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Mol Biol Rep ; 39(12): 10723-9, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23053969

ABSTRACT

This study examined firstly the possible association of G241R and K469E single nucleotide polymorphisms (SNPs) of ICAM-1 gene with the occurrence of Hashimoto thyroiditis (HT). G241R and K469E SNPs in DNA from peripheral blood leukocytes of 190 HT and 247 healthy controls were investigated by real-time PCR combined with melting curve analysis using fluorescence-labeled hybridization probes. There was a significant increase of ICAM-1 241R allele frequency in patients with HT compared with healthy controls (P = 0.04, OR = 1.84, 95 % CI = 1.00-3.37). Regarding ICAM-1 K469E polymorphism, patients homozygous for E allele had 1.73-fold increased risk for developing HT according to KK homozygotes (P = 0.04, 95 % CI = 1.00-3.01). The 469E allele frequency was higher in HT patients according to controls, however the difference was at borderline significance (P = 0.05, OR = 1.30, 95 % CI = 1.00-1.70). No associations between polymorphisms and HT phenotypes were observed. We suggest that the G241R and K469E SNPs of ICAM-1 gene may be related to occurrence of HT. However, more studies with larger sample size including other loci of the ICAM-1 gene are necessary to support our findings before any definite statement can be made about the relationship between HT and ICAM-1 polymorphism.


Subject(s)
Amino Acid Substitution/genetics , Genetic Predisposition to Disease , Hashimoto Disease/genetics , Intercellular Adhesion Molecule-1/genetics , Polymorphism, Single Nucleotide/genetics , Adolescent , Adult , Aged , Case-Control Studies , Female , Gene Frequency/genetics , Hashimoto Disease/blood , Humans , Intercellular Adhesion Molecule-1/blood , Lipids/blood , Male , Middle Aged , Thyroid Hormones/blood , Young Adult
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