Widespread Cortical Thickness Is Associated With Neuroactive Steroid Levels.
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2019-01
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Background:Neuroactive steroids are endogenous molecules with regenerative and neuroprotective actions. Both cortical thickness and many neuroactive steroid levels decline with age and are decreased in several neuropsychiatric disorders. However, a systematic examination of the relationship between serum neuroactive steroid levels and in vivo measures of cortical thickness in humans is lacking. Methods:Peripheral serum levels of seven neuroactive steroids were assayed in United States military veterans. All (n = 143) subsequently underwent high-resolution structural MRI, followed by parcellelation of the cortical surface into 148 anatomically defined regions. Regression modeling was applied to test the association between neuroactive steroid levels and hemispheric total gray matter volume as well as region-specific cortical thickness. False discovery rate (FDR) correction was used to control for Type 1 error from multiple testing. Results:Neuroactive steroid levels of allopregnanolone and pregnenolone were positively correlated with gray matter thickness in multiple regions of cingulate, parietal, and occipital association cortices (r = 0.20-0.47; p < 0.05; FDR-corrected). Conclusion:Positive associations between serum neuroactive steroid levels and gray matter cortical thickness are found in multiple brain regions. If these results are confirmed, neuroactive steroid levels and cortical thickness may help in monitoring the clinical response in future intervention studies of neuroregenerative therapies.
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Morey, Rajendra A, Sarah L Davis, Courtney C Haswell, Jennifer C Naylor, Jason D Kilts, Steven T Szabo, Larry J Shampine, Gillian J Parke, et al. (2019). Widespread Cortical Thickness Is Associated With Neuroactive Steroid Levels. Frontiers in Neuroscience, 13. p. 1118. 10.3389/fnins.2019.01118 Retrieved from https://hdl.handle.net/10161/21230.
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Scholars@Duke

Jennifer C. Naylor

Jason David Kilts

Delin Sun
I am interested in the neuropsychological and behavioral correlates of posttraumatic stress disorder (PTSD) and adolescent trauma. With a multidisciplinary background in psychology, physics, and biology, I have specific training and expertise in neuroimaging methods and secondary data analysis of neural changes in PTSD and childhood trauma. I systematically study PTSD-related structural and functional brain images using methods that focus on different levels including regional changes, connectivity, and brain networks, respectively, to build a complete behavioral-brain map. I also study the relationship between adolescent brain development and trauma as well as alcohol by using brain structure network graphs, longitudinal studies, and machine learning research methods. Besides, I utilize neuroimaging and neurophysiological techniques to investigate the neural underpinnings of social cognitive and affective functions in both healthy volunteers and patients with mental disorders including excessive internet usage, smoking addiction, Alzheimer’s Disease, and depression. I have successfully collaborated with researchers locally or from other institutions and have had several peer-reviewed publications in each project.
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