Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and Management

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Movement Disorders Pub Date : 2026-03-02 Epub Date: 2025-12-04 DOI:10.1002/mds.70140
Wei Luo MD, PhD, Zhidong Cen MD, PhD, Huiberdina Koek MD, Miryam Carecchio MD, PhD, Isao Hozumi MD, PhD, Wan-Jin Chen MD, PhD, Amit Batla MD, FRCP, Alexander Balck MD, Francesca Magrinelli MD, PhD, Dehao Yang MD, PhD, Xuewen Cheng PhD, Ana Westenberger PhD, Akiyoshi Kakita MD, PhD, Liam Chen MD, PhD, Christian Lambert PhD, Jing-Yu Liu PhD, Annika Keller PhD, João Ricardo Mendes de Oliveira MD, Zhi-Qi Xiong PhD, Henry Houlden MD, PhD, Kailash P. Bhatia MD, FRCP, Christine Klein MD, Gaël Nicolas MD, PhD
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引用次数: 0

Abstract

Our understanding of primary brain calcification (PBC) has accelerated with the identification of seven causative genes over the past 13 years, vastly expanding knowledge of the molecular underpinnings of this disorder. Despite this progress, a lack of standardized clinical definitions, variable presentations, and heterogeneous calcification patterns has perpetuated inconsistencies in diagnosis and patient care. To address these challenges, an international expert panel undertook a comprehensive process—combining systematic literature review, virtual and in-person expert discussions, and iterative Delphi consensus questionnaires—to develop unified recommendations. These consensus guidelines encompass terminology, diagnostic criteria, neuroimaging protocols, clinical evaluation standards, genetic testing approaches, and management strategies. Notably, PBC is recommended as the clinical standard, with new diagnostic criteria, including the use of a computed tomography–based total calcification score and a three-tiered diagnostic algorithm (possible, probable, definite PBC). A systematic review of 27 symptoms and signs identified 19 as most closely linked with PBC, guiding more focused clinical assessment. Recommendations strongly support comprehensive next-generation sequencing for genetic testing, favoring whole genome over exome or targeted panels to maximize diagnostic yield. Multidisciplinary management priorities are outlined in four key principles centering on individualized care, symptom relief, genetic counseling, and ongoing monitoring. Widespread adoption of these unified guidelines will facilitate consistent diagnosis, enable comparative international data collection, and lay the groundwork for large-scale collaborative research—including future randomized controlled trials of symptomatic and disease-modifying PBC therapies. This consensus fosters clarity and consistency, creating a framework for improved patient care and scientific discovery. © 2025 International Parkinson and Movement Disorder Society.

原发性脑钙化:关于命名、诊断、评估和管理的国际共识
在过去的13年里,我们对原发性脑钙化(PBC)的理解随着7种致病基因的鉴定而加速,极大地扩展了对这种疾病分子基础的认识。尽管取得了这些进展,但缺乏标准化的临床定义、可变的表现和异质的钙化模式,导致了诊断和患者护理的不一致。为了应对这些挑战,一个国际专家小组进行了一个全面的过程,结合了系统的文献综述,虚拟和面对面的专家讨论,以及迭代的德尔菲共识问卷,以制定统一的建议。这些共识指南包括术语、诊断标准、神经影像学协议、临床评估标准、基因检测方法和管理策略。值得注意的是,PBC被推荐为临床标准,具有新的诊断标准,包括使用基于计算机断层扫描的总钙化评分和三层诊断算法(可能的、可能的、确定的PBC)。对27种症状和体征进行系统回顾,确定了19种与PBC最密切相关的症状和体征,指导更有针对性的临床评估。建议强烈支持全面的下一代基因检测测序,支持全基因组测序,而不是外显子组或靶向组,以最大限度地提高诊断产量。多学科管理的重点概述了四个关键原则,即个体化护理、症状缓解、遗传咨询和持续监测。这些统一指南的广泛采用将促进一致的诊断,使比较国际数据收集成为可能,并为大规模合作研究奠定基础,包括未来对症状性和疾病改变性PBC治疗的随机对照试验。这种共识促进了清晰度和一致性,为改善患者护理和科学发现创造了框架。©2025国际帕金森和运动障碍学会。
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
Movement Disorders
Movement Disorders 医学-临床神经学
CiteScore
13.30
自引率
8.10%
发文量
371
审稿时长
12 months
期刊介绍: Movement Disorders publishes a variety of content types including Reviews, Viewpoints, Full Length Articles, Historical Reports, Brief Reports, and Letters. The journal considers original manuscripts on topics related to the diagnosis, therapeutics, pharmacology, biochemistry, physiology, etiology, genetics, and epidemiology of movement disorders. Appropriate topics include Parkinsonism, Chorea, Tremors, Dystonia, Myoclonus, Tics, Tardive Dyskinesia, Spasticity, and Ataxia.
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