Literature DB >> 34453583

An ethical analysis of divergent clinical approaches to the application of genetic testing for autism and schizophrenia.

E Morris1,2, M O'Donovan3, A Virani2,4, J Austin5,6.   

Abstract

Genetic testing to identify genetic syndromes and copy number variants (CNVs) via whole genome platforms such as chromosome microarray (CMA) or exome sequencing (ES) is routinely performed clinically, and is considered by a variety of organizations and societies to be a "first-tier" test for individuals with developmental delay (DD), intellectual disability (ID), or autism spectrum disorder (ASD). However, in the context of schizophrenia, though CNVs can have a large effect on risk, genetic testing is not typically a part of routine clinical care, and no clinical practice guidelines recommend testing. This raises the question of whether CNV testing should be similarly performed for individuals with schizophrenia. Here we consider this proposition in light of the history of genetic testing for ID/DD and ASD, and through the application of an ethical analysis designed to enable robust, accountable and justifiable decision-making. Using a systematic framework and application of relevant bioethical principles (beneficence, non-maleficence, autonomy, and justice), our examination highlights that while CNV testing for the indication of ID has considerable benefits, there is currently insufficient evidence to suggest that overall, the potential harms are outweighed by the potential benefits of CNV testing for the sole indications of schizophrenia or ASD. However, although the application of CNV tests for children with ASD or schizophrenia without ID/DD is, strictly speaking, off-label use, there may be clinical utility and benefits substantive enough to outweigh the harms. Research is needed to clarify the harms and benefits of testing in pediatric and adult contexts. Given that genetic counseling has demonstrated benefits for schizophrenia, and has the potential to mitigate many of the potential harms from genetic testing, any decisions to implement genetic testing for schizophrenia should involve high-quality evidence-based genetic counseling.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Year:  2021        PMID: 34453583     DOI: 10.1007/s00439-021-02349-1

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  77 in total

Review 1.  Genetic investigation for adults with intellectual disability: opportunities and challenges.

Authors:  Kate Baker; F Lucy Raymond; Nick Bass
Journal:  Curr Opin Neurol       Date:  2012-04       Impact factor: 5.710

2.  Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia.

Authors:  Kate Baker; Gregory Costain; Wai Lun Alan Fung; Anne S Bassett
Journal:  Lancet Psychiatry       Date:  2014-09-05       Impact factor: 27.083

3.  Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.

Authors:  Anne Andermann; Ingeborg Blancquaert; Sylvie Beauchamp; Véronique Déry
Journal:  Bull World Health Organ       Date:  2008-04       Impact factor: 9.408

Review 4.  Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue.

Authors:  Michael J Ackerman
Journal:  Heart Rhythm       Date:  2015-07-02       Impact factor: 6.343

5.  Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's disease.

Authors:  E W Almqvist; R R Brinkman; S Wiggins; M R Hayden
Journal:  Clin Genet       Date:  2003-10       Impact factor: 4.438

6.  High rate of disease-related copy number variations in childhood onset schizophrenia.

Authors:  K Ahn; N Gotay; T M Andersen; A A Anvari; P Gochman; Y Lee; S Sanders; S Guha; A Darvasi; J T Glessner; H Hakonarson; T Lencz; M W State; Y Y Shugart; J L Rapoport
Journal:  Mol Psychiatry       Date:  2013-05-21       Impact factor: 15.992

Review 7.  Schizophrenia and 22q11.2 deletion syndrome.

Authors:  Anne S Bassett; Eva W C Chow
Journal:  Curr Psychiatry Rep       Date:  2008-04       Impact factor: 5.285

8.  Detection of hemizygosity at the elastin locus by FISH analysis as a diagnostic test in both classical and atypical cases of Williams syndrome.

Authors:  I Borg; J D Delhanty; M Baraitser
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

9.  Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray.

Authors:  Erin L Baldwin; Ji-Yun Lee; Douglas M Blake; Brian P Bunke; Chad R Alexander; Amy L Kogan; David H Ledbetter; Christa L Martin
Journal:  Genet Med       Date:  2008-06       Impact factor: 8.822

10.  Risk communication in genetic counseling: Exploring uptake and perception of recurrence numbers, and their impact on patient outcomes.

Authors:  K Borle; E Morris; A Inglis; J Austin
Journal:  Clin Genet       Date:  2018-06-12       Impact factor: 4.296

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.