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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00064532
Other study ID # 1226
Secondary ID R01HL074338
Status Completed
Phase N/A
First received July 8, 2003
Last updated December 2, 2014
Start date July 2003
Est. completion date June 2008

Study information

Verified date November 2013
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

To assess the associations of serum sex hormones with the presence and progression of subclinical atherosclerosis.


Description:

BACKGROUND:

Throughout their lifetime, men are at higher risk of coronary heart disease (CHD) than women, however, after menopause this difference is attenuated. This observation suggests that endogenous sex hormones could be associated with CHD risk. There is some evidence indicating that the effect of sex hormones on CHD risk could be mediated, in part, by alterations in lipid levels or other CHD risk factors. However, other evidence supports an independent relationship of circulating hormone levels with CHD risk.

DESIGN NARRATIVE:

The study, which is ancillary to MESA, will examine the associations of serum sex hormone concentrations with the presence and progression of subclinical atherosclerosis in 3,259 male and 2,802 postmenopausal female participants of the Multi-Ethnic Study of Atherosclerosis (MESA). Subclinical atherosclerosis will be identified using both coronary artery calcium (CAC) and carotid intimal-medial wall thickness (IMT). Progression will be identified by the change in CAC over 3.5 years. Circulating concentrations of total (and free) testosterone (T), dehydroepiandrosterone (DHEA), 17 beta-estradiol (E2), and sex hormone binding globulin (SHBG) in stored serum samples collected at the MESA baseline exam will be assessed. Laboratory results will be merged with existing demographic, anthropometric, lifestyle, CHD risk factor, and subclinical disease data collected in MESA. Cross-sectional and prospective methods of statistical analysis will be used to assess the proposed associations. MESA is particularly well suited for disentangling the effects of hormonal factors and CHD risk factors on subclinical atherosclerosis because of the availability of high-quality data, serum samples, and CAC and IMT measurements in a large multi-ethnic population of men and women.


Recruitment information / eligibility

Status Completed
Enrollment 6173
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender Both
Age group 45 Years to 84 Years
Eligibility Exclusion Criteria:

- Age younger than 45 or older than 84 years

- Physician-diagnosed heart attack

- Physician-diagnosed angina or taking nitroglycerin

- Physician-diagnosed stroke or TIA

- Physician-diagnosed heart failure

- Current atrial fibrillation

- Having undergone procedures related to cardiovascular disease (CABG, angioplasty, valve replacement, pacemaker or defibrillator implantation, any surgery on the heart or arteries)

- Active treatment for cancer

- Pregnancy

- Any serious medical condition which would prevent long-term participation

- Weight >300 pounds

- Cognitive inability as judged by the interviewer

- Living in a nursing home or on the waiting list for a nursing home

- Plans to leave the community within five years

- Language barrier (speaks other than English, Spanish, Cantonese or Mandarin)

- Chest CT scan in the past year

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Northwestern University National Heart, Lung, and Blood Institute (NHLBI)

Outcome

Type Measure Description Time frame Safety issue
Primary Coronary artery calcium Baseline No
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