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OpenTrials
Completed

NCT Number: NCT01869816

CTRP3 and Progranulin in Patients With Coronary Artery Disease

Visceral obesity is the one of the major causes of cardiovascular morbidity and mortality in industrialized countries. Adipose tissue secretes various kinds of bioactive molecules termed adipokines which contribute to the development of obesity-related disorders including cardiovascular disease (CVD). Progranulin and CTRP3 are recently discovered novel adipokines. Therefore, the investigators tried to compare circulating CTRP-3 and progranulin levels in patients with CAD and investigated whether CTRP-3 or progranulin is significantly associated with CAD prevalence after adjustment for well-known CAD risk factors.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Korea University Guro Hospital Dept. of Endocrinology

Seoul, South Korea

About this study

CTRP-3 (synonyms CORS-26, cartducin and cartonectin) is a potent anti-inflammatory adipokine that inhibits proinflammatory pathways in monocytes and adipocytes. Using a recently developed enzymelinked immunosorbent assay (ELISA), we reported that circulating CTRP-3 levels were elevated in patients with glucose metabolism dysregulation.

Progranulin was identified as a key adipokine mediating high fat diet-induced insulin resistance and obesity through interleukin-6 (IL-6) in adipose tissue. We previously reported that progranulin levels were significantly higher in individuals with type 2 diabetes and were associated with macrophage infiltration in omental adipose tissue. Moreover, the expression of progranulin reduces inflammation and its degradation into granulins peptides enhances inflammation in atherosclerotic plaque, which may contribute to the progression of atherosclerosis There has been no previous report on the implication of CTRP-3 or progranulin in humans with cardiovascular disease (CAD). In the present study, we compared circulating CTRP-3 and progranulin levels in patients with CAD and investigated whether CTRP-3 or progranulin is significantly associated with CAD prevalence after adjustment for well known CAD risk factors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • acute myocardial infarction
  • unstable angina
  • stable angina pectoris

Exclusion criteria

For control group, we exclude the participants who had

  • a history of CVD (myocardial infarction, unstable angina, stroke, or cardiovascular revascularization)
  • type 2 diabetes
  • stage 2 hypertension (resting blood pressure, ≥160/100 mmHg)
  • malignancy
  • severe renal or hepatic disease

Treatment and study plan

Primary outcomes

  1. CTRP3

    Time frame: 16 months

    CTRP3 (ng/ml)

Secondary outcomes

  1. SBP

    Time frame: 16 months

    SBP (mmHg)

  2. LDL cholesterol

    Time frame: 16 months

    LDL (mg/dl)

  3. hsCRP

    Time frame: 16 months

    hsCRP (mg/dl)

  4. creatinine

    Time frame: 16 months

    creatinine (mg/dl)

Sponsors and collaborators

Lead sponsor

Korea University

Other

Registry information

Official study title

Implications of C1q/TNF-related Protein-3(CTRP-3) and Progranulin in Patients With Acutecoronary Syndrome and Stable Angina Pectoris

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Jun 5, 2013
Registry last updated
Sep 2, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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