Genetic Polymorphisms of Stromal Interaction Molecule 1 Associated with the Erythrocyte Sedimentation Rate and C-Reactive Protein in HLA-B27 Positive Ankylosing Spondylitis Patients
Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In...
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Published in | PloS one Vol. 7; no. 12; p. e49698 |
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14.12.2012
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Abstract | Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In this study, we enrolled 361 AS patients and selected four tagging single nucleotides polymorphisms (tSNPs) at STIM1 gene. The correlation between STIM1 genetic polymorphisms and AS activity index (BASDAI, BASFI, BAS-G) as well as laboratory parameters of inflammation (erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)) were tested. Our results indicated that HLA-B27 positive AS patients who are carrying the minor allele homozygous G/G genotype of SNP rs3750996 significantly associated with a higher level of ESR in serum. Furthermore, rs3750996/rs3750994 pairwise allele analysis indicated that G-C haplotypes also significantly correlated with higher level of ESR as well as CRP. These findings provide a better understanding of STIM1 genetic contribution to the pathogenesis of AS. |
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AbstractList | Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In this study, we enrolled 361 AS patients and selected four tagging single nucleotides polymorphisms (tSNPs) at STIM1 gene. The correlation between STIM1 genetic polymorphisms and AS activity index (BASDAI, BASFI, BAS-G) as well as laboratory parameters of inflammation (erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)) were tested. Our results indicated that HLA-B27 positive AS patients who are carrying the minor allele homozygous G/G genotype of SNP rs3750996 significantly associated with a higher level of ESR in serum. Furthermore, rs3750996/rs3750994 pairwise allele analysis indicated that G-C haplotypes also significantly correlated with higher level of ESR as well as CRP. These findings provide a better understanding of STIM1 genetic contribution to the pathogenesis of AS. Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In this study, we enrolled 361 AS patients and selected four tagging single nucleotides polymorphisms (tSNPs) at STIM1 gene. The correlation between STIM1 genetic polymorphisms and AS activity index (BASDAI, BASFI, BAS-G) as well as laboratory parameters of inflammation (erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)) were tested. Our results indicated that HLA-B27 positive AS patients who are carrying the minor allele homozygous G/G genotype of SNP rs3750996 significantly associated with a higher level of ESR in serum. Furthermore, rs3750996/rs3750994 pairwise allele analysis indicated that G-C haplotypes also significantly correlated with higher level of ESR as well as CRP. These findings provide a better understanding of STIM1 genetic contribution to the pathogenesis of AS.Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In this study, we enrolled 361 AS patients and selected four tagging single nucleotides polymorphisms (tSNPs) at STIM1 gene. The correlation between STIM1 genetic polymorphisms and AS activity index (BASDAI, BASFI, BAS-G) as well as laboratory parameters of inflammation (erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)) were tested. Our results indicated that HLA-B27 positive AS patients who are carrying the minor allele homozygous G/G genotype of SNP rs3750996 significantly associated with a higher level of ESR in serum. Furthermore, rs3750996/rs3750994 pairwise allele analysis indicated that G-C haplotypes also significantly correlated with higher level of ESR as well as CRP. These findings provide a better understanding of STIM1 genetic contribution to the pathogenesis of AS. Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still unclear. Genetics factors such as human leukocyte antigen HLA-B27 and ERAP1 have been widely reported to associate to AS susceptibility. In this study, we enrolled 361 AS patients and selected four tagging single nucleotides polymorphisms (tSNPs) at STIM1 gene. The correlation between STIM1 genetic polymorphisms and AS activity index (BASDAI, BASFI, BAS-G) as well as laboratory parameters of inflammation (erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)) were tested. Our results indicated that HLA-B27 positive AS patients who are carrying the minor allele homozygous G/G genotype of SNP rs3750996 significantly associated with a higher level of ESR in serum. Furthermore, rs3750996/rs3750994 pairwise allele analysis indicated that G-C haplotypes also significantly correlated with higher level of ESR as well as CRP. These findings provide a better understanding of STIM1 genetic contribution to the pathogenesis of AS. |
Audience | Academic |
Author | Wong, Ruey-Hong Wu, Shyh-Jong Huang, Chun-Huang Jan, Ming-Shiou Wei, James Cheng-Chung Chang, Wei-Chiao Hsu, Yu-Wen Hung, Kuo-Sheng Juan, Yung-Shun |
AuthorAffiliation | 8 Department of Urology, Kaohsiung municipal Hsiao-Kang Hospital and College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan 5 Department of Public Health, Chung Shan Medical University, Taichung, Taiwan 2 Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan 7 Department of Medical Laboratory Science and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung, Taiwan 6 Institute of Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan 1 Division of Allergy, Immunology and Rheumatology, Department of Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan Institut Jacques Monod, France 3 Department of Neurosurgery, Center of Excellence for Clinical Trial and Research, Graduate Institute of Injury Prevention and Control, Taipei Medical University, Wan Fang Medical Center, Taipei, Taiwan 4 Department of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan 9 Department of Pharmacy |
AuthorAffiliation_xml | – name: 4 Department of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan – name: 6 Institute of Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan – name: Institut Jacques Monod, France – name: 7 Department of Medical Laboratory Science and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung, Taiwan – name: 3 Department of Neurosurgery, Center of Excellence for Clinical Trial and Research, Graduate Institute of Injury Prevention and Control, Taipei Medical University, Wan Fang Medical Center, Taipei, Taiwan – name: 2 Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan – name: 8 Department of Urology, Kaohsiung municipal Hsiao-Kang Hospital and College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan – name: 1 Division of Allergy, Immunology and Rheumatology, Department of Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan – name: 9 Department of Pharmacy, Taipei Medical University-Wanfang Hospital, Taipei, Taiwan – name: 5 Department of Public Health, Chung Shan Medical University, Taichung, Taiwan |
Author_xml | – sequence: 1 givenname: James Cheng-Chung surname: Wei fullname: Wei, James Cheng-Chung – sequence: 2 givenname: Kuo-Sheng surname: Hung fullname: Hung, Kuo-Sheng – sequence: 3 givenname: Yu-Wen surname: Hsu fullname: Hsu, Yu-Wen – sequence: 4 givenname: Ruey-Hong surname: Wong fullname: Wong, Ruey-Hong – sequence: 5 givenname: Chun-Huang surname: Huang fullname: Huang, Chun-Huang – sequence: 6 givenname: Ming-Shiou surname: Jan fullname: Jan, Ming-Shiou – sequence: 7 givenname: Shyh-Jong surname: Wu fullname: Wu, Shyh-Jong – sequence: 8 givenname: Yung-Shun surname: Juan fullname: Juan, Yung-Shun – sequence: 9 givenname: Wei-Chiao surname: Chang fullname: Chang, Wei-Chiao |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: JW KH YH HW WC. Performed the experiments: YH CH MJ SW. Analyzed the data: YH CH YJ KH HW WC. Contributed reagents/materials/analysis tools: WC YJ JW KH. Wrote the paper: WC HW JW YH. |
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Snippet | Ankylosing spondylitis (AS) is a chronic inflammation of the sacroiliac joints, spine and peripheral joints. The development of ankylosing spondylitis is still... |
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SubjectTerms | Adolescent Adult Aged Alleles Ankylosing spondylitis Antigens Arthritis B cells Biology Blood Sedimentation C-reactive protein C-Reactive Protein - genetics Deoxyribonucleic acid DNA Enzymes Erythrocyte sedimentation rate Erythrocytes Genes Genetic aspects Genetics Genotype Haplotypes Histocompatibility antigen HLA HLA antigens HLA-B27 Antigen - biosynthesis Homozygote Hospitals Humans Immunology Inflammation Interleukin-6 - metabolism Joint diseases Laboratories Leukocytes Medical research Medical schools Medicine Membrane Proteins - genetics Membrane Proteins - metabolism Middle Aged Neoplasm Proteins - genetics Neoplasm Proteins - metabolism Nucleotides Pathogenesis Patients Pharmacy Polymorphism, Genetic Polymorphism, Single Nucleotide Proteins Sequence Analysis, DNA Severity of Illness Index Single nucleotide polymorphisms Single-nucleotide polymorphism Spine Spondylitis Spondylitis, Ankylosing - diagnosis Spondylitis, Ankylosing - genetics STIM1 protein Stromal Interaction Molecule 1 Studies Tagging Tumor Necrosis Factor-alpha - metabolism Tumor necrosis factor-TNF |
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Title | Genetic Polymorphisms of Stromal Interaction Molecule 1 Associated with the Erythrocyte Sedimentation Rate and C-Reactive Protein in HLA-B27 Positive Ankylosing Spondylitis Patients |
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