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Meta-analysis of diffusion tensor imaging studies shows altered fractional anisotropy occurring in distinct brain areas in association with depression

DOI: 10.1186/2045-5380-1-3

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Abstract:

Major depressive disorder (MDD) is one of the most common human diseases, with a lifetime prevalence of 16% and an annual incidence of 6.6% [1]. It is a major cause of long-term disability, with approximately 800,000 individuals worldwide dying each year as a result of suicide, a high proportion of whom have or had MDD [2]. The World Health Organization (WHO) estimates that more people die each year as a result of suicide than in all the armed conflicts worldwide [2]. Even with treatment, approximately 40% of patients do not respond to the first antidepressant prescribed, and 20% experience chronic depression [3]. Many theories exist regarding the pathophysiological basis of MDD, though it remains unresolved. However, recent studies have highlighted many interesting neuronal processes occurring concurrently in the brains of patients with MDD, and these processes may interact with one another to increase or decrease an individual's susceptibility to depression. MDD is believed to originate from a combination of a susceptible genotype, chronic stress and an adverse developmental environment, leading to alterations in the biochemistry, neuroplasticity and structure in the brain [3-7]. Recent advances in neuroimaging techniques have allowed us to study the microstructural changes occurring both prior to and as a result of this disorder.Magnetic resonance diffusion tensor imaging (DTI) is a novel neuroimaging technique that can evaluate both the orientation and the diffusion characteristics of white matter (WM) tracts in vivo [8]. DTI is sensitive to the diffusion patterns of water molecules and produces a three-dimensional image of the brain as a function of this water diffusion [9]. By measuring the direction and magnitude of restricted tissue water motility (diffusion anisotropy), the orientation of WM tracts in the brain can be determined [10], allowing the investigator to assess microstructural changes occurring in response to individual genotypes and environmental

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