Brunel University London: Study finds no evidence of genetic legacy in children of UK’s nuclear test veterans

Military men who had been present when British nuclear weapons were tested in the 1950s and 60s are no more likely to pass on to their descendants more changes to their DNA in comparison to other veterans, a study has found.

The findings, published today in the journal Scientific Reports, are from the first study looking into whether there is a genetic legacy associated with having been present at the test sites, including Christmas Island and the Australian outback.

Supported by the Nuclear Community Charity Fund (NCCF), the study addresses questions raised by the nuclear test veteran community, with further findings to follow later this year.

“Changes to the human genome – our genetic information – happen naturally as part of having children, when our DNA is handed down with slight imperfections here and there,” said Dr Rhona Anderson, the study lead from Brunel University London, and Director of the Centre for Health Effects of Radiological and Chemical Agents. “So our study set out to see whether or not the amount and type of genetic changes seen in the children of nuclear test veterans, when compared to their parents, is as would be expected in families more generally.”

To do this, the researchers analysed blood samples from 30 family trios: the father, the mother and their surviving biological child conceived soonest after the father returned from nuclear test sites. For comparison purposes, samples were analysed from a matched control group of 30 family trios of veterans of similar age and military service who hadn’t been at test sites. All were invited to the study through their GPs in a multi-step recruitment process.

Dr Alex Moorhouse and colleagues from the University of Leicester, led by Professor Yuri Dubrova, extracted DNA from each sample and sequenced and analysed the whole genome, producing a readout of each participant’s genetic information. All the samples were processed blind, so the researchers didn’t know whether they were analysing blood from a nuclear test veteran or control family trio. Comparing the readouts between the generations meant the researchers could identify different types of newly arising germline genetic changes, such as when building blocks of DNA swap places or are deleted, and then count them.

Once the samples were revealed as being part of the veteran group or control group, the study team, including researchers at the London School of Hygiene & Tropical Medicine, were able to make comparisons.

They compared their data with previous studies of how often newly arising germline genetic changes happen in humans more generally. The researchers also compared the nuclear test veteran family group with the control family group, focusing on genetic changes collectively known as single nucleotide variants, structural variants and clustered mutations, and a particular type where DNA building blocks are inserted or deleted, known as indels.

The researchers found that, for each comparison, the number and type of genetic changes were in line with what would be expected naturally, with no significant differences between the nuclear test veteran and control groups. “Our study shows no significant increases in the frequency of newly arising genetic changes in the offspring of nuclear test veteran fathers,” Dr Anderson said. “This result should reassure the study participants and the wider nuclear test veteran community.”

A paper published earlier this month by the researchers revealed that a higher proportion of the nuclear test veterans in the study said that at least one of their children or grandchildren had been born with a congenital anomaly – sometimes known as birth defects, such as of the heart or of the limbs – and that a higher proportion of control veterans reported chemical or radiation exposure through their jobs.

However, these differences are not explained by the genetic analysis carried out on the family members studied in these two groups. “Overall, our findings may reflect the low radiation doses thought to be received by the nuclear test veterans. Another consideration is the time gap between the date of last attendance at a test site and when the next child was conceived,” Professor Dubrova said.

When analysing the genetic changes seen in the nuclear test veteran and control groups, the researchers spotted that one particular pattern of changes to the DNA building blocks – known as SBS16, a mutation signature – differed between the groups, happening more often in the nuclear test veteran family trios.

“That this signature is present more for nuclear test veteran families is most likely explained by it being a feature of a small group of the study’s participants,” Dr Anderson said. “However, we cannot rule out with sufficient confidence that this could be a random occurrence unrelated to the background of these families.”

Additional papers from the Genetic and Cytogenetic Family Trio study will report the results of a cytogenetic analysis comparing the nuclear test veteran and control groups, and will be published later this year.

‘No evidence of increased mutations in the germline of a group of British nuclear test veterans’, by Alexander Moorhouse, Martin Scholze, Nicolas Sylvius, Clare Gillham, Christine Rake, Julian Peto, Rhona Anderson and Yuri Dubrova, is published in Scientific Reports.

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