Serum irisin: A prognostic marker for severe acne vulgaris
• 2018
معلومات البحث
المؤلفون
Amany I. Mustafa MD1 | Ola S. El‐Shimi MD2
الكلمات المفتاحية
acne vulgaris, insulin resistance, irisin
المجلة العلمية
Not Available
الناشر
Not Available
المجلد
Not Available
العدد
Not Available
الصفحات
Not Available
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Background: Acne vulgaris is a common chronic inflammatory skin disease involving
pilosebaceous units. Adipokines are secreted by adipose tissue and function as signaling
networks communicating it with different organs. They may have role in
pathogenesis of acne vulgaris and the associated insulin resistance. Irisin, a hormone
like myokine, is one of adipokines with anti‐inflammatory, anti‐oxidant, and antidiabetic
effects.
Aims: We aimed at evaluation of serum irisin level in patients with acne vulgaris to
assess its correlation with disease pathogenesis.
Patients and Methods: Serum irisin level was measured by an ELISA technique in
60 acne vulgaris patients and 60 apparently healthy controls. Insulin resistance was
calculated by Homeostasis Model Assessment of Insulin Resistance index.
Results: Serum irisin level was significantly lower in acne vulgaris patients than control
group (P < 0.001). It showed a significant negative correlation with insulin resistance
among patients (P 0.012). Moreover, it was decreasing significantly with the
increase in disease severity (P 0.004).
Conclusions: Our results revealed that lower serum irisin not only to be a biomarker
of disease pathogenesis but also to be a potential prognostic predictor for severity
in acne vulgaris.
pilosebaceous units. Adipokines are secreted by adipose tissue and function as signaling
networks communicating it with different organs. They may have role in
pathogenesis of acne vulgaris and the associated insulin resistance. Irisin, a hormone
like myokine, is one of adipokines with anti‐inflammatory, anti‐oxidant, and antidiabetic
effects.
Aims: We aimed at evaluation of serum irisin level in patients with acne vulgaris to
assess its correlation with disease pathogenesis.
Patients and Methods: Serum irisin level was measured by an ELISA technique in
60 acne vulgaris patients and 60 apparently healthy controls. Insulin resistance was
calculated by Homeostasis Model Assessment of Insulin Resistance index.
Results: Serum irisin level was significantly lower in acne vulgaris patients than control
group (P < 0.001). It showed a significant negative correlation with insulin resistance
among patients (P 0.012). Moreover, it was decreasing significantly with the
increase in disease severity (P 0.004).
Conclusions: Our results revealed that lower serum irisin not only to be a biomarker
of disease pathogenesis but also to be a potential prognostic predictor for severity
in acne vulgaris.
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