Detailseite
Projekt Druckansicht

Einfluss der Ultrastruktur auf die Fraktureigenschaften humanen Knochengewebes in physiologischen und pathologischen Zuständen

Fachliche Zuordnung Orthopädie, Unfallchirurgie, rekonstruktive Chirurgie
Förderung Förderung von 2013 bis 2018
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 227070813
 
Erstellungsjahr 2018

Zusammenfassung der Projektergebnisse

Aging and bone diseases are associated with an increased risk of fracture. Therefore, it is important to understand the origins of such disease-related deterioration in bone's mechanical properties. The mechanical integrity of bone derives from its hierarchical structure, which in healthy states is able to resist bone fracture and tolerate damage. Indeed, the mechanisms through which bone derives its mechanical properties are related to bone quality parameters. Comprehensive bone quality assessment in healthy and diseased cases was carried out to provide new data on bone's cellular activities, structural changes and mechanical resistance. In this context, we have used an integrated approach combining experimental bone quality assessment tools and clinical medical technology by using high resolution peripheral quantitative microcomputed tomography (HR-pQCT), dual energy x-ray absorptiometry (DXA), microcomputed tomography, bone histomorphometry, synchrotron small-angle X-ray scattering (SAXS) / wide-angle X-ray diffraction (WAXD), backscattered electron imaging (BSE), microanalysis (EDX, µXRF), reference point indentation/nanoindentation, Raman and Fourier Transform Infrared spectroscopy (FTIR). Although healthy bone tissue can generally resist physiological loading environments, certain conditions such as aging and disease can significantly increase the risk of fracture in patients. Specifically, the reduced mechanical integrity originates from various alterations to the hierarchical structure of bone tissue. With this program, we have analyzed how human bone structure resists fracture in healthy bone and how changes to the bone structure due to aging, osteoporosis, osteoporosis treatment and changed collagen matrix properties can affect the mechanical integrity of bone tissue.

Projektbezogene Publikationen (Auswahl)

  • Osteocytic canalicular networks: morphological implications for altered mechanosensitivity. ACS Nano. 2013 Sep 24;7(9):7542-51
    Milovanovic P, Zimmermann EA, Hahn M, Djonic D, Püschel K, Djuric M, Amling M, Busse B
    (Siehe online unter https://doi.org/10.1021/nn401360u)
  • Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae. Eur Cell Mater. 2014 Sep 22;28:152-63
    Krause M, Soltau M, Zimmermann EA, Hahn M, Kornet J, Hapfelmeier A, Breer S, Morlock M, Wulff B, Püschel K, Glueer CC, Amling M, Busse B
    (Siehe online unter https://doi.org/10.22203/eCM.v028a12)
  • Fracture resistance of human cortical bone across multiple length-scales at physiological strain rates. Biomaterials. 2014 Jul;35(21):5472-81
    Zimmermann EA, Gludovatz B, Schaible E, Busse B, Ritchie RO
    (Siehe online unter https://doi.org/10.1016/j.biomaterials.2014.03.066)
  • Multi-level characterization of human femoral cortices and their underlying osteocyte network reveal trends in quality of young, aged, osteoporotic and antiresorptive-treated bone. Biomaterials. 2015 Mar;45:46-55
    Milovanovic P, Zimmermann EA, Riedel C, vom Scheidt A, Herzog L, Krause M, Djonic D, Djuric M, Püschel K, Amling M, Ritchie RO, Busse B
    (Siehe online unter https://doi.org/10.1016/j.biomaterials.2014.12.024)
  • Intrinsic mechanical behavior of femoral cortical bone in young, osteoporotic and bisphosphonate-treated individuals in low- and high energy fracture conditions. Sci Rep. 2016 Feb 16;6:21072
    Zimmermann EA, Schaible E, Gludovatz B, Schmidt FN, Riedel C, Krause M, Vettorazzi E, Acevedo C, Hahn M, Püschel K, Tang S, Amling M, Ritchie RO, Busse B
    (Siehe online unter https://doi.org/10.1038/srep21072)
  • Assessment of collagen quality associated with non-enzymatic cross-links in human bone using Fourier-transform infrared imaging. Bone. 2017 Apr;97:243-251
    Schmidt FN, Zimmermann EA, Campbell GM, Sroga GE, Püschel K, Amling M, Tang SY, Vashishth D, Busse B
    (Siehe online unter https://doi.org/10.1016/j.bone.2017.01.015)
  • Atypical fracture with long-term bisphosphonate therapy is associated with altered cortical composition and reduced fracture resistance. Proc Natl Acad Sci USA. 2017 Aug 15;114(33):8722-8727
    Lloyd AA, Gludovatz B, Riedel C, Luengo EA, Saiyed R, Marty E, Lorich DG, Lane JM, Ritchie RO, Busse B, Donnelly E
    (Siehe online unter https://doi.org/10.1073/pnas.1704460114)
  • The Formation of Calcified Nanospherites during Micropetrosis Represents a Unique Mineralization Mechanism in Aged Human Bone. Small. 2017 Jan;13(3)
    Milovanovic P, Zimmermann EA, Vom Scheidt A, Hoffmann B, Sarau G, Yorgan T, Schweizer M, Amling M, Christiansen S, Busse B
    (Siehe online unter https://doi.org/10.1002/smll.201602215)
  • Bone tissue aging affects mineralization of cement lines. Bone. 2018 May;110:187-193
    Milovanovic P, Vom Scheidt A, Mletzko K, Sarau G, Püschel K, Djuric M, Amling M, Christiansen S, Busse B
    (Siehe online unter https://doi.org/10.1016/j.bone.2018.02.004)
  • Inter-site variability of the osteocyte lacunar network in the cortical bone underpins fracture susceptibility of the superolateral femoral neck. Bone. 2018 Jul;112:187-193
    Rolvien T, Vom Scheidt A, Stockhausen KE, Milovanovic P, Djonic D, Hubert J, Hawellek T, Wacker A, Jebens V, Püschel K, Zimmermann EA, Djuric M, Amling M, Busse B
    (Siehe online unter https://doi.org/10.1016/j.bone.2018.04.018)
 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung