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Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome
BACKGROUND: Postural tachycardia syndrome (POTS) is a disorder of chronic orthostatic intolerance accompanied by excessive orthostatic tachycardia. Patients with POTS commonly have comorbid conditions such as attention deficit hyperactivity disorder, depression, or fibromyalgia that are treated with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835251/ https://www.ncbi.nlm.nih.gov/pubmed/24002370 http://dx.doi.org/10.1161/JAHA.113.000395 |
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author | Green, Elizabeth A. Raj, Vidya Shibao, Cyndya A. Biaggioni, Italo Black, Bonnie K. Dupont, William D. Robertson, David Raj, Satish R. |
author_facet | Green, Elizabeth A. Raj, Vidya Shibao, Cyndya A. Biaggioni, Italo Black, Bonnie K. Dupont, William D. Robertson, David Raj, Satish R. |
author_sort | Green, Elizabeth A. |
collection | PubMed |
description | BACKGROUND: Postural tachycardia syndrome (POTS) is a disorder of chronic orthostatic intolerance accompanied by excessive orthostatic tachycardia. Patients with POTS commonly have comorbid conditions such as attention deficit hyperactivity disorder, depression, or fibromyalgia that are treated with medications that inhibit the norepinephrine reuptake transporter (NRI). NRI medications can increase sympathetic nervous system tone, which may increase heart rate (HR) and worsen symptoms in POTS patients. We sought to determine whether NRI with atomoxetine increases standing tachycardia or worsens the symptom burden in POTS patients. METHODS AND RESULTS: Patients with POTS (n=27) underwent an acute drug trial of atomoxetine 40 mg and placebo on separate mornings in a randomized, crossover design. Blood pressure (BP), HR, and symptoms were assessed while seated and after standing prior to and hourly for 4 hours following study drug administration. Atomoxetine significantly increased standing HR compared with placebo (121±17 beats per minute versus 105±15 beats per minute; P=0.001) in POTS patients, with a trend toward higher standing systolic BP (P=0.072). Symptom scores worsened with atomoxetine compared to placebo (+4.2 au versus −3.5 au; P=0.028) from baseline to 2 hours after study drug administration. CONCLUSION: Norepinephrine reuptake inhibition with atomoxetine acutely increased standing HR and symptom burden in patients with POTS. CLINICAL TRIALS REGISTRATION: URL: http://clinicaltrials.gov. Unique identifier: NCT00262470. |
format | Online Article Text |
id | pubmed-3835251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38352512013-11-25 Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome Green, Elizabeth A. Raj, Vidya Shibao, Cyndya A. Biaggioni, Italo Black, Bonnie K. Dupont, William D. Robertson, David Raj, Satish R. J Am Heart Assoc Original Research BACKGROUND: Postural tachycardia syndrome (POTS) is a disorder of chronic orthostatic intolerance accompanied by excessive orthostatic tachycardia. Patients with POTS commonly have comorbid conditions such as attention deficit hyperactivity disorder, depression, or fibromyalgia that are treated with medications that inhibit the norepinephrine reuptake transporter (NRI). NRI medications can increase sympathetic nervous system tone, which may increase heart rate (HR) and worsen symptoms in POTS patients. We sought to determine whether NRI with atomoxetine increases standing tachycardia or worsens the symptom burden in POTS patients. METHODS AND RESULTS: Patients with POTS (n=27) underwent an acute drug trial of atomoxetine 40 mg and placebo on separate mornings in a randomized, crossover design. Blood pressure (BP), HR, and symptoms were assessed while seated and after standing prior to and hourly for 4 hours following study drug administration. Atomoxetine significantly increased standing HR compared with placebo (121±17 beats per minute versus 105±15 beats per minute; P=0.001) in POTS patients, with a trend toward higher standing systolic BP (P=0.072). Symptom scores worsened with atomoxetine compared to placebo (+4.2 au versus −3.5 au; P=0.028) from baseline to 2 hours after study drug administration. CONCLUSION: Norepinephrine reuptake inhibition with atomoxetine acutely increased standing HR and symptom burden in patients with POTS. CLINICAL TRIALS REGISTRATION: URL: http://clinicaltrials.gov. Unique identifier: NCT00262470. Blackwell Publishing Ltd 2013-10-25 /pmc/articles/PMC3835251/ /pubmed/24002370 http://dx.doi.org/10.1161/JAHA.113.000395 Text en © 2013 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an Open Access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Green, Elizabeth A. Raj, Vidya Shibao, Cyndya A. Biaggioni, Italo Black, Bonnie K. Dupont, William D. Robertson, David Raj, Satish R. Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title | Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title_full | Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title_fullStr | Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title_full_unstemmed | Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title_short | Effects of Norepinephrine Reuptake Inhibition on Postural Tachycardia Syndrome |
title_sort | effects of norepinephrine reuptake inhibition on postural tachycardia syndrome |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835251/ https://www.ncbi.nlm.nih.gov/pubmed/24002370 http://dx.doi.org/10.1161/JAHA.113.000395 |
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