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Evaluation of Two Different Pamidronate Treatment Protocols in Children with Osteogenesis Imperfecta

Year 2014, Volume: 39 Issue: 3, 532 - 539, 22.07.2014
https://doi.org/10.17826/cutf.46470

Abstract

Purpose: Osteogenesis imperfecta is an inherited disorder of connective tissue. Children with this condition suffer from recurrent fractures, deformities, osteoporosis and pain. Over the recent years, pamidronate became the standard treatment choice. However the optimal dose and interval have not been defined yet. The main of this study was to compare of two different pamidronate regime. Materials and Methods: 12 patients aged 42.3 ± 37.4 months were studied. At the beginning patients had received pamidronate infusion at a dose of 1.5 mg/kg/day once, every two months with duration of 23.5 ± 9.0 months (first protocol), than switched to a dose of 1mg/kg/day for three consecutive days, every three months with duration of 18.5 ± 5.1 months (second protocol). The bone mineral density Z-score was evaluated yearly. Results: Annual fracture rate decreased from 6.3 ± 5.5 to 1.1 ± 1.3 (p=0.001) in the first and from 1.1 ± 1.3 to 0.0 ± 0.0 (p

References

  • Van Dijk FS, Pals G, van Rijn RR, Nikkels PG, Cobben JM: Classification of Osteogenesis Imperfecta revisited. Eur J Med Genet. 2010;53: 1–5.
  • Mungan NÖ, Gürbüz F, Mengen E, Özgür Ö, Topaloglu AK, Yüksel B. Comparison of Calcitonin and Pamidronate Treatments in Children with Osteogenesis Imperfecta. Cukurova Med J. 2013;38:667-74. van Dijk FS, Cobben JM, Kariminejad A, Maugeri A, Nikkels PG, van Rijn RR, Pals G. Osteogenesis Imperfecta: A Review with Clinical Examples. Mol Syndromol. 2011;2:1-20.
  • Steiner RD, Pepin MG, Byers PH: Osteogenesis Imperfecta, in Pagon RA, Bird TD, Dolan CR, Stephens K (eds): GeneReviews (University of Washington, Seattle 1993). http://www.ncbi.nlm.nih.gov/books/NBK1116/
  • Sillence DO, Senn A, Danks DM: Genetic heterogeneity in osteogenesis imperfecta. J Med Genet. 1979;16:101–16.
  • Glorieux FH, Rauch F, Plotkin H et al: Type V osteogenesis imperfecta: a new form of brittle bone disease. J Bone Miner Res. 2000;15:1650–8.
  • Glorieux FH, Ward LM, Rauch F, Lalic L, Roughly PJ, Travers R: Osteogenesis imperfecta type VI: a form of brittle bone disease with mineralization defect. J Bone Miner Res. 2002;17:30–7.
  • Byers PH, Bonadio JF, Steinmann B. Osteogenesis imperfecta: update and perspective. Am J Med Genet. 1984;17:429-35.
  • Barnes AM, Chang W, Morello R, Cabral WA, Weis M, et al: Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta. N Engl J Med. 2006;355: 2757–64.
  • Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, et al: CRTAP is required for prolyl 3-hydroxylation and mutations cause recessive osteogenesis imperfecta. Cell. 2006;127:291–304.
  • Cabral WA, Chang W, Barnes AM, Weis M, Scott MA, et al: Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta. Nat Genet. 2007;39:359–65.
  • Van Dijk FS, Nesbitt IM, Zwikstra EH, Nikkels PG, Piersma SR, et al: PPIB mutations cause severe osteogenesis imperfecta. Am J Hum Genet. 2009;85: 521–
  • Barnes AM, Carter EM, Cabral WA, Weis M, Chang W, et al: Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding. N Engl J Med. 2010;362:521–8.
  • Christiansen HE, Schwarze U, Pyott SM, Al- Swaid A, Al Balwi M, et al: Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:389–98.
  • Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, et al: Mutations in the gene encoding the RER protein FKBP65 cause autosomal recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:551–9.
  • Lapunzina P, Aglan M, Temtamy S, Caparrós Martin JA, Valencia M, et al: Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta. Am J Hum Genet. 2010;87:110–14.
  • Becker J, Semler O, Gilissen C, Li Y, Bolz HJ, et al: Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal recessive osteogenesis imperfecta. Am J Hum Genet. 2011;88:362–71.
  • Glorieux FH, Bishop NJ, Plotkin H, Chabot G, Lanoue G, Travers R: Cyclic administration of pamidronate in children with severe osteogenesis imperfecta. N Engl J Med. 1998;339:947–52.
  • Lindsay R. Modeling the benefits of pamidronate in children with osteogenesis imperfecta. J Clin Invest. 2002;110:1239-43.
  • Glorieux FH. The use of bisphosphonates in children with osteogenesis imperfecta. J Pediatr Endocrinol Metab. 2001;14: 1491-5.
  • Lee YS, Low SL, Lim AL, Loke KY. Cyclic pamidronate infusion improves bone mineralization and reduces fracture incidence in osteogenesis imperfecta. Eur J Pediatr. 2001;1:1-4.
  • Moriwake T, Seino Y. Recent progress in diagnosis and treatment of osteogenesis imperfecta. Acta Pediatr Jpn. 1997;39:521-7.
  • Gandrud LM, Cheung JC, Daniels MW, Bachrach LK. Low-dose intravenous pamidronate reduces fractures in childhood osteoporosis. J Pediatr Endocrinol Metab. 2003;16:887– 92.
  • Steelman J, Zeitler P. Treatment of symptomatic pediatric osteoporosis with cyclic single-day intravenous pamidronate infusions. J Pediatr. 2003;142:417–423.
  • Plotkin H, Coughlin S, Kreikemeier R, Heldt K, Bruzoni M, et al. Low doses of pamidronate to treat osteopenia in children with severe cerebral palsy: a pilot study. Dev Med Child Neurol. 2006;48:709–12.
  • Bachrach SJ, Kecskemethy HH, Harcke HT, Lark RK, Miller F, et al. Pamidronate treatment and posttreatment bone density in children with spastic quadriplegic cerebral palsy. J Clin Densitom. 2006;9:167–74.
  • Vasikaran SD. Bisphosphonates: an overview with special reference to alendronate. Ann Clin Biochem. 2001;38:608-23.
  • Plotkin H, Rauch F, Bishop NJ, et al. Pamidronate treatment of severe osteogenesis imperfecta in children under 3 years of age. J Clin Endocrinol Metab. 2000;85:1846-50.
  • Astrom E, Soderhall S. Beneficial effect of long term intravenous bisphosphonate treatment of osteogenesis imperfecta. Arch Dis Child. 2002;86:356-64.
  • Zacharin M, Baterman J. Pamidronate treatment of osteogenesis imperfecta - lack of correlation between clinical severity, age at onset of treatment, predicted collagen mutation and treatment response. J Pediatr Endocrinol Metab. 2002;15:163-74.
  • Guillot M, Eckart P, Desrosieres H, Amiour M, alJazayri Z. Osteogenesis imperfecta: a new, early therapeutic approach with bisphosphonate. A case report. Arch Pediatr. 2001;8:172-5.
  • Gökşen D, Coker M, Darcan S, Köse T, Kara S. Low-dose intravenous pamidronate treatment in osteogenesis imperfecta. Turk J Pediatr. 2006;48:124-9.
  • Martinez-Soto T, Pacaud D, Stephure D, Trussell R, Huang C. Treatment of symptomatic osteoporosis in children: a comparison of two pamidronate dosage regimens. J Pediatr Endocrinol Metab. 2011;24:271
  • Brumsen C, Hamdy NA, Papapoulos SE. Long-term effects of bisphosphonates on the growing skeleton. Studies of young patients with severe osteoporosis. Medicine. 1997;76:266-8.
  • Marni JF, Heeger S, Lynch KA, Decaro KR, Bohach D, Gibson KS, Warman ML. Intravenous bisphosphonate therapy in children and adolescents with osteogenesis imperfecta. Pediatrics. 2003;111:573-8.
  • Banerjee I, Shortland GJ, Ewans WD, Gregory JW. Osteogenesis imperfecta and intravenous pamidroate. Arch Dis Child. 2002;349: 562-63.
  • Landsmeer-Beker EA, Massa GG, MaaswinkelMooy PD, van de Kamp JJ, Papapoulos SE. Treatment of osteogenesis imperfecta with the bisphosphonate olpadronate. Eur J Pediatr. 1997;156:792-4.
  • Gonzalez E, Pavia C, Ros J, Villaronga M, Valls C, Escola J. Efficacy of low dose schedule pamidronate infusion in children with osteogenesis imperfecta. J Pediatr Endocrinol Metab. 2001;14:529-33.
  • Shapiro JR, Mccarthy EF, Rossiter K, Ernest K, Gelman R, Fedarko N, Santiago HT, Bober M. The effect of intravenous pamidroate on bone mineral density, bone histomorphometry, and parameters of bone turnover in adults with type 1A osteogenesis imperfecta. Calc Tissue Intl. 2003;72:103-12.
  • Monpetit K, Plotkin H, Rauch F, Bilodeau N, Cloutier S, Rabzel M, Glorieux FH. Rapid increase in grip force after start of pamidronate therapy in children and adolescents with severe osteogenesis imperfecta. Pediatrics. 2003;111:601-7.
  • Rauch F, Plotkin H, Travers R, Zeitlin L, Glorieux FH. Osteogenesis imperfecta types I, III, and IV: effect of pamidronate therapy on bone and mineral metabolism. J Clin Endocrinol Metab. 2003;88:986
  • Yazışma Adresi / Address for Correspondence: Dr. Fatih GÜRBÜZ Çukurova Üniversitesi Tıp Fakültesi, Çocuk Endokrinolojisi Bilim Dalı, ADANA Email: fggurbuz@yahoo.com G eliş tarihi/Received on: 20.01.2014
  • Kabul tarihi/Accepted on:27.02.2014

Osteogenezis İmperfekta Olan Çocuklarda İki Farklı Pamidronat Protokolünün Değerlendirilmesi

Year 2014, Volume: 39 Issue: 3, 532 - 539, 22.07.2014
https://doi.org/10.17826/cutf.46470

Abstract

Amaç: Osteogenezis imperfekta bağ dokusunun kalıtsal bir hastalığıdır. Bu durumdaki çocuklar tekrarlayan kırıklar, deformiteler, osteoporosis ve ağrıdan yakınırlar. Son yıllarda pamidronat standart tedavi tercihi olmuştur. Ancak, optimal doz ve aralık henüz tam olarak belirlenmemiştir. Bu çalışmada amaç, iki farklı pamidronat tedavi rejiminin karşılaştırılmasıdır. Materyal ve Metod: Yaşları 42.3 ± 37.4 ay arasında değişen toplam 12 hastada yapıldı. Başlangıçta her iki ayda bir defa 1.5 mg/kg/gün dozunda 23.5 ± 9.0 ay pamidromat infüzyonu uygulandı (ilk protokol), daha sonra üçer aylık aralarla 3 gün üstüste 1 mg/kg/gün 18.5 ± 5.1 ay dozuna geçildi (ikinci protokol). Kemik mineral dansitesi z-skoru yıllık değerlendirildi. Bulgular: Yıllık kırık oranı ilk protokolde 6.3 ± 5.5"den 1.1 ± 1.3"e (p=0.001), ikinci protokolde 1.1 ± 1.3"den 0.0 ± 0.0"a (p

References

  • Van Dijk FS, Pals G, van Rijn RR, Nikkels PG, Cobben JM: Classification of Osteogenesis Imperfecta revisited. Eur J Med Genet. 2010;53: 1–5.
  • Mungan NÖ, Gürbüz F, Mengen E, Özgür Ö, Topaloglu AK, Yüksel B. Comparison of Calcitonin and Pamidronate Treatments in Children with Osteogenesis Imperfecta. Cukurova Med J. 2013;38:667-74. van Dijk FS, Cobben JM, Kariminejad A, Maugeri A, Nikkels PG, van Rijn RR, Pals G. Osteogenesis Imperfecta: A Review with Clinical Examples. Mol Syndromol. 2011;2:1-20.
  • Steiner RD, Pepin MG, Byers PH: Osteogenesis Imperfecta, in Pagon RA, Bird TD, Dolan CR, Stephens K (eds): GeneReviews (University of Washington, Seattle 1993). http://www.ncbi.nlm.nih.gov/books/NBK1116/
  • Sillence DO, Senn A, Danks DM: Genetic heterogeneity in osteogenesis imperfecta. J Med Genet. 1979;16:101–16.
  • Glorieux FH, Rauch F, Plotkin H et al: Type V osteogenesis imperfecta: a new form of brittle bone disease. J Bone Miner Res. 2000;15:1650–8.
  • Glorieux FH, Ward LM, Rauch F, Lalic L, Roughly PJ, Travers R: Osteogenesis imperfecta type VI: a form of brittle bone disease with mineralization defect. J Bone Miner Res. 2002;17:30–7.
  • Byers PH, Bonadio JF, Steinmann B. Osteogenesis imperfecta: update and perspective. Am J Med Genet. 1984;17:429-35.
  • Barnes AM, Chang W, Morello R, Cabral WA, Weis M, et al: Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta. N Engl J Med. 2006;355: 2757–64.
  • Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, et al: CRTAP is required for prolyl 3-hydroxylation and mutations cause recessive osteogenesis imperfecta. Cell. 2006;127:291–304.
  • Cabral WA, Chang W, Barnes AM, Weis M, Scott MA, et al: Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta. Nat Genet. 2007;39:359–65.
  • Van Dijk FS, Nesbitt IM, Zwikstra EH, Nikkels PG, Piersma SR, et al: PPIB mutations cause severe osteogenesis imperfecta. Am J Hum Genet. 2009;85: 521–
  • Barnes AM, Carter EM, Cabral WA, Weis M, Chang W, et al: Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding. N Engl J Med. 2010;362:521–8.
  • Christiansen HE, Schwarze U, Pyott SM, Al- Swaid A, Al Balwi M, et al: Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:389–98.
  • Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, et al: Mutations in the gene encoding the RER protein FKBP65 cause autosomal recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:551–9.
  • Lapunzina P, Aglan M, Temtamy S, Caparrós Martin JA, Valencia M, et al: Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta. Am J Hum Genet. 2010;87:110–14.
  • Becker J, Semler O, Gilissen C, Li Y, Bolz HJ, et al: Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal recessive osteogenesis imperfecta. Am J Hum Genet. 2011;88:362–71.
  • Glorieux FH, Bishop NJ, Plotkin H, Chabot G, Lanoue G, Travers R: Cyclic administration of pamidronate in children with severe osteogenesis imperfecta. N Engl J Med. 1998;339:947–52.
  • Lindsay R. Modeling the benefits of pamidronate in children with osteogenesis imperfecta. J Clin Invest. 2002;110:1239-43.
  • Glorieux FH. The use of bisphosphonates in children with osteogenesis imperfecta. J Pediatr Endocrinol Metab. 2001;14: 1491-5.
  • Lee YS, Low SL, Lim AL, Loke KY. Cyclic pamidronate infusion improves bone mineralization and reduces fracture incidence in osteogenesis imperfecta. Eur J Pediatr. 2001;1:1-4.
  • Moriwake T, Seino Y. Recent progress in diagnosis and treatment of osteogenesis imperfecta. Acta Pediatr Jpn. 1997;39:521-7.
  • Gandrud LM, Cheung JC, Daniels MW, Bachrach LK. Low-dose intravenous pamidronate reduces fractures in childhood osteoporosis. J Pediatr Endocrinol Metab. 2003;16:887– 92.
  • Steelman J, Zeitler P. Treatment of symptomatic pediatric osteoporosis with cyclic single-day intravenous pamidronate infusions. J Pediatr. 2003;142:417–423.
  • Plotkin H, Coughlin S, Kreikemeier R, Heldt K, Bruzoni M, et al. Low doses of pamidronate to treat osteopenia in children with severe cerebral palsy: a pilot study. Dev Med Child Neurol. 2006;48:709–12.
  • Bachrach SJ, Kecskemethy HH, Harcke HT, Lark RK, Miller F, et al. Pamidronate treatment and posttreatment bone density in children with spastic quadriplegic cerebral palsy. J Clin Densitom. 2006;9:167–74.
  • Vasikaran SD. Bisphosphonates: an overview with special reference to alendronate. Ann Clin Biochem. 2001;38:608-23.
  • Plotkin H, Rauch F, Bishop NJ, et al. Pamidronate treatment of severe osteogenesis imperfecta in children under 3 years of age. J Clin Endocrinol Metab. 2000;85:1846-50.
  • Astrom E, Soderhall S. Beneficial effect of long term intravenous bisphosphonate treatment of osteogenesis imperfecta. Arch Dis Child. 2002;86:356-64.
  • Zacharin M, Baterman J. Pamidronate treatment of osteogenesis imperfecta - lack of correlation between clinical severity, age at onset of treatment, predicted collagen mutation and treatment response. J Pediatr Endocrinol Metab. 2002;15:163-74.
  • Guillot M, Eckart P, Desrosieres H, Amiour M, alJazayri Z. Osteogenesis imperfecta: a new, early therapeutic approach with bisphosphonate. A case report. Arch Pediatr. 2001;8:172-5.
  • Gökşen D, Coker M, Darcan S, Köse T, Kara S. Low-dose intravenous pamidronate treatment in osteogenesis imperfecta. Turk J Pediatr. 2006;48:124-9.
  • Martinez-Soto T, Pacaud D, Stephure D, Trussell R, Huang C. Treatment of symptomatic osteoporosis in children: a comparison of two pamidronate dosage regimens. J Pediatr Endocrinol Metab. 2011;24:271
  • Brumsen C, Hamdy NA, Papapoulos SE. Long-term effects of bisphosphonates on the growing skeleton. Studies of young patients with severe osteoporosis. Medicine. 1997;76:266-8.
  • Marni JF, Heeger S, Lynch KA, Decaro KR, Bohach D, Gibson KS, Warman ML. Intravenous bisphosphonate therapy in children and adolescents with osteogenesis imperfecta. Pediatrics. 2003;111:573-8.
  • Banerjee I, Shortland GJ, Ewans WD, Gregory JW. Osteogenesis imperfecta and intravenous pamidroate. Arch Dis Child. 2002;349: 562-63.
  • Landsmeer-Beker EA, Massa GG, MaaswinkelMooy PD, van de Kamp JJ, Papapoulos SE. Treatment of osteogenesis imperfecta with the bisphosphonate olpadronate. Eur J Pediatr. 1997;156:792-4.
  • Gonzalez E, Pavia C, Ros J, Villaronga M, Valls C, Escola J. Efficacy of low dose schedule pamidronate infusion in children with osteogenesis imperfecta. J Pediatr Endocrinol Metab. 2001;14:529-33.
  • Shapiro JR, Mccarthy EF, Rossiter K, Ernest K, Gelman R, Fedarko N, Santiago HT, Bober M. The effect of intravenous pamidroate on bone mineral density, bone histomorphometry, and parameters of bone turnover in adults with type 1A osteogenesis imperfecta. Calc Tissue Intl. 2003;72:103-12.
  • Monpetit K, Plotkin H, Rauch F, Bilodeau N, Cloutier S, Rabzel M, Glorieux FH. Rapid increase in grip force after start of pamidronate therapy in children and adolescents with severe osteogenesis imperfecta. Pediatrics. 2003;111:601-7.
  • Rauch F, Plotkin H, Travers R, Zeitlin L, Glorieux FH. Osteogenesis imperfecta types I, III, and IV: effect of pamidronate therapy on bone and mineral metabolism. J Clin Endocrinol Metab. 2003;88:986
  • Yazışma Adresi / Address for Correspondence: Dr. Fatih GÜRBÜZ Çukurova Üniversitesi Tıp Fakültesi, Çocuk Endokrinolojisi Bilim Dalı, ADANA Email: fggurbuz@yahoo.com G eliş tarihi/Received on: 20.01.2014
  • Kabul tarihi/Accepted on:27.02.2014
There are 42 citations in total.

Details

Primary Language Turkish
Journal Section Research
Authors

Neslihan Önenli Mungan This is me

Fatih Gürbüz This is me

Eda Mengen This is me

Özden Özgür This is me

Ali Kemal Topaloğlu This is me

Bilgin Yüksel This is me

Publication Date July 22, 2014
Published in Issue Year 2014 Volume: 39 Issue: 3

Cite

MLA Mungan, Neslihan Önenli et al. “Osteogenezis İmperfekta Olan Çocuklarda İki Farklı Pamidronat Protokolünün Değerlendirilmesi”. Cukurova Medical Journal, vol. 39, no. 3, 2014, pp. 532-9, doi:10.17826/cutf.46470.