» Articles » PMID: 20040244

Hippocampal Subdivision and Amygdalar Volumes in Patients in an At-risk Mental State for Schizophrenia

Overview
Specialty Psychiatry
Date 2009 Dec 31
PMID 20040244
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Altered Volumes of the Amygdala and Hippocampus in the Brain of Suicidal Patients with First Episode Schizophrenia.

Sen M, Karamustafalioglu N, Celikkiran P, Ansen G, Sakul B, Namli M Psychiatr Q. 2025; .

PMID: 40000589 DOI: 10.1007/s11126-025-10124-y.


Multipronged investigation of morphometry and connectivity of hippocampal network in relation to risk for psychosis using ultrahigh field MRI.

Prasad K, Muldoon B, Theis N, Iyengar S, Keshavan M Schizophr Res. 2023; 256:88-97.

PMID: 37196534 PMC: 10363272. DOI: 10.1016/j.schres.2023.05.002.


Elucidating gut microbiota-hippocampus interactions in emerging psychosis: A new perspective for the development of early interventions for memory impairments.

Iseli G, Ulrich S, Schmidt A Front Psychiatry. 2023; 14:1098019.

PMID: 37032923 PMC: 10076719. DOI: 10.3389/fpsyt.2023.1098019.


Childhood Trauma, the HPA Axis and Psychiatric Illnesses: A Targeted Literature Synthesis.

Murphy F, Nasa A, Cullinane D, Raajakesary K, Gazzaz A, Sooknarine V Front Psychiatry. 2022; 13:748372.

PMID: 35599780 PMC: 9120425. DOI: 10.3389/fpsyt.2022.748372.


Altered amygdala shape trajectories and emotion recognition in youth at familial high risk of schizophrenia who develop psychosis.

Guimond S, Mothi S, Makowski C, Chakravarty M, Keshavan M Transl Psychiatry. 2022; 12(1):202.

PMID: 35562339 PMC: 9106712. DOI: 10.1038/s41398-022-01957-3.


References
1.
Ongur D, Cullen T, Wolf D, Rohan M, Barreira P, Zalesak M . The neural basis of relational memory deficits in schizophrenia. Arch Gen Psychiatry. 2006; 63(4):356-65. DOI: 10.1001/archpsyc.63.4.356. View

2.
McGlashan T . Early detection and intervention in schizophrenia: research. Schizophr Bull. 1996; 22(2):327-45. DOI: 10.1093/schbul/22.2.327. View

3.
Pantelis C, Velakoulis D, McGorry P, Wood S, Suckling J, Phillips L . Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison. Lancet. 2003; 361(9354):281-8. DOI: 10.1016/S0140-6736(03)12323-9. View

4.
Bogerts B, Falkai P, Haupts M, Greve B, Ernst S, Heinzmann U . Post-mortem volume measurements of limbic system and basal ganglia structures in chronic schizophrenics. Initial results from a new brain collection. Schizophr Res. 1990; 3(5-6):295-301. DOI: 10.1016/0920-9964(90)90013-w. View

5.
McDonald C, Marshall N, Sham P, Bullmore E, Schulze K, Chapple B . Regional brain morphometry in patients with schizophrenia or bipolar disorder and their unaffected relatives. Am J Psychiatry. 2006; 163(3):478-87. DOI: 10.1176/appi.ajp.163.3.478. View