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Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss
OBJECTIVE: To explore the effects of anti-tumour necrosis factor (TNF)α antibody therapy on bone mineral density (BMD) of the lumbar spine and femur neck in patients with rheumatoid arthritis (RA). METHODS: A total of 50 patients with active RA (DAS28⩾3.2) who started adalimumab (40 mg subcutaneousl...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BMJ Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945478/ https://www.ncbi.nlm.nih.gov/pubmed/18408246 http://dx.doi.org/10.1136/ard.2008.091611 |
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author | Wijbrandts, C A Klaasen, R Dijkgraaf, M G W Gerlag, D M van Eck-Smit, B L F Tak, P P |
author_facet | Wijbrandts, C A Klaasen, R Dijkgraaf, M G W Gerlag, D M van Eck-Smit, B L F Tak, P P |
author_sort | Wijbrandts, C A |
collection | PubMed |
description | OBJECTIVE: To explore the effects of anti-tumour necrosis factor (TNF)α antibody therapy on bone mineral density (BMD) of the lumbar spine and femur neck in patients with rheumatoid arthritis (RA). METHODS: A total of 50 patients with active RA (DAS28⩾3.2) who started adalimumab (40 mg subcutaneously/2 weeks) were included in an open label prospective study. All patients used stable methotrexate and were allowed to use prednisone (⩽10 mg/day). The BMD of the lumbar spine and femur neck was measured before and 1 year after start of treatment. RESULTS: Disease activity at baseline (28-joint Disease Activity Score (DAS28)) and disease duration were inversely correlated with femoral neck BMD and lumbar spine BMD (p<0.05). Mean BMD of lumbar spine and femur neck remained unchanged after 1 year of adalimumab therapy (+0.3% and +0.3%, respectively). Of interest, a beneficial effect of prednisone on change in femur neck BMD was observed with a relative increase with prednisone use (+2.5%) compared to no concomitant prednisone use (−0.7%), (p = 0.015). CONCLUSION: In contrast to the progressive bone loss observed after conventional disease-modifying antirheumatic drug therapy, TNF blockade may result in an arrest of general bone loss. Consistent with previous observations, the data also suggest that the net effect of low-dose corticosteroids on BMD in RA may be beneficial, possibly resulting from their anti-inflammatory effects. |
format | Text |
id | pubmed-2945478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29454782010-09-30 Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss Wijbrandts, C A Klaasen, R Dijkgraaf, M G W Gerlag, D M van Eck-Smit, B L F Tak, P P Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVE: To explore the effects of anti-tumour necrosis factor (TNF)α antibody therapy on bone mineral density (BMD) of the lumbar spine and femur neck in patients with rheumatoid arthritis (RA). METHODS: A total of 50 patients with active RA (DAS28⩾3.2) who started adalimumab (40 mg subcutaneously/2 weeks) were included in an open label prospective study. All patients used stable methotrexate and were allowed to use prednisone (⩽10 mg/day). The BMD of the lumbar spine and femur neck was measured before and 1 year after start of treatment. RESULTS: Disease activity at baseline (28-joint Disease Activity Score (DAS28)) and disease duration were inversely correlated with femoral neck BMD and lumbar spine BMD (p<0.05). Mean BMD of lumbar spine and femur neck remained unchanged after 1 year of adalimumab therapy (+0.3% and +0.3%, respectively). Of interest, a beneficial effect of prednisone on change in femur neck BMD was observed with a relative increase with prednisone use (+2.5%) compared to no concomitant prednisone use (−0.7%), (p = 0.015). CONCLUSION: In contrast to the progressive bone loss observed after conventional disease-modifying antirheumatic drug therapy, TNF blockade may result in an arrest of general bone loss. Consistent with previous observations, the data also suggest that the net effect of low-dose corticosteroids on BMD in RA may be beneficial, possibly resulting from their anti-inflammatory effects. BMJ Publishing Group 2008-04-13 /pmc/articles/PMC2945478/ /pubmed/18408246 http://dx.doi.org/10.1136/ard.2008.091611 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Clinical and Epidemiological Research Wijbrandts, C A Klaasen, R Dijkgraaf, M G W Gerlag, D M van Eck-Smit, B L F Tak, P P Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title | Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title_full | Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title_fullStr | Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title_full_unstemmed | Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title_short | Bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
title_sort | bone mineral density in rheumatoid arthritis patients 1 year after adalimumab therapy: arrest of bone loss |
topic | Clinical and Epidemiological Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945478/ https://www.ncbi.nlm.nih.gov/pubmed/18408246 http://dx.doi.org/10.1136/ard.2008.091611 |
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