4.5 Article

Differences in regional brain metabolism associated with specific formulations of hormone therapy in postmenopausal women at risk for AD

Journal

PSYCHONEUROENDOCRINOLOGY
Volume 36, Issue 4, Pages 502-513

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.psyneuen.2010.08.002

Keywords

PET; Estrogen formulations; Postmenopausal; Hormone therapy; AD; Verbal memory

Funding

  1. National Institute on Aging [R01 AG22008]
  2. National Center for Research Resources, National Institutes of Health [M01 RR-00070]

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Differential cerebral metabolic effects of various hormone therapy formulations, and their associations with cognitive status, remain to be established. The principal aim of the current study was to assess relationships between regional cerebral metabolism and estrogen-based hormone therapies. Postmenopausal women (n = 53) at elevated risk for Alzheimer's disease (AD) were on estrogen-containing hormone therapy for at least one year prior to enrollment in a prospective, randomized clinical trial. Subjects underwent an FDG-PET scan, along with neuropsychological, medical, and demographic assessments at time of enrollment, to be repeated one year following randomization to hormone therapy continuation versus discontinuation, and results from analyses of the baseline assessments are reported here. Across all subjects, years of endogenous estrogen exposure correlated most closely with metabolism in right superior frontal gyrus (p < 0.0005). Women taking 17 beta-estradiol (E) performed three standard deviations higher in verbal memory than women taking conjugated equine estrogen (CEE), and their verbal memory performance positively correlated with metabolism in Wernicke's (p = 0.003) and auditory association (p = 0.002) areas. Women taking progesterone-plus-estrogen had lower metabolism than women taking unopposed estrogen within the mesial and inferior lateral temporal regions (p < 0.0005) and the inferior frontal cortex, contralateral to Broca's area (p < 0.0005). In conclusion, particular areas of relatively preserved metabolism were seen in women with more years of endogenous estrogen exposure, as well as in women taking estradiol-based formulations or estrogen therapies unopposed by progesterone, together suggesting regionally specific neuroprotective estrogenic effects. (c) 2010 Elsevier Ltd. All rights reserved.

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