HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

An association study between the Clara cell secretory protein CC16 A38G polymorphism and asthma phenotypes.

AbstractBACKGROUND:
Previously, an association has been reported between an increased risk of asthma and a polymorphism in the Clara cell secretory protein (CC16) gene [namely, an adenine to guanine substitution in the CC16 gene at position 38 (A38G) downstream from the transcription initiation site within the noncoding region of exon 1]. Homozygous individuals for the polymorphic sequence (AA genotype) were reported to have a significant (6.9 fold) increased risk of developing asthma. This finding has not been confirmed independently.
OBJECTIVE:
To validate the association of CC16 A38G polymorphism to asthma in a separate well-characterized population through a case-control study.
METHODS:
We conducted an association study using a sample of 217 unrelated Northern European Caucasians. Individuals were clinically characterized by a validated respiratory questionnaire, spirometry and bronchial reactivity measurement, and genotyped for the A38G polymorphism using PCR and restriction digestion. Association analysis was performed using the nonparametric Chi-squared tests.
RESULTS:
In the unselected population, 43.3% participants were homozygous for the CC16*G allele and 45.4% were heterozygous (AG). We observed no significant difference in the distribution of positive bronchial reactivity to methacholine (at FEV1 PC20 of </= 8 mg/mL) across the three genotypes. Homozygous individuals for the CC16*A allele did not demonstrate an increased risk of asthma when compared to heterozygous or GG homozygotes. In addition, no significant difference was observed in the distribution of the CC16*A or *G alleles in the asthmatics vs. non-asthmatics.
CONCLUSION:
CC16 polymorphism A38G does not influence the predisposition to asthma in this sample.
AuthorsA H Mansur, A A Fryer, M Hepple, R C Strange, M A Spiteri
JournalClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology (Clin Exp Allergy) Vol. 32 Issue 7 Pg. 994-9 (Jul 2002) ISSN: 0954-7894 [Print] England
PMID12100044 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Proteins
  • SCGB1A1 protein, human
  • Uteroglobin
Topics
  • Adolescent
  • Adult
  • Asthma (genetics)
  • Bronchial Hyperreactivity (genetics)
  • Chromosome Mapping
  • Female
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Phenotype
  • Polymorphism, Genetic
  • Proteins (genetics)
  • Uteroglobin

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: