Bone Fracture Risk is Not Associated with the Use of Glucagon-Like Peptide-1 Receptor Agonists: A Population-Based Cohort Analysis

Verfasser / Beitragende:
[Johanna Driessen, Ronald Henry, Hein van Onzenoort, Arief Lalmohamed, Andrea Burden, Daniel Prieto-Alhambra, Cees Neef, Hubert Leufkens, Frank de Vries]
Ort, Verlag, Jahr:
2015
Enthalten in:
Calcified Tissue International, 97/2(2015-08-01), 104-112
Format:
Artikel (online)
ID: 605520968
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024 7 0 |a 10.1007/s00223-015-9993-5  |2 doi 
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245 0 0 |a Bone Fracture Risk is Not Associated with the Use of Glucagon-Like Peptide-1 Receptor Agonists: A Population-Based Cohort Analysis  |h [Elektronische Daten]  |c [Johanna Driessen, Ronald Henry, Hein van Onzenoort, Arief Lalmohamed, Andrea Burden, Daniel Prieto-Alhambra, Cees Neef, Hubert Leufkens, Frank de Vries] 
520 3 |a Glucagon-like Peptide-1 receptor agonists (GLP1-ra) are a relatively new class of anti-hyperglycemic drugs which may positively affect bone metabolism and thereby decrease (osteoporotic) bone fracture risk. Data on the effect of GLP1-ra on fracture risk are scarce and limited to clinical trial data only. The aim of this study was to investigate, in a population-based cohort, the association between the use of GLP1-ra and bone fracture risk. We conducted a population-based cohort study, with the use of data from the Clinical Practice Research Datalink (CPRD) database (2007-2012). The study population (N=216,816) consisted of all individuals with type 2 diabetes patients with at least one prescription for a non-insulin anti-diabetic drug and were over 18years of age. Cox proportional hazards models were used to estimate the hazard ratio of fracture in GLP1-ra users versus never-GLP1-ra users. Time-dependent adjustments were made for age, sex, lifestyle, comorbidity and the use of other drugs. There was no decreased risk of fracture with current use of GLP1-ra compared to never-GLP1-ra use (adjusted HR 0.99, 95% CI 0.82-1.19). Osteoporotic fracture risk was also not decreased by current GLP1-ra use (adjusted HR 0.97; 95% CI 0.72-1.32). In addition, stratification according to cumulative dose did not show a decreased bone fracture risk with increasing cumulative GLP1-ra dose. We showed in a population-based cohort study that GLP1-ra use is not associated with a decreased bone fracture risk compared to users of other anti-hyperglycemic drugs. Future research is needed to elucidate the potential working mechanisms of GLP1-ra on bone. 
540 |a The Author(s), 2015 
690 7 |a GLP1-ra  |2 nationallicence 
690 7 |a Fracture  |2 nationallicence 
690 7 |a Diabetes mellitus type 2  |2 nationallicence 
690 7 |a Cohort study  |2 nationallicence 
690 7 |a CPRD  |2 nationallicence 
700 1 |a Driessen  |D Johanna  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
700 1 |a Henry  |D Ronald  |u Department of Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands  |4 aut 
700 1 |a van Onzenoort  |D Hein  |u Department of Clinical Pharmacy and Toxicology, Maastricht University Medical Centre+, Maastricht, The Netherlands  |4 aut 
700 1 |a Lalmohamed  |D Arief  |u Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, The Netherlands  |4 aut 
700 1 |a Burden  |D Andrea  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
700 1 |a Prieto-Alhambra  |D Daniel  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Oxford NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, UK  |4 aut 
700 1 |a Neef  |D Cees  |u Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands  |4 aut 
700 1 |a Leufkens  |D Hubert  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
700 1 |a de Vries  |D Frank  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
773 0 |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 97/2(2015-08-01), 104-112  |x 0171-967X  |q 97:2<104  |1 2015  |2 97  |o 223 
856 4 0 |u https://doi.org/10.1007/s00223-015-9993-5  |q text/html  |z Onlinezugriff via DOI 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Driessen  |D Johanna  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Henry  |D Ronald  |u Department of Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a van Onzenoort  |D Hein  |u Department of Clinical Pharmacy and Toxicology, Maastricht University Medical Centre+, Maastricht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lalmohamed  |D Arief  |u Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Burden  |D Andrea  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Prieto-Alhambra  |D Daniel  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Oxford NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Neef  |D Cees  |u Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Leufkens  |D Hubert  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a de Vries  |D Frank  |u Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 97/2(2015-08-01), 104-112  |x 0171-967X  |q 97:2<104  |1 2015  |2 97  |o 223