M. Ito et al., Clinico-laboratory characteristics of patients with dermatomyositis accompanied by rapidly progressive interstitial lung disease, CLIN RHEUMA, 18(6), 1999, pp. 462-467
The clinico-laboratory features of 16 patients with dermatomyositis (DM) we
re compared between patients with accompanying rapidly progressive intersti
tial lung disease (RP-TLD, n = 7) and those with chronic interstitial lung
disease (C-ILD, n = 9), and also between deceased (seven RP-ILD and three C
-ILD) and living patients (six C-ILD). The extent of muscle weakness of the
extremities and frequency of autoantibody positivity were significantly lo
wer in DM patients with RP-ILD than in DM patients with C-ILD. Furthermore,
significantly lower serum ceatine kinase/lactate dehydrogenase levels (0.2
6+/-0.27) were found in the 10 patients who died than in the six living pat
ients (1.21+/-1.09). A higher CD4+/CD8+ T-lymphocyte ratio in the periphera
l blood (3.51+/-2.65) was detected in the four DM patients with RP-ILD who
died than in the six living DM patients with C-ILD (1.22+/-0.49).