Estrogen Use in Protection From Cognitive Decline

Completed

• Conditions: Aging; Menopause

• Registration Number: NCT00097058
• Lead Sponsor: Stanford University

Brief Summary

This study is designed to assess the effects of estrogen therapy among postmenopausal women at risk for cognitive decline.

Detailed Description

A total of 71 postmenopausal women ages 50-65 on estrogen therapy will be randomized to continue or discontinue use of estrogen and will be followed for two years.

Participants will undergo PET and MRI scans and neuropsychological assessments initially and at the end of the two-year follow-up period. These procedures will allow us to evaluate brain metabolism and cognitive performance at baseline and two years following continuation or discontinuation of estrogen therapy.

We hypothesize that women who discontinue estrogen will show more evidence of decline than those who continue estrogen. This project will expand current knowledge of effects of estrogen by 1) determining whether estrogen use among postmenopausal women at risk for cognitive decline is protective of brain metabolism, 2) identifying early predictors for cognitive decline, and 3) developing guidelines for estrogen use in postmenopausal women.

Study Timeline

• Study Start: 2003-08
• Study First Submitted: 2004-11-17
• Study First Submitted QC: 2004-11-17
• Study First Posted: 2004-11-18
• Status Verified: 2014-11
• Primary Completion: 2014-11
• Study Completion: 2014-11
• Last Update Submitted: 2014-11-17
• Last Update Posted: 2014-11-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 71

Inclusion Criteria

• Women between the ages of 45 and 65
• Currently on hormone replacement
• One year or more post complete cessation of menses
• Willing to sign the Human Subject Protection Consent form prior to enrollment in the study
• Willing to be randomized to continue or discontinue estrogen therapy
• Adequately visually and auditorially acute to allow neuropsychological testing
• Beyond 8 years of educational achievement to allow adequate neuropsychological testing
• Willing to undergo brain imaging
• At risk for cognitive decline, as defined by one or more of the following: Personal or family history of mood disorder, Hypothyroidism, Diabetes, Family history of Alzheimer's, APOE-4 allele

Exclusion Criteria

• Diagnosis of possible or probable Alzheimer's disease or dementia
• Cerebrovascular disease or uncontrolled hypertension (systolic BP >170 or diastolic BP >100)
• History of myocardial infarction within previous year or unstable heart disease
• History of significant liver disease, pulmonary disease, or current cancer
• Contraindication for MRI (metal in body, claustrophobia, etc.)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Changes in cognition and brain metabolism	Baseline and 24 months

Trial Locations

Locations (1)

Stanford University School of Medicine, Dept. of Psychiatry and Behavioral Sciences; 🇺🇸 Stanford, California, United States