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寻找帕金森病α-突触核蛋白病理学的外周活检指标

The Search for a Peripheral Biopsy Indicator of α-Synuclein Pathology for Parkinson Disease.

作者信息

Lee John M, Derkinderen Pascal, Kordower Jeffrey H, Freeman Roy, Munoz David G, Kremer Thomas, Zago Wagner, Hutten Samantha J, Adler Charles H, Serrano Geidy E, Beach Thomas G

机构信息

Department of Pathology, NorthShore University Health System, University of Chicago, Pritzker School of Medicine, Evanston, Illinois, USA.

Inserm, U913, Nantes F-44035; Nantes University, Nantes F-44035; Department of Neurology, CHU Nantes, Nantes F-44093, France.

出版信息

J Neuropathol Exp Neurol. 2017 Jan 1;76(1):2-15. doi: 10.1093/jnen/nlw103.

Abstract

The neuropathological hallmark of Parkinson disease (PD) is abnormal accumulation of α-synuclein (α-syn). Demonstrating pathological α-syn in live patients would be useful for identifying and monitoring PD patients. To date, however, imaging and biofluid approaches have not permitted premortem assessment of pathological α-syn. α-syn pathology in the peripheral nervous system of patients with PD has been demonstrated in studies dating back more than 40 years. More recent work suggests that colon, submandibular gland and skin biopsies could be useful as expedient biomarkers but histological differentiation of pathological and normal peripheral α-syn has been challenging and multiple research groups have reported variable results. A variety of immunohistochemical methods have been employed but almost all studies to date originated at single centers with no independent, blinded replication. To address these issues, the Michael J. Fox Foundation for Parkinson's Research sponsored a series of meetings and investigations by several research groups with relevant experience. The major finding reported herein was that biopsies can be used to distinguish PD patients from normal subjects. However, full assessment of the clinical potential of biopsy will only be achieved through large, multicenter trials in which both the initial detection methodology and histology have been assessed by blinded panels of pathologists.

摘要

帕金森病(PD)的神经病理学标志是α-突触核蛋白(α-syn)的异常积聚。在活体患者中证实病理性α-syn对于识别和监测PD患者将很有帮助。然而,迄今为止,成像和生物流体方法尚未允许对病理性α-syn进行生前评估。早在40多年前的研究中就已证实PD患者外周神经系统中存在α-syn病理学变化。最近的研究表明,结肠、下颌下腺和皮肤活检作为便捷的生物标志物可能有用,但病理性和正常外周α-syn的组织学区分一直具有挑战性,多个研究小组报告的结果各不相同。已经采用了多种免疫组织化学方法,但迄今为止几乎所有研究都来自单一中心,没有独立的、盲法重复研究。为了解决这些问题,迈克尔·J·福克斯帕金森研究基金会赞助了一系列会议以及几个有相关经验的研究小组开展的调查。本文报告的主要发现是活检可用于区分PD患者和正常受试者。然而只有通过大型多中心试验才能全面评估活检的临床潜力,在这些试验中,初始检测方法和组织学都要由病理学家组成的盲法小组进行评估。

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