Effects of intravenous pamidronate treatment in infants with osteogenesis imperfecta: Clinical and histomorphometric outcome

被引:95
作者
Munns, CFJ
Rauch, F
Travers, R
Glorieux, FH
机构
[1] Shriners Hosp Children, Genet Unit, Montreal, PQ H3G 1A6, Canada
[2] McGill Univ, Montreal, PQ, Canada
关键词
bisphosphonate; bone fragility; histomorphometry; osteoporosis; pediatric;
D O I
10.1359/JBMR.050213
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Clinical and histomorphometric outcome was compared between children with OI who had received pamidronate since infancy and age-matched patients who had never received pamidronate. Pamidronate was associated with improved vertebral shape and mass, higher cortical width, increased cancellous bone volume, and suppressed bone turnover. Introduction: Observations in small patient series indicate that infants with severe osteogenesis imperfecta (01) benefit from treatment with cyclical intravenous pamidronate. However, detailed analyses of outcome are lacking for this age group. Materials and Methods: Clinical outcome was evaluated in 29 children with OI types I (n = 3), III (n = 14), or IV (n = 12) who started pamidronate therapy before 2 years of age (age at treatment onset: median, 6 months; range, 2 weeks to 23 months) and who had completed 3 years of treatment (total annual pamidronate dose, 9 mg/kg). They were compared with a historical control group of 29 untreated children with severe 01 who were matched for 01 type and age at the 3-year treatment time-point. In addition, iliac bone histomorphometry was compared between 24 pamidronate-treated patients and 24 age-matched 01 patients who had not received pamidronate. Results: Morphometric evaluation of lumbar vertebrae (L-1-L-4) showed that the shape of vertebral bodies was better preserved in pamidronate-treated patients. This was accompanied by significantly higher lumbar spine areal and volumetric BMD (+110 and +96%, respectively) and a larger vertebral bone volume (+26%) on densitometry. Regarding mobility function, the Pediatric Evaluation of Disability Inventory gross motor score was 50% greater in the pamidronate group (p < 0.001). Iliac bone histomorphometry showed 61% higher cortical width and 89% higher cancellous bone volume in pamidronate-treated patients. Bone formation rate per bone surface in the pamidronate group was only 17% that of untreated patients. Conclusions: In conclusion, this study suggests that cyclical pamidronate treatment started in infancy leads to improved bone strength and better gross motor function but also suppresses bone turnover markedly. It is therefore prudent to reserve pamidronate treatment to infant OI patients who present with a moderate to severe phenotype.
引用
收藏
页码:1235 / 1243
页数:9
相关论文
共 26 条
[1]
Beneficial effect of long term intravenous bisphosphonate treatment of osteogenesis imperfecta [J].
Åström, E ;
Söderhäll, S .
ARCHIVES OF DISEASE IN CHILDHOOD, 2002, 86 (05) :356-364
[2]
BLECK EE, 1981, CLIN ORTHOP RELAT R, V159, P111
[3]
Pamidronate treatment of severe osteogenesis imperfecta in a newborn infant [J].
Chien, YH ;
Chu, SY ;
Hsu, CC ;
Hwu, WL .
JOURNAL OF INHERITED METABOLIC DISEASE, 2002, 25 (07) :593-595
[4]
Intravenous pamidronate treatment of children under 36 months of age with osteogenesis imperfecta [J].
DiMeglio, LA ;
Ford, L ;
McClintock, C ;
Peacock, M .
BONE, 2004, 35 (05) :1038-1045
[5]
Intravenous bisphosphonate therapy in children with osteogenesis imperfecta [J].
Falk, MJ ;
Heeger, S ;
Lynch, KA ;
DeCaro, KR ;
Bohach, D ;
Gibson, KS ;
Warman, ML .
PEDIATRICS, 2003, 111 (03) :573-578
[6]
Fazzalari NL, 1997, ANAT REC, V248, P1
[7]
CONCURRENT AND CONSTRUCT-VALIDITY OF THE PEDIATRIC EVALUATION OF DISABILITY INVENTORY [J].
FELDMAN, AB ;
HALEY, SM ;
CORYELL, J .
PHYSICAL THERAPY, 1990, 70 (10) :602-610
[8]
Normative data for iliac bone histomorphometry in growing children [J].
Glorieux, FH ;
Travers, R ;
Taylor, A ;
Bowen, JR ;
Rauch, F ;
Norman, M ;
Parfitt, AM .
BONE, 2000, 26 (02) :103-109
[9]
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
[10]
Greulich W.W., 1971, RADIOGRAPHIC ATLAS S