Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice

被引:16
|
作者
Shkedi-Rafid, Shiri [1 ]
Fenwick, Angela [1 ]
Dheensa, Sandi [1 ]
Lucassen, Anneke M. [1 ]
机构
[1] Univ Southampton, Fac Med, Acad Dept Clin Genet, CELS, Southampton SO16 5YA, Hants, England
基金
英国惠康基金;
关键词
SATISFACTION; ATTITUDES;
D O I
10.1038/ejhg.2014.221
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study set out to explore the attitudes of a representative sample of the British public towards genetic testing in children to predict disease in the future. We sought opinions about genetic testing for adult-onset conditions for which no prevention/treatment is available during childhood, and about genetic 'carrier' status to assess future reproductive risks. The study also examined participants' level of agreement with the reasons professional organisations give in favour of deferring such testing. Participants (n = 2998) completed a specially designed questionnaire, distributed by email. Nearly half of the sample (47%) agreed that parents should be able to test their child for adult-onset conditions, even if there is no treatment or prevention at time of testing. This runs contrary to professional guidance about genetic testing in children. Testing for carrier status was supported by a larger proportion (60%). A child's future ability to decide for her/himself if and when to be tested was the least supported argument in favour of deferring testing.
引用
收藏
页码:1281 / 1285
页数:5
相关论文
共 50 条
  • [31] Adult-onset hyperinsulinaemic hypoglycaemia in clinical practice: diagnosis, aetiology and management
    Challis, Benjamin G.
    Powlson, Andrew S.
    Casey, Ruth T.
    Pearson, Carla
    Lam, Brian Y.
    Ma, Marcella
    Pitfield, Deborah
    Yeo, Giles S. H.
    Godfrey, Edmund
    Cheow, Heok K.
    Chatterjee, V. Krishna
    Carroll, Nicholas R.
    Shaw, Ashley
    Buscombe, John R.
    Simpson, Helen L.
    ENDOCRINE CONNECTIONS, 2017, 6 (07): : 540 - 548
  • [32] HORMONE TESTING IN WOMEN WITH ADULT-ONSET AMENORRHEA
    LAUFER, MR
    FLOOR, AE
    PARSONS, KE
    KUNTZ, KM
    BARBIERI, RL
    GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1995, 40 (03) : 200 - 203
  • [33] Adult-onset hypomyelinating leukodystrophies: a clinical and genetic study of 15 individuals
    Salsano, E.
    Di Bella, D.
    Magri, S.
    Farina, L.
    Pareyson, D.
    Taroni, F.
    EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 : 74 - 74
  • [34] Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases
    Gaggiano, Carla
    Rigante, Donato
    Vitale, Antonio
    Lucherini, Orso Maria
    Fabbiani, Alessandra
    Capozio, Giovanna
    Marzo, Chiara
    Gelardi, Viviana
    Grosso, Salvatore
    Frediani, Bruno
    Renieri, Alessandra
    Cantarini, Luca
    MEDIATORS OF INFLAMMATION, 2019, 2019
  • [35] Adult-Onset Genetic Leukoencephalopathies With Movement Disorders
    Fu, Mu -Hui
    Chang, Yung -Yee
    JOURNAL OF MOVEMENT DISORDERS, 2023, 16 (02) : 115 - 132
  • [36] Genetic Analysis of Adult-Onset Autoimmune Diabetes
    Howson, Joanna M. M.
    Rosinger, Silke
    Smyth, Deborah J.
    Boehm, Bernhard O.
    Todd, John A.
    DIABETES, 2011, 60 (10) : 2645 - 2653
  • [37] PREVALENCE OF ADULT-ONSET IDDM IN THE US POPULATION
    HARRIS, MI
    ROBBINS, DC
    DIABETES CARE, 1994, 17 (11) : 1337 - 1340
  • [38] Genetic testing for susceptibility to adult-onset cancer - The process and content of informed consent
    Geller, G
    Botkin, JR
    Green, MJ
    Press, N
    Biesecker, B
    Wilfond, B
    Grana, G
    Daly, MB
    Schneider, K
    Kahn, MJE
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (18): : 1467 - 1474
  • [39] Clinical course of adult-onset cervical dystonia
    Jovic, J. S.
    Ivanovic, N.
    Svetel, M. V.
    Pekmezovic, T.
    Kostic, V. S.
    EUROPEAN JOURNAL OF NEUROLOGY, 2005, 12 : 93 - 93
  • [40] Adult-onset adrenoleukodystrophy: a clinical and neuropsychological study
    Luda, E
    Barisone, MG
    NEUROLOGICAL SCIENCES, 2001, 22 (01) : 21 - 25