Shalita A R, Smith J G, Parish L C, Sofman M S, Chalker D K
Department of Dermatology, State University of New York, College of Medicine, Brooklyn, USA.
Int J Dermatol. 1995 Jun;34(6):434-7. doi: 10.1111/j.1365-4362.1995.tb04449.x.
Systemic and topical antimicrobials are effective in the treatment of inflammatory acne vulgaris; however, widespread use of these agents is becoming increasingly associated with the emergence of resistant pathogens raising concerns about microorganism resistance and highlighting the need for alternative nonantimicrobial agents for the treatment of acne. Nicotinamide gel provides potent antiinflammatory activity without the risk of inducing bacterial resistance.
In our double-blind investigation, the safety and efficacy of topically applied 4% nicotinamide gel was compared to 1% clindamycin gel for the treatment of moderate inflammatory acne vulgaris. Seventy-six patients were randomly assigned to apply either 4% nicotinamide gel (n = 38) or 1% clindamycin gel (n = 38) twice daily for 8 weeks. Efficacy was evaluated at 4 and 8 weeks using a Physician's Global Evaluation, Acne Lesion Counts, and an Acne Severity Rating.
After 8 weeks, both treatments produced comparable (P = 0.19) beneficial results in the Physician's Global Evaluation of Inflammatory Acne; 82% of the patients treated with nicotinamide gel and 68% treated with clindamycin gel were improved. Both treatments produced statistically similar reductions in acne lesions (papules/pustules; -60%, nicotinamide vs. -43%, clindamycin, P = 0.168), and acne severity (-52% nicotinamide group vs. -38% clindamycin group, P = 0.161).
These data demonstrate that 4% nicotinamide gel is of comparable efficacy to 1% clindamycin gel in the treatment of acne vulgaris. Because topical clindamycin, like other antimicrobials, is associated with emergence of resistant microorganisms, nicotinamide gel is a desirable alternative treatment for acne vulgaris.
全身性和局部性抗菌药物在治疗炎性寻常痤疮方面有效;然而,这些药物的广泛使用与耐药病原体的出现越来越相关,引发了对微生物耐药性的担忧,并凸显了需要替代的非抗菌药物来治疗痤疮。烟酰胺凝胶具有强大的抗炎活性,且无诱导细菌耐药性的风险。
在我们的双盲研究中,将局部应用4%烟酰胺凝胶与1%克林霉素凝胶治疗中度炎性寻常痤疮的安全性和有效性进行了比较。76名患者被随机分配,每天两次分别涂抹4%烟酰胺凝胶(n = 38)或1%克林霉素凝胶(n = 38),持续8周。在第4周和第8周时,使用医生整体评估、痤疮皮损计数和痤疮严重程度评分来评估疗效。
8周后,在医生对炎性痤疮的整体评估中,两种治疗产生了相当的(P = 0.19)有益效果;使用烟酰胺凝胶治疗的患者中有82%病情改善,使用克林霉素凝胶治疗的患者中有68%病情改善。两种治疗在痤疮皮损(丘疹/脓疱;烟酰胺组减少60%,克林霉素组减少43%,P = 0.168)和痤疮严重程度(烟酰胺组降低52%,克林霉素组降低38%,P = 0.161)方面的降低在统计学上相似。
这些数据表明,4%烟酰胺凝胶在治疗寻常痤疮方面与1%克林霉素凝胶疗效相当。由于局部使用克林霉素与其他抗菌药物一样,与耐药微生物的出现有关,烟酰胺凝胶是寻常痤疮理想的替代治疗方法。