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雌激素水平影响围绝经期膝关节骨关节炎疼痛的机制及非药物措施

The Mechanism by Which Estrogen Level Affects Knee Osteoarthritis Pain in Perimenopause and Non-Pharmacological Measures.

作者信息

Zhao Huiying, Yu Fan, Wu Wei

机构信息

School of Exercise and Health, Shanghai University of Sports, Shanghai 200438, China.

School of Athletic Performance, Shanghai University of Sports, Shanghai 200438, China.

出版信息

Int J Mol Sci. 2025 Mar 7;26(6):2391. doi: 10.3390/ijms26062391.


DOI:10.3390/ijms26062391
PMID:40141035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11942494/
Abstract

Perimenopausal women have fluctuating estrogen levels, which often trigger a range of symptoms of perimenopausal syndromes as estrogen levels decrease. Changes in perimenopausal estrogen levels are closely related to pain in knee osteoarthritis (KOA), which has long been a research area of great interest in perimenopausal women. In recent years, it has been found that perimenopausal estrogen levels have an important role in KOA pain, namely, that estrogen can affect KOA pain through the regulation of inflammatory responses, inhibition of cellular senescence and apoptosis, and modulation of neurotransmitters, which may provide new ideas for KOA treatment. This study aims to describe the mechanism of estrogen level on knee osteoarthritis pain in perimenopause and related non-pharmacological measures, such as physical therapy, physical factor therapy, traditional Chinese medicine, and diet, which can provide a reference for the study and treatment of pain in perimenopausal women with KOA.

摘要

围绝经期女性的雌激素水平波动较大,随着雌激素水平下降,常引发一系列围绝经期综合征症状。围绝经期雌激素水平的变化与膝关节骨关节炎(KOA)疼痛密切相关,长期以来一直是围绝经期女性备受关注的研究领域。近年来发现,围绝经期雌激素水平在KOA疼痛中起重要作用,即雌激素可通过调节炎症反应、抑制细胞衰老和凋亡以及调节神经递质来影响KOA疼痛,这可能为KOA治疗提供新思路。本研究旨在阐述围绝经期雌激素水平对膝关节骨关节炎疼痛的作用机制以及相关非药物措施,如物理治疗、物理因子治疗、中医和饮食等,可为围绝经期KOA女性疼痛的研究和治疗提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/a4f7f0fddc3d/ijms-26-02391-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/4887dae00b00/ijms-26-02391-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/1113fe718154/ijms-26-02391-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/a4f7f0fddc3d/ijms-26-02391-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/4887dae00b00/ijms-26-02391-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/1113fe718154/ijms-26-02391-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d98/11942494/a4f7f0fddc3d/ijms-26-02391-g003.jpg

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[1]
The Mechanism by Which Estrogen Level Affects Knee Osteoarthritis Pain in Perimenopause and Non-Pharmacological Measures.

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引用本文的文献

[1]
Age-Dependent Meniscal and Chondral Damage in Eastern European Women Undergoing First-Time Knee Arthroscopy.

Healthcare (Basel). 2025-7-26

本文引用的文献

[1]
Knee adipose tissue: from its implication in osteoarthritis to its supposed role in tissue engineering.

NPJ Aging. 2025-2-3

[2]
Follicle-stimulating hormone: More than a marker for menopause: FSH as a frontier for women's mental health.

Psychiatry Res. 2025-3

[3]
Icaritin alleviates motor impairment and osteoporosis in Parkinson's disease mice via the ER-PI3K/Akt pathway.

Sci Rep. 2025-1-25

[4]
Menopause-induced 17β-estradiol and progesterone loss increases senescence markers, matrix disassembly and degeneration in mouse cartilage.

Nat Aging. 2025-1

[5]
Identification of biomarkers for knee osteoarthritis through clinical data and machine learning models.

Sci Rep. 2025-1-11

[6]
High-resolution microCT analysis of sclerotic subchondral bone beneath bone-on-bone wear grooves in severe osteoarthritis.

Bone. 2025-4

[7]
Physiological premature aging of ovarian blood vessels leads to decline in fertility in middle-aged mice.

Nat Commun. 2025-1-2

[8]
Construction and validation of a senescence-related gene signature for early prediction and treatment of osteoarthritis based on bioinformatics analysis.

Sci Rep. 2024-12-30

[9]
Exploring the effects of estrogen deficiency and aging on organismal homeostasis during menopause.

Nat Aging. 2024-12

[10]
Effects of three types of resistance training on knee osteoarthritis: A systematic review and network meta-analysis.

PLoS One. 2024-12-5

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