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Risk Factors and Relationship of Cutaneous and Uveal Melanocytic Lesions in Monozygotic and Dizygotic Twin Pairs

机译:单卵双胎和双卵双胎的皮肤和葡萄膜黑色素细胞病变的危险因素及其关系

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摘要

BACKGROUND: The similar genetic background of a pair of twins, and the similar environmental impacts to which they are exposed allow an exact and objective investigation of various constitutional and environmental factors in naevus development. As far as we are aware, this is the first published survey that simultaneously examines cutaneous and ocular pigmented lesions in an appreciable sample of identical and non-identical twins. METHODS: 172 pairs of twins of Caucasian origin were included in this study. A whole-body skin examination and a detailed ophthalmological examination were performed to determine the density of melanocytic lesions. A standardized questionnaire was used to assess the data relating to constitutional, sun exposure and other variables. RESULTS: A notably high proportion of the subjects (36.78%) manifested one or more clinically atypical melanocytic naevi (CAMNs), and approximately one-third (31.4%) of them at least one benign uveal pigmented lesion (BUPL). The incidence of iris freckles (IFs), iris naevi (INs) and choroidal naevi (CHNs) proved to be 25.35%, 5.98% and 3.52%, respectively. The interclass correlation coefficients for common melanocytic naevi (CMNs), CAMNs, and INs were 0.77, 0.76 and 0.86 in monozygotic twins, as compared with 0.5, 0.27 and 0.25 in dizygotic twin pairs, respectively. A statistically significant correlation was found between the prevalence of CAMNs and that of INs. CONCLUSIONS: This significant correlation suggests the existence of a subgroup of Caucasian people with an increased susceptibility to both cutaneous and ocular naevus formation. There is accumulating evidence that, besides the presence of cutaneous atypical naevi, INs can serve as a marker of a predisposed phenotype at risk of uveal melanoma. The correlation between cutaneous and ocular pigmented lesions underlines the need for the adequate ophthalmological screening of subjects with CAMNs and INs.
机译:背景:一对双胞胎的相似遗传背景,以及它们所遭受的相似环境影响,使得可以准确,客观地研究痣发育中的各种体质和环境因素。据我们所知,这是首次发表的调查,该调查同时检查了相当多的相同和不同双胞胎样本中的皮肤和眼部色素性病变。方法:本研究包括172对来自白种人的双胞胎。进行全身皮肤检查和详细的眼科检查以确定黑素细胞病变的密度。使用标准化的问卷来评估与体质,日晒和其他变量有关的数据。结果:相当高比例的受试者(36.78%)表现出一种或多种临床上非典型的黑素细胞痣(CAMNs),其中约三分之一(31.4%)至少表现出一种葡萄膜良性病变(BUPL)。虹膜雀斑(IFs),虹膜naevi(INs)和脉络膜naevi(CHNs)的发生率分别为25.35%,5.98%和3.52%。单卵双生双胞胎中常见的黑素细胞痣(CMNs),CAMNs和IN的类间相关系数分别为0.77、0.76和0.86,而双卵双生双胞胎中的组间相关系数分别为0.5、0.27和0.25。在CAMN和IN的患病率之间发现了统计学上显着的相关性。结论:这种显着的相关性表明存在一个高加索人亚组,其对皮肤和眼内痣形成的敏感性增加。有越来越多的证据表明,除了存在皮肤非典型性痣外,INs还可以作为易患葡萄膜黑色素瘤的易感表型的标志物。皮肤和眼部色素沉着病变之间的相关性强调了对有CAMNs和INs的受试者进行适当的眼科筛查的必要性。

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