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Evaluation of Raman Spectroscopy for Fracture Resistance Assessment

The age-related risk of skeletal fracture is a significant problem in modern medicine, such that both hip fracture and osteoporotic fracture are listed in the World Health Organization top 12 sources of disease burden, with nearly 9 million osteoporotic fractures in the year 2000 alone. Dual energy X-ray absorptiometry or (DXA) is the clinical gold standard in the diagnosis of fracture risk for disease like osteoporosis. However, DXA based assessment of areal bone mineral density does not explain the age related increase in fracture risk. Despite the excellence in advances of X-ray based technologies and complementary etiological factors (FRAX), the DXA method is fundamentally limited to the assessment of the mineral phase of bone. Therefore growing efforts to improve fracture risk assessment have led to the development of several complementary tools to analyze bone quality beyond its mineral density.
At the core of this interchange between laboratory science and clinical diagnosis, Raman Spectroscopy (RS) has become a critical tool for measuring bone composition. The stable chemical composition and crystalline nature of bone tissue makes RS a powerful tool suited for the needs of bone assessment. Despite significant work in identifying the RS features of bone tissue, little evidence correlates RS to fracture resistance of bone. This thesis focuses on the evaluation of RS as a clinically relevant tool for bone fracture resistance assessment. I will detail how I established the technique of manipulating light polarization to concurrently measure both the organization and composition of bone according to optical theory, despite the complications of biological tissue. Application of the methods will show how RS measures of organization explain bone brittleness when measures of composition do not. Finally, I will detail how multivariate expressions of RS describing the interplay between organization and composition led to the first nondestructive explanation of fracture toughness in the largest human sample study to date. The analysis reveals that fracture toughness is driven by microstructural heterogeneity and not bulk composition, with significant implications for our understanding of clinical fracture resistance and future designs applications of RS instruments to material quality.

Identiferoai:union.ndltd.org:VANDERBILT/oai:VANDERBILTETD:etd-11172014-160844
Date18 November 2014
CreatorsMakowski, Alexander James
ContributorsJeffry S. Nyman, Anita Mahadevan-Jansen, E. Duco Jansen, Florent Elefteriou, Jeffrey M. Davidson
PublisherVANDERBILT
Source SetsVanderbilt University Theses
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.library.vanderbilt.edu/available/etd-11172014-160844/
Rightsunrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.

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