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Study Description

This substudy phs000503 WHISE contains phenotypes only for the Sight Examination study. Summary level phenotypes for the WHI Cohort study participants can be viewed at the top-level study page phs000200 WHI Cohort. Individual level phenotype data and molecular data for all WHI top-level study and substudies are available by requesting Authorized Access to the WHI Cohort study phs000200.

Women enrolled in the Women's Health Initiative (WHI) Hormone Replacement Therapy (HRT) Clinical Trial (CT) were included in this study. In WHI, participants who did not have a hysterectomy before enrollment into the WHI HRT CT were randomly assigned to either conjugated equine estrogens with progestin (CEE P) (0.625 mg/d of CEE and 2.5 mg/d of progestin) or a placebo. Those without a uterus were randomly assigned to either CEE (0.625 mg/d) or a placebo. Participants in the WHISE Study were recruited an average of 5.1 years after randomization into the WHI HRT CT. Participants included 4688 women who consented to participate in the WHISE Study; 4347 completed enrollment with photographs of at least 1 eye. The purpose of the study was to evaluate the effects of HRT on age-related macular degeneration.

Authorized Access
Publicly Available Data
  Link to other NCBI resources related to this study
Study Inclusion/Exclusion Criteria

Inclusion Criteria

  1. Women aged 65 years or older enrolled in the WHI HRT Clinical Trial.
  2. Speak and read English or Spanish, agree to complete study questionnaires and two eye examinations with fundus photography, and sign the informed consent document
  3. Patient has at least one eye that can be dilated for the purpose of retinal fundus photography

Exclusion Criteria

  1. Allergies to dilating eye drops
  2. Other known contraindications for the administration of dilating eye drops
  3. Any reason that the participant cannot be subjected to retinal fundus photography

Selected Publications
Diseases/Traits Related to Study (MeSH terms)
Authorized Data Access Requests
Study Attribution
  • Principal Investigator
    • Mary N. Haan, PhD. Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.