Serum Levels of Surfactant Proteins A and D Are Useful Biomarkers for Interstitial Lung Disease in Patients with Progressive Systemic Sclerosis

2000 ◽  
Vol 162 (1) ◽  
pp. 258-263 ◽  
Author(s):  
HIROKI TAKAHASHI ◽  
YOSHIO KUROKI ◽  
HIROSHI TANAKA ◽  
TSUKASA SAITO ◽  
KEIZO KUROKAWA ◽  
...  
Thorax ◽  
2015 ◽  
Vol 70 (Suppl 3) ◽  
pp. A92.2-A92
Author(s):  
M Kokosi ◽  
P Saunders ◽  
K Karagiannis ◽  
F Chua ◽  
TM Maher ◽  
...  

Radiology ◽  
1990 ◽  
Vol 176 (3) ◽  
pp. 755-759 ◽  
Author(s):  
H Schurawitzki ◽  
R Stiglbauer ◽  
W Graninger ◽  
C Herold ◽  
D Pölzleitner ◽  
...  

2021 ◽  
Vol 10 (4) ◽  
pp. 660
Author(s):  
Ai Kuzumi ◽  
Ayumi Yoshizaki ◽  
Satoshi Ebata ◽  
Takemichi Fukasawa ◽  
Asako Yoshizaki-Ogawa ◽  
...  

Systemic sclerosis (SSc) is a multisystem fibrotic disorder with autoimmune background. Accumulating evidence has highlighted the importance of T helper (Th) 2 cells in the pathogenesis of SSc and its complications. Because thymus and activation-regulated chemokine (TARC) is a potent chemoattractant for Th2 cells, we measured serum TARC levels in SSc patients and analyzed their correlation with interstitial lung disease (ILD), a major complication of SSc. Serum TARC levels were significantly elevated in patients with SSc, especially in those with the diffuse subtype, compared with healthy controls. In particular, dcSSc patients with SSc-associated ILD (SSc-ILD) showed higher TARC levels than those without SSc-ILD. However, there was no significant correlation between serum TARC levels and pulmonary function in SSc patients. Serum TARC levels did not correlate with serum levels of interleukin-13, an important Th2 cytokine, either. Furthermore, in the longitudinal study, serum TARC levels did not predict the onset or progression of SSc-ILD in patients with SSc. These results were in contrast with those of KL-6 and surfactant protein D, which correlated well with the onset, severity, and progression of SSc-ILD. Overall, these results suggest that serum TARC levels are not suitable for monitoring the disease activity of SSc-ILD.


2021 ◽  
pp. jrheum.201625
Author(s):  
Gonçalo Boleto ◽  
Jérôme Avouac ◽  
Yannick Allanore

Despite recent advances in the management of systemic sclerosis–associated interstitial lung disease (SSc-ILD), it remains the most common cause of death and a significant contributor to morbidity.1,2 SSc-ILD is characterized by a wide spectrum of disease courses, with some patients having limited nonprogressive fibrosis, whereas others develop rapid and extensive fibrosis leading to respiratory failure.3


CHEST Journal ◽  
1985 ◽  
Vol 88 (4) ◽  
pp. 263S-265 ◽  
Author(s):  
J. Ohar ◽  
C. Polatty ◽  
A. Robichaud ◽  
A. Fowler ◽  
G. Vetrovec ◽  
...  

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