关于自闭症遗传学的有影响力的文章是否显示出与自闭症群体接触的证据?

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Heidi Kristiina Kaljusto, Emma Wilson, Sue Fletcher-Watson
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引用次数: 0

摘要

对自闭症的病因学和遗传基础的调查继续推动着许多自闭症研究,然而,这些研究与自闭症患者的优先事项不一致的报告正在出现。让自闭症患者参与研究过程是将他们的观点纳入考虑的关键途径。我们调查了有影响力的遗传自闭症研究是否通过发表的文章文本中的指标显示了与自闭症社区接触的证据。通过对提到“自闭症”或“自闭”的文章摘要进行文本挖掘,我们发现与自闭症相关的渐进式术语的流行程度最低。我们还设计了一个新的评级系统来评估自闭症社区参与的三个标志:非污名化语言的存在,参考社区优先事项,以及参与性方法的使用。我们在主要的自闭症和遗传期刊上回顾了149篇文章。在所有三个标志中都发现了与自闭症社区接触的最小证据。专注于自闭症的遗传学研究人员应该抓住机会与自闭症群体接触,使他们的工作与他们的优先事项更紧密地结合起来,从而产生科学和道德上的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do Influential Articles on the Genetics of Autism Show Evidence of Engagement With the Autistic Community?

Investigations into the etiology and genetic basis of autism continue to drive much autism research, yet reports are emerging of this research not aligning with priorities of autistic people. Engagement of autistic people in the research process is a key way to take their perspectives on board. We investigated whether influential genetic autism research shows evidence of engagement with the autistic community via indicators in published article texts. Through text mining of the abstracts of articles mentioning the words "autism" or "autistic," we found minimal prevalence of progressive terminology associated with autism. We also devised a novel rating system to assess three hallmarks of autistic community engagement: presence of non-stigmatizing language, referencing community priorities, and the use of participatory methods. We reviewed 149 articles within leading autism and genetic journals. Minimal evidence of engagement with the autistic community was found within all three hallmarks. Genetics researchers focused on autism should embrace opportunities to engage with the autistic community to bring their work into closer alignment with their priorities, yielding scientific and moral benefits.

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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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