PET PET
  • My Account
  • Subscribe
Become a Friend Donate
  • About Us
    • People
    • Press Office
    • Our History
  • Get Involved
    • Become a Friend of PET
    • Volunteer
    • Campaigns
    • Writing Scheme
    • Partnership and Sponsorship
    • Advertise with Us
  • Donate
    • Become a Friend of PET
  • BioNews
    • News
    • Comment
    • Reviews
    • Elsewhere
    • Topics
    • Glossary
    • Newsletters
  • Events
    • Upcoming Events
    • Previous Events
  • Engagement
    • Policy and Projects
      • Resources
    • Education
  • Jobs & Opportunities
  • Contact Us
  • About Us
    • People
    • Press Office
    • Our History
  • Get Involved
    • Become a Friend of PET
    • Volunteer
    • Campaigns
    • Writing Scheme
    • Partnership and Sponsorship
    • Advertise with Us
  • Donate
    • Become a Friend of PET
  • BioNews
    • News
    • Comment
    • Reviews
    • Elsewhere
    • Topics
    • Glossary
    • Newsletters
  • Events
    • Upcoming Events
    • Previous Events
  • Engagement
    • Policy and Projects
      • Resources
    • Education
  • Jobs & Opportunities
  • Contact Us
  • My Account
  • Subscribe
  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements
PETBioNewsNewsReport warns against universal screening of babies' genomes

BioNews

Report warns against universal screening of babies' genomes

Published 17 August 2018 posted in News and appears in BioNews 963

Author

Shaoni Bhattacharya

Science Editor
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.

The universal screening of babies' genomes at birth is not 'inevitable', according to a new report from a US bioethics organisation...

The universal screening of babies' genomes at birth is not 'inevitable', according to a new report from a US bioethics organisation.

As the cost of genome sequencing falls, doctors and researchers are debating whether screening at birth would help plan personalised medical care and be a useful public health measure. But experts at the US non-profit organisation, the Hastings Centre in Garrison, New York, are urging that the use of this technology in newborns should be 'nuanced and attentive to context'.

While it is too early to screen every baby's genome, they added that there could be 'considerable benefit in using targeted sequencing to screen for or detect specific conditions'.

The report is unequivocal about universal screening. It recommends: 'Genome-wide sequencing should not be implemented as a universal, public health screening tool in newborns. Sequencing the entire genome may result in the return of genetic data of unknown or uncertain significance and may not yield actionable results.'

'Genomics is a powerful tool, but the results it returns are still not fully understood and have not been proven to advance health outside of very specific clinical situations,' said Josephine Johnston, director of research at the Hastings Centre, and co-editor of the report. 'The recommendations embrace the use of genomics to aid in the diagnosis of sick newborns, but they draw a sharp distinction between that kind of focused clinical use and population screening.'

The report also advised health professionals to warn parents against using direct-to-consumer (DTC) genome testing on their newborns. It said: 'The use of DTC genomic testing in children conflicts with clinical and professional guidelines, which limit testing to clinical contexts and for conditions that manifest during childhood.'

'Sequencing the genome of every newborn could cause parents to worry needlessly about their healthy baby,' added co-editor Professor Barbara Koenig at the University of California, San Francisco and a Hastings Centre Fellow.

The document is the result of a four-year interdisciplinary investigation funded by the US National Institutes of Health.

Related Articles

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
Comment
11 November 2019 • 5 minutes read

Let's grasp this opportunity to examine the potential future of screening

by Nick Meade and 1 others

Twenty thousand babies are to have their genomes sequenced at birth in an NHS-based pilot announced by Matt Hancock on Monday 4 November at the Genomics England Research Conference...

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
News
26 July 2019 • 2 minutes read

Call for genome sequencing pilot in newborn screening

by Rachel Siden

A new report has called for genome sequencing to be trialled alongside the nine tests that currently comprise newborn screening in the UK...

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
News
4 January 2019 • 2 minutes read

US newborn genomic sequencing trial publishes first findings

by Dr Barbara Kramarz

A whole-genome sequencing trial for newborns in the US has published its initial results, detecting a genetic childhood-onset condition in almost 10 percent of babies...

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
Comment
15 October 2018 • 5 minutes read

Whose genome is it anyway? Big Data and your DNA

by Annabel Slater

DNA is effectively data. If we are concerned about the data stored on our phones and computers, on social media sites and government servers, should we extend our concern to our DNA? ...

Image by Alan Handyside via the Wellcome Collection. Depicts a human egg soon after fertilisation, with the two parental pronuclei clearly visible.
CC0 1.0
Image by Alan Handyside via the Wellcome Collection. Depicts a human egg soon after fertilisation, with the two parental pronuclei clearly visible.
News
10 August 2018 • 3 minutes read

Genetic screening of embryos makes no difference to births

by Dr Charlott Repschläger

Pre-implantation genetic testing of embryos does not improve IVF birth rates in older women, found the largest study of its kind yet...

PET BioNews
News
15 June 2018 • 2 minutes read

Genetic test identifies very highest risk men for prostate cancer

by Dr Charlott Repschläger

Sixty-three novel gene variants linked to prostate cancer in men have been discovered...

Image by Alan Handyside via the Wellcome Collection. Depicts a human egg soon after fertilisation, with the two parental pronuclei clearly visible.
CC0 1.0
Image by Alan Handyside via the Wellcome Collection. Depicts a human egg soon after fertilisation, with the two parental pronuclei clearly visible.
Comment
8 May 2018 • 4 minutes read

The case for mandatory fertility counselling

by Anthony Ryb

Should everyone stepping through their doctor's door enquiring about fertility treatment receive a counselling session? Probably not, although in most situations it would certainly be useful for them. Should everyone who has decided to go ahead with ferti

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
News
1 March 2018 • 2 minutes read

Genome studies shed light on childhood cancers

by Dr Nicoletta Charolidi

Two separate genomic studies of childhood cancers reveal differences compared with adult cancers, potentially opening new therapeutic avenues...

Leave a Reply Cancel reply

You must be logged in to post a comment.

« Special rules for US gene therapy trials relaxed

Data-Label The UK's Leading Supplier Of Medical Labels & Asset Labels

RetiringDentist.co.uk The UK's Leading M&A Company.

Find out how you can advertise here
easyfundraising
amazon

This month in BioNews

  • Popular
  • Recent
13 June 2022 • 2 minutes read

Drop in diversity of blood stem cells leads to old-age health issues

8 August 2022 • 2 minutes read

Placenta and organ formation observed in mouse embryo models

8 August 2022 • 2 minutes read

Complex structures of the human heart bioengineered

8 August 2022 • 1 minute read

Brain tumour gene also linked to childhood cancers

8 August 2022 • 2 minutes read

Lower hormone doses may improve IVF egg quality

8 August 2022 • 2 minutes read

Boosting muscle cell production of gene therapy proteins

Subscribe to BioNews and other PET updates for free.

Subscribe
  • Twitter
  • Facebook
  • Instagram
  • LinkedIn
  • YouTube
  • RSS
Wellcome
Website redevelopment supported by Wellcome.

Website by Impact Media Impact Media

  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements

© 1992 - 2022 Progress Educational Trust. All rights reserved.

Limited company registered in England and Wales no 07405980 • Registered charity no 1139856

Subscribe to BioNews and other PET updates for free.

Subscribe
PET PET

PET is an independent charity that improves choices for people affected by infertility and genetic conditions.

  • Twitter
  • Facebook
  • Instagram
  • LinkedIn
  • YouTube
  • RSS
Wellcome
Website redevelopment supported by Wellcome.

Navigation

  • About Us
  • Get Involved
  • Donate
  • BioNews
  • Events
  • Engagement
  • Jobs & Opportunities
  • Contact Us

BioNews

  • News
  • Comment
  • Reviews
  • Elsewhere
  • Topics
  • Glossary
  • Newsletters

Other

  • My Account
  • Subscribe

Website by Impact Media Impact Media

  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements

© 1992 - 2022 Progress Educational Trust. All rights reserved.

Limited company registered in England and Wales no 07405980 • Registered charity no 1139856