Impact of Proton-Pump Inhibitor Use on Gut Microbiota Composition and Other Markers of Health in Older Adults

Abstract Background The composition and diversity of the gut microbiota interact with the host immune system to prevent infection and limit accumulation of pathogen-related toxins. Proton-pump inhibitors (PPIs) may affect the gut microbiota by directly targeting bacterial proton pumps and/or affecti...

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Veröffentlicht in:Open forum infectious diseases 2017-10, Vol.4 (suppl_1), p.S234-S234
Hauptverfasser: Reveles, Kelly R, Moore, R Joel, Cosimi, Reese A, Ryan, Caitlin N, Chan, Luisa S, Haynes, Wanda L
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container_issue suppl_1
container_start_page S234
container_title Open forum infectious diseases
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creator Reveles, Kelly R
Moore, R Joel
Cosimi, Reese A
Ryan, Caitlin N
Chan, Luisa S
Haynes, Wanda L
description Abstract Background The composition and diversity of the gut microbiota interact with the host immune system to prevent infection and limit accumulation of pathogen-related toxins. Proton-pump inhibitors (PPIs) may affect the gut microbiota by directly targeting bacterial proton pumps and/or affecting the microenvironment of the flora; however, the extent to which PPIs alter gut microbiota composition and other markers of health is unknown. Methods This was a prospective study of healthy volunteers from San Antonio, TX from June to November 2016. Included subjects were ≥60 years old and had no recent use of medications known to affect the gut microbiota. Participants provided a blood and stool sample at baseline, completed a 14-day course of omeprazole 20mg daily, then provided a follow-up blood and stool sample. Stool 16s rRNA sequences were classified into operational taxonomic units (OTUs) via Mothur’s Bayesian classifier and referenced to the Greengenes database. OTU richness and Shannon diversity were compared between samples using the Wilcoxon signed rank test. Abundance-weighted sample differences were calculated using the Bray-Curtis dissimilarity. PERMANOVA was used to assess the impact of PPI use on β diversity. Systemic inflammatory markers (interleukin [IL]-6, IL-10, and tumor necrosis factor [TNF]-alpha) and insulin-like growth factor (IGF-1) were analyzed using ELISA and compared using the paired t-test. Results A total of 24 subjects completed the study (mean age 71 years; 63% female). OTU richness (P = 0.32) and Shannon diversity (P = 0.28) were similar between pre- and post-PPI samples. PPI use was associated with significantly lower abundance of Actinobacteria, Lachnospiraceae, Erysipelotrichaceae, and Bifidobacteriaceae. Β diversity was significantly associated with PPI use (P < 0.0001). PPI use was associated with a significant increase in mean IL-10 (5.7 vs. 4.7, P = 0.0385) and decrease in mean IGF-1 (87.5 vs. 94.8, P = 0.0185), while TNF-alpha (1.4 vs. 1.4, P = 0.9180) and IL-6 (4.6 vs. 3.4, P = 0.0808) were statistically similar between groups. Conclusion Short-term, over-the-counter PPI use was associated with significant changes in gut microbiota composition and other markers of health in older adults. Disclosures All authors: No reported disclosures.
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Proton-pump inhibitors (PPIs) may affect the gut microbiota by directly targeting bacterial proton pumps and/or affecting the microenvironment of the flora; however, the extent to which PPIs alter gut microbiota composition and other markers of health is unknown. Methods This was a prospective study of healthy volunteers from San Antonio, TX from June to November 2016. Included subjects were ≥60 years old and had no recent use of medications known to affect the gut microbiota. Participants provided a blood and stool sample at baseline, completed a 14-day course of omeprazole 20mg daily, then provided a follow-up blood and stool sample. Stool 16s rRNA sequences were classified into operational taxonomic units (OTUs) via Mothur’s Bayesian classifier and referenced to the Greengenes database. OTU richness and Shannon diversity were compared between samples using the Wilcoxon signed rank test. Abundance-weighted sample differences were calculated using the Bray-Curtis dissimilarity. PERMANOVA was used to assess the impact of PPI use on β diversity. Systemic inflammatory markers (interleukin [IL]-6, IL-10, and tumor necrosis factor [TNF]-alpha) and insulin-like growth factor (IGF-1) were analyzed using ELISA and compared using the paired t-test. Results A total of 24 subjects completed the study (mean age 71 years; 63% female). OTU richness (P = 0.32) and Shannon diversity (P = 0.28) were similar between pre- and post-PPI samples. PPI use was associated with significantly lower abundance of Actinobacteria, Lachnospiraceae, Erysipelotrichaceae, and Bifidobacteriaceae. Β diversity was significantly associated with PPI use (P &lt; 0.0001). PPI use was associated with a significant increase in mean IL-10 (5.7 vs. 4.7, P = 0.0385) and decrease in mean IGF-1 (87.5 vs. 94.8, P = 0.0185), while TNF-alpha (1.4 vs. 1.4, P = 0.9180) and IL-6 (4.6 vs. 3.4, P = 0.0808) were statistically similar between groups. Conclusion Short-term, over-the-counter PPI use was associated with significant changes in gut microbiota composition and other markers of health in older adults. Disclosures All authors: No reported disclosures.</description><identifier>ISSN: 2328-8957</identifier><identifier>EISSN: 2328-8957</identifier><identifier>DOI: 10.1093/ofid/ofx163.491</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><ispartof>Open forum infectious diseases, 2017-10, Vol.4 (suppl_1), p.S234-S234</ispartof><rights>The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,861,27905,27906</link.rule.ids></links><search><creatorcontrib>Reveles, Kelly R</creatorcontrib><creatorcontrib>Moore, R Joel</creatorcontrib><creatorcontrib>Cosimi, Reese A</creatorcontrib><creatorcontrib>Ryan, Caitlin N</creatorcontrib><creatorcontrib>Chan, Luisa S</creatorcontrib><creatorcontrib>Haynes, Wanda L</creatorcontrib><title>Impact of Proton-Pump Inhibitor Use on Gut Microbiota Composition and Other Markers of Health in Older Adults</title><title>Open forum infectious diseases</title><description>Abstract Background The composition and diversity of the gut microbiota interact with the host immune system to prevent infection and limit accumulation of pathogen-related toxins. Proton-pump inhibitors (PPIs) may affect the gut microbiota by directly targeting bacterial proton pumps and/or affecting the microenvironment of the flora; however, the extent to which PPIs alter gut microbiota composition and other markers of health is unknown. Methods This was a prospective study of healthy volunteers from San Antonio, TX from June to November 2016. Included subjects were ≥60 years old and had no recent use of medications known to affect the gut microbiota. Participants provided a blood and stool sample at baseline, completed a 14-day course of omeprazole 20mg daily, then provided a follow-up blood and stool sample. Stool 16s rRNA sequences were classified into operational taxonomic units (OTUs) via Mothur’s Bayesian classifier and referenced to the Greengenes database. OTU richness and Shannon diversity were compared between samples using the Wilcoxon signed rank test. Abundance-weighted sample differences were calculated using the Bray-Curtis dissimilarity. PERMANOVA was used to assess the impact of PPI use on β diversity. Systemic inflammatory markers (interleukin [IL]-6, IL-10, and tumor necrosis factor [TNF]-alpha) and insulin-like growth factor (IGF-1) were analyzed using ELISA and compared using the paired t-test. Results A total of 24 subjects completed the study (mean age 71 years; 63% female). OTU richness (P = 0.32) and Shannon diversity (P = 0.28) were similar between pre- and post-PPI samples. PPI use was associated with significantly lower abundance of Actinobacteria, Lachnospiraceae, Erysipelotrichaceae, and Bifidobacteriaceae. Β diversity was significantly associated with PPI use (P &lt; 0.0001). PPI use was associated with a significant increase in mean IL-10 (5.7 vs. 4.7, P = 0.0385) and decrease in mean IGF-1 (87.5 vs. 94.8, P = 0.0185), while TNF-alpha (1.4 vs. 1.4, P = 0.9180) and IL-6 (4.6 vs. 3.4, P = 0.0808) were statistically similar between groups. Conclusion Short-term, over-the-counter PPI use was associated with significant changes in gut microbiota composition and other markers of health in older adults. 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Proton-pump inhibitors (PPIs) may affect the gut microbiota by directly targeting bacterial proton pumps and/or affecting the microenvironment of the flora; however, the extent to which PPIs alter gut microbiota composition and other markers of health is unknown. Methods This was a prospective study of healthy volunteers from San Antonio, TX from June to November 2016. Included subjects were ≥60 years old and had no recent use of medications known to affect the gut microbiota. Participants provided a blood and stool sample at baseline, completed a 14-day course of omeprazole 20mg daily, then provided a follow-up blood and stool sample. Stool 16s rRNA sequences were classified into operational taxonomic units (OTUs) via Mothur’s Bayesian classifier and referenced to the Greengenes database. OTU richness and Shannon diversity were compared between samples using the Wilcoxon signed rank test. Abundance-weighted sample differences were calculated using the Bray-Curtis dissimilarity. PERMANOVA was used to assess the impact of PPI use on β diversity. Systemic inflammatory markers (interleukin [IL]-6, IL-10, and tumor necrosis factor [TNF]-alpha) and insulin-like growth factor (IGF-1) were analyzed using ELISA and compared using the paired t-test. Results A total of 24 subjects completed the study (mean age 71 years; 63% female). OTU richness (P = 0.32) and Shannon diversity (P = 0.28) were similar between pre- and post-PPI samples. PPI use was associated with significantly lower abundance of Actinobacteria, Lachnospiraceae, Erysipelotrichaceae, and Bifidobacteriaceae. Β diversity was significantly associated with PPI use (P &lt; 0.0001). PPI use was associated with a significant increase in mean IL-10 (5.7 vs. 4.7, P = 0.0385) and decrease in mean IGF-1 (87.5 vs. 94.8, P = 0.0185), while TNF-alpha (1.4 vs. 1.4, P = 0.9180) and IL-6 (4.6 vs. 3.4, P = 0.0808) were statistically similar between groups. Conclusion Short-term, over-the-counter PPI use was associated with significant changes in gut microbiota composition and other markers of health in older adults. Disclosures All authors: No reported disclosures.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/ofid/ofx163.491</doi><oa>free_for_read</oa></addata></record>
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title Impact of Proton-Pump Inhibitor Use on Gut Microbiota Composition and Other Markers of Health in Older Adults
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