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Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events

IMPORTANCE: The prevalence of antiphospholipid antibodies (aPL) and their association with future atherosclerotic cardiovascular disease (ASCVD) risk has yet to be thoroughly investigated. OBJECTIVE: To determine the association between measurements of aPL at a single time point and ASCVD risk in a...

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Autores principales: Zuo, Yu, Navaz, Sherwin, Liang, Wenying, Li, Chun, Ayers, Colby R., Rysenga, Christine E., Harbaugh, Alyssa, Norman, Gary L., Solow, E. Blair, Bermas, Bonnie, Akinmolayemi, Oludamilola, Rohatgi, Anand, Karp, David R., Knight, Jason S., de Lemos, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074226/
https://www.ncbi.nlm.nih.gov/pubmed/37014642
http://dx.doi.org/10.1001/jamanetworkopen.2023.6530
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author Zuo, Yu
Navaz, Sherwin
Liang, Wenying
Li, Chun
Ayers, Colby R.
Rysenga, Christine E.
Harbaugh, Alyssa
Norman, Gary L.
Solow, E. Blair
Bermas, Bonnie
Akinmolayemi, Oludamilola
Rohatgi, Anand
Karp, David R.
Knight, Jason S.
de Lemos, James A.
author_facet Zuo, Yu
Navaz, Sherwin
Liang, Wenying
Li, Chun
Ayers, Colby R.
Rysenga, Christine E.
Harbaugh, Alyssa
Norman, Gary L.
Solow, E. Blair
Bermas, Bonnie
Akinmolayemi, Oludamilola
Rohatgi, Anand
Karp, David R.
Knight, Jason S.
de Lemos, James A.
author_sort Zuo, Yu
collection PubMed
description IMPORTANCE: The prevalence of antiphospholipid antibodies (aPL) and their association with future atherosclerotic cardiovascular disease (ASCVD) risk has yet to be thoroughly investigated. OBJECTIVE: To determine the association between measurements of aPL at a single time point and ASCVD risk in a diverse population. DESIGN, SETTING, AND PARTICIPANTS: This cohort study measured 8 aPL (anticardiolipin [aCL] IgG/IgM/IgA, anti–beta-2 glycoprotein I [aβ2GPI] IgG/IgM/IgA, and antiphosphatidylserine/prothrombin [aPS/PT] IgG/IgM) by solid-phase assays in plasma from participants of the Dallas Heart Study (DHS) phase 2, a multiethnic, population-based cohort study. Blood samples were collected between 2007 and 2009. The median follow-up was 8 years. Statistical analysis was performed from April 2022 to January 2023. MAIN OUTCOMES AND MEASURES: Associations of aPL with future ASCVD events (defined as first nonfatal myocardial infarction, first nonfatal stroke, coronary revascularization, or death from cardiovascular cause) were assessed by Cox proportional hazards models, adjusting for known risk factors, medications, and multiple comparisons. RESULTS: Among the 2427 participants (mean [SD] age, 50.6 [10.3] years; 1399 [57.6%] female; 1244 [51.3%] Black, 339 [14.0%] Hispanic, and 796 [32.8%] White), the prevalence of any positive aPL tested at a single time point was 14.5% (353 of 2427), with approximately one-third of those detected at a moderate or high titer; aCL IgM had the highest prevalence (156 individuals [6.4%]), followed by aPS/PT IgM (88 [3.4%]), aβ2GPI IgM (63 [2.6%]), and aβ2GPI IgA (62 [2.5%]). The IgA of aCL (adjusted hazard ratio [HR], 4.92; 95% CI, 1.52-15.98) and aβ2GPI (HR, 2.91; 95% CI, 1.32-6.41) were independently associated with future ASCVD events. The risk further increased when applying a positivity threshold of at least 40 units (aCL IgA: HR, 9.01 [95% CI, 2.73-29.72]; aβ2GPI IgA: HR, 4.09 [95% CI, 1.45-11.54]). Levels of aβ2GPI IgA negatively correlated with cholesterol efflux capacity (r = −0.055; P = .009) and positively correlated with circulating oxidized LDL (r = 0.055; P = .007). aβ2GPI IgA–positive plasma was associated with an activated endothelial cell phenotype as evidenced by increased surface expression of surface E-selectin, intercellular adhesion molecule-1, and vascular cell adhesion molecule-1. CONCLUSIONS AND RELEVANCE: In this population-based cohort study, aPL detectable by solid-phase assays were present in a substantial proportion of adults; positive aCL IgA and aβ2GPI IgA at a single time point were independently associated with future ASCVD events. Longitudinal studies with serial aPL measurements are needed to further explore these findings.
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spelling pubmed-100742262023-04-06 Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events Zuo, Yu Navaz, Sherwin Liang, Wenying Li, Chun Ayers, Colby R. Rysenga, Christine E. Harbaugh, Alyssa Norman, Gary L. Solow, E. Blair Bermas, Bonnie Akinmolayemi, Oludamilola Rohatgi, Anand Karp, David R. Knight, Jason S. de Lemos, James A. JAMA Netw Open Original Investigation IMPORTANCE: The prevalence of antiphospholipid antibodies (aPL) and their association with future atherosclerotic cardiovascular disease (ASCVD) risk has yet to be thoroughly investigated. OBJECTIVE: To determine the association between measurements of aPL at a single time point and ASCVD risk in a diverse population. DESIGN, SETTING, AND PARTICIPANTS: This cohort study measured 8 aPL (anticardiolipin [aCL] IgG/IgM/IgA, anti–beta-2 glycoprotein I [aβ2GPI] IgG/IgM/IgA, and antiphosphatidylserine/prothrombin [aPS/PT] IgG/IgM) by solid-phase assays in plasma from participants of the Dallas Heart Study (DHS) phase 2, a multiethnic, population-based cohort study. Blood samples were collected between 2007 and 2009. The median follow-up was 8 years. Statistical analysis was performed from April 2022 to January 2023. MAIN OUTCOMES AND MEASURES: Associations of aPL with future ASCVD events (defined as first nonfatal myocardial infarction, first nonfatal stroke, coronary revascularization, or death from cardiovascular cause) were assessed by Cox proportional hazards models, adjusting for known risk factors, medications, and multiple comparisons. RESULTS: Among the 2427 participants (mean [SD] age, 50.6 [10.3] years; 1399 [57.6%] female; 1244 [51.3%] Black, 339 [14.0%] Hispanic, and 796 [32.8%] White), the prevalence of any positive aPL tested at a single time point was 14.5% (353 of 2427), with approximately one-third of those detected at a moderate or high titer; aCL IgM had the highest prevalence (156 individuals [6.4%]), followed by aPS/PT IgM (88 [3.4%]), aβ2GPI IgM (63 [2.6%]), and aβ2GPI IgA (62 [2.5%]). The IgA of aCL (adjusted hazard ratio [HR], 4.92; 95% CI, 1.52-15.98) and aβ2GPI (HR, 2.91; 95% CI, 1.32-6.41) were independently associated with future ASCVD events. The risk further increased when applying a positivity threshold of at least 40 units (aCL IgA: HR, 9.01 [95% CI, 2.73-29.72]; aβ2GPI IgA: HR, 4.09 [95% CI, 1.45-11.54]). Levels of aβ2GPI IgA negatively correlated with cholesterol efflux capacity (r = −0.055; P = .009) and positively correlated with circulating oxidized LDL (r = 0.055; P = .007). aβ2GPI IgA–positive plasma was associated with an activated endothelial cell phenotype as evidenced by increased surface expression of surface E-selectin, intercellular adhesion molecule-1, and vascular cell adhesion molecule-1. CONCLUSIONS AND RELEVANCE: In this population-based cohort study, aPL detectable by solid-phase assays were present in a substantial proportion of adults; positive aCL IgA and aβ2GPI IgA at a single time point were independently associated with future ASCVD events. Longitudinal studies with serial aPL measurements are needed to further explore these findings. American Medical Association 2023-04-04 /pmc/articles/PMC10074226/ /pubmed/37014642 http://dx.doi.org/10.1001/jamanetworkopen.2023.6530 Text en Copyright 2023 Zuo Y et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Zuo, Yu
Navaz, Sherwin
Liang, Wenying
Li, Chun
Ayers, Colby R.
Rysenga, Christine E.
Harbaugh, Alyssa
Norman, Gary L.
Solow, E. Blair
Bermas, Bonnie
Akinmolayemi, Oludamilola
Rohatgi, Anand
Karp, David R.
Knight, Jason S.
de Lemos, James A.
Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title_full Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title_fullStr Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title_full_unstemmed Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title_short Prevalence of Antiphospholipid Antibodies and Association With Incident Cardiovascular Events
title_sort prevalence of antiphospholipid antibodies and association with incident cardiovascular events
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074226/
https://www.ncbi.nlm.nih.gov/pubmed/37014642
http://dx.doi.org/10.1001/jamanetworkopen.2023.6530
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