Establishing a Collaborative Genomic Repository for Adult Burn Survivors: A Burn Model System Feasibility Study.

IF 1 Q4 CRITICAL CARE MEDICINE European burn journal Pub Date : 2024-11-06 DOI:10.3390/ebj5040034
Stephen Sibbett, Jamie Oh, Gretchen Carrougher, Lara Muffley, Nathaniel Ashford, Maiya Pacleb, Samuel Mandell, Jeffrey Schneider, Steven Wolf, Barclay Stewart, Nicole S Gibran
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Abstract

In this study, we aimed to integrate a genetic repository with an existing longitudinal national burn database. We set out two primary objectives, namely (1) to develop standard operating procedures for genetic sample collection and storage, DNA isolation, and data integration into an existing multicenter database; and (2) to demonstrate the feasibility of correlating genetic variation to functional outcomes in a pilot study, using the catechol-O-methyltransferase (COMT) gene. Dubbed the worrier/warrior gene, COMT variants have been associated with varying phenotypes of post-traumatic stress, wellbeing, and resilience. Between August 2018 and July 2020, COMT variants were identified for 111 participants from three sites and correlated with their outcome data. We found no association between COMT variants and functional outcomes, likely due to the inadequate sample size. We also asked all potential participants why they consented to or refused genetic analysis. A thematic analysis of responses revealed altruism and personal interest/enthusiasm in the study as top reasons for consenting. Privacy concerns were the most common reason for refusal. In conclusion, we successfully developed standard operating procedures for genetic sample collection and storage, DNA isolation, and data integration into an existing database, and we demonstrated the feasibility of conducting a multicenter collaborative study using a centralized lab location.

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建立成人烧伤幸存者的协作基因组库:一项烧伤模型系统可行性研究。
在这项研究中,我们的目标是整合遗传库与现有的纵向国家烧伤数据库。我们设定了两个主要目标,即(1)制定遗传样本收集和存储、DNA分离和数据集成到现有多中心数据库的标准操作程序;(2)利用儿茶酚o -甲基转移酶(COMT)基因,在一项初步研究中证明遗传变异与功能结果相关的可行性。被称为忧虑者/战士基因的COMT变异与创伤后压力、幸福感和复原力的不同表型有关。在2018年8月至2020年7月期间,来自三个地点的111名参与者发现了COMT变异,并与他们的结果数据相关联。我们发现COMT变异与功能预后之间没有关联,可能是由于样本量不足。我们还询问了所有潜在参与者同意或拒绝基因分析的原因。对调查结果的主题分析显示,利他主义和个人兴趣/热情是同意调查结果的主要原因。隐私问题是最常见的拒绝理由。总之,我们成功地开发了遗传样本收集和存储、DNA分离和数据集成到现有数据库的标准操作程序,并且我们证明了使用集中实验室位置进行多中心协作研究的可行性。
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