Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes

被引:3
作者
Miller, Ilana M. [1 ]
Lewis, Katie L. [1 ]
Lawal, Tokunbor A. [1 ,3 ]
Ng, David [1 ]
Johnston, Jennifer J. [1 ]
Biesecker, Barbara B. [2 ,4 ]
Biesecker, Leslie G. [1 ]
机构
[1] NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA
[2] NHGRI, Social & Behav Res Branch, NIH, Bethesda, MD 20892 USA
[3] NINR, Tissue Injury Branch, NIH, Bethesda, MD 20892 USA
[4] Res Triangle Inst, Raleigh, NC USA
关键词
Health behaviors; Healthcare use; Genome sequencing; Psychological reactions; Variants of uncertain significance; UNKNOWN SIGNIFICANCE; RISK PERCEPTION; BRCA2; VARIANTS; CANCER; IMPACT; WOMEN; DECISIONS; WORRY;
D O I
10.1038/s41436-018-0083-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Studies on returning variants of uncertain significance (VUS) results have predominantly included patients with a personal or family history of cancer and cancer-associated gene VUS. This study examined health behaviors among participants with cardiomyopathy-associated gene VUS, but without a personal history of cardiomyopathy. Methods: Sixty-eight eligible participants without apparent cardiomyopathy but with VUS in cardiomyopathy-associated genes completed a survey of health behaviors, disclosure, distress, uncertainty, positive experiences, decisional conflict, and perceived value. The medical records of participants who reported cardiac testing because of their VUS were reviewed for testing indication(s). Results: Two participants had cardiac testing due to their VUS alone. Four had cardiac testing because of their VUS and other clinical indications. Twelve changed health behaviors, including one participant who was subsequently diagnosed with cardiomyopathy. Distress, uncertainty, and decisional conflict were low (means = 1.2, 4.2, and 24.5 (scale ranges = 0-30, 0-45, and 15-75), respectively), and positive experiences and perceived value were moderate (means = 12.4 and 14.4 (scale ranges = 0-20 and 4-20), respectively). Greater perceived value was associated with greater likelihood to engage in health behaviors (P = 0.04). Conclusion: Positive VUS results can be returned to apparently unaffected individuals with modest use of healthcare resources, minimal behavioral changes, and favorable psychological reactions.
引用
收藏
页码:748 / 752
页数:5
相关论文
共 20 条
  • [1] Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' views
    Bertier, Gabrielle
    Hetu, Martin
    Joly, Yann
    [J]. BMC MEDICAL GENOMICS, 2016, 9
  • [2] The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine
    Biesecker, Leslie G.
    Mullikin, James C.
    Facio, Flavia M.
    Turner, Clesson
    Cherukuri, Praveen F.
    Blakesley, Robert W.
    Bouffard, Gerard G.
    Chines, Peter S.
    Cruz, Pedro
    Hansen, Nancy F.
    Teer, Jamie K.
    Maskeri, Baishali
    Young, Alice C.
    Manolio, Teri A.
    Wilson, Alexander F.
    Finkel, Toren
    Hwang, Paul
    Arai, Andrew
    Remaley, Alan T.
    Sachdev, Vandana
    Shamburek, Robert
    Cannon, Richard O.
    Green, Eric D.
    [J]. GENOME RESEARCH, 2009, 19 (09) : 1665 - 1674
  • [3] When parents disclose BRCA1/2 test results: Their communication and perceptions of offspring response
    Bradbury, Angela R.
    Patrick-Miller, Linda
    Egleston, Brian L.
    Olopade, Olufunmilayo I.
    Daly, Mary B.
    Moore, Cynthia W.
    Sands, Colleen B.
    Schmidheiser, Helen
    Kondamudi, Preethi K.
    Feigon, Maia
    Ibe, Comfort N.
    Daugherty, Christopher K.
    [J]. CANCER, 2012, 118 (13) : 3417 - 3425
  • [4] A brief assessment of concerns associated with genetic testing for cancer: The Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire
    Cella, D
    Hughes, C
    Peterman, A
    Chang, CH
    Peshkin, BN
    Schwartz, MD
    Wenzel, L
    Lemke, A
    Marcus, AC
    Lerman, C
    [J]. HEALTH PSYCHOLOGY, 2002, 21 (06) : 564 - 572
  • [5] Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress
    Culver, J. O.
    Brinkerhoff, C. D.
    Clague, J.
    Yang, K.
    Singh, K. E.
    Sand, S. R.
    Weitzel, J. N.
    [J]. CLINICAL GENETICS, 2013, 84 (05) : 464 - 472
  • [6] Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study
    Facio, Flavia M.
    Eidem, Haley
    Fisher, Tyler
    Brooks, Stephanie
    Linn, Amy
    Kaphingst, Kimberly A.
    Biesecker, Leslie G.
    Biesecker, Barbara B.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2013, 21 (03) : 261 - 265
  • [7] Comparison of risk management strategies between women testing positive for a BRCA variant of unknown significance and women with known BRCA deleterious mutations
    Garcia, Christine
    Lyon, Liisa
    Littell, Ramey D.
    Powell, C. Bethan
    [J]. GENETICS IN MEDICINE, 2014, 16 (12) : 896 - 902
  • [8] A systematic review of perceived risks, psychological and behavioral impacts of genetic testing
    Heshka, Jodi T.
    Palleschi, Crystal
    Howley, Heather
    Wilson, Brenda
    Wells, Philip S.
    [J]. GENETICS IN MEDICINE, 2008, 10 (01) : 19 - 32
  • [9] Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
    Jarvik, Gail P.
    Amendola, Laura M.
    Berg, Jonathan S.
    Brothers, Kyle
    Clayton, Ellen W.
    Chung, Wendy
    Evans, Barbara J.
    Evans, James P.
    Fullerton, Stephanie M.
    Gallego, Carlos J.
    Garrison, Nanibaa' A.
    Gray, Stacy W.
    Holm, Ingrid A.
    Kullo, Iftikhar J.
    Lehmann, Lisa Soleymani
    McCarty, Cathy
    Prows, Cynthia A.
    Rehm, Heidi L.
    Sharp, Richard R.
    Salama, Joseph
    Sanderson, Saskia
    Van Driest, Sara L.
    Williams, Marc S.
    Wolf, Susan M.
    Wolf, Wendy A.
    Burke, Wylie
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 94 (06) : 818 - 826
  • [10] A general framework for estimating the relative pathogenicity of human genetic variants
    Kircher, Martin
    Witten, Daniela M.
    Jain, Preti
    O'Roak, Brian J.
    Cooper, Gregory M.
    Shendure, Jay
    [J]. NATURE GENETICS, 2014, 46 (03) : 310 - +