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Ho, T. C.

Publications and source records attributed to Ho, T. C..

2 recordsLinked to original sources

Subcortical Shape Alterations in Major Depressive Disorder: Findings from the ENIGMA Major Depressive Disorder Working Group

Alterations in regional subcortical brain volumes have been widely investigated as part of the efforts of an international consortium, ENIGMA, to determine reliable structural brain signatures for Major Depressive Disorder (MDD). Given that subcortical structures are comprised of distinct subfields, we sought to build significantly from prior work to precisely map localized MDD-related differences in subcortical regions using shape analysis. In this meta-analysis of subcortical shape from the ENIGMA-MDD working group, we compared 1,781 patients with MDD and 2,953 healthy controls (CTL) on individual measures of shape metrics (thickness and surface area) on the surface of seven bilateral subcortical structures: nucleus accumbens, amygdala, caudate, hippocampus, pallidum, putamen, and thalamus. Harmonized data processing and statistical analyses were conducted locally at each site, and findings were aggregated by meta-analysis. Relative to CTL, patients with MDD had lower surface area in the subiculum of the hippocampus, the basolateral amygdala, and the nucleus accumbens shell. Relative to CTL, patients with adolescent-onset MDD ([≤] 21 years) had lower thickness and surface area of the subiculum of the hippocampus and the basolateral amygdala. Relative to first-episode MDD, recurrent MDD patients had lower thickness and surface area in the CA1 of the hippocampus and the basolateral amygdala. Our results suggest that previously reported MDD-associated volumetric differences may be localized to specific subfields of these structures that have been shown to be sensitive to the effects of stress, with important implications for mapping treatments to patients based on specific neural targets and key clinical features.

neuroscience

Sex differences in the effects of gonadal hormones on white matter microstructure development in adolescence

Adolescence, the transition between childhood and adulthood, is characterized by rapid brain development in white matter (WM) that is attributed in part to surges in gonadal hormones. To date, however, there have been no longitudinal investigations of the effects of gonadal hormones on WM development in adolescents. We acquired T1-weighted and diffusion-weighted MRIs at two timepoints and saliva samples from 80 adolescents (52 females [11.10{+/-}1.05 years at Time 1; 12.75{+/-}1.37 years at Time 2] and 28 males [ages 11.91{+/-}0.88 years at Time 1; 13.79{+/-}0.95 years at Time 2] who were matched on pubertal stage at Time 1. We estimated mean fractional anisotropy (FA) from 10 major WM tracts and assayed levels of testosterone (in both sexes) and estradiol (in females only). We used linear regression models to test whether interactions between sex and changes in testosterone levels significantly explained changes in FA. Sex significantly moderated the associations between changes in testosterone and changes in FA within the corpus callosum, inferior fronto-occipital fasciculus (IFOF), uncinate fasciculus (UF), and cingulum cingulate (all ps<0.05): whereas these associations were positive in females, they were not significant in males. Females also exhibited positive associations between changes in estradiol and changes in UF, IFOF, and corticospinal FA (all ps<0.05). Our findings indicate that sex differences in WM microstructure of tracts supporting cognitive control, response inhibition, and emotion regulation are explained by differences in changes in testosterone, and have important implications for understanding sex differences in brain development and psychosocial behaviors during the pubertal transition.

neuroscience