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Genetic contributions to brain fiber architecture and neuroanatomical alterations in alcohol dependent individuals : a correlation study

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1928/10884

Genetic contributions to brain fiber architecture and neuroanatomical alterations in alcohol dependent individuals : a correlation study

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Title: Genetic contributions to brain fiber architecture and neuroanatomical alterations in alcohol dependent individuals : a correlation study
Author: Kulkarny, Vibhati
Advisor(s): Perrone-Bizzozero, Nora
Hutchison, Kent
Committee Member(s): Allan, Andrea
Wilson, Michael
Department: University of New Mexico. Biomedical Sciences Graduate Program
Subject(s): Alcohol Dependence
Neuroimaging
Magnetic Resonance Imaging
Diffusion Tensor Imaging
Genetics
Single Nucleotide Polymorphsims
LC Subject(s): Alcoholism--Genetic aspects
Alcoholism--Imaging.
Alcoholism--Pathophysiology
Alcohol--Physiological effect.
Neurofibrils--Physiology.
Degree Level: Doctoral
Abstract: Alcohol dependence (AD) is a complex addictive disorder, affecting 5.4% of the general population during a lifetime (Kessler, 2005) and has a complex heterogenous phenotype, with behavioral, morphological, and genetic components. Alcohol use can cause gray matter and white matter tissue damage. The extent of alcoholism’s effect on brain matter structure in young adults is less known. Assessement of low and high alcohol dependent individuals was derived from DSM-IV. FSL based Magnetic Resonance Imaging (MRI) and quantitative fiber tracking derived from diffusion tensor imaging (DTI) assessed morphological alterations of 6 gray matter structures involved in addiction and 10 white matter structures that show connectivity of these structures in 26 low AD and 19 high AD individuals. Candidate SNPs were chosen relating to synaptic plasticity and myelination (BDNF, NTRK2, NFKB1, MAG, OLIG2) and each individual was genotyped. Alcohol dependence affected the volumes of the caudate-putamen, the accumbens, the amygdala and the hippocampus. The uncinate fasciculus was also affected by level og AD, showing smaller mean diffusivity (MD), quantified separately for axial diffusivity (AxD), a marker of axonal intergrity, and radial diffusivity (RD), a marker of myelin integrity. Exploratory associations of AD, morphological alterations and SNPs, showed significant correlations and trends, but was not well defined due to a small subject population. The present research shows evidence that behavioral diseases are associated with identifiable neuroanatomic alterations, and do form relationships with specific SNPs. Additional information is needed when studying a specific, yet multifactorial disease, such as AD, but nonetheless, we advocate the use of neuroimaging measures in genetic studies.
Graduation Date: May 2010
URI: http://hdl.handle.net/1928/10884

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