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Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study

OBJECTIVE: Antipsychotics may increase serum prolactin, which has particularly been observed with risperidone. Further, hyperprolactinemia has been linked to osteoporosis‐related fractures. Therefore, we investigated fracture risk in a nationwide cohort exposed to antipsychotics. METHODS: Swedish re...

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Autores principales: Clapham, E., Bodén, R., Reutfors, J., Svensson, T., Ramcharran, D., Qiu, H., Kieler, H., Bahmanyar, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973241/
https://www.ncbi.nlm.nih.gov/pubmed/31545521
http://dx.doi.org/10.1111/acps.13101
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author Clapham, E.
Bodén, R.
Reutfors, J.
Svensson, T.
Ramcharran, D.
Qiu, H.
Kieler, H.
Bahmanyar, S.
author_facet Clapham, E.
Bodén, R.
Reutfors, J.
Svensson, T.
Ramcharran, D.
Qiu, H.
Kieler, H.
Bahmanyar, S.
author_sort Clapham, E.
collection PubMed
description OBJECTIVE: Antipsychotics may increase serum prolactin, which has particularly been observed with risperidone. Further, hyperprolactinemia has been linked to osteoporosis‐related fractures. Therefore, we investigated fracture risk in a nationwide cohort exposed to antipsychotics. METHODS: Swedish registers were used to identify adults with two consecutive dispensations of risperidone (n = 38 211), other atypical antipsychotics not including paliperidone (n = 60 691), or typical antipsychotics (n = 17 445) within three months between 2006 and 2013. An osteoporosis‐related fracture was defined as a non‐open hip/femur fracture in primary analyses. Cox regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: Risperidone users were on average older (mean age of 68, 44, and 63 years for risperidone, other atypical antipsychotics, and typical antipsychotics respectively). Compared with other atypical antipsychotics, there was no association between risperidone and osteoporosis‐related fractures in the overall (HR = 1.04, CI: 0.91–1.19) or age‐stratified analyses. A significantly increased risk of typical antipsychotics (HR = 1.24, CI: 1.07–1.45) compared with other atypical antipsychotics remained for ages >45 years. CONCLUSION: Risperidone does not appear to be associated with an increased risk of osteoporosis‐related fracture compared with other atypical antipsychotic agents as a group. For typical antipsychotics, a moderately elevated risk of hip fractures was noted compared with other atypical antipsychotics, possibly because of residual confounding.
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spelling pubmed-69732412020-01-27 Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study Clapham, E. Bodén, R. Reutfors, J. Svensson, T. Ramcharran, D. Qiu, H. Kieler, H. Bahmanyar, S. Acta Psychiatr Scand Original Articles OBJECTIVE: Antipsychotics may increase serum prolactin, which has particularly been observed with risperidone. Further, hyperprolactinemia has been linked to osteoporosis‐related fractures. Therefore, we investigated fracture risk in a nationwide cohort exposed to antipsychotics. METHODS: Swedish registers were used to identify adults with two consecutive dispensations of risperidone (n = 38 211), other atypical antipsychotics not including paliperidone (n = 60 691), or typical antipsychotics (n = 17 445) within three months between 2006 and 2013. An osteoporosis‐related fracture was defined as a non‐open hip/femur fracture in primary analyses. Cox regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: Risperidone users were on average older (mean age of 68, 44, and 63 years for risperidone, other atypical antipsychotics, and typical antipsychotics respectively). Compared with other atypical antipsychotics, there was no association between risperidone and osteoporosis‐related fractures in the overall (HR = 1.04, CI: 0.91–1.19) or age‐stratified analyses. A significantly increased risk of typical antipsychotics (HR = 1.24, CI: 1.07–1.45) compared with other atypical antipsychotics remained for ages >45 years. CONCLUSION: Risperidone does not appear to be associated with an increased risk of osteoporosis‐related fracture compared with other atypical antipsychotic agents as a group. For typical antipsychotics, a moderately elevated risk of hip fractures was noted compared with other atypical antipsychotics, possibly because of residual confounding. John Wiley and Sons Inc. 2019-10-11 2020-01 /pmc/articles/PMC6973241/ /pubmed/31545521 http://dx.doi.org/10.1111/acps.13101 Text en © 2019 The Authors. Acta Psychiatrica Scandinavica Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Clapham, E.
Bodén, R.
Reutfors, J.
Svensson, T.
Ramcharran, D.
Qiu, H.
Kieler, H.
Bahmanyar, S.
Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title_full Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title_fullStr Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title_full_unstemmed Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title_short Exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
title_sort exposure to risperidone versus other antipsychotics and risk of osteoporosis‐related fractures: a population‐based study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973241/
https://www.ncbi.nlm.nih.gov/pubmed/31545521
http://dx.doi.org/10.1111/acps.13101
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