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The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants

BACKGROUND: It is unclear whether C-reactive protein (CRP) is causally related to coronary heart disease (CHD). Genetic variants that are known to be associated with CRP levels can be used to provide causal inference of the effect of CRP on CHD. Our objective was to examine the association between C...

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Autores principales: Lawlor, Debbie A., Harbord, Roger M., Timpson, Nic J., Lowe, Gordon D. O., Rumley, Ann, Gaunt, Tom R., Baker, Ian, Yarnell, John W. G., Kivimäki, Mika, Kumari, Meena, Norman, Paul E., Jamrozik, Konrad, Hankey, Graeme J., Almeida, Osvaldo P., Flicker, Leon, Warrington, Nicole, Marmot, Michael G., Ben-Shlomo, Yoav, Palmer, Lyle J., Day, Ian N. M., Ebrahim, Shah, Smith, George Davey
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2507759/
https://www.ncbi.nlm.nih.gov/pubmed/18714384
http://dx.doi.org/10.1371/journal.pone.0003011
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author Lawlor, Debbie A.
Harbord, Roger M.
Timpson, Nic J.
Lowe, Gordon D. O.
Rumley, Ann
Gaunt, Tom R.
Baker, Ian
Yarnell, John W. G.
Kivimäki, Mika
Kumari, Meena
Norman, Paul E.
Jamrozik, Konrad
Hankey, Graeme J.
Almeida, Osvaldo P.
Flicker, Leon
Warrington, Nicole
Marmot, Michael G.
Ben-Shlomo, Yoav
Palmer, Lyle J.
Day, Ian N. M.
Ebrahim, Shah
Smith, George Davey
author_facet Lawlor, Debbie A.
Harbord, Roger M.
Timpson, Nic J.
Lowe, Gordon D. O.
Rumley, Ann
Gaunt, Tom R.
Baker, Ian
Yarnell, John W. G.
Kivimäki, Mika
Kumari, Meena
Norman, Paul E.
Jamrozik, Konrad
Hankey, Graeme J.
Almeida, Osvaldo P.
Flicker, Leon
Warrington, Nicole
Marmot, Michael G.
Ben-Shlomo, Yoav
Palmer, Lyle J.
Day, Ian N. M.
Ebrahim, Shah
Smith, George Davey
author_sort Lawlor, Debbie A.
collection PubMed
description BACKGROUND: It is unclear whether C-reactive protein (CRP) is causally related to coronary heart disease (CHD). Genetic variants that are known to be associated with CRP levels can be used to provide causal inference of the effect of CRP on CHD. Our objective was to examine the association between CRP genetic variant +1444C>T (rs1130864) and CHD risk in the largest study to date of this association. METHODS AND RESULTS: We estimated the association of CRP genetic variant +1444C>T (rs1130864) with CRP levels and with CHD in five studies and then pooled these analyses (N = 18,637 participants amongst whom there were 4,610 cases). CRP was associated with potential confounding factors (socioeconomic position, physical activity, smoking and body mass) whereas genotype (rs1130864) was not associated with these confounders. The pooled odds ratio of CHD per doubling of circulating CRP level after adjustment for age and sex was 1.13 (95%CI: 1.06, 1.21), and after further adjustment for confounding factors it was 1.07 (95%CI: 1.02, 1.13). Genotype (rs1130864) was associated with circulating CRP; the pooled ratio of geometric means of CRP level among individuals with the TT genotype compared to those with the CT/CC genotype was 1.21 (95%CI: 1.15, 1.28) and the pooled ratio of geometric means of CRP level per additional T allele was 1.14 (95%CI: 1.11, 1.18), with no strong evidence in either analyses of between study heterogeneity (I(2) = 0%, p>0.9 for both analyses). There was no association of genotype (rs1130864) with CHD: pooled odds ratio 1.01 (95%CI: 0.88, 1.16) comparing individuals with TT genotype to those with CT/CC genotype and 0.96 (95%CI: 0.90, 1.03) per additional T allele (I(2)<7.5%, p>0.6 for both meta-analyses). An instrumental variables analysis (in which the proportion of CRP levels explained by rs1130864 was related to CHD) suggested that circulating CRP was not associated with CHD: the odds ratio for a doubling of CRP level was 1.04 (95%CI: 0.61, 1.80). CONCLUSIONS: We found no association of a genetic variant, which is known to be related to CRP levels, (rs1130864) and having CHD. These findings do not support a causal association between circulating CRP and CHD risk, but very large, extended, genetic association studies would be required to rule this out.
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spelling pubmed-25077592008-08-20 The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants Lawlor, Debbie A. Harbord, Roger M. Timpson, Nic J. Lowe, Gordon D. O. Rumley, Ann Gaunt, Tom R. Baker, Ian Yarnell, John W. G. Kivimäki, Mika Kumari, Meena Norman, Paul E. Jamrozik, Konrad Hankey, Graeme J. Almeida, Osvaldo P. Flicker, Leon Warrington, Nicole Marmot, Michael G. Ben-Shlomo, Yoav Palmer, Lyle J. Day, Ian N. M. Ebrahim, Shah Smith, George Davey PLoS One Research Article BACKGROUND: It is unclear whether C-reactive protein (CRP) is causally related to coronary heart disease (CHD). Genetic variants that are known to be associated with CRP levels can be used to provide causal inference of the effect of CRP on CHD. Our objective was to examine the association between CRP genetic variant +1444C>T (rs1130864) and CHD risk in the largest study to date of this association. METHODS AND RESULTS: We estimated the association of CRP genetic variant +1444C>T (rs1130864) with CRP levels and with CHD in five studies and then pooled these analyses (N = 18,637 participants amongst whom there were 4,610 cases). CRP was associated with potential confounding factors (socioeconomic position, physical activity, smoking and body mass) whereas genotype (rs1130864) was not associated with these confounders. The pooled odds ratio of CHD per doubling of circulating CRP level after adjustment for age and sex was 1.13 (95%CI: 1.06, 1.21), and after further adjustment for confounding factors it was 1.07 (95%CI: 1.02, 1.13). Genotype (rs1130864) was associated with circulating CRP; the pooled ratio of geometric means of CRP level among individuals with the TT genotype compared to those with the CT/CC genotype was 1.21 (95%CI: 1.15, 1.28) and the pooled ratio of geometric means of CRP level per additional T allele was 1.14 (95%CI: 1.11, 1.18), with no strong evidence in either analyses of between study heterogeneity (I(2) = 0%, p>0.9 for both analyses). There was no association of genotype (rs1130864) with CHD: pooled odds ratio 1.01 (95%CI: 0.88, 1.16) comparing individuals with TT genotype to those with CT/CC genotype and 0.96 (95%CI: 0.90, 1.03) per additional T allele (I(2)<7.5%, p>0.6 for both meta-analyses). An instrumental variables analysis (in which the proportion of CRP levels explained by rs1130864 was related to CHD) suggested that circulating CRP was not associated with CHD: the odds ratio for a doubling of CRP level was 1.04 (95%CI: 0.61, 1.80). CONCLUSIONS: We found no association of a genetic variant, which is known to be related to CRP levels, (rs1130864) and having CHD. These findings do not support a causal association between circulating CRP and CHD risk, but very large, extended, genetic association studies would be required to rule this out. Public Library of Science 2008-08-20 /pmc/articles/PMC2507759/ /pubmed/18714384 http://dx.doi.org/10.1371/journal.pone.0003011 Text en Lawlor et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lawlor, Debbie A.
Harbord, Roger M.
Timpson, Nic J.
Lowe, Gordon D. O.
Rumley, Ann
Gaunt, Tom R.
Baker, Ian
Yarnell, John W. G.
Kivimäki, Mika
Kumari, Meena
Norman, Paul E.
Jamrozik, Konrad
Hankey, Graeme J.
Almeida, Osvaldo P.
Flicker, Leon
Warrington, Nicole
Marmot, Michael G.
Ben-Shlomo, Yoav
Palmer, Lyle J.
Day, Ian N. M.
Ebrahim, Shah
Smith, George Davey
The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title_full The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title_fullStr The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title_full_unstemmed The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title_short The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants
title_sort association of c-reactive protein and crp genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2507759/
https://www.ncbi.nlm.nih.gov/pubmed/18714384
http://dx.doi.org/10.1371/journal.pone.0003011
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