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Association Between Osteopontin Gene Polymorphisms and Cerebral Palsy in a Chinese Population

Shang, Q. (author)
Zhou, C. C. (author)
Liu, D. Z. (author)
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Li, W. X. (author)
Chen, M. J. (author)
Xu, Y. R. (author)
Wang, F. (author)
Bi, D. (author)
Zhang, X. L. (author)
Zhao, X. Z. (author)
Wang, L. (author)
Zhu, Changlian, 1964 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering,Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Xing, Q. H. (author)
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 (creator_code:org_t)
2016-04-25
2016
English.
In: Neuromolecular Medicine. - : Springer Science and Business Media LLC. - 1535-1084 .- 1559-1174. ; 18:2, s. 232-238
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Cerebral palsy (CP) is a neurological disorder affecting movement and posture that develops as a complication of prenatal, perinatal, and postnatal brain injury. Such non-progressive brain injury is often accompanied by neonatal encephalopathy and inflammation. The widely expressed soluble cytokine osteopontin (OPN) plays an important role in inflammation and neurological protection. Therefore, it is of great interest to study the relationship between CP and genetic variants of OPN. To explore the genetic association between OPN gene single nucleotide polymorphisms (SNPs) and CP in the Chinese Han population, five SNPs (rs2853744, rs2853749, rs11728697, rs4754, and rs1126616) were genotyped among 715 CP patients and 658 healthy controls using the MassArray platform. Statistical analysis was performed using the online SHEsis program, and Bonferroni correction was applied as necessary. We found an association between rs1126616 and global CP (corrected allelic P = 0.0006 and genotypic P = 0.0011 after Bonferroni correction). The other SNPs were not statistically associated with CP or any of its subgroups. By testing a relatively large sample size, our study demonstrates that the OPN gene SNP rs1126616 is statistically associated with CP. We suspect that the OPN gene might be a susceptibility factor for CP.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

Cerebral palsy
Osteopontin
Association
SNP
near-term infants
brain-injury
inflammation
risk
spp1
urolithiasis
immunity
update
damage
shesis
Neurosciences & Neurology

Publication and Content Type

ref (subject category)
art (subject category)

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