Kang Sewon, Bergfeld Wilma, Gottlieb Alice B, Hickman Janet, Humeniuk John, Kempers Steven, Lebwohl Mark, Lowe Nicholas, McMichael Amy, Milbauer James, Phillips Tania, Powers Jerold, Rodriguez David, Savin Ronald, Shavin Joel, Sherer Daniel, Silvis Nancy, Weinstein Richard, Weiss Jonathan, Hammerberg Craig, Fisher Gary J, Nighland Marge, Grossman Rachel, Nyirady Judit
Department of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.
Am J Clin Dermatol. 2005;6(4):245-53. doi: 10.2165/00128071-200506040-00005.
Long-term (>1 year) placebo-controlled studies of tretinoin in the treatment of photodamaged skin have not been conducted. Recently, we conducted a 2-year placebo-controlled study of tretinoin emollient cream 0.05%, including histopathologic assessment of safety and analysis of markers of collagen deposition.
The objective of the study was to determine the long-term safety and efficacy of tretinoin emollient cream 0.05% in the treatment of moderate to severe facial photodamage.
A total of 204 subjects were treated with tretinoin or placebo (vehicle emollient cream) applied to the entire face once a day for up to 2 years. Clinical and histologic effects were assessed at regularly scheduled clinic visits.
Treatment with tretinoin resulted in significantly greater improvement relative to placebo in clinical signs of photodamage (fine and coarse wrinkling, mottled hyperpigmentation, lentigines, and sallowness), overall photodamage severity, and investigator's global assessment of clinical response (p<0.05). Histologic evaluation showed no increase in keratinocytic or melanocytic atypia, dermal elastosis, or untoward effects on stratum corneum following treatment with tretinoin compared with placebo. Immunohistochemistry studies, conducted at three study centers, showed a significant increase relative to placebo in facial procollagen 1C terminal, a marker for procollagen synthesis, at month 12 (p=0.0074).
Long-term treatment with tretinoin emollient cream 0.05% is safe and effective in subjects with moderate to severe facial photodamage.
尚未进行过维甲酸治疗光损伤皮肤的长期(>1年)安慰剂对照研究。最近,我们开展了一项为期2年的关于0.05%维甲酸润肤霜的安慰剂对照研究,包括安全性的组织病理学评估和胶原蛋白沉积标志物分析。
本研究的目的是确定0.05%维甲酸润肤霜治疗中度至重度面部光损伤的长期安全性和有效性。
总共204名受试者接受维甲酸或安慰剂(赋形剂润肤霜)治疗,每天一次全脸涂抹,持续长达2年。在定期安排的门诊就诊时评估临床和组织学效果。
与安慰剂相比,维甲酸治疗在光损伤的临床体征(细纹和粗纹、斑驳色素沉着、雀斑和皮肤发黄)、总体光损伤严重程度以及研究者对临床反应的整体评估方面有显著更大的改善(p<0.05)。组织学评估显示,与安慰剂相比,维甲酸治疗后角质形成细胞或黑素细胞异型性、真皮弹性组织变性或对角质层的不良影响均未增加。在三个研究中心进行的免疫组织化学研究显示,与安慰剂相比,在第12个月时,面部前胶原1C末端(前胶原合成的标志物)显著增加(p=0.0074)。
0.05%维甲酸润肤霜长期治疗中度至重度面部光损伤受试者是安全有效的。