Joint Analysis of SNPs and Proteins Identifies Regulatory IL18 Gene Variations Decreasing the Chance of Spastic Cerebral Palsy. Issue 1 (4th September 2012)

• Record Type: Journal Article
• Authors: Hollegaard, Mads Vilhelm; Skogstrand, Kristin; Thorsen, Poul; Nørgaard‐Pedersen, Bent; Hougaard, David Michael; Grove, Jakob
• Is Part Of: Human mutation. Volume 34:Issue 1(2013:Jan.)
• Page Start: 143
• Page End: 148
• Publication Date: 2012-09-04
• Subjects: Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.22173
• Languages: English
• ISSNs: 1059-7794

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Cerebral palsy (CP) is a permanent disorder, affecting 2–3 per 1, 000 live born children, disturbing movement and posture. Spastic limbs affects about 70–80% of the CP children, and this group is the target of our study. CP is considered a multifactorial condition believed to be provoked by, for example, preterm birth, infection during pregnancy, neural disorders, and genetics, to mention some. Interestingly, the cytokine network is believed to be involved in many of these disorders. In this study, including 203 spastic CP cases and 167 controls, we measured the levels of 25 cytokine proteins, and genotyped 159 SNPs in their gene loci. Using logistic regression, we estimated the genetic association of SNP genotypes to spastic CP. In addition, fitting a Tobit regression model for each protein and each SNP in the respective gene loci, we estimated three regression coefficients corresponding three different effects of the genetic variation on the protein level. Intriguingly, two <italic>IL18</italic> loci SNPs (rs549908:A&gt;C and rs1290349:C&gt;A) showed a protective effect against spastic CP, and interestingly both were associated to a decreased epidemiological expression of IL‐18 protein. By joining protein data to genetic information, we have provided new data suggesting <italic>IL18</italic>'s involvement in the pathogenesis of spastic CP.</p> </abstract>