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The Use of Antidepressants and the Risk of Idiopathic Pulmonary Arterial Hypertension
Affiliation:1. Policlinico S Orsola-Malpighi University Hospital, Bologna, Italy;2. University Hospital, Grenoble, France;3. CHU Bordeaux – Bordeaux University, Bordeaux, France;4. Alessandro Manzoni Hospital, Lecco, Italy;5. University Hospital Rennes, Rennes, France;6. Le Confluent Nouvelle Clinique Nantaises, Nantes, France;7. Medtronic plc, Minneapolis, MN, USA;8. Medtronic Bakken Research Center, Maastricht, The Netherlands;9. University Hospital Southampton, Southampton, United Kingdom;1. Division of Imaging Sciences and Biomedical Engineering, King''s College London, London, United Kingdom;2. Cardiovascular Department, Guy''s and St Thomas'' NHS Foundation Trust, London, United Kingdom;3. Medtronic Ltd, United Kingdom
Abstract:BackgroundSerotonin has been implicated in the development of idiopathic pulmonary arterial hypertension (IPAH). Drugs modulating serotonin pathways, including antidepressants, have been associated with the incidence of IPAH, with conflicting reports as to the direction of the effect. We aimed to determine whether antidepressant exposure is associated with the incidence of IPAH.MethodsA nested case-control study was conducted using the United Kingdom Clinical Practice Research Datalink and the Hospital Episodes Statistics repository between January 1, 1988 and September 30, 2011. Incident cases of IPAH were identified and matched to all controls in the case's risk set on age, sex, general practice, and date of registration with the practice. Rate ratios (RRs) and 95% confidence intervals (CIs) were estimated for the use of antidepressants on the risk of IPAH, with an 18-month lag period before the diagnosis.ResultsOne hundred ninety-five IPAH cases were identified (incidence 3.84/million per year). Use of any antidepressant was associated with a 67% increased risk of IPAH (RR, 1.67; 95% CI, 1.17-2.37). The rate of IPAH was similar across antidepressant classes, whether with selective serotonin reuptake inhibitors (SSRIs) (RR, 1.67; 95% CI, 1.09-2.57) or non-SSRI antidepressants (RR, 1.66; 95% CI, 1.07-2.59). In sensitivity and exploratory analyses, no change in risk was observed with different lag times, serotonin transporter affinities, or durations of exposure.ConclusionsThe use of antidepressants was associated with a significantly increased risk of IPAH. However, the consistency of this risk across all antidepressants and absence of a dose-response relationship suggests a noncausal association.
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