@article{1a666a82b68a46fcbc7879e37355cab9,
title = "Early visual processing and adaptation as markers of disease, not vulnerability: EEG evidence from 22q11.2 deletion syndrome, a population at high risk for schizophrenia",
abstract = "We investigated visual processing and adaptation in 22q11.2 deletion syndrome (22q11.2DS), a condition characterized by an increased risk for schizophrenia. Visual processing differences have been described in schizophrenia but remain understudied early in the disease course. Electrophysiology was recorded during a visual adaptation task with different interstimulus intervals to investigate visual processing and adaptation in 22q11.2DS (with (22q+) and without (22q−) psychotic symptoms), compared to control and idiopathic schizophrenia groups. Analyses focused on early windows of visual processing. While increased amplitudes were observed in 22q11.2DS in an earlier time window (90–140 ms), decreased responses were seen later (165–205 ms) in schizophrenia and 22q+. 22q11.2DS, and particularly 22q−, presented increased adaptation effects. We argue that while amplitude and adaptation in the earlier time window may reflect specific neurogenetic aspects associated with a deletion in chromosome 22, amplitude in the later window may be a marker of the presence of psychosis and/or of its chronicity/severity.",
author = "Francisco, {Ana A.} and Foxe, {John J.} and Horsthuis, {Douwe J.} and Sophie Molholm",
note = "Funding Information: We wish to thank Dr. Juliana Bates, who performed the clinical assessments, and Alaina Berruti for her help with data collection. Additionally, we thank Chloe Ifrah and Ilana Deyneko for their assistance at different stages of the project. We would also like to acknowledge the role of the Jacobi Medical Center, the Montefiore-Einstein Regional Center for 22q11.2 Deletion Syndrome, and the OnTrackNY program at Montefiore in recruitment, and the Rose F. Kennedy Intellectual and Developmental Disability Research Center for all its support. We extend our most sincere gratitude to the participants and their families for their interest, their involvement, and their time. This work was supported in part by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), under award numbers U54 HD090260 and P50 HD105352. Work on rare diseases at the University of Rochester (UR) collaboration site is supported in part through the UR Intellectual and Developmental Disabilities Research Center (UR-IDDRC), which is funded by a center grant from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD P50 HD103536 to JJF). Funding Information: We wish to thank Dr. Juliana Bates, who performed the clinical assessments, and Alaina Berruti for her help with data collection. Additionally, we thank Chloe Ifrah and Ilana Deyneko for their assistance at different stages of the project. We would also like to acknowledge the role of the Jacobi Medical Center, the Montefiore-Einstein Regional Center for 22q11.2 Deletion Syndrome, and the OnTrackNY program at Montefiore in recruitment, and the Rose F. Kennedy Intellectual and Developmental Disability Research Center for all its support. We extend our most sincere gratitude to the participants and their families for their interest, their involvement, and their time. This work was supported in part by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), under award numbers U54 HD090260 and P50 HD105352. Work on rare diseases at the University of Rochester (UR) collaboration site is supported in part through the UR Intellectual and Developmental Disabilities Research Center (UR-IDDRC), which is funded by a center grant from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD P50 HD103536 to JJF). Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
month = dec,
doi = "10.1038/s41537-022-00240-0",
language = "English (US)",
volume = "8",
journal = "Schizophrenia",
issn = "2334-265X",
publisher = "Nature Publishing Group",
number = "1",
}