Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study

Background/Aims: Chronic Obstructive Pulmonary Disease (COPD) is characterized by airway inflammation, in which contributes to loss of lung function. Systemic inflammation is also a feature of COPD contributing to many associated co-morbidities. Statins, omega-3 fatty acids (docosahexanoic acid, DHA...

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Main Authors: Evan J. Williams, Katherine J. Baines, Joanne M. Smart, Peter G. Gibson, Lisa G. Wood
Format: Article
Language:English
Published: Elsevier 2016-09-01
Series:Journal of Nutrition & Intermediary Metabolism
Online Access:http://www.sciencedirect.com/science/article/pii/S2352385915300128
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spelling doaj-ad32a641fbc440fdb4205ab7ac6a41432020-11-24T23:19:47ZengElsevierJournal of Nutrition & Intermediary Metabolism2352-38592016-09-015C869510.1016/j.jnim.2016.04.006Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot studyEvan J. Williams0Katherine J. Baines1Joanne M. Smart2Peter G. Gibson3Lisa G. Wood4Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute and University of Newcastle, NSW, 2305, AustraliaPriority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute and University of Newcastle, NSW, 2305, AustraliaPriority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute and University of Newcastle, NSW, 2305, AustraliaPriority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute and University of Newcastle, NSW, 2305, AustraliaPriority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute and University of Newcastle, NSW, 2305, AustraliaBackground/Aims: Chronic Obstructive Pulmonary Disease (COPD) is characterized by airway inflammation, in which contributes to loss of lung function. Systemic inflammation is also a feature of COPD contributing to many associated co-morbidities. Statins, omega-3 fatty acids (docosahexanoic acid, DHA and eicosapentanoic acid, EPA) and lycopene have been shown to decrease systemic inflammation; however their combined effects have not been investigated. This study aims to identify changes in systemic and airway inflammation induced by statins alone or in combination with DHA, EPA and lycopene in COPD. Methods: COPD patients (n = 11) received rosuvastatin (20 mg/day) for 4 weeks, then a combination of rosuvastatin (20 mg/day), DHA and EPA (1.5 g/day) and lycopene (45 mg/day) for 8 weeks. Blood and sputum were collected and lung function measured by spirometry at baseline, week 4 and 12. Plasma fatty acids were measured using gas chromatography, while plasma carotenoids were analysed using high-performance liquid chromatography. Plasma CRP and IL-6 concentrations were measured using ELISA; and peripheral blood gene expression was measured using the nCounter™ GX Human Inflammation Kit 2. Results: Following the interventions, clinical characteristics and plasma IL-6 and CRP were unchanged. Sputum neutrophil proportion and absolute count was increased and macrophage proportion decreased by rosuvastatin (P = 0.020 and P = 0.015; respectively). Rosuvastatin increased LTB4R and decreased CXCL10 and AGER gene expression in white blood cells. The addition of lycopene and omega-3 fatty acids decreased LTB4R and increased CXCL10 to basal levels, whilst combined use of interventions increased ALOX15 blood gene expression. Conclusion: This study shows that rosuvastatin, omega-3 fatty acids and lycopene have some anti-inflammatory effects systemically, but rosuvastatin may increase airway neutrophils, which would be undesirable in COPD patients, warranting further investigation.http://www.sciencedirect.com/science/article/pii/S2352385915300128
collection DOAJ
language English
format Article
sources DOAJ
author Evan J. Williams
Katherine J. Baines
Joanne M. Smart
Peter G. Gibson
Lisa G. Wood
spellingShingle Evan J. Williams
Katherine J. Baines
Joanne M. Smart
Peter G. Gibson
Lisa G. Wood
Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
Journal of Nutrition & Intermediary Metabolism
author_facet Evan J. Williams
Katherine J. Baines
Joanne M. Smart
Peter G. Gibson
Lisa G. Wood
author_sort Evan J. Williams
title Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
title_short Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
title_full Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
title_fullStr Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
title_full_unstemmed Rosuvastatin, lycopene and omega-3 fatty acids: A potential treatment for systemic inflammation in COPD; a pilot study
title_sort rosuvastatin, lycopene and omega-3 fatty acids: a potential treatment for systemic inflammation in copd; a pilot study
publisher Elsevier
series Journal of Nutrition & Intermediary Metabolism
issn 2352-3859
publishDate 2016-09-01
description Background/Aims: Chronic Obstructive Pulmonary Disease (COPD) is characterized by airway inflammation, in which contributes to loss of lung function. Systemic inflammation is also a feature of COPD contributing to many associated co-morbidities. Statins, omega-3 fatty acids (docosahexanoic acid, DHA and eicosapentanoic acid, EPA) and lycopene have been shown to decrease systemic inflammation; however their combined effects have not been investigated. This study aims to identify changes in systemic and airway inflammation induced by statins alone or in combination with DHA, EPA and lycopene in COPD. Methods: COPD patients (n = 11) received rosuvastatin (20 mg/day) for 4 weeks, then a combination of rosuvastatin (20 mg/day), DHA and EPA (1.5 g/day) and lycopene (45 mg/day) for 8 weeks. Blood and sputum were collected and lung function measured by spirometry at baseline, week 4 and 12. Plasma fatty acids were measured using gas chromatography, while plasma carotenoids were analysed using high-performance liquid chromatography. Plasma CRP and IL-6 concentrations were measured using ELISA; and peripheral blood gene expression was measured using the nCounter™ GX Human Inflammation Kit 2. Results: Following the interventions, clinical characteristics and plasma IL-6 and CRP were unchanged. Sputum neutrophil proportion and absolute count was increased and macrophage proportion decreased by rosuvastatin (P = 0.020 and P = 0.015; respectively). Rosuvastatin increased LTB4R and decreased CXCL10 and AGER gene expression in white blood cells. The addition of lycopene and omega-3 fatty acids decreased LTB4R and increased CXCL10 to basal levels, whilst combined use of interventions increased ALOX15 blood gene expression. Conclusion: This study shows that rosuvastatin, omega-3 fatty acids and lycopene have some anti-inflammatory effects systemically, but rosuvastatin may increase airway neutrophils, which would be undesirable in COPD patients, warranting further investigation.
url http://www.sciencedirect.com/science/article/pii/S2352385915300128
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