根据arrival指南报告Niemann-Pick C型疾病领域的临床前基因治疗研究。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Charlotte Laurfelt Munch Rasmussen, Annette Burkhart, Torben Moos, Louiza Bohn Thomsen
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引用次数: 0

摘要

几十年来,人们一直强调在报道动物研究时缺乏必要的信息,导致可重复性较低。ARRIVE(动物研究:体内实验报告)指南于2010年首次发布,旨在改进动物研究报告,使体内研究更加透明,从而提高科学质量。尽管得到了科学界的认可,但仍然需要不断改进动物研究报告,不幸的是,在尼曼-皮克C型病(NPC)领域也是如此。NPC是一种脂质储存紊乱,由Npc1或Npc2基因突变引起。尽管经过多年的研究,这种致命的疾病仍然无法治愈。2020年,发布了最新版本的ARRIVE指南(ARRIVE 2.0),描述了报告临床前研究时应包括的十个最基本要素。在这里,我们系统地回顾了在一系列研究基因治疗作为鼻咽癌治疗策略的临床前研究中,使用“arrival Essential 10”检查表对arrival指南的遵守情况。审阅的论文中没有一篇符合ARRIVE 2.0指南。缺乏关于样本量、随机化、盲法和统计方法的信息。希望新更新的ARRIVE指南能够帮助研究人员在未来计划和发表体内实验。编辑、审稿人和研究人员都需要更多地认识到包括这些基本项目的重要性,以便在科学界完全认可《到达》指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reporting preclinical gene therapy studies in the field of Niemann-Pick type C disease according to the ARRIVE guidelines.

The lack of essential information when reporting animal studies causing lower reproducibility has been stressed for decades. The ARRIVE (Animal Research: Reporting of In Vivo Experiments) guidelines were first published in 2010, to improve reporting of animal research, making in vivo studies more transparent thereby improving the scientific quality. Regardless of an endorsement from the scientific community, there is still a continuous need to improve animal research reporting, which unfortunately also is the case in the field of Niemann-Pick type C disease (NPC). NPC is a lipid storage disorder, caused by mutations in either the Npc1 or Npc2 gene. Despite years of research, no cure for this fatal disease exists. In 2020, an updated version of the ARRIVE guidelines (ARRIVE 2.0), was published, describing the ten most essential elements to be included when reporting pre-clinical studies. Here we systematically reviewed the compliance with the ARRIVE guidelines using the "ARRIVE Essential 10" checklist in a series of pre-clinical studies investigating gene therapy as a treatment strategy for NPC. None of the reviewed papers fulfilled the ARRIVE 2.0 guidelines. Information regarding sample size, randomization, blinding, and statistical methodology was lacking. Hopefully, the newly updated ARRIVE guidelines will aid researchers in planning and publishing in vivo experiments in the future. More awareness of the importance of including these essential items is needed, both from editors, reviewers and researchers, for complete endorsement of the ARRIVE guidelines in the scientific community.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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