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双重特异性磷酸酶 22 与皮肤损伤程度和生物制剂治疗史有关,而在治疗过程中其水平的持续升高反映了银屑病患者的更好预后。

Dual specificity phosphatase 22 relates to skin lesion degree and biologics history, while its longitudinal elevation during treatment reflects better outcome in psoriasis patients.

机构信息

Department of Dermatology, Renmin Hospital, Hubei University of Medicine, Shiyan, China.

出版信息

J Clin Lab Anal. 2022 Feb;36(2):e24199. doi: 10.1002/jcla.24199. Epub 2021 Dec 31.

DOI:10.1002/jcla.24199
PMID:34973040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8841189/
Abstract

BACKGROUND

Dual specificity phosphatase 22 (DUSP22) plays an important role in the regulation of immune and inflammation, but its correlation with clinical features and treatment outcome in psoriasis patients is still unclear. This study was to investigate the longitudinal change of DUSP22 with time, as well as its association with disease activity and treatment response in psoriasis patients.

METHODS

Totally, 120 psoriasis patients, 50 patients with other skin inflammations as disease controls (DCs), and 50 health controls (HCs) were recruited. Serum samples were collected from psoriasis patients at baseline, month (M)1, M3, and M6 after initiation of etanercept-based treatment as well as from DCs and HCs after enrollment to assess DUSP22 level by enzyme-linked immunosorbent assay.

RESULTS

DUSP22 was lower in psoriasis patients than in HCs and DCs (both p < 0.001). Besides, in psoriasis patients, DUSP22 was associated with lower psoriasis area severity index (PASI) score (p = 0.001) and systemic biological treatment history (p = 0.023), but not with other demographics, disease characteristics, or treatment history (all p>0.05). In addition, DUSP22 was increased with time (p < 0.001) in total patients. Moreover, DUSP22 at M3 (p = 0.004) and M6 (p < 0.001) was higher in response patients than in non-response patients evaluated by PASI 75. Additionally, DUSP22 at M3 (p < 0.001) and M6 (p = 0.003) was also increased in response patients compared with non-response patients evaluated by PASI 90.

CONCLUSION

DUSP22 decreases and negatively correlates with disease activity, while its longitudinal elevation with time reflects satisfactory treatment response in psoriasis patients.

摘要

背景

双特异性磷酸酶 22(DUSP22)在免疫和炎症调节中发挥着重要作用,但它与银屑病患者的临床特征和治疗结果的相关性尚不清楚。本研究旨在探讨 DUSP22 随时间的纵向变化及其与银屑病患者疾病活动度和治疗反应的关系。

方法

共招募 120 例银屑病患者、50 例其他皮肤炎症患者作为疾病对照组(DCs)和 50 名健康对照者(HCs)。在开始依那西普治疗后的基线、第 1、3 和 6 个月以及 DCs 和 HCs 入组时,采集银屑病患者的血清样本,通过酶联免疫吸附试验评估 DUSP22 水平。

结果

银屑病患者的 DUSP22 水平低于 HCs 和 DCs(均 p<0.001)。此外,在银屑病患者中,DUSP22 与较低的银屑病面积严重指数(PASI)评分(p=0.001)和全身生物治疗史(p=0.023)相关,但与其他人口统计学、疾病特征或治疗史无关(均 p>0.05)。此外,DUSP22 在所有患者中随时间增加(p<0.001)。此外,在通过 PASI75 评估的反应患者中,M3(p=0.004)和 M6(p<0.001)时的 DUSP22 更高,而非反应患者。此外,在通过 PASI90 评估的反应患者中,M3(p<0.001)和 M6(p=0.003)时的 DUSP22 也高于非反应患者。

结论

DUSP22 降低且与疾病活动度呈负相关,而其随时间的纵向升高反映了银屑病患者治疗反应良好。

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JKAP correlates with lower disease risk and inflammation, and its increment during etanercept treatment associates with commendable treatment efficiency in rheumatoid arthritis patients.
JNK 通路相关磷酸酶在炎症性肠病儿童中表达水平较低,与炎症、疾病活动和辅助性 T 细胞 17 细胞呈负相关。
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JNK pathway-associated phosphatase associates with rheumatoid arthritis risk, disease activity, and its longitudinal elevation relates to etanercept treatment response.JNK 通路相关磷酸酶与类风湿关节炎风险、疾病活动度相关,其纵向升高与依那西普治疗反应相关。
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