2 results match your criteria: "6 Center for Pulmonary Functional Imaging.[Affiliation]"

Article Synopsis
  • Interstitial lung abnormalities (ILA) are detected via chest CT scans and may indicate early pulmonary fibrosis; the study investigates their patterns in relation to disease progression and mortality risk.
  • An analysis of 5,320 individuals revealed that 10% had ILA, with 73% of these showing progression over five years, influenced by factors like age and genetic makeup.
  • Certain imaging patterns, especially definitive fibrosis, significantly predicted both progression of ILA and increased risk of death, highlighting the importance of CT findings in patient prognosis.
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Rationale: Galectin-3 (Gal-3) has been implicated in the development of pulmonary fibrosis in experimental studies, and Gal-3 levels have been found to be elevated in small studies of human pulmonary fibrosis.

Objectives: We sought to study whether circulating Gal-3 concentrations are elevated early in the course of pulmonary fibrosis.

Methods: We examined 2,596 Framingham Heart Study participants (mean age, 57 yr; 54% women; 14% current smokers) who underwent Gal-3 assessment using plasma samples and pulmonary function testing between 1995 and 1998.

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