Serum Sex Hormone Levels and Subclinical Atherosclerosis - Ancillary to MESA

NCT ID: NCT00064532

Last Updated: 2014-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

6173 participants

Study Classification

OBSERVATIONAL

Study Start Date

2003-07-31

Study Completion Date

2008-06-30

Brief Summary

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

Detailed Description

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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.

Conditions

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Cardiovascular Diseases Atherosclerosis Coronary Arteriosclerosis Coronary Disease Heart Diseases

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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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
Minimum Eligible Age

45 Years

Maximum Eligible Age

84 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role collaborator

Northwestern University

OTHER

Sponsor Role lead

Responsible Party

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Kiang Liu

Professor in Preventive Medicine and Geriatrics and Internal Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Susan Gapstur

Role: PRINCIPAL_INVESTIGATOR

Northwestern University

Other Identifiers

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R01HL074338

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1226

Identifier Type: -

Identifier Source: org_study_id