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Vitamin D3 supplementation in adults with bronchiectasis: A pilot study
Vitamin D supplementation prevents acute respiratory infections and, through modulating innate and adaptive immunity, could have a potential role in bronchiectasis management. The primary aims of this pilot study were to assess serum 25-hydroxyvitamin D (25(OH)D) levels in New Zealand adults with br...
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Published in: | Chronic respiratory disease 2018-11, Vol.15 (4), p.384-392 |
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description | Vitamin D supplementation prevents acute respiratory infections and, through modulating innate and adaptive immunity, could have a potential role in bronchiectasis management. The primary aims of this pilot study were to assess serum 25-hydroxyvitamin D (25(OH)D) levels in New Zealand adults with bronchiectasis, and their 25(OH)D levels after vitamin D3 supplementation. Adults with bronchiectasis received an initial 2.5 mg vitamin D3 oral loading dose and 0.625 mg vitamin D3 weekly for 24 weeks. The primary outcome was serum 25(OH)D levels before and after vitamin D3 supplementation. Secondary outcomes (time to first infective exacerbation, exacerbation frequency, spirometry, health-related quality of life measures, sputum bacteriology and cell counts and chronic rhinosinusitis) were also assessed. This study is registered with the Australian New Zealand Clinical Trials Registry (ACTRN 12612001222831). The initial, average 25(OH)D level was 71 nmol/L (95% confidence interval (CI): [58, 84]), rising to 218 nmol/L (95% CI: [199, 237]) at 12 weeks and 205 nmol/L (95% CI: [186, 224]) at 24 weeks. The initial serum cathelicidin level was 25 nmol/L (95% CI: [17, 33]), rising to 102 nmol/L (95% CI: [48, 156]) at 12 weeks and 151 nmol/L (95% CI: [97, 205]) at 24 weeks. Over the 24-week study period, we observed statistically significant changes of 1.11 (95% CI: [0.08, 2.14]) in the Leicester Cough Questionnaire and −1.97 (95% CI: [−3.71, −0.23]) in the Dartmouth COOP charts score. No significant adverse effects were recorded. Many New Zealand adults with bronchiectasis have adequate 25(OH)D levels. Weekly vitamin D3 supplementation significantly improved 25(OH)D levels. |
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The primary aims of this pilot study were to assess serum 25-hydroxyvitamin D (25(OH)D) levels in New Zealand adults with bronchiectasis, and their 25(OH)D levels after vitamin D3 supplementation. Adults with bronchiectasis received an initial 2.5 mg vitamin D3 oral loading dose and 0.625 mg vitamin D3 weekly for 24 weeks. The primary outcome was serum 25(OH)D levels before and after vitamin D3 supplementation. Secondary outcomes (time to first infective exacerbation, exacerbation frequency, spirometry, health-related quality of life measures, sputum bacteriology and cell counts and chronic rhinosinusitis) were also assessed. This study is registered with the Australian New Zealand Clinical Trials Registry (ACTRN 12612001222831). The initial, average 25(OH)D level was 71 nmol/L (95% confidence interval (CI): [58, 84]), rising to 218 nmol/L (95% CI: [199, 237]) at 12 weeks and 205 nmol/L (95% CI: [186, 224]) at 24 weeks. The initial serum cathelicidin level was 25 nmol/L (95% CI: [17, 33]), rising to 102 nmol/L (95% CI: [48, 156]) at 12 weeks and 151 nmol/L (95% CI: [97, 205]) at 24 weeks. Over the 24-week study period, we observed statistically significant changes of 1.11 (95% CI: [0.08, 2.14]) in the Leicester Cough Questionnaire and −1.97 (95% CI: [−3.71, −0.23]) in the Dartmouth COOP charts score. No significant adverse effects were recorded. Many New Zealand adults with bronchiectasis have adequate 25(OH)D levels. Weekly vitamin D3 supplementation significantly improved 25(OH)D levels.</description><identifier>ISSN: 1479-9731</identifier><identifier>ISSN: 1479-9723</identifier><identifier>EISSN: 1479-9731</identifier><identifier>DOI: 10.1177/1479972318761646</identifier><identifier>PMID: 29490469</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Clinical outcomes ; Clinical trials ; Dietary supplements ; Immune system ; Lung diseases ; Original Papers ; Quality of life ; Respiration ; Rhinitis ; Sinusitis ; Vitamin D</subject><ispartof>Chronic respiratory disease, 2018-11, Vol.15 (4), p.384-392</ispartof><rights>The Author(s) 2018</rights><rights>The Author(s) 2018. This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2018 2018 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3416-9ef3c3a9d5546b7f9949f2bfbfd82e3f8b96f0b5fd5eb65d040a301a1a7868ad3</citedby><orcidid>0000-0002-5071-7654</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234573/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2420559911?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21966,25753,27853,27924,27925,37012,44590,44945,45333,53791,53793</link.rule.ids></links><search><creatorcontrib>Bartley, Jim</creatorcontrib><creatorcontrib>Garrett, Jeff</creatorcontrib><creatorcontrib>Camargo, Carlos A</creatorcontrib><creatorcontrib>Scragg, Robert</creatorcontrib><creatorcontrib>Vandal, Alain</creatorcontrib><creatorcontrib>Sisk, Rose</creatorcontrib><creatorcontrib>Milne, David</creatorcontrib><creatorcontrib>Tai, Ray</creatorcontrib><creatorcontrib>Jeon, Gene</creatorcontrib><creatorcontrib>Cursons, Ray</creatorcontrib><creatorcontrib>Wong, Conroy</creatorcontrib><title>Vitamin D3 supplementation in adults with bronchiectasis: A pilot study</title><title>Chronic respiratory disease</title><addtitle>Chron Respir Dis</addtitle><description>Vitamin D supplementation prevents acute respiratory infections and, through modulating innate and adaptive immunity, could have a potential role in bronchiectasis management. The primary aims of this pilot study were to assess serum 25-hydroxyvitamin D (25(OH)D) levels in New Zealand adults with bronchiectasis, and their 25(OH)D levels after vitamin D3 supplementation. Adults with bronchiectasis received an initial 2.5 mg vitamin D3 oral loading dose and 0.625 mg vitamin D3 weekly for 24 weeks. The primary outcome was serum 25(OH)D levels before and after vitamin D3 supplementation. Secondary outcomes (time to first infective exacerbation, exacerbation frequency, spirometry, health-related quality of life measures, sputum bacteriology and cell counts and chronic rhinosinusitis) were also assessed. This study is registered with the Australian New Zealand Clinical Trials Registry (ACTRN 12612001222831). The initial, average 25(OH)D level was 71 nmol/L (95% confidence interval (CI): [58, 84]), rising to 218 nmol/L (95% CI: [199, 237]) at 12 weeks and 205 nmol/L (95% CI: [186, 224]) at 24 weeks. The initial serum cathelicidin level was 25 nmol/L (95% CI: [17, 33]), rising to 102 nmol/L (95% CI: [48, 156]) at 12 weeks and 151 nmol/L (95% CI: [97, 205]) at 24 weeks. Over the 24-week study period, we observed statistically significant changes of 1.11 (95% CI: [0.08, 2.14]) in the Leicester Cough Questionnaire and −1.97 (95% CI: [−3.71, −0.23]) in the Dartmouth COOP charts score. No significant adverse effects were recorded. Many New Zealand adults with bronchiectasis have adequate 25(OH)D levels. Weekly vitamin D3 supplementation significantly improved 25(OH)D levels.</description><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Dietary supplements</subject><subject>Immune system</subject><subject>Lung diseases</subject><subject>Original Papers</subject><subject>Quality of life</subject><subject>Respiration</subject><subject>Rhinitis</subject><subject>Sinusitis</subject><subject>Vitamin D</subject><issn>1479-9731</issn><issn>1479-9723</issn><issn>1479-9731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><recordid>eNp9kctLAzEYxIMotlbvHgOeV_POxoNQfFSh4EW9hmQ3aVO2u-smq_S_d0sLPg6evo-ZH8PAAHCO0SXGUl5hJpWShOJcCiyYOADjrZQpSfHhj38ETmJcIUSUFOwYjIhiCjGhxmD2FpJZhxreURj7tq3c2tXJpNDUcFBN2Vcpws-QltB2TV0sgyuSiSFewylsQ9UkGFNfbk7BkTdVdGf7OwGvD_cvt4_Z_Hn2dDudZwVlWGTKeVpQo0rOmbDSq6GIJ9ZbX-bEUZ9bJTyy3JfcWcFLxJChCBtsZC5yU9IJuNnltr1du7IYynam0m0X1qbb6MYE_dupw1Ivmg8tCGVc0iHgYh_QNe-9i0mvmr6rh86aMII4VwrjfymMFeJSUTRQ2Y6KZuG-CYz0dh39dx36BaZZgDE</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Bartley, Jim</creator><creator>Garrett, Jeff</creator><creator>Camargo, Carlos A</creator><creator>Scragg, Robert</creator><creator>Vandal, Alain</creator><creator>Sisk, Rose</creator><creator>Milne, David</creator><creator>Tai, Ray</creator><creator>Jeon, Gene</creator><creator>Cursons, Ray</creator><creator>Wong, Conroy</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>K9.</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5071-7654</orcidid></search><sort><creationdate>20181101</creationdate><title>Vitamin D3 supplementation in adults with bronchiectasis: A pilot study</title><author>Bartley, Jim ; 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The primary aims of this pilot study were to assess serum 25-hydroxyvitamin D (25(OH)D) levels in New Zealand adults with bronchiectasis, and their 25(OH)D levels after vitamin D3 supplementation. Adults with bronchiectasis received an initial 2.5 mg vitamin D3 oral loading dose and 0.625 mg vitamin D3 weekly for 24 weeks. The primary outcome was serum 25(OH)D levels before and after vitamin D3 supplementation. Secondary outcomes (time to first infective exacerbation, exacerbation frequency, spirometry, health-related quality of life measures, sputum bacteriology and cell counts and chronic rhinosinusitis) were also assessed. This study is registered with the Australian New Zealand Clinical Trials Registry (ACTRN 12612001222831). The initial, average 25(OH)D level was 71 nmol/L (95% confidence interval (CI): [58, 84]), rising to 218 nmol/L (95% CI: [199, 237]) at 12 weeks and 205 nmol/L (95% CI: [186, 224]) at 24 weeks. The initial serum cathelicidin level was 25 nmol/L (95% CI: [17, 33]), rising to 102 nmol/L (95% CI: [48, 156]) at 12 weeks and 151 nmol/L (95% CI: [97, 205]) at 24 weeks. Over the 24-week study period, we observed statistically significant changes of 1.11 (95% CI: [0.08, 2.14]) in the Leicester Cough Questionnaire and −1.97 (95% CI: [−3.71, −0.23]) in the Dartmouth COOP charts score. No significant adverse effects were recorded. Many New Zealand adults with bronchiectasis have adequate 25(OH)D levels. Weekly vitamin D3 supplementation significantly improved 25(OH)D levels.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29490469</pmid><doi>10.1177/1479972318761646</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5071-7654</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Clinical outcomes Clinical trials Dietary supplements Immune system Lung diseases Original Papers Quality of life Respiration Rhinitis Sinusitis Vitamin D |
title | Vitamin D3 supplementation in adults with bronchiectasis: A pilot study |
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