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dc.contributor.authorGümüş, Evren
dc.contributor.authorTemiz, Ebru
dc.contributor.authorSarıkaya, Baran
dc.contributor.authorYüksekdağ, Özgür
dc.contributor.authorSipahioğlu, Serkan
dc.contributor.authorGönel, Ataman
dc.date.accessioned2020-11-20T14:30:06Z
dc.date.available2020-11-20T14:30:06Z
dc.date.issued2020
dc.identifier.issn0019-5413
dc.identifier.issn1998-3727
dc.identifier.urihttps://doi.org/10.1007/s43465-020-00235-y
dc.identifier.urihttps://hdl.handle.net/20.500.12809/359
dc.descriptionWOS: 000564212500004en_US
dc.description.abstractObjective 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 (CX3CR1), ubiquinol-cytochrome c reductase complex assembly factor 1 (UQCC1) and growth/differentiation factor 5 (GDF5), 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 ofCX3CR1rs3732378 andUQCC1rs6060373, which have been shown to be associated with DDH in different populations. In addition, we aimed to investigate theBMP-2rs235768 polymorphism which has not been investigated in the etiology of DDH. Methods 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. Results ForCX3CR1rs3732378 polymorphism, significant differences were observed in genotypes and allele frequencies (p < 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. Conclusions 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 betweenBMP-2rs235768 polymorphism and DDH. Our study revealed a clear relationship betweenCX3CR1rs3732378 polymorphism and DDH in Turkish population.en_US
dc.description.sponsorshipHarran UniversitesiHarran University [18239]en_US
dc.description.sponsorshipFunding was provided by Harran Universitesi (Grant No. 18239).en_US
dc.item-language.isoengen_US
dc.publisherSpringer Heidelbergen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDevelopmental Dysplasia of the Hipen_US
dc.subjectSingle-Nucleotide Polymorphismen_US
dc.subjectBMP-2en_US
dc.subjectUQCC1en_US
dc.subjectCX3CR1en_US
dc.titleThe Association BetweenBMP-2,UQCC1andCX3CR1Polymorphisms and the Risk of Developmental Dysplasia of the Hipen_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.identifier.doi10.1007/s43465-020-00235-y
dc.relation.journalIndian Journal of Orthopaedicsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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