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In the wall lies the truth: a systematic review of diagnostic markers in intracranial aneurysms

机译:在墙上谎言说明:对颅内动脉瘤诊断标志物的系统审查

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Abstract Objective : Despite recent advances in molecular biology and genetics, the development of intracranial aneurysms (IA) is still poorly understood.?Elucidation of the processes occurring in the IA wall is essential for a better understanding of IA pathophysiology. We sought to analyze the current evidence from histological, molecular and genetic studies of IA. Methods : We systematically searched PubMed, Scopus, Web of Science and Cochrane Library for articles published before Mar 1, 2019 reporting on different diagnostic markers in human IA specimens. Expression of the markers in IA wall (vs. healthy arterial wall) and association with the rupture status were analyzed. The quality of the included studies and the level of the evidence for the markers were incorporated into the final data assessment. Results: We included 123 studies reporting on analyses of 3476 IA (median 19 IA/study) published between 1966 and 2018. Based on microscopic, biochemical, genetic and biomechanical analyses, data on 358 diagnostic targets in the IA wall were collected. We developed a scale to distribute the diagnostic markers according to their specificity for IA or healthy arterial wall, as well as for ruptured or unruptured IA. We identified different functional pathways, which might reflect the intrinsic and extrinsic processes underlying IA pathophysiology. Conclusions: Multiple histological and molecular markers and the related functional pathways contributing to the development of IA might present promising targets for future therapeutic interventions. Because of?small numbers of IA samples in each study, 89% of the analyzed diagnostic markers presented with the lowest level of evidence. This underlines the need for the initiation of a multi‐centric prospective histological IA register for pooled data analysis.
机译:摘要目的:尽管分子生物学和遗传学的最近进步,但颅内动脉瘤(IA)的发展仍然很清楚.IA墙壁发生的过程阐明对于更好地了解IA病理生理学至关重要。我们试图分析来自IA的组织学,分子和遗传研究的当前证据。方法:我们系统地搜索了2019年3月1日前发表的文章的PubMed,Scopus,科学和Cochrane图书馆,报告了人类IA标本的不同诊断标志。分析了IA壁(与健康动脉壁)中标记的表达及与破裂状态相关联。所包含的研究质量和标记证据的水平纳入最终数据评估。结果:我们在1966年至2018年间公布的3476岁(中位数19 IA / Studio)的分析包括123项研究。基于显微镜,生化,遗传和生物力学分析,收集了IA墙358件诊断靶标的数据。我们开发了根据其对IA或健康动脉壁的特异性分发诊断标志物的规模,以及破裂或未破裂的IA。我们确定了不同的功能途径,这可能反映了IA病理生理学的内在和外在过程。结论:多种组织学和分子标记和有助于IA的发展的相关功能途径可能呈现未来治疗干预措施的有希望的目标。因为每项研究中少量的IA样本,89%的分析诊断标记呈现出最低的证据。这强调了对汇集数据分析的多维预期组织学IA寄存器启动的需要。

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