Estrogen Administration for the Treatment of NASH in Postmenopausal Women

Description

Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States. Despite this, the treatment options remain limited. Preclinical and preliminary clinical data suggest that estrogen deficiency plays an important role in the pathology of steatosis, inflammation and fibrosis in non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Post-menopausal women are a growing population with particularly high risk of NASH due to their lack of estrogen. This study will examine the effect of estradiol on hepatic fibrosis and fat in post-menopausal women with NASH.

Conditions

NASH - Nonalcoholic Steatohepatitis

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Study Overview

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Study Details

Study overview

Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States. Despite this, the treatment options remain limited. Preclinical and preliminary clinical data suggest that estrogen deficiency plays an important role in the pathology of steatosis, inflammation and fibrosis in non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Post-menopausal women are a growing population with particularly high risk of NASH due to their lack of estrogen. This study will examine the effect of estradiol on hepatic fibrosis and fat in post-menopausal women with NASH.

Estrogen Administration for the Treatment of NASH in Postmenopausal Women

Estrogen Administration for the Treatment of NASH in Postmenopausal Women

Condition
NASH - Nonalcoholic Steatohepatitis
Intervention / Treatment

-

Contacts and Locations

Boston

Massachusetts General Hospital, Boston, Massachusetts, United States, 02114

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Postmenopausal women 45-70 years old
  • * NASH by biopsy or NAFLD by imaging within 6 months of screen
  • * Hepatitis C antibody and hepatitis B surface antigen negative
  • * Negative mammogram within 1 year
  • * Heavy alcohol use
  • * Use of NASH pharmacotherapies within 12 months of study entry
  • * Known cirrhosis, stage 4 fibrosis on biopsy, or clinical evidence of cirrhosis or portal hypertension on imaging or exam
  • * Participation in NASH clinical trial within 6 months of study entry
  • * Chronic use of corticosteroids, methotrexate, amiodarone, or tamoxifen within 6 months of entry
  • * Known diagnosis of chronic liver disease other than NAFLD or found on biopsy
  • * Contraindication to liver biopsy including INR \> 1.5, platelets \< 50,000/mL, ascites, chronic anticoagulation (other than aspirin), biliary obstruction, peritonitis, inability to lie supine for 30 minutes
  • * Hgb \< 10.0 g/dL or glomerular filtration rate \< 60 mL/min
  • * Contraindications to estrogen therapy
  • * Any vaginal bleeding, including spotting, within the last year
  • * Active malignancy
  • * Severe chronic illness
  • * Use of estrogen or progesterone within a year of baseline visit
  • * Routine MRI exclusion criteria such as the presence of a pacemaker or cerebral aneurysm clip

Ages Eligible for Study

45 Years to 70 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Massachusetts General Hospital,

Karen K. Miller, MD, PRINCIPAL_INVESTIGATOR, Massachsuetts General Hospital

Study Record Dates

2027-05-31