Expression of transforming growth factor-β after different non-invasive facial rejuvenation modalities

Background Transforming growth factor‐β (TGF‐β) is a major regulator of the synthesis of extracellular matrix (ECM) proteins in human skin as it stimulates fibroblast proliferation and collagen production. Perturbed TGF‐β expression may play a key role in the pathogenesis of skin aging. Objectives T...

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Veröffentlicht in:International journal of dermatology 2015-04, Vol.54 (4), p.396-404
Hauptverfasser: El-Domyati, Moetaz, El-Ammawi, Tarek S., Medhat, Walid, Moawad, Osama, Mahoney, Mỹ G., Uitto, Jouni
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Sprache:eng
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Zusammenfassung:Background Transforming growth factor‐β (TGF‐β) is a major regulator of the synthesis of extracellular matrix (ECM) proteins in human skin as it stimulates fibroblast proliferation and collagen production. Perturbed TGF‐β expression may play a key role in the pathogenesis of skin aging. Objectives This study was conducted to objectively evaluate the effects of different modalities of non‐invasive facial rejuvenation on TGF‐β expression and to correlate its level with that of newly synthesized collagen. Methods A total of 36 patients with Fitzpatrick skin types III and IV were divided into six groups. Each group of six patients was subjected to a different non‐invasive modality for the treatment of skin aging, including radiofrequency (RF), Nd:YAG 1320‐nm laser and Er:YAG 2940‐nm laser mini‐peels, intense pulsed light (IPL), mesotherapy injection, and electro‐optical synergy (ELOS). Skin biopsies were obtained before treatment, at the end of treatment, and at three months post‐treatment. In addition, biopsies were obtained from 30 control subjects. Levels of TGF‐β were quantitatively evaluated using computerized image analysis of immunostained sections. Results The expression of TGF‐β was statistically significantly increased (P  0.05) were observed in TGF‐β level in response to IPL or mesotherapy treatments in comparison with baseline. The level of TGF‐β was positively correlated (P 
ISSN:0011-9059
1365-4632
DOI:10.1111/ijd.12435