Histomorphometry and Bone Matrix Mineralization Before and After Bisphosphonate Treatment in Boys With Duchenne Muscular Dystrophy: A Paired Transiliac Biopsy Study

被引:35
作者
Misof, Barbara M. [1 ,2 ]
Roschger, Paul [1 ,2 ]
McMillan, Hugh J. [3 ]
Ma, Jinhui [4 ]
Klaushofer, Klaus [1 ,2 ]
Rauch, Frank [5 ]
Ward, Leanne M. [3 ]
机构
[1] Hanusch Hosp WGKK, Ludwig Boltzmann Inst Osteol, Vienna, Austria
[2] Hanusch Hosp, Dept Med 1, AUVA Trauma Ctr Meidling, Vienna, Austria
[3] Univ Ottawa, Childrens Hosp Eastern Ontario, Dept Pediat, Ottawa, ON, Canada
[4] Univ Ottawa, Childrens Hosp Eastern Ontario, Sch Epidemiol Publ Hlth & Prevent Med, Res Inst, Ottawa, ON, Canada
[5] McGill Univ, Shriners Hosp Montreal, Dept Pediat, Montreal, PQ, Canada
关键词
DUCHENNE MUSCULAR DYSTROPHY; INTRAVENOUS BISPHOSPHONATE TREATMENT; HISTOMORPHOMETRY; PAIRED TRANSILIAC BONE BIOPSY; QUANTITATIVE BACKSCATTER ELECTRON IMAGING; BONE MINERALIZATION DENSITY DISTRIBUTION (BMDD); DENSITY DISTRIBUTION; OSTEOGENESIS IMPERFECTA; VERTEBRAL FRACTURES; NORMATIVE DATA; OSTEOPOROSIS; RISEDRONATE; ADOLESCENTS; ALENDRONATE; OSTEOCLASTS; TURNOVER;
D O I
10.1002/jbmr.2756
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Duclienne muscular dystrophy (DMD) is a genetic disorder causing progressive muscle weakness. To prolong independent ambulation, DMD patients are treated with glucocorticaids, which, in turn, can increase bone fragility. In a cohort with vertebral fractures, intravenous bisphosphonate (iv BP) therapy stabilized vertebrae and reduced back pain. To characterize the effects of glucocorticoid therapy and bisphosphonate treatment on bone tissue and material properties, paired transiliac biopsy samples (before and after on average 2.4 years of iv BP) from 9 boys with DMD were studied for histomorphometry and bone mineralization density distribution (BMDD) and compared to reference values. Before iv BP, the boys had low cancellous bone volume (BV/TV) and cortical thickness (Ct.Wi) (both on average 56% of the healthy average,p <0.001 versus reference), and mineralizing surface (MS/BS) in the lower normal range (on average 74% of the healthy average). The average degree of mineralization of cancellous (Cn.Cal\ilean) and cortical compartments (Ct.CaMean) was 21.48 (20.70, 21.90) wt% and 20.42 (19.32, 21.64) wt%, respectively (median [25th, 75th percentiles]), which was not different from reference. After iv BP, BV/TV and Ct.Wi were, on average, unchanged. However, at the individual patient level, BV/TV Z-scores increased in 2, remained unchanged in 4, and declined in 3 patients. Additionally, on average, MS/BS decreased (-85%,p < 0.001), Cn.CaMean (+2.7%) increased, whereas the heterogeneity of cancellous (Cn.CaWidth -19%) and cortical bone mineralization (Ct.CaWidth -8%, all p < 0.05) decreased versus baseline. The changes in bone mineralization are consistent with the antiresorptive action of iv BP. At the same time, our observations point to the need for novel therapies with less or absent bone turnover suppression, including the fact that bone turnover was low even before bisphosphonate therapy, that bone turnover declined further (as expected) with treatment, and that declines in trabecular bone volume were observed in some boys despite bisphosphonate therapy. (C) 2015 American Society for Bone and Mineral Research.
引用
收藏
页码:1060 / 1069
页数:10
相关论文
共 37 条
[1]
Determining mineral content variations in bone using backscattered electron imaging [J].
Bloebaum, RD ;
Skedros, JG ;
Vajda, EG ;
Bachus, KN ;
Constantz, BR .
BONE, 1997, 20 (05) :485-490
[2]
The degree of mineralization of bone tissue measured by computerized quantitative contact microradiography [J].
Boivin, G ;
Meunier, PJ .
CALCIFIED TISSUE INTERNATIONAL, 2002, 70 (06) :503-511
[3]
Influence of remodeling on the mineralization of bone tissue [J].
Boivin, G. ;
Farlay, D. ;
Bala, Y. ;
Doublier, A. ;
Meunier, P. J. ;
Delmas, P. D. .
OSTEOPOROSIS INTERNATIONAL, 2009, 20 (06) :1023-1026
[4]
Long-term risedronate treatment normalizes mineralization and continues to preserve trabecular architecture: Sequential triple biopsy studies with micro-computed tomography [J].
Borah, B ;
Dufresne, TE ;
Ritman, EL ;
Jorgensen, SM ;
Liu, S ;
Chmielewski, PA ;
Phipps, RJ ;
Zhou, XJ ;
Sibonga, JD ;
Turner, RT .
BONE, 2006, 39 (02) :345-352
[5]
BACKSCATTERED ELECTRON IMAGING OF SKELETAL TISSUES [J].
BOYDE, A ;
JONES, SJ .
METABOLIC BONE DISEASE & RELATED RESEARCH, 1984, 5 (03) :145-150
[6]
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management [J].
Bushby, Katharine ;
Finkel, Richard ;
Birnkrant, David J. ;
Case, Laura E. ;
Clemens, Paula R. ;
Cripe, Linda ;
Kaul, Ajay ;
Kinnett, Kathi ;
McDonald, Craig ;
Pandya, Shree ;
Poysky, James ;
Shapiro, Frederic ;
Tomezsko, Jean ;
Constantin, Carolyn .
LANCET NEUROLOGY, 2010, 9 (01) :77-93
[7]
Canalis E, 1996, J CLIN ENDOCR METAB, V81, P3441, DOI 10.1210/jc.81.10.3441
[8]
Effects of Odanacatib on the Radius and Tibia of Postmenopausal Women: Improvements in Bone Geometry, Microarchitecture, and Estimated Bone Strength [J].
Cheung, Angela M. ;
Majumdar, Sharmila ;
Brixen, Kim ;
Chapurlat, Roland ;
Fuerst, Thomas ;
Engelke, Klaus ;
Dardzinski, Bernard ;
Cabal, Antonio ;
Verbruggen, Nadia ;
Ather, Shabana ;
Rosenberg, Elizabeth ;
de Papp, Anne E. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2014, 29 (08) :1786-1794
[9]
Large Osteoclasts in Pediatric Osteogenesis Imperfecta Patients Receiving Intravenous Pamidronate [J].
Cheung, Moira S. ;
Glorieux, Francis H. ;
Rauch, Frank .
JOURNAL OF BONE AND MINERAL RESEARCH, 2009, 24 (04) :669-674
[10]
Regional Changes in Bone Area and Bone Mineral Content in Boys with Duchenne Muscular Dystrophy Receiving Corticosteroid Therapy [J].
Crabtree, Nicola J. ;
Roper, Helen ;
McMurchie, Heather ;
Shaw, Nicholas J. .
JOURNAL OF PEDIATRICS, 2010, 156 (03) :450-U154