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激素治疗引起不规则出血的机制:基质金属蛋白酶及其组织抑制剂的作用

Mechanisms of irregular bleeding with hormone therapy: the role of matrix metalloproteinases and their tissue inhibitors.

作者信息

Hickey M, Crewe J, Mahoney L A, Doherty D A, Fraser I S, Salamonsen L A

机构信息

School of Women's and Infants' Health, University of Western Australia, King Edward Memorial Hospital, Subiaco, Perth, Western Australia 6008.

出版信息

J Clin Endocrinol Metab. 2006 Aug;91(8):3189-98. doi: 10.1210/jc.2005-2748. Epub 2006 May 9.

Abstract

CONTEXT

Irregular bleeding is common in users of combined hormone therapy (HT) and often leads to invasive and expensive investigations to exclude underlying pathology. The mechanisms of HT-related bleeding are poorly understood. Endometrial matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are believed to regulate bleeding during the normal menstrual cycle and are known to be altered in breakthrough bleeding with progestogen-only contraception.

OBJECTIVE

The aim of this study was to determine how HT exposure alters endometrial production of MMP-1, -3, -9, and -14 and their tissue inhibitors TIMP-1, -2, -3, and -4 and to determine the relationship between MMP and TIMP production and bleeding patterns in HT users. Endometrial leukocytes regulating MMP production and activation were also assessed.

DESIGN

A prospective observational study was conducted between 2003 and 2005.

SETTING AND PATIENTS

The study occurred at a tertiary referral menopause clinic at King Edward Memorial Hospital, Western Australia, and included 25 postmenopausal women not taking HT and 73 women taking combined HT.

INTERVENTIONS

Endometrium was obtained during and outside bleeding episodes.

MAIN OUTCOME MEASURES

We assessed production of MMP-1, -3, -9, and -14 and their tissue inhibitors TIMP-1, -2, -3, and -4 and their relationship to bleeding patterns in HT users.

RESULTS

All MMPs studied, with the exception of MMP-9, were expressed at low levels in postmenopausal endometrium. Increases in both MMP-3 and -9 localization were seen in association with irregular bleeding, but these did not reach statistical significance. Endometrial production of TIMP-1 was significantly increased in association with bleeding. Endometrial leukocytes were not related to bleeding, with the exception of uterine natural killer cells, which were significantly increased during bleeding, as previously published.

CONCLUSIONS

Irregular bleeding in HT users is associated with a distinct pattern of MMP and TIMP production that differs from that seen in normal menstrual bleeding and from that seen in contraceptive-related breakthrough bleeding. This suggests that the endometrial balance between MMP and TIMP contributes to vascular breakdown with HT but by a different mechanism than that seen in normal menstruation or in breakthrough bleeding.

摘要

背景

不规则出血在联合激素疗法(HT)使用者中很常见,常常需要进行侵入性且昂贵的检查以排除潜在病变。与HT相关的出血机制尚不清楚。子宫内膜基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs)被认为在正常月经周期中调节出血,并且已知在仅使用孕激素避孕导致的突破性出血中会发生改变。

目的

本研究的目的是确定HT暴露如何改变子宫内膜MMP-1、-3、-9和-14及其组织抑制剂TIMP-1、-2、-3和-4的产生,并确定MMP和TIMP产生与HT使用者出血模式之间的关系。还评估了调节MMP产生和激活的子宫内膜白细胞。

设计

2003年至2005年进行了一项前瞻性观察研究。

地点和患者

该研究在西澳大利亚爱德华国王纪念医院的三级转诊更年期诊所进行,包括25名未使用HT的绝经后妇女和73名使用联合HT的妇女。

干预措施

在出血期间和出血期外获取子宫内膜。

主要观察指标

我们评估了MMP-1、-3、-9和-14及其组织抑制剂TIMP-1、-2、-3和-4的产生及其与HT使用者出血模式的关系。

结果

除MMP-9外,所有研究的MMP在绝经后子宫内膜中均低水平表达。MMP-3和-9的定位增加与不规则出血有关,但未达到统计学意义。TIMP-1的子宫内膜产生与出血显著增加有关。子宫内膜白细胞与出血无关,但子宫自然杀伤细胞除外,如先前发表的那样,其在出血期间显著增加。

结论

HT使用者的不规则出血与MMP和TIMP产生的独特模式有关,这与正常月经出血以及与避孕相关的突破性出血中所见的模式不同。这表明MMP和TIMP之间的子宫内膜平衡导致HT引起的血管破裂,但其机制与正常月经或突破性出血中所见的不同。

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