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CLINICAL CASE SEMINAR |
Department of Endocrinology (K.S.), St. Vincents Hospital and St. Vincents Clinic; Immunology and Infectious Diseases Unit (S.P., D.A.C.), St. Vincents Hospital; National Centre for HIV Epidemiology and Clinical Research (S.P., D.A.C.), University of New South Wales; and Holdsworth House General Practice (A.G.), Darlinghurst, New South Wales 2010, Australia; and 407 Doctors General Practice (M.M.), Surry Hills, New South Wales 2010, Australia
Address all correspondence and requests for reprints to: Dr. Katherine Samaras, MBBS, FRACP, Ph.D., Diabetes and Obesity Group, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, New South Wales, 2010, Australia. E-mail: k.samaras{at}garvan.org.au.
Ritonavir, a protease inhibitor (PI), is a potent inhibitor of cytochrome P450 3A4. This pharmacological effect, even at low doses (
200 mg/d), is used to "boost" levels of other PIs in the treatment of HIV infection and facilitate once or twice daily dosing with reduced pill burden. Six patients with preexisting HIV-lipodystrophy developed symptomatic Cushings syndrome when treated with inhaled fluticasone at varying doses for asthma while concurrently treated with low-dose ritonavir-boosted PI antiretroviral therapy (ART) regimens for HIV infection. There was evidence of adrenal suppression in all patients on stimulation studies. After the withdrawal of inhaled fluticasone, four patients became symptomatic of hypocortisolism, and three required oral corticosteroid support for several months. Other complications included evidence of osteoporosis (n = 3), crush fractures (n = 1), and exacerbation of preexisting type 2 diabetes mellitus (n = 1). In part, the diagnosis of fluticasone-induced Cushings syndrome was delayed because all patients had preexisting body composition changes of ART-associated lipodystrophy, masking the Cushings features. Practitioners should be aware of the impact on the adrenal axis of coadministration of PI-based ART regimens with inhaled corticosteroids and the potential for exacerbating or even inducing other metabolic conditions, such as osteoporosis or diabetes.
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