Clinical characteristics and cytokine profiles of central‐compartment‐type chronic rhinosinusitis

Author(s):  
Yi‐Tsen Lin ◽  
Chih‐Feng Lin ◽  
Chun‐Kang Liao ◽  
Bor‐Luen Chiang ◽  
Te‐Huei Yeh
ORL ◽  
2013 ◽  
Vol 75 (1) ◽  
pp. 37-45 ◽  
Author(s):  
Yuhui Ouyang ◽  
Erzhong Fan ◽  
Ying Li ◽  
Xiangdong Wang ◽  
Luo Zhang

2019 ◽  
Vol 7 (2) ◽  
pp. 30 ◽  
Author(s):  
Sonya Marcus ◽  
John M. DelGaudio ◽  
Lauren T. Roland ◽  
Sarah K. Wise

A few chronic rhinosinusitis (CRS) variants have demonstrated a strong association with environmental allergy, including allergic fungal rhinosinusitis (AFRS) and central compartment atopic disease (CCAD). However, the overall relationship between CRS and allergy remains poorly defined. The goal of this review is to evaluate the relationship between CRS and allergy with a focus on specific CRS variants.


2006 ◽  
Vol 33 (4) ◽  
pp. 403-408 ◽  
Author(s):  
Hyo Yeol Kim ◽  
Hun-Jong Dhong ◽  
Seung Kyu Chung ◽  
Young-Jun Chung ◽  
Myung-Gu Kim

2016 ◽  
Vol 43 (4) ◽  
pp. 738-744 ◽  
Author(s):  
Hidenaga Kawasumi ◽  
Takahisa Gono ◽  
Eiichi Tanaka ◽  
Hirotaka Kaneko ◽  
Yasushi Kawaguchi ◽  
...  

Objective.It has been reported that organizing pneumonia (OP) develops when patients with rheumatoid arthritis (RA) are treated with biologic disease-modifying antirheumatic drugs (bDMARD). However, the clinical characteristics and pathophysiology of OP in RA remain unknown in patients treated with bDMARD. We investigated the clinical characteristics and cytokine profiles of patients with RA-OP treated with bDMARD or conventional synthetic DMARD (csDMARD).Methods.Twenty-four patients with RA who had developed OP were enrolled. These patients included 12 treated with bDMARD (bDMARD-OP subset) and 12 treated with csDMARD (csDMARD-OP subset). We compared the clinical characteristics and cytokine profiles between the patients with OP (OP subset, n = 24) and non-OP patients (non-OP subset, n = 29).Results.There was no significant difference in clinical characteristics between the OP subset and the non-OP subset. Four patients developed OP within 2 months of bDMARD administration. In the other 8 patients, OP developed more than 1 year after the initiation of bDMARD. OP improved with corticosteroid treatment in all bDMARD-OP patients. After OP improved, bDMARD were readministered in 6 patients, and no OP recurrence was observed in any of these patients. Our multivariate analysis revealed that serum levels of interferon-α (IFN-α), interleukin (IL)-1β, IL-6, IL-8, and interferon-γ–inducible protein 10 were significantly associated with the development of OP, although these cytokines tended to be lower in the bDMARD-OP subset than in the csDMARD-OP subset.Conclusion.OP is unlikely to be fatal in patients treated with bDMARD or csDMARD. IFN-α and proinflammatory cytokines are associated with the pathophysiology of OP in RA.


2012 ◽  
Vol 61 (1) ◽  
pp. 115-122 ◽  
Author(s):  
Takayuki Sejima ◽  
Gabriele Holtappels ◽  
Hisashi Kikuchi ◽  
Shoichiro Imayoshi ◽  
Keiichi Ichimura ◽  
...  

Author(s):  
Myoung Su Choi ◽  
No Sun Park ◽  
Seung-Gu Park ◽  
Ho Yun Lee ◽  
Dong Sik Chang ◽  
...  

Author(s):  
Tsung-Hua Wu ◽  
Nancy M Wang ◽  
Fang-Ching Liu ◽  
Hui-Hsien Pan ◽  
Fang-Liang Huang ◽  
...  

Abstract Background The factors to predict the progression of Mycoplasma pneumoniae infection remain inconclusive. Therefore, we investigated macrolide resistance prevalence, M. pneumoniae genotype, and clinical characteristics of childhood M. pneumoniae respiratory tract infections in Taiwan. Methods A total of 295 children hospitalized with respiratory tract infections with positive serological M. pneumoniae immunoglobulin M test results were enrolled in this 3-year prospective study. Oropharyngeal swabs were obtained for M. pneumoniae cultures and PCR tests. All M. pneumoniae specimens were further characterized by P1 typing, multilocus variable-number tandem-repeat analysis (MLVA), and macrolide resistance genotyping. The clinical characteristics and blood cytokine profiles were analyzed accordingly. Results Of 138 M. pneumoniae specimens, type I P1 was the predominant (136/138, 98.6%). MLVA type P (4-4-5-7-2) was the leading strain (42/138, 30.4%), followed by type J, U, A, and X. The overall macrolide-resistant rate was 38.4% (53/138); the resistance rate increased dramatically yearly: 10.6% in 2017, 47.5% in 2018, and 62.5% in 2019 (P < .001). All macrolide-resistant M. pneumoniae (MRMP) harbored the A2063G mutation and were MLVA type 4-5-7-2 (49/53, 92.5%), especially type U and X. No significant differences in clinical symptoms, duration of hospital stay, and radiographic findings were identified among patients between MRMP and macrolide-sensitive M. pneumoniae (MSMP) groups. Patients with MRMP infection had more febrile days before and during hospitalization; higher IL-13 and IL-33 levels than patients with MSMP infection (P < .005). Conclusions MRMP surged in Taiwan throughout the study period, but macrolide resistance was not a determinant factor of clinical severity.


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