TY - JOUR
T1 - Differences in the neural correlates of schizophrenia with positive and negative formal thought disorder in patients with schizophrenia in the ENIGMA dataset
AU - Sharkey, Rachel J.
AU - Bacon, Chelsea
AU - Peterson, Zeru
AU - Rootes-Murdy, Kelly
AU - Salvador, Raymond
AU - Pomarol-Clotet, Edith
AU - Karuk, Andriana
AU - Homan, Philipp
AU - Ji, Ellen
AU - Omlor, Wolfgang
AU - Homan, Stephanie
AU - Georgiadis, Foivos
AU - Kaiser, Stefan
AU - Kirschner, Matthias
AU - Ehrlich, Stefan
AU - Dannlowski, Udo
AU - Grotegerd, Dominik
AU - Goltermann, Janik
AU - Meinert, Susanne
AU - Kircher, Tilo
AU - Stein, Frederike
AU - Brosch, Katharina
AU - Krug, Axel
AU - Nenadic, Igor
AU - Sim, Kang
AU - Spalletta, Gianfranco
AU - Banaj, Nerisa
AU - Sponheim, Scott R.
AU - Demro, Caroline
AU - Ramsay, Ian S.
AU - King, Margaret
AU - Quidé, Yann
AU - Green, Melissa Jane
AU - Nguyen, Dana
AU - Preda, Adrian
AU - Calhoun, Vince
AU - Turner, Jessica
AU - van Erp, Theo
AU - Nickl-Jockschat, Thomas
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024
Y1 - 2024
N2 - Formal thought disorder (FTD) is a clinical key factor in schizophrenia, but the neurobiological underpinnings remain unclear. In particular, the relationship between FTD symptom dimensions and patterns of regional brain volume loss in schizophrenia remains to be established in large cohorts. Even less is known about the cellular basis of FTD. Our study addresses these major obstacles by enrolling a large multi-site cohort acquired by the ENIGMA Schizophrenia Working Group (752 schizophrenia patients and 1256 controls), to unravel the neuroanatomy of FTD in schizophrenia and using virtual histology tools on implicated brain regions to investigate the cellular basis. Based on the findings of previous clinical and neuroimaging studies, we decided to separately explore positive, negative and total formal thought disorder. We used virtual histology tools to relate brain structural changes associated with FTD to cellular distributions in cortical regions. We identified distinct neural networks positive and negative FTD. Both networks encompassed fronto-occipito-amygdalar brain regions, but positive and negative FTD demonstrated a dissociation: negative FTD showed a relative sparing of orbitofrontal cortical thickness, while positive FTD also affected lateral temporal cortices. Virtual histology identified distinct transcriptomic fingerprints associated for both symptom dimensions. Negative FTD was linked to neuronal and astrocyte fingerprints, while positive FTD also showed associations with microglial cell types. These results provide an important step towards linking FTD to brain structural changes and their cellular underpinnings, providing an avenue for a better mechanistic understanding of this syndrome.
AB - Formal thought disorder (FTD) is a clinical key factor in schizophrenia, but the neurobiological underpinnings remain unclear. In particular, the relationship between FTD symptom dimensions and patterns of regional brain volume loss in schizophrenia remains to be established in large cohorts. Even less is known about the cellular basis of FTD. Our study addresses these major obstacles by enrolling a large multi-site cohort acquired by the ENIGMA Schizophrenia Working Group (752 schizophrenia patients and 1256 controls), to unravel the neuroanatomy of FTD in schizophrenia and using virtual histology tools on implicated brain regions to investigate the cellular basis. Based on the findings of previous clinical and neuroimaging studies, we decided to separately explore positive, negative and total formal thought disorder. We used virtual histology tools to relate brain structural changes associated with FTD to cellular distributions in cortical regions. We identified distinct neural networks positive and negative FTD. Both networks encompassed fronto-occipito-amygdalar brain regions, but positive and negative FTD demonstrated a dissociation: negative FTD showed a relative sparing of orbitofrontal cortical thickness, while positive FTD also affected lateral temporal cortices. Virtual histology identified distinct transcriptomic fingerprints associated for both symptom dimensions. Negative FTD was linked to neuronal and astrocyte fingerprints, while positive FTD also showed associations with microglial cell types. These results provide an important step towards linking FTD to brain structural changes and their cellular underpinnings, providing an avenue for a better mechanistic understanding of this syndrome.
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U2 - 10.1038/s41380-024-02563-z
DO - 10.1038/s41380-024-02563-z
M3 - Article
C2 - 38671214
AN - SCOPUS:85191702564
SN - 1359-4184
JO - Molecular psychiatry
JF - Molecular psychiatry
ER -