HMGB1-RAGE- moesin axis may be indicted for acne vulgaris
• 2021
معلومات البحث
المؤلفون
Rehab Mohammed Salem MD1 | Asmaa Adel El-fallah
MD2 | Rasha Shaker MD3
الكلمات المفتاحية
acne, HMGB 1, moesin
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: High-mobility
group box 1 (HMGB1)-receptor
for advanced glycation end
(RAGE)-moesin
axis could be implicated in induction of inflammation. However, there
is a scarcity in literature discussing the role of this axis in inflammatory skin disorders.
Aims: The aim of the present study was to evaluate the serum levels of HMGB1 and
moesin in patients with inflammatory acne vulgaris.
Patients/Methods: This comparative cross-sectional
study included 66 inflammatory
acne vulgaris patients classified according to Global Acne Grading System (GAGS) into
three groups (22 patients each): mild, moderate, and severe acne vulgaris. In addition,
82 acne-free
individuals were included as a control group. Serum HMGB 1 and moesin
levels were measured using enzyme-linked
immunosorbent assay kits.
Results: High-mobility
group box 1 and moe sin serum levels in acne patients were
significantly higher than the levels in control subjects (p = 0.04, 0.0005 respectively).
Serum levels of both markers in severe acne patients and in those with post-acne
scarring were elevated when compared to the levels in the other groups, and however,
this elevation was significant only for moesin levels. There was a significant positive
correlation between the serum levels of HMGB1 and moesin in the studied patient's
sample (r = 0.3079, p = 0.011).
Conclusion: High-mobility
group box 1-receptor
for advanced glycation end-moesin
axis may be implicated in acne vulgaris pathogenesis, and it may be a promising therapeutic
target.
group box 1 (HMGB1)-receptor
for advanced glycation end
(RAGE)-moesin
axis could be implicated in induction of inflammation. However, there
is a scarcity in literature discussing the role of this axis in inflammatory skin disorders.
Aims: The aim of the present study was to evaluate the serum levels of HMGB1 and
moesin in patients with inflammatory acne vulgaris.
Patients/Methods: This comparative cross-sectional
study included 66 inflammatory
acne vulgaris patients classified according to Global Acne Grading System (GAGS) into
three groups (22 patients each): mild, moderate, and severe acne vulgaris. In addition,
82 acne-free
individuals were included as a control group. Serum HMGB 1 and moesin
levels were measured using enzyme-linked
immunosorbent assay kits.
Results: High-mobility
group box 1 and moe sin serum levels in acne patients were
significantly higher than the levels in control subjects (p = 0.04, 0.0005 respectively).
Serum levels of both markers in severe acne patients and in those with post-acne
scarring were elevated when compared to the levels in the other groups, and however,
this elevation was significant only for moesin levels. There was a significant positive
correlation between the serum levels of HMGB1 and moesin in the studied patient's
sample (r = 0.3079, p = 0.011).
Conclusion: High-mobility
group box 1-receptor
for advanced glycation end-moesin
axis may be implicated in acne vulgaris pathogenesis, and it may be a promising therapeutic
target.
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