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

医学 多学科方法 基因检测 清晰 神经影像学 梅德林 鉴定(生物学) 系统回顾 临床试验 德尔菲法 随机对照试验 重症监护医学 遗传咨询 外显子组 外显子组测序 心理学 科学证据 最佳实践 神经认知 诊断试验
作者
Wei Luo,Zhidong Cen,Huiberdina L. Koek,Miryam Carecchio,Isao Hozumi,Wan‐Jin Chen,Amit Batla,Alexander Balck,Francesca Magrinelli,Dehao Yang,Xuewen Cheng,Ana Westenberger,Akiyoshi Kakita,Liam Chen,Christian Lambert,Jing Yu Liu,Annika Keller,João Ricardo Mendes de Oliveira,Zhi‐Qi Xiong,Henry Houlden
出处
期刊:Movement Disorders [Wiley]
卷期号:41 (2): 315-336 被引量:7
标识
DOI:10.1002/mds.70140
摘要

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.
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