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趋化因子能否用作子宫内膜异位症的生物标志物?一项系统评价。

Can chemokines be used as biomarkers for endometriosis? A systematic review.

作者信息

Borrelli G M, Abrão M S, Mechsner S

机构信息

Department of Gynecology, Charité, Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

出版信息

Hum Reprod. 2014 Feb;29(2):253-66. doi: 10.1093/humrep/det401. Epub 2013 Nov 27.

Abstract

STUDY QUESTION

Can we use chemokines as biomarkers to diagnose patients with endometriosis in clinical practice?

SUMMARY ANSWER

Some chemokines, especially CXCL8 (IL-8), CCL-2 (MCP-1) and CCL5 (RANTES), have the potential to work as biomarkers to identify patients with endometriosis but their accuracy could be improved by combination with other non-inflammatory markers in a panel of biomarkers.

WHAT IS ALREADY KNOWN

The need for a good marker to diagnose endometriosis has increased in recent years and research in this field has intensified. Chemokines have been reported to be associated with endometriosis in several studies over the last 20 years. Many of these studies measured one or more chemokines in peritoneal fluid (PF) and peripheral blood (PB) or through endometrial biopsies in patients with and without endometriosis.

STUDY DESIGN, SIZE, DURATION: A systematic review was done on all published studies that compared chemokine concentrations in patients with and without endometriosis to evaluate their potential as biomarkers for the disease.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Using MEDLINE database from December 1993 to August 2013 and the MeSH terms 'Endometriosis' and 'Chemokines', we identified relevant studies to include in the present review, which was based on the PRISMA statement. Studies that measured at least one chemokine in patients with endometriosis and matching controls in PB, PF or endometrial samples were included. We did not include samples from ectopic lesions. All review articles as well as studies with animals and those not written in English were excluded from this systematic review. The studies were assessed using a modified version of the Quality Assessment of Diagnostic Accuracy Studies criteria. Two authors independently assessed studies for inclusion and risk of bias, and extracted data.

MAIN RESULTS AND THE ROLE OF CHANCE

After inclusion and exclusion criteria, 62 studies were selected to be included in this systematic review. A total of 27 different chemokines or their receptors were evaluated in the reviewed studies. The most studied chemokines (including their receptors) were CXCL8 (51.6%), CCL2 (38.7%) and CCL5 (19.3%) (% of studies). CXCL8 (IL-8) appears to have the best results among all the other chemokines as a marker for endometriosis.

LIMITATIONS, REASONS FOR CAUTION: Some studies included have low power due to small sample size and study designs vary in the assessment criteria for the markers, the state of the patients (e.g. phase of the cycle and stage of disease) and the nature of the controls.

WIDER IMPLICATIONS OF THE FINDINGS

Our findings could guide future research in this field to select the chemokines with the best potential, and to stimulate better-designed studies to determine whether they can become a useful diagnostic tool in clinical practice.

STUDY FUNDING/COMPETING INTEREST(S): There was no funding to support this systematic review. The authors have no competing interest to declare.

摘要

研究问题

在临床实践中,我们能否将趋化因子用作生物标志物来诊断子宫内膜异位症患者?

总结答案

一些趋化因子,尤其是CXCL8(白细胞介素-8)、CCL-2(单核细胞趋化蛋白-1)和CCL5(调节激活正常T细胞表达和分泌因子),有潜力作为生物标志物来识别子宫内膜异位症患者,但通过与生物标志物组合中的其他非炎症标志物联合使用,其准确性可能会提高。

已知信息

近年来,对用于诊断子宫内膜异位症的良好标志物的需求有所增加,该领域的研究也日益深入。在过去20年的多项研究中,趋化因子已被报道与子宫内膜异位症有关。这些研究中有许多在患有和未患有子宫内膜异位症的患者的腹腔液(PF)、外周血(PB)或通过子宫内膜活检来测量一种或多种趋化因子。

研究设计、规模、持续时间:对所有已发表的比较患有和未患有子宫内膜异位症患者趋化因子浓度的研究进行了系统综述,以评估其作为该疾病生物标志物的潜力。

参与者/材料、设置、方法:使用1993年12月至2013年8月的MEDLINE数据库以及主题词“子宫内膜异位症”和“趋化因子”,我们确定了相关研究以纳入本综述,该综述基于PRISMA声明。纳入了在子宫内膜异位症患者以及PB、PF或子宫内膜样本中的匹配对照中测量至少一种趋化因子的研究。我们未纳入来自异位病变的样本。所有综述文章以及动物研究和非英文撰写的研究均被排除在本系统综述之外。使用诊断准确性研究质量评估标准的修改版对研究进行评估。两位作者独立评估研究的纳入情况和偏倚风险,并提取数据。

主要结果及机遇的作用

经过纳入和排除标准后,选择了62项研究纳入本系统综述。在综述研究中总共评估了27种不同的趋化因子或其受体。研究最多的趋化因子(包括其受体)是CXCL8(51.6%)(研究占比)、CCL2(38.7%)和CCL5(19.3%)。作为子宫内膜异位症的标志物,CXCL8(白细胞介素-8)在所有其他趋化因子中似乎具有最佳结果。

局限性、谨慎原因:一些纳入的研究由于样本量小而效力较低,并且研究设计在标志物的评估标准、患者状态(例如月经周期阶段和疾病分期)以及对照性质方面存在差异。

研究结果的更广泛影响

我们的研究结果可以指导该领域未来的研究,以选择最具潜力的趋化因子,并推动设计更完善的研究,以确定它们是否能够成为临床实践中有用的诊断工具。

研究资金/利益冲突:没有资金支持本系统综述。作者没有利益冲突需要声明。

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