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  Vol. 302 No. 13, October 7, 2009 TABLE OF CONTENTS
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Effects of Iron Supplementation and Depletion on Hypoxic Pulmonary Hypertension

Two Randomized Controlled Trials

Thomas G. Smith, MBBS, DPhil; Nick P. Talbot, BMBCh, DPhil; Catherine Privat, BSc; Maria Rivera-Ch, PhD; Annabel H. Nickol, MBBS, PhD; Peter J. Ratcliffe, BMBCh, MD; Keith L. Dorrington, DM, DPhil; Fabiola León-Velarde, PhD; Peter A. Robbins, BMBCh, DPhil

JAMA. 2009;302(13):1444-1450.

Context  Hypoxia is a major cause of pulmonary hypertension in respiratory disease and at high altitude. Recent work has established that the effect of hypoxia on pulmonary arterial pressure may depend on iron status, possibly acting through the transcription factor hypoxia-inducible factor, but the pathophysiological and clinical importance of this interaction is unknown.

Objective  To determine whether increasing or decreasing iron availability modifies altitude-induced hypoxic pulmonary hypertension.

Design, Setting, and Participants  Two randomized, double-blind, placebo-controlled protocols conducted in October-November 2008. In the first protocol, 22 healthy sea-level resident men (aged 19-60 years) were studied over 1 week of hypoxia at Cerro de Pasco, Peru (altitude 4340 m). In the second protocol, 11 high-altitude resident men (aged 30-59 years) diagnosed with chronic mountain sickness were studied over 1 month of hypoxia at Cerro de Pasco, Peru.

Intervention  In the first protocol, participants received intravenous infusions of Fe(III)-hydroxide sucrose (200 mg) or placebo on the third day of hypoxia. In the second protocol, patients underwent staged isovolemic venesection of 2 L of blood. Two weeks later, patients received intravenous infusions of Fe(III)-hydroxide sucrose (400 mg) or placebo, which were subsequently crossed over.

Main Outcome Measure  Effect of varying iron availability on pulmonary artery systolic pressure (PASP) assessed by Doppler echocardiography.

Results  In the sea-level resident protocol, approximately 40% of the pulmonary hypertensive response to hypoxia was reversed by infusion of iron, which reduced PASP by 6 mm Hg (95% confidence interval [CI], 4-8 mm Hg), from 37 mm Hg (95% CI, 34-40 mm Hg) to 31 mm Hg (95% CI, 29-33 mm Hg; P = .01). In the chronic mountain sickness protocol, progressive iron deficiency induced by venesection was associated with an approximately 25% increase in PASP of 9 mm Hg (95% CI, 4-14 mm Hg), from 37 mm Hg (95% CI, 30-44 mm Hg) to 46 mm Hg (95% CI, 40-52 mm Hg; P = .003). During the subsequent crossover period, no acute effect of iron replacement on PASP was detected.

Conclusion  Hypoxic pulmonary hypertension may be attenuated by iron supplementation and exacerbated by iron depletion.

Trial Registration  clinicaltrials.gov Identifier: NCT00952302


Author Affiliations: Department of Physiology, Anatomy, and Genetics (Drs Smith, Talbot, Nickol, Dorrington, and Robbins) and Nuffield Department of Clinical Medicine (Dr Ratcliffe), University of Oxford, Oxford, England; Nuffield Department of Anaesthetics, John Radcliffe Hospital, Headington, Oxford, England (Drs Smith and Dorrington); Oxford Centre for Respiratory Medicine, Churchill Hospital, Oxford, England (Drs Talbot and Nickol); and High Altitude Adaptation Laboratory, Cayetano Heredia University, Lima, Peru (Drs Rivera-Ch and León-Velarde and Ms Privat).



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