Fig. 4: Alterations in peak alpha frequency (PAF) supportive of thalamocortical dysrhythmia in FXS patients. | Communications Biology

Fig. 4: Alterations in peak alpha frequency (PAF) supportive of thalamocortical dysrhythmia in FXS patients.

From: Neocortical localization and thalamocortical modulation of neuronal hyperexcitability contribute to Fragile X Syndrome

Fig. 4

The slowing of alpha oscillations have been observed across scalp potentials and intraoperative recordings and is suggestive of abnormalities in thalamocortical activity in several neuropsychiatric conditions. a Bar plots (model estimated mean ± standard error of least-squared mean estimates) comparing regional PAF by groups matched by sex. Scatter plot of observed subject-level PAF values are superimposed over model estimates. Participants with FXS (n = 70) have slower PAF across all cortical regions than controls (n = 71). b Line plots ± standard error of least-squared mean estimates comparing the within-subject distribution of PAF across posterior-anterior cortical regions. Males with FXS have a relatively even distribution of PAF across the posterior-anterior axis with no prominent central elevation as seen in matched controls. c Visualization of mean FXS-control differences of PAF by cortical node. Participants with FXS have broadly reduced PAF with the most prominent reductions in central and parietal nodes. See Supplementary Fig. 3 for node atlas. d The severity of anxiety is inversely associated with PAF. Visualization of cortex plotting age-corrected Spearman correlations in full-mutation, non-mosaic males (FM; n = 27; r(25) = −0.41 to −0.53, p ≤ 0.05). FM full mutation, FXS non-mosaic males, LO left occipital. Horizontal black bars: FDR-adjusted, post-hoc testing; *adj. p ≤ 0.05; **adj. p ≤ 0.01; ***adj. p. ≤ 1 × 10−5.

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