ArticleTomography (Ann Arbor, Mich.)2017
Correcting Nonpathological Variation in Longitudinal Parametric Response Maps of CT Scans in COPD Subjects: SPIROMICS.
Article in Tomography (Ann Arbor, Mich.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01969344 (Subpopulations and Intermediate Outcome Measures in COPD Study), which is not on this map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Subpopulations and Intermediate Outcome Measures in COPD Study
Who cites it
1 citing paper in PubMed.
- Imaging in animal models: bridging experimental findings and human pathophysiology.Critical care (London, England) · 2025Review
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Authors and funding
8 authors.
Funding
Abstract
Small airways disease (SAD) is one of the leading causes of airflow limitations in patients diagnosed with chronic obstructive pulmonary disease (COPD). Parametric response mapping (PRM) of computed tomography (CT) scans allows for the quantification of this previously invisible COPD component. Although PRM is being investigated as a diagnostic tool for COPD, variability in the longitudinal measurements of SAD by PRM has been reported. Here, we show a method for correcting longitudinal PRM data because of non-pathological variations in serial CT scans. In this study, serial whole-lung high-resolution CT scans over a 30-day interval were obtained from 90 subjects with and without COPD accrued as part of SPIROMICS. It was assumed in all subjects that the COPD did not progress between examinations. CT scans were acquired at inspiration and expiration, spatially aligned to a single geometric frame, and analyzed using PRM. By modeling variability in longitudinal CT scans, our method could identify, at the voxel-level, shifts in PRM classification over the 30-day interval. In the absence of any correction, PRM generated serial percent volumes of functional SAD with differences as high as 15%. Applying the correction strategy significantly mitigated this effect with differences ~1%. At the voxel-level, significant differences were found between baseline PRM classifications and the follow-up map computed with and without correction (
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