Literature DB >> 21946608

Association of serum a disintegrin and metalloproteinase with thrombospodin motif 4 levels with the presence and severity of coronary artery disease.

Liming Chen1, Le Yang, Yanping Zha, Lianqun Cui.   

Abstract

OBJECTIVE: A disintegrin and metalloproteinase with thrombospodin motif 4 (ADAMTS4) has been shown to be an important player in atherosclerosis. However, the clinical significance of measuring serum ADAMTS4 levels has not been fully elucidated. We therefore investigate whether serum ADAMTS4 levels are associated with the presence and severity of coronary artery disease (CAD).
METHODS: Serum levels of ADAMTS4 were measured in 192 patients undergoing elective coronary angiography for suspected CAD, the severity of CAD was determined by the number of diseased vessels and the severity score of coronary stenosis.
RESULTS: Patients with CAD showed significantly higher levels of ADAMTS4 than did patients with normal coronary arteries [57.82 (48.96-70.32) vs. 46.55 (41.16-51.72) ng/ml, P<0.001]. ADAMTS4 levels increased with the number of diseased vessels (P<0.05) and significantly associated with severity score of stenosis (rs=0.601, P<0.001). In the multivariate analysis, ADAMTS4 levels were found to be independently correlated with the presence and severity of CAD. Receiver-operating characteristic analysis revealed that a cut-off of serum ADAMTS4 levels of 51.63 ng/ml could predict CAD with a 76% sensitivity and a 69% specificity. ADAMTS4 levels were significantly lower in patients with statin treatment than in those without it [47.49 (42.30, 57.09) vs. 56.39 (47.05, 68.94) ng/ml, P<0.05].
CONCLUSION: In conclusion, serum ADAMTS4 levels are associated with the presence and the severity of CAD, ADAMTS4 might serve as an independent factor for predicting CAD. Statin therapy reduces the serum levels of ADAMTS4.
© 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins

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Year:  2011        PMID: 21946608     DOI: 10.1097/MCA.0b013e32834c7565

Source DB:  PubMed          Journal:  Coron Artery Dis        ISSN: 0954-6928            Impact factor:   1.439


  8 in total

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Review 2.  A Disintegrin and Metalloproteinase (ADAM) and ADAM with thrombospondin motifs (ADAMTS) family in vascular biology and disease.

Authors:  Sheng Zhong; Raouf A Khalil
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3.  ADAM and ADAMTS disintegrin and metalloproteinases as major factors and molecular targets in vascular malfunction and disease.

Authors:  HaiFeng Yang; Raouf A Khalil
Journal:  Adv Pharmacol       Date:  2022-01-24

4.  Regulation of ADAMTS-1, -4 and -5 expression in human macrophages: differential regulation by key cytokines implicated in atherosclerosis and novel synergism between TL1A and IL-17.

Authors:  Tim G Ashlin; Alvin P L Kwan; Dipak P Ramji
Journal:  Cytokine       Date:  2013-07-13       Impact factor: 3.861

5.  A novel association between TGFb1 and ADAMTS4 in coronary artery disease: A new potential mechanism in the progression of atherosclerosis and diabetes.

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6.  ADAMTS proteases in cardiovascular physiology and disease.

Authors:  Salvatore Santamaria; Rens de Groot
Journal:  Open Biol       Date:  2020-12-23       Impact factor: 6.411

7.  The anti-atherogenic cytokine interleukin-33 inhibits the expression of a disintegrin and metalloproteinase with thrombospondin motifs-1, -4 and -5 in human macrophages: Requirement of extracellular signal-regulated kinase, c-Jun N-terminal kinase and phosphoinositide 3-kinase signaling pathways.

Authors:  Tim G Ashlin; Melanie L Buckley; Rebecca C Salter; Jason L Johnson; Alvin P L Kwan; Dipak P Ramji
Journal:  Int J Biochem Cell Biol       Date:  2013-11-22       Impact factor: 5.085

8.  Loss of ADAMTS4 reduces high fat diet-induced atherosclerosis and enhances plaque stability in ApoE(-/-) mice.

Authors:  Saran Kumar; Mo Chen; Yan Li; Fiona H S Wong; Chung Wee Thiam; Md Zakir Hossain; Kian Keong Poh; Satoshi Hirohata; Hiroko Ogawa; Véronique Angeli; Ruowen Ge
Journal:  Sci Rep       Date:  2016-08-05       Impact factor: 4.379

  8 in total

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