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. 2024 Feb 8;49(5):814–823. doi: 10.1038/s41386-024-01812-7

Table 3.

Associations between clinical variables and GMV within all BD patients.

Variable Negative Positive
Number of depressive episodes ptfce-FWE = 0.162 ptfce-FWE = 0.589
Number of (hypo-) manic episodes ptfce-FWE = 0.427 ptfce-FWE = 0.831
Number of psychiatric hospitalizations ptfce-FWE = 0.132 ptfce-FWE = 0.999
Time since first psychiatric hospitalization ptfce-FWE = 0.416 ptfce-FWE = 0.785
Time since first symptoms ptfce-FWE = 0.329 ptfce-FWE = 0.646
Age of Onset ptfce-FWE = 0.646 ptfce-FWE = 0.329
Psychotic symptoms (yes vs. no)a ptfce-FWE = 0.356
Medication Load ptfce-FWE = 0.072 ptfce-FWE = 0.999
PRS-CS-auto (mean φ = 1.29×10-4) for BD ptfce-FWE = 0.571 ptfce-FWE = 0.314
Childhood Adversityb ptfce-FWE = 0.098 ptfce-FWE = 0.988
Body Mass Index ptfce-FWE = 0.546 ptfce-FWE = 0.621

p-values are considered significant at p < 0.005, correcting for multiple testing by the Bonferroni procedure, aaccording to pairwise comparison (t-test) comparing patients with and without lifetime psychotic symptoms across both BD subtype groups, bmeasured by the Childhood Trauma Questionnaire (CTQ).

BD bipolar disorder, BD-I bipolar disorder subtype I, BD-II bipolar disorder subtype 2, GMV gray matter volumes, PRS polygenic risk score.