Use of aldosterone antagonists to inhibit myocardial fibrosis
AssigneeThe Curators of the University of Missouri
InventorKarl T. Weber
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Abstract
This invention discloses a method of using an aldosterone antagonist such as spironolactone, at a dosage which does not disrupt a patient's normal electrolyte and water-retention balance, to inhibit myocardial fibrosis, including left ventricular hypertrophy (LVH).
Claims20
A method of inhibiting aldosterone-mediated myocardial fibrosis, comprising administering to a patient in need thereof an aldosterone antagonist which suppresses activity at aldosterone receptors in a mammalian body, wherein said aldosterone antagonist is administered in a quantity that is therapeutically effective in suppressing aldosterone-mediated myocardial fibrosis without substantially disrupting the water-retention balance of the body.
A method of inhibiting aldosterone-mediated myocardial fibrosis in a patient at risk of myocardial fibrosis, comprising administering to a patient in need thereof an aldosterone antagonist which suppresses activity at aldosterone receptors in a mammalian body, wherein said aldosterone antagonist is administered in a quantity that is therapeutically effective in suppressing aldosterone-mediated myocardial fibrosis without substantially increasing sodium excretion by the body.
A method of inhibiting aldosterone-mediated deposition of pathological concentrations of collagen, comprising administering to a patient in need thereof an aldosterone antagonist which suppresses activity at aldosterone receptors in a mammalian body, wherein said aldosterone antagonist is administered in a quantity that is therapeutically effective in suppressing aldosterone-mediated deposition of pathological concentrations of collagen without substantially increasing sodium excretion by the body.
A method of inhibiting aldosterone-mediated reactive fibrosis, comprising administering to a patient in need thereof an aldosterone antagonist which suppresses activity at aldosterone receptors in a mammalian body, wherein said aldosterone antagonist is administered in a quantity that is therapeutically effective in suppressing reactive fibrosis without substantially increasing sodium excretion by the body.
A method of inhibiting aldosterone-mediated perivascular fibrosis, comprising administering to a patient in need thereof an aldosterone antagonist which suppresses activity at aldosterone receptors in a mammalian body, wherein said aldosterone antagonist is administered in a quantity that is therapeutically effective in suppressing perivascular fibrosis without substantially increasing sodium excretion by the body.
Dependencies are inferred from the claim text.