4.7 Article

Implications of C1q/TNF-related protein-3 (CTRP-3) and progranulin in patients with acute coronary syndrome and stable angina pectoris

Journal

CARDIOVASCULAR DIABETOLOGY
Volume 13, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/1475-2840-13-14

Keywords

C1q/tumor necrosis factor-related protein-3; Progranulin; Coronary artery disease; Acute coronary syndrome; Stable angina pectoris; Adipokines

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea
  2. Ministry of Education, Science and Technology [2012006363]
  3. Brain Korea 21 Project of the Ministry of Education and Human Resources Development, Republic of Korea
  4. Korean Health Technology R&D Project, Ministry for Health, Welfare & Family Affairs, Republic of Korea [A070001]
  5. Korea University
  6. National Research Foundation of Korea [2012R1A1A2006363] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Background: C1q/TNF-related protein-3 (CTRP-3), an adiponectin paralog, and progranulin were recently identified as novel adipokines which may link obesity with glucose dysregulation and subclinical inflammation. We analyzed the relationship between CTRP-3, progranulin and coronary artery disease (CAD) in Korean men and women. Methods: Circulating CTRP-3 and progranulin levels were examined in 362 Korean adults with acute coronary syndrome (ACS, n = 69), stable angina pectoris (SAP, n = 85), and control subjects (n = 208) along with various kinds of cardiometabolic risk factors. Results: CTRP-3 concentrations were significantly decreased in patients with ACS or SAP compared to control subjects (P <0.001, respectively), whereas progranulin and adiponectin levels were similar. Correlation analysis adjusted for age and gender exhibited that CTRP-3 levels showed significant negative relationship with glucose (r = -0.110, P = 0.041) and high sensitive C-reactive protein (hsCRP) levels (r = -0.159, P = 0.005), and positive relationship with HDL-cholesterol (r = 0.122, P = 0.025) and adiponectin levels (r = 0.194, P < 0.001). In a multivariate logistic regression analysis, the odds ratio for CAD risk was 5.14 (95% CI, 1.83-14.42) in the second, and 9.04 (95% CI, 2.81-29.14) in the first tertile of CTRP-3 levels compared to third tertile after adjusting for other cardiometabolic risk variables. Conclusions: Patients with ACS or SAP had significantly lower circulating CTRP-3 concentrations compared to control subjects, although progranulin levels were not different. These results suggest the possibility that CTRP-3 might be useful for assessing the risk of CAD.

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