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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-ad32a641fbc440fdb4205ab7ac6a4143 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT evanjwilliams rosuvastatinlycopeneandomega3fattyacidsapotentialtreatmentforsystemicinflammationincopdapilotstudy AT katherinejbaines rosuvastatinlycopeneandomega3fattyacidsapotentialtreatmentforsystemicinflammationincopdapilotstudy AT joannemsmart rosuvastatinlycopeneandomega3fattyacidsapotentialtreatmentforsystemicinflammationincopdapilotstudy AT peterggibson rosuvastatinlycopeneandomega3fattyacidsapotentialtreatmentforsystemicinflammationincopdapilotstudy AT lisagwood rosuvastatinlycopeneandomega3fattyacidsapotentialtreatmentforsystemicinflammationincopdapilotstudy |
_version_ |
1725576858655784960 |