Harman, Sherman

Abstract INTRODUCTION Associations of short‐term use of menopausal hormone therapy (mHT) with Alzheimer's disease (AD) and structural magnetic resonance imaging (MRI) biomarkers were investigated 10 years after an mHT trial. METHODS Recently menopausal women with good cardiovascular health were randomized to oral conjugated equine estrogens (oCEE) or transdermal 17β‐estradiol (tE2) and micronized progesterone, or placebo for 4 years. Amyloid beta (Aβ) on positron emission tomography, hippocampal atrophy, and dorsolateral prefrontal cortex thickness on MRI were assessed 10 years after completion of the mHT trial ( n = 266). RESULTS Aβ and structural MRI biomarkers were not different in the oCEE and tE2 groups compared to placebo. Apolipoprotein E ε4 status did not modify the findings. DISCUSSION There was no evidence of adverse effects or benefits associated with 4 years of use of oral or transdermal mHT on Aβ and structural MRI biomarkers in relatively healthy women, 10 years after mHT. Findings support the long‐term safety of short‐term use of mHT on brain health. CLINICAL TRIALS REGISTRATION NCT00154180 Kronos Early Estrogen Prevention Study (KEEPS) Highlights There were no menopausal hormone therapy–related adverse effects or benefits on amyloid beta and magnetic resonance imaging biomarkers in the long term. Apolipoprotein E ε4 carrier status did not modify these findings. Findings align with neutral cognitive and cerebrovascular outcomes in this cohort.

Abstract Evidence suggests that early postmenopausal hormone treatment (MHT) may attenuate metabolic effects on dementia pathogenesis. Using Kronos Early Estrogen Prevention Study (KEEPS) and KEEPS-Continuation data, we investigated heterogeneity in the associations between longitudinal central adiposity (CA), MHT, and cognition, hypothesizing that CA would be related to cognition and that MHT would favorably alter this relationship. KEEPS participants (previously randomized to 48 months treatment with placebo or HT with oral conjugated equine estrogens + progesterone or transdermal 17-β-estradiol+ progesterone) were recruited for KEEPS-Continuation ~10 years post-randomization. Cognitive tests from both studies were analyzed as four-factor scores. Using the original KEEPS data (n=662), growth mixture modeling identified distinct CA trajectories (classes) across 48 months of MHT, which predicted cognition at 48 months and ~10 years, adjusting for covariates. Adiposity trajectories included “low-CA” and “high-CA” classes. Low-CA women exhibited stable low-CA throughout MHT. High-CA women’s adiposity was initially elevated but declined significantly after 48 months of MHT. After adjusting for covariates, the high (versus low) CA class predicted significantly lower cognitive factors scores at month 48 with one exception – Verbal-Learning & Memory. Ten years later, high-CA women (n=299) scored significantly lower on two factors. MHT predicted neither CA trajectories nor cognitive performance at 48 months or 10 years later. Adiposity levels significantly declined in the high-CA class on MHT but not placebo and was associated with diminished cognitive function. CA influenced short-and long-term cognition. Organ/tissue studies should examine how heterogeneity in adiposity levels interacts with MHT and other factors driving dementia pathogenesis.