Platelet Count and Mean Platelet Volume at the Time of and After Acute Myocardial Infarction

Author:

Amraotkar Alok Ravindra1,Song David Day2,Otero Diana3,Trainor Patrick James14,Ismail Imtiaz5,Kothari Vallari6,Singh Ayesha2,Moore Joseph B.1,Rai Shesh Nath57,DeFilippis Andrew Paul189

Affiliation:

1. Division of Cardiovascular Medicine, University of Louisville, Louisville, KY, USA

2. School of Medicine, University of Louisville, Louisville, KY, USA

3. Bronx Program, Icahn School of Medicine at Mount Sinai, Bronx, NY, USA

4. Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA

5. Department of Medicine, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA

6. Department of Internal Medicine, Henry Ford Hospital, Detroit, MI, USA

7. Biostatistics Shared Facility, J. G. Brown Cancer Center, University of Louisville, Louisville, KY, USA

8. KentuckyOne Health Jewish Hospital, Louisville, KY, USA

9. Ciccarone Center for the Prevention of Heart Disease, Johns Hopkins University, Baltimore, MD, USA

Abstract

Platelet count has been shown to be lower and mean platelet volume (MPV) to be higher in acute myocardial infarction (MI). However, it is not known whether these changes persist post-MI or if these measures are able to distinguish between acute thrombotic and non-thrombotic MI. Platelet count and MPV were measured in 80 subjects with acute MI (thrombotic and non-thrombotic) and stable coronary artery disease (CAD) at cardiac catheterization (acute phase) and at >3-month follow-up (quiescent phase). Subjects were stratified using stringent clinical, biochemical, histological, and angiographic criteria. Outcome measures were compared between groups by analysis of variance. Forty-seven subjects met criteria for acute MI with clearly defined thrombotic (n = 22) and non-thrombotic (n = 12) subsets. Fourteen subjects met criteria for stable CAD. No significant difference was observed in platelet count between subjects with acute MI and stable CAD at the acute or quiescent phase. MPV was higher in acute MI (9.18 ± 1.21) compared to stable CAD (8.13 ± 0.66; P = 0.003) at the acute phase but not at the quiescent phase (8.48 ± 0.58 vs 8.94 ± 1.42; P = 0.19). No difference in platelet count or MPV was detected between thrombotic and non-thrombotic subsets at acute or quiescent phases. The power to detect differences in these measures between thrombotic and non-thrombotic subsets was 58%. Higher MPV at the time of acute MI is not observed by 3 months post-MI (quiescent phase). Platelet count and MPV do not differ in subjects with thrombotic versus non-thrombotic MI. Further investigation is warranted to evaluate the utility of these measures in the diagnosis of acute MI.

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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