Impact of Hemoglobin A1c Levels on Residual Platelet Reactivity and Outcomes After Insertion of Coronary Drug-Eluting Stents (from the ADAPT-DES Study)
An increasing hemoglobin A1c (HbA1c) level portends an adverse cardiovascular prognosis; however, the association between glycemic control, platelet reactivity, and outcomes after percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is unknown. We sought to investigate whether HbA...
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Published in | The American journal of cardiology Vol. 117; no. 2; pp. 192 - 200 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.01.2016
Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0002-9149 1879-1913 |
DOI | 10.1016/j.amjcard.2015.10.037 |
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Abstract | An increasing hemoglobin A1c (HbA1c) level portends an adverse cardiovascular prognosis; however, the association between glycemic control, platelet reactivity, and outcomes after percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is unknown. We sought to investigate whether HbA1c levels are associated with high platelet reactivity (HPR) in patients loaded with clopidogrel and aspirin, thereby constituting an argument for intensified antiplatelet therapy in patients with poor glycemic control. In the prospective, multicenter Assessment of Dual Antiplatelet Therapy With Drug Eluting Stents registry, HbA1c levels were measured as clinically indicated in 1,145 of 8,582 patients, stratified by HbA1c <6.5% (n = 551, 48.12%), 6.5% to 8.5% (n = 423, 36.9%), and >8.5% (n = 171, 14.9%). HPR on clopidogrel and aspirin was defined after PCI as P2Y12 reaction units (PRU) >208 and aspirin reaction units >550, respectively. HPR on clopidogrel was frequent (48.3%), whereas HPR on aspirin was not (3.9%). Patients with HbA1c >8.5% were younger, more likely non-Caucasian, had a greater body mass index, and more insulin-treated diabetes and acute coronary syndromes. Proportions of PRU >208 (42.5%, 50.2%, and 62.3%, p <0.001) and rates of definite or probable stent thrombosis (ST; 0.9%, 2.7%, and 4.2%, p = 0.02) increased progressively with HbA1c groups. Clinically relevant bleeding was greatest in the intermediate HbA1c group (8.2% vs 13.1% vs 9.5%, p = 0.04). In adjusted models that included PRU, high HbA1c levels (>8.5) remained associated with ST (hazard ratio 3.92, 95% CI 1.29 to 12.66, p = 0.02) and cardiac death (hazard ratio 4.24, 95% CI 1.41 to 12.70) but not bleeding at 2-year follow-up. There was no association between aspirin reaction units >550 and HbA1c levels. In conclusion, in this large-scale study, HbA1c and HPR were positively associated, but the clinical effect on adverse outcome was driven by poor glycemic control, which predicted ST and cardiac death after PCI regardless of PRU levels, warranting efforts to improve glycemic control after DES implantation in patients with diabetes mellitus. |
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AbstractList | An increasing hemoglobin A1c (HbA1c) level portends an adverse cardiovascular prognosis; however, the association between glycemic control, platelet reactivity, and outcomes after percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is unknown. We sought to investigate whether HbA1c levels are associated with high platelet reactivity (HPR) in patients loaded with clopidogrel and aspirin, thereby constituting an argument for intensified antiplatelet therapy in patients with poor glycemic control. In the prospective, multicenter Assessment of Dual Antiplatelet Therapy With Drug Eluting Stents registry, HbA1c levels were measured as clinically indicated in 1,145 of 8,582 patients, stratified by HbA1c <6.5% (n = 551, 48.12%), 6.5% to 8.5% (n = 423, 36.9%), and >8.5% (n = 171, 14.9%). HPR on clopidogrel and aspirin was defined after PCI as P2Y12 reaction units (PRU) >208 and aspirin reaction units >550, respectively. HPR on clopidogrel was frequent (48.3%), whereas HPR on aspirin was not (3.9%). Patients with HbA1c >8.5% were younger, more likely non-Caucasian, had a greater body mass index, and more insulin-treated diabetes and acute coronary syndromes. Proportions of PRU >208 (42.5%, 50.2%, and 62.3%, p <0.001) and rates of definite or probable stent thrombosis (ST; 0.9%, 2.7%, and 4.2%, p = 0.02) increased progressively with HbA1c groups. Clinically relevant bleeding was greatest in the intermediate HbA1c group (8.2% vs 13.1% vs 9.5%, p = 0.04). In adjusted models that included PRU, high HbA1c levels (>8.5) remained associated with ST (hazard ratio 3.92, 95% CI 1.29 to 12.66, p = 0.02) and cardiac death (hazard ratio 4.24, 95% CI 1.41 to 12.70) but not bleeding at 2-year follow-up. There was no association between aspirin reaction units >550 and HbA1c levels. In conclusion, in this large-scale study, HbA1c and HPR were positively associated, but the clinical effect on adverse outcome was driven by poor glycemic control, which predicted ST and cardiac death after PCI regardless of PRU levels, warranting efforts to improve glycemic control after DES implantation in patients with diabetes mellitus. An increasing hemoglobin A1c (HbA1c) level portends an adverse cardiovascular prognosis; however, the association between glycemic control, platelet reactivity, and outcomes after percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is unknown. We sought to investigate whether HbA1c levels are associated with high platelet reactivity (HPR) in patients loaded with clopidogrel and aspirin, thereby constituting an argument for intensified antiplatelet therapy in patients with poor glycemic control. In the prospective, multicenter Assessment of Dual Antiplatelet Therapy With Drug Eluting Stents registry, HbA1c levels were measured as clinically indicated in 1,145 of 8,582 patients, stratified by HbA1c <6.5% (n = 551, 48.12%), 6.5% to 8.5% (n = 423, 36.9%), and >8.5% (n = 171, 14.9%). HPR on clopidogrel and aspirin was defined after PCI as P2Y12 reaction units (PRU) >208 and aspirin reaction units >550, respectively. HPR on clopidogrel was frequent (48.3%), whereas HPR on aspirin was not (3.9%). Patients with HbA1c >8.5% were younger, more likely non-Caucasian, had a greater body mass index, and more insulin-treated diabetes and acute coronary syndromes. Proportions of PRU >208 (42.5%, 50.2%, and 62.3%, p <0.001) and rates of definite or probable stent thrombosis (ST; 0.9%, 2.7%, and 4.2%, p = 0.02) increased progressively with HbA1c groups. Clinically relevant bleeding was greatest in the intermediate HbA1c group (8.2% vs 13.1% vs 9.5%, p = 0.04). In adjusted models that included PRU, high HbA1c levels (>8.5) remained associated with ST (hazard ratio 3.92, 95% CI 1.29 to 12.66, p = 0.02) and cardiac death (hazard ratio 4.24, 95% CI 1.41 to 12.70) but not bleeding at 2-year follow-up. There was no association between aspirin reaction units >550 and HbA1c levels. In conclusion, in this large-scale study, HbA1c and HPR were positively associated, but the clinical effect on adverse outcome was driven by poor glycemic control, which predicted ST and cardiac death after PCI regardless of PRU levels, warranting efforts to improve glycemic control after DES implantation in patients with diabetes mellitus. |
Author | Brodie, Bruce R. Litherland, Claire Duffy, Peter L. Yu, Jennifer Henry, Timothy D. Clemmensen, Peter Schoos, Mikkel M. Cox, David A. Weisz, Giora Stone, Gregg W. Witzenbichler, Bernhard Neumann, Franz-Josef Kirtane, Ajay J. Metzger, D. Christopher Dangas, George D. Stuckey, Thomas D. Maehara, Akiko Mazzaferri, Ernest L. Mehran, Roxana Rinaldi, Michael J. |
Author_xml | – sequence: 1 givenname: Mikkel M. surname: Schoos fullname: Schoos, Mikkel M. organization: The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York – sequence: 2 givenname: George D. surname: Dangas fullname: Dangas, George D. organization: The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York – sequence: 3 givenname: Roxana orcidid: 0000-0002-5546-262X surname: Mehran fullname: Mehran, Roxana organization: The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York – sequence: 4 givenname: Ajay J. surname: Kirtane fullname: Kirtane, Ajay J. organization: Clinical Trials Center, Cardiovascular Research Foundation, New York, New York – sequence: 5 givenname: Jennifer surname: Yu fullname: Yu, Jennifer organization: The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York – sequence: 6 givenname: Claire surname: Litherland fullname: Litherland, Claire organization: Clinical Trials Center, Cardiovascular Research Foundation, New York, New York – sequence: 7 givenname: Peter surname: Clemmensen fullname: Clemmensen, Peter organization: Department of Cardiology, Nykoebing F Hospital, Institute of Regional Health Research, University of Southern Denmark, Denmark – sequence: 8 givenname: Thomas D. surname: Stuckey fullname: Stuckey, Thomas D. organization: LeBauer Cardiovascular Research Foundation/Cone Health, Greensboro, North Carolina – sequence: 9 givenname: Bernhard surname: Witzenbichler fullname: Witzenbichler, Bernhard organization: Department of Cardiology and Pneumology, Helios Amper-Klinikum, Dachau, Germany – sequence: 10 givenname: Giora surname: Weisz fullname: Weisz, Giora organization: Clinical Trials Center, Cardiovascular Research Foundation, New York, New York – sequence: 11 givenname: Michael J. surname: Rinaldi fullname: Rinaldi, Michael J. organization: Sanger Heart & Vascular Institute/Carolinas HealthCare System, Charlotte, North Carolina – sequence: 12 givenname: Franz-Josef surname: Neumann fullname: Neumann, Franz-Josef organization: Department of Cardiology and Angiology II, Universitäts-Herzzentrum Freiburg Bad Krozingen, Bad Krozingen, Germany – sequence: 13 givenname: D. Christopher surname: Metzger fullname: Metzger, D. Christopher organization: Wellmont CVA Heart Institute, Kingsport, Tennessee – sequence: 14 givenname: Timothy D. surname: Henry fullname: Henry, Timothy D. organization: Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota – sequence: 15 givenname: David A. surname: Cox fullname: Cox, David A. organization: Lehigh Valley Health Network, Allentown, Pennsylvania – sequence: 16 givenname: Peter L. surname: Duffy fullname: Duffy, Peter L. organization: Reid Heart Center, FirstHealth of the Carolinas, Pinehurst, North Carolina – sequence: 17 givenname: Bruce R. surname: Brodie fullname: Brodie, Bruce R. organization: LeBauer Cardiovascular Research Foundation/Cone Health, Greensboro, North Carolina – sequence: 18 givenname: Ernest L. orcidid: 0000-0002-5532-0306 surname: Mazzaferri fullname: Mazzaferri, Ernest L. organization: The Ohio State University Wexner Medical Center, Columbus, Ohio – sequence: 19 givenname: Akiko surname: Maehara fullname: Maehara, Akiko organization: Clinical Trials Center, Cardiovascular Research Foundation, New York, New York – sequence: 20 givenname: Gregg W. surname: Stone fullname: Stone, Gregg W. email: gs2184@columbia.edu organization: Clinical Trials Center, Cardiovascular Research Foundation, New York, New York |
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Copyright | 2016 Elsevier Inc. Elsevier Inc. Copyright © 2016 Elsevier Inc. All rights reserved. Copyright Elsevier Limited Jan 15, 2016 |
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