The Answer ALS return of results study: Answering the duty to disclose

被引:0
|
作者
Roggenbuck, Jennifer [1 ]
Kaschalk, Mackenzie [1 ]
Eustace, Rory [1 ]
Vicini, Leah [2 ]
Gokun, Yevgeniya [3 ]
Harms, Matthew B. [4 ]
Kolb, Stephen J. [1 ,5 ]
机构
[1] Ohio State Univ, Wexner Med Ctr, Dept Neurol, Columbus, OH USA
[2] Ohio State Univ, Genet Counseling Grad Program, Coll Med, Columbus, OH USA
[3] Ohio State Univ, Med Ctr, Dept Biostat, Columbus, OH USA
[4] Columbia Univ Vagelos Coll Phys & Surg, Dept Neurol, New York, NY USA
[5] Ohio State Univ, Dept Biol Chem & Pharmacol, Wexner Med Ctr, Columbus, OH USA
关键词
Genetics of ALS; return of results; patient engagement in genomic research; AMYOTROPHIC-LATERAL-SCLEROSIS; EXOME; PREFERENCES; DELIVERY; UPDATE;
D O I
10.1080/21678421.2024.2385004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The Return of Answer ALS Results (RoAR) Study was designed to provide a mechanism for participants in Answer ALS, a large, prospectively designed natural history and biorepository study to receive select clinical genetic testing results and study participants' experience with the results disclosure. Methods: Participants consented to receive results of five ALS genes (C9orf72, SOD1, FUS, TARDP, TBK1) and/or 59 medically actionable genes as designated by the American College of Medical Genetics. Patient-reported genetic testing outcomes were measured via a post-disclosure survey. Results: Of 645 eligible Answer ALS enrollees, 143 (22%) enrolled and completed participation in RoAR. Pathogenic variants were identified in 22/143 (15.4%) participants, including 13/143 (9.0%) in ALS genes and 9/143 (6.3%) in ACMG genes. Participant-reported measures of result utility indicated the research result disclosure was as or more successful than published patient-reported outcomes of result disclosure the clinical setting. Conclusions: This study serves as a model of a "disclosure study" to share results from genomic research with participants who were not initially offered the option to receive results, and our findings can inform the design of future, large scale genomic projects to empower research participants to access their genetic information.
引用
收藏
页码:743 / 750
页数:8
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