采用有效的招聘和留用策略,让多样化的儿科人群参与基因组学研究。

IF 8.1 1区 生物学 Q1 GENETICS & HEREDITY
Michelle A Ramos, Katherine E Bonini, Laura Scarimbolo, Nicole R Kelly, Beverly Insel, Sabrina A Suckiel, Kaitlyn Brown, Miranda Di Biase, Katie M Gallagher, Jessenia Lopez, Karla López Aguiñiga, Priya N Marathe, Estefany Maria, Jacqueline A Odgis, Jessica E Rodriguez, Michelle A Rodriguez, Nairovylex Ruiz, Monisha Sebastin, Nicole M Yelton, Charlotte Cunningham-Rundles, Melvin Gertner, Irma Laguerre, Thomas V McDonald, Patricia E McGoldrick, Mimsie Robinson, Arye Rubinstein, Lisa H Shulman, Trinisha Williams, Steven M Wolf, Elissa G Yozawitz, Randi E Zinberg, Noura S Abul-Husn, Laurie J Bauman, George A Diaz, Bart S Ferket, John M Greally, Vaidehi Jobanputra, Bruce D Gelb, Eimear E Kenny, Melissa P Wasserstein, Carol R Horowitz
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引用次数: 0

摘要

临床基因组学研究中的代表性不足限制了研究结果的普遍性和科学发现的效益。我们描述了在一项儿科基因组测序研究中,以患者为中心、数据驱动的招募和保留策略所产生的影响。我们与利益相关者委员会合作,对其子女接受了基因组测试的成年人进行了形成性研究,并对研究方法和材料进行了试点和修订。我们的方法包括种族、民族和语言一致的研究人员、关系互动、研究访问的灵活性以及以数据为依据的质量改进。在 1656 名符合条件的儿童中,只有 6.5%的儿童拒绝接受研究。他们的父母/法定监护人中有 76.9% 为非白人,65.6% 的儿童享有公共医疗保险,49.9% 的儿童生活在联邦贫困线以下,52.8% 的儿童居住在医疗服务不足的地区。在入选者中,87.3%的人完成了所有研究程序。报名者和拒绝报名者之间、保留者和失去随访者之间没有社会人口学方面的差异。我们概述了利益相关者参与的方法,这些方法可能导致了不同家庭的成功注册和保留。这些方法可为未来旨在吸引和留住基因组医学研究中代表性不足的人群的研究计划提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research.

Underrepresentation in clinical genomics research limits the generalizability of findings and the benefits of scientific discoveries. We describe the impact of patient-centered, data-driven recruitment and retention strategies in a pediatric genome sequencing study. We collaborated with a stakeholder board, conducted formative research with adults whose children had undergone genomic testing, and piloted and revised study approaches and materials. Our approaches included racially, ethnically, and linguistically congruent study staff, relational interactions, study visit flexibility, and data-informed quality improvement. Of 1,656 eligible children, only 6.5% declined. Their parents/legal guardians were 76.9% non-White, 65.6% had public health insurance for the child, 49.9% lived below the federal poverty level, and 52.8% resided in a medically underserved area. Among those enrolled, 87.3% completed all study procedures. There were no sociodemographic differences between those who enrolled and declined or between those retained and lost to follow-up. We outline stakeholder-engaged approaches that may have led to the successful enrollment and retention of diverse families. These approaches may inform future research initiatives aiming to engage and retain underrepresented populations in genomics medicine research.

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来源期刊
CiteScore
14.70
自引率
4.10%
发文量
185
审稿时长
1 months
期刊介绍: The American Journal of Human Genetics (AJHG) is a monthly journal published by Cell Press, chosen by The American Society of Human Genetics (ASHG) as its premier publication starting from January 2008. AJHG represents Cell Press's first society-owned journal, and both ASHG and Cell Press anticipate significant synergies between AJHG content and that of other Cell Press titles.
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