Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disease that resembles rapid aging, with young children displaying hardened blood vessels, fragile bones and wrinkles among other symptoms. It usually results in death during the teenage years from heart attack or stroke.

Dr. William Stanford and his colleagues recently showed that cells from individuals with HGPS can be genetically reprogrammed, turning them into stem cells that don’t show any signs of aging.

They then directed the HGPS stem cells to produce new blood vessels cells, and were able to observe the start of the aging process in fast forward.

Their research could lead to a better understanding of the molecular basis of aging, as well as new treatments for HGPS, cardiovascular disease and other age–related diseases.

The research paper was published in the journal Aging Cell.