Clinical Characteristics of Parkinsonism in HTLV-1-Associated Myelopathy.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Mika Dozono, Satoshi Nozuma, Shota Hirakata, Takashi Yoshida, Daisuke Kodama, Masakazu Tanaka, Eiji Matsuura, Ryuji Kubota, Hiroshi Takashima
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引用次数: 0

Abstract

Objective: Human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is the classic neurological manifestation of HTLV-1 infection; however, this virus has also been associated with other neurological disorders. Concurrent parkinsonism is relatively rare and presents diagnostic challenges. The present study aimed to identify the clinical characteristics of HAM/TSP with parkinsonism.

Methods: This retrospective study included HAM/TSP patients hospitalized in Kagoshima University Hospital from January 2000 to March 2022. Clinical and laboratory findings of the HAM/TSP patients with parkinsonism (P-HAM) were collected from the medical records and compared with HAM/TSP patients without parkinsonism (typical HAM/TSP [T-HAM]). P-HAM cases were defined as patients presenting with any combination of rigidity, resting tremor, bradykinesia, and/or postural instability, with these symptoms not attributed to HAM/TSP.

Results: Of 246 HAM/TSP patients, 11 (4.5%) presented with parkinsonism. Compared with T-HAM, the age of onset was significantly older (65.0 vs. 48.8 years, p = 0.001) in patients with P-HAM. Moreover, despite a shorter illness duration (8.5 vs. 12.5 years, p = 0.151), the Osame Motor Disability Score was significantly higher in P-HAM cases than in T-HAM cases (6.3 vs. 4.6, p = 0.0132), and all P-HAM cases had scores ≥ 4. Laboratory findings showed no differences between the groups.

Interpretation: In our cohort, 4.5% of HAM/TSP patients had concomitant parkinsonism, which was associated with a later age of onset and greater disease severity. The coexistence of parkinsonism in HAM/TSP may be underrecognized, and our findings expand the clinical spectrum of neurological disease with HTLV-1 infection.

htlv -1相关性脊髓病帕金森病的临床特征。
目的:人嗜t淋巴病毒1型(HTLV-1)相关脊髓病/热带痉挛性截瘫(HAM/TSP)是HTLV-1感染的典型神经学表现;然而,这种病毒也与其他神经系统疾病有关。并发性帕金森氏症是相对罕见的,并提出诊断挑战。本研究旨在探讨HAM/TSP与帕金森病的临床特征。方法:回顾性研究2000年1月至2022年3月鹿儿岛大学附属医院住院的HAM/TSP患者。从医疗记录中收集伴有帕金森病(P-HAM)的HAM/TSP患者的临床和实验室结果,并与无帕金森病的HAM/TSP患者(典型的HAM/TSP [T-HAM])进行比较。P-HAM病例定义为出现强直、静息性震颤、运动迟缓和/或姿势不稳定的任何组合,且这些症状不归因于HAM/TSP的患者。结果:246例HAM/TSP患者中,11例(4.5%)表现为帕金森病。与T-HAM相比,p - ham患者的发病年龄明显更大(65.0岁vs 48.8岁,p = 0.001)。此外,尽管p - ham患者病程较短(8.5年vs. 12.5年,p = 0.151),但p - ham患者的Osame运动障碍评分明显高于T-HAM患者(6.3年vs. 4.6年,p = 0.0132),且所有p - ham患者的得分均≥4分。实验室结果显示两组之间没有差异。解释:在我们的队列中,4.5%的HAM/TSP患者伴有帕金森病,这与发病年龄较晚和疾病严重程度较高有关。HAM/TSP中帕金森病的共存可能被低估,我们的研究结果扩大了HTLV-1感染神经系统疾病的临床范围。
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来源期刊
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology Medicine-Neurology (clinical)
CiteScore
9.10
自引率
1.90%
发文量
218
审稿时长
8 weeks
期刊介绍: Annals of Clinical and Translational Neurology is a peer-reviewed journal for rapid dissemination of high-quality research related to all areas of neurology. The journal publishes original research and scholarly reviews focused on the mechanisms and treatments of diseases of the nervous system; high-impact topics in neurologic education; and other topics of interest to the clinical neuroscience community.
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