
Common genetic variants contribute to idiopathic pulmonary fibrosis (IPF) risk, and polygenic risk scores (PRSs) were developed with and without the MUC5B region. The PRSs demonstrated associations with IPF, and the combined genetic predictors significantly improved risk prediction over clinical models. The PRS without MUC5B also showed associations with interstitial lung abnormalities (ILA) and ILA progression.
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