Effect of n–3 Polyunsaturated Fatty Acids in Asthma after Low-Dose Allergen Challenge
Background: We investigated the anti-inflammatory potential of n–3 polyunsaturated fatty acids (PUFA) on specific bronchial inflammation. Allergic asthmatics were challenged using a low-dose allergen provocation model. Methods: Our parallel double-blinded study randomly assigned 23 house dust mite-a...
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creator | Schubert, R. Kitz, R. Beermann, C. Rose, M.A. Lieb, A. Sommerer, P.C. Moskovits, J. Alberternst, H. Böhles, H.J. Schulze, J. Zielen, S. |
description | Background: We investigated the anti-inflammatory potential of n–3 polyunsaturated fatty acids (PUFA) on specific bronchial inflammation. Allergic asthmatics were challenged using a low-dose allergen provocation model. Methods: Our parallel double-blinded study randomly assigned 23 house dust mite-allergic asthmatics (aged 22–29 years; 13 females, 10 males) to dietary supplementation with either an n–3 PUFA-enriched fat blend (0.69 g/day) or placebo for 5 weeks. After 3 weeks, the patients were challenged daily with low doses of mite allergen for 2 weeks. Primary outcome parameters were effects on lung function (forced expiratory volume in 1 s, FEV 1 ) and exhaled nitric oxide (eNO) as a marker of bronchial inflammation. Results: Even before the bronchial challenge, eNO was significantly lower in the n–3 PUFA group (p = 0.014). Levels of eNO increased during allergen exposure in both groups, but differences in means were significantly lower in the n–3 PUFA group (p = 0.022). During the low-dose allergen challenge, there were no differences between the groups with regard to symptoms, FEV 1 or the allergen dose required to induce deterioration of lung function (PD 20 ). Numbers of sputum eosinophils did not differ significantly, while serum eosinophils (10.1 ± 0.1.84 vs. 5.79 ± 0.69%) as well as changes in eosinophilic cationic protein (20.5 ± 9.93 vs. –1.68 ± 4.36 ng/ml) and in vitro cysteinyl leukotriene release (2,889 ± 872 vs. 1,120 ± 173 ng/ml) were significantly lower in the n–3 PUFA group (p < 0.05 each). Conclusion: Our results provide evidence that dietary supplementation with n–3 PUFA is able to reduce bronchial inflammation even after low-dose allergen challenge. |
doi_str_mv | 10.1159/000170386 |
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Allergic asthmatics were challenged using a low-dose allergen provocation model. Methods: Our parallel double-blinded study randomly assigned 23 house dust mite-allergic asthmatics (aged 22–29 years; 13 females, 10 males) to dietary supplementation with either an n–3 PUFA-enriched fat blend (0.69 g/day) or placebo for 5 weeks. After 3 weeks, the patients were challenged daily with low doses of mite allergen for 2 weeks. Primary outcome parameters were effects on lung function (forced expiratory volume in 1 s, FEV 1 ) and exhaled nitric oxide (eNO) as a marker of bronchial inflammation. Results: Even before the bronchial challenge, eNO was significantly lower in the n–3 PUFA group (p = 0.014). Levels of eNO increased during allergen exposure in both groups, but differences in means were significantly lower in the n–3 PUFA group (p = 0.022). During the low-dose allergen challenge, there were no differences between the groups with regard to symptoms, FEV 1 or the allergen dose required to induce deterioration of lung function (PD 20 ). Numbers of sputum eosinophils did not differ significantly, while serum eosinophils (10.1 ± 0.1.84 vs. 5.79 ± 0.69%) as well as changes in eosinophilic cationic protein (20.5 ± 9.93 vs. –1.68 ± 4.36 ng/ml) and in vitro cysteinyl leukotriene release (2,889 ± 872 vs. 1,120 ± 173 ng/ml) were significantly lower in the n–3 PUFA group (p < 0.05 each). Conclusion: Our results provide evidence that dietary supplementation with n–3 PUFA is able to reduce bronchial inflammation even after low-dose allergen challenge.</description><identifier>ISSN: 1018-2438</identifier><identifier>EISSN: 1423-0097</identifier><identifier>DOI: 10.1159/000170386</identifier><identifier>PMID: 19001792</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adult ; Allergies ; Antigens, Dermatophagoides - immunology ; Asthma ; Asthma - diet therapy ; Asthma - immunology ; Asthma - physiopathology ; Biological and medical sciences ; Breath Tests ; Bronchial Provocation Tests ; Cell Count ; Chronic obstructive pulmonary disease, asthma ; Cysteine - metabolism ; Dietary supplements ; Double-Blind Method ; Eosinophils - cytology ; Erythrocytes - metabolism ; Fatty acids ; Fatty Acids, Omega-3 - blood ; Fatty Acids, Omega-3 - metabolism ; Fatty Acids, Omega-3 - therapeutic use ; Female ; Forced Expiratory Volume - physiology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Immune system ; Immunopathology ; Leukocyte Count ; Leukocytes - cytology ; Leukocytes - immunology ; Leukocytes - metabolism ; Leukotrienes - metabolism ; Male ; Medical sciences ; Nitric Oxide - metabolism ; Original Paper ; Pneumology ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Sputum - cytology ; Treatment Outcome ; Young Adult</subject><ispartof>International archives of allergy and immunology, 2009-01, Vol.148 (4), p.321-329</ispartof><rights>2008 S. Karger AG, Basel</rights><rights>2009 INIST-CNRS</rights><rights>Copyright 2008 S. Karger AG, Basel.</rights><rights>Copyright (c) 2009 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-cd5fcec6fe328718e6252026fa0cf208ce7c98f9e6942d66893105b9c0031ded3</citedby><cites>FETCH-LOGICAL-c458t-cd5fcec6fe328718e6252026fa0cf208ce7c98f9e6942d66893105b9c0031ded3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21213481$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19001792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schubert, R.</creatorcontrib><creatorcontrib>Kitz, R.</creatorcontrib><creatorcontrib>Beermann, C.</creatorcontrib><creatorcontrib>Rose, M.A.</creatorcontrib><creatorcontrib>Lieb, A.</creatorcontrib><creatorcontrib>Sommerer, P.C.</creatorcontrib><creatorcontrib>Moskovits, J.</creatorcontrib><creatorcontrib>Alberternst, H.</creatorcontrib><creatorcontrib>Böhles, H.J.</creatorcontrib><creatorcontrib>Schulze, J.</creatorcontrib><creatorcontrib>Zielen, S.</creatorcontrib><title>Effect of n–3 Polyunsaturated Fatty Acids in Asthma after Low-Dose Allergen Challenge</title><title>International archives of allergy and immunology</title><addtitle>Int Arch Allergy Immunol</addtitle><description>Background: We investigated the anti-inflammatory potential of n–3 polyunsaturated fatty acids (PUFA) on specific bronchial inflammation. Allergic asthmatics were challenged using a low-dose allergen provocation model. Methods: Our parallel double-blinded study randomly assigned 23 house dust mite-allergic asthmatics (aged 22–29 years; 13 females, 10 males) to dietary supplementation with either an n–3 PUFA-enriched fat blend (0.69 g/day) or placebo for 5 weeks. After 3 weeks, the patients were challenged daily with low doses of mite allergen for 2 weeks. Primary outcome parameters were effects on lung function (forced expiratory volume in 1 s, FEV 1 ) and exhaled nitric oxide (eNO) as a marker of bronchial inflammation. Results: Even before the bronchial challenge, eNO was significantly lower in the n–3 PUFA group (p = 0.014). Levels of eNO increased during allergen exposure in both groups, but differences in means were significantly lower in the n–3 PUFA group (p = 0.022). During the low-dose allergen challenge, there were no differences between the groups with regard to symptoms, FEV 1 or the allergen dose required to induce deterioration of lung function (PD 20 ). Numbers of sputum eosinophils did not differ significantly, while serum eosinophils (10.1 ± 0.1.84 vs. 5.79 ± 0.69%) as well as changes in eosinophilic cationic protein (20.5 ± 9.93 vs. –1.68 ± 4.36 ng/ml) and in vitro cysteinyl leukotriene release (2,889 ± 872 vs. 1,120 ± 173 ng/ml) were significantly lower in the n–3 PUFA group (p < 0.05 each). Conclusion: Our results provide evidence that dietary supplementation with n–3 PUFA is able to reduce bronchial inflammation even after low-dose allergen challenge.</description><subject>Adult</subject><subject>Allergies</subject><subject>Antigens, Dermatophagoides - immunology</subject><subject>Asthma</subject><subject>Asthma - diet therapy</subject><subject>Asthma - immunology</subject><subject>Asthma - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Breath Tests</subject><subject>Bronchial Provocation Tests</subject><subject>Cell Count</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Cysteine - metabolism</subject><subject>Dietary supplements</subject><subject>Double-Blind Method</subject><subject>Eosinophils - cytology</subject><subject>Erythrocytes - metabolism</subject><subject>Fatty acids</subject><subject>Fatty Acids, Omega-3 - blood</subject><subject>Fatty Acids, Omega-3 - metabolism</subject><subject>Fatty Acids, Omega-3 - therapeutic use</subject><subject>Female</subject><subject>Forced Expiratory Volume - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunopathology</subject><subject>Leukocyte Count</subject><subject>Leukocytes - cytology</subject><subject>Leukocytes - immunology</subject><subject>Leukocytes - metabolism</subject><subject>Leukotrienes - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nitric Oxide - metabolism</subject><subject>Original Paper</subject><subject>Pneumology</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunopathology</topic><topic>Leukocyte Count</topic><topic>Leukocytes - cytology</topic><topic>Leukocytes - immunology</topic><topic>Leukocytes - metabolism</topic><topic>Leukotrienes - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nitric Oxide - metabolism</topic><topic>Original Paper</topic><topic>Pneumology</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Sputum - cytology</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schubert, R.</creatorcontrib><creatorcontrib>Kitz, R.</creatorcontrib><creatorcontrib>Beermann, C.</creatorcontrib><creatorcontrib>Rose, M.A.</creatorcontrib><creatorcontrib>Lieb, A.</creatorcontrib><creatorcontrib>Sommerer, P.C.</creatorcontrib><creatorcontrib>Moskovits, J.</creatorcontrib><creatorcontrib>Alberternst, H.</creatorcontrib><creatorcontrib>Böhles, H.J.</creatorcontrib><creatorcontrib>Schulze, J.</creatorcontrib><creatorcontrib>Zielen, S.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>International archives of allergy and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schubert, R.</au><au>Kitz, R.</au><au>Beermann, C.</au><au>Rose, M.A.</au><au>Lieb, A.</au><au>Sommerer, P.C.</au><au>Moskovits, J.</au><au>Alberternst, H.</au><au>Böhles, H.J.</au><au>Schulze, J.</au><au>Zielen, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of n–3 Polyunsaturated Fatty Acids in Asthma after Low-Dose Allergen Challenge</atitle><jtitle>International archives of allergy and immunology</jtitle><addtitle>Int Arch Allergy Immunol</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>148</volume><issue>4</issue><spage>321</spage><epage>329</epage><pages>321-329</pages><issn>1018-2438</issn><eissn>1423-0097</eissn><abstract>Background: We investigated the anti-inflammatory potential of n–3 polyunsaturated fatty acids (PUFA) on specific bronchial inflammation. Allergic asthmatics were challenged using a low-dose allergen provocation model. Methods: Our parallel double-blinded study randomly assigned 23 house dust mite-allergic asthmatics (aged 22–29 years; 13 females, 10 males) to dietary supplementation with either an n–3 PUFA-enriched fat blend (0.69 g/day) or placebo for 5 weeks. After 3 weeks, the patients were challenged daily with low doses of mite allergen for 2 weeks. Primary outcome parameters were effects on lung function (forced expiratory volume in 1 s, FEV 1 ) and exhaled nitric oxide (eNO) as a marker of bronchial inflammation. Results: Even before the bronchial challenge, eNO was significantly lower in the n–3 PUFA group (p = 0.014). Levels of eNO increased during allergen exposure in both groups, but differences in means were significantly lower in the n–3 PUFA group (p = 0.022). During the low-dose allergen challenge, there were no differences between the groups with regard to symptoms, FEV 1 or the allergen dose required to induce deterioration of lung function (PD 20 ). Numbers of sputum eosinophils did not differ significantly, while serum eosinophils (10.1 ± 0.1.84 vs. 5.79 ± 0.69%) as well as changes in eosinophilic cationic protein (20.5 ± 9.93 vs. –1.68 ± 4.36 ng/ml) and in vitro cysteinyl leukotriene release (2,889 ± 872 vs. 1,120 ± 173 ng/ml) were significantly lower in the n–3 PUFA group (p < 0.05 each). Conclusion: Our results provide evidence that dietary supplementation with n–3 PUFA is able to reduce bronchial inflammation even after low-dose allergen challenge.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>19001792</pmid><doi>10.1159/000170386</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Allergies Antigens, Dermatophagoides - immunology Asthma Asthma - diet therapy Asthma - immunology Asthma - physiopathology Biological and medical sciences Breath Tests Bronchial Provocation Tests Cell Count Chronic obstructive pulmonary disease, asthma Cysteine - metabolism Dietary supplements Double-Blind Method Eosinophils - cytology Erythrocytes - metabolism Fatty acids Fatty Acids, Omega-3 - blood Fatty Acids, Omega-3 - metabolism Fatty Acids, Omega-3 - therapeutic use Female Forced Expiratory Volume - physiology Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Immune system Immunopathology Leukocyte Count Leukocytes - cytology Leukocytes - immunology Leukocytes - metabolism Leukotrienes - metabolism Male Medical sciences Nitric Oxide - metabolism Original Paper Pneumology Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Sputum - cytology Treatment Outcome Young Adult |
title | Effect of n–3 Polyunsaturated Fatty Acids in Asthma after Low-Dose Allergen Challenge |
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