Skip to main content

Table 1 Overview of cortical thinning studies comparing young patients with psychosis, bipolar disorder and controls

From: Cortical thinning in young psychosis and bipolar patients correlate with common neurocognitive deficits

Author

Sample (age, years ± SD)

Regions of cortical thinning

White et al. (2003)

42 Childhood/adolescent-onset psychosis (17.7 ± 1.7)

• Mean cortical thickness

24 Controls (17.7 ± 2.0)

• Frontal, temporal, and parietal sulci; temporal gyri

Narr et al. (2005a, b)

72 First episode psychosis (25.1 ± 4.7)

• Frontal, temporal and parietal lobes (significance set at p < 0.05, uncorrected)

78 Controls (27.3 ± 6.6)

• Fronto-polar, occipital lobes in patients with little or no prior antipsychotic medication

Rais et al. (2010)

32 Early schizophrenia, non-cannabis users (23.3 ± 5.1)

• Same at baseline

19 Early schizophrenia, cannabis users (21.8 ± 3.9)

• Five-year follow-up schizophrenia patients: right supplementary motor cortex, inferior frontal  cortex, superior temporal gyrus, angular gyrus, cuneus and postcentral gyrus

31 Controls (24.7 ± 6.7)

Crespo-Facorro et al. (2011)

142 First episode psychosis (29.7 ± 8.7)

• Frontal, temporal and parietal lobes (group contrast only, not significant when covarying  for gender)

83 Controls (27.6 ± 7.6)

Jung et al. (2011)

29 Ultra-high risk (UHR) of psychosis (22.2 ± 4.3)

• Mean cortical thickness: (controls = UHR) > schizophrenia

31 Schizophrenia (24.3 ± 4.2)

• Schizophrenia vs controls: bilateral insular, inferior frontal, STG, PCC and ACC; left superior  frontal, inferior temporal and precuneus; right parahippocampal, inferior parietal, lingual and  precentral cortices

29 Controls (23.2 ± 2.7)

• UHR vs controls: bilateral ACC and parahippocampal and medial frontal cortices; left STG;  right lingual, inferior frontal, parietal and middle temporal cortices

• Schizophrenia vs UHR: bilateral medial frontal cortex; left STG, superior frontal,  parahippocampal and inferior temporal cortices; right insula, uncus, PCC and precentral and  middle temporal cortices

Lyoo et al. (2006b)

25 Bipolar disorder (33.8 ± 9.6)

• Bilateral postcentral cortex; left DLPFC, ACC, PCC, occipital cortex; right orbitofrontal, angular  and fusiform cortices

21 Controls (31.5 ± 9.7)

• Bipolar I to bipolar II

Rimol et al. (2010, 2012)

173 Schizophrenia (32.3 ± 9.0)

• Schizophrenia vs controls: bilateral lateral and medial frontal lobe, temporal lobe, precuneus,  parahippocampal and fusiform gyri, precentral gyrus, lateral and medial occipital lobe, lingual  gyrus; left ACC, STG, middle temporal gyrus, inferior parietal and lingual gyrus; right medial  orbitofrontal, entorhinal, supramarginal and inferior parietal cortices, isthmus of PCC

139 Bipolar disorder (35.4 ± 11.3)

207 Controls (36.2 ± 9.7)

• Bipolar vs controls, schizophrenia: no significant findings

• Bipolar I vs controls: bilateral lateral and medial frontal lobes; left orbitofrontal, posterior STG,  inferior parietal gyrus; right superior frontal gyrus, supramarginal, parietal, inferior temporal  and parahippocampal gyrus

• Bipolar I vs schizophrenia: no significant findings

Foland-Ross et al. (2011)

34 Bipolar I disorder (38.1 ± 12.0)

• Bilateral prefrontal cortex; left ACC and dorsomedial, ventrolateral, frontopolar cortices

31 Controls (37.8 ± 13.1)

• No difference between patients treated with or without lithium

  1. ACC, anterior cingulate cortex; DLPFC, dorsolateral prefrontal cortex; PCC, posterior cingulate cortex; STG, superior temporal gyrus; UHR, ultra-high risk.