Gumus Evren, Temiz Ebru, Sarikaya Baran, Yuksekdag Ozgur, Sipahioglu Serkan, Gonel Ataman
Department of Medical Genetics, Faculty of Medicine, University of Harran, Sanliurfa, Turkey.
Department of Medical Genetics, Faculty of Medicine, University of Mugla Sitki Kocman, Mugla, 48000 Turkey.
Indian J Orthop. 2020 Aug 29;55(1):169-175. doi: 10.1007/s43465-020-00235-y. eCollection 2021 Feb.
Developmental dysplasia of the hip (DDH) is a complicated skeletal disease ranging from subluxation to complete dislocation of the hip as a result of insufficient development of the acetabulum and femur. To date, numerous genes such as C-X3-C motif chemokine receptor 1 (), ubiquinol-cytochrome c reductase complex assembly factor 1 () and growth/differentiation factor 5 (), have been investigated to elucidate the underlying genetic etiology. Turkish population is one of the communities where DDH patients frequently observed, but almost no study has been conducted to elucidate the genetic etiology. In our study, we aimed to investigate the polymorphism of rs3732378 and rs6060373, which have been shown to be associated with DDH in different populations. In addition, we aimed to investigate the - rs235768 polymorphism which has not been investigated in the etiology of DDH.
Overall, 168 subjects (68 participants in the patient group, 100 participants in the control group) were investigated. The participants with following evidence and symptoms were excluded from the two groups: any systemic syndrome, another congenital anomaly, hereditary diseases, breech presentation, history of oligohydramnios, swaddling and high birth weight (> 4000 g). 3 single-nucleotide polymorphisms (SNP) were examined by qRT-PCR method.
For rs3732378 polymorphism, significant differences were observed in genotypes and allele frequencies (< 0.0001). This condition was associated with a 12-fold increased risk in recessive modeling and 75-fold increased risk in dominant modeling. There was no significant relationship between DDH and the other two polymorphisms.
Our work is the first study to investigate DDH and genetic polymorphisms in Turkish population where DDH is observed quite frequently. It is also the first study to investigate the relationship between - rs235768 polymorphism and DDH. Our study revealed a clear relationship between rs3732378 polymorphism and DDH in Turkish population.
发育性髋关节发育不良(DDH)是一种复杂的骨骼疾病,由于髋臼和股骨发育不足,可导致髋关节从半脱位到完全脱位。迄今为止,人们已经研究了许多基因,如C-X3-C基序趋化因子受体1()、泛醇-细胞色素c还原酶复合体组装因子1()和生长/分化因子5(),以阐明潜在的遗传病因。土耳其人群是经常观察到DDH患者的群体之一,但几乎没有研究致力于阐明其遗传病因。在我们的研究中,我们旨在调查rs3732378和rs6060373的多态性,这两种多态性已被证明在不同人群中与DDH相关。此外,我们旨在研究尚未在DDH病因中进行调查的rs235768多态性。
总共调查了168名受试者(患者组68名参与者,对照组100名参与者)。两组中具有以下证据和症状的参与者被排除:任何全身综合征、另一种先天性异常、遗传性疾病、臀位、羊水过少病史、襁褓包裹和高出生体重(>4000克)。通过qRT-PCR方法检测3个单核苷酸多态性(SNP)。
对于rs3732378多态性,在基因型和等位基因频率方面观察到显著差异(<0.0001)。这种情况在隐性模型中与风险增加12倍相关,在显性模型中与风险增加75倍相关。DDH与其他两种多态性之间没有显著关系。
我们的工作是第一项在DDH相当常见的土耳其人群中研究DDH和基因多态性的研究。这也是第一项研究rs235768多态性与DDH之间关系的研究。我们的研究揭示了土耳其人群中rs3732378多态性与DDH之间的明确关系。