Intravenous Pamidronate Treatment Improves Growth in Prepubertal Osteogenesis Imperfecta Patients

被引:3
作者
Heino, Terhi J. [1 ]
Astrom, Eva [2 ]
Laurencikas, Evaldas [1 ]
Savendahl, Lars [1 ]
Soderhall, Stefan [3 ]
机构
[1] Karolinska Inst, Astrid Lindgren Childrens Hosp, Pediat Endocrinol Unit, Dept Womens & Childrens Hlth, Stockholm, Sweden
[2] Karolinska Inst, Astrid Lindgren Childrens Hosp, Pediat Neurol Unit, Dept Womens & Childrens Hlth, Stockholm, Sweden
[3] Karolinska Inst, Astrid Lindgren Childrens Hosp, Pediat Oncol Unit, Dept Womens & Childrens Hlth, Stockholm, Sweden
来源
HORMONE RESEARCH IN PAEDIATRICS | 2011年 / 75卷 / 05期
关键词
Osteogenesis imperfecta; Bisphosphonate; Vertebral growth; BISPHOSPHONATE TREATMENT; MOUSE MODEL; CHILDREN; THERAPY; OSTEOPOROSIS; ALENDRONATE; INFANTS; BONE; ADOLESCENTS; SKELETAL;
D O I
10.1159/000323370
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Pamidronate is widely used to treat pediatric patients with osteogenesis imperfecta (OI). We aimed at delineating the effects of monthly pamidronate therapy on the growth of different body segments in prepubertal OI patients. Methods: The study included 14 prepubertal patients (12 boys, 2 girls) with mild forms of OI (type I and IV). The mean age at treatment start was 7: 8 years: months (3: 7-11:0). Pamidronate was given as monthly intravenous infusions. The patients were measured 1 year before, at treatment start and 1 and 2 years after treatment start. Results: Height standard deviation score (SDS) and sitting height SDS significantly increased (p < 0.05) during the first year of treatment when compared to the pre-treatment year. No further improvement was detected during the second year of treatment. However, when plotted on disease-specific growth charts (untreated patients with the same OI types), height gain was significant during the first (p < 0.001) and second (p < 0.05) years of treatment. All patients increased their bone mineral density throughout the follow-up. Conclusion: Monthly pamidronate improves the growth of prepubertal patients with mild OI, where the most prominent growth stimulation is seen in the upper body segment. Copyright (c) 2011 S. Karger AG, Basel
引用
收藏
页码:354 / 361
页数:8
相关论文
共 31 条
[11]  
Delemarre-van de Waal H, 2005, ENDOCRIN DEV, V8, P1, DOI 10.1159/000084082
[12]  
DiMeglio LA, 2005, J PEDIATR ENDOCR MET, V18, P43
[13]   Benefits of pamidronate in children with osteogenesis imperfecta: an open prospective study [J].
Forin, W ;
Arabi, A ;
Guigonis, V ;
Filipe, G ;
Bensman, A ;
Roux, C .
JOINT BONE SPINE, 2005, 72 (04) :313-318
[14]   Intravenous neridronate in children with osteogenesis imperfecta:: A randomized controlled study [J].
Gatti, D ;
Antoniazzi, F ;
Prizzi, R ;
Braga, V ;
Rossini, M ;
Tatò, L ;
Viapiana, O ;
Adami, S .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (05) :758-763
[15]   Cyclic administration of pamidronate in children with severe osteogenesis imperfecta [J].
Glorieux, FH ;
Bishop, NJ ;
Plotkin, H ;
Chabot, G ;
Lanoue, G ;
Travers, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (14) :947-952
[16]   Effects of alendronate and pamidronate on cultured rat metatarsal bones:: Failure to prevent dexamethasone-induced growth retardation [J].
Heino, Terhi J. ;
Chagin, Andrei S. ;
Takigawa, Masaharu ;
Savendahl, Lars .
BONE, 2008, 42 (04) :702-709
[17]   Vertebral morphometry in children and adolescents with osteogenesis imperfecta: Effect of intravenous pamidronate treatment [J].
Land, Christof ;
Rauch, Frank ;
Munns, Craig F. ;
Sahebjam, Solmaz ;
Glorieux, Francis H. .
BONE, 2006, 39 (04) :901-906
[18]   Cyclic pamidronate infusion improves bone mineralisation and reduces fracture incidence in osteogenesis imperfecta [J].
Lee, YS ;
Low, SL ;
Lim, LA ;
Loke, KY .
EUROPEAN JOURNAL OF PEDIATRICS, 2001, 160 (11) :641-644
[19]   Anthropometry of patients with osteogenesis imperfecta [J].
Lund, AM ;
Müller, J ;
Skovby, F .
ARCHIVES OF DISEASE IN CHILDHOOD, 1999, 80 (06) :524-528
[20]   Alendronate treatment for infants with osteogenesis imperfecta: Demonstration of efficacy in a mouse model [J].
McCarthy, EA ;
Raggio, CL ;
Hossack, MD ;
Miller, EA ;
Jain, S ;
Boskey, AL ;
Camacho, NP .
PEDIATRIC RESEARCH, 2002, 52 (05) :660-670