Lin Pei-Chin, Su Yi-Ning, Liao Yu-Mei, Chang Tai-Tsung, Tsai Shih-Pien, Shu Hsiu-Lan, Chiou Shyh-Shin
Division of Pediatric Hematology and Oncology, Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan; Department of Pediatrics, School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan.
Kaohsiung J Med Sci. 2014 Apr;30(4):187-93. doi: 10.1016/j.kjms.2013.12.003. Epub 2014 Jan 6.
Hemophilia B (HB) is an X-linked recessive disorder characterized by mutations in the clotting factor IX (FIX) gene that result in FIX deficiency. Previous studies have shown a wide variation of FIX gene mutations in HB. Although the quality of life in HB has greatly improved mainly because of prophylactic replacement therapy with FIX concentrates, there exists a significant burden on affected families and the medical care system. Accurate detection of FIX gene mutations is critical for genetic counseling and disease prevention in HB. In this study, we used denaturing high-performance liquid chromatography (DHPLC), which has proved to be a highly informative and practical means of detecting mutations, for the molecular diagnosis of our patients with HB. Ten Taiwanese families affected by HB were enrolled. We used the DHPLC technique followed by direct sequencing of suspected segments to detect FIX gene mutations. In all, 11 FIX gene mutations (8 point mutations, 2 small deletions/insertions, and 1 large deletion), including two novel mutations (exon6 c.687-695, del 9 mer and c.460-461, ins T) were found. According to the HB pedigrees, 25% and 75% of our patients were defined as familial and sporadic HB cases, respectively. We show that DHPLC is a highly sensitive and cost-effective method for FIX gene analysis and can be used as a convenient system for disease prevention.
血友病B(HB)是一种X连锁隐性疾病,其特征是凝血因子IX(FIX)基因突变导致FIX缺乏。先前的研究表明,HB中FIX基因突变存在广泛差异。尽管主要由于使用FIX浓缩物进行预防性替代治疗,HB患者的生活质量有了很大提高,但受影响家庭和医疗系统仍承受着巨大负担。准确检测FIX基因突变对于HB的遗传咨询和疾病预防至关重要。在本研究中,我们使用变性高效液相色谱法(DHPLC)对HB患者进行分子诊断,该方法已被证明是一种检测突变的信息丰富且实用的手段。招募了10个受HB影响的台湾家庭。我们采用DHPLC技术,随后对可疑片段进行直接测序以检测FIX基因突变。总共发现了11种FIX基因突变(8个点突变、2个小缺失/插入和1个大缺失),包括两种新突变(外显子6 c.687 - 695,del 9 mer和c.460 - 461,ins T)。根据HB谱系,我们的患者分别有25%和75%被定义为家族性和散发性HB病例。我们表明,DHPLC是一种用于FIX基因分析的高度灵敏且经济高效的方法,可作为一种方便的疾病预防系统。