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Evaluation of alpha-synuclein immunohistochemical methods for the detection of Lewy-type synucleinopathy in gastrointestinal biopsies

机译:评价α-突触核蛋白免疫组织化学方法检测胃肠道活检中路易型突触核蛋白病

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摘要

The observation showing that Lewy type synucleinopathy (LTS), the pathological hallmark of Parkinson’s disease (PD), is found in the gut of almost all PD subjects led to a substantial amount of research to develop a diagnostic procedure in living patients based on endoscopically obtained gastrointestinal biopsies. However, the existing studies have provided conflicting results regarding the sensitivity and specificity of gastrointestinal biopsies for the detection of LTS. We therefore undertook a multi-center staining and blinded judging of a common set of slides from colonic biopsies to determine the optimal protocol for the detection of LTS. Four different immunohistochemical methods, developed in four separate expert laboratories, were evaluated for their sensitivity and specificity to detect enteric LTS. Test sets of formalin-fixed, paraffin-embedded sections from biopsies of 9 PD subjects and 3 controls were stained with the 4 methods and graded by 4 different observers. Four types of staining morphology (granular staining in the lamina propria, perivascular/vascular wall staining in the submucosa, lacy-granular pattern in the submucosa and epithelial cell nuclear staining) were variably observed in the slides stained by the 4 methods. Positive alpha-synuclein staining was observed by all 5 judges in most of the slides from control cases, regardless of the staining methods that were used. Moreover, none of the tested method or staining pattern had a specificity and sensitivity more than 80 % regarding to PD. Overall, our study suggest that the tested methods are not adequate for the prediction of PD using gastrointestinal biopsies. Future studies are warranted to test new immunostaining methods.Electronic supplementary materialThe online version of this article (doi:10.1186/s40478-016-0305-8) contains supplementary material, which is available to authorized users.
机译:观察表明几乎在所有PD受试者的肠道中都发现了路易型突触核蛋白病(LTS),这是帕金森氏病(PD)的病理学特征,导致大量研究开发了基于内窥镜检查获得的活体患者诊断方法胃肠活检。然而,现有研究在胃肠活检对LTS检测的敏感性和特异性方面提供了矛盾的结果。因此,我们对来自结肠活检的一组普通玻片进行了多中心染色和盲法判断,以确定用于检测LTS的最佳方案。评估了在四个独立的专家实验室中开发的四种不同的免疫组织化学方法的敏感性和特异性,以检测肠溶性LTS。用4种方法对9例PD受试者和3例对照的活检标本进行福尔马林固定,石蜡包埋切片的测试集进行染色,并由4位不同的观察者进行分级。在用4种方法染色的玻片中,观察到了四种类型的染色形态(固有层的颗粒染色,粘膜下层的血管周围/血管壁染色,粘膜下层的蕾丝-颗粒状染色和上皮细胞核染色)。无论采用哪种染色方法,对照病例中的大多数玻片上的所有5名法官均观察到了阳性的α-突触核蛋白染色。而且,相对于PD,所测试的方法或染色方式均没有超过80%的特异性和敏感性。总体而言,我们的研究表明,所测试的方法不足以通过胃肠道活检来预测PD。有必要进行进一步的研究以测试新的免疫染色方法。电子补充材料本文的在线版本(doi:10.1186 / s40478-016-0305-8)包含补充材料,授权用户可以使用。

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