Cheong Hyun Sub, Park Choon-Sik, Kim Lyoung Hyo, Park Byung Lae, Uh Soo-Taek, Kim Yong Hooun, Lym Gune-Il, Lee Jong-Young, Lee Jong-Keuk, Kim Hung Tae, Ryu Ha-Jung, Han Bok Ghee, Kim Jun Woo, Park Chan, Kimm Kuchan, Shin Hyoung Doo, Oh Bermseok
Department of Genetic Epidemiology, SNP Genetics, Inc., WooLim Lion's Valley, 371-28, Seoul 153-803, Republic of Korea.
Biochem Biophys Res Commun. 2005 Sep 9;334(4):1219-25. doi: 10.1016/j.bbrc.2005.07.019.
The chemokine (C-X-C motif) receptor 3 (CXCR3) gene, on chromosome Xq13, is known to have critical roles in inflammatory and immune responses. In an effort to discover polymorphisms have been implicated in asthma, we investigated the genetic polymorphisms in CXCR3 to evaluate it as a potential candidate gene for a host genetic study of asthma. Statistical analysis revealed that one SNP in intron 1, c.12+234G > A, showed significant association with the risk of asthma development (P = 0.007, OR = 0.81). By subgroup analyses stratified by gender and atopic status, the genetic effect of c.12+234G > A on asthma was more apparent among male atopic subjects (P = 0.0009, OR = 0.61). Our findings suggest that polymorphisms in CXCR3 might be one of the genetic factors for the risk of asthma development, especially in male atopic subjects. CXCR3 variation/haplotype information identified in this study will provide valuable information and insight into strategies for the control of asthma and its subgroup, atopy.