Frequency and clinical significance of anticentromere and anti Scl-70 antibodies in an English connective tissue disease population

1983 ◽  
Vol 3 (1) ◽  
pp. 19-21 ◽  
Author(s):  
L. J. Catoggio ◽  
R. P. Skinner ◽  
P. J. Maddison
Rheumatology ◽  
2019 ◽  
Vol 58 (Supplement_3) ◽  
Author(s):  
Kristina E N Clark ◽  
Corrado Campochiaro ◽  
Lauren V Host ◽  
Jennifer Harvey ◽  
Christopher P Denton ◽  
...  

2021 ◽  
Vol 11 (2) ◽  
pp. 78-79
Author(s):  
Nikolay Cherkasov ◽  
Yuliya Lutsenko

This research aims to study levels of laminin and elastine in 64 children with undifferentiated connective tissue disease (UCTD). All the children underwent clinical, laboratory and instrumental examination. It was found that changes in the levels of laminin and elastin are directly related to the severity of UCTD in children. Thus, clinical values of laminin and elastin levels can serve as additional criteria of UCTD severity. Using them, along with early detection of the phenotypic and visceral signs, helps prevent the development of severe forms of the disease.


2021 ◽  
Author(s):  
Xianhua Gui ◽  
Hui Ding ◽  
ShenYun Shi ◽  
Jingjing Ding ◽  
Mei Huang ◽  
...  

Abstract Background: Soluble mannose receptor, sCD206, is a marker of alternatively activated macrophages. Activated macrophages play important roles in connective tissue disease (CTD) and lung fibrosis. Interstitial lung disease (ILD) is a common complication of CTD, which leads to poor prognosis, especially in a pattern with usual interstitial pneumonia (UIP). Similarly, idiopathic pulmonary fibrosis (IPF) is also characterized by UIP. Compared with IPF, the prognosis of CTD-associated UIP is tightly correlated with early treatment. In the present study, we aimed to evaluate the clinical significance of sCD206 in discriminating CTD-associated UIP from IPF. Methods: The serum level of sCD206 was determined in 48 patients with CTD-associated UIP, 54 IPF patients and 27 healthy controls. The clinical significance of sCD206 was also evaluated. Result: Patients with CTD-associated UIP had a higher level of sCD206 compared with healthy controls and IPF patients (p<0.001, p<0.001, respectively). A cutoff value of sCD206 at 523.8 ng/mL could be a useful marker for distinguishing CTD-associated UIP from IPF. Moreover, 15 decedents with CTD-associated UIP exhibited a greater level of sCD206 compared with 33 survivors (p=0.030), and the elevated sCD206 level was associated with a higher mortality rate (log-rank test, p=0.003). Age and gender-adjusted multivariate Cox regression analysis showed that sCD206 (>444.2 ng/mL) was an independent predictor of survival (p= 0.026). Conclusions: Collectively, the serum level of sCD206 could be a useful marker for distinguishing CTD-associated UIP from IPF and associated with a poor survival of CTD-associated UIP.


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