Melo Uirá S, Santos Silvana, Cavalcanti Hannalice G, Andrade Wagner T, Dantas Vitor G, Rosa Marine Rd, Mingroni-Netto Regina C
Departamento de Genética e Biologia Evolutiva da Universidade de São Paulo, São Paulo, Brazil.
Núcleo de Estudos em Genética e Educação da Universidade Estadual da Paraíba,Paraíba, Brazil.
Int J Mol Epidemiol Genet. 2014 Feb 17;5(1):11-21. eCollection 2014.
The overall aim of this study was to estimate the contribution of genetic factors to the etiology of hearing loss (HL) in two counties in the Brazilian northeastern region. A cross-sectional study, based on the key informant approach (KI) was conducted in Queimadas and Gado Bravo counties (Paraíba, Northeast Brazil). The sample consisted of 182 patients with HL. Genetic screening of the most frequent mutations associated with HL was performed for all samples. DFNB1 mutations were the most frequently found in both counties. The c.35delG mutation was detected in homozygosis in seven non-syndromic probands in Queimadas (7/76, 9.2%) and only a single homozygote with this mutation was found in Gado Bravo (1/44, 2.3%). We also detected the del(GJB6-D13S1854) mutation in non-syndromic probands from Gado Bravo (2/44, 4.5%). The c.189C>A (p.TyrY63*) mutation in the CLRN1 gene was detected in homozygosis in 21/23 Usher syndrome patients from Gado Bravo and it was not found in Queimadas. Cases with probable genetic etiology contributed approximately to half of HL probands in each county (54.6% in Gado Bravo and 45.7% in Queimadas). We confirm the importance of DFNB1 locus to non-syndromic HL but we show that the frequency of mutations in the northeastern region differs somewhat from those reported in southeastern Brazil and other populations. In addition, the extremely high frequency of individuals with Usher syndrome with c.189C>A variation in CLRN1 indicates the need for a specific screening of this mutation.
本研究的总体目标是评估遗传因素对巴西东北部两个县听力损失(HL)病因的影响。采用关键信息提供者方法(KI),在奎马达斯县和加多布拉沃县(巴西东北部帕拉伊巴州)开展了一项横断面研究。样本包括182例HL患者。对所有样本进行了与HL相关的最常见突变的基因筛查。DFNB1突变在两个县均最为常见。在奎马达斯县,7例非综合征先证者中检测到纯合子c.35delG突变(7/76,9.2%),而在加多布拉沃县仅发现1例该突变的纯合子(1/44,2.3%)。我们还在加多布拉沃县的非综合征先证者中检测到del(GJB6-D13S1854)突变(2/44,4.5%)。在加多布拉沃县的21/23例Usher综合征患者中检测到CLRN1基因的纯合子c.189C>A(p.TyrY63*)突变,奎马达斯县未发现。每个县中可能由遗传病因导致的病例约占HL先证者的一半(加多布拉沃县为54.6%,奎马达斯县为45.7%)。我们证实了DFNB1位点对非综合征HL的重要性,但表明东北地区的突变频率与巴西东南部及其他人群报道的有所不同。此外,CLRN1基因c.189C>A变异的Usher综合征患者频率极高,表明需要对该突变进行特异性筛查。