Influence of interleukin-6 gene −174G>C polymorphism on development of atherosclerosis: A meta-analysis of 50 studies involving 33,514 subjects

Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Sci...

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Published inGene Vol. 529; no. 1; pp. 94 - 103
Main Authors Yin, Yan-Wei, Li, Jing-Cheng, Zhang, Meng, Wang, Jing-Zhou, Li, Bing-Hu, Liu, Yun, Liao, Shao-Qiong, Zhang, Ming-Jie, Gao, Chang-Yue, Zhang, Li-Li
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 15.10.2013
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Online AccessGet full text
ISSN0378-1119
1879-0038
1879-0038
DOI10.1016/j.gene.2013.07.074

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Abstract Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene −174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene −174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94–1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85–1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84–1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97–1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene −174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06–1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61–0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38–0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45–0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00–1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04–1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene −174GC polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution. •We performed a meta-analysis to derive a more precise estimation of the relationship.•Our study has the potential to detect small effects in genetic association studies.•Our study suggests that IL-6 gene −174G>C polymorphism is associated with AS risk.
AbstractList Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene −174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene −174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94–1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85–1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84–1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97–1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene −174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06–1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61–0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38–0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45–0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00–1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04–1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene −174GC polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution.
Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene -174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene -174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene -174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94-1.11, p =0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85-1.21, p =0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84-1.12, p =0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97-1.17, p =0.18). In the subgroup analyses, significant associations were found between the IL-6 gene -174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06-1.41, p =0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61-0.93, p =0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38-0.81, p =0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45-0.79, p =0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00-1.18, p =0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04-1.27, p =0.005). In summary, the present meta-analysis suggests that the IL-6 gene -174GC polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution.
Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene −174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene −174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94–1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85–1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84–1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97–1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene −174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06–1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61–0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38–0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45–0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00–1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04–1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene −174GC polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution. •We performed a meta-analysis to derive a more precise estimation of the relationship.•Our study has the potential to detect small effects in genetic association studies.•Our study suggests that IL-6 gene −174G>C polymorphism is associated with AS risk.
Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene -174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene -174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene -174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94-1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85-1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84-1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97-1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene -174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06-1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61-0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38-0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45-0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00-1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04-1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene -174G C polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution.Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene -174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene -174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene -174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94-1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85-1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84-1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97-1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene -174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06-1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61-0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38-0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45-0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00-1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04-1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene -174G C polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution.
Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene -174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene -174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene -174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94-1.11, p=0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85-1.21, p=0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84-1.12, p=0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97-1.17, p=0.18). In the subgroup analyses, significant associations were found between the IL-6 gene -174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06-1.41, p=0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61-0.93, p=0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38-0.81, p=0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45-0.79, p=0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00-1.18, p=0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04-1.27, p=0.005). In summary, the present meta-analysis suggests that the IL-6 gene -174G C polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution.
Author Liao, Shao-Qiong
Zhang, Li-Li
Wang, Jing-Zhou
Yin, Yan-Wei
Zhang, Ming-Jie
Gao, Chang-Yue
Li, Jing-Cheng
Zhang, Meng
Li, Bing-Hu
Liu, Yun
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2013 Elsevier B.V. All rights reserved.
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ID FETCH-LOGICAL-c361t-26342a9e4a4df0414e62ff5823d592da13bce81bc109b5d2b8c574c49925a0653
IEDL.DBID AIKHN
ISSN 0378-1119
1879-0038
IngestDate Fri Sep 05 05:43:29 EDT 2025
Fri Sep 05 07:06:34 EDT 2025
Fri Sep 05 09:06:05 EDT 2025
Mon Jul 21 06:04:04 EDT 2025
Tue Jul 01 01:22:41 EDT 2025
Thu Apr 24 22:56:45 EDT 2025
Wed Dec 27 19:17:59 EST 2023
Fri Feb 23 02:23:20 EST 2024
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords RAO
AAA
PAOD
OR
RAS
CI
CAD
PRISMA
MeSH
IS
TIA
IL-6
Interleukin-6
Meta-analysis
AS
PAD
NOS
HWE
Atherosclerosis
MI
CVDs
CHD
Polymorphism
coronary artery disease
Preferred Reporting Items for Systematic Reviews and Meta-analyses
myocardial infarction
odds ratio
abdominal aortic aneurysm
Newcastle-Ottawa Scale
Hardy–Weinberg equilibrium
ischemic stroke
Medical Subject Heading
retinal artery occlusion
peripheral artery occlusive disease
cardiovascular diseases
peripheral Arterial Disease
transient ischemic attack, CAS carotid artery stenosis
renal artery stenosis
confidence interval
coronary heart disease
Language English
License 2013 Elsevier B.V. All rights reserved.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c361t-26342a9e4a4df0414e62ff5823d592da13bce81bc109b5d2b8c574c49925a0653
Notes http://dx.doi.org/10.1016/j.gene.2013.07.074
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content type line 23
PMID 23954871
PQID 1431296517
PQPubID 23479
PageCount 10
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crossref_primary_10_1016_j_gene_2013_07_074
fao_agris_US201500044846
elsevier_sciencedirect_doi_10_1016_j_gene_2013_07_074
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– reference: - Gene. 2014 Jan 25;534(2):456
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Snippet Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but...
Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene -174G>C polymorphism and atherosclerotic diseases, but...
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SubjectTerms Alleles
Atherosclerosis
Atherosclerosis - genetics
clinical trials
confidence interval
Databases, Factual
epidemiological studies
Ethnic Groups - genetics
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Interleukin-6
Interleukin-6 - genetics
Meta-analysis
nationalities and ethnic groups
Odds Ratio
Polymorphism
Polymorphism, Genetic
risk
Risk Factors
Sensitivity and Specificity
Title Influence of interleukin-6 gene −174G>C polymorphism on development of atherosclerosis: A meta-analysis of 50 studies involving 33,514 subjects
URI https://dx.doi.org/10.1016/j.gene.2013.07.074
https://www.ncbi.nlm.nih.gov/pubmed/23954871
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