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Scleroderma-related interstitial lung disease based on HRCT: predictors of lung function decline

The extent of lung involvement visualized by high-resolution computed tomography ( HRCT ) is a predictor of decline in forced vital capacity ( FVC ) in scleroderma-interstitial lung disease.
The objective of a study was to evaluate the performance of three different HRCT-defined staging systems in the Scleroderma Lung Study I ( SLS I ) over a 1-year period.

Researchers assessed two visual semiquantitative scores: the maximum fibrosis score ( MaxFib, the fibrosis score in the zone of maximal lung involvement ) and visual assessment of total lung involvement ( TLI ) as proposed by Goh and Wells.
In addition, researchers evaluated the computer-aided diagnosis and calculated the quantitative percentage with fibrosis ( QLF ) and total lung involvement.

The mean duration of the disease was 3.2 years, and the mean FVC was 67.7 %.

Regardless of the staging system used, a greater degree of fibrosis / total lung involvement on HRCT scans was associated with a greater decline in FVC in the placebo group.

Using the MaxFib and QLF, the mean absolute changes in FVC from baseline were 0.1 % and -1.4 %, respectively, in less than 25% lung involvement versus a change of -6.2% and -6.9%, respectively, with more than 25% involvement ( negative score denotes worsening in FVC ).

Conversely, Cyclophosphamide was able to stabilize decline in FVC in subjects with greater degree of involvement detected by HRCT.
Using the visual MaxFib and QLF, the mean absolute improvements in FVC were 1.2 and 1.1, respectively, with more than 25% involvement.

In conclusion, HRCT-defined lung involvement was a predictor of decline in FVC in SLS I. ( Xagena )

Khanna D et al, Arthritis Res Ther 2015;17:372. doi: 10.1186/s13075-015-0872-2.