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      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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          Abstract

          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 ( P for 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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          Most cited references41

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          An estimate of the worldwide prevalence and disability associated with osteoporotic fractures.

          The aim of this study was to quantify the global burden of osteoporotic fracture worldwide. The incidence of hip fractures was identified by systematic review and the incidence of osteoporotic fractures was imputed from the incidence of hip fractures in different regions of the world. Excess mortality and disability weights used age- and sex-specific data from Sweden to calculate the Disability Adjusted Life Years (DALYs) lost due to osteoporotic fracture. In the year 2000 there were an estimated 9.0 million osteoporotic fractures of which 1.6 million were at the hip, 1.7 million at the forearm and 1.4 million were clinical vertebral fractures. The greatest number of osteoporotic fractures occurred in Europe (34.8%). The total DALYs lost was 5.8 million of which 51% were accounted for by fractures that occurred in Europe and the Americas. World-wide, osteoporotic fractures accounted for 0.83% of the global burden of non-communicable disease and was 1.75% of the global burden in Europe. In Europe, osteoporotic fractures accounted for more DALYs lost than common cancers with the exception of lung cancer. For chronic musculo-skeletal disorders the DALYs lost in Europe due to osteoporosis (2.0 million) were less than for osteoarthrosis (3.1 million) but greater than for rheumatoid arthritis (1.0 million). We conclude that osteoporotic fractures are a significant cause of morbidity and mortality, particularly in the developed countries.
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            Trends in Prescription Drug Use Among Adults in the United States From 1999-2012.

            It is important to document patterns of prescription drug use to inform both clinical practice and research.
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              Clinical practice. Vitamin B12 deficiency.

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                Author and article information

                Contributors
                kmcfm@hanmail.net
                jinnie@neca.re.kr
                Journal
                BMC Geriatr
                BMC Geriatr
                BMC Geriatrics
                BioMed Central (London )
                1471-2318
                15 October 2020
                15 October 2020
                2020
                : 20
                : 407
                Affiliations
                [1 ]GRID grid.411134.2, ISNI 0000 0004 0474 0479, Department of Family Medicine, , Korea University Ansan Hospital, Korea University College of Medicine, ; 123, Jeokgeum-ro, Danwon-gu, Ansan-si, Gyeonggi-do 15355 Republic of Korea
                [2 ]National Evidence-based Healthcare Collaborating Agency, Seoul, Republic of Korea
                [3 ]GRID grid.411947.e, ISNI 0000 0004 0470 4224, Department of Biostatics, , Catholic University College of Medicine, ; Seoul, Republic of Korea
                [4 ]GRID grid.263765.3, ISNI 0000 0004 0533 3568, Department of Statistics and Actuarial Science, , Soongsil University, ; Seoul, Republic of Korea
                Author information
                http://orcid.org/0000-0001-7421-4501
                Article
                1794
                10.1186/s12877-020-01794-3
                7565339
                33059626
                0da95eaf-1e5d-4272-a11c-4ab2fa6771c5
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 21 April 2020
                : 27 September 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003670, National Evidence-based Healthcare Collaborating Agency;
                Award ID: NA17-004
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                Geriatric medicine
                proton-pump inhibitor,osteoporosis,fracture,peptic ulcer disease,gastroesophageal reflux disease

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