Sabbagh Audrey, Pasmant Eric, Laurendeau Ingrid, Parfait Béatrice, Barbarot Sébastien, Guillot Bernard, Combemale Patrick, Ferkal Salah, Vidaud Michel, Aubourg Patrick, Vidaud Dominique, Wolkenstein Pierre
Faculté des Sciences Pharmaceutiques et Biologiques, UMR745 INSERM, Université Paris Descartes, Paris 75006, France.
Hum Mol Genet. 2009 Aug 1;18(15):2768-78. doi: 10.1093/hmg/ddp212. Epub 2009 May 5.
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder which displays considerable inter- and intra-familial variability in phenotypic expression. To evaluate the genetic component of variable expressivity in NF1, we examined the phenotypic correlations between affected relatives in 750 NF1 patients from 275 multiplex families collected through the NF-France Network. Twelve NF1-related clinical features, including five quantitative traits (number of café-au-lait spots of small size and of large size, and number of cutaneous, subcutaneous and plexiform neurofibromas) and seven binary ones, were scored. All clinical features studied, with the exception of neoplasms, showed significant familial aggregation after adjusting for age and sex. For most of them, patterns of familial correlations indicated a strong genetic component with no apparent influence of the constitutional NF1 mutation. Heritability estimates of the five quantitative traits ranged from 0.26 to 0.62. Moreover, we investigated for the first time the role of the normal NF1 allele in the variable expression of NF1 through a family-based association study. Nine tag SNPs in NF1 were genotyped in 1132 individuals from 313 NF1 families. No significant deviations of transmission of any of the NF1 variants to affected offspring was found for any of the 12 clinical features examined, based on single marker or haplotype analysis. Taken together, our results provided evidence that genetic modifiers, unlinked to the NF1 locus, contribute to the variable expressivity of the disease.
1型神经纤维瘤病(NF1)是一种常见的常染色体显性疾病,其表型表达在家族间和家族内均表现出显著差异。为了评估NF1可变表达的遗传成分,我们通过法国神经纤维瘤病网络收集了275个多重家庭的750例NF1患者,研究了受影响亲属之间的表型相关性。对12种与NF1相关的临床特征进行了评分,包括5个数量性状(小尺寸和大尺寸咖啡牛奶斑的数量,以及皮肤、皮下和丛状神经纤维瘤的数量)和7个二元性状。除肿瘤外,所有研究的临床特征在调整年龄和性别后均显示出显著的家族聚集性。对于大多数特征,家族相关性模式表明存在强大的遗传成分,而NF1构成性突变没有明显影响。5个数量性状的遗传度估计值在0.26至0.62之间。此外,我们首次通过基于家系的关联研究调查了正常NF1等位基因在NF1可变表达中的作用。在来自313个NF1家庭的1132名个体中,对NF1中的9个标签单核苷酸多态性进行了基因分型。基于单标记或单倍型分析,在所检查的12种临床特征中,未发现任何NF1变体向受影响后代的传递存在显著偏差。综上所述,我们的结果表明,与NF1基因座不连锁的遗传修饰因子促成了该疾病的可变表达。