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Extract Interstitial lung disease (ILD) has a complex, multifactorial aetiology involving genetic susceptibility and environmental exposures [1]. While some ILDs have well-recognised environmental triggers, including hypersensitivity pneumonitis which is commonly associated with exposure to organic antigens or pneumoconiosis secondary to occupational exposures such as silica or asbestos [2], identification of environmental risk factors remains elusive for many other ILDs, including idiopathic pulmonary fibrosis (IPF).
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Zhao et al. (2026) studied this question.
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