Soy Food and Coronary Heart Disease in Women

Sponsor
Vanderbilt University Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT00241735
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
135,896
44

Study Details

Study Description

Brief Summary

To investigate whether soy food intake reduces risk of non-fatal myocardial infarction (MI) and fatal coronary heart disease in Chinese women.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    BACKGROUND:

    Coronary heart disease (CHD) is the leading cause of death in the US and many other countries. Estrogen deficiency plays a significant role in the development of coronary heart disease (CHD) in postmenopausal women. Recently, a series of randomized clinical trials evaluating the effects of hormone replacement therapy (HRT) on CHD yielded surprisingly deleterious results, shifting clinical decision-making from a position of presumed benefit to one of potential harm. Soy food is emerging as a promising natural substitute for HRT, given its estrogenic properties and potential lipids benefits. However, data directly linking soy food intake to the clinical endpoints of CHD are lacking.

    DESIGN NARRATIVE:

    The study will evaluate the association of soy food consumption with CHD using resources from the Shanghai Women's Health Study (SWHS), an ongoing prospective cohort study of 75,000 Chinese women who were recruited from 1997 to 2000 and who completed two extensive dietary assessments at baseline. The investigators will verify all CHD events identified in this cohort during the follow-up and longitudinally analyze the association between soy food intake and CHD risk, overall, and according to conventional CHD risk factors. In addition, they will conduct a nested case-control study to evaluate the association of urinary isoflavonoids (a biomarker of soy intake) and risk of CHD, and to investigate whether soy and CHD associations are modified by baseline levels of lipids and plasma C-reactive protein, two well established risk markers of CHD. In the United States, the sale of soy products has increased more than 3-fold in recent decades, and the proportion of people reporting soy product consumption at least once a week nearly doubled in the last six years. However, the overall intake level of soy food in the US population is still low, and women who consume soy food regularly are likely to be highly selective. Furthermore, it is difficult, if at all possible, to assess usual soy food intake in the US population because soy protein is added to many American food products. Informative studies on the association between soy food intake and CHD risk are better conducted in Chinese and other Asian populations, where soy food is part of traditional dietary practice. The SWHS with its wealth of data on dietary and lifestyle factors and biological samples provides a unique and unparalleled opportunity to prospectively investigate the effects of soy food intake on the risk of CHD, and to identify those most likely to benefit from consumption of soy food.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    135896 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Study Start Date :
    Sep 1, 2005
    Actual Primary Completion Date :
    May 1, 2009
    Actual Study Completion Date :
    May 1, 2009

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A to 100 Years
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      No

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • Vanderbilt University Medical Center
      • National Heart, Lung, and Blood Institute (NHLBI)

      Investigators

      • Principal Investigator: Xiao Shu, Vanderbilt University Medical Center

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Vanderbilt University Medical Center
      ClinicalTrials.gov Identifier:
      NCT00241735
      Other Study ID Numbers:
      • 1311
      • R01HL079123
      First Posted:
      Oct 19, 2005
      Last Update Posted:
      Sep 14, 2017
      Last Verified:
      Sep 1, 2017
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Sep 14, 2017