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Adverse effects of benfluorex on heart valves and pulmonary circulation
Author(s) -
Szymanski Catherine,
Andréjak Michel,
Peltier Marcel,
Maréchaux Sylvestre,
Tribouilloy Christophe
Publication year - 2014
Publication title -
pharmacoepidemiology and drug safety
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.023
H-Index - 96
eISSN - 1099-1557
pISSN - 1053-8569
DOI - 10.1002/pds.3642
Subject(s) - medicine , valvular heart disease , cardiology , adverse effect , stimulation , blockade , receptor
Benfluorex is responsible for the development of restrictive valvular regurgitation due to one of its metabolites, norfenfluramine. The 5‐HT 2B receptor, expressed on heart valves, acts as culprit receptor for drug‐induced valvular heart disease (VHD). Stimulation of this receptor leads to the upregulation of target genes involved in the proliferation and stimulation of valvular interstitial cells through different intracellular pathways. Valve lesions essentially involve the mitral and/or aortic valves. The randomised prospective REGULATE trial shows a threefold increase in the incidence of valvular regurgitation in patients exposed to benfluorex. A cross‐sectional trial shows that about 7% of patients without a history of VHD previously exposed to benfluorex present echocardiographic features of drug‐induced VHD. The excess risks of hospitalisation for cardiac valvular insufficiency and of valvular replacement surgery were respectively estimated to 0.5 per 1000 and 0.2 per 1000 exposed patients per year. Recent data strongly suggest an aetiological link between benfluorex exposure and pulmonary arterial hypertension (PAH). The PAH development may be explained by serotonin, which creates a pulmonary vasoconstriction through potassium‐channel blockade. Further studies should be conducted to determine the subsequent course of benfluorex‐induced VHD and PAH, and to identify genetic, biological and clinical factors that determine individual susceptibility to developing such adverse effects. Copyright © 2014 John Wiley & Sons, Ltd.