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Inflammatory biomarker changes in healthy adults secondary to electronic cigarette use: A scoping review

Context There has been a global increase in the use of electronic cigarettes (EC). However, to our knowledge, no review has summarized or categorized changes in inflammatory biomarkers after EC use in the extant literature. Objective To evaluate changes in general, cardiopulmonary, and oxidative str...

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Published in:Immunity, Inflammation and Disease Inflammation and Disease, 2024-02, Vol.12 (2), p.e1170-n/a
Main Authors: Boss, Shawn, Bertolio, Michael, Lipke, Laura
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description Context There has been a global increase in the use of electronic cigarettes (EC). However, to our knowledge, no review has summarized or categorized changes in inflammatory biomarkers after EC use in the extant literature. Objective To evaluate changes in general, cardiopulmonary, and oxidative stress‐related inflammatory biomarkers in healthy adults who use ECs. Methods A scoping review was conducted according to the Arksey and O'Malley framework. PubMed and MEDLINE (Ovid) databases were used for our search. After initial pilot searches and discussions, we performed a final search with medical subject headings and plain language terms related to inflammation, biomarkers, ECs, and adult humans. All full‐text articles, gray literature, and primary studies dating from the inception of the searched databases to the present were included. Studies of human participants with known confounding medical histories were excluded. Results Thirty‐seven studies met the inclusion criteria. After short‐term (1 month) use, ECs containing nicotine produced mixed results. Two commonly measured biomarkers in this group, matrix metalloproteinase‐9 (MMP‐9) and interleukin‐6 (IL‐6), were elevated in 75% and 60% of measured instances, respectively. Conclusion The results of studies evaluated in our scoping review suggested that short‐term use of nicotine‐containing ECs may result in increased CV and oxidative stress inflammation, contributing to potential CV or neurologic disease development. The results of studies evaluated in our scoping review also suggested that long‐term use of nicotine‐containing ECs resulted in no significant changes in general inflammatory biomarker levels. A rigorous systematic review and meta‐analysis is necessary to corroborate our findings and to determine the effect of long‐term EC use on MMP‐9 and IL‐6 levels. The current review summarizes changes in inflammatory biomarkers in adults after the use of electronic cigarettes. Cardiovascular, pulmonary, general, and oxidative‐stress biomarkers reported in the extant literature on this topic are reviewed.
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However, to our knowledge, no review has summarized or categorized changes in inflammatory biomarkers after EC use in the extant literature. Objective To evaluate changes in general, cardiopulmonary, and oxidative stress‐related inflammatory biomarkers in healthy adults who use ECs. Methods A scoping review was conducted according to the Arksey and O'Malley framework. PubMed and MEDLINE (Ovid) databases were used for our search. After initial pilot searches and discussions, we performed a final search with medical subject headings and plain language terms related to inflammation, biomarkers, ECs, and adult humans. All full‐text articles, gray literature, and primary studies dating from the inception of the searched databases to the present were included. Studies of human participants with known confounding medical histories were excluded. Results Thirty‐seven studies met the inclusion criteria. After short‐term (&lt;1 month) use, ECs containing nicotine moderately increased cardiovascular (CV) and oxidative stress markers of inflammation. Of all reported results, 50% of CV biomarkers were increased, and 64% of oxidative stress markers were increased. After long‐term (&gt;1 month) use, ECs containing nicotine produced mixed results. Two commonly measured biomarkers in this group, matrix metalloproteinase‐9 (MMP‐9) and interleukin‐6 (IL‐6), were elevated in 75% and 60% of measured instances, respectively. Conclusion The results of studies evaluated in our scoping review suggested that short‐term use of nicotine‐containing ECs may result in increased CV and oxidative stress inflammation, contributing to potential CV or neurologic disease development. The results of studies evaluated in our scoping review also suggested that long‐term use of nicotine‐containing ECs resulted in no significant changes in general inflammatory biomarker levels. A rigorous systematic review and meta‐analysis is necessary to corroborate our findings and to determine the effect of long‐term EC use on MMP‐9 and IL‐6 levels. The current review summarizes changes in inflammatory biomarkers in adults after the use of electronic cigarettes. Cardiovascular, pulmonary, general, and oxidative‐stress biomarkers reported in the extant literature on this topic are reviewed.</description><identifier>ISSN: 2050-4527</identifier><identifier>EISSN: 2050-4527</identifier><identifier>DOI: 10.1002/iid3.1170</identifier><identifier>PMID: 38353387</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Adult ; Biomarkers ; Cardiology ; cardiovascular disease ; Citation management software ; Confounding (Statistics) ; Content analysis ; Digital libraries ; Dissertations &amp; theses ; Electronic cigarettes ; Electronic Nicotine Delivery Systems ; e‐cig ; Grey literature ; Humans ; Inflammation ; Interleukin-6 ; Investigations ; Matrix Metalloproteinase 9 ; Nicotine ; Oxidative stress ; Physiology ; pulmonary disease ; Review ; vape ; Vaping - adverse effects</subject><ispartof>Immunity, Inflammation and Disease, 2024-02, Vol.12 (2), p.e1170-n/a</ispartof><rights>2024 The Authors. published by John Wiley &amp; Sons Ltd.</rights><rights>2024 The Authors. 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However, to our knowledge, no review has summarized or categorized changes in inflammatory biomarkers after EC use in the extant literature. Objective To evaluate changes in general, cardiopulmonary, and oxidative stress‐related inflammatory biomarkers in healthy adults who use ECs. Methods A scoping review was conducted according to the Arksey and O'Malley framework. PubMed and MEDLINE (Ovid) databases were used for our search. After initial pilot searches and discussions, we performed a final search with medical subject headings and plain language terms related to inflammation, biomarkers, ECs, and adult humans. All full‐text articles, gray literature, and primary studies dating from the inception of the searched databases to the present were included. Studies of human participants with known confounding medical histories were excluded. Results Thirty‐seven studies met the inclusion criteria. After short‐term (&lt;1 month) use, ECs containing nicotine moderately increased cardiovascular (CV) and oxidative stress markers of inflammation. Of all reported results, 50% of CV biomarkers were increased, and 64% of oxidative stress markers were increased. After long‐term (&gt;1 month) use, ECs containing nicotine produced mixed results. Two commonly measured biomarkers in this group, matrix metalloproteinase‐9 (MMP‐9) and interleukin‐6 (IL‐6), were elevated in 75% and 60% of measured instances, respectively. Conclusion The results of studies evaluated in our scoping review suggested that short‐term use of nicotine‐containing ECs may result in increased CV and oxidative stress inflammation, contributing to potential CV or neurologic disease development. The results of studies evaluated in our scoping review also suggested that long‐term use of nicotine‐containing ECs resulted in no significant changes in general inflammatory biomarker levels. A rigorous systematic review and meta‐analysis is necessary to corroborate our findings and to determine the effect of long‐term EC use on MMP‐9 and IL‐6 levels. The current review summarizes changes in inflammatory biomarkers in adults after the use of electronic cigarettes. 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theses</topic><topic>Electronic cigarettes</topic><topic>Electronic Nicotine Delivery Systems</topic><topic>e‐cig</topic><topic>Grey literature</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Interleukin-6</topic><topic>Investigations</topic><topic>Matrix Metalloproteinase 9</topic><topic>Nicotine</topic><topic>Oxidative stress</topic><topic>Physiology</topic><topic>pulmonary disease</topic><topic>Review</topic><topic>vape</topic><topic>Vaping - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boss, Shawn</creatorcontrib><creatorcontrib>Bertolio, Michael</creatorcontrib><creatorcontrib>Lipke, Laura</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Journals</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>Health &amp; 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However, to our knowledge, no review has summarized or categorized changes in inflammatory biomarkers after EC use in the extant literature. Objective To evaluate changes in general, cardiopulmonary, and oxidative stress‐related inflammatory biomarkers in healthy adults who use ECs. Methods A scoping review was conducted according to the Arksey and O'Malley framework. PubMed and MEDLINE (Ovid) databases were used for our search. After initial pilot searches and discussions, we performed a final search with medical subject headings and plain language terms related to inflammation, biomarkers, ECs, and adult humans. All full‐text articles, gray literature, and primary studies dating from the inception of the searched databases to the present were included. Studies of human participants with known confounding medical histories were excluded. Results Thirty‐seven studies met the inclusion criteria. After short‐term (&lt;1 month) use, ECs containing nicotine moderately increased cardiovascular (CV) and oxidative stress markers of inflammation. Of all reported results, 50% of CV biomarkers were increased, and 64% of oxidative stress markers were increased. After long‐term (&gt;1 month) use, ECs containing nicotine produced mixed results. Two commonly measured biomarkers in this group, matrix metalloproteinase‐9 (MMP‐9) and interleukin‐6 (IL‐6), were elevated in 75% and 60% of measured instances, respectively. Conclusion The results of studies evaluated in our scoping review suggested that short‐term use of nicotine‐containing ECs may result in increased CV and oxidative stress inflammation, contributing to potential CV or neurologic disease development. The results of studies evaluated in our scoping review also suggested that long‐term use of nicotine‐containing ECs resulted in no significant changes in general inflammatory biomarker levels. A rigorous systematic review and meta‐analysis is necessary to corroborate our findings and to determine the effect of long‐term EC use on MMP‐9 and IL‐6 levels. The current review summarizes changes in inflammatory biomarkers in adults after the use of electronic cigarettes. Cardiovascular, pulmonary, general, and oxidative‐stress biomarkers reported in the extant literature on this topic are reviewed.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38353387</pmid><doi>10.1002/iid3.1170</doi><tpages>18</tpages><orcidid>https://orcid.org/0009-0004-1095-4489</orcidid><oa>free_for_read</oa></addata></record>
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source PubMed Central (Open Access); Publicly Available Content (ProQuest); Wiley Open Access
subjects Adult
Biomarkers
Cardiology
cardiovascular disease
Citation management software
Confounding (Statistics)
Content analysis
Digital libraries
Dissertations & theses
Electronic cigarettes
Electronic Nicotine Delivery Systems
e‐cig
Grey literature
Humans
Inflammation
Interleukin-6
Investigations
Matrix Metalloproteinase 9
Nicotine
Oxidative stress
Physiology
pulmonary disease
Review
vape
Vaping - adverse effects
title Inflammatory biomarker changes in healthy adults secondary to electronic cigarette use: A scoping review
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