Proton pump inhibitors use and the risk of fatty liver disease: A nationwide cohort study

Background and Aim Proton pump inhibitor (PPI)‐induced hypochondria can change the composition of the gut microbiota, inducing overgrowth of small bowel bacteria, which has been suggested to promote the development of fatty liver disease through the gut‐liver axis. In this study, we aimed to investi...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2021-05, Vol.36 (5), p.1235-1243
Hauptverfasser: Pyo, Jeung Hui, Kim, Tae Jun, Lee, Hyuk, Choi, Sung Chul, Cho, Soo‐Jin, Choi, Yoon‐Ho, Min, Yang Won, Min, Byung‐Hoon, Lee, Jun Haeng, Kang, Minwoong, Lee, Yeong Chan, Kim, Jae J
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container_end_page 1243
container_issue 5
container_start_page 1235
container_title Journal of gastroenterology and hepatology
container_volume 36
creator Pyo, Jeung Hui
Kim, Tae Jun
Lee, Hyuk
Choi, Sung Chul
Cho, Soo‐Jin
Choi, Yoon‐Ho
Min, Yang Won
Min, Byung‐Hoon
Lee, Jun Haeng
Kang, Minwoong
Lee, Yeong Chan
Kim, Jae J
description Background and Aim Proton pump inhibitor (PPI)‐induced hypochondria can change the composition of the gut microbiota, inducing overgrowth of small bowel bacteria, which has been suggested to promote the development of fatty liver disease through the gut‐liver axis. In this study, we aimed to investigate the association between PPI use and the risk of fatty liver disease. Methods A retrospective cohort study was conducted using the Korean National Health Insurance Service‐National Sample Cohort, a nationwide population‐based representative sample, from January 1, 2002, to December 31, 2015. PPI use was identified from treatment claims and considered as a time‐varying variable. Results During 1 463 556 person‐years of follow‐up, 75 727 patients had at least one PPI prescription, and 3735 patients developed fatty liver disease. The hazard ratio for fatty liver disease comparing PPI users with non‐PPI users was 1.68 (95% confidence interval, 1.61–1.75). When adjusted for multiple confounders, including age, sex, body mass index, smoking, alcohol intake, exercise, income level, and comorbidities, the association was still significant (hazard ratio, 1.50; 95% confidence interval, 1.44–1.57). After considering the amounts of PPIs stratified by cumulative defined daily dose, the dose–response effect was observed until 180 days. Subgroup analysis also revealed that PPI use was correlated to an increased risk of fatty liver disease. Conclusions This current national wide cohort study suggests that PPI use was associated with an increased risk of fatty liver disease compared with non‐use of PPIs. Clinicians should consider fatty liver as a potential risk when prescribing PPI.
doi_str_mv 10.1111/jgh.15236
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In this study, we aimed to investigate the association between PPI use and the risk of fatty liver disease. Methods A retrospective cohort study was conducted using the Korean National Health Insurance Service‐National Sample Cohort, a nationwide population‐based representative sample, from January 1, 2002, to December 31, 2015. PPI use was identified from treatment claims and considered as a time‐varying variable. Results During 1 463 556 person‐years of follow‐up, 75 727 patients had at least one PPI prescription, and 3735 patients developed fatty liver disease. The hazard ratio for fatty liver disease comparing PPI users with non‐PPI users was 1.68 (95% confidence interval, 1.61–1.75). When adjusted for multiple confounders, including age, sex, body mass index, smoking, alcohol intake, exercise, income level, and comorbidities, the association was still significant (hazard ratio, 1.50; 95% confidence interval, 1.44–1.57). After considering the amounts of PPIs stratified by cumulative defined daily dose, the dose–response effect was observed until 180 days. Subgroup analysis also revealed that PPI use was correlated to an increased risk of fatty liver disease. Conclusions This current national wide cohort study suggests that PPI use was associated with an increased risk of fatty liver disease compared with non‐use of PPIs. Clinicians should consider fatty liver as a potential risk when prescribing PPI.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/jgh.15236</identifier><identifier>PMID: 32886822</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Body mass index ; Cohort analysis ; Cohort study ; Confidence intervals ; Dosage ; Drug dosages ; Fatty liver ; Fatty liver disease ; Intestinal microflora ; Liver diseases ; Microbiota ; Proton pump inhibitor ; Proton pump inhibitors ; Small intestine</subject><ispartof>Journal of gastroenterology and hepatology, 2021-05, Vol.36 (5), p.1235-1243</ispartof><rights>2020 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd</rights><rights>2020 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd.</rights><rights>2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley &amp; Sons Australia, Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-a93270663da31f67b84246f5ea601cddc8f341131235f4c1ed99b4b81dab41b13</citedby><cites>FETCH-LOGICAL-c3536-a93270663da31f67b84246f5ea601cddc8f341131235f4c1ed99b4b81dab41b13</cites><orcidid>0000-0003-4271-7205 ; 0000-0001-8101-9034</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjgh.15236$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjgh.15236$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32886822$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pyo, Jeung Hui</creatorcontrib><creatorcontrib>Kim, Tae Jun</creatorcontrib><creatorcontrib>Lee, Hyuk</creatorcontrib><creatorcontrib>Choi, Sung Chul</creatorcontrib><creatorcontrib>Cho, Soo‐Jin</creatorcontrib><creatorcontrib>Choi, Yoon‐Ho</creatorcontrib><creatorcontrib>Min, Yang Won</creatorcontrib><creatorcontrib>Min, Byung‐Hoon</creatorcontrib><creatorcontrib>Lee, Jun Haeng</creatorcontrib><creatorcontrib>Kang, Minwoong</creatorcontrib><creatorcontrib>Lee, Yeong Chan</creatorcontrib><creatorcontrib>Kim, Jae J</creatorcontrib><title>Proton pump inhibitors use and the risk of fatty liver disease: A nationwide cohort study</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background and Aim Proton pump inhibitor (PPI)‐induced hypochondria can change the composition of the gut microbiota, inducing overgrowth of small bowel bacteria, which has been suggested to promote the development of fatty liver disease through the gut‐liver axis. In this study, we aimed to investigate the association between PPI use and the risk of fatty liver disease. Methods A retrospective cohort study was conducted using the Korean National Health Insurance Service‐National Sample Cohort, a nationwide population‐based representative sample, from January 1, 2002, to December 31, 2015. PPI use was identified from treatment claims and considered as a time‐varying variable. Results During 1 463 556 person‐years of follow‐up, 75 727 patients had at least one PPI prescription, and 3735 patients developed fatty liver disease. The hazard ratio for fatty liver disease comparing PPI users with non‐PPI users was 1.68 (95% confidence interval, 1.61–1.75). When adjusted for multiple confounders, including age, sex, body mass index, smoking, alcohol intake, exercise, income level, and comorbidities, the association was still significant (hazard ratio, 1.50; 95% confidence interval, 1.44–1.57). After considering the amounts of PPIs stratified by cumulative defined daily dose, the dose–response effect was observed until 180 days. Subgroup analysis also revealed that PPI use was correlated to an increased risk of fatty liver disease. Conclusions This current national wide cohort study suggests that PPI use was associated with an increased risk of fatty liver disease compared with non‐use of PPIs. 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Kim, Tae Jun ; Lee, Hyuk ; Choi, Sung Chul ; Cho, Soo‐Jin ; Choi, Yoon‐Ho ; Min, Yang Won ; Min, Byung‐Hoon ; Lee, Jun Haeng ; Kang, Minwoong ; Lee, Yeong Chan ; Kim, Jae J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-a93270663da31f67b84246f5ea601cddc8f341131235f4c1ed99b4b81dab41b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Body mass index</topic><topic>Cohort analysis</topic><topic>Cohort study</topic><topic>Confidence intervals</topic><topic>Dosage</topic><topic>Drug dosages</topic><topic>Fatty liver</topic><topic>Fatty liver disease</topic><topic>Intestinal microflora</topic><topic>Liver diseases</topic><topic>Microbiota</topic><topic>Proton pump inhibitor</topic><topic>Proton pump inhibitors</topic><topic>Small intestine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pyo, Jeung Hui</creatorcontrib><creatorcontrib>Kim, Tae Jun</creatorcontrib><creatorcontrib>Lee, Hyuk</creatorcontrib><creatorcontrib>Choi, Sung Chul</creatorcontrib><creatorcontrib>Cho, Soo‐Jin</creatorcontrib><creatorcontrib>Choi, Yoon‐Ho</creatorcontrib><creatorcontrib>Min, Yang Won</creatorcontrib><creatorcontrib>Min, Byung‐Hoon</creatorcontrib><creatorcontrib>Lee, Jun Haeng</creatorcontrib><creatorcontrib>Kang, Minwoong</creatorcontrib><creatorcontrib>Lee, Yeong Chan</creatorcontrib><creatorcontrib>Kim, Jae J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pyo, Jeung Hui</au><au>Kim, Tae Jun</au><au>Lee, Hyuk</au><au>Choi, Sung Chul</au><au>Cho, Soo‐Jin</au><au>Choi, Yoon‐Ho</au><au>Min, Yang Won</au><au>Min, Byung‐Hoon</au><au>Lee, Jun Haeng</au><au>Kang, Minwoong</au><au>Lee, Yeong Chan</au><au>Kim, Jae J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proton pump inhibitors use and the risk of fatty liver disease: A nationwide cohort study</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2021-05</date><risdate>2021</risdate><volume>36</volume><issue>5</issue><spage>1235</spage><epage>1243</epage><pages>1235-1243</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background and Aim Proton pump inhibitor (PPI)‐induced hypochondria can change the composition of the gut microbiota, inducing overgrowth of small bowel bacteria, which has been suggested to promote the development of fatty liver disease through the gut‐liver axis. In this study, we aimed to investigate the association between PPI use and the risk of fatty liver disease. Methods A retrospective cohort study was conducted using the Korean National Health Insurance Service‐National Sample Cohort, a nationwide population‐based representative sample, from January 1, 2002, to December 31, 2015. PPI use was identified from treatment claims and considered as a time‐varying variable. Results During 1 463 556 person‐years of follow‐up, 75 727 patients had at least one PPI prescription, and 3735 patients developed fatty liver disease. The hazard ratio for fatty liver disease comparing PPI users with non‐PPI users was 1.68 (95% confidence interval, 1.61–1.75). When adjusted for multiple confounders, including age, sex, body mass index, smoking, alcohol intake, exercise, income level, and comorbidities, the association was still significant (hazard ratio, 1.50; 95% confidence interval, 1.44–1.57). After considering the amounts of PPIs stratified by cumulative defined daily dose, the dose–response effect was observed until 180 days. Subgroup analysis also revealed that PPI use was correlated to an increased risk of fatty liver disease. Conclusions This current national wide cohort study suggests that PPI use was associated with an increased risk of fatty liver disease compared with non‐use of PPIs. Clinicians should consider fatty liver as a potential risk when prescribing PPI.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32886822</pmid><doi>10.1111/jgh.15236</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4271-7205</orcidid><orcidid>https://orcid.org/0000-0001-8101-9034</orcidid></addata></record>
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subjects Body mass index
Cohort analysis
Cohort study
Confidence intervals
Dosage
Drug dosages
Fatty liver
Fatty liver disease
Intestinal microflora
Liver diseases
Microbiota
Proton pump inhibitor
Proton pump inhibitors
Small intestine
title Proton pump inhibitors use and the risk of fatty liver disease: A nationwide cohort study
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