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体内脑雌激素受体密度与神经内分泌衰老的关系及其与认知和症状的关系。

In vivo brain estrogen receptor density by neuroendocrine aging and relationships with cognition and symptomatology.

机构信息

Department of Neurology, Weill Cornell Medicine, 402 East 70th Street, LH-404, New York, NY, 10021, USA.

Department of Radiology, Weill Cornell Medicine, New York, NY, USA.

出版信息

Sci Rep. 2024 Jun 20;14(1):12680. doi: 10.1038/s41598-024-62820-7.


DOI:10.1038/s41598-024-62820-7
PMID:38902275
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11190148/
Abstract

17β-estradiol, the most biologically active estrogen, exerts wide-ranging effects in brain through its action on estrogen receptors (ERs), influencing higher-order cognitive function and neurobiological aging. However, our knowledge of ER expression and regulation by neuroendocrine aging in the living human brain is limited. This in vivo brain F-fluoroestradiol (F-FES) Positron Emission Tomography (PET) study of healthy midlife women reveals progressively higher ER density over the menopause transition in estrogen-regulated networks. Effects were independent of age, plasma estradiol and sex hormone binding globulin, and were highly consistent, correctly classifying all women as being postmenopausal or premenopausal. Higher ER density in target regions was associated with poorer memory performance for both postmenopausal and perimenopausal groups, and predicted presence of self-reported mood and cognitive symptoms after menopause. These findings provide novel insights on brain ER density modulation by female neuroendocrine aging, with clinical implications for women's health.

摘要

17β-雌二醇是生物活性最强的雌激素,通过与雌激素受体(ER)结合,在大脑中发挥广泛的作用,影响高级认知功能和神经生物学衰老。然而,我们对活体人类大脑中神经内分泌衰老对 ER 表达和调节的了解有限。本项针对健康中年女性的体内 F-氟雌二醇(F-FES)正电子发射断层扫描(PET)研究显示,在雌激素调节网络中,ER 密度在绝经过渡期间逐渐升高。这些效应独立于年龄、血浆雌二醇和性激素结合球蛋白,且高度一致,正确地将所有女性归类为绝经后或绝经前。目标区域的 ER 密度越高,绝经后和围绝经期组的记忆表现越差,并且可以预测绝经后自我报告的情绪和认知症状的出现。这些发现为女性神经内分泌衰老对大脑 ER 密度的调节提供了新的见解,对女性健康具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/9326c741b13c/41598_2024_62820_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/b400e3f2be69/41598_2024_62820_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/1388e9edfe37/41598_2024_62820_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/0e1080648b2f/41598_2024_62820_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/9326c741b13c/41598_2024_62820_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/b400e3f2be69/41598_2024_62820_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/1388e9edfe37/41598_2024_62820_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/0e1080648b2f/41598_2024_62820_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1081/11190148/9326c741b13c/41598_2024_62820_Fig4_HTML.jpg

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In vivo brain estrogen receptor density by neuroendocrine aging and relationships with cognition and symptomatology.

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引用本文的文献

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Sex differences in brain glucose metabolism in alzheimer's disease: A voxel-based study.

Geroscience. 2025-9-5

[2]
Microglia and Chek2 contribute to sex-specific organization of the adult zebrafish brain.

bioRxiv. 2025-8-21

[3]
Estrogen regulation of the nucleus accumbens as a gateway to understanding menopause associated metabolic dysfunction.

NPJ Womens Health. 2025

[4]
Postmortem tissue biomarkers of menopausal transition.

Mol Psychiatry. 2025-8-27

[5]
Association Between Menopause Age and Estradiol-Based Hormone Therapy With Cognitive Performance in Cognitively Normal Women in the CLSA.

Neurology. 2025-9-23

[6]
Leveraging high-resolution brain imaging and (epi)genomic approaches to improve women's mental health.

Neuropsychopharmacology. 2025-8-26

[7]
Quantitative and simplified [18F] fluoroestradiol positron emission tomography (PET) measures of brain estrogen receptor expression.

Eur J Nucl Med Mol Imaging. 2025-8-7

[8]
Impact of Myocardial Infarction on Cerebral Homeostasis: Exploring the Protective Role of Estrogen.

J Cardiovasc Aging. 2025-6

[9]
White matter micro- and macrostructural properties in midlife individuals at risk for Alzheimer's disease: Associations with sex and menopausal status.

bioRxiv. 2025-6-13

[10]
Associations between objective sleep metrics and brain structure in cognitively unimpaired adults: interactions with sex and Alzheimer's biomarkers.

Alzheimers Dement. 2025-6

本文引用的文献

[1]
Systematic review and meta-analysis of the effects of menopause hormone therapy on cognition.

Front Endocrinol (Lausanne). 2024

[2]
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Front Aging Neurosci. 2023-10-23

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Ovarian steroid hormones: A long overlooked but critical contributor to brain aging and Alzheimer's disease.

Front Aging Neurosci. 2022-7-19

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Menopause Status Moderates Sex Differences in Tau Burden: A Framingham PET Study.

Ann Neurol. 2022-7

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Endogenous and Exogenous Estrogen Exposures: How Women's Reproductive Health Can Drive Brain Aging and Inform Alzheimer's Prevention.

Front Aging Neurosci. 2022-3-9

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Essays Biochem. 2021-12-17

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Sci Rep. 2021-6-9

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Supervised clustering for TSPO PET imaging.

Eur J Nucl Med Mol Imaging. 2021-12

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Eur J Nucl Med Mol Imaging. 2021-8

[10]
Interactions Between Age, Sex, Menopause, and Brain Structure at Midlife: A UK Biobank Study.

J Clin Endocrinol Metab. 2021-1-23

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