Interleukin 6 (rs1800795) gene polymorphism is associated with cardiovascular diseases: a meta-analysis of 74 studies with 86,229 subjects
Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 ( ) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the (rs1800795)...
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Published in | EXCLI journal Vol. 18; pp. 331 - 355 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Leibniz Research Centre for Working Environment and Human Factors
01.01.2019
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Subjects | |
Online Access | Get full text |
ISSN | 1611-2156 1611-2156 |
DOI | 10.17179/excli2019-1248 |
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Abstract | Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 (
) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the
(rs1800795) gene polymorphism and CVD. We systematically searched in the PubMed, Web of Sciences, and Scopus databases. The analyses were performed using five study groups based on (1) a combined pool of the overall populations, (2) the country of birth, (3) the continent of birth, (4) the diagnosis and (5) both location (country or continent) and diagnosis. The analysis included the allelic, homozygote, heterozygote, dominant and recessive models. The meta-analysis showed that -174
(rs1800795) is a risk factor for CVD (
: OR=1.06, CI 95%=1.02-1.10. Z p value <0.0001; homozygous: OR=1.11, CI 95%=1.03-1.19, Z p value= 0.002;
: OR=1.08, CI 95%=1.03-1.21, Z p value= 0.003;
: OR= 1.12, CI 95%= 1.07-1.18, Z p value= 0.001) and that this risk increases in the Chinese population. Additionally, we found that carriers of the
allele of 174
(rs1800795) polymorphism have an increase in the risk of coronary artery disease under the hereditary models assessed in the study. Using robust data, we found that
(rs1800795) -174
gene polymorphism is associated with CVD risk. |
---|---|
AbstractList | Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 (
IL-6
) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the
IL-6
(rs1800795) gene polymorphism and CVD. We systematically searched in the PubMed, Web of Sciences, and Scopus databases. The analyses were performed using five study groups based on (1) a combined pool of the overall populations, (2) the country of birth, (3) the continent of birth, (4) the diagnosis and (5) both location (country or continent) and diagnosis. The analysis included the allelic, homozygote, heterozygote, dominant and recessive models. The meta-analysis showed that -174
G>C
(rs1800795) is a risk factor for CVD (
allelic
: OR=1.06, CI 95%=1.02-1.10. Z p value <0.0001; homozygous: OR=1.11, CI 95%=1.03-1.19, Z p value= 0.002;
heterozygous
: OR=1.08, CI 95%=1.03-1.21, Z p value= 0.003;
dominant
: OR= 1.12, CI 95%= 1.07-1.18, Z p value= 0.001) and that this risk increases in the Chinese population. Additionally, we found that carriers of the
C
allele of 174
G>C
(rs1800795) polymorphism have an increase in the risk of coronary artery disease under the hereditary models assessed in the study. Using robust data, we found that
IL-6
(rs1800795) -174
G>C
gene polymorphism is associated with CVD risk. Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 (IL-6) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the IL-6 (rs1800795) gene polymorphism and CVD. We systematically searched in the PubMed, Web of Sciences, and Scopus databases. The analyses were performed using five study groups based on (1) a combined pool of the overall populations, (2) the country of birth, (3) the continent of birth, (4) the diagnosis and (5) both location (country or continent) and diagnosis. The analysis included the allelic, homozygote, heterozygote, dominant and recessive models. The meta-analysis showed that -174G>C (rs1800795) is a risk factor for CVD (allelic: OR=1.06, CI 95%=1.02-1.10. Z p value <0.0001; homozygous: OR=1.11, CI 95%=1.03-1.19, Z p value= 0.002; heterozygous: OR=1.08, CI 95%=1.03-1.21, Z p value= 0.003; dominant: OR= 1.12, CI 95%= 1.07-1.18, Z p value= 0.001) and that this risk increases in the Chinese population. Additionally, we found that carriers of the C allele of 174G>C (rs1800795) polymorphism have an increase in the risk of coronary artery disease under the hereditary models assessed in the study. Using robust data, we found that IL-6 (rs1800795) -174G>C gene polymorphism is associated with CVD risk.Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 (IL-6) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the IL-6 (rs1800795) gene polymorphism and CVD. We systematically searched in the PubMed, Web of Sciences, and Scopus databases. The analyses were performed using five study groups based on (1) a combined pool of the overall populations, (2) the country of birth, (3) the continent of birth, (4) the diagnosis and (5) both location (country or continent) and diagnosis. The analysis included the allelic, homozygote, heterozygote, dominant and recessive models. The meta-analysis showed that -174G>C (rs1800795) is a risk factor for CVD (allelic: OR=1.06, CI 95%=1.02-1.10. Z p value <0.0001; homozygous: OR=1.11, CI 95%=1.03-1.19, Z p value= 0.002; heterozygous: OR=1.08, CI 95%=1.03-1.21, Z p value= 0.003; dominant: OR= 1.12, CI 95%= 1.07-1.18, Z p value= 0.001) and that this risk increases in the Chinese population. Additionally, we found that carriers of the C allele of 174G>C (rs1800795) polymorphism have an increase in the risk of coronary artery disease under the hereditary models assessed in the study. Using robust data, we found that IL-6 (rs1800795) -174G>C gene polymorphism is associated with CVD risk. Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 ( ) gene polymorphisms have been associated with several components of the CVD. Thus, in this study, we thoroughly reviewed and meta-analyzed evidence on the association between the (rs1800795) gene polymorphism and CVD. We systematically searched in the PubMed, Web of Sciences, and Scopus databases. The analyses were performed using five study groups based on (1) a combined pool of the overall populations, (2) the country of birth, (3) the continent of birth, (4) the diagnosis and (5) both location (country or continent) and diagnosis. The analysis included the allelic, homozygote, heterozygote, dominant and recessive models. The meta-analysis showed that -174 (rs1800795) is a risk factor for CVD ( : OR=1.06, CI 95%=1.02-1.10. Z p value <0.0001; homozygous: OR=1.11, CI 95%=1.03-1.19, Z p value= 0.002; : OR=1.08, CI 95%=1.03-1.21, Z p value= 0.003; : OR= 1.12, CI 95%= 1.07-1.18, Z p value= 0.001) and that this risk increases in the Chinese population. Additionally, we found that carriers of the allele of 174 (rs1800795) polymorphism have an increase in the risk of coronary artery disease under the hereditary models assessed in the study. Using robust data, we found that (rs1800795) -174 gene polymorphism is associated with CVD risk. |
Author | Vargas-Alarcón, Gilberto Reyes-López, Pedro A Rodríguez-Pérez, José Manuel Cazarín-Santos, Benny Giovanni Tovilla-Zárate, Carlos Alfonso Hernández-Díaz, Yazmín Pérez-Hernández, Nonanzit López-Narvaez, María Lilia Borgonio-Cuadra, Verónica Marusa Blachman-Braun, Ruben García-Flores, Esbeidy Juárez-Rojop, Isela Esther Posadas-Sánchez, Rosalinda González-Castro, Thelma Beatriz |
AuthorAffiliation | 1 Multidisciplinary Academic Division of Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Jalpa de Méndez, Tabasco, Mexico 2 Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico 6 Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico 3 Multidisciplinary Academic Division of Comalcalco, Universidad Juárez Autónoma de Tabasco, Comalcalco, Tabasco, Mexico 5 General Hospital de Yajalón Manuel Velasco Siles, Secretaría de Salud, Yajalón, Chiapas, Mexico 8 Division of Research, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico 7 Department of Genetics, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Mexico City, Mexico 4 Academic Division of Health Sciences, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico |
AuthorAffiliation_xml | – name: 2 Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – name: 5 General Hospital de Yajalón Manuel Velasco Siles, Secretaría de Salud, Yajalón, Chiapas, Mexico – name: 3 Multidisciplinary Academic Division of Comalcalco, Universidad Juárez Autónoma de Tabasco, Comalcalco, Tabasco, Mexico – name: 1 Multidisciplinary Academic Division of Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Jalpa de Méndez, Tabasco, Mexico – name: 4 Academic Division of Health Sciences, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico – name: 6 Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – name: 7 Department of Genetics, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Mexico City, Mexico – name: 8 Division of Research, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico |
Author_xml | – sequence: 1 givenname: Thelma Beatriz surname: González-Castro fullname: González-Castro, Thelma Beatriz organization: Multidisciplinary Academic Division of Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Jalpa de Méndez, Tabasco, Mexico – sequence: 2 givenname: Yazmín surname: Hernández-Díaz fullname: Hernández-Díaz, Yazmín organization: Multidisciplinary Academic Division of Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Jalpa de Méndez, Tabasco, Mexico – sequence: 3 givenname: Nonanzit surname: Pérez-Hernández fullname: Pérez-Hernández, Nonanzit organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 4 givenname: Carlos Alfonso surname: Tovilla-Zárate fullname: Tovilla-Zárate, Carlos Alfonso organization: Multidisciplinary Academic Division of Comalcalco, Universidad Juárez Autónoma de Tabasco, Comalcalco, Tabasco, Mexico – sequence: 5 givenname: Isela Esther surname: Juárez-Rojop fullname: Juárez-Rojop, Isela Esther organization: Academic Division of Health Sciences, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico – sequence: 6 givenname: María Lilia surname: López-Narvaez fullname: López-Narvaez, María Lilia organization: General Hospital de Yajalón Manuel Velasco Siles, Secretaría de Salud, Yajalón, Chiapas, Mexico – sequence: 7 givenname: Ruben surname: Blachman-Braun fullname: Blachman-Braun, Ruben organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 8 givenname: Rosalinda surname: Posadas-Sánchez fullname: Posadas-Sánchez, Rosalinda organization: Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 9 givenname: Gilberto surname: Vargas-Alarcón fullname: Vargas-Alarcón, Gilberto organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 10 givenname: Esbeidy surname: García-Flores fullname: García-Flores, Esbeidy organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 11 givenname: Benny Giovanni surname: Cazarín-Santos fullname: Cazarín-Santos, Benny Giovanni organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 12 givenname: Verónica Marusa surname: Borgonio-Cuadra fullname: Borgonio-Cuadra, Verónica Marusa organization: Department of Genetics, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Mexico City, Mexico – sequence: 13 givenname: Pedro A surname: Reyes-López fullname: Reyes-López, Pedro A organization: Division of Research, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico – sequence: 14 givenname: José Manuel surname: Rodríguez-Pérez fullname: Rodríguez-Pérez, José Manuel organization: Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31338006$$D View this record in MEDLINE/PubMed |
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Keywords | genetic association meta-analysis polymorphism cardiovascular diseases inflammation IL-6 |
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) gene polymorphisms have been associated with... Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 (IL-6) gene polymorphisms have been associated with... Cardiovascular diseases (CVD) are group of complex and multifactorial pathologies, in which interleukin-6 ( IL-6 ) gene polymorphisms have been associated with... |
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Title | Interleukin 6 (rs1800795) gene polymorphism is associated with cardiovascular diseases: a meta-analysis of 74 studies with 86,229 subjects |
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