Gasdermin A (GSDMA) 组织表达、血清和尿液浓度与银屑病临床病理结果的关系。

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-07-01 DOI:10.5826/dpc.1403a177
Julia Nowowiejska, Anna Baran, Anna Pryczynicz, Justyna Magdalena Hermanowicz, Beata Sieklucka, Dariusz Pawlak, Iwona Flisiak
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摘要

导言:银屑病是一种多发且无法治愈的皮肤病,是当代皮肤病学的一个重要问题,尽管其发病机制仍不明确。Gasdermin A(GSDMA)是gasdermin蛋白家族的成员之一,它能在细胞膜上形成孔隙,导致细胞死亡,这种细胞死亡被称为脓毒症:我们的目的是研究 GSDMA 在银屑病患者中的作用:研究对象包括60名活动性斑块型银屑病患者和30名性别和年龄匹配的无皮肤病志愿者。采用酶联免疫吸附法评估所有参与者血清和尿液样本中的 GSDMA 浓度。免疫组化法评估了 GSDMA 在组织中的表达:结果:与对照组相比,患者血清中的 GSDMA 浓度明显升高,而尿液中的 GSDMA/肌酐比值则明显降低。与非皮损患者皮肤和无皮肤病的健康皮肤相比,银屑病斑块中的 GSDMA 组织表达更为突出。GSDMA血清浓度与谷丙转氨酶活性呈强负相关。GSDMA与PASI或银屑病持续时间无关:结论:研究结果表明,GSDMA 可能与银屑病有关。GSDMA过度表达可能会导致角质细胞过度增殖,并引发银屑病皮肤炎症。血清中的 GSDMA 可能成为银屑病的生物标志物,而尿液中的 GSDMA 目前还不能。
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Gasdermin A (GSDMA) Tissue Expression, Serum and Urinary Concentrations with Clinicopathologic Outcome in Psoriasis.

Introduction: Psoriasis is a frequent and incurable skin disease that is an important issue in contemporary dermatology, although its pathogenesis is still uncertain. Gasdermin A (GSDMA) is a member of the gasdermin protein family which are able to cause pore formation in cellular membranes leading to cell death called pyroptosis.

Objective: Our aim was to investigate the role of GSDMA in psoriatic patients.

Method: The study enrolled 60 patients with active plaque-type psoriasis and 30 sex- and age-matched volunteers without dermatoses. GSDMA concentration was assessed in serum and urine samples of all participants using ELISA. GSDMA tissue expression was assessed by immunohistochemistry.

Results: GSDMA serum concentration was significantly higher in patients compared to controls, whereas urinary GSDMA/creatinine ratio was insignificantly lower. GSDMA tissue expression was more prominent in psoriatic plaque compared to non-lesional patients' skin and healthy skin of subjects without dermatoses. There was a strong negative correlation between GSDMA serum concentration and ALT activity. GSDMA did not correlate with PASI or psoriasis duration.

Conclusions: Obtained results point to the probable involvement of GSDMA in psoriasis. GSDMA overexpression may probably lead to keratinocytes hyperproliferation and be responsible for triggering inflammation in psoriatic skin. Serum GSDMA could become psoriasis biomarker, whereas urinary GSDMA, not at this point.

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