Hippocampal subdivision and amygdalar volumes in patients in an at-risk mental state for schizophrenia
BACKGROUND: Accumulating evidence from postmortem and magnetic resonance imaging (MRI) studies suggests that abnormalities of medial temporal lobe structures are critically involved in the pathogenesis of schizophrenia. It is still unclear, however, whether certain abnormalities are already present in individuals at ultra high-risk (UHR) for transition into psychosis. Recent studies involving patients at UHR showed contradictory results for hippocampal volume, and only 1 study reported that amygdalar volume was unchanged between healthy patients and those at UHR. Furthermore, no subregions of the hippocampus have been investigated in people at UHR.
METHODS: We recruited 29 UHR patients, 23 first-episode patients and 29 age- and sex-matched healthy controls. We measured hippocampal and amygdalar volumes from MRI scans by use of BRAINS2 to manually trace the regions of interest. The hippocampi were divided in 2 regions: head and corpus/tail.
RESULTS: Patients at UHR had significantly smaller volumes of the hippocampus corpus and tail bilaterally, but not of the head, compared with healthy controls. Group differences for the right hippocampus corpus and tail volume remained significant after we controlled for whole brain volume and other covariates. We found that UHR patients who later developed psychosis had smaller right hippocampus corpus and tail volumes than did those who did not develop psychosis. First-episode patients had significantly smaller left amygdalar volumes than did healthy individuals or those at UHR.
LIMITATIONS: Our study had a small sample size, and we were unable to control for the effects of medication.
CONCLUSION: Our findings suggest that parts of the hippocampal-amygdalar complex are involved in the pathogenesis of schizophrenia. Reduction of hippocampus corpus and tail volumes may be indicative of the prodromal phase of schizophrenia and represent risk factors for transition into psychosis. Further investigations are needed to determine whether structural changes of the left amygdala play a role during transition from the prodromal phase to the first manifest episode of schizophrenia.
| Errataetall: |
CommentIn: J Psychiatry Neurosci. 2010 May;35(3):214-5; author reply 215. - PMID 20420772 |
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| Medienart: |
E-Artikel |
| Erscheinungsjahr: |
2010 |
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| Erschienen: |
2010 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:35 |
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| Enthalten in: |
Journal of psychiatry & neuroscience : JPN - 35(2010), 1 vom: 30. Jan., Seite 33-40 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Witthaus, Henning [VerfasserIn] |
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| Themen: |
Antipsychotic Agents |
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| Anmerkungen: |
Date Completed 01.03.2010 Date Revised 20.10.2021 published: Print CommentIn: J Psychiatry Neurosci. 2010 May;35(3):214-5; author reply 215. - PMID 20420772 Citation Status MEDLINE |
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| Förderinstitution / Projekttitel: |
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NLM194036596 |
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| 100 | 1 | |a Witthaus, Henning |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Hippocampal subdivision and amygdalar volumes in patients in an at-risk mental state for schizophrenia |
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| 500 | |a CommentIn: J Psychiatry Neurosci. 2010 May;35(3):214-5; author reply 215. - PMID 20420772 | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a BACKGROUND: Accumulating evidence from postmortem and magnetic resonance imaging (MRI) studies suggests that abnormalities of medial temporal lobe structures are critically involved in the pathogenesis of schizophrenia. It is still unclear, however, whether certain abnormalities are already present in individuals at ultra high-risk (UHR) for transition into psychosis. Recent studies involving patients at UHR showed contradictory results for hippocampal volume, and only 1 study reported that amygdalar volume was unchanged between healthy patients and those at UHR. Furthermore, no subregions of the hippocampus have been investigated in people at UHR | ||
| 520 | |a METHODS: We recruited 29 UHR patients, 23 first-episode patients and 29 age- and sex-matched healthy controls. We measured hippocampal and amygdalar volumes from MRI scans by use of BRAINS2 to manually trace the regions of interest. The hippocampi were divided in 2 regions: head and corpus/tail | ||
| 520 | |a RESULTS: Patients at UHR had significantly smaller volumes of the hippocampus corpus and tail bilaterally, but not of the head, compared with healthy controls. Group differences for the right hippocampus corpus and tail volume remained significant after we controlled for whole brain volume and other covariates. We found that UHR patients who later developed psychosis had smaller right hippocampus corpus and tail volumes than did those who did not develop psychosis. First-episode patients had significantly smaller left amygdalar volumes than did healthy individuals or those at UHR | ||
| 520 | |a LIMITATIONS: Our study had a small sample size, and we were unable to control for the effects of medication | ||
| 520 | |a CONCLUSION: Our findings suggest that parts of the hippocampal-amygdalar complex are involved in the pathogenesis of schizophrenia. Reduction of hippocampus corpus and tail volumes may be indicative of the prodromal phase of schizophrenia and represent risk factors for transition into psychosis. Further investigations are needed to determine whether structural changes of the left amygdala play a role during transition from the prodromal phase to the first manifest episode of schizophrenia | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 7 | |a Antipsychotic Agents |2 NLM | |
| 700 | 1 | |a Mendes, Ute |e verfasserin |4 aut | |
| 700 | 1 | |a Brüne, Martin |e verfasserin |4 aut | |
| 700 | 1 | |a Ozgürdal, Seza |e verfasserin |4 aut | |
| 700 | 1 | |a Bohner, Georg |e verfasserin |4 aut | |
| 700 | 1 | |a Gudlowski, Yehonala |e verfasserin |4 aut | |
| 700 | 1 | |a Kalus, Peter |e verfasserin |4 aut | |
| 700 | 1 | |a Andreasen, Nancy |e verfasserin |4 aut | |
| 700 | 1 | |a Heinz, Andreas |e verfasserin |4 aut | |
| 700 | 1 | |a Klingebiel, Randolf |e verfasserin |4 aut | |
| 700 | 1 | |a Juckel, Georg |e verfasserin |4 aut | |
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