Thromb Haemost 2000; 83(05): 688-692
DOI: 10.1055/s-0037-1613893
Review Article
Schattauer GmbH

Pravastatin: An Antithrombotic Effect Independent of the Cholesterol-lowering Effect

George Dangas
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
2   The Cardiovascular Research Foundation, New York, NY
,
Donald A. Smith
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
Allen H. Unger
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
John H. Shao
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
Perwaiz Meraj
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
Carl Fier
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
Adam M. Cohen
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
John T. Fallon
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
Juan J. Badimon
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
,
John A. Ambrose
3   Saint Vincents Hospital Medical Center, New York, NY, USA
1   From the Cardiovascular Institute, Mount Sinai Medical Center, New York, NY
› Author Affiliations
This study was supported in part by a research grant from Bristol-Myers Squibb Company, Princeton, NJ, and by grant 5 M01 RR00071 to the Mount Sinai General Clinical Research Center from the National Center for Research Resources, National Institutes of Health, Bethesda, MD
Further Information

Publication History

Received 23 August 1999

Accepted after resubmission 21 January 2000

Publication Date:
08 December 2017 (online)

Summary

Lipid-lowering with statins reduces blood thrombogenicity. However, it is unknown whether this is purely due to LDL-cholesterol reduction, or it is related to a statin or agent specific effect. We investigated the relationship between reduction in blood thrombogenicity and the magnitude of low-density lipoprotein cholesterol (LDL-C) during pravastatin therapy.

We prospectively followed for 6 months 57 hyperlipidemic patients who initiated therapy with pravastatin, and 36 patients who were randomized into placebo plus diet. Pravastatin-treated patients were grouped according to the LDL-C reduction at 6 months; (i) “adequate LDL-C reduction”: LDL-C reduction >30% from baseline or LDL-C<125 mg/dl (n = 38; LDL-C reduction 74 ± 4 mg/dl; 6-month LDL-C 119 ± 5 mg/dl); (ii) “inadequate LDL-C reduction”: neither of the above criteria (n = 19; LDL-C reduction 31 ± 5 mg/dl; 6-month LDL-C 158 ± 6 mg/dl). Placebo patients were divided into those “with LDL-C reduction” (n = 17, mean reduction 21 ± 5 mg/dl) and those “without LDL reduction” (n = 19).

The following parameters were altered at 6 months in both patients with “adequate” and “inadequate” LDL-C reduction: (1) tissue plasminogen activator decreased by 1.4 ± 0.4 and 1.5 ± 0.5 ng/ml respectively (p = NS); (2) plasminogen activator inhibitor-1 decreased by 8.7 ± 2.0 and 10.1 ± 2.7 ng/ml respectively (p = NS); (3) thrombus formation under dynamic flow conditions decreased by 3.5 ± 0.9 and 2.8 ± 1.2 µm2 × 103 respectively (p = NS). In contrast, no significant changes from baseline were noted in placebo-treated patients, regardless of their LDL-C reduction category, and multivariate analysis eliminated LDL-C reduction as an independent predictor of reduction in thrombogenicity.

Therefore, the reduction in thrombogenicity was not proportional to the magnitude of LDL-C reduction suggesting that a class or agent specific property is primarily responsible for the pro-fibrinolytic/antithrombotic effects observed.

 
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