The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta

Osteogenesis imperfecta (OI) is characterized by different signs including increased bone fragility, short stature, blue sclera, abnormal tooth growth and often secondary immobility. No curative therapy has been found for this rare disease up to now, and different pharmacological substances have bee...

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Main Authors: Ingmar Ipach, Torsten Kluba, Petra Wolf, Bertram Pontz, Falk Mittag
Format: Article
Language:English
Published: Open Medical Publishing 2012-09-01
Series:Orthopedic Reviews
Subjects:
Online Access:http://www.pagepress.org/journals/index.php/or/article/view/4246
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author Ingmar Ipach
Torsten Kluba
Petra Wolf
Bertram Pontz
Falk Mittag
author_facet Ingmar Ipach
Torsten Kluba
Petra Wolf
Bertram Pontz
Falk Mittag
author_sort Ingmar Ipach
collection DOAJ
description Osteogenesis imperfecta (OI) is characterized by different signs including increased bone fragility, short stature, blue sclera, abnormal tooth growth and often secondary immobility. No curative therapy has been found for this rare disease up to now, and different pharmacological substances have been tried as treatment for severe forms of OI. Promising results were seen with intravenous bisphosphonates in the treatment of patients with OI. The aim of present study was to show the effect of intravenous ibandronate therapy on bone density and bone metabolism markers. We analyzed the data of 27 patients with the diagnosis of OI who were treated off-label with intravenous ibandronate. Ibandronate was administered by intravenous infusion every three months at a dosage of 0.3-2 mg. Bone turnover markers and bone density were measured before starting therapy and every three months during treatment. Bone density was measured by using an ultrasound imaging system providing an accurate image of the calcaneus and by evaluating broadband ultrasound attenuation (BUA). Twenty-seven patients were treated with intravenous iban- dronate during the observation period. 18 were female. The mean age of all patients was 23.9 years ± 19.6 (range 4-63). Seventeen patients were categorized to have OI Type I, 5 patients to have OI Type III and 5 patients to have OI Type IV. There was a statistically significant decrease in total alkaline phosphatase (P<0.0001). We detected also a statistically significant decrease in the ratio urinary deoxypyridinoline/urinary creatinine (P=0.0048) and the ratio urinary pyridinoline/urinary creatinine (P<0.0001) respectively. There was also a statistically significant increase in serum magnesium (P=0.034) and BUA (P=0.0071). No statistically significant changes were seen for total serum calcium (P=0.16), the ratio of urine calcium/urine creatinine (P=0.29), alkaline phosphatase (isoform bone) (P=0.3), procollagen-I-peptide (P=0.5), osteocalcin (P=0.9), serum phosphatase (P=0.71), parathormone (P=0.11) and the ratio urine phosphatase/urine creatinine (P=0.58) Therapy with ibandronate in patients with OI leads to a normalisation of bone turnover markers and increasing bone density. Therefore serum alkaline phosphatase and bone density are possible parameters to monitor bisphosphonate treatment in patients with OI.
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spelling doaj.art-452ed7375bbf434ab8707d5995b252a12022-12-21T19:50:43ZengOpen Medical PublishingOrthopedic Reviews2035-82372035-81642012-09-0143e29e2910.4081/or.2012.e292258The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfectaIngmar Ipach0Torsten Kluba1Petra Wolf2Bertram Pontz3Falk Mittag4Department of Orthopaedic Surgery, Tuebingen University Hospital, TuebingenDepartment of Orthopaedic Surgery, Tuebingen University Hospital, TuebingenDepartment of Medical Statistics and Epidemiology, Technical University of MunichTechnical University of Munich Children’s Hospital, MunichDepartment of Orthopaedic Surgery, Tuebingen University Hospital, TuebingenOsteogenesis imperfecta (OI) is characterized by different signs including increased bone fragility, short stature, blue sclera, abnormal tooth growth and often secondary immobility. No curative therapy has been found for this rare disease up to now, and different pharmacological substances have been tried as treatment for severe forms of OI. Promising results were seen with intravenous bisphosphonates in the treatment of patients with OI. The aim of present study was to show the effect of intravenous ibandronate therapy on bone density and bone metabolism markers. We analyzed the data of 27 patients with the diagnosis of OI who were treated off-label with intravenous ibandronate. Ibandronate was administered by intravenous infusion every three months at a dosage of 0.3-2 mg. Bone turnover markers and bone density were measured before starting therapy and every three months during treatment. Bone density was measured by using an ultrasound imaging system providing an accurate image of the calcaneus and by evaluating broadband ultrasound attenuation (BUA). Twenty-seven patients were treated with intravenous iban- dronate during the observation period. 18 were female. The mean age of all patients was 23.9 years ± 19.6 (range 4-63). Seventeen patients were categorized to have OI Type I, 5 patients to have OI Type III and 5 patients to have OI Type IV. There was a statistically significant decrease in total alkaline phosphatase (P<0.0001). We detected also a statistically significant decrease in the ratio urinary deoxypyridinoline/urinary creatinine (P=0.0048) and the ratio urinary pyridinoline/urinary creatinine (P<0.0001) respectively. There was also a statistically significant increase in serum magnesium (P=0.034) and BUA (P=0.0071). No statistically significant changes were seen for total serum calcium (P=0.16), the ratio of urine calcium/urine creatinine (P=0.29), alkaline phosphatase (isoform bone) (P=0.3), procollagen-I-peptide (P=0.5), osteocalcin (P=0.9), serum phosphatase (P=0.71), parathormone (P=0.11) and the ratio urine phosphatase/urine creatinine (P=0.58) Therapy with ibandronate in patients with OI leads to a normalisation of bone turnover markers and increasing bone density. Therefore serum alkaline phosphatase and bone density are possible parameters to monitor bisphosphonate treatment in patients with OI.http://www.pagepress.org/journals/index.php/or/article/view/4246osteogenesis imperfecta, bisphospho- nate, ibandronate, bone density, bone turnover markers
spellingShingle Ingmar Ipach
Torsten Kluba
Petra Wolf
Bertram Pontz
Falk Mittag
The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
Orthopedic Reviews
osteogenesis imperfecta, bisphospho- nate, ibandronate, bone density, bone turnover markers
title The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
title_full The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
title_fullStr The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
title_full_unstemmed The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
title_short The influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
title_sort influence of ibandronate treatment on bone density and biochemical bone markers in patients with osteogenesis imperfecta
topic osteogenesis imperfecta, bisphospho- nate, ibandronate, bone density, bone turnover markers
url http://www.pagepress.org/journals/index.php/or/article/view/4246
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