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Variants of the OLI...
Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic-Ischemic Encephalopathy
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Sun, L. Y. (författare)
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Xia, L. (författare)
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Wang, M. T. (författare)
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Zhu, D. N. (författare)
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Wang, Y. G. (författare)
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Bi, D. (författare)
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Song, J. (författare)
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Ma, C. Y. (författare)
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Gao, C. (författare)
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Zhang, X. L. (författare)
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Sun, Y. Y. (författare)
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Wang, X. Y. (författare)
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- Zhu, Changlian, 1964 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology
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Xing, Q. H. (författare)
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(creator_code:org_t)
- 2018-09-03
- 2019
- Engelska.
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Ingår i: Neuromolecular Medicine. - : Springer Science and Business Media LLC. - 1535-1084 .- 1559-1174. ; 21:1, s. 75-84
- Relaterad länk:
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https://gup.ub.gu.se...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Cerebral palsy (CP) is a leading cause of neurological disability among young children. Congenial and adverse perinatal clinical conditions, such as genetic factors, perinatal infection, and asphyxia, are risk factors for CP. Oligodendrocyte transcription factor (OLIG2) is a protein that is expressed in brain oligodendrocyte cells and is involved in neuron repair after brain injury. In this study, we employed a Chinese Han cohort of 763 CP infants and 738 healthy controls to study the association of OLIG2 gene polymorphisms with CP. We found marginal association of the SNP rs6517135 with CP (p=0.044) at the genotype level, and the association was greatly strengthened when we focused on the subgroup of CP infants who suffered from hypoxic-ischemic encephalopathy (HIE) after birth, with p=0.003 (OR=0.558) at the allele level and p=0.007 at the genotype level, indicating a risk-associated role of the T allele of the SNP rs6517135 under HIE conditions. The haplotype CTTG for rs6517135-rs1005573-rs6517137-rs9653711 in OLIG2 was also significantly associated with the occurrence of CP in infants with HIE (p=0.01, OR=0.521). Our results indicate that in the Han Chinese population, the polymorphisms of OLIG2 were associated with CP, especially in patients who had suffered HIE injury. This finding could be used to develop personalized care for infants with high susceptibility to CP.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
Nyckelord
- Cerebral palsy
- OLIG2
- HIE
- SNP
- Hypoxia
- Ischemia
- white-matter injury
- transcription factor
- gestational-age
- birth-weight
- lineage
- prevalence
- expression
- differentiation
- erythropoietin
- proliferation
- Neurosciences & Neurology
- ates of america
- v103
- p12469
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
Till lärosätets databas
- Av författaren/redakt...
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Sun, L. Y.
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Xia, L.
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Wang, M. T.
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Zhu, D. N.
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Wang, Y. G.
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Bi, D.
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visa fler...
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Song, J.
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Ma, C. Y.
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Gao, C.
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Zhang, X. L.
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Sun, Y. Y.
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Wang, X. Y.
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Zhu, Changlian, ...
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Xing, Q. H.
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visa färre...
- Om ämnet
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- MEDICIN OCH HÄLSOVETENSKAP
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MEDICIN OCH HÄLS ...
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och Klinisk medicin
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och Neurologi
- Artiklar i publikationen
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Neuromolecular M ...
- Av lärosätet
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Göteborgs universitet