Phan Tai A, Halliday Gary M, Barnetson Ross Stc, Damian Diona L
Department of Medicine (Dermatology), Melanoma and Skin Cancer Research Institute, Royal Prince Alfred Hospital, University of Sydney, Sydney, Australia.
Photodermatol Photoimmunol Photomed. 2006 Aug;22(4):174-80. doi: 10.1111/j.1600-0781.2006.00226.x.
BACKGROUND/PURPOSE: This study aimed to determine the relationship between various measures of constitutive skin pigmentation and erythema caused by solar-simulated UV (ssUV), 290 and 310 nm UV.
Skin pigmentation was assessed clinically by skin typing as well as objectively by measurement of the melanin index (MI) by reflectance spectroscopy. Subjects having Fitzpatrick skin types I-IV were exposed to graded doses of ssUV and either narrowband 310 nm (n=70) or 290 nm (n=69) UV, and assessed 24 h after exposure. Minimal erythema dose (MED) was assessed visually as the lowest dose that caused minimally perceptible erythema. Susceptibility to further development of erythema with higher exposure doses was measured by the gradient of erythema dose-response curves. This was determined by linear regression using reflectance spectrometry data beyond the MED.
Although there was considerable variation within each skin type, MI and ssUV MED increased with increasing Fitzpatrick skin type. MI correlated with ssUV MED and 310 nm UV MED, but not 290 nm UV MED. There was also a significant negative correlation between MI and erythema dose-response gradients caused by ssUV, 310 and 290 nm UV.
Melanin situated near the basal epidermis may not protect from the initial development of threshold erythema caused by 290 nm UV because it penetrates poorly past the stratum corneum and is not well absorbed by melanin in vivo compared with 310 nm UV. Higher erythemal 290 nm UV doses may reach basal epidermal melanin, which may then afford protection against further 290 nm UV erythema.
背景/目的:本研究旨在确定内源性皮肤色素沉着的各种指标与模拟阳光紫外线(ssUV)、290纳米和310纳米紫外线引起的红斑之间的关系。
通过皮肤分型对皮肤色素沉着进行临床评估,并通过反射光谱法测量黑色素指数(MI)进行客观评估。将Fitzpatrick皮肤分型为I-IV型的受试者暴露于分级剂量的ssUV以及窄带310纳米(n = 70)或290纳米(n = 69)紫外线,并在暴露后24小时进行评估。最小红斑剂量(MED)通过肉眼评估,即引起最小可察觉红斑的最低剂量。通过红斑剂量反应曲线的斜率来测量更高暴露剂量下红斑进一步发展的易感性。这是通过使用超过MED的反射光谱数据进行线性回归来确定的。
尽管每种皮肤类型内部存在相当大的差异,但MI和ssUV MED随着Fitzpatrick皮肤类型的增加而增加。MI与ssUV MED和310纳米紫外线MED相关,但与290纳米紫外线MED无关。MI与ssUV、310纳米和290纳米紫外线引起的红斑剂量反应梯度之间也存在显著的负相关。
位于基底表皮附近的黑色素可能无法保护皮肤免受290纳米紫外线引起的阈值红斑的初始发展,因为它穿过角质层的能力较差,并且与310纳米紫外线相比,在体内黑色素对其吸收不佳。更高剂量的290纳米紫外线红斑可能会到达基底表皮黑色素,然后这可能提供针对进一步290纳米紫外线红斑的保护。