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The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy
BACKGROUND: The aim of the present study was to assess whether the efficacy of bisphosphonate treatment is influenced by PTH levels measured in newly diagnosed osteoporotic patients and to identify the threshold value, beyond which PTH level negatively influences therapeutic efficacy. METHODS: One h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529113/ https://www.ncbi.nlm.nih.gov/pubmed/23227959 http://dx.doi.org/10.1186/1471-2474-13-244 |
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author | Kincse, Gyöngyvér Varga, József Somogyi, Péter Szodoray, Péter Surányi, Péter Gaál, János |
author_facet | Kincse, Gyöngyvér Varga, József Somogyi, Péter Szodoray, Péter Surányi, Péter Gaál, János |
author_sort | Kincse, Gyöngyvér |
collection | PubMed |
description | BACKGROUND: The aim of the present study was to assess whether the efficacy of bisphosphonate treatment is influenced by PTH levels measured in newly diagnosed osteoporotic patients and to identify the threshold value, beyond which PTH level negatively influences therapeutic efficacy. METHODS: One hundred and thirty-eight osteoporotic patients were enrolled into the study. All subjects underwent laboratory screening, bone densitometry with DEXA, and x-ray imaging. The changes in bone density were evaluated after a mean follow-up period of 13.37 ± 1.29 months. Correlation analysis was performed on the clinical data of patients, the percentage changes of BMD values, and the PTH levels measured at the beginning of study, using SPSS software. RESULTS: The mean age of the subjects was 64.82 ± 10.51 years, and the female-to-male ratio was 116/22. Baseline BMD value measured with AP DEXA scanning was 0.854 ± 0.108 g/cm(2) in the L(1-4) vertebrae and 0.768 ± 0.115 g/cm(2) in the left femoral neck. By the end of the follow-up period, these values changed to 0.890 ± 0.111 g/cm(2) and 0.773 ± 0.111 g/cm(2), respectively. We found a statistically significant, negative correlation between PTH levels and the percentage changes of lumbar BMD values measured at the end of the follow-up (correlation coefficient R(2) = 0.121, p < 0.0001). The analysis of frequency histograms suggested that negative effects on bone might be expected above a PTH level of 60 pg/mL (7.3 pmol/L). CONCLUSION: Our findings imply that a baseline PTH level over 60 ng/mL can reduce the efficacy of bisphosphonate treatment. |
format | Online Article Text |
id | pubmed-3529113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35291132013-01-03 The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy Kincse, Gyöngyvér Varga, József Somogyi, Péter Szodoray, Péter Surányi, Péter Gaál, János BMC Musculoskelet Disord Research Article BACKGROUND: The aim of the present study was to assess whether the efficacy of bisphosphonate treatment is influenced by PTH levels measured in newly diagnosed osteoporotic patients and to identify the threshold value, beyond which PTH level negatively influences therapeutic efficacy. METHODS: One hundred and thirty-eight osteoporotic patients were enrolled into the study. All subjects underwent laboratory screening, bone densitometry with DEXA, and x-ray imaging. The changes in bone density were evaluated after a mean follow-up period of 13.37 ± 1.29 months. Correlation analysis was performed on the clinical data of patients, the percentage changes of BMD values, and the PTH levels measured at the beginning of study, using SPSS software. RESULTS: The mean age of the subjects was 64.82 ± 10.51 years, and the female-to-male ratio was 116/22. Baseline BMD value measured with AP DEXA scanning was 0.854 ± 0.108 g/cm(2) in the L(1-4) vertebrae and 0.768 ± 0.115 g/cm(2) in the left femoral neck. By the end of the follow-up period, these values changed to 0.890 ± 0.111 g/cm(2) and 0.773 ± 0.111 g/cm(2), respectively. We found a statistically significant, negative correlation between PTH levels and the percentage changes of lumbar BMD values measured at the end of the follow-up (correlation coefficient R(2) = 0.121, p < 0.0001). The analysis of frequency histograms suggested that negative effects on bone might be expected above a PTH level of 60 pg/mL (7.3 pmol/L). CONCLUSION: Our findings imply that a baseline PTH level over 60 ng/mL can reduce the efficacy of bisphosphonate treatment. BioMed Central 2012-12-10 /pmc/articles/PMC3529113/ /pubmed/23227959 http://dx.doi.org/10.1186/1471-2474-13-244 Text en Copyright ©2012 Kincse et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kincse, Gyöngyvér Varga, József Somogyi, Péter Szodoray, Péter Surányi, Péter Gaál, János The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title | The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title_full | The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title_fullStr | The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title_full_unstemmed | The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title_short | The impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
title_sort | impact of secondary hyperparathyroidism on the efficacy of antiresorptive therapy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529113/ https://www.ncbi.nlm.nih.gov/pubmed/23227959 http://dx.doi.org/10.1186/1471-2474-13-244 |
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