methods and results: We assessed carotid intima media thickness (IMT), body mass index (BMI), and other cardiovascular risk factors in 622 healthy volunteers. Using flow-cytometry, we differentiated monocytes into CD14++CD16 and CD16+ cells, which we further subdivided into CD14++CD16+ and CD14(+)CD16+ cells. Body mass index was significantly correlated with carotid IMT. High CD16+ monocyte counts were significantly associated with both higher BMI and increased carotid IMT. Adjustment for CD16+ monocyte counts weakened the correlation between BMI and carotid IMT, suggesting that the increase in CD16+ monocyte numbers in obesity may partly explain the association between obesity and IMT.

Conclusion: Our results reveal a significant univariate association between CD16+ monocytes and both obesity and subclinical atherosclerosis in low-risk individuals. They are in line with recent observations that CD16+ monocytes show high endothelial affinity and a potent capacity to invade vascular lesions and to transform into pro-inflammatory cytokine producing macrophages.

Key Words: Immunology • Monocytes • Subclinical atherosclerosis • Obesity


{dagger} The first two authors contributed equally to the study.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.