Comparing proton pump inhibitors with histamin-2 receptor blockers regarding the risk of osteoporotic fractures: a nested case-control study of more than 350,000 Korean patients with GERD and peptic ulcer disease

Background Patients with peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD) are more likely to receive long-term therapy with proton pump inhibitors (PPIs). This study aimed to investigate the risk of osteoporotic fractures in PPI users compared to histamine-2 receptor antagonist...

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Veröffentlicht in:BMC geriatrics 2020-10, Vol.20 (1), p.407-11, Article 407
Hauptverfasser: Park, Joo-Hyun, Lee, Jessie, Yu, Su-Yeon, Jung, Jin-Hyung, Han, Kyungdo, Kim, Do-Hoon, Rhee, Jinnie
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container_issue 1
container_start_page 407
container_title BMC geriatrics
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creator Park, Joo-Hyun
Lee, Jessie
Yu, Su-Yeon
Jung, Jin-Hyung
Han, Kyungdo
Kim, Do-Hoon
Rhee, Jinnie
description Background Patients with peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD) are more likely to receive long-term therapy with proton pump inhibitors (PPIs). This study aimed to investigate the risk of osteoporotic fractures in PPI users compared to histamine-2 receptor antagonist (H2RA) users and the association between fractures and the duration and regular use of PPI. Methods A population-based, nationwide nested case-control study from January 2006 to December 2015 was performed using Korean National Health Insurance Service claims data. We included patients >= 50 years of age, without previous fractures, newly prescribed with PPI or H2RA, and diagnosed with PUD or GERD from 2006 to 2015. Patients with osteoporotic fracture (n = 59,240) were matched with the non-fracture control group (n = 296,200) at a 1:5 ratio based on sex, age, cohort entry date, follow-up duration, and bisphosphonate use. The osteoporotic fractures were defined using the diagnostic codes of claims data (M80, M81, M82, M484, M485, S220, S221, S320, S327, S422, S423, S525, S526, S72). Results The higher the cumulative use of PPIs, the higher the osteoporotic fracture risk (Pfor trend < 0.001). The risk of osteoporotic fracture in the patients whose cumulative use of PPI was more than 1 year was higher than that of others (OR: 1.42, 95% CI: 1.32-1.52). Patients who regularly used PPI in the recent 1 year had a higher risk of osteoporotic fracture than exclusive H2RA users (OR: 1.37, 95% CI: 1.26-1.50). Conclusions The risk of osteoporotic fracture increased with the duration of PPI use, especially when PPI was used for >= 1 year and regularly in the recent 1 year.
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This study aimed to investigate the risk of osteoporotic fractures in PPI users compared to histamine-2 receptor antagonist (H2RA) users and the association between fractures and the duration and regular use of PPI. Methods A population-based, nationwide nested case-control study from January 2006 to December 2015 was performed using Korean National Health Insurance Service claims data. We included patients &gt;= 50 years of age, without previous fractures, newly prescribed with PPI or H2RA, and diagnosed with PUD or GERD from 2006 to 2015. Patients with osteoporotic fracture (n = 59,240) were matched with the non-fracture control group (n = 296,200) at a 1:5 ratio based on sex, age, cohort entry date, follow-up duration, and bisphosphonate use. The osteoporotic fractures were defined using the diagnostic codes of claims data (M80, M81, M82, M484, M485, S220, S221, S320, S327, S422, S423, S525, S526, S72). Results The higher the cumulative use of PPIs, the higher the osteoporotic fracture risk (Pfor trend &lt; 0.001). The risk of osteoporotic fracture in the patients whose cumulative use of PPI was more than 1 year was higher than that of others (OR: 1.42, 95% CI: 1.32-1.52). Patients who regularly used PPI in the recent 1 year had a higher risk of osteoporotic fracture than exclusive H2RA users (OR: 1.37, 95% CI: 1.26-1.50). Conclusions The risk of osteoporotic fracture increased with the duration of PPI use, especially when PPI was used for &gt;= 1 year and regularly in the recent 1 year.</description><identifier>ISSN: 1471-2318</identifier><identifier>EISSN: 1471-2318</identifier><identifier>DOI: 10.1186/s12877-020-01794-3</identifier><identifier>PMID: 33059626</identifier><language>eng</language><publisher>LONDON: Springer Nature</publisher><subject><![CDATA[Age ; Aged ; Aged, 80 and over ; Anti-Ulcer Agents - administration & dosage ; Anti-Ulcer Agents - adverse effects ; Bisphosphonates ; Body mass index ; Case-Control Studies ; Enzyme Inhibitors - administration & dosage ; Enzyme Inhibitors - adverse effects ; Exercise ; Female ; Fracture ; Fractures ; Gastroesophageal reflux ; Gastroesophageal Reflux - drug therapy ; Gastroesophageal Reflux - epidemiology ; Gastroesophageal reflux disease ; Geriatrics ; Geriatrics & Gerontology ; Gerontology ; Histamine H2 Antagonists - administration & dosage ; Histamine H2 Antagonists - adverse effects ; Histamine H2 receptors ; Hormone replacement therapy ; Humans ; Life Sciences & Biomedicine ; Male ; Medical screening ; Older people ; Osteoporosis ; Osteoporotic Fractures - chemically induced ; Osteoporotic Fractures - epidemiology ; Peptic Ulcer - drug therapy ; Peptic Ulcer - epidemiology ; Peptic ulcer disease ; Peptic ulcers ; Physical fitness ; Population Surveillance ; Prescription drugs ; Proton pump inhibitors ; Proton Pump Inhibitors - administration & dosage ; Proton Pump Inhibitors - adverse effects ; Proton-pump inhibitor ; Republic of Korea - epidemiology ; Risk factors ; Science & Technology ; Sex ratio ; Treatment Outcome ; Ulcers]]></subject><ispartof>BMC geriatrics, 2020-10, Vol.20 (1), p.407-11, Article 407</ispartof><rights>2020. 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This study aimed to investigate the risk of osteoporotic fractures in PPI users compared to histamine-2 receptor antagonist (H2RA) users and the association between fractures and the duration and regular use of PPI. Methods A population-based, nationwide nested case-control study from January 2006 to December 2015 was performed using Korean National Health Insurance Service claims data. We included patients &gt;= 50 years of age, without previous fractures, newly prescribed with PPI or H2RA, and diagnosed with PUD or GERD from 2006 to 2015. Patients with osteoporotic fracture (n = 59,240) were matched with the non-fracture control group (n = 296,200) at a 1:5 ratio based on sex, age, cohort entry date, follow-up duration, and bisphosphonate use. The osteoporotic fractures were defined using the diagnostic codes of claims data (M80, M81, M82, M484, M485, S220, S221, S320, S327, S422, S423, S525, S526, S72). Results The higher the cumulative use of PPIs, the higher the osteoporotic fracture risk (Pfor trend &lt; 0.001). The risk of osteoporotic fracture in the patients whose cumulative use of PPI was more than 1 year was higher than that of others (OR: 1.42, 95% CI: 1.32-1.52). Patients who regularly used PPI in the recent 1 year had a higher risk of osteoporotic fracture than exclusive H2RA users (OR: 1.37, 95% CI: 1.26-1.50). Conclusions The risk of osteoporotic fracture increased with the duration of PPI use, especially when PPI was used for &gt;= 1 year and regularly in the recent 1 year.</description><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Ulcer Agents - administration &amp; dosage</subject><subject>Anti-Ulcer Agents - adverse effects</subject><subject>Bisphosphonates</subject><subject>Body mass index</subject><subject>Case-Control Studies</subject><subject>Enzyme Inhibitors - administration &amp; dosage</subject><subject>Enzyme Inhibitors - adverse effects</subject><subject>Exercise</subject><subject>Female</subject><subject>Fracture</subject><subject>Fractures</subject><subject>Gastroesophageal reflux</subject><subject>Gastroesophageal Reflux - drug therapy</subject><subject>Gastroesophageal Reflux - epidemiology</subject><subject>Gastroesophageal reflux disease</subject><subject>Geriatrics</subject><subject>Geriatrics &amp; Gerontology</subject><subject>Gerontology</subject><subject>Histamine H2 Antagonists - administration &amp; dosage</subject><subject>Histamine H2 Antagonists - adverse effects</subject><subject>Histamine H2 receptors</subject><subject>Hormone replacement therapy</subject><subject>Humans</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Male</subject><subject>Medical screening</subject><subject>Older people</subject><subject>Osteoporosis</subject><subject>Osteoporotic Fractures - chemically induced</subject><subject>Osteoporotic Fractures - epidemiology</subject><subject>Peptic Ulcer - drug therapy</subject><subject>Peptic Ulcer - epidemiology</subject><subject>Peptic ulcer disease</subject><subject>Peptic ulcers</subject><subject>Physical fitness</subject><subject>Population Surveillance</subject><subject>Prescription drugs</subject><subject>Proton pump inhibitors</subject><subject>Proton Pump Inhibitors - administration &amp; dosage</subject><subject>Proton Pump Inhibitors - adverse effects</subject><subject>Proton-pump inhibitor</subject><subject>Republic of Korea - epidemiology</subject><subject>Risk factors</subject><subject>Science &amp; 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Lee, Jessie ; Yu, Su-Yeon ; Jung, Jin-Hyung ; Han, Kyungdo ; Kim, Do-Hoon ; Rhee, Jinnie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-576b1658b1f1dc90d62ce4ed3cdc8ca2309e4aa946327975c1271b507dd12bd23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Ulcer Agents - administration &amp; dosage</topic><topic>Anti-Ulcer Agents - adverse effects</topic><topic>Bisphosphonates</topic><topic>Body mass index</topic><topic>Case-Control Studies</topic><topic>Enzyme Inhibitors - administration &amp; dosage</topic><topic>Enzyme Inhibitors - adverse effects</topic><topic>Exercise</topic><topic>Female</topic><topic>Fracture</topic><topic>Fractures</topic><topic>Gastroesophageal reflux</topic><topic>Gastroesophageal Reflux - drug therapy</topic><topic>Gastroesophageal Reflux - epidemiology</topic><topic>Gastroesophageal reflux disease</topic><topic>Geriatrics</topic><topic>Geriatrics &amp; Gerontology</topic><topic>Gerontology</topic><topic>Histamine H2 Antagonists - administration &amp; dosage</topic><topic>Histamine H2 Antagonists - adverse effects</topic><topic>Histamine H2 receptors</topic><topic>Hormone replacement therapy</topic><topic>Humans</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Male</topic><topic>Medical screening</topic><topic>Older people</topic><topic>Osteoporosis</topic><topic>Osteoporotic Fractures - chemically induced</topic><topic>Osteoporotic Fractures - epidemiology</topic><topic>Peptic Ulcer - drug therapy</topic><topic>Peptic Ulcer - epidemiology</topic><topic>Peptic ulcer disease</topic><topic>Peptic ulcers</topic><topic>Physical fitness</topic><topic>Population Surveillance</topic><topic>Prescription drugs</topic><topic>Proton pump inhibitors</topic><topic>Proton Pump Inhibitors - administration &amp; dosage</topic><topic>Proton Pump Inhibitors - adverse effects</topic><topic>Proton-pump inhibitor</topic><topic>Republic of Korea - epidemiology</topic><topic>Risk factors</topic><topic>Science &amp; Technology</topic><topic>Sex ratio</topic><topic>Treatment Outcome</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Joo-Hyun</creatorcontrib><creatorcontrib>Lee, Jessie</creatorcontrib><creatorcontrib>Yu, Su-Yeon</creatorcontrib><creatorcontrib>Jung, Jin-Hyung</creatorcontrib><creatorcontrib>Han, Kyungdo</creatorcontrib><creatorcontrib>Kim, Do-Hoon</creatorcontrib><creatorcontrib>Rhee, Jinnie</creatorcontrib><collection>Web of Knowledge</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science - Social Sciences Citation Index – 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Social Sciences Citation Index</collection><collection>Web of Science Primary (SCIE, SSCI &amp; AHCI)</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>Calcium &amp; 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This study aimed to investigate the risk of osteoporotic fractures in PPI users compared to histamine-2 receptor antagonist (H2RA) users and the association between fractures and the duration and regular use of PPI. Methods A population-based, nationwide nested case-control study from January 2006 to December 2015 was performed using Korean National Health Insurance Service claims data. We included patients &gt;= 50 years of age, without previous fractures, newly prescribed with PPI or H2RA, and diagnosed with PUD or GERD from 2006 to 2015. Patients with osteoporotic fracture (n = 59,240) were matched with the non-fracture control group (n = 296,200) at a 1:5 ratio based on sex, age, cohort entry date, follow-up duration, and bisphosphonate use. The osteoporotic fractures were defined using the diagnostic codes of claims data (M80, M81, M82, M484, M485, S220, S221, S320, S327, S422, S423, S525, S526, S72). Results The higher the cumulative use of PPIs, the higher the osteoporotic fracture risk (Pfor trend &lt; 0.001). The risk of osteoporotic fracture in the patients whose cumulative use of PPI was more than 1 year was higher than that of others (OR: 1.42, 95% CI: 1.32-1.52). Patients who regularly used PPI in the recent 1 year had a higher risk of osteoporotic fracture than exclusive H2RA users (OR: 1.37, 95% CI: 1.26-1.50). Conclusions The risk of osteoporotic fracture increased with the duration of PPI use, especially when PPI was used for &gt;= 1 year and regularly in the recent 1 year.</abstract><cop>LONDON</cop><pub>Springer Nature</pub><pmid>33059626</pmid><doi>10.1186/s12877-020-01794-3</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4358-4208</orcidid><orcidid>https://orcid.org/0000-0001-5488-5068</orcidid><orcidid>https://orcid.org/0000-0001-7421-4501</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Aged
Aged, 80 and over
Anti-Ulcer Agents - administration & dosage
Anti-Ulcer Agents - adverse effects
Bisphosphonates
Body mass index
Case-Control Studies
Enzyme Inhibitors - administration & dosage
Enzyme Inhibitors - adverse effects
Exercise
Female
Fracture
Fractures
Gastroesophageal reflux
Gastroesophageal Reflux - drug therapy
Gastroesophageal Reflux - epidemiology
Gastroesophageal reflux disease
Geriatrics
Geriatrics & Gerontology
Gerontology
Histamine H2 Antagonists - administration & dosage
Histamine H2 Antagonists - adverse effects
Histamine H2 receptors
Hormone replacement therapy
Humans
Life Sciences & Biomedicine
Male
Medical screening
Older people
Osteoporosis
Osteoporotic Fractures - chemically induced
Osteoporotic Fractures - epidemiology
Peptic Ulcer - drug therapy
Peptic Ulcer - epidemiology
Peptic ulcer disease
Peptic ulcers
Physical fitness
Population Surveillance
Prescription drugs
Proton pump inhibitors
Proton Pump Inhibitors - administration & dosage
Proton Pump Inhibitors - adverse effects
Proton-pump inhibitor
Republic of Korea - epidemiology
Risk factors
Science & Technology
Sex ratio
Treatment Outcome
Ulcers
title Comparing proton pump inhibitors with histamin-2 receptor blockers regarding the risk of osteoporotic fractures: a nested case-control study of more than 350,000 Korean patients with GERD and peptic ulcer disease
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