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Predicting the risk of pulmonary deterioration in sarcoidosis
  1. Elizabeth V Arkema1,
  2. Pernilla Lindin Darlington2,3,
  3. Yvette C Cozier4,5
  1. Correspondence to Dr Elizabeth V Arkema; Elizabeth.Arkema@ki.se

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In sarcoidosis, any organ may be affected, and the majority of cases have pulmonary involvement. The disease course in pulmonary sarcoidosis varies considerably, from complete resolution to chronic disease and/or pulmonary fibrosis. The heterogeneity of sarcoidosis is a major challenge in treatment decision-making, and the hope is that subgrouping patients into phenotypes may help to provide the right care for the right patient. In this issue of Thorax, Sharp et al 1 provide evidence that sarcoidosis phenotypes, based on pulmonary function tests (PFTs), predict lung function decline over time. They found that individuals with a restrictive pulmonary phenotype had a greater 3-year loss in pulmonary function compared with those without impairment. Furthermore, black individuals had a less favourable course compared with white individuals who improved in pulmonary function over time.

The study by Sharp et al included longitudinal data with several years of follow-up, which is an improvement over previous studies which were based on cross-sectional data. Prognosis prediction in sarcoidosis is challenging due to the wide variation across patients, and many studies have not been replicated. Previous studies have examined different blood-based biomarkers, but it is still unclear whether these are reliable and useful to predict progression to fibrosis. Some more recent …

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Footnotes

  • X @elizabetharkema, @@yyandtd

  • Contributors All authors wrote and edited the manuscript.

  • Funding EA is supported by grants from the Swedish Research Council (Vetenskapsrådet 2022-00826), Swedish Heart-Lung Foundation (Hjärt-lungfonden 20200452, 20240059) and the Sven and Ebba Hagberg Prize and Karolinska Institutet’s research funds. PLD is supported by grants from the Swedish Heart-Lung Foundation (Hjärt-lungfonden 20240059) and the Swedish Respiratory Society (Svensk Lungmedicinsk Förening). YC is supported by grant CA164974 from the National Institutes of Health (NIH) and National Cancer Institute (NCI).

  • Competing interests None declared.

  • Provenance and peer review Commissioned; externally peer reviewed.

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