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DOI 10.1186/s12895-020-00111-0

Медицинская библиотека · BMC dermatology · 2020

The role of insulin-like growth factor in Acrochordon Etiopathology.

Köseoğlu Hanife Gündoğdu, Bozca Burçin Cansu, Başsorgun Cumhur İbrahim, Sarı Ramazan, Akbaş Sadıka Halide, Karakaş Ayşe Akman

СтатьяНаблюдательное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

There are reports that acrochordon (skin tag), the most common fibroepithelial tumor of the skin, may be associated with metabolic syndrome components, particularly insulin metabolism disorders. However, to the best of our knowledge, there is no study examining its association with insulin resistance and tissue levels of insulin-like growth factor 1 receptor (IGF-1R) and insulin-like growth factor 2 receptor (IGF-2R).

METHODS

Thirty patients with at least one acrochordon in their body who had no known history of diabetes mellitus and a control group comprised 30 individuals who had no acrochordon or no known history of diabetes mellitus were included. The tissue expression of IGF-1R and IGF-2R were investigated via immunohistochemical assessment in both groups.

RESULTS

In the group with acrochordon, IGF-1R and IGF-2R expression was found to be significantly higher compared to the control group (p < 0,01). Using logistic regression analysis, an increase in serum insulin, serum IGF-1 and HOMA-IR levels was found to be associated with the expression levels of IGF-1R and IGF-2R.

CONCLUSION

These findings support the view that insulin metabolism disorders should be evaluated in patients with acrochordon. Our study indicates that IGF receptors may have an effect on acrochordon pathogenesis and that acrochordon etiology and related conditions can be clarified by detection of parameters that influence receptor levels.

Для цитирования: Köseoğlu Hanife Gündoğdu, Bozca Burçin Cansu, Başsorgun Cumhur İbrahim, Sarı Ramazan, Akbaş Sadıka Halide, Karakaş Ayşe Akman. The role of insulin-like growth factor in Acrochordon Etiopathology.. BMC dermatology. 2020. DOI: 10.1186/s12895-020-00111-0.

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