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DOI 10.4103/ijt.ijt_9_19

Медицинская библиотека · International journal of trichology · 2019

Tumor Necrosis Factor-like Weak Inducer of Apoptosis: A Novel Serum Marker in Patients with Severe Alopecia.

Al Taweel Abdul-Aziz Ibrahim, Hamed Ahmed Mohamed, Abdelrahman Amira Mohamed Noureldin, Hassan Mona Nady Ibrahim

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Аннотация

BACKGROUND

Alopecia areata (AA) is a common form of nonscarring hair loss of scalp and/or body. Genetic predisposition, autoimmunity, and environmental factors play a major role in the etiopathogenesis of AA. Tumor necrosis factor-like weak inducer of apoptosis (TWEAK) is a multifunctional cytokine expressed on various cell types and tissues and acts through binding to its sole receptor factor-inducible 14 (Fn14). TWEAK/Fn14 activation contributes to various pathological processes, including cell proliferation and death, angiogenesis, carcinogenesis, and inflammation.

AIM: The aim of this current study was to measure serum levels of TWEAK in patients with AA and to assess the correlation between it and severity of the disease.

SUBJECTS AND

METHODS

This study included 50 patients who had patchy AA, in addition to 50 apparently healthy controls. Severity of AA was assessed using Severity of Alopecia Tool Score. Serum TWEAK levels in all participants were determined using ELISA technique and were correlated with the severity of the disease.

RESULTS

Mean serum levels of TWEAK were significantly higher in AA patients, with a positive significant correlation between serum levels of TWEAK and severity of the disease.

CONCLUSION

TWEAK as a novel marker of many autoimmune inflammatory dermatological diseases, could be a promising marker in the diagnosis of AA, and also can be used as a prognostic marker for its severity.

Для цитирования: Al Taweel Abdul-Aziz Ibrahim, Hamed Ahmed Mohamed, Abdelrahman Amira Mohamed Noureldin, Hassan Mona Nady Ibrahim. Tumor Necrosis Factor-like Weak Inducer of Apoptosis: A Novel Serum Marker in Patients with Severe Alopecia.. International journal of trichology. 2019. DOI: 10.4103/ijt.ijt_9_19.
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