Lessons from KEEPS: the Kronos Early Estrogen Prevention Study.

Department of Surgery, Mayo Clinic College of Medicine, Rochester, MN, USA. Department of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine, Rochester, MN, USA. Department of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, USA. Department of Obstetrics and Gynecology, New York University Grossman School of Medicine, New York, NY, USA. Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Division of Geriatrics, Department of Medicine, Wisconsin Alzheimer's Disease Research Center, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA. Utah Lipid Center, Salt Lake City, UT, USA. Department of Internal Medicine, Division of Women's Health Internal Medicine, Mayo Clinic, AZ, USA. Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, San Francisco, CA, USA. Department of Acute & Chronic Care, School of Nursing, Department of Epidemiology & Biostatistics, Milken Institute School of Public Health, The George Washington University, Washington DC, USA. Department of Radiology, Mayo Clinic College of Medicine, Rochester, MN, USA. Kronos Longevity Research Institute, Phoenix, AZ, USA. Phoenix Veterans Administration Health Care System, Phoenix, AZ, USA.

Climacteric : the journal of the International Menopause Society. 2021;(2):139-145

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Abstract

The Kronos Early Estrogen Prevention Study (KEEPS) was a randomized, double-blind, placebo-controlled trial designed to determine the effects of hormone treatments (menopausal hormone treatments [MHTs]) on the progression of carotid intima-medial thickness (CIMT) in recently menopausal women. Participants less than 3 years from menopause and without a history of overt cardiovascular disease (CVD), defined as no clinical CVD events and coronary artery calcium < 50 Agatston units, received either oral conjugated equine estrogens (0.45 mg/day) or transdermal 17β-estradiol (50 µg/day), both with progesterone (200 mg/day for 12 days/month), or placebo pills and patches for 4 years. Although MHT did not decrease the age-related increase in CIMT, KEEPS provided other important insights about MHT effects. Both MHTs versus placebo reduced the severity of menopausal symptoms and maintained bone density, but differed in efficacy regarding mood/anxiety, sleep, sexual function, and deposition of β-amyloid in the brain. Additionally, genetic variants in enzymes for metabolism and uptake of estrogen affected the efficacy of MHT for some aspects of symptom relief. KEEPS provides important information for use of MHT in clinical practice, including type, dose, and mode of delivery of MHT recently after menopause, and how genetic variants in hormone metabolism may affect MHT efficacy on specific outcomes.

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Publication Type : Randomized Controlled Trial

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