Irish Independent

Controvers­ial ‘three-parent’ babies get green light in UK

■ Doctors say IVF method will help prevent inherited diseases

- Jennifer Cockerell

FERTILITY doctors in the UK have been given permission to create the country’s first “three-parent” babies to help prevent women passing on inherited diseases to their children.

Two women being treated at the Newcastle Fertility Centre at Life will now receive mitochondr­ial replacemen­t therapy (MRT) after being deemed suitable by the UK’s Human Fertilisat­ion and Embryology Authority (HFEA).

The aim of the treatment is to prevent women passing on defective genes in the mitochondr­ia – tiny rod-like power plants in cells which supply energy.

But the technique, which involves giving a woman an IVF baby with DNA from three individual­s, is highly controvers­ial.

The baby will have nuclear DNA from its mother and father, which define characteri­stics such as personalit­y and eye colour. In addition, it will have a tiny amount of mitochondr­ial DNA provided by a female donor – the third “parent”.

An estimated one in 200 children is born with defective mitochondr­ial DNA (mtDNA).

Britain became the first country in the world to formally allow MRT when the HFEA gave a cautious green light to the procedure last year.

Approval of the Newcastle clinic’s facilities, equipment and staff was announced by the HFEA in March, but separate appraisals are still needed to assess the suitabilit­y of each candidate.

These have to take account of medical history and personal biology to ensure that the procedure is safe and likely to meet with success.

A HFEA spokeswoma­n said: “Our Statutory Approvals Committee has considered applicatio­ns from the Newcastle Fertility Centre at Life, part of Newcastle upon Tyne Hospitals NHS Foundation Trust, for the use of mitochondr­ial donation in treatment for two patients, both of which have been approved.”

Dr Jeremy Farrar, director of the Wellcome Trust, which funds medical research in the UK, welcomed the news.

“It is wonderful that after more than a decade of research, public consultati­on, scientific and legal review, the first women are now taking the next steps to being able to have this treatment and a healthy baby,” he said.

“Our best wishes go to families setting out on their exciting and momentous journey.”

The director of the Progress Educationa­l Trust, Sarah Norcross, said: “The granting of licences to treat two women in the UK is the latest mile- stone in seeking to help parents avoid passing on mitochondr­ial disease to their children.

“The pace at which these treatments are being rolled out may seem slow, but this highly regulated and measured approach will ensure the highest standards of treatment and follow-up research. Options which for many years have been tantalisin­gly out of reach to patients are now a step closer.”

In 2015, British politician­s paved the way for the change by voting to alter the Human Fertilisat­ion and Embryology Act which sets the legal framework for fertility research and treatment. Mitochondr­ial replacemen­t has been made an exception to the general rule which outlaws tampering with “germline” inherited DNA.

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