TY - JOUR
T1 - Associations between pituitary-ovarian hormones and cognition in recently menopausal women independent of type of hormone therapy
AU - Kling, Juliana M.
AU - Dowling, N. Maritza
AU - Bimonte-Nelson, Heather
AU - Gleason, Carey E.
AU - Kantarci, Kejal
AU - Stonnington, Cynthia M.
AU - Harman, S. Mitch
AU - Naftolin, Frederick
AU - Pal, Lubna
AU - Cedars, Marcelle
AU - Manson, Jo Ann E.
AU - James, Taryn T.
AU - Brinton, Eliot A.
AU - Miller, Virginia M.
N1 - Funding Information: The study was supported in part by a Mayo Clinic Mentored Research Award Grant NIA RF1 AG057547 to KK, CEG and VMM; NIA AG028084 , ADHS14-052688 , and the NIA AG028084 and NIH Alzheimer's Disease Centers P30AG019610 to HBN; P50 AG033514 to CEG; and the Mayo Clinic Foundation for Research and Education. KEEPS was funded by grants from the Aurora Foundation to the Kronos Longevity Research Institute, from the National Institutes of Health (NIH) HL90639 to VMM, Mayo Clinic CTSA 1 UL1 RR024150 , the Mayo Foundation , Brigham and Women's Hospital / Harvard Medical School CTSA, CTSA UL1 RR024139 and UCSF CTSA UL1 RR024131 from the National Center for Advancing Translational Sciences (NCATS), a component of the National Institutes of Health (NIH) and NIH Roadmap for Medical Research. The manuscript's contents are solely the responsibility of the authors and do not necessarily represent the official view of NCATS or NIH. Information on NCRR is available at http://www.ncrr.nih.gov . Study medications were supplied in part by Bayer Health Care and by Abbott Pharmaceuticals. Steroid hormone assays were funded by a grant from Pfizer Corp. Funding for FSH:LH assays was made available through support offered by the Department of Obstetrics, Gynecology & Reproductive Sciences at Yale and the Benneck-Polan Family Foundation GRECC Manuscript # 004-2019. Funding Information: The study was supported in part by a Mayo Clinic Mentored Research Award Grant NIA RF1 AG057547 to KK, CEG and VMM; NIA AG028084, ADHS14-052688, and the NIA AG028084 and NIH Alzheimer's Disease Centers P30AG019610 to HBN; P50 AG033514 to CEG; and the Mayo Clinic Foundation for Research and Education. KEEPS was funded by grants from the Aurora Foundation to the Kronos Longevity Research Institute, from the National Institutes of Health (NIH) HL90639 to VMM, Mayo Clinic CTSA 1 UL1 RR024150, the Mayo Foundation, Brigham and Women's Hospital/Harvard Medical School CTSA, CTSA UL1 RR024139 and UCSF CTSA UL1 RR024131 from the National Center for Advancing Translational Sciences (NCATS), a component of the National Institutes of Health (NIH) and NIH Roadmap for Medical Research. The manuscript's contents are solely the responsibility of the authors and do not necessarily represent the official view of NCATS or NIH. Information on NCRR is available at http://www.ncrr.nih.gov. Study medications were supplied in part by Bayer Health Care and by Abbott Pharmaceuticals. Steroid hormone assays were funded by a grant from Pfizer Corp. Funding for FSH:LH assays was made available through support offered by the Department of Obstetrics, Gynecology & Reproductive Sciences at Yale and the Benneck-Polan Family Foundation GRECC Manuscript # 004-2019. Publisher Copyright: © 2022 Elsevier B.V.
PY - 2023/1
Y1 - 2023/1
N2 - Objectives: To examine associations of pituitary-ovarian hormone levels with cognition before and after different formulations of hormone therapy (HT) or placebo independent of treatment group. Methods: Recently menopausal, healthy women were randomized to 0.45 mg/day oral conjugated equine estrogens (o-CEE, n = 109), 50 μg/day transdermal 17β (tE2, n = 107) or placebo pills and patches (n = 146); women on active treatment received oral 200 mg/day micronized progesterone for 12 days per month. Levels of estrone, 17β-estradiol, follicle stimulating hormone, luteinizing hormone, androstenedione, and testosterone were determined prior to and after 48 months of study participation. Neuropsychological testing was administered at baseline, and months 18, 36 and 48. Latent growth curve models controlling for education level, age, APOE allele status, waist circumference, and treatment examined the trajectories of each cognitive domain after accounting for the effect of hormone levels at baseline and months 18, 36 and 48. A linear multivariate mixed model examined the effect of changes in hormone levels on changes in trajectories of complex attention tasks with varying degrees of difficulty. Results: All women were adherent to treatment at month 48. Higher baseline estrone levels were associated with poorer global cognition, auditory attention and working memory, visual attention, and executive function, but not working memory. Higher levels of baseline 17β-E2 were associated with poorer cognitive performance, with marginal significance at baseline in speeded language and mental flexibility (p = 0.013). Other hormone levels were not associated with cognition. Controlling for all treatments, hormone levels at baseline and at month 48 did not have any significant correlation with cognitive trajectories over time. In healthy, recently menopausal women, baseline estrone levels were inversely associated with selected cognitive factors independent of two types of HT or placebo during 4 years of follow-up. Baseline levels of the other pituitary-ovarian hormones studied were not associated with baseline cognition, nor were changes in any hormones associated with changes in cognition during the study. The marginal association between estradiol levels and cognitive factors warrants further investigation. ClinicalTrials.gov numbers: NCT00154180, NCT00623311.
AB - Objectives: To examine associations of pituitary-ovarian hormone levels with cognition before and after different formulations of hormone therapy (HT) or placebo independent of treatment group. Methods: Recently menopausal, healthy women were randomized to 0.45 mg/day oral conjugated equine estrogens (o-CEE, n = 109), 50 μg/day transdermal 17β (tE2, n = 107) or placebo pills and patches (n = 146); women on active treatment received oral 200 mg/day micronized progesterone for 12 days per month. Levels of estrone, 17β-estradiol, follicle stimulating hormone, luteinizing hormone, androstenedione, and testosterone were determined prior to and after 48 months of study participation. Neuropsychological testing was administered at baseline, and months 18, 36 and 48. Latent growth curve models controlling for education level, age, APOE allele status, waist circumference, and treatment examined the trajectories of each cognitive domain after accounting for the effect of hormone levels at baseline and months 18, 36 and 48. A linear multivariate mixed model examined the effect of changes in hormone levels on changes in trajectories of complex attention tasks with varying degrees of difficulty. Results: All women were adherent to treatment at month 48. Higher baseline estrone levels were associated with poorer global cognition, auditory attention and working memory, visual attention, and executive function, but not working memory. Higher levels of baseline 17β-E2 were associated with poorer cognitive performance, with marginal significance at baseline in speeded language and mental flexibility (p = 0.013). Other hormone levels were not associated with cognition. Controlling for all treatments, hormone levels at baseline and at month 48 did not have any significant correlation with cognitive trajectories over time. In healthy, recently menopausal women, baseline estrone levels were inversely associated with selected cognitive factors independent of two types of HT or placebo during 4 years of follow-up. Baseline levels of the other pituitary-ovarian hormones studied were not associated with baseline cognition, nor were changes in any hormones associated with changes in cognition during the study. The marginal association between estradiol levels and cognitive factors warrants further investigation. ClinicalTrials.gov numbers: NCT00154180, NCT00623311.
KW - Cognition
KW - Menopausal hormone therapy
KW - Menopause
KW - Pituitary ovarian hormones
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U2 - https://doi.org/10.1016/j.maturitas.2022.10.002
DO - https://doi.org/10.1016/j.maturitas.2022.10.002
M3 - Article
C2 - 36395695
SN - 0378-5122
VL - 167
SP - 113
EP - 122
JO - Maturitas
JF - Maturitas
ER -