Inserm, U913, Nantes, F-44035, France.
Nantes University, Nantes, F-44035, France.
Acta Neuropathol Commun. 2016 Apr 4;4:35. doi: 10.1186/s40478-016-0305-8.
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.
观察表明,路易体型突触核蛋白病(LTS)是帕金森病(PD)的病理标志,几乎所有 PD 患者的肠道中都存在 LTS,这促使大量研究致力于开发基于内窥镜获得的胃肠道活检的活体患者诊断程序。然而,现有的研究对于胃肠道活检检测 LTS 的敏感性和特异性提供了相互矛盾的结果。因此,我们进行了一项多中心染色和盲法判断,对来自结肠活检的常见切片进行了评估,以确定检测 LTS 的最佳方案。评估了四个不同的免疫组织化学方法,这些方法是在四个独立的专家实验室中开发的,以评估它们检测肠内 LTS 的敏感性和特异性。使用四种方法对来自 9 名 PD 患者和 3 名对照者的福尔马林固定、石蜡包埋切片的测试集进行染色,并由 4 名不同的观察者进行评分。在由四种方法染色的切片中观察到四种类型的染色形态(固有层中的颗粒状染色、黏膜下层中的血管壁周围/血管壁染色、黏膜下层中的花边状颗粒状模式和上皮细胞核染色)。所有 5 名裁判者在大多数对照病例的切片中都观察到了所有方法的 alpha-synuclein 阳性染色,无论使用哪种染色方法。此外,在所测试的方法或染色模式中,没有一种方法的特异性和敏感性超过 80%,可以用于 PD 的预测。总体而言,我们的研究表明,所测试的方法不能用于使用胃肠道活检来预测 PD。需要进行未来的研究来测试新的免疫染色方法。