Abstract | BACKGROUND: METHODS: Totally, 103 active AS patients who underwent celecoxib treatment for 12 weeks were enrolled. Then, pre-treatment serum TNF-α, IL-1β, IL-6, IL-8, IL-17A, IL-21, IL-23, IL-32, ICAM-1, and VEGF were detected by enzyme-linked immunosorbent assay. Besides, the ASAS 20 response was assessed at week 2 (W2), week 6 (W6), and week 12 ( W12). Based on the ASAS 20 response at W12, patients were divided into responders and non-responders. RESULTS: After celecoxib treatment, 53 (51.3%), 58 (56.3%), and 60 (58.3%) patients achieved ASAS 20 response at W2, W6, and W12, respectively. Furthermore, IL-1β (P = 0.019), IL-6 (P = 0.004), and IL-17A (P = 0.007) levels were higher, while TNF-α (P = 0.086), IL-8 (P = 0.143), IL-21 (P = 0.687), IL-23 (P = 0.329), IL-32 (P = 0.216), ICAM-1 (P = 0.119), and VEGF (P = 0.732) levels were similar in responders compared with non-responders. Subsequent multivariate logistic regression analysis revealed that among these inflammatory cytokines, only IL-6 (P = 0.019) independently predicted higher ASAS 20 response to celecoxib at W12, and it had a fair value for predicting ASAS 20 response to celecoxib at W12 (area under the curve: 0.666, 95% confidence interval: 0.561-0.771) by receiver-operating characteristic curve analysis. CONCLUSION: Serum IL-1β, IL-6, and IL-17A serve as indicators for predicting clinical response to celecoxib in AS patients, which may assist with the optimization of personalized treatment.
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Authors | Yang Zhang, Chao Ning, Huijie Zhou, Yingjie Yan, Fulai Liu, Yayun Huang |
Journal | Irish journal of medical science
(Ir J Med Sci)
Vol. 190
Issue 2
Pg. 631-638
(May 2021)
ISSN: 1863-4362 [Electronic] Ireland |
PMID | 32955700
(Publication Type: Journal Article)
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Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- IL17A protein, human
- IL1B protein, human
- Interleukin-17
- Interleukin-1beta
- Interleukin-6
- Celecoxib
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Topics |
- Adult
- Anti-Inflammatory Agents, Non-Steroidal
(blood, pharmacology, therapeutic use)
- Celecoxib
(blood, pharmacology, therapeutic use)
- Female
- Humans
- Interleukin-17
(blood, metabolism, therapeutic use)
- Interleukin-1beta
(metabolism)
- Interleukin-6
(metabolism)
- Male
- Spondylitis, Ankylosing
(blood, drug therapy, pathology)
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