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Diagnosis of osteoporosis in statin-treated patients is dose-dependent
OBJECTIVE: Whether HMG-CoA-reductase inhibition, the main mechanism of statins, plays a role in the pathogenesis of osteoporosis, is not entirely known so far. Consequently, this study was set out to investigate the relationship of different kinds and dosages of statins with osteoporosis, hypothesis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900255/ https://www.ncbi.nlm.nih.gov/pubmed/31558481 http://dx.doi.org/10.1136/annrheumdis-2019-215714 |
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author | Leutner, Michael Matzhold, Caspar Bellach, Luise Deischinger, Carola Harreiter, Jürgen Thurner, Stefan Klimek, Peter Kautzky-Willer, Alexandra |
author_facet | Leutner, Michael Matzhold, Caspar Bellach, Luise Deischinger, Carola Harreiter, Jürgen Thurner, Stefan Klimek, Peter Kautzky-Willer, Alexandra |
author_sort | Leutner, Michael |
collection | PubMed |
description | OBJECTIVE: Whether HMG-CoA-reductase inhibition, the main mechanism of statins, plays a role in the pathogenesis of osteoporosis, is not entirely known so far. Consequently, this study was set out to investigate the relationship of different kinds and dosages of statins with osteoporosis, hypothesising that the inhibition of the synthesis of cholesterol could influence sex-hormones and therefore the diagnosis of osteoporosis. METHODS: Medical claims data of all Austrians from 2006 to 2007 was used to identify all patients treated with statins to compute their daily defined dose averages of six different types of statins. We applied multiple logistic regression to analyse the dose-dependent risks of being diagnosed with osteoporosis for each statin individually. RESULTS: In the general study population, statin treatment was associated with an overrepresentation of diagnosed osteoporosis compared with controls (OR: 3.62, 95% CI 3.55 to 3.69, p<0.01). There was a highly non-trivial dependence of statin dosage with the ORs of osteoporosis. Osteoporosis was underrepresented in low-dose statin treatment (0–10 mg per day), including lovastatin (OR: 0.39, CI 0.18 to 0.84, p<0.05), pravastatin (OR: 0.68, 95% CI 0.52 to 0.89, p<0.01), simvastatin (OR: 0.70, 95% CI 0.56 to 0.86, p<0.01) and rosuvastatin (OR: 0.69, 95% CI 0.55 to 0.87, p<0.01). However, the exceeding of the 40 mg threshold for simvastatin (OR: 1.64, 95% CI 1.31 to 2.07, p<0.01), and the exceeding of a 20 mg threshold for atorvastatin (OR: 1.78, 95% CI 1.41 to 2.23, p<0.01) and for rosuvastatin (OR: 2.04, 95% CI 1.31 to 3.18, p<0.01) was related to an overrepresentation of osteoporosis. CONCLUSION: Our results show that the diagnosis of osteoporosis in statin-treated patients is dose-dependent. Thus, osteoporosis is underrepresented in low-dose and overrepresented in high-dose statin treatment, demonstrating the importance of future studies’ taking dose-dependency into account when investigating the relationship between statins and osteoporosis. |
format | Online Article Text |
id | pubmed-6900255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-69002552019-12-23 Diagnosis of osteoporosis in statin-treated patients is dose-dependent Leutner, Michael Matzhold, Caspar Bellach, Luise Deischinger, Carola Harreiter, Jürgen Thurner, Stefan Klimek, Peter Kautzky-Willer, Alexandra Ann Rheum Dis Osteoporosis OBJECTIVE: Whether HMG-CoA-reductase inhibition, the main mechanism of statins, plays a role in the pathogenesis of osteoporosis, is not entirely known so far. Consequently, this study was set out to investigate the relationship of different kinds and dosages of statins with osteoporosis, hypothesising that the inhibition of the synthesis of cholesterol could influence sex-hormones and therefore the diagnosis of osteoporosis. METHODS: Medical claims data of all Austrians from 2006 to 2007 was used to identify all patients treated with statins to compute their daily defined dose averages of six different types of statins. We applied multiple logistic regression to analyse the dose-dependent risks of being diagnosed with osteoporosis for each statin individually. RESULTS: In the general study population, statin treatment was associated with an overrepresentation of diagnosed osteoporosis compared with controls (OR: 3.62, 95% CI 3.55 to 3.69, p<0.01). There was a highly non-trivial dependence of statin dosage with the ORs of osteoporosis. Osteoporosis was underrepresented in low-dose statin treatment (0–10 mg per day), including lovastatin (OR: 0.39, CI 0.18 to 0.84, p<0.05), pravastatin (OR: 0.68, 95% CI 0.52 to 0.89, p<0.01), simvastatin (OR: 0.70, 95% CI 0.56 to 0.86, p<0.01) and rosuvastatin (OR: 0.69, 95% CI 0.55 to 0.87, p<0.01). However, the exceeding of the 40 mg threshold for simvastatin (OR: 1.64, 95% CI 1.31 to 2.07, p<0.01), and the exceeding of a 20 mg threshold for atorvastatin (OR: 1.78, 95% CI 1.41 to 2.23, p<0.01) and for rosuvastatin (OR: 2.04, 95% CI 1.31 to 3.18, p<0.01) was related to an overrepresentation of osteoporosis. CONCLUSION: Our results show that the diagnosis of osteoporosis in statin-treated patients is dose-dependent. Thus, osteoporosis is underrepresented in low-dose and overrepresented in high-dose statin treatment, demonstrating the importance of future studies’ taking dose-dependency into account when investigating the relationship between statins and osteoporosis. BMJ Publishing Group 2019-12 2019-09-26 /pmc/articles/PMC6900255/ /pubmed/31558481 http://dx.doi.org/10.1136/annrheumdis-2019-215714 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Osteoporosis Leutner, Michael Matzhold, Caspar Bellach, Luise Deischinger, Carola Harreiter, Jürgen Thurner, Stefan Klimek, Peter Kautzky-Willer, Alexandra Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title | Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title_full | Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title_fullStr | Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title_full_unstemmed | Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title_short | Diagnosis of osteoporosis in statin-treated patients is dose-dependent |
title_sort | diagnosis of osteoporosis in statin-treated patients is dose-dependent |
topic | Osteoporosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900255/ https://www.ncbi.nlm.nih.gov/pubmed/31558481 http://dx.doi.org/10.1136/annrheumdis-2019-215714 |
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