Effects of 1 year of daily teriparatide treatment on iliacal bone mineralization density distribution (BMDD) in postmenopausal osteoporotic women previously treated with alendronate or risedronate
Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before a...
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Published in | Journal of bone and mineral research Vol. 25; no. 11; pp. 2297 - 2303 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.11.2010
Wiley Oxford University Press |
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Online Access | Get full text |
ISSN | 0884-0431 1523-4681 1523-4681 |
DOI | 10.1002/jbmr.198 |
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Abstract | Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1‐34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.CaLow +25.9%, Ct.CaLow +62.0%, both p < .05) and Ct. heterogeneity of mineralization (Ct.CaWidth +22.8%, p < .001). PriorRIS patients showed increased mineralization heterogeneity (Cn.CaWidth +14.8%, p < .05, and Ct.CaWidth +15.8%, p < .001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.CaWidth and Ct.CaWidth (+10.7%, p < .01, and +19.6%, p < .001, respectively) as well as increased Cn.CaLow and Ct.CaLow (+18.2%, p < .05, and +36.6%, p < .01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action. © 2010 American Society for Bone and Mineral Research. |
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AbstractList | Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1-34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.CaLow +25.9%, Ct.CaLow +62.0%, both p<.05) and Ct. heterogeneity of mineralization (Ct.CaWidth +22.8%, p<.001). PriorRIS patients showed increased mineralization heterogeneity (Cn.CaWidth +14.8%, p<.05, and Ct.CaWidth +15.8%, p<.001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.CaWidth and Ct.CaWidth (+10.7%, p<.01, and +19.6%, p<.001, respectively) as well as increased Cn.CaLow and Ct.CaLow (+18.2%, p<.05, and +36.6%, p<.01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action. © 2010 American Society for Bone and Mineral Research. Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1-34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.Ca(Low) +25.9%, Ct.Ca(Low) +62.0%, both p < .05) and Ct. heterogeneity of mineralization (Ct.Ca(Width) +22.8%, p < .001). PriorRIS patients showed increased mineralization heterogeneity (Cn.Ca(Width) +14.8%, p < .05, and Ct.Ca(Width) +15.8%, p < .001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.Ca(Width) and Ct.Ca(Width) (+10.7%, p < .01, and +19.6%, p < .001, respectively) as well as increased Cn.Ca(Low) and Ct.Ca(Low) (+18.2%, p < .05, and +36.6%, p < .01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action. Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1-34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.Ca sub(Low) +25.9%, Ct.Ca sub(Low) +62.0%, both p<.05) and Ct. heterogeneity of mineralization (Ct.Ca sub(Width) +22.8%, p<.001). PriorRIS patients showed increased mineralization heterogeneity (Cn.Ca sub(Width) +14.8%, p<.05, and Ct.Ca sub(Width) +15.8%, p<.001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.Ca sub(Width) and Ct.Ca sub(Width) (+10.7%, p<.01, and +19.6%, p<.001, respectively) as well as increased Cn.Ca sub(Low) and Ct.Ca sub(Low) (+18.2%, p<.05, and +36.6%, p<.01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action. copyright 2010 American Society for Bone and Mineral Research. Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1-34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.Ca(Low) +25.9%, Ct.Ca(Low) +62.0%, both p < .05) and Ct. heterogeneity of mineralization (Ct.Ca(Width) +22.8%, p < .001). PriorRIS patients showed increased mineralization heterogeneity (Cn.Ca(Width) +14.8%, p < .05, and Ct.Ca(Width) +15.8%, p < .001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.Ca(Width) and Ct.Ca(Width) (+10.7%, p < .01, and +19.6%, p < .001, respectively) as well as increased Cn.Ca(Low) and Ct.Ca(Low) (+18.2%, p < .05, and +36.6%, p < .01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action.Anabolic treatment with teriparatide of postmenopausal osteoporotic patients previously treated with bisphosphonates is a new therapeutic approach. However, its effects on the bone mineralization density distribution (BMDD) are unknown. We studied paired transiliac bone biopsy samples taken before and after 1 year of treatment with recombinant human parathyroid hormone peptide 1-34 (teriparatide) from 16 osteoporotic women treated with either alendronate (priorALN) or risedronate (priorRIS) for at least 2 years and subsequently treated for 12 months with teriparatide. Cancellous (Cn.) and cortical (Ct.) BMDD values were measured using quantitative backscattered electron imaging. At baseline, BMDD values of priorALN and priorRIS women were similar and within the normal range. One year of teriparatide treatment caused significant effects on the BMDD. Analyzing changes from baseline for each bisphosphonate group separately, priorALN patients revealed increases in the portion of low mineralized bone areas (Cn.Ca(Low) +25.9%, Ct.Ca(Low) +62.0%, both p < .05) and Ct. heterogeneity of mineralization (Ct.Ca(Width) +22.8%, p < .001). PriorRIS patients showed increased mineralization heterogeneity (Cn.Ca(Width) +14.8%, p < .05, and Ct.Ca(Width) +15.8%, p < .001). Analysis of the influence of the prior bisphosphonate treatment showed that the BMDD response to 1 year of teriparatide treatment did not depend on the type of prior bisphosphonate. In consequence, priorALN and priorRIS groups were combined. The pooled groups revealed increased Cn.Ca(Width) and Ct.Ca(Width) (+10.7%, p < .01, and +19.6%, p < .001, respectively) as well as increased Cn.Ca(Low) and Ct.Ca(Low) (+18.2%, p < .05, and +36.6%, p < .01, respectively). In summary, our findings indicate a significant effect of teriparatide on BMDD when administered subsequent to a bisphosphonate in agreement with teriparatide's anabolic action. |
Author | Misof, Barbara M Klaushofer, Klaus Fratzl‐Zelman, Nadja Blouin, Stéphane Paschalis, Eleftherios P Roschger, Paul |
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CitedBy_id | crossref_primary_10_1016_S1169_8330_11_70041_2 crossref_primary_10_1185_03007995_2015_1074063 crossref_primary_10_1016_j_bone_2011_08_015 crossref_primary_10_1016_j_rdc_2011_07_007 crossref_primary_10_1016_j_bonr_2017_02_006 crossref_primary_10_1016_j_bone_2017_10_013 crossref_primary_10_1007_s00223_014_9901_4 crossref_primary_10_3109_13697137_2015_1016378 crossref_primary_10_1002_jbmr_2188 crossref_primary_10_14341_osteo2015220_24 crossref_primary_10_1002_jbmr_2124 crossref_primary_10_1210_jc_2013_1172 crossref_primary_10_1002_jbmr_2588 crossref_primary_10_1016_j_bone_2021_115900 crossref_primary_10_1097_MD_0000000000003626 crossref_primary_10_1007_s00198_015_3446_x crossref_primary_10_1016_j_bone_2014_07_014 crossref_primary_10_1097_MD_0000000000019042 crossref_primary_10_1007_s12018_016_9220_6 crossref_primary_10_1016_j_bone_2018_02_001 crossref_primary_10_1016_j_jbspin_2011_09_014 crossref_primary_10_1007_s00223_015_0074_6 crossref_primary_10_1016_j_bone_2017_03_049 crossref_primary_10_1080_14656566_2020_1717468 crossref_primary_10_1007_s00198_015_3334_4 crossref_primary_10_1007_s00198_016_3812_3 crossref_primary_10_1002_jbmr_2454 crossref_primary_10_1016_j_bone_2013_01_032 crossref_primary_10_1016_j_bone_2015_04_013 crossref_primary_10_1016_j_bone_2014_02_002 crossref_primary_10_1007_s11914_014_0218_z crossref_primary_10_1016_j_bonr_2020_100253 |
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Copyright | Copyright © 2010 American Society for Bone and Mineral Research 2015 INIST-CNRS 2010 American Society for Bone and Mineral Research. |
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Keywords | BONE MINERALIZATION DENSITY Diseases of the osteoarticular system Antiresorptive agent Diphosphonic acid derivatives Bisphosphonates Density Osteoarticular system Alendronic acid Osteoporosis Osteoforming Vertebrata Mammalia Treatment POSTMENOPAUSAL OSTEOPOROSIS Risedronic acid Mineralization Imaging Distribution Postmenopause Female Bone Teriparatide QUANTITATIVE BACKSCATTERED ELECTRON IMAGING (QBEI) |
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SubjectTerms | Alendronate - therapeutic use Biological and medical sciences bisphosphonates Bone Density - drug effects Bone Density Conservation Agents - pharmacology Bone Density Conservation Agents - therapeutic use bone mineralization density Calcification, Physiologic - drug effects Drug Administration Schedule Etidronic Acid - analogs & derivatives Etidronic Acid - therapeutic use Female Fundamental and applied biological sciences. Psychology Humans Ilium - drug effects Ilium - pathology Osteoporosis, Postmenopausal - drug therapy Osteoporosis, Postmenopausal - physiopathology postmenopausal osteoporosis quantitative backscattered electron imaging (QBEI) Risedronate Sodium Skeleton and joints teriparatide Teriparatide - pharmacology Teriparatide - therapeutic use Treatment Outcome Vertebrates: osteoarticular system, musculoskeletal system |
Title | Effects of 1 year of daily teriparatide treatment on iliacal bone mineralization density distribution (BMDD) in postmenopausal osteoporotic women previously treated with alendronate or risedronate |
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