Clinical and Molecular Effects on Mature Burn Scars After Treatment With a Fractional CO2 Laser
AUTHORS: Le Qu, M.D.,1,2,4 Austin Liu, M.D.,2 Li Zhou, M.D.,1,2,3 Chundi He, M.D., Ph.D,4 Peter H. Grossman, M.D.,5 Ronald L. Moy, M.D.,6 Qing-Sheng Mi, M.D., Ph.D,1,2,3 David Ozog, M.D.
RESEARCH SITES: 1Henry Ford Immunology Program, Henry Ford Hospital, Detroit, Michigan, 2Department of Dermatology, Henry Ford Hospital, Detroit, Michigan, 3Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan, 4Department of Dermatology, No. 1 Hospital of China Medical University, Shenyang, PR China, 5Grossman Burn Center, West Hills, California, 6David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles, California
PUBLICATION: Lasers Surg. Med.44:517–524, 2012
YEAR: 2012
BACKGROUND AND OBJECTIVE: There have been several case reports of improvement in the appearance of mature burn scars following treatment with fractional CO2 lasers. However, the biochemical mechanisms responsible for these improvements have not been elucidated.
MATERIALS AND METHODS: Ten patients with mature, full thickness, hypertrophic burn scars received initial treatment with a fractional CO2 laser. Clinical improvement was measured with Vancouver Scar Scale as well as Patient and Observer Scar Assessment Scale. Fresh tissue samples were obtained before the initial treatment and 48 hours after the first treatment for TaqMan Real-time RT-PCR analyses. Expressions of several scar-related biological markers, including types I and III procollagen, matrix metalloproteinase (MMP)-1, -13, transforming growth factor (TGF)-b1, b2, b3, and basic fibroblast growth factor (bFGF), as well as microRNA miR-17-92 cluster, were investigated.
RESULTS: There were significant improvements in both observer and subject ratings in all scales. Both types I and III procollagen mRNA levels were dramatically down-regulated after treatment, but the ratio of types I/ III procollagen mRNA was not different. The expression of MMP-1 was significantly up-regulated after treatment, while TGF-b2, – b3, and bFGF levels were significantly down-regulated. Expression of miR-18a and miR-19a were dramatically up- regulated (P < 0.05) after treatment.
CONCLUSIONS: Our study indicated that fractional CO2 resulted in clinical improvement of mature burn scar. Alteration of types I and III procollagen, MMP-1, TGF-b2, -b3, bFGF, as well as miRNAs miR-18a and miR-19a expression may be responsible for the clinical improvement after treatment. Our finding may have implications for novel treatments and further our understanding of fractional CO2 laser treatment.