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虹膜色素病变作为皮肤黑色素瘤风险的标志物:一项澳大利亚病例对照研究。

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case-control study.

机构信息

Dermatology Research Centre, The University of Queensland, UQ Diamantina Institute, Translational Research Institute, Brisbane, 4102, Australia.

Department of Dermatology, Emory University School of Medicine, Atlanta, 30309, GA, U.S.A.

出版信息

Br J Dermatol. 2018 May;178(5):1119-1127. doi: 10.1111/bjd.16323. Epub 2018 Apr 6.

Abstract

BACKGROUND

Iris naevi and iris freckles have a frequency of 4% and 50% in the European population, respectively. They are associated with dysplastic naevi, but few studies have examined their link to cutaneous melanoma.

OBJECTIVES

To assess whether iris pigmented lesions are a predictive indicator for cutaneous melanoma.

METHODS

This is a melanoma case-control study of 1254 European-background Australians. Sun exposure and melanoma history, a saliva sample for DNA analysis and eye photographs taken with a digital camera were collected from 1117 participants. Iris images were assessed by up to four trained observers for the number of iris pigmented lesions. The data were analysed for correlations between iris pigmented lesions and melanoma history.

RESULTS

Case participants over the age of 40 had similar numbers of iris pigmented lesions to age matched controls (mean 5·7 vs. 5·2, P = 0·02), but in younger case and control participants there was a greater difference (mean 3·96 vs. 2·19, P = 0·004). A logistic regression adjusted for age, sex, skin, hair and eye colour, skin freckling and naevus count found that the presence of three or more iris pigmented lesions increases the melanoma risk 1·45-fold [95% confidence interval (CI) 1·07-1·95]. HERC2/OCA2 rs12913832 and IRF4 rs12203592 influenced both eye colour and the number of iris pigmented lesions. On the HERC2/OCA2 A/A and A/G genotype background there was an increasing proportion of blue eye colour when carrying the IRF4 T allele (P = 3 × 10 ) and a higher number of iris pigmented lesions with the IRF4 T/T homozygote (P = 3 × 10 ).

CONCLUSIONS

Iris pigmented lesion count provides additional predictive information for melanoma risk above that from conventional risk factors.

摘要

背景

虹膜痣和虹膜雀斑在欧洲人群中的发生率分别为 4%和 50%。它们与发育不良痣有关,但很少有研究探讨它们与皮肤黑色素瘤的联系。

目的

评估虹膜色素病变是否是皮肤黑色素瘤的预测指标。

方法

这是一项针对 1254 名欧洲背景的澳大利亚人的黑色素瘤病例对照研究。从 1117 名参与者中收集了阳光暴露和黑色素瘤病史、唾液样本进行 DNA 分析以及使用数码相机拍摄的眼部照片。多达四名经过培训的观察者评估了虹膜图像中虹膜色素病变的数量。分析了虹膜色素病变与黑色素瘤病史之间的相关性。

结果

年龄在 40 岁以上的病例参与者的虹膜色素病变数量与年龄匹配的对照组相似(平均 5.7 对 5.2,P=0.02),但在较年轻的病例和对照组参与者中,差异更大(平均 3.96 对 2.19,P=0.004)。调整年龄、性别、皮肤、头发和眼睛颜色、皮肤雀斑和痣数量后进行的逻辑回归发现,存在 3 个或更多虹膜色素病变会使黑色素瘤风险增加 1.45 倍(95%置信区间 1.07-1.95)。HERC2/OCA2 rs12913832 和 IRF4 rs12203592 影响眼睛颜色和虹膜色素病变的数量。在 HERC2/OCA2 A/A 和 A/G 基因型背景下,携带 IRF4 T 等位基因时蓝色眼睛的比例增加(P=3×10),携带 IRF4 T/T 纯合子时虹膜色素病变的数量增加(P=3×10)。

结论

虹膜色素病变计数提供了超过传统危险因素的黑色素瘤风险的额外预测信息。

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