Large international study validates genetic risk score for diagnosing and predicting pulmonary fibrosis outcomes
By
Susan Murphy
Summary
Researchers have validated a polygenic risk score tool that can help diagnose idiopathic pulmonary fibrosis (IPF) and predict which patients face the highest risk of severe outcomes like death or needing a lung transplant. The international study, co-led by Mayo Clinic and Brigham and Women's Hospital, analyzed data from over 570,000 people and is one of the largest real-world evaluations of a genetic risk score for IPF. The findings were published in the American Journal of Respiratory and Critical Care Medicine.
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Key quotes
· 3 pulledResearchers have validated a genetic scoring tool that may help physicians diagnose idiopathic pulmonary fibrosis and identify which patients are at greatest risk for severe outcomes, including death or the need for a lung transplant.
The findings come from a new international study of more than 570,000 people co-led by Mayo Clinic and Brigham and Women's Hospital.
Published in the American Journal of Respiratory and Critical Care Medicine, the study is one of the largest real-world evaluations of a polygenic risk score for idiopathic pulmonary fibrosis.
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