Abstract

Psoriasis refers to genetically deterministic chronic inflammatory dermatoses, which are characterized by systemic immuno-mediated inflammatory response with preferential activation of the IL -23/-17 axis, growth deviation and keratinocyte differentiation.Material and methods. There were 21 patients under supervision with moderate to severe plaque psoriasis. Nine (42.8 %) patients did not receive previous systemic therapy; 3 (14.2 %) patients received apremilast at a dose of 30 mg twice a day during a year, 4 (19.0 %) patients were prescribed methotrexate at a dose of 15 mg subcutaneously weekly, for at least a year; 5 (23.8 %) patients received secukinumab at 300 mg subcutaneously once every 4 weeks for a year. All patients had a lost of effect or had developed side effects, which determined a change in therapeutic tactics.Results. Among the patients who were earlier not receiving treatment treatment after therapy with netakimab was started, the PASI index made 3.5 ± 1.1 (decrease by 94.4 %), the PASI index at the patients who were earlier receiving sekukinumab was 4.5 ± 1.1 (decrease by 81.9 %), among the patients who were earlier receiving the methotrexate the PASI index was 8.5 ± 1.3 (decrease by 89.9 %), at the patients who were earlier receiving apremilast the PASI index was 9.5 ± 2.1 (decrease by 86.3 %).Conclusions. Improvement in skin symptoms was accompanied by improvement of patients’ quality of life. Thus, the DLQI decreased by 77.9 % in the group of patients who had not previously received systemic therapy, by 77.4 % and 76.4 % in patients who had previously received sekukinumab and methotrexate therapy, respectively, and by 85.2 % in the group of patients who had previously received apremilast.

Highlights

  • Psoriasis refers to genetically deterministic chronic inflammatory dermatoses, which are characterized by systemic immuno-mediated inflammatory response with preferential activation of the IL -23/-17 axis, growth deviation and keratinocyte differentiation

  • The DLQI decreased by 77.9 % in the group of patients who had not previously received systemic therapy, by 77.4 % and 76.4 % in patients who had previously received sekukinumab and methotrexate therapy, respectively, and by 85.2 % in the group of patients who had previously received apremilast

  • А. Эффективность препарата нетакимаб в реальной клинической практике у пациентов с тяжелыми формами псориаза Медицинский алфавит.2020; (6):

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Summary

Оригинальные статьи

Наиболее привлекательной в плане блокады иммунопатогенеза псориаза мишенью является ИЛ‐17, так как именно данный цитокин вызывает чрезмерный упреждающий воспалительный ответ в кератиноцитах. В свете современных данных о патогенезе псориаза, его ассоциации с коморбидной патологией, дерматоз рассматривается как системное воспалительное заболевание, при этом наиболее часто отмечается поражение опорно-двигательного аппарата – псориатический артрит (ПсА) – выявляется у 30–40 % пациентов со среднетяжелым и тяжелым псориазом [1]. Наиболее привлекательной в плане блокады иммунопатогенеза псориаза мишенью является ИЛ‐17, так как именно данный цитокин вызывает упреждающий воспалительный ответ в кератиноцитах. С появлением генно-инженерных биологических препаратов (ГИБП) в значительной степени изменились наши возможности по контролю над псориазом, появились возможности для управления системным воспалением, а при наличии предикторов тяжелого течения или развитии коморбидной патологии может быть рассмотрена стратегия профилактической направленности ГИБП [3, 4]. Министерство здравоохранения Российской Федерации одобрило включение препарата в 2020 году в списки жизненно необ-

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