Dong Zhaoying, Du Xinyi, Wang Ling, Zou Xiaoya, Zuo Hongzhou, Yan Yong, Chen Guojun, Cheng Oumei, Zhang Yong
Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Ultrasound Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
J Cent Nerv Syst Dis. 2024 Jul 29;16:11795735241259429. doi: 10.1177/11795735241259429. eCollection 2024.
Parkinson's disease (PD) is a common degenerative disease caused by abnormal accumulation of α-synuclein. The glymphatic pathway is essential for removing macromolecular proteins including α-synuclein from the brain, which flows into deep cervical lymph nodes (DCLNs) through meningeal lymphatics. As a terminal station for the cerebral lymphatic system drainage, DCLNs can be easily assessed clinically.
Although the drainage function of the cerebral lymphatic system is impaired in PD, the correlation between DCLNs and PD remains unknown.
Single-center retrospective cross-sectional study.
The size of the DCLNs were measured using ultrasound. The Movement Disorder Society Sponsored Revision Unified Parkinson's Disease Rating Scale and other scales were used to assess PD motor and non-motor symptoms.
Compared with the healthy control (HC) and the atypical Parkinson's disease (AP) groups, the size of the second and third DCLNs in the Parkinson's disease (PD) group was significantly smaller ( < .05). The width diameter of the third DCLN (DCLN3(y)) was significantly smaller in the PD group than in the AP group ( = .014). DCLN3(y) combined with a variety of clinical features improved the sensitivity of AP identification (sensitivity = .813).
DCLNs were able to distinguish HC, PD and AP and were mainly located in Robbins ΙΙA level. PD and AP were associated with different factors that influenced the size of the DCLNs. DCLN3(y) plays an important role in differentiating PD from AP, which, combined with other clinical features, has the ability to distinguish PD from AP; in particular, the sensitivity of AP diagnosis was improved.
帕金森病(PD)是一种由α-突触核蛋白异常积聚引起的常见退行性疾病。类淋巴系统对于从大脑中清除包括α-突触核蛋白在内的大分子蛋白质至关重要,这些蛋白质通过脑膜淋巴管流入颈深淋巴结(DCLNs)。作为脑淋巴系统引流的终点站,DCLNs在临床上易于评估。
尽管PD患者脑淋巴系统的引流功能受损,但DCLNs与PD之间的相关性仍不清楚。
单中心回顾性横断面研究。
采用超声测量DCLNs的大小。使用运动障碍协会赞助修订的统一帕金森病评定量表和其他量表评估PD的运动和非运动症状。
与健康对照(HC)组和非典型帕金森病(AP)组相比,帕金森病(PD)组第二和第三DCLNs的大小明显更小(P<0.05)。PD组第三DCLN(DCLN3(y))的宽度直径明显小于AP组(P = 0.014)。DCLN3(y)结合多种临床特征提高了AP识别的敏感性(敏感性 = 0.813)。
DCLNs能够区分HC、PD和AP,且主要位于Robbins ΙΙA水平。PD和AP与影响DCLNs大小的不同因素相关。DCLN3(y)在区分PD与AP方面起重要作用,其与其他临床特征相结合有能力区分PD与AP;特别是提高了AP诊断的敏感性。