Phenotypic and population differences in the association between CILP and lumbar disc disease
IM Virtanen, YQ Song, KMC Cheung… - Journal of medical …, 2007 - jmg.bmj.com
Journal of medical genetics, 2007•jmg.bmj.com
Background: Lumbar disc disease (LDD) is one of the leading causes of disability in the
working-age population. A functional single-nucleotide polymorphism (SNP),+ 1184T→ C, in
exon 8 of the cartilage intermediate layer protein gene (CILP) was recently identified as a
risk factor for LDD in the Japanese population (odds ratio (OR) 1.61, 95% CI 1.31 to 1.98),
with implications for impaired transforming growth factorβ1 signalling. Aim: To validate this
finding in two different ethnic cohorts with LDD. Methods: This SNP and flanking SNPs were …
working-age population. A functional single-nucleotide polymorphism (SNP),+ 1184T→ C, in
exon 8 of the cartilage intermediate layer protein gene (CILP) was recently identified as a
risk factor for LDD in the Japanese population (odds ratio (OR) 1.61, 95% CI 1.31 to 1.98),
with implications for impaired transforming growth factorβ1 signalling. Aim: To validate this
finding in two different ethnic cohorts with LDD. Methods: This SNP and flanking SNPs were …
Background: Lumbar disc disease (LDD) is one of the leading causes of disability in the working-age population. A functional single-nucleotide polymorphism (SNP), +1184T→C, in exon 8 of the cartilage intermediate layer protein gene (CILP) was recently identified as a risk factor for LDD in the Japanese population (odds ratio (OR) 1.61, 95% CI 1.31 to 1.98), with implications for impaired transforming growth factorβ1 signalling.
Aim: To validate this finding in two different ethnic cohorts with LDD.
Methods: This SNP and flanking SNPs were analysed in 243 Finnish patients with symptoms of LDD and 259 controls, and in 348 Chinese subjects with MRI-defined LDD and 343 controls.
Results and conclusion: The results showed no evidence of association in the Finnish (OR = 1.35, 95% CI 0.97 to 1.87; p = 0.14) or the Chinese (OR = 1.05, 95% CI 0.77 to 1.43; p = 0.71) samples, suggesting that cartilage intermediate layer protein gene is not a major risk factor for symptoms of LDD in Caucasians or in the general population that included individuals with or without symptoms.
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