Thromb Haemost 1985; 54(03): 700-703
DOI: 10.1055/s-0038-1660101
Original Article
Schattauer GmbH Stuttgart

White Blood Cell Count and Haematocrit as Predictors of Coronary Recurrence after Myocardial Infarction

Authors

  • G D O Lowe

    The University Department of Medicine, Royal Infirmary, Glasgow, UK and the Maryland Medical Research Institute, Baltimore, USA
  • S G Machado

    The University Department of Medicine, Royal Infirmary, Glasgow, UK and the Maryland Medical Research Institute, Baltimore, USA
  • W F Krol

    The University Department of Medicine, Royal Infirmary, Glasgow, UK and the Maryland Medical Research Institute, Baltimore, USA
  • B A Barton

    The University Department of Medicine, Royal Infirmary, Glasgow, UK and the Maryland Medical Research Institute, Baltimore, USA
  • C D Forbes

    The University Department of Medicine, Royal Infirmary, Glasgow, UK and the Maryland Medical Research Institute, Baltimore, USA
Further Information

Publication History

Received 11 March 1985

Accepted 22 August 1985

Publication Date:
19 July 2018 (online)

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Summary

Baseline white blood cell count (WCC) and haematocrit were examined in relation to recurrent coronary events and to all-cause mortality in 2026 persons enrolled in the first Persantin-Aspirin Reinfarction Study (PARIS-1) 2-60 months after myocardial infarction. WCC was strongly related to coronary recurrence (relative risk 3.5 for men with WCC ≥ 9 × 109/1 vs men with WCC < 5 × 109/1) and total mortality (relative risk 2.6). No such relationships were found for haematocrit. WCC correlated also with cigarette-smoking, diuretic use, serum cholesterol and uric acid; however, the associations with coronary recurrence and total mortality persisted on multiple linear and logistic regression analysis including these variables and treatment group (p <0.001). WCC is therefore an easily-measured prognostic variable in survivors of myocardial infarction. Furthermore, we suggest that white blood cells may promote myocardial ischaemia by capillary plugging and/or release of toxic oxygen metabolites.