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Article

Adropin is associated with hyperhomocysteine and coronary atherosclerosis

  • Authors:
    • Liang‑Ping Zhao
    • Tao You
    • Siew‑Pang Chan
    • Jian‑Chang Chen
    • Wei‑Ting Xu
  • View Affiliations / Copyright

    Affiliations: Department of Cardiology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, P.R. China, Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Republic of Singapore
  • Pages: 1065-1070
    |
    Published online on: December 23, 2015
       https://doi.org/10.3892/etm.2015.2954
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Abstract

Homocysteine has been recognized as a risk factor for atherosclerosis and cardiovascular diseases. Adropin is a newly‑identified energy homeostasis protein with a potential protective effect against coronary artery disease (CAD). This study attempted to measure the correlation between serum homocysteine and adropin levels in patients with CAD, and to ascertain how the two hormones could affect the severity of coronary atherosclerosis. A cohort of CAD patients who had undergone coronary angiography was prospectively recruited. The serum homocysteine and adropin levels of the patients were measured and the severity of coronary atherosclerosis was quantified with the SYNTAX score. The data were analyzed with a generalized structural equation model. In total, 170 consecutive patients were recruited with a mean serum homocysteine level of 15.9±8.3 µmol/l, and 76 (44.7%) patients were identified as hyperhomocysteinemic with a serum homocysteine level >15 µmol/l. Serum homocysteine level was found to be significantly negatively correlated with serum adropin level (r=‑0.169, P=0.028). Patients with hyperhomocysteinemia had lower serum adropin levels and higher SYNTAX scores than patients without hyperhomocysteinemia. Further analysis with a generalized structural equation model showed that adropin was significantly associated with hyperhomocysteinemia (adjusted odds ratio: 0.95, 95% confidence interval: 0.93 to 0.98; P=0.002), which in turn was significantly associated with the SYNTAX score (coefficient: 4.71, 95% confidence interval: 1.39 to 8.03; P=0.005). In conclusion, the serum homocysteine level was inversely correlated with the serum adropin level in patients with CAD. A low serum adropin level was associated with hyperhomocysteinemia and more severe coronary atherosclerosis, as reflected by a higher SYNTAX score.
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Copy and paste a formatted citation
Spandidos Publications style
Zhao LP, You T, Chan SP, Chen JC and Xu WT: Adropin is associated with hyperhomocysteine and coronary atherosclerosis. Exp Ther Med 11: 1065-1070, 2016.
APA
Zhao, L., You, T., Chan, S., Chen, J., & Xu, W. (2016). Adropin is associated with hyperhomocysteine and coronary atherosclerosis. Experimental and Therapeutic Medicine, 11, 1065-1070. https://doi.org/10.3892/etm.2015.2954
MLA
Zhao, L., You, T., Chan, S., Chen, J., Xu, W."Adropin is associated with hyperhomocysteine and coronary atherosclerosis". Experimental and Therapeutic Medicine 11.3 (2016): 1065-1070.
Chicago
Zhao, L., You, T., Chan, S., Chen, J., Xu, W."Adropin is associated with hyperhomocysteine and coronary atherosclerosis". Experimental and Therapeutic Medicine 11, no. 3 (2016): 1065-1070. https://doi.org/10.3892/etm.2015.2954
Copy and paste a formatted citation
x
Spandidos Publications style
Zhao LP, You T, Chan SP, Chen JC and Xu WT: Adropin is associated with hyperhomocysteine and coronary atherosclerosis. Exp Ther Med 11: 1065-1070, 2016.
APA
Zhao, L., You, T., Chan, S., Chen, J., & Xu, W. (2016). Adropin is associated with hyperhomocysteine and coronary atherosclerosis. Experimental and Therapeutic Medicine, 11, 1065-1070. https://doi.org/10.3892/etm.2015.2954
MLA
Zhao, L., You, T., Chan, S., Chen, J., Xu, W."Adropin is associated with hyperhomocysteine and coronary atherosclerosis". Experimental and Therapeutic Medicine 11.3 (2016): 1065-1070.
Chicago
Zhao, L., You, T., Chan, S., Chen, J., Xu, W."Adropin is associated with hyperhomocysteine and coronary atherosclerosis". Experimental and Therapeutic Medicine 11, no. 3 (2016): 1065-1070. https://doi.org/10.3892/etm.2015.2954
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