The Daily Telegraph

Arthritis sufferers can blame it on Ice Age man

- By Sarah Knapton

FOR the 10 million Britons suffering from arthritis, it may be cold comfort, but they may not be alive today were it not for their aching limbs.

Researcher­s have discovered that a gene mutation that increases the risk of arthritis evolved during the most recent Ice Age to help protect our ancestors from frostbite.

Around half of all Europeans carry a variant of the GDF5 gene, which nearly doubles the chance of developing painful joints, and also reduces their height by approximat­ely 1cm.

Although it may seem like an evolutiona­ry disadvanta­ge to be shorter and less mobile, in fact it helped early humans to ward off the freezing temperatur­es of the north as they ventured out of Africa around 50,000 years ago. Being short and stocky helped our ancestors withstand the bitter cold and reduced the risk of life-threatenin­g bone fractures when slipping on ice.

And because arthritis usually appears after reproducti­ve age, it would not have proved detrimenta­l to starting a family, so the mutation was passed on. Dr David Kingsley, professor of developmen­tal biology at Stanford University, said: “This gene variant is present in billions of people, and it’s likely responsibl­e for millions of cases of arthritis around the globe.

“Many people think of osteoarthr­itis as a kind of wear-and-tear disease, but there’s clearly a genetic component at work here as well.

“It’s possible that climbing around in cold environmen­ts was enough of a risk factor to select for a protective variant even if it brought along an increased likelihood of an age-related disease like arthritis.”

Researcher­s first linked a mutated form of GDF5 to arthritis and height in the Nineties. They discovered it was being controlled by genetic machinery which tells the gene to turn off bone growth. In the new study they looked at people who submitted their DNA for the 1,000 Genomes project and noticed that the gene variant was more common in Europeans, but rare in Africans.

The research was published in the journal Nature Genetics.

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