Insight into the relationship between forced vital capacity and transfer of the lungs for carbon monoxide in patients with idiopathic pulmonary fibrosis.

Respir Med Res

Service Hospitalier Universitaire Pneumologie Physiologie, Pôle Thorax et Vaisseaux, Centre Hospitalier Universitaire Grenoble Alpes, Grenoble, France; Laboratoire HP2, INSERM U1300, Université Grenoble Alpes, Grenoble, France. Electronic address:

Published: November 2023

AI Article Synopsis

  • Forced vital capacity (FVC) and lung transfer of carbon monoxide (TLCO) are both important tests for measuring how bad a lung disease called idiopathic pulmonary fibrosis (IPF) is, but TLCO is better at showing the disease's severity.
  • * In a study of 430 IPF patients, many with "normal" FVC actually had "abnormal" TLCO, meaning FVC alone might not tell the whole story about lung health.
  • * The research found that most patients with a decline in TLCO also had a decline in FVC, but the opposite was not true, suggesting TLCO should be given more attention in monitoring IPF.

Article Abstract

Background: Forced vital capacity (FVC) is routinely used to quantify the severity and identify the progression of idiopathic pulmonary fibrosis (IPF). Although less commonly used, lung transfer of carbon monoxide (TLCO) correlates better with the severity of IPF than does FVC.

Methods: Aiming at studying how FVC behaves in relation to TLCO, we analysed cross-sectional data from 430 IPF patients, of which 221 had at least 2 assessments (performed 2.4 ± 1.9 years apart) available for longitudinal analyses. Thresholds for identifying "abnormal" FVC and TLCO values were the statistically-defined lower limits of normal (LLN). For patients with longitudinal data, mean annual absolute declines of FVC and TLCO were calculated.

Results: The correlation between FVC and TLCO (%predicted) was weak (R=0.21). FVC was "abnormal" (i.e.,
Conclusion: In IPF, a "normal" FVC should be viewed with caution as it is most often associated with an "abnormal" TLCO, a parameter that is strongly correlated with the morphological extent of the disease. Only 1/3 of the patients with a FVC-based progression criterion also had a TLCO progression criterion. In contrast, 2/3 of patients with a TLCO progression criterion also had a FVC progression criterion.

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Source
http://dx.doi.org/10.1016/j.resmer.2023.101042DOI Listing

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