Cited by 39Rheumatoid Arthritis Research and TherapiesGenetic Associations and EpidemiologyAutoimmune and Inflammatory Disorders Research

Interleukin-6-174G > C (rs1800795) polymorphism distribution and its association with rheumatoid arthritis: a case-control study and meta-analysis

Dar, Sajad Ahmad, Haque, Shafiul, Mandal, Raju Kumar, Singh, Taru, Wahid, Mohd, Jawed, Arshad, Panda, Aditya K., Akhter, Naseem +7 more·2017·Autoimmunity

Abstract

The association of interleukin-6 (IL-6)-174G > C (rs1800795) single nucleotide polymorphism (SNP) with the risk of acquiring rheumatoid arthritis (RA) is a relevant issue because of conflicting and consensus lacking reports published in literature. We investigated IL-6-174G > C promoter polymorphism in 34 RA patients, attending a tertiary care hospital in north India. We also performed a meta-analysis, of the previously published studies reporting this genetic relationship, in overall population, and independently in Asian and Caucasian ethnicities to further elucidate this association. A total of 13 studies, including the current one, involving 3291 RA cases and 3812 controls were analyzed. Out of the 13 studies, 6 were from Asian, 6 from Caucasian and 1 from a mixed population. Our case-control study showed significant association of IL-6-174G > C SNP with increased RA risk: allelic (OR = 3.750, 95% CI = 1.800-7.813, p C SNP in overall population: allelic (OR = 1.650, 95% CI = 1.169-2.329, p = 0.004); homozygous (OR = 1.380, 95% CI = 0.906-2.101, p = 0.133); heterozygous (OR = 1.559, 95% CI = 1.001-2.428, p = 0.049); dominant (OR = 1.663, 95% CI = 1.078-2.567, p = 0.022); and recessive (OR = 1.366, 95% CI = 0.964-1.935, p = 0.079). Subgroup analysis also showed this polymorphism to be associated with increased RA risk in Asian population: allelic (OR = 3.724, 95% CI = 1.361-10.190, p = 0.010); dominant (OR = 3.823, 95% CI = 1.320-11.074, p = 0.013); and recessive (OR = 4.35…

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Crossref · 10.1080/08916934.2016.1261833

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  • GWAS, meta-analysis, exome analysis and SNP mapping have associated IL-6, IL-6R and gp130 with inflammatory diseases such as RA and coronary artery disease.

    “Genome-wide association studies (GWAS), meta-analysis, exome analysis and single nucleotide polymorphism (SNP) mapping have associated IL-6, IL-6R and gp130 with inflammatory diseases such as RA and coronary artery disease (263–269).”

    From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [263]

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Authors
Dar, S. A., Haque, S., Mandal, R. K., Singh, T., Wahid, M., Jawed, A., Panda, A. K., Akhter, N., Lohani, M., Areeshi, M. Y., Rai, G., Datt, S., Bhattacharya, S. N., Ramachandran, V. G., & Das, S.
Affiliations
  • University of Delhi (IN)
  • Jazan University (SA)
  • Central University of Jharkhand (IN)
  • ,
Corresponding author
Das, Shukla
Venue
Autoimmunity
Published
2016-12-23
Volume
50
Issue
3
Pages
158-169
ISSN
  • 0891-6934 (ISSN-L)
  • 1607-842X
OpenAlex
W2565946906
Cited by
38
References
0
Citations by year
2026: 1 · 2025: 2 · 2024: 5 · 2023: 3 · 2022: 8 · 2021: 6 · 2020: 7 · 2019: 1 · 2018: 4 · 2017: 1
FWCI
2.13
Type
journal article
Language
en
Open access
closed
Locations
  • Autoimmunity (publishedVersion)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Funders
University Grants Commission
Topics
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Health Sciences › Medicine › Hematology › Autoimmune and Inflammatory Disorders Research
Keywords
rheumatoid arthritis, interleukin-6, IL-6 -174 G/C polymorphism, rs1800795, promoter polymorphism, genetic susceptibility, single nucleotide polymorphisms, disease risk association, Asian populations, Caucasian population, ethnic differences in genetic association, meta-analysis of genetic association studies
MeSH terms
Alleles, Arthritis, Rheumatoid, Genotype, Humans, Interleukin-6, Odds Ratio, Case-Control Studies, Publication Bias, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Population Groups, Genetic Association Studies

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