Background: The prevalence of idiopathic pulmonary fibrosis (IPF) is higher in men, a previously not well-understood sex bias that extends across severity and mortality. Mosaic loss of chromosome Y (mLOY) in blood is male-specific and associated with adverse outcomes, including IPF. In mLOY-mice, enhanced TGF-β signaling has been reported to contribute to fibrosis of internal organs, but it is not known if such mLOY-driven disease mechanism exists in humans.
Methods: We focused here on IPF in men to investigate if mLOY contributes to fibrotic disease processes in humans, as demonstrated in mouse models. To this end, we investigated mLOY as a risk factor for male IPF in epidemiological and clinical datasets, as well as by re-analyses of published single-cell RNA sequencing (scRNAseq) datasets.
Results: We find that men with mLOY in blood display an increased risk for IPF diagnosis and death caused by IPF in UK Biobank, and that mLOY is associated with reduced lung functions in two cohorts. Approximately 80% of the male excess in IPF prevalence occurs in the group of men with mLOY in blood leukocytes. Notably, scRNAseq analyses support that pulmonary leukocytes with Y loss exacerbate IPF by upregulating profibrotic genes and enhancing TGF-β signaling.
Conclusions: Our results contribute to explaining the profound sex bias in IPF and replicate a mLOY-driven profibrotic disease mechanism first identified in mice. Male IPF patients with mLOY represent a subgroup that may benefit from treatment with TGF-β inhibitors.
Idiopathic pulmonary fibrosis (IPF) is a lung disease that affects more men than women, but the reason for this sex difference has been unclear. Here we show that a male-specific genetic change, called mosaic loss of chromosome Y (mLOY), increases the risk of IPF in men. We analyzed large health databases and genetic data, finding that men with mLOY in their blood had a higher risk of developing IPF, worse lung function, and were more likely to die from the disease. Studies in mice have shown that when some white blood cells lose the Y chromosome, it can lead to increased scarring (fibrosis) in the lungs and other internal organs. In this study, we show that the same process can also happen in men. These findings help explain why IPF is more common in men and suggest that men with mLOY could benefit from targeted treatments.
© 2025. The Author(s).