Bertrand Nassar, Hafid Belhadj-Tahar, Weiyang Jin, Guanghua Yang
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This study evaluates the safety and efficacy of a new dermocosmetic formulation combining poly-<span>l</span>-lysine biovectors with vitamins A and C.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A single-arm, open-label study was conducted on 20 patients diagnosed with AD, including 14 women and 6 men aged between 24 and 63, with skin phototypes of Fitzpatrick I–VI. Treatment involved sequential application of poly-<span>l</span>-lysine G2/vitamin C in the morning and poly-<span>l</span>-lysine G3/vitamin A in the evening for 28 days, on the face, hands, and body. Outcomes were assessed using the Dermatology Life Quality Index (DLQI) and SCORAD scores. Additional assessments included a visual analog scale for pruritus and sleep disturbance, as well as patient self-report questionnaires on skin improvement and treatment satisfaction.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The treatment was well-tolerated, with no adverse effects and no relapses of AD. After 28 days, patients showed a significant reduction in DLQI (−61.8%, Cohen's <i>d</i> = 1.20) and SCORAD (−41.8%, Cohen's <i>d</i> = 1.05) scores. Objective improvements included reductions in erythema (−50%), dryness (−60%), and pruritus (−50%).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>This study demonstrates the potential of poly-<span>l</span>-lysine-based dermocosmetics combined with vitamins A and C to improve the symptoms and quality of life of patients suffering from AD. The formulations were well-tolerated and effective in restoring the skin barrier and reducing inflammation. Further large-scale controlled studies are needed to validate these results and explore long-term efficacy.</p>\n </section>\n </div>","PeriodicalId":36518,"journal":{"name":"Health Science Reports","volume":"8 4","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/hsr2.70676","citationCount":"0","resultStr":"{\"title\":\"A Prospective Open-Label Study of Tolerance and Effectiveness of Sequential Dermocosmetic Treatments Combining Poly-l-Lysine Biovectors With Vitamins A and C\",\"authors\":\"Bertrand Nassar, Hafid Belhadj-Tahar, Weiyang Jin, Guanghua Yang\",\"doi\":\"10.1002/hsr2.70676\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background and Objectives</h3>\\n \\n <p>Atopic dermatitis (AD) is a common chronic inflammatory skin condition, affecting 15%–20% of children and up to 10% of adults. 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引用次数: 0
摘要
背景和目的特应性皮炎(AD)是一种常见的慢性炎症性皮肤病,影响15%-20%的儿童和高达10%的成人。它对患者的生活质量产生重大影响,并对医疗保健系统构成相当大的负担。治疗策略旨在恢复皮肤屏障,减少炎症,达到生理和体内平衡。本研究评估了一种将聚赖氨酸生物载体与维生素a和c结合的新型皮肤化妆品配方的安全性和有效性。方法对20例AD患者进行单臂、开放标签研究,其中女性14例,男性6例,年龄24 ~ 63岁,皮肤光型为Fitzpatrick I-VI。治疗包括在早晨使用聚赖氨酸G2/维生素C,在晚上使用聚赖氨酸G3/维生素A,连续使用28天,涂抹于面部、手部和身体。使用皮肤病生活质量指数(DLQI)和SCORAD评分评估结果。其他评估包括瘙痒和睡眠障碍的视觉模拟量表,以及患者关于皮肤改善和治疗满意度的自我报告问卷。结果治疗耐受性好,无不良反应,无AD复发。28天后,患者DLQI评分(- 61.8%,Cohen’s d = 1.20)和SCORAD评分(- 41.8%,Cohen’s d = 1.05)均显著降低。客观改善包括红斑(- 50%)、干燥(- 60%)和瘙痒(- 50%)的减少。结论以聚赖氨酸为基础的皮肤化妆品联合维生素A和C可改善AD患者的症状和生活质量。该配方耐受性良好,在恢复皮肤屏障和减少炎症方面有效。需要进一步的大规模对照研究来验证这些结果并探索长期疗效。
A Prospective Open-Label Study of Tolerance and Effectiveness of Sequential Dermocosmetic Treatments Combining Poly-l-Lysine Biovectors With Vitamins A and C
Background and Objectives
Atopic dermatitis (AD) is a common chronic inflammatory skin condition, affecting 15%–20% of children and up to 10% of adults. It has a significant impact on patients' quality of life and represents a considerable burden on healthcare systems. Management strategies aim to restore the skin barrier, reduce inflammation, and achieve physiological and homeostatic balance. This study evaluates the safety and efficacy of a new dermocosmetic formulation combining poly-l-lysine biovectors with vitamins A and C.
Methods
A single-arm, open-label study was conducted on 20 patients diagnosed with AD, including 14 women and 6 men aged between 24 and 63, with skin phototypes of Fitzpatrick I–VI. Treatment involved sequential application of poly-l-lysine G2/vitamin C in the morning and poly-l-lysine G3/vitamin A in the evening for 28 days, on the face, hands, and body. Outcomes were assessed using the Dermatology Life Quality Index (DLQI) and SCORAD scores. Additional assessments included a visual analog scale for pruritus and sleep disturbance, as well as patient self-report questionnaires on skin improvement and treatment satisfaction.
Results
The treatment was well-tolerated, with no adverse effects and no relapses of AD. After 28 days, patients showed a significant reduction in DLQI (−61.8%, Cohen's d = 1.20) and SCORAD (−41.8%, Cohen's d = 1.05) scores. Objective improvements included reductions in erythema (−50%), dryness (−60%), and pruritus (−50%).
Conclusion
This study demonstrates the potential of poly-l-lysine-based dermocosmetics combined with vitamins A and C to improve the symptoms and quality of life of patients suffering from AD. The formulations were well-tolerated and effective in restoring the skin barrier and reducing inflammation. Further large-scale controlled studies are needed to validate these results and explore long-term efficacy.