Camptocormia in Parkinson's disease: state of the art and future directions.

IF 4.6 2区 医学 Q1 CLINICAL NEUROLOGY
Valeria Sajin, Mark Goodall, Antonella Macerollo
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Abstract

Camptocormia is a frequent axial postural deformity in Parkinson's disease (PD) that is prevalent in up to 18% in the PD population. Camptocormic PD patients have a lower quality of life and higher risks of falls, back pain and spondylarthrosis. Camptocormia is probably induced by brain changes caused by PD. Despite the myopathic changes in camptocormic PD patients' spine muscles and camptocormia's clinical similarity with dystonic postures, its pathophysiology seems to be different from myopathy and dystonia. The exact pathogenesis is however unclear. There is no consensus for treatment of PD-related camptocormia, although some nonpharmacological (e.g., backpack weight, back extensors and physiotherapy), pharmacological (e.g., levodopa, istradefylline and botulinum toxin) and surgical approaches (surgical corrections and deep brain stimulation) were elaborated upon with variable effects. There are still many gaps in data regarding clinical predictors, pathophysiology, the treatment and prevention of camptocormia. Multicenter studies (particularly on nonpharmacological therapy, on preventing strategies, and on favorizing factors) are needed. We identified an unexpectedly limited number of publications on camptocormia in PD. As of August 2025, the search strategy with MeSH terms related to camptocormia, on PubMed returned only 220 results. After screening, only 138 of the titles and abstracts were relevant to the topics. Of all these publications, only 27 (19.6%) were reviews, and more than half of which (15 reviews) focused on some characteristics of camptocormia (e.g., surgical treatment, deep brain stimulation, and prevalence or etiology) but did not elucidate on all its complex aspects. The present narrative review aims to describe different aspects of camptocormia ranging from its prevalence to the pathophysiology and treatment possibilities and provide a comprehensive image of this disorder.

帕金森病中的喜树病:现状和未来方向。
喜树畸形是帕金森病(PD)中一种常见的轴位畸形,在PD人群中患病率高达18%。喜喜剧性PD患者的生活质量较低,跌倒、背痛和脊椎关节病的风险较高。喜树病可能是由PD引起的大脑变化引起的。尽管喜树病PD患者脊柱肌肉的肌病性改变和喜树病与肌张力障碍姿势的临床相似性,但其病理生理似乎不同于肌病和肌张力障碍。然而,确切的发病机制尚不清楚。对于pd相关喜树病的治疗尚无共识,尽管一些非药物(如背包负重、背部伸肌和物理治疗)、药物(如左旋多巴、伊斯特福林和肉毒杆菌毒素)和手术方法(手术矫正和深部脑刺激)都有不同的效果。关于喜树病的临床预测、病理生理、治疗和预防等方面的数据仍有许多空白。需要多中心研究(特别是非药物治疗、预防策略和有利因素)。我们意外地发现,PD中关于喜树虫病的出版物数量有限。截至2025年8月,在PubMed上搜索与喜树虫相关的MeSH术语,只返回220个结果。经过筛选,只有138个标题和摘要与主题相关。在所有这些出版物中,只有27篇(19.6%)是综述,其中一半以上(15篇)的重点是喜树病的一些特征(例如,手术治疗、深部脑刺激和患病率或病因),但没有阐明其所有复杂的方面。本综述旨在描述喜树病的不同方面,从患病率到病理生理和治疗可能性,并提供这种疾病的综合形象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neurology
Journal of Neurology 医学-临床神经学
CiteScore
10.00
自引率
5.00%
发文量
558
审稿时长
1 months
期刊介绍: The Journal of Neurology is an international peer-reviewed journal which provides a source for publishing original communications and reviews on clinical neurology covering the whole field. In addition, Letters to the Editors serve as a forum for clinical cases and the exchange of ideas which highlight important new findings. A section on Neurological progress serves to summarise the major findings in certain fields of neurology. Commentaries on new developments in clinical neuroscience, which may be commissioned or submitted, are published as editorials. Every neurologist interested in the current diagnosis and treatment of neurological disorders needs access to the information contained in this valuable journal.
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