Fatty acid β-oxidation disorders (FAODs), the most frequent group of inborn errors of metabolism, are clinically heterogeneous and clear genotype-phenotype correlations have not been described. Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency and short chain acyl-CoA dehydrogenase (SCAD) deficiency result from mutations on the ACADVL and ACADS genes, respectively. Multiple mutations have been described in both disorders. Acute symptoms are often induced by physiological stress such as fasting, but the pathophysiologic mechanism underlying disease symptoms and phenotypic heterogeneity remains unknown. The aim of this dissertation was to explore the biological changes induced by genetic mutations and the gene-gene interactions and environmental effects on these defects.
Proteomic changes in SCAD and VLCAD deficient mice, as well as the changes induced by fasting in VLCAD deficiency, were measured quantitatively using a combination of proteomics techniques. Broad mitochondrial dysfunction and derangements in multiple energy metabolism related proteins were altered in SCAD deficiency, indicating a complex mechanism for development of symptoms. Overall, a pattern associated with hepatotoxicity implicated in mitochondrial dysfunction and alteration of fatty acid metabolism was identified. Affected pathways converge on disorders with neurologic symptoms, suggesting that even asymptomatic individuals with SCAD deficiency may be at risk to develop more severe symptoms. Several candidate biomarkers were suggested through Ingenuity Pathway Analysis. Numerous proteomic changes were characterized in VLCAD deficient mice in both fed and fasting states, and relevant biological pathway were identified. Fasting in both deficient and wild type animals induced alterations in several proteins. The pattern of alterations induced by fasting was different in VLCAD deficient mice from that in wild type animals. Mitochondrial chaperonins HSP60 and HSP10 altered differently in VLCAD deficient mice depending on the feeding state. Fasting altered an apparent compensatory increase in oxidative phosphorylation seen in the fed state. Thus, environmental factors and gene-environment interaction play important roles in the pathogenesis of VLCAD deficiency. The diversity of protein changes in variable pathways due to deficiencies in SCAD and VLCAD may help explain the phenotypic heterogeneity in patients.
These proteomic studies present new paradigm for exploring the mechanisms of disease, gene-environment interactions, and their contribution to gene-gene interactions in FAODs, one group of the mandatory target diseases in newborn screening program. The results advanced the knowledge about FAODs and offered the benefits for the improvement in the diagnosis and treatment of theses disorders of great public health interest. Future characterization of functionally interactive genes and association studies in humans will provide further insight into disease mechanism. Further studies on candidate biomarkers are necessary to identify novel markers for prognosis prediction, adjunct diagnosis and therapy guidance in patients.
| Identifer | oai:union.ndltd.org:PITT/oai:PITTETD:etd-07242011-140146 |
| Date | 23 September 2011 |
| Creators | Wang, Wei |
| Contributors | Jerry Vockley, Robert Ferrell, Billy Day, David Finegold, Michael Barmada |
| Publisher | University of Pittsburgh |
| Source Sets | University of Pittsburgh |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.library.pitt.edu/ETD/available/etd-07242011-140146/ |
| Rights | restricted, 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 University of Pittsburgh 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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