• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

孕激素受体状态预测内异症孕激素治疗的反应。

Progesterone Receptor Status Predicts Response to Progestin Therapy in Endometriosis.

机构信息

Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, Yale University, New Haven, Connecticut.

出版信息

J Clin Endocrinol Metab. 2018 Dec 1;103(12):4561-4568. doi: 10.1210/jc.2018-01227.

DOI:10.1210/jc.2018-01227
PMID:30357380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6226602/
Abstract

CONTEXT

Progestin-based therapy is the first-line treatment for managing endometriosis-associated pain. However, response to progestins is currently variable and unpredictable. Predictive markers for response to progestin-based therapy would allow for a personalized approach to endometriosis treatment.

OBJECTIVE

We hypothesize that progesterone receptor (PR) levels in endometriotic lesions determine response to progestin-based therapy.

DESIGN

Retrospective cohort study.

SETTING

Academic center.

PATIENTS

Fifty-two subjects with histologically confirmed endometriosis and a previous documented response to hormonal therapy were included.

INTERVENTIONS

Immunohistochemistry was performed on sections of endometriotic lesions using a rabbit polyclonal IgG for detection of PR-A/B.

MAIN OUTCOME MEASURES

The Histo (H)-score was used for quantifying PR status. Response to progestin-based therapies was determined from review of the electronic medical record.

RESULTS

H-score was higher in responders compared with nonresponders. Subjects were categorized into three groups: high (H-score > 80, n = 7), medium (H-score 6 to 80, n = 28), and low (H-score ≤ 5, n = 17) PR status. The threshold of PR > 80 was associated with a 100% positive predictive value. The threshold of PR < 5 was associated with a 94% negative predictive value.

CONCLUSION

PR status is strongly associated with response to progestin-based therapy. Receptor status in endometriosis could be used to tailor hormonal-based regimens after surgery, and negate trialing progestin-based therapy to determine resistance. Ascertainment of PR status may allow for a novel, targeted, precision-based approach to treating endometriosis.

摘要

背景

孕激素为基础的治疗是管理子宫内膜异位症相关疼痛的一线治疗方法。然而,目前孕激素的反应是可变的和不可预测的。孕激素反应的预测标志物将允许子宫内膜异位症治疗的个性化方法。

目的

我们假设子宫内膜异位症病变中的孕激素受体(PR)水平决定了孕激素为基础的治疗反应。

设计

回顾性队列研究。

设置

学术中心。

患者

52 名组织学证实的子宫内膜异位症患者,且之前有激素治疗反应的记录。

干预措施

使用针对 PR-A/B 的兔多克隆 IgG 对子宫内膜异位症病变的切片进行免疫组化。

主要观察指标

使用 Histo(H)评分来量化 PR 状态。通过审查电子病历来确定孕激素为基础的治疗反应。

结果

与无反应者相比,反应者的 H 评分更高。将受试者分为三组:高(H 评分>80,n=7)、中(H 评分 6 至 80,n=28)和低(H 评分≤5,n=17)PR 状态。PR>80 的阈值与 100%的阳性预测值相关。PR<5 的阈值与 94%的阴性预测值相关。

结论

PR 状态与孕激素为基础的治疗反应密切相关。受体状态可用于在手术后调整激素为基础的方案,并消除孕激素为基础的治疗试验以确定耐药性。PR 状态的确定可能允许一种新的、有针对性的、基于精准的治疗子宫内膜异位症的方法。

相似文献

1
Progesterone Receptor Status Predicts Response to Progestin Therapy in Endometriosis.孕激素受体状态预测内异症孕激素治疗的反应。
J Clin Endocrinol Metab. 2018 Dec 1;103(12):4561-4568. doi: 10.1210/jc.2018-01227.
2
Progesterone receptor status predicts aggressiveness of human endometriotic lesions in murine avatars.孕激素受体状态可预测人子宫内膜异位症病变在小鼠模型中的侵袭性。
F S Sci. 2025 Feb;6(1):65-72. doi: 10.1016/j.xfss.2024.10.004. Epub 2024 Oct 10.
3
Progesterone receptor ligands for the treatment of endometriosis: the mechanisms behind therapeutic success and failure.孕激素受体配体治疗子宫内膜异位症:治疗成功和失败的背后机制。
Hum Reprod Update. 2020 Jun 18;26(4):565-585. doi: 10.1093/humupd/dmaa009.
4
Inflammation influences steroid hormone receptors targeted by progestins in endometrial stromal cells from women with endometriosis.炎症会影响子宫内膜异位症女性子宫内膜基质细胞中孕激素作用的甾体激素受体。
J Reprod Immunol. 2016 Sep;117:30-8. doi: 10.1016/j.jri.2016.06.004. Epub 2016 Jun 17.
5
Estrogen receptor-α immunoreactivity predicts symptom severity and pain recurrence in deep endometriosis.雌激素受体-α免疫反应可预测深部子宫内膜异位症的症状严重程度和疼痛复发。
Fertil Steril. 2020 Jun;113(6):1224-1231.e1. doi: 10.1016/j.fertnstert.2020.01.036. Epub 2020 May 13.
6
Efficacy, safety and recurrence of new progestins and selective progesterone receptor modulator for the treatment of endometriosis: a comparison study in mice.新孕激素和选择性孕激素受体调节剂治疗子宫内膜异位症的疗效、安全性和复发:小鼠比较研究。
Reprod Biol Endocrinol. 2018 Apr 3;16(1):32. doi: 10.1186/s12958-018-0347-9.
7
Progesterone receptor ligands for the treatment of endometriosis.用于治疗子宫内膜异位症的孕激素受体配体。
Minerva Obstet Gynecol. 2023 Jun;75(3):288-297. doi: 10.23736/S2724-606X.22.05157-0. Epub 2022 Oct 18.
8
Promoter hypermethylation of progesterone receptor isoform B (PR-B) in endometriosis.子宫内膜异位症中孕激素受体B亚型(PR-B)的启动子高甲基化
Epigenetics. 2006 Apr-Jun;1(2):106-11. doi: 10.4161/epi.1.2.2766. Epub 2006 Apr 1.
9
Abundance and Localization of Progesterone Receptor Isoforms in Endometrium in Women With and Without Endometriosis and in Peritoneal and Ovarian Endometriotic Implants.有和没有子宫内膜异位症的女性子宫内膜中孕激素受体亚型的丰度和定位,以及腹膜和卵巢子宫内膜异位植入物中的情况
Reprod Sci. 2015 Sep;22(9):1153-61. doi: 10.1177/1933719115585145. Epub 2015 Jun 2.
10
Progestin effects on expression of AKR1C1-AKR1C3, SRD5A1 and PGR in the Z-12 endometriotic epithelial cell line.孕激素对 Z-12 子宫内膜异位症上皮细胞系 AKR1C1-AKR1C3、SRD5A1 和 PGR 表达的影响。
Chem Biol Interact. 2013 Feb 25;202(1-3):218-25. doi: 10.1016/j.cbi.2012.10.028. Epub 2012 Nov 23.

引用本文的文献

1
Pathophysiology of Endometriosis: Insights from Immunohistochemical Analysis of Ectopic and Eutopic Tissues.子宫内膜异位症的病理生理学:来自异位和在位组织免疫组化分析的见解
Int J Mol Sci. 2025 Jun 22;26(13):5998. doi: 10.3390/ijms26135998.
2
The role of long non-coding ribonucleic acid HOXA11-AS in endometriosis therapy.长链非编码核糖核酸HOXA11-AS在子宫内膜异位症治疗中的作用
Reprod Biol Endocrinol. 2025 Jun 2;23(1):83. doi: 10.1186/s12958-025-01420-0.
3
The effect of combined oral contraceptive pills on angiogenesis in endometriotic lesions.复方口服避孕药对子宫内膜异位症病灶血管生成的影响。
Hormones (Athens). 2025 Feb 21. doi: 10.1007/s42000-025-00636-4.
4
Single-cell transcriptomic atlas of different endometriosis indicating that an interaction between endometriosis-associated mesothelial cells (EAMCs) and ectopic stromal cells may influence progesterone resistance.不同子宫内膜异位症的单细胞转录组图谱表明,子宫内膜异位症相关间皮细胞(EAMCs)与异位基质细胞之间的相互作用可能会影响孕激素抵抗。
Clin Transl Med. 2025 Feb;15(2):e70216. doi: 10.1002/ctm2.70216.
5
Prospects for potential therapy targeting immune‑associated factors in endometriosis (Review).针对子宫内膜异位症中免疫相关因子的潜在治疗前景(综述)
Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2024.13422. Epub 2024 Dec 24.
6
Exploring the Shared Pathogenesis Mechanisms of Endometriosis and Cancer: Stemness and Targeted Treatments of Its Molecular Pathways-A Narrative Review.探索子宫内膜异位症和癌症的共同发病机制:干性及其分子途径的靶向治疗——一篇叙述性综述
Int J Mol Sci. 2024 Nov 27;25(23):12749. doi: 10.3390/ijms252312749.
7
Exploring the Role of MicroRNAs in Progesterone and Estrogen Receptor Expression in Endometriosis.探索微小RNA在子宫内膜异位症中孕酮和雌激素受体表达中的作用。
Biomedicines. 2024 Sep 28;12(10):2218. doi: 10.3390/biomedicines12102218.
8
The role of progesterone and estrogen receptors in treatment choice after endometriosis surgery: A cross-sectional study.孕激素和雌激素受体在子宫内膜异位症手术后治疗选择中的作用:一项横断面研究。
Int J Reprod Biomed. 2024 Sep 12;22(7):567-578. doi: 10.18502/ijrm.v22i7.16970. eCollection 2024 Jul.
9
Endometriosis: Molecular Pathophysiology and Recent Treatment Strategies-Comprehensive Literature Review.子宫内膜异位症:分子病理生理学与近期治疗策略——综合文献综述
Pharmaceuticals (Basel). 2024 Jun 24;17(7):827. doi: 10.3390/ph17070827.
10
Long-Term Maintenance of Viable Human Endometrial Epithelial Cells to Analyze Estrogen and Progestin Effects.长期维持有活力的人子宫内膜上皮细胞以分析雌激素和孕激素的作用。
Cells. 2024 May 9;13(10):811. doi: 10.3390/cells13100811.

本文引用的文献

1
Predictive biomarkers may allow precision therapy of endometriosis.预测性生物标志物可能使子宫内膜异位症的精准治疗成为可能。
J Endometr Pelvic Pain Disord. 2017 Oct;9(4):279-285. doi: 10.5301/jeppd.5000311. Epub 2017 Aug 11.
2
Human Endometriosis Tissue Microarray Reveals Site-specific Expression of Estrogen Receptors, Progesterone Receptor, and Ki67.人子宫内膜异位症组织芯片揭示雌激素受体、孕激素受体和Ki67的位点特异性表达。
Appl Immunohistochem Mol Morphol. 2019 Aug;27(7):491-500. doi: 10.1097/PAI.0000000000000663.
3
Endometriosis alters brain electrophysiology, gene expression and increases pain sensitization, anxiety, and depression in female mice.子宫内膜异位症改变了雌性小鼠的大脑电生理学、基因表达,并增加了疼痛敏感性、焦虑和抑郁。
Biol Reprod. 2018 Aug 1;99(2):349-359. doi: 10.1093/biolre/ioy035.
4
Heterogeneity of estrogen receptor α and progesterone receptor distribution in lesions of deep infiltrating endometriosis of untreated women or during exposure to various hormonal treatments.未接受治疗的女性或在接受各种激素治疗期间,深部浸润性子宫内膜异位症病变中雌激素受体α和孕激素受体分布的异质性。
Gynecol Endocrinol. 2018 Aug;34(8):651-655. doi: 10.1080/09513590.2018.1433160. Epub 2018 Jan 31.
5
Systemic Inflammation Induced by microRNAs: Endometriosis-Derived Alterations in Circulating microRNA 125b-5p and Let-7b-5p Regulate Macrophage Cytokine Production.系统性炎症诱导的 microRNAs:来源于子宫内膜异位症的循环 microRNA125b-5p 和 Let-7b-5p 的改变调节巨噬细胞细胞因子的产生。
J Clin Endocrinol Metab. 2018 Jan 1;103(1):64-74. doi: 10.1210/jc.2017-01199.
6
Treatment of Endometriosis-Associated Pain with Elagolix, an Oral GnRH Antagonist.Elagolix,一种口服 GnRH 拮抗剂,治疗子宫内膜异位症相关疼痛。
N Engl J Med. 2017 Jul 6;377(1):28-40. doi: 10.1056/NEJMoa1700089. Epub 2017 May 19.
7
Incremental direct and indirect cost burden attributed to endometriosis surgeries in the United States.在美国,子宫内膜异位症手术导致的直接和间接增量成本负担。
Fertil Steril. 2017 May;107(5):1181-1190.e2. doi: 10.1016/j.fertnstert.2017.03.020.
8
Progesterone resistance in endometriosis: origins, consequences and interventions.子宫内膜异位症中的孕激素抵抗:起源、后果及干预措施
Acta Obstet Gynecol Scand. 2017 Jun;96(6):623-632. doi: 10.1111/aogs.13156.
9
Low Body Mass Index in Endometriosis Is Promoted by Hepatic Metabolic Gene Dysregulation in Mice.小鼠肝脏代谢基因失调促进子宫内膜异位症患者低体重指数的发生
Biol Reprod. 2016 Dec;95(6):115. doi: 10.1095/biolreprod.116.142877. Epub 2016 Sep 14.
10
Challenges in the development of novel therapeutic strategies for treatment of endometriosis.子宫内膜异位症新型治疗策略开发中的挑战。
Expert Opin Ther Targets. 2016;20(5):593-600. doi: 10.1517/14728222.2016.1118461. Epub 2015 Dec 19.