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PETBioNewsNewsDelay to avoiding mitochondrial disease in babies

BioNews

Delay to avoiding mitochondrial disease in babies

Published 31 October 2012 posted in News and appears in BioNews 605

Author

MacKenna Roberts

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.

Further research is needed into the safety and effectiveness of techniques to prevent children being born with mitochondrial disease, a Human Fertilisation and Embryology Authority (HFEA) report has concluded...

Further research is needed into the safety and effectiveness of techniques to prevent children being born with mitochondrial disease, a Human Fertilisation and Embryology Authority (HFEA) report has concluded.

The report was commissioned by UK Health Secretary Andrew Lansley to inform his decision about whether to hold a public consultation on the issue.

The HFEA-appointed panel that wrote the report requested that three experimental hurdles be cleared before permitting the techniques to be used to treat patients. The panel did not find evidence that the treatments were unsafe.

The Progress Educational Trust, Medical Research Council, Wellcome Trust and other bodies wrote an open letter to UK Health Secretary Andrew Lansley after the report's publication.

The letter urged the UK Government to publish a timetable for the drafting of regulations so that the techniques can be used in the clinic once the committee's hurdles have been vaulted.

Dr Robin Lovell-Badge, co-chair of the review panel, defended its conclusions. Dr Lovell-Badge anticipates that the further experimentation requirements will take little over a year to be met.

'Some people seem to be taking our report as negative and hesitant - it wasn't meant to be at all. It was meant to say, just gather a little bit more information', he said.

The report reviewed two techniques - maternal spindle transfer and pronuclear transfer. Both involve exchanging defective mitochondria with healthy mitochondria from a donor egg. The healthy donor egg's mitochondrial DNA would be passed to future generations in place of the mother's defective mitochondrial DNA.

The panel did not consider the ethical and legal implications of these techniques, only their safety and effectiveness.

It is illegal in the UK to alter nuclear DNA in a human embryo. But Parliament included regulation making powers in the Human Fertilisation and Embryology Act 2008 to allow techniques to avoid mitochondrial disease to be used in the clinic if they could be shown to be safe and effective.

Unlike nuclear DNA, mitochondrial DNA only encodes information for cell function, not distinguishing characteristics such as appearance or personality.

Mitochondrial diseases can include fatal liver, neurological and heart conditions. They to the birth of about 100 severely disabled children every year.

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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.
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10 April 2013 • 2 minutes read

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Mitochondria don't normally get much press attention, they like to keep a low profile generating energy in the cells and leave nuclear DNA to grab the headlines...

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.
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The advent of PGD extended the scope of IVF beyond the treatment of infertility. PGD is predominantly used to prevent transmission of genetic defects arising from mutations in nuclear DNA. However, it can also be used to reduce the risk of transmitting mutations in mitochondrial DNA (mtDNA), which cause a range of debilitating and life-threatening diseases...

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.
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17 October 2012 • 3 minutes read

HFEA asks scientists for advice on mitochondrial disease treatment

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Health Secretary, Andrew Lansley has asked the Human Fertilisation and Embryology Authority (HFEA) to convene an expert group 'to assess the effectiveness and safety' of a fertility treatment that would enable children to be born without potentially devastating, incurable mitochondrial diseases.

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.
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2 June 2011 • 3 minutes read

PGD could offer new hope for mitochondrial disease parents

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Women at risk of passing on mitochondrial disease to their children could use PGD to give birth to an unaffected child. The scientists at Maastricht University Medical Centre in the Netherlands claim their work has the potential to prevent the transmission of mitochondrial diseases...

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.
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Pronuclear transfer may give families affected by mitochondrial disease a choice

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Research at Newcastle University funded by the Muscular Dystrophy Campaign has shown that it might be possible to prevent mitochondrial diseases being passed from mother to child...

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.
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New IVF technique could prevent transmission of mitochondrial disorders

by Ruth Pidsley

A team of researchers at Newcastle University in the UK has been successful in attempts to transfer genetic material from one newly fertilised human egg to another without carrying over the egg's mitochondria (the energy-producing structures of a cell)...

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