Hormone therapy and Alzheimer disease dementia

Huibo Shao, John C.S. Breitner, Rachel A. Whitmer, Junmin Wang, Kathleen M. Hayden, Heidi J. Wengreen, Chris Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ron Munger, Kathleen A. Welsh‐Bohmer, Peter P. Zandi, James C. Anthony(Michigan State University), Erin D. Bigler(Brigham Young University), Ron Brookmeyer(UCLA Health), James Burke(Duke University), Eric J. Christopher(Duke University), Jane P. Gagliardi(Duke University), Robert C. Green(Utah State University), Michael J. Helms(Duke University), Christine Hulette(Duke University), Ara Khachaturian(Dementia Australia), Liz Klein(Utah State University), Carol Leslie(Utah State University), Constantine G. Lyketsos(Johns Hopkins University), John C. Morris(McGill University), Chiadi U. Onyike(Johns Hopkins University), Truls Østbye(Duke University), Ron Petersen(Utah State University), Kathy Piercy(Utah State University), Carl F. Pieper(Duke University), Brenda L. Plassman(Duke University), Peter V. Rabins(Johns Hopkins University), Pritham Raj(Duke University), Ingmar Skoog(University of Gothenburg), David C. Steffens(Duke University), Martin H. Steinberg(Johns Hopkins University), Marty Toohill(Utah State University), Leslie Toone(Utah State University), Jeannette J. Townsend(University of Utah), Michael Williams(Duke University), Bonita W. Wyse(Utah State University)
Neurology
October 25, 2012
Cited by 264Open Access
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Abstract

OBJECTIVES: Observational studies suggest reduced risk of Alzheimer disease (AD) in users of hormone therapy (HT), but trials show higher risk. We examined whether the association of HT with AD varies with timing or type of HT use. METHODS: Between 1995 and 2006, the population-based Cache County Study followed 1,768 women who had provided a detailed history on age at menopause and use of HT. During this interval, 176 women developed incident AD. Cox proportional hazard models evaluated the association of HT use with AD, overall and in relation to timing, duration of use, and type (opposed vs unopposed) of HT. RESULTS: Women who used any type of HT within 5 years of menopause had 30% less risk of AD (95% confidence interval 0.49-0.99), especially if use was for 10 or more years. By contrast, AD risk was not reduced among those who had initiated HT 5 or more years after menopause. Instead, rates were increased among those who began "opposed" estrogen-progestin compounds within the 3 years preceding the Cache County Study baseline (adjusted hazard ratio 1.93; 95% confidence interval 0.94-3.96). This last hazard ratio was similar to the ratio of 2.05 reported in randomized trial participants assigned to opposed HT. CONCLUSIONS: Association of HT use and risk of AD may depend on timing of use. Although possibly beneficial if taken during a critical window near menopause, HT (especially opposed compounds) initiated in later life may be associated with increased risk. The relation of AD risk to timing and type of HT deserves further study.


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