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A polymorphic variant of the endoglin gene is associated with increased risk for intracranial aneurysms in a Korean population

Cited 8 time in Web of Science Cited 9 time in Scopus
Authors
Joo, Sung-Pil; Lee, Jung-Kil; Kim, Tae-Sun; Kim, Myeong-Kyu; Lee, Il-Kwon; Seo, Bo-Ra; Kim, Jae-Hyoo; Kim, Soo-Han; Oh, Chang-Wan
Issue Date
2008-04-29
Publisher
Elsevier
Citation
Surg Neurol. 2008;70(1):39-44
Keywords
AdolescentAdultAgedAged, 80 and overAntigens, CD/*geneticsAsian Continental Ancestry Group/*geneticsCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansIntracranial Aneurysm/diagnosis/*ethnology/*geneticsKoreaMaleMiddle AgedMutagenesis, Insertional/geneticsPolymorphism, Single Nucleotide/*geneticsReceptors, Cell Surface/*geneticsRisk Assessment
Abstract
BACKGROUND: Endoglin is a component of the transforming growth factor-beta receptor complex and is predominantly expressed on the cell surface of endothelial cells. It plays an important role in vascular growth and development. There have been conflicting reports on whether a polymorphic variant, in the endoglin gene, is associated with risk for IAs. In this study, we investigated whether polymorphisms of the endoglin gene are associated with the development of cerebral aneurysms in a Korean population. METHODS: This was a hospital-based, case-control study conducted at the Chonnam University Hospital, Gwangju, Korea. The study population consisted of 342 patients who had been treated for intracranial aneurysm and 253 healthy, hospital-based controls. Two polymorphic loci were amplified by polymerase chain reaction. The well-known in/del in intron 7 of the endoglin gene and the rs1800956 coding nonsynonymous SNP were amplified by PCR and analyzed by MADGE or the pyrosequencing system. RESULTS: The endoglin insertion polymorphism was not associated with IAs in comparisons between cases and controls (OR, 0.11 [95% CI, 0.79-1.57] vs OR, 0.88 [95% CI, 0.50-1.56]). An association was found with rs1800956 in the heterozygous type (OR, 1.71); however, the association was not evident for the homozygous type. These differences were statistically significant. In addition, the C allele was significantly associated with an increased risk for IAs (OR, 1.73). CONCLUSION: The rs1800956 (G/C transversion with D366H substitution, National Center for Biotechnology Information SNP database) of endoglin may play an important role in the pathogenesis of IAs in the Korean population. However, the in/del of intron 7 was not associated with an increased risk for IAs, which is consistent with the findings of previous reports.
ISSN
0090-3019 (Print)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=18440621

http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6TCB-4SCTMV4-W-1&_cdi=5166&_user=168665&_orig=search&_coverDate=07%2F31%2F2008&_sk=999299998&view=c&wchp=dGLbVtb-zSkWb&md5=9649ae68b850033ee7471dc894ca2f39&ie=/sdarticle.pdf

http://hdl.handle.net/10371/68412
DOI
https://doi.org/10.1016/j.surneu.2008.01.060
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College of Medicine/School of Medicine (의과대학/대학원)Neurosurgery (신경외과학전공)Journal Papers (저널논문_신경외과학전공)
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