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DOI 10.1159/000066348

Медицинская библиотека · Kidney & blood pressure research · 2002

Effect of spironolactone on impaired fibrinolysis of hypertensive patients.

Vautier-Rit S, Subtil D, Vaast P, Dufour P, Valat A S, Bourgeot P, Puech F

Клиническое исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND/AIMS: Angiotensin-converting enzyme inhibitors and angiotensin II receptor antagonists have beneficial effects on impaired fibrinolytic activity of hypertensive patients. The aim of the study was to evaluate the effect of antialdosterone treatment on impaired fibrinolysis of hypertensive patients.

METHODS

Fourteen hypertensive outpatients and 14 normotensive healthy volunteers participated in this study. Blood samples for plasminogen activator inhibitor-1 (PAI-1) antigen and tissue plasminogen activator (t-PA) antigen were obtained at baseline in all patients and control subjects. Then all hypertensive patients used spironolactone 50 mg/day for a week. Blood samples were again obtained after a week of spironolactone treatment.

RESULTS

The mean basal plasma level of PAI-1 of hypertensive patients was higher than those of the normotensive control group (60.98 +/- 4.2 vs. 24.09 +/- 1.61 ng/ml, p < 0.01) The mean basal t-PA level was similar in the hypertensive and control subjects (7.49 +/- 0.65 vs. 8.78 +/- 0.92 ng/ml, p > 0.05). The mean PAI-1 level decreased after a week of spironolactone treatment (60.98 +/- 4.2 vs. 42.99 +/- 7.98 ng/ml, p < 0.05). The mean plasma t-PA level of hypertensive patients increased after spironolactone treatment (7.49 +/- 0.65 vs. 11.09 +/- 1.33 ng/ml, p < 0.05).

CONCLUSION

This study shows that spironolactone improves impaired fibrinolysis in systemic hypertension. It provides evidence for a direct link between aldosterone and the fibrinolytic system in humans.

Для цитирования: Vautier-Rit S, Subtil D, Vaast P, Dufour P, Valat A S, Bourgeot P, Puech F. Effect of spironolactone on impaired fibrinolysis of hypertensive patients.. Kidney & blood pressure research. 2002. DOI: 10.1159/000066348.

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