Skip to main content
OpenTrials
Completed

NCT Number: NCT01268046

Aging and Estrogen on Cortical Function

This study will focus on how estrogen affects parts of the brain associated with memory and how the effect of estrogen is altered with aging in postmenopausal women.

Completed

Looking for future studies?

Notify Me

Key information

Age range

45 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Reproductive Endocrine Unit, Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

The broad goal of this proposal is to determine the effect of aging on areas of the brain whose function is impacted by gonadal steroids in women. The overarching hypothesis is that aging differentially alters the effects of estrogen on the brain. Our preliminary data indicated that aging alters the effect of estrogen on brain regions involved in cognition and thus, the current study focused on the impact of aging on functional changes induced by estrogen in cortical and subcortical areas associated with verbal working memory and declarative/episodic memory.

As our model, we will use women in whom the absence of gonadal function makes it possible to control the duration and amount of estrogen exposure, specifically postmenopausal women who are younger (45-55) or older (65-80) who receive either oral or transdermal estradiol to achieve premenopausal early follicular phase estradiol levels.. We evaluate the effects of low dose estrogen exposure at 48 hr and 1 month to determine whether the short-term changes in brain regions involved in cognition with low dose estrogen exposure seen in our preliminary studies are confirmed and whether changes with short-term estrogen exposure persist with more prolonged exposure, a finding that would have enormous clinical relevance. These studies, using sophisticated neuroimaging tools (structural and functional magnetic resonance imaging [MRI] and [18F] 2-fluoro-2-deoxy-D-glucose positron emission tomography [FDG-PET]), provide a unique window into the brain in women.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • young postmenopausal (age 45-55) or older (age 65-80) postmenopausal women
  • otherwise healthy, non-obese women with normal blood pressure and a history of normal menopause, defined by the absence of menses for at least 12 months
  • prescription hormone replacement treatment discontinued at least 3 months before study
  • Normal or corrected normal vision
  • Intelligence quotient (IQ) > 70 on the Wechsler Adult Reading Test (WTAR)*
  • Absence of Mild Cognitive Impairment (MCI) and depression on the Mini Mental State Examination (MMSE)** and Beck Depression Inventory II (BDI-II).***
  • Normal mammogram or breast MRI within the past 2 years

Exclusion criteria

  • On gonadal hormone replacement medication, herbal supplements and/or over the counter menopause treatment within three months of study
  • History of radiotherapy or chemotherapy.
  • Absolute contraindications to the use of physiologic replacement doses of estrogen and/or history of coronary artery disease
  • History of breast cancer, blood clot, pulmonary embolus, hypercoagulability and stroke.
  • On centrally acting medications
  • History of head trauma and/or neurologic disorder
  • Contraindication to MRI (eg. metal implants) or PET imaging (eg. PET imaging studies in the previous 12 months)
  • Concurrent participation in research studies involving medications and/or PET scans.
  • Left handedness.
  • Current breast lump(s) or family/genetic history of breast cancer in younger women (< 40 years old).
  • Current smoking

Treatment and study plan

Estradiol oral capsule

Drug

1 oral capsule (1 mg estradiol) administered daily for one month

Other names: Micronized Estradiol, Estradiol

transderman estrogen patch

Drug

transdermal estrogen patch (50 mcg/day) for one month

Other names: Climara, Estraderm, Estrogen patch

trasdermal placebo patch

Drug

transdermal placebo patch with patch change every 84 hr for one month

Other names: Placebo patch

Placebo oral capsule

Drug

placebo oral capsule administered daily for one month.

Other names: Placebo capsule

Primary outcomes

  1. Functional Magnetic Resonance Imaging (fMRI) Changes in Response to Estrogen and Aging - Dorsolateral Pre-frontal Cortex (DLPFC)

    Time frame: baseline to 1 month

    Change in extracted beta coefficients of the blood oxygen level dependent (BOLD) signal response to a cognitive task (N-back) in the DLPFC (x,y,z coordinates = -34 44 16) from baseline to 1 month as a function of aging and estrogen (young vs older and estrogen vs placebo). A positive change indicates an increase in oxygen utilization (inferring increased neuronal functioning) between baseline and treatment during the cognitive task, while a negative change indicates a decrease in oxygen utilization between baseline and treatment during the cognitive task.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

The Effect of Low Dose Estrogen on Cortical Function as a Function of Age in Postmenopausal Women.

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Dec 29, 2010
Registry last updated
Aug 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.