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EPSTI1 polymorphisms are associated with systemic lupus erythmatosus
- 작성일2018-02-14
- 최종수정일2018-02-14
- 담당부서연구기획과
- 연락처043-719-8033
- 2,810
Genes & Genomics, 2017, 01, 445─451, DOI: https://doi.org/https://doi.org/10.1007/s13258-017-0515-x
EPSTI1 polymorphisms are associated with systemic lupus erythmatosus
Ji Su Mo, Soo Cheon Chae
Abstract
Epithelial stromal interaction 1 (EPSTI1) is an interferon (IFN) response gene, which was originally identified as a stromal fibroblast-induced gene in breast cancer. Our previous study using a customized SNP chip found evidence of an association between EPSTI1 and susceptibility to the chronic inflammatory disease, systematic lupus erythematosus (SLE). This study aimed to validate whether polymorphisms in EPSTI1 are associated with susceptibility to SLE. We analyzed genotype and allele frequencies of SNPs at EPSTI1 using genomic DNA from 119 patients with SLE and 512 healthy controls. We found that the genotype frequencies of rs1044856 and rs1359184 in patients with SLE were significantly different from those found in the control group (P = 0.03 and P = 0.01, respectively). In addition, we found that genotype and allele frequencies of rs1359184 in female patients with SLE were significantly different from those found in female controls (P = 0.02 and P = 0.04, respectively). We identified two major haplotypes in EPSTI1 that were significantly different between patients with SLE and healthy controls (P = 0.01 and P = 0.05, respectively). Furthermore, we found that rs1359184 and rs1044856 in EPSTI1 were associated with antinuclear antibody (ANA) and erythrocyte sedimentation rate (ESR) levels in patients with SLE (P = 0.0035 and P = 0.021, respectively). Our findings indicate that polymorphisms in EPSTI1 are associated with susceptibility to SLE and that haplotypes at EPSTI1 may be useful genetic markers for SLE.
- DOI: https://doi.org/https://doi.org/10.1007/s13258-017-0515-x
- ISBN or ISSN: 2092-9293
- 본 연구는 질병관리본부 연구개발과제(과제번호 2017-보건의료생물자원종합관리) 연구비를 지원받아 수행되었습니다.
- This research was supported by a fund(code 2017-보건의료생물자원종합관리) by Research of Korea Centers for Disease Control and Prevention.
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