4.4 Article

Time to harmonize mitochondrial syndrome nomenclature and classification: A consensus from the North American Mitochondrial Disease Consortium (NAMDC)

期刊

MOLECULAR GENETICS AND METABOLISM
卷 136, 期 2, 页码 125-131

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymgme.2022.05.001

关键词

Mitochondrial disease; Mitochondrial disorders; Oxidative-phosphorylation; Mitochondrial DNA

资金

  1. North American Mitochondrial Disease Consortium (NAMDC)
  2. Rare Diseases Clinical Research Network (RDCRN) , an initiative of the Office of Rare Diseases Research (ORDR)
  3. National Center for Advancing Translational Sciences (NCATS)
  4. National Institute of Neurological Dis-orders and Stroke (NINDS) [NIH U54 NS078059]
  5. Eunice Kennedy Shriver National Institute of Child Health and Development (NICHD)
  6. Office of Dietary Supplements (ODS)
  7. NCATS
  8. United Mitochondrial Disease Foundation (UMDF)
  9. J. Willard and Alice S. Marriott Family Foundation

向作者/读者索取更多资源

The objective of this study is to harmonize terminology in mitochondrial medicine by proposing revised clinical criteria for primary mitochondrial syndromes. The North American Mitochondrial Disease Consortium (NAMDC) established a Diagnostic Criteria Committee comprised of experts from various fields to reach a consensus on mitochondrial disease definitions. The revised criteria are expected to standardize the diagnosis and categorization of mitochondrial diseases.
Objective: To harmonize terminology in mitochondrial medicine, we propose revised clinical criteria for primary mitochondrial syndromes. Methods: The North American Mitochondrial Disease Consortium (NAMDC) established a Diagnostic Criteria Committee comprised of members with diverse expertise. It included clinicians, researchers, diagnostic laboratory directors, statisticians, and data managers. The Committee conducted a comprehensive literature review, an evaluation of current clinical practices and diagnostic modalities, surveys, and teleconferences to reach consensus on syndrome definitions for mitochondrial diseases. The criteria were refined after manual application to patients enrolled in the NAMDC Registry. Results: By building upon published diagnostic criteria and integrating recent advances, NAMDC has generated updated consensus criteria for the clinical definition of classical mitochondrial syndromes. Conclusions: Mitochondrial diseases are clinically, biochemically, and genetically heterogeneous and therefore challenging to classify and diagnose. To harmonize terminology, we propose revised criteria for the clinical definition of mitochondrial disorders. These criteria are expected to standardize the diagnosis and categorization of mitochondrial diseases, which will facilitate future natural history studies and clinical trials.(C) 2022 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据