Accelerated mineralization kinetics in children with osteogenesis imperfecta type 1

被引:6
作者
Misof, Barbara M. [1 ,2 ,3 ]
Roschger, Paul [1 ,2 ]
Maehr, Matthias [1 ,2 ]
Fratzl-Zelman, Nadja [1 ,2 ,3 ]
Glorieux, Francis H. [4 ,5 ]
Hartmann, Markus A. [1 ,2 ,3 ]
Rauch, Frank [4 ,5 ]
Blouin, Stephane [1 ,2 ,3 ]
机构
[1] Hanusch Hosp OEGK, Ludwig Boltzmann Inst Osteol, Vienna, Austria
[2] Hanusch Hosp, AUVA Trauma Ctr Meidling, Med Dept 1, Vienna, Austria
[3] Vienna Bone & Growth Ctr, Vienna, Austria
[4] Shriners Hosp Children, Montreal, PQ H4A 0A9, Canada
[5] McGill Univ, Montreal, PQ H4A 0A9, Canada
关键词
Osteogenesis imperfecta type 1; Children; Transiliac biopsy sample; Mineralization kinetics; Bone matrix mineralization; Quantitative backscattered electron imaging (qBEI); Double fluorescent labeling; ILIAC BONE HISTOMORPHOMETRY; DENSITY DISTRIBUTION; PARATHYROID-HORMONE; NORMATIVE DATA; TURNOVER; BISPHOSPHONATES; OSTEOPOROSIS; ADOLESCENTS; MECHANISMS; BIOPSIES;
D O I
10.1016/j.bone.2022.116580
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Not much is known about the time course of mineralization in newly formed bone from healthy individuals nor in patients with bone disease. To investigate the early phase of mineral accumulation in human bone, we measured the mean mineralization content between double fluorescence labels (CaYoung) with quantitative backscattered electron imaging (qBEI) in human transiliac biopsy samples. Fluorescent labels for histomorpho-metric evaluation were administered over two 2-day periods separated by a 10-day-free interval, 4-5 days before biopsy procedure. We compared n = 19 children with osteogenesis imperfecta type 1 (OI, 6 girls/13 boys, age -range 2.2-14.1 years) with both a reference group of n = 38 healthy children (REF, 24 girls/14 boys, age-range 1.5-20.9 years) and an age-matched subgroup (n = 17) of the latter (CON, 5 girls/12 boys, age-range 2.0-14.7 years).We observed significantly higher levels of CaYoung in OI type 1 compared to CON and REF in both cortical bone (Ct.CaYoung, +8.3 % and +7.0 %, respectively) and cancellous bone (Cn.CaYoung, +6.5 % and +4.9 %, all p < 0.001). When comparing cortical and cancellous compartments intra-individually, we found a significantly higher Cn.CaYoung than Ct.CaYoung in REF (2.3 +/- 2.9 %, p < 0.001), but not in the OI group (0.6 +/- 1.6 %, not significant). In the REF group, n = 7 samples also contained double labels in primary woven bone (which is deposited at the external cortex during growth/lateral drift of the iliac crest). This primary woven bone in REF had a higher CaYoung than secondary osteonal bone (4.9 +/- 2.7 %).Our findings suggest that bone in OI has an accelerated mineral accumulation compared to healthy bone. This is reflecting the overall increased bone mineralization in OI as reported previously, and indicates that the higher levels of mineralization than those seen in healthy individuals are already achieved in OI type 1 early after onset of mineralization.
引用
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页数:8
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共 44 条
[1]   Aging of microstructural compartments in human compact bone [J].
Akkus, O ;
Polyakova-Akkus, A ;
Adar, F ;
Schaffler, MB .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (06) :1012-1019
[2]   3D Interrelationship between Osteocyte Network and Forming Mineral during Human Bone Remodeling [J].
Ayoubi, Mahdi ;
van Tol, Alexander F. ;
Weinkamer, Richard ;
Roschger, Paul ;
Brugger, Peter C. ;
Berzlanovich, Andrea ;
Bertinetti, Luca ;
Roschger, Andreas ;
Fratzl, Peter .
ADVANCED HEALTHCARE MATERIALS, 2021, 10 (12)
[3]   Time sequence of secondary mineralization and microhardness in cortical and cancellous bone from ewes [J].
Bala, Yohann ;
Farlay, Delphine ;
Delmas, Pierre D. ;
Meunier, Pierre J. ;
Boivin, Georges .
BONE, 2010, 46 (04) :1204-1212
[4]   Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation [J].
Blouin, Stephane ;
Fratzl-Zelman, Nadja ;
Glorieux, Francis H. ;
Roschger, Paul ;
Klaushofer, Klaus ;
Marini, Joan C. ;
Rauch, Frank .
JOURNAL OF BONE AND MINERAL RESEARCH, 2017, 32 (09) :1884-1892
[5]   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
[6]   The mineralization density of iliac crest bone from children with osteogenesis imperfecta [J].
Boyde, A ;
Travers, R ;
Glorieux, FH ;
Jones, SJ .
CALCIFIED TISSUE INTERNATIONAL, 1999, 64 (03) :185-190
[7]   Bone turnover markers in patients with osteogenesis imperfecta [J].
Braga, V ;
Gatti, D ;
Rossini, M ;
Colapietro, F ;
Battaglia, E ;
Viaplana, O ;
Adami, S .
BONE, 2004, 34 (06) :1013-1016
[8]   Altered lacunar and vascular porosity in osteogenesis imperfecta mouse bone as revealed by synchrotron tomography contributes to bone fragility [J].
Carriero, A. ;
Doube, M. ;
Vogt, M. ;
Busse, B. ;
Zustin, J. ;
Levchuk, A. ;
Schneider, P. ;
Mueller, R. ;
Shefelbine, S. J. .
BONE, 2014, 61 :116-124
[9]   Dynamics of the transition from osteoblast to osteocyte [J].
Dallas, Sarah L. ;
Bonewald, Lynda F. .
SKELETAL BIOLOGY AND MEDICINE, 2010, 1192 :437-443
[10]   New perspectives on osteogenesis imperfecta [J].
Forlino, Antonella ;
Cabral, Wayne A. ;
Barnes, Aileen M. ;
Marini, Joan C. .
NATURE REVIEWS ENDOCRINOLOGY, 2011, 7 (09) :540-557