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DOI 10.1093/ced/llae363

Медицинская библиотека · Clinical and experimental dermatology · 2024

Elevation of serum carcinoembryonic antigen as a possible predictor of response to pulse methylprednisolone in acquired idiopathic generalized anhidrosis.

Sakiyama Tomoki, Endo Yuichiro, Nakamizo Satoshi, Kabashima Kenji

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Аннотация

BACKGROUND

Acquired idiopathic generalized anhidrosis (AIGA) is a rare disorder primarily observed in Asian populations, particularly in Japan. Although pulse methylprednisolone therapy is an effective treatment for AIGA, predictors of therapeutic response remain poorly defined.

OBJECTIVES

To identify factors that predict the efficacy of pulse methylprednisolone therapy in patients with AIGA.

METHODS

Data obtained from 32 patients with AIGA were assessed based on clinical, histopathological and serological examinations. Statistical analyses were conducted to explore predictors of response to pulse methylprednisolone therapy.

RESULTS

The average age of participants was 32.1 years (SD 12.3); 66% were male and 34% female. The response to pulse methylprednisolone therapy was closely associated with the time from the onset to start of therapy (Wilcoxson's rank sum test, P = 0.02, n = 27), with earlier intervention resulting in a better outcome. Notably, male patients and patients presenting with severe symptoms at diagnosis responded better to treatment. High serum carcinoembryonic antigen (CEA) levels and histological evidence of inflammation around sweat glands also correlated with a positive therapeutic response.

CONCLUSIONS

Earlier intervention, elevated serum CEA levels and inflammation around sweat glands are potential indicators of a successful response to pulse methylprednisolone therapy in patients with AIGA.

Для цитирования: Sakiyama Tomoki, Endo Yuichiro, Nakamizo Satoshi, Kabashima Kenji. Elevation of serum carcinoembryonic antigen as a possible predictor of response to pulse methylprednisolone in acquired idiopathic generalized anhidrosis.. Clinical and experimental dermatology. 2024. DOI: 10.1093/ced/llae363.

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