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The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review

BACKGROUND: Psoriasis (Ps) is a multisystem inflammatory disease associated with several comorbidities; however, its effect on bone health remains uncertain. This systematic review aimed to evaluate the risks of osteopenia (OPe) and osteoporosis (OP) in psoriasis. METHODS: A systematic search was pe...

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Autores principales: Schauer, Anna, Uthayakumar, Aarthy K., Boardman, Glenn, Bunker, Christopher B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892432/
https://www.ncbi.nlm.nih.gov/pubmed/36751315
http://dx.doi.org/10.1002/ski2.169
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author Schauer, Anna
Uthayakumar, Aarthy K.
Boardman, Glenn
Bunker, Christopher B.
author_facet Schauer, Anna
Uthayakumar, Aarthy K.
Boardman, Glenn
Bunker, Christopher B.
author_sort Schauer, Anna
collection PubMed
description BACKGROUND: Psoriasis (Ps) is a multisystem inflammatory disease associated with several comorbidities; however, its effect on bone health remains uncertain. This systematic review aimed to evaluate the risks of osteopenia (OPe) and osteoporosis (OP) in psoriasis. METHODS: A systematic search was performed for published studies evaluating cutaneous Ps and psoriatic arthritis (PsA) compared with healthy control groups utilizing a validated bone mineral density (BMD) assessment score. Meta‐analysis was performed using a random‐effects model; pooled estimates and their confidence intervals (CIs) were calculated. For analysis, Ps and PsA groups were combined due to the small number of studies. RESULTS: Twenty‐one studies were included for final analysis; three Ps only, 15 PsA and three both. There was a significant difference between psoriatic disease (combination Ps and PsA group) compared with controls relating to an association with OP/OPe, with an overall odds ratio (OR) of 1.71 (95% CI 1.07–2.74: p‐value = 0.026). The Ps group had significantly lower BMD than the control group at both the lumbar spine and femoral neck (mean difference −0.04; 95% CI −0.090 to 0.002 and −0.03; 95% CI −0.059 to 0.003 respectively). CONCLUSION: Putative risks of OPe and OP in both Ps and PsA are supported but not confirmed. Significant heterogeneity of reported data limits definitive conclusions in this meta‐analysis. This review contributes to the further understanding of Ps as a multisystem disease and future management of potential comorbidities, but highlights key gaps in the literature. Further studies addressing standardised OP reporting, specific disease group characteristics comparing Ps with PsA, patient characteristics and medication use, are required in order to make more certain conclusions with greater clinical impact.
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spelling pubmed-98924322023-02-06 The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review Schauer, Anna Uthayakumar, Aarthy K. Boardman, Glenn Bunker, Christopher B. Skin Health Dis Systematic Reviews BACKGROUND: Psoriasis (Ps) is a multisystem inflammatory disease associated with several comorbidities; however, its effect on bone health remains uncertain. This systematic review aimed to evaluate the risks of osteopenia (OPe) and osteoporosis (OP) in psoriasis. METHODS: A systematic search was performed for published studies evaluating cutaneous Ps and psoriatic arthritis (PsA) compared with healthy control groups utilizing a validated bone mineral density (BMD) assessment score. Meta‐analysis was performed using a random‐effects model; pooled estimates and their confidence intervals (CIs) were calculated. For analysis, Ps and PsA groups were combined due to the small number of studies. RESULTS: Twenty‐one studies were included for final analysis; three Ps only, 15 PsA and three both. There was a significant difference between psoriatic disease (combination Ps and PsA group) compared with controls relating to an association with OP/OPe, with an overall odds ratio (OR) of 1.71 (95% CI 1.07–2.74: p‐value = 0.026). The Ps group had significantly lower BMD than the control group at both the lumbar spine and femoral neck (mean difference −0.04; 95% CI −0.090 to 0.002 and −0.03; 95% CI −0.059 to 0.003 respectively). CONCLUSION: Putative risks of OPe and OP in both Ps and PsA are supported but not confirmed. Significant heterogeneity of reported data limits definitive conclusions in this meta‐analysis. This review contributes to the further understanding of Ps as a multisystem disease and future management of potential comorbidities, but highlights key gaps in the literature. Further studies addressing standardised OP reporting, specific disease group characteristics comparing Ps with PsA, patient characteristics and medication use, are required in order to make more certain conclusions with greater clinical impact. John Wiley and Sons Inc. 2022-09-21 /pmc/articles/PMC9892432/ /pubmed/36751315 http://dx.doi.org/10.1002/ski2.169 Text en © 2022 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Systematic Reviews
Schauer, Anna
Uthayakumar, Aarthy K.
Boardman, Glenn
Bunker, Christopher B.
The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title_full The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title_fullStr The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title_full_unstemmed The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title_short The risk of osteopenia/osteoporosis and psoriatic disease: A systematic review
title_sort risk of osteopenia/osteoporosis and psoriatic disease: a systematic review
topic Systematic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892432/
https://www.ncbi.nlm.nih.gov/pubmed/36751315
http://dx.doi.org/10.1002/ski2.169
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