Title of article :
A disintegrin and metalloproteinase 33 (ADAM33) gene polymorphism association with asthma in Egyptian children
Author/Authors :
el-falaki, m.m. Cairo University - pediatrics department, Egypt , wilson, m.m. Cairo University - clinical and chemical pathology department, Egypt , ezzat, g.m. Fayoum University - clinical and chemical pathology department, Egypt , mokhtar, d.a. Cairo University - clinical and chemical pathology department, Egypt , el baz, m.s. Cairo University - pediatrics department, Egypt , hamed, d.h. Cairo University - pediatrics department, Egypt
Abstract :
A disintegrin and metalloproteinase-encoding gene (ADAM33),was recently identified as an asthma susceptibility gene. ADAM33 protein is expressed in smooth muscle cells of bronchi and pulmonary fibroblasts,playing a major role in airway remodeling. Earlier studies,have mostly confirmed a link between ADAM33 and asthma as well as bronchial hyperresponsiveness. This work studied a group of Egyptian asthmatic children for 3 ADAM33 single nucleotide polymorphisms (SNPs),previously identified as putative risk alleles: T1 G . A(rs2280091),T2 A . G(rs2280090),V4 G . C(rs2787094) using Polymerase Chain Reaction - restriction fragment length polymorphism (PCRRFLP) with emphasis on their relation to clinical (severity,smoking,family history,and atopic manifestations) and laboratory data (Ig Immunoglobulin E (Ig E) level and absolute eosinophilia) and pulmonary functions. Sixty (3-12. years old) asthmatic children and 32 matched controls were recruited. The genotype distribution for the SNPs showed no significant difference between the patients and the controls. A higher frequency of the (AA) genotype of T1 polymorphism was found in controls (75%) than in patients (41%),while the (AG) variant was higher in cases (46.6%) than in controls (21.9%) but with no statistically significant difference. Also the (GG) genotype was higher in cases (11.6%) than in controls (3.1%) but with no statistical significance. The allelic frequencies of T1 showed a higher (A) allele in controls (85.93%) than cases (65%) and higher (G) allele in cases (35%) than controls (14.06%),showing a high significant difference. No correlation was found between (T1,T2,and V4) and the demographic,clinical and laboratory parameters,except SNP T1 showing a positive correlation with Ig E level,and SNP V4 showing a positive correlation with passive smoking as a precipitating factor and borderline significance with absolute eosinophilia. In conclusion,no significant association was detected between these SNPs and asthma susceptibility in this study. © 2012.
Keywords :
ADAM33 , Asthma , Eosinophilia , Ig E , PCR , Polymorphism , RFLP
Journal title :
Egyptian Journal of Medical Human Genetics
Journal title :
Egyptian Journal of Medical Human Genetics