4.7 Article

Postmenopausal hormone therapy, type 2 diabetes mellitus, and brain volumes

Journal

NEUROLOGY
Volume 85, Issue 13, Pages 1131-1138

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000001816

Keywords

-

Funding

  1. National Heart, Lung, and Blood Institute of the NIH, U.S. Department of Health and Human Services
  2. Wyeth Pharmaceuticals, Inc., St. Davids, PA
  3. [HHSN268200464221C]
  4. [N01-WH-4-4221]

Ask authors/readers for more resources

Objective:To examine whether the effect of postmenopausal hormone therapy (HT) on brain volumes in women aged 65-79 years differs depending on type 2 diabetes status during postintervention follow-up of a randomized controlled clinical trial.Methods:The Women's Health Initiative randomized clinical trials assigned women to HT (0.625 mg/day conjugated equine estrogens with or without 2.5 mg/day medroxyprogesterone acetate) or placebo for an average of 5.6 years. A total of 1,402 trial participants underwent brain MRI 2.4 years after the trials; these were repeated in 699 women 4.7 years later. General linear models were used to assess the interaction between diabetes status and HT assignment on brain volumes.Results:Women with diabetes at baseline or during follow-up who had been assigned to HT compared to placebo had mean decrement in total brain volume of -18.6 mL (95% confidence interval [CI] -29.6, -7.6). For women without diabetes, this mean decrement was -0.4 (95% CI -3.8, 3.0) (interaction p = 0.002). This interaction was evident for total gray matter (p < 0.001) and hippocampal (p = 0.006) volumes. It was not evident for changes in brain volumes over follow-up or for ischemic lesion volumes and was not influenced by diabetes duration or oral medications.Conclusions:For women aged 65 years or older who are at increased risk for brain atrophy due to type 2 diabetes, prescription of postmenopausal HT is associated with lower gray matter (total and hippocampal) volumes. Interactions with diabetes and insulin resistance may explain divergent findings on how estrogen influences brain volume among older women.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Geriatrics & Gerontology

Sex-Related Differences in Brain Volumes and Cerebral Blood Flow Among Overweight and Obese Adults With Type 2 Diabetes: Exploratory Analyses From the Action for Health in Diabetes Brain Magnetic Resonance Imaging Study

Mark A. Espeland, Kathleen M. Hayden, Samuel N. Lockhart, Hussein N. Yassine, Siobhan Hoscheidt, Sevil Yasar, Jose A. Luchsinger, Rebecca H. Neiberg, Roberta Diaz Brinton, Owen Carmichael

JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES (2020)

Article Clinical Neurology

Allopregnanolone Reverses Bioenergetic Deficits in Female Triple Transgenic Alzheimer's Mouse Model

Tian Wang, Jia Yao, Shuhua Chen, Zisu Mao, Roberta Diaz Brinton

NEUROTHERAPEUTICS (2020)

Article Biochemistry & Molecular Biology

Von Willebrand factor A domain-containing protein 8 (VWA8) localizes to the matrix side of the inner mitochondrial membrane

Moulun Luo, Wuqiong Ma, Zoe Sand, Jean Finlayson, Tian Wang, Roberta Diaz Brinton, Wayne T. Willis, Lawrence J. Mandarino

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2020)

Article Multidisciplinary Sciences

Evidence in support of chromosomal sex influencing plasma based metabolome vs APOE genotype influencing brain metabolome profile in humanized APOE male and female mice

Yuan Shang, Aarti Mishra, Tian Wang, Yiwei Wang, Maunil Desai, Shuhua Chen, Zisu Mao, Loi Do, Adam S. Bernstein, Theodore P. Trouard, Roberta D. Brinton

PLOS ONE (2020)

Article Multidisciplinary Sciences

Association of combination statin and antihypertensive therapy with reduced Alzheimer's disease and related dementia risk

Douglas Barthold, Geoffrey Joyce, Roberta Diaz Brinton, Whitney Wharton, Patrick Gavin Kehoe, Julie Zissimopoulos

PLOS ONE (2020)

Article Multidisciplinary Sciences

Alternatives to amyloid for Alzheimer's disease therapies-a symposium report

Jennifer Cable, David M. Holtzman, Bradley T. Hyman, Malu Gamez Tansey, Marco Colonna, Manolis Kellis, Roberta D. Brinton, Marilyn Albert, Cheryl L. Wellington, Sangram S. Sisodia, Rudolph E. Tanzi

ANNALS OF THE NEW YORK ACADEMY OF SCIENCES (2020)

Article Biochemistry & Molecular Biology

Mitochondria-Targeted Therapeutics for Alzheimer's Disease: The Good, the Bad, the Potential

Yashi Mi, Guoyuan Qi, Roberta Diaz Brinton, Fei Yin

Summary: The paper summarizes the importance, recent advances, critical issues, and future directions of Alzheimer's disease (AD) therapeutics. The authors emphasize that emerging non-energetic aspects of mitochondria targeting strategies may have the potential to modify AD risk and progression.

ANTIOXIDANTS & REDOX SIGNALING (2021)

Article Multidisciplinary Sciences

Midlife Chronological and Endocrinological Transitions in Brain Metabolism: System Biology Basis for Increased Alzheimer's Risk in Female Brain

Yiwei Wang, Yuan Shang, Aarti Mishra, Eliza Bacon, Fei Yin, Roberta Brinton

SCIENTIFIC REPORTS (2020)

Review Clinical Neurology

Drug therapies for chronic conditions and risk of Alzheimer's disease and related dementias: A scoping review

Johanna Thunell, Yi Chen, Geoffrey Joyce, Douglas Barthold, Paul G. Shekelle, Roberta Diaz Brinton, Julie Zissimopoulos

Summary: The study identified 29 drug classes associated with increasing or decreasing ADRD risk, with a need for further research in certain areas. Some areas of study still have limited evidence and require more data to support conclusions.

ALZHEIMERS & DEMENTIA (2021)

Article Cell Biology

ApoE4 Impairs Neuron-Astrocyte Coupling of Fatty Acid Metabolism

Guoyuan Qi, Yashi Mi, Xiaojian Shi, Haiwei Gu, Roberta Diaz Brinton, Fei Yin

Summary: This study reveals the detrimental effects of ApoE4 on fatty acid metabolism in neurons and astrocytes, leading to lipid accumulation and energy imbalance. ApoE4 decreases the transport efficiency of neuronal lipids, compromising metabolic and synaptic support from astrocytes to neurons.

CELL REPORTS (2021)

Review Obstetrics & Gynecology

Precision hormone therapy: identification of positive responders

Y. J. Kim, R. D. Brinton

Summary: The therapeutic impact of MHT remains under debate, with variations in neurodegenerative diseases among individuals. Characteristics of women in observational studies and clinical trials, as well as different MHT treatments and regimens, may impact outcomes. Precision hormone therapy in the future will require identification of symptomatic women appropriate for MHT and personalized treatment based on genetic profile and health risks.

CLIMACTERIC (2021)

Article Behavioral Sciences

Epigenetics of the developing and aging brain: Mechanisms that regulate onset and outcomes of brain reorganization

Eliza R. Bacon, Roberta Diaz Brinton

Summary: Brain development is a lifelong process that undergoes significant cognitive changes during critical periods of transition. Environmental factors can impact embryonic development, puberty, and reproductive senescence. Epigenetic marks, such as DNA methylation and histone modifications, play a role in how early events affect development, cognition, and health outcomes.

NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2021)

Article Oncology

Androgen-targeting therapeutics mitigate the adverse effect of GnRH agonist on the risk of neurodegenerative disease in men treated for prostate cancer

Gregory L. Branigan, Georgina Torrandell-Haro, Maira Soto, Edward P. Gelmann, Francesca Vitali, Kathleen E. Rodgers, Roberta Diaz Brinton

Summary: This study investigated the impact of androgen-targeting therapeutics on the risk of neurodegenerative diseases in men with prostate cancer. It found that GnRH agonists were associated with increased NDD risk, while abiraterone acetate was associated with decreased risk. These findings suggest potential strategies for mitigating the risk of NDD in prostate cancer patients.

CANCER MEDICINE (2022)

Article Endocrinology & Metabolism

Loss of fatty acid degradation by astrocytic mitochondria triggers neuroinflammation and neurodegeneration

Yashi Mi, Guoyuan Qi, Francesca Vitali, Yuan Shang, Adam C. Raikes, Tian Wang, Yan Jin, Roberta D. Brinton, Haiwei Gu, Fei Yin

Summary: Mi, Qi et al. have identified a mechanism in which defective oxidative phosphorylation in astrocytes disrupts astroglial lipid homeostasis, leading to neuronal damage and microglial reactivity. This mechanism involves the accumulation of lipid droplets in astrocytes, which triggers neurodegeneration resembling Alzheimer's disease. The study reveals the importance of astrocytic oxidative phosphorylation in fatty acid degradation and lipid homeostasis maintenance, and highlights the role of astrocyte dysfunction in neuroinflammation and neurodegeneration.

NATURE METABOLISM (2023)

Article Obstetrics & Gynecology

Retrospective analysis of phytoSERM for management of menopause-associated vasomotor symptoms and cognitive decline: a pilot study on pharmacogenomic effects of mitochondrial haplogroup and APOE genotype on therapeutic efficacy

Yiwei Wang, Gerson Hernandez, Wendy J. Mack, Lon S. Schneider, Fei Yin, Roberta D. Brinton

MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY (2020)

No Data Available