Plasma Albumin and Incident Cardiovascular Disease: Results From the CGPS and an Updated Meta-Analysis

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

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Plasma Albumin and Incident Cardiovascular Disease : Results From the CGPS and an Updated Meta-Analysis. / Ronit, Andreas; Kirkegaard-Klitbo, Ditte M; Dohlmann, Tine L; Lundgren, Jens; Sabin, Caroline A; Phillips, Andrew N; Nordestgaard, Børge G; Afzal, Shoaib.

I: Arteriosclerosis, Thrombosis, and Vascular Biology, Bind 40, Nr. 2, 02.2020, s. 473-482.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Ronit, A, Kirkegaard-Klitbo, DM, Dohlmann, TL, Lundgren, J, Sabin, CA, Phillips, AN, Nordestgaard, BG & Afzal, S 2020, 'Plasma Albumin and Incident Cardiovascular Disease: Results From the CGPS and an Updated Meta-Analysis', Arteriosclerosis, Thrombosis, and Vascular Biology, bind 40, nr. 2, s. 473-482. https://doi.org/10.1161/ATVBAHA.119.313681

APA

Ronit, A., Kirkegaard-Klitbo, D. M., Dohlmann, T. L., Lundgren, J., Sabin, C. A., Phillips, A. N., Nordestgaard, B. G., & Afzal, S. (2020). Plasma Albumin and Incident Cardiovascular Disease: Results From the CGPS and an Updated Meta-Analysis. Arteriosclerosis, Thrombosis, and Vascular Biology, 40(2), 473-482. https://doi.org/10.1161/ATVBAHA.119.313681

Vancouver

Ronit A, Kirkegaard-Klitbo DM, Dohlmann TL, Lundgren J, Sabin CA, Phillips AN o.a. Plasma Albumin and Incident Cardiovascular Disease: Results From the CGPS and an Updated Meta-Analysis. Arteriosclerosis, Thrombosis, and Vascular Biology. 2020 feb.;40(2):473-482. https://doi.org/10.1161/ATVBAHA.119.313681

Author

Ronit, Andreas ; Kirkegaard-Klitbo, Ditte M ; Dohlmann, Tine L ; Lundgren, Jens ; Sabin, Caroline A ; Phillips, Andrew N ; Nordestgaard, Børge G ; Afzal, Shoaib. / Plasma Albumin and Incident Cardiovascular Disease : Results From the CGPS and an Updated Meta-Analysis. I: Arteriosclerosis, Thrombosis, and Vascular Biology. 2020 ; Bind 40, Nr. 2. s. 473-482.

Bibtex

@article{a91c545567e844768bba60e31116c2ea,
title = "Plasma Albumin and Incident Cardiovascular Disease: Results From the CGPS and an Updated Meta-Analysis",
abstract = "OBJECTIVE: We studied the association of plasma albumin with cardiovascular disease (CVD) and explored potential mechanisms behind the association in the CGPS (Copenhagen General Population Study). We also performed a meta-analysis to summarize the association between plasma albumin and CVD in individuals without preexisting CVD. Approach and Results: We included 100 520 individuals without prior CVD with 8247 incident CVD events developed during a median follow-up of 8.5 years. Rates of CVD outcomes were calculated using Cox regression and Fine and Gray competing-risks regression. The association of plasma albumin and CVD was approximately linear and confounder adjustment had little influence on the effect estimates, except for some attenuation after CRP (C-reactive protein) adjustment. In analyses according to subtypes of CVD events, the hazard ratios for each 10 g/L lower plasma albumin were 1.17 (95% CI, 1.08-1.28) for ischemic heart disease, 1.25 (95% CI, 1.09-1.43) for myocardial infarction, 1.37 (95% CI, 1.21-1.54) for any stroke, and 1.46 (95% CI, 1.28-1.68) for ischemic stroke. In the meta-analysis, we combined estimates from prospective and nested case-control studies investigating the association of plasma albumin with CVD. The meta-analysis included 14 studies with 150 652 individuals (12 studies reported events totaling 11 872). The risk ratio for a CVD event per 10 g/L lower plasma albumin was 1.96 (95% CI, 1.43-2.68) in previous studies and 1.85 (95% CI, 1.39-2.47) including our study with 57% weight in the meta-analysis. Exploratory analyses of the mechanism of the association indicated that it was probably not due to fatty acid binding but may be due to the regulation of plasma albumin by inflammation.CONCLUSIONS: There is a robust, independent association of low plasma albumin with CVD, partly explained by plasma albumin as a negative acute-phase reactant.CLINICAL TRIAL REGISTRATION: URL: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=95796. Unique identifier: CRD42018095796.",
keywords = "Biomarkers/blood, Cardiovascular Diseases/blood, Global Health, Humans, Incidence, Risk Assessment/methods, Risk Factors, Serum Albumin/metabolism",
author = "Andreas Ronit and Kirkegaard-Klitbo, {Ditte M} and Dohlmann, {Tine L} and Jens Lundgren and Sabin, {Caroline A} and Phillips, {Andrew N} and Nordestgaard, {B{\o}rge G} and Shoaib Afzal",
year = "2020",
month = feb,
doi = "10.1161/ATVBAHA.119.313681",
language = "English",
volume = "40",
pages = "473--482",
journal = "Arteriosclerosis, Thrombosis, and Vascular Biology",
issn = "1079-5642",
publisher = "Lippincott Williams & Wilkins",
number = "2",

}

RIS

TY - JOUR

T1 - Plasma Albumin and Incident Cardiovascular Disease

T2 - Results From the CGPS and an Updated Meta-Analysis

AU - Ronit, Andreas

AU - Kirkegaard-Klitbo, Ditte M

AU - Dohlmann, Tine L

AU - Lundgren, Jens

AU - Sabin, Caroline A

AU - Phillips, Andrew N

AU - Nordestgaard, Børge G

AU - Afzal, Shoaib

PY - 2020/2

Y1 - 2020/2

N2 - OBJECTIVE: We studied the association of plasma albumin with cardiovascular disease (CVD) and explored potential mechanisms behind the association in the CGPS (Copenhagen General Population Study). We also performed a meta-analysis to summarize the association between plasma albumin and CVD in individuals without preexisting CVD. Approach and Results: We included 100 520 individuals without prior CVD with 8247 incident CVD events developed during a median follow-up of 8.5 years. Rates of CVD outcomes were calculated using Cox regression and Fine and Gray competing-risks regression. The association of plasma albumin and CVD was approximately linear and confounder adjustment had little influence on the effect estimates, except for some attenuation after CRP (C-reactive protein) adjustment. In analyses according to subtypes of CVD events, the hazard ratios for each 10 g/L lower plasma albumin were 1.17 (95% CI, 1.08-1.28) for ischemic heart disease, 1.25 (95% CI, 1.09-1.43) for myocardial infarction, 1.37 (95% CI, 1.21-1.54) for any stroke, and 1.46 (95% CI, 1.28-1.68) for ischemic stroke. In the meta-analysis, we combined estimates from prospective and nested case-control studies investigating the association of plasma albumin with CVD. The meta-analysis included 14 studies with 150 652 individuals (12 studies reported events totaling 11 872). The risk ratio for a CVD event per 10 g/L lower plasma albumin was 1.96 (95% CI, 1.43-2.68) in previous studies and 1.85 (95% CI, 1.39-2.47) including our study with 57% weight in the meta-analysis. Exploratory analyses of the mechanism of the association indicated that it was probably not due to fatty acid binding but may be due to the regulation of plasma albumin by inflammation.CONCLUSIONS: There is a robust, independent association of low plasma albumin with CVD, partly explained by plasma albumin as a negative acute-phase reactant.CLINICAL TRIAL REGISTRATION: URL: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=95796. Unique identifier: CRD42018095796.

AB - OBJECTIVE: We studied the association of plasma albumin with cardiovascular disease (CVD) and explored potential mechanisms behind the association in the CGPS (Copenhagen General Population Study). We also performed a meta-analysis to summarize the association between plasma albumin and CVD in individuals without preexisting CVD. Approach and Results: We included 100 520 individuals without prior CVD with 8247 incident CVD events developed during a median follow-up of 8.5 years. Rates of CVD outcomes were calculated using Cox regression and Fine and Gray competing-risks regression. The association of plasma albumin and CVD was approximately linear and confounder adjustment had little influence on the effect estimates, except for some attenuation after CRP (C-reactive protein) adjustment. In analyses according to subtypes of CVD events, the hazard ratios for each 10 g/L lower plasma albumin were 1.17 (95% CI, 1.08-1.28) for ischemic heart disease, 1.25 (95% CI, 1.09-1.43) for myocardial infarction, 1.37 (95% CI, 1.21-1.54) for any stroke, and 1.46 (95% CI, 1.28-1.68) for ischemic stroke. In the meta-analysis, we combined estimates from prospective and nested case-control studies investigating the association of plasma albumin with CVD. The meta-analysis included 14 studies with 150 652 individuals (12 studies reported events totaling 11 872). The risk ratio for a CVD event per 10 g/L lower plasma albumin was 1.96 (95% CI, 1.43-2.68) in previous studies and 1.85 (95% CI, 1.39-2.47) including our study with 57% weight in the meta-analysis. Exploratory analyses of the mechanism of the association indicated that it was probably not due to fatty acid binding but may be due to the regulation of plasma albumin by inflammation.CONCLUSIONS: There is a robust, independent association of low plasma albumin with CVD, partly explained by plasma albumin as a negative acute-phase reactant.CLINICAL TRIAL REGISTRATION: URL: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=95796. Unique identifier: CRD42018095796.

KW - Biomarkers/blood

KW - Cardiovascular Diseases/blood

KW - Global Health

KW - Humans

KW - Incidence

KW - Risk Assessment/methods

KW - Risk Factors

KW - Serum Albumin/metabolism

U2 - 10.1161/ATVBAHA.119.313681

DO - 10.1161/ATVBAHA.119.313681

M3 - Review

C2 - 31852221

VL - 40

SP - 473

EP - 482

JO - Arteriosclerosis, Thrombosis, and Vascular Biology

JF - Arteriosclerosis, Thrombosis, and Vascular Biology

SN - 1079-5642

IS - 2

ER -

ID: 250488230