Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study

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Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study. / Ver Loren van Themaat, Anna Hester; Oranje, Bob; Larsen, Kit Melissa; Tomasevic, Leo; Korsgaard Johnsen, Line; Elgaard Thorup, Anne Amalie; Plessen, Kerstin Jessica; Siebner, Hartwig Roman; Nordentoft, Merete.

In: Schizophrenia Research, Vol. 246, 2022, p. 187-194.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ver Loren van Themaat, AH, Oranje, B, Larsen, KM, Tomasevic, L, Korsgaard Johnsen, L, Elgaard Thorup, AA, Plessen, KJ, Siebner, HR & Nordentoft, M 2022, 'Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study', Schizophrenia Research, vol. 246, pp. 187-194. https://doi.org/10.1016/j.schres.2022.06.035

APA

Ver Loren van Themaat, A. H., Oranje, B., Larsen, K. M., Tomasevic, L., Korsgaard Johnsen, L., Elgaard Thorup, A. A., Plessen, K. J., Siebner, H. R., & Nordentoft, M. (2022). Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study. Schizophrenia Research, 246, 187-194. https://doi.org/10.1016/j.schres.2022.06.035

Vancouver

Ver Loren van Themaat AH, Oranje B, Larsen KM, Tomasevic L, Korsgaard Johnsen L, Elgaard Thorup AA et al. Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study. Schizophrenia Research. 2022;246:187-194. https://doi.org/10.1016/j.schres.2022.06.035

Author

Ver Loren van Themaat, Anna Hester ; Oranje, Bob ; Larsen, Kit Melissa ; Tomasevic, Leo ; Korsgaard Johnsen, Line ; Elgaard Thorup, Anne Amalie ; Plessen, Kerstin Jessica ; Siebner, Hartwig Roman ; Nordentoft, Merete. / Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study. In: Schizophrenia Research. 2022 ; Vol. 246. pp. 187-194.

Bibtex

@article{32775db79a9943cb92eade897980548e,
title = "Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study",
abstract = "Background: Infrequent deviants in a rapid sequence of sounds elicit a negative cortical potential over the frontocentral midline (mismatch negativity, MMN) followed by a positive deflection (P3a). Both cortical potentials are consistently attenuated in patients with schizophrenia (SZ), and, to a lesser degree, in patients with bipolar disorder (BP). Objective: Since it is unclear when MMN and P3a deficits arise relative to the emergence of symptoms, we examined whether MMN and P3a alterations are already detectable in children with familial high risk. Methods: Using 128-channel electroencephalography, we recorded auditory MMN and P3a evoked by a deviation in sound duration, frequency, or both in 51 children with familial high-risk for SZ (FHR-SZ), 41 children with familial high-risk for BP (FHR-BP), and 39 population-based children (PBC) at a mean age of 12.10. Results: MMN amplitude evoked by a duration deviant was larger in children with FHR-BP compared to PBC and FHR-SZ. P3a amplitude in response to a duration ∗ frequency deviant was larger in children with FHR-BP compared to children with FHR-SZ, but not compared to PBC. MMN- and P3a-peak latency did not differ between groups. Conclusions: At an age of around 12 years, children with FHR-BP display enhanced neural sensitivity to change detection of duration deviants, while FHR-SZ showed a normal response pattern. Longitudinal recordings in high-risk children during adolescence are required to elucidate the temporal trajectories of MMN and P3a responses and how they relate to the emergence of first clinical symptoms in SZ and BP.",
keywords = "Electroencephalography, Mismatch negativity, Neurodevelopment, Offspring",
author = "{Ver Loren van Themaat}, {Anna Hester} and Bob Oranje and Larsen, {Kit Melissa} and Leo Tomasevic and {Korsgaard Johnsen}, Line and {Elgaard Thorup}, {Anne Amalie} and Plessen, {Kerstin Jessica} and Siebner, {Hartwig Roman} and Merete Nordentoft",
note = "Publisher Copyright: {\textcopyright} 2022 Elsevier B.V.",
year = "2022",
doi = "10.1016/j.schres.2022.06.035",
language = "English",
volume = "246",
pages = "187--194",
journal = "Schizophrenia Research",
issn = "0920-9964",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Mismatch negativity and P3a amplitude in children with familial high risk of schizophrenia or bipolar disorder – A Danish register-based EEG study

AU - Ver Loren van Themaat, Anna Hester

AU - Oranje, Bob

AU - Larsen, Kit Melissa

AU - Tomasevic, Leo

AU - Korsgaard Johnsen, Line

AU - Elgaard Thorup, Anne Amalie

AU - Plessen, Kerstin Jessica

AU - Siebner, Hartwig Roman

AU - Nordentoft, Merete

N1 - Publisher Copyright: © 2022 Elsevier B.V.

PY - 2022

Y1 - 2022

N2 - Background: Infrequent deviants in a rapid sequence of sounds elicit a negative cortical potential over the frontocentral midline (mismatch negativity, MMN) followed by a positive deflection (P3a). Both cortical potentials are consistently attenuated in patients with schizophrenia (SZ), and, to a lesser degree, in patients with bipolar disorder (BP). Objective: Since it is unclear when MMN and P3a deficits arise relative to the emergence of symptoms, we examined whether MMN and P3a alterations are already detectable in children with familial high risk. Methods: Using 128-channel electroencephalography, we recorded auditory MMN and P3a evoked by a deviation in sound duration, frequency, or both in 51 children with familial high-risk for SZ (FHR-SZ), 41 children with familial high-risk for BP (FHR-BP), and 39 population-based children (PBC) at a mean age of 12.10. Results: MMN amplitude evoked by a duration deviant was larger in children with FHR-BP compared to PBC and FHR-SZ. P3a amplitude in response to a duration ∗ frequency deviant was larger in children with FHR-BP compared to children with FHR-SZ, but not compared to PBC. MMN- and P3a-peak latency did not differ between groups. Conclusions: At an age of around 12 years, children with FHR-BP display enhanced neural sensitivity to change detection of duration deviants, while FHR-SZ showed a normal response pattern. Longitudinal recordings in high-risk children during adolescence are required to elucidate the temporal trajectories of MMN and P3a responses and how they relate to the emergence of first clinical symptoms in SZ and BP.

AB - Background: Infrequent deviants in a rapid sequence of sounds elicit a negative cortical potential over the frontocentral midline (mismatch negativity, MMN) followed by a positive deflection (P3a). Both cortical potentials are consistently attenuated in patients with schizophrenia (SZ), and, to a lesser degree, in patients with bipolar disorder (BP). Objective: Since it is unclear when MMN and P3a deficits arise relative to the emergence of symptoms, we examined whether MMN and P3a alterations are already detectable in children with familial high risk. Methods: Using 128-channel electroencephalography, we recorded auditory MMN and P3a evoked by a deviation in sound duration, frequency, or both in 51 children with familial high-risk for SZ (FHR-SZ), 41 children with familial high-risk for BP (FHR-BP), and 39 population-based children (PBC) at a mean age of 12.10. Results: MMN amplitude evoked by a duration deviant was larger in children with FHR-BP compared to PBC and FHR-SZ. P3a amplitude in response to a duration ∗ frequency deviant was larger in children with FHR-BP compared to children with FHR-SZ, but not compared to PBC. MMN- and P3a-peak latency did not differ between groups. Conclusions: At an age of around 12 years, children with FHR-BP display enhanced neural sensitivity to change detection of duration deviants, while FHR-SZ showed a normal response pattern. Longitudinal recordings in high-risk children during adolescence are required to elucidate the temporal trajectories of MMN and P3a responses and how they relate to the emergence of first clinical symptoms in SZ and BP.

KW - Electroencephalography

KW - Mismatch negativity

KW - Neurodevelopment

KW - Offspring

U2 - 10.1016/j.schres.2022.06.035

DO - 10.1016/j.schres.2022.06.035

M3 - Journal article

C2 - 35797883

AN - SCOPUS:85134611314

VL - 246

SP - 187

EP - 194

JO - Schizophrenia Research

JF - Schizophrenia Research

SN - 0920-9964

ER -

ID: 329291630