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Publication Date:
November 2011
ISSN:
1437-4331
DOI:
10.1515/cclm.2011.805

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Clinical Chemistry and Laboratory Medicine (CCLM)

Published in Association with the International Federation of Clinical Chemistry and Laboratory Medicine and the European Federation of Clinical Chemistry and Laboratory Medicine

Editor-in-Chief: Plebani, Mario

Editorial Board Member: Lippi, Giuseppe / Gillery, Philippe / Kazmierczak, Steven / Lackner, Karl J. / Melichar, Bohuslav / Siest, Gérard / Whitfield, John B. / Abi Fadel, Marianne / Alvarez Menendez, Francisco V. / Azzazy, Hassan M.E. / Diamandis, Eleftherios P. / Eckardstein, Arnold / Favaloro, Emmanuel J. / Griesmacher, Andrea / Herrmann, Wolfgang / Hoffmann, Johannes J.M.L. / Hooijkaas, Herbert / Ichihara, Kiyoshi / Kaabachi, Naziha / Kim, Jeong-Ho / Korte, Wolfgang / Kroupis, Christos / Lai, Leslie Charles / Lam, Wai Kei Christopher / Marc, Janja / Miyoshi, Eiji / Özben, Tomris / Palicka, Vladimir / Panteghini, Mauro / Queralto, Jose M. / Scartezini, Marileia / Simundic, Ana-Maria / Tsongalis, Gregory J. / Wallemacq, Pierre E. / Yan, Shengkai / Young, Ian S. / Chiu, Rossa Wai Kwun / Ghosh, Debabrata / Kappelmayer, Janos / Lehmann, Sylvain / Sypniewska, Grazyna

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Elevated plasma matrix metalloproteinase-9 protein and its gene polymorphism in patients with community-acquired pneumonia

Ting-Yen Chiang1, a / Ling-Yuh Shyu2, 3, a / Thomas-Chang Yao Tsao1 / Ming-Hsien Chien4, 5 / Shih-Ming Tsao1, 3, 6 / Yuan-Ti Lee1, 3, 6 / 3, 7

1School of Medicine, Chung Shan Medical University, Taichung, Taiwan

2Department of Parasitology, School of Medicine, Chung Shan Medical University, Taiwan

3Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan

4Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan

5Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

6Division of Infectious Diseases, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan

7Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan

aTing-Yen Chiang and Ling-Yuh Shyu contributed equally to this article.

Corresponding authors: Shun-Fa Yang or Shih-Ming Tsao or Yuan-Ti Lee, Institute of Medicine, Chung Shan Medical University, 110, Section 1, Chien-Kuo N. Road, Taichung, Taiwan Phone: +886-4-24739595 ext. 34253, Fax: +886-4-24723229

Citation Information: Clinical Chemistry and Laboratory Medicine. Volume 50, Issue 3, Pages 449–454, ISSN (Online) 1437-4331, ISSN (Print) 1434-6621, DOI: 10.1515/cclm.2011.805, November 2011

Publication History:
Received:
2011-09-14
Accepted:
2011-11-08
Published Online:
2011-11-23

Abstract

Background: The purpose here was to detect the association among plasma matrix metalloproteinase-9 (MMP-9) concentration, single nucleotide polymorphisms (SNPs) of MMP-9 gene and community-acquired pneumonia (CAP).

Methods: The enzyme-linked immunosorbent assay (ELISA) and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) were, respectively used to measure the plasma MMP-9 level and its gene polymorphisms.

Results: The level of plasma of MMP-9 was elevated in patients with CAP as compared to that of normal controls and decreased significantly after treatment. Plasma MMP-9 concentration was significantly correlated with white blood cell (WBC) and neutrophil counts in patients with CAP. No significant difference was found in the genotypes distribution of MMP-9 SNPs, rs3918242, rs17576 or rs2274756, between patients with CAP and normal controls. Plasma MMP-9 concentration was not associated with MMP-9 polymorphism. When the cut-off level of the plasma MMP-9 concentration was set to be 105.02 ng/mL, the odds ratio of plasma MMP-9 for CAP risk was 9.86 (95% confident interval: 4.27–22.75). Plasma MMP-9 level may act as a prediction marker for CAP.

Conclusions: Elevated plasma MMP-9 could be a biological marker for the diagnosis and be a new strategy for target therapy of community-acquired pneumonia.

Keywords: community-acquired pneumonia; gene polymorphism; metalloproteinase-9 (MMP-9)

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