Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-26T07:38:32.017Z Has data issue: false hasContentIssue false

Paracingulate sulcus morphology in men with early-onset schizophrenia

Published online by Cambridge University Press:  02 January 2018

Jean-Bernard Le Provost
Affiliation:
Frédéric Joliot Hospital Department, Orsay
David Bartrés-Faz
Affiliation:
Frédéric Joliot Hospital Department, Orsay
Marie-Laure Paillère-Martinot*
Affiliation:
Frédéric Joliot Hospital Department, Orsay
Eric Artiges
Affiliation:
Frédéric Joliot Hospital Department, Orsay
Sabina Pappata
Affiliation:
Frédéric Joliot Hospital Department, Orsay
Christophe Recasens
Affiliation:
Albert Chenevier Hospital, Créteil, France
Mercedes Pérez-Gómez
Affiliation:
Department of Psychiatry and Psychobiology, University of Barcelona
Miquel Bernardo
Affiliation:
Hospital Clinic i Provincial de Barcelona, Spain
Imma Baeza
Affiliation:
Hospital Clinic i Provincial de Barcelona, Spain
Frank Bayle
Affiliation:
Sainte-Anne Hospital, Paris
Jean-Luc Martinot
Affiliation:
Frédéric Joliot Hospital Deparment, Orsay, France
*
Jean-Luc Martinot, ERM 0205 Imagerie Cérébrale en Psychiatrie, INSERM-CEA, Service Hospitalier Frédéric Joliot, 4 Place du Général Leclerc, 91401 ORSAY Cedex, France. Tel: 1698 67719; fax: 1698 67816; e-mail: martinot@shfj.cea.fr
Rights & Permissions [Opens in a new window]

Abstract

Background

Cingulate dysfunction has been reported in schizophrenia. Although the paracingulate sulcus (PCS) is known to be asymmetric in healthy people, little information is available about its morphology in schizophrenia.

Aims

To search for morphological anomalies of the PCS in men with early-onset schizophrenia.

Method

The PCS was examined in magnetic resonance images of the brains of men with schizophrenia and 100 healthy men.

Results

A significant asymmetry was found in the brains of healthy volunteers, whose sulci were more frequent and more marked in the left hemisphere. In contrast, the sulcus was as frequent in the right as in the left hemisphere in the patient group. Moreover, patients displayed significantly more rightward asymmetry, and overall less-asymmetrical patterns than the comparison group.

Conculsions

Since the PCS has developed at 36 weeks of gestation, these findings suggest an impaired maturation of the cingulate region during the third trimester.

Type
Papers
Copyright
Copyright © Royal College of Psychiatrists, 2003 

Reversals, reductions or absence of normal cerebral asymmetries have been described in schizophrenia in several structures such as the planum temporale (Reference Rossi, Stratta and MatteiRossi et al, 1992; Reference Barta, Pearlson and BrillBarta et al, 1997), the Sylvian fissure (Reference Crow, Brown and BurtonCrow et al, 1992; Reference Falkaï, Bogerts and GreveFalkaï et al, 1995), both occipital and frontal lobes (Reference Bilder, Houwei and BogertsBilder et al, 1994), and the cerebral ventricles (Reference Crow, Ball and BloomCrow et al, 1989a ). Moreover, people with early-onset schizophrenia might be more likely to exhibit reduced brain asymmetries (Reference Crow, Colter and FrithCrow et al, 1989b ). Cerebral sulcal and gyral patterns and their asymmetries may provide a robust marker of the contribution of neurodevelopmental factors to the aetiology of schizophrenia. Indeed, cerebral sulci are formed during the second and third trimesters (Reference Chi, Dooling and GillesChi et al, 1977; Reference HuangHuang, 1991) and remain relatively stable after birth (Reference Armstrong, Schleicher and OmranArmstrong et al, 1995; Reference Magnotta, Andreasen and SchultMagnotta et al, 1999), whereas other brain measurements such as cerebral volumes can vary with ageing, life experiences, nutrition (Reference Dalman and CullbergDalman & Cullberg, 1999), substance misuse (Reference Pfefferbaum, Sullivan and MathalonPfefferbaum et al, 1997; Reference Wilson, Mathew and TurkingtonWilson et al, 2000) and even neuroleptic medication (Reference Chakos, Lieberman and BilderChakos et al, 1994). Yücel et al (Reference Yücel, Stuart and Maruff2002a ) reported a lack of leftward paracingulate sulcus asymmetry among right-handed men with schizophrenia compared with a control group. Since these findings are relevant to the study of the neurobiological aspects of schizophrenia, they need replication in independent samples. Our hypothesis was that the asymmetric patterns of the paracingulate sulcus observed in healthy individuals would be disrupted in men with early-onset schizophrenia. Such abnormalities could provide evidence of abnormal neurodevelopment of paralimbic areas in schizophrenia.

METHOD

Study participants

The study included 40 right-handed male patients (mean age 27.2 years, s.d=6.6) fulfilling DSM-IV criteria for schizophrenia (American Psychiatric Association, 1994), with clinical onset before age 25 years (Reference Crow, Colter and FrithCrow et al, 1989b ; Reference Corrigal and MurrayCorrigal & Murray, 1994). Patients were recruited from the psychiatric departments of several hospitals in the Paris area of France, and from Barcelona in Spain. Clinical ratings and review of research and medical records were performed by senior psychiatrists (M.B., I.B., M.-L.P.-M., C.R. and J.-L.M.). Clinical symptoms were assessed by means of the Scale for the Assessment of Positive Symptoms (SAPS; Reference AndreasenAndreasen, 1984) (mean score 27.5, s.d.=17.6) and the Scale for the Assessment of Negative Symptoms (SANS; Reference AndreasenAndreasen, 1982) (mean score 53, s.d.=25.6). The comparison group included 100 right-handed healthy male volunteers (mean age 28.5 years, s.d.=7.7), with no family history of psychiatric disorders. All participants were examined to exclude medical conditions, including substance misuse, and all were found to be right handed according to Annett's questionnaire (Reference AnnettAnnett, 1970).

Magnetic resonance imaging

Whole-brain T 1-weighted images were acquired using a 1.5 T magnetic resonance imaging (MRI) scanner. A three-dimensional inversion-recovery-prepared fast-spoiled gradient echo sequence was used with the following scanning parameters: 256 × 256 matrix, 124 or 248 contiguous slices of 1.5-mm or 0.6-mm thickness, field of view 24 cm × 24 cm, flip angle 10°, echo time 2.2 ms, T 1 600 ms, repetition time 12.5 ms. Everyone who was scanned first gave written informed consent, according to the local ethics committee requirements.

Paracingulate sulcus rating

The paracingulate sulcus extends dorsally and parallel to the cingulate sulcus, lying in the medial walls of the frontal lobes. Measurements were made using the method of describing paracingulate sulcus patterns defined by Yücel et al (Reference Yücel, Stuart and Maruff2001) in healthy adults. The origin of the paracingulate sulcus was defined as the point where the sulcus extends posteriorly, from a coronal plane parallel to the line through the anterior commissure, and perpendicular to the line through the anterior and posterior commissures (Reference Yücel, Stuart and MaruffYücel et al, 2001). The paracingulate sulcus was classified as ‘prominent’ if the sulcus extended at least 40 mm and exhibited no more than 20 mm of interruptions between its origin and a coronal plane passing through the anterior commissure (Fig. 1c ). If interruptions exceeded 20 mm and the length was at least 20 mm, the paracingulate sulcus was classified as ‘present’ (Fig. 1b ). Finally, when no clearly horizontal sulcus parallel to the cingulate sulcus could be found or was less than 20 mm in length, it was classified as ‘absent’ (Fig. 1a ). Leftward asymmetry was defined as a ‘prominent’ pattern in the left hemisphere with a ‘present’ or ‘absent’ pattern in the right hemisphere, or as ‘present’ left and ‘absent’ right patterns. Conversely, rightward asymmetry was defined as a right ‘prominent’ pattern occurring with a left ‘present’ or ‘absent’ pattern, or as a right ‘present’ pattern and a left ‘absent’ pattern. Symmetry of the paracingulate sulcus was rated when the same pattern was observed in both hemispheres. Two independent raters, masked to participant status, examined the images. Intrarater reliability was assessed by one examiner (J.-B.L.P.), who examined all cases (κ=0.92). Interrater reliability was assessed by using a second rater (D.B.-F.) to evaluate 70 randomly chosen participants (κ=0.90).

Fig. 1 Magnetic resonance images of the cingulate sulcus (black arrow) and paracingulate sulcus (white arrow): T 1-weighted sagittal views showing the distinct paracingulate sulcus patterns evaluated in this study; (a) absent, (b) present, (c) prominent.

Intragroup asymmetry was assessed using McNemar's test for symmetry. Hemispheric differences for paracingulate sulcus presence were assessed within each group using χ2 tests. Afterwards, between-group differences for rightward/leftward asymmetry rates were also assessed using χ2. Statistical significance was set at P=0.05. Correlations between clinical scores and paracingulate sulcus patterns were searched for in the patient group, using the Spearman rank order statistic.

RESULTS

Within-group comparisons

Healthy volunteers had a significant paracingulate sulcus asymmetry (McNemar's test χ2=31.47, P<0.00001, d.f.=3). The presence of a paracingulate sulcus (‘prominent’ or ‘present’) was more frequent in the left hemisphere than in the right (χ2=30.5, P<0.001) and it was more often defined as ‘prominent’ than ‘present’ in the left hemisphere (χ2=6.7, P=0.009). In participants with schizophrenia however, no significant asymmetry was detected (McNemar's test χ2=2.33, P=0.51, d.f.=3). The frequency of a paracingulate sulcus (‘prominent’ or ‘present’) did not differ between left and right hemispheres (χ2=0.05, P=0.82). When a ‘prominent’ paracingulate sulcus was found, it was equally frequent on both sides (χ2=1.13, P=0.29).

Between-group comparisons

Paracingulate sulcus patterns (Table 1) were more often leftwardly asymmetric in healthy participants than in patients (χ2=7.48, P=0.006). In contrast, patients had more rightward asymmetric patterns (χ2=4.84, P=0.03). The incidence rates of a symmetrical pattern were similar in both groups (χ2=1.12, P=0.29).

Table 1 Hemispheric distribution of the morphological patterns of the paracingulate sulcus in healthy men and men with schizophrenia. Values are percentages of cases presenting distinct patterns of paracingulate sulcus morphology in both left and right hemispheres

Clinical correlates

The presence or absence of paracingulate sulcus, either in the right or left hemisphere, was not related to any clinical measure (SANS and SAPS scores). Spearman correlation tests were applied to search for relationships between asymmetry or symmetry of the paracingulate sulcus (leftward, rightward or symmetrical) and clinical measures. No significant correlation was observed.

DISCUSSION

The main finding of this study was a lack of paracingulate sulcus asymmetry among male patients with early-onset schizophrenia; this was due to both the less-frequent leftward asymmetry and the more-frequent rightward asymmetry of paracingulate sulcus patterns than in healthy participants.

Patient characteristics

The characteristics of our patient sample (all men, with disease onset before 25 years of age) may have influenced the findings. These patients were chosen because previous studies have reported more-frequent brain anomalies in early-onset cases (Reference Crow, Colter and FrithCrow et al, 1989b ) and an interaction between diagnosis and gender on frontal lobe measurements in patients with schizophrenia (Reference Highley, Esiri and McDonaldHighley et al, 1998). Moreover, previous investigations conducted in normal individuals have found gender differences in paracingulate sulcus patterns, as well as in intrasulcal paracingulate sulcus grey matter volumes (Reference Paus, Tomaiuolo and OtakyPaus et al, 1996a ; Reference Yücel, Stuart and MaruffYücel et al, 2001). Therefore, it is possible that different findings would be observed in older or female patients. Thus, it should be stated that our results pertain to a homogeneous category of patients (right-handed, male, with early-onset disease) and may not be generalisable to other types of patient with schizophrenia.

Consistent replication

The finding of an asymmetric pattern of the paracingulate sulcus in healthy individuals is consistent with previous anatomical MRI reports (Paus et al, Reference Paus, Tomaiuolo and Otaky1996a , Reference Paus, Otaky and Caramanos b ; Reference Yücel, Stuart and MaruffYücel et al, 2001). Furthermore, our results replicate those reported by Yücel et al (Reference Yücel, Stuart and Maruff2002a ) and extend to an independent sample of earlyonset cases, indicating that the reduction of leftward paracingulate sulcus asymmetry might be a robust finding. They are also complementary to reports of grey matter volume reductions in the cingulate, suggesting an involvement of the cingulate and paracingulate region in the pathophysiology of schizophrenic disorders (Reference Albanese, Merlo and MascittiAlbanese et al, 1995; Reference Wright, Ellison and SharmaWright et al, 1999; Reference Paillère-Martinot, Caclin and ArtigesPaillère-Martinot et al, 2001; Reference Sigmundsson, Suckling and MaierSigmundsson et al, 2001). Further evidence implicating these limbic or paralimbic regions in schizophrenia comes from functional findings demonstrating abnormal brain activity in these regions in response to cognitive demands (e.g. Reference Carter, Mintun and NicholsCarter et al, 1997; Reference Artiges, Martinot and VerdysArtiges et al, 2000) and from a report showing that brain activity patterns during a cognitive task depend on the underlying morphology of the paracingulate sulcus (Reference Yücel, Pantelis and StuartYücel et al, 2002b ).

Folding and connectivity

Functional neuroimaging studies indicate that schizophrenia is characterised by an alteration of brain connectivity (e.g. Reference Fletcher, McKenna and FristonFletcher et al, 1999; Reference Spence, Grasby and LiddleSpence et al, 2000). Notably, it has been suggested that gyral-shape studies might be an interesting alternative method of searching for disturbances of brain connectivity in the disorder (Reference Highley, Walker and EsiriHighley et al, 2001). Indeed, brain gyrification indexes in humans would reflect the density of intrinsic connectivity (Reference Welker, Jones and PetersWelker, 1990). A proposed mechanism derived from the tension-based morphogenesis theory explains cortical folding as depending on differences in mechanical tension along axons, dendrites or glial processes connecting different brain regions (Reference van Essenvan Essen, 1997). Thus, the presence of a prominent paracingulate sulcus could indicate a marked local connectivity within the paralimbic cortex (Brodmann's area 32) and adjacent regions (Brodmann's areas 6, 8 and 9). In contrast, the reduction in paracingulate sulcus folding, more frequently observed in the left hemisphere in our patients, could be the consequence of weaker local connectivity in these areas. According to this model, people with sulcogyral anomalies would be more likely to exhibit dysfunctional cingulate or paracingulate connectivity.

Folding during the third trimester

It has been historically proposed that losses, absences or reversals of hemispheric asymmetries could denote indexes of brain dysmaturation (Reference Crichton-BrowneCrichton-Browne, 1879) in mental disturbances (Reference SouthardSouthard, 1915). A corpus of theories postulate that the absence of right shift (Reference AnnettAnnett, 1999) or the loss of the physiological asymmetry in the ontogenetically recent heteromodal cortices (Reference Pearlson, Petty and RossPearlson et al, 1996; Reference CrowCrow, 1999) might result from genetic factors that would enhance the vulnerability to schizophrenia. An anomaly in the paracingulate sulcus pattern in patients supports these theories. Indeed, the paracingulate sulcus develops by 36 weeks of gestation, when major cerebral asymmetry has already been established. Thus, as a tertiary sulcus, it depends on the pattern of regional gyrification previously established by primary and secondary sulci (Reference Armstrong, Schleicher and OmranArmstrong et al, 1995). Consequently, evidence of altered paracingulate development in people with schizophrenia may reflect abnormalities in the course of neurodevelopment occurring, at the earliest, during week 32 of gestation, when secondary sulci are forming — i.e. during the third trimester. Folding peculiarities in this paralimbic region during the third trimester do not preclude more wide-spread and earlier anomalies in folding symmetry, which remain to be investigated (Vogeley et al, Reference Vogeley, Scheider-Axmann and Pfeiffer2000, Reference Vogeley, Tepest and Pfeiffer2001). Consequently, sulcogyral measurements can be used to explore hypotheses (e.g. Reference Crow, Ball and BloomCrow et al, 1989a ; Reference Bilder, Houwei and BogertsBilder et al, 1994) that disturbances in brain development during the second and third trimesters are related to vulnerability to schizophrenic disorders.

Clinical Implications and Limitations

CLINICAL IMPLICATIONS

  1. Abnormal maturation of the paralimbic area may occur during the third trimester of gestation.

  2. The study provides further evidence of abnormal development of the cerebral hemispheres in schizophrenia.

  3. Reduced cerebral asymmetry could be a vulnerability factor for schizophrenia.

LIMITATIONS

  1. The investigation was restricted to male patients with early-onset disease.

  2. Continuous measures of the sulcus length were not available, and there was no interrater assessment of schizophrenia symptom rating scales.

  3. The findings cannot address the issue of anatomic specificity of the paracingulate sulcus since the characteristics of other sulci were not assessed.

Acknowledgement

The authors thank M. C. Bourdel for thoughtful statistical comments.

Footnotes

Declaration of interest

The Fondation pour la Recherche Médicale supported J.-B.L.P.; D.B.-F. was supported by a post-doctoral grant from the Spanish Ministry of Education and Culture (MEC/Fulbright) and by an INSERM research fellowship.

References

Albanese, A. M., Merlo, A. B., Mascitti, T. A., et al (1995) Inversion of the hemispheric laterality of the anterior cingulate gyrus in schizophrenics. Biological Psychiatry, 38, 1321.CrossRefGoogle ScholarPubMed
American Psychiatric Association (1994) Diagnostic and Statistical Manual of Mental Disorders (4th edn) (DSM–IV). Washington, DC: APA.Google Scholar
Andreasen, N. C. (1982) The Scale for the Assessment of Negative Symptoms (SANS). Iowa, IA: University of Iowa.Google Scholar
Andreasen, N. C. (1984) The Scale for the Assessment of Positive Symptoms (SAPS). Iowa, IA: University of Iowa.Google Scholar
Annett, M. (1970) A classification of hand preference by association analysis. British Journal of Psychology, 61, 303321.CrossRefGoogle ScholarPubMed
Annett, M. (1999) The theory of an agnosic right shift gene in schizophrenia and autism. Schizophrenia Research, 19, 177182.CrossRefGoogle Scholar
Armstrong, E., Schleicher, A., Omran, H., et al (1995) The ontogeny of human gyrification. Cerebral Cortex, 1, 5663.CrossRefGoogle Scholar
Artiges, E., Martinot, J. L., Verdys, M., et al (2000) Altered hemispheric functional dominance during word generation in negative schizophrenia. Schizophrenia Bulletin, 26, 709721.CrossRefGoogle ScholarPubMed
Barta, P. E., Pearlson, G. D., Brill, L. B. I., et al (1997) Planum temporale asymmetry reversal in schizophrenia: replication and relationship to grey matter abnormalities. American Journal of Psychiatry, 154, 661667.Google Scholar
Bilder, R. M., Houwei, W., Bogerts, B., et al (1994) Absence of regional hemispheric asymmetry in first episode schizophrenia. American Journal of Psychiatry, 151, 14371447.Google ScholarPubMed
Carter, C. S., Mintun, M., Nichols, T., et al (1997) Anterior cingulate gyrus dysfunction and selective attention deficits in schizophrenia: an [15O] H2O PET study during single trial stroop task performance. American Journal of Psychiatry, 154, 16701675.CrossRefGoogle ScholarPubMed
Chakos, J. A., Lieberman, R. M., Bilder, M., et al (1994) Increase in caudate nuclei volumes of first-episode schizophrenic patients taking antipsychotic drugs. American Journal of Psychiatry, 151, 14301436.Google ScholarPubMed
Chi, J. G., Dooling, E. C. & Gilles, F. H. (1977) Gyral development of the human brain. Annals of Neurology, 1, 8693.CrossRefGoogle ScholarPubMed
Corrigal, R. J. & Murray, R. M. (1994) Twin concordance for congenital a d adult-onset psychoses: a preliminary study of the validity of a novel classification of schizophrenia. Acta Psychiatrica Scandinavica, 89, 142145.CrossRefGoogle Scholar
Crichton-Browne, J. (1879) On the weight of the brain and its component parts in the insane. Brain, 2, 4267.CrossRefGoogle Scholar
Crow, T. J. (1999) Commentary on Annett, Yeo et al, Klar, Saugstad and Orr: cerebral asymmetry, language and psychosis – the case for a Homo sapiens-specific sex-linked gene for brain growth. Schizophrenia Research, 39, 219231.CrossRefGoogle Scholar
Crow, T. J., Ball, J., Bloom, S. R., et al (1989a) Schizophrenia as an anomaly of development of cerebral asymmetry. A postmortem study and a proposal concerning the genetic basis of the disease. Archives of General Psychiatry, 46, 11451150.CrossRefGoogle Scholar
Crow, T. J., Colter, N., Frith, C. D., et al (1989b) Developmental arrest of cerebral asymmetry in early onset schizophrenia. Psychiatry Research, 29, 247253.CrossRefGoogle ScholarPubMed
Crow, T. J., Brown, R., Burton, C. J., et al (1992) Loss of Sylvian asymmetry in schizophrenia: findings in the Runwell 2 series of brains. Schizophrenia Research, 6, 152153.CrossRefGoogle Scholar
Dalman, C. & Cullberg, J. (1999) Neonatal hyperbilirubinaemia – a vulnerability factor for mental disorder? Acta Psychiatrica Scandinavica, 100, 469471.CrossRefGoogle ScholarPubMed
Falkaï, P., Bogerts, B., Greve, B., et al (1995) Loss of Sylvian fissure asymmetry in schizophrenia. A quantitative post-mortem study. Schizophrenia Research, 7, 2332.CrossRefGoogle Scholar
Fletcher, P., McKenna, P. J., Friston, K. J., et al (1999) Abnormal cingulate modulation of fronto-temporal connectivity in schizophrenia. Neuroimage, 9, 337342.CrossRefGoogle ScholarPubMed
Highley, J. R., Esiri, M. M., McDonald, B., et al (1998) Anomalies of cerebral asymmetry in schizophrenia interact with gender and age of onset: a post-mortem study. Schizophrenia Research, 34, 1325.CrossRefGoogle ScholarPubMed
Highley, J. R., Walker, M. A., Esiri, M. M., et al (2001) Schizophrenia and the frontal lobes: post-mortem stereological study of tissue volume. British Journal of Psychiatry, 178, 337343.CrossRefGoogle ScholarPubMed
Huang, C. C. (1991) Sonographic cerebral sulcal development in premature newborns. Brain and Development, 13, 2731.CrossRefGoogle ScholarPubMed
Magnotta, V. A., Andreasen, N. C., Schult, S. K., et al (1999) Quantitative in vivo measurement of gyrification in the human brain: changes associated with aging. Cerebral Cortex, 19, 151160.CrossRefGoogle Scholar
Paillère-Martinot, M. L., Caclin, A., Artiges, E., et al (2001) Cerebral gray matter reductions and clinical correlates in patients with early onset schizophrenia. Schizophrenia Research, 50, 1926.CrossRefGoogle ScholarPubMed
Paus, T., Tomaiuolo, F., Otaky, N., et al (1996a) Human cingulate and paracingulate sulci: pattern, variability, asymmetry and probabilistic map. Cerebral Cortex, 6, 207214.CrossRefGoogle ScholarPubMed
Paus, T., Otaky, N., Caramanos, Z., et al (1996b) In vivo morphometry of the intrasulcal gray matter in the human cingulate, paracingulate, and superior-rostral sulci: hemispheric asymmetries, gender differences and probability maps. Journal of Comparative Neurology, 376, 664673.3.0.CO;2-M>CrossRefGoogle ScholarPubMed
Pearlson, G. D., Petty, R. G., Ross, C. A., et al (1996) Schizophrenia: a disease of heteromodal association cortex? Neuropsychopharmacology, 14, 117.CrossRefGoogle ScholarPubMed
Pfefferbaum, A., Sullivan, E. V., Mathalon, D. H., et al (1997) Frontal lobe volume loss observed with magnetic resonance imaging in older chronic alcoholics. Alcoholism, Clinical and Experimental Research, 21, 521529.CrossRefGoogle ScholarPubMed
Rossi, A., Stratta, P., Mattei, P., et al (1992) Planum temporale in schizophrenia: a magnetic resonance study. Schizophrenia Research, 7, 1922.CrossRefGoogle ScholarPubMed
Sigmundsson, T., Suckling, J., Maier, M., et al (2001) Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms. American Journal of Psychiatry, 158, 234243.CrossRefGoogle ScholarPubMed
Southard, E. E. (1915) On the topographical distribution of cortex lesions and anomalies in dementia praecox, with some account of their functional significance. American Journal of Insanity, 71, 603671.Google Scholar
Spence, S. A., Grasby, P. M., Liddle, P. F., et al (2000) Functional anatomy of verbal fluency in people with schizophrenia and those at genetic risk. Focal dysfunction and distributed disconnectivity reappraised. British Journal of Psychiatry, 176, 5260.CrossRefGoogle ScholarPubMed
van Essen, D. C. (1997) A tension-based theory of morphogenesis and compact wiring in the central nervous system. Nature, 385, 313318.CrossRefGoogle ScholarPubMed
Vogeley, K. V., Scheider-Axmann, T., Pfeiffer, U., et al (2000) Disturbed gyrification of the prefrontal region in male schizophrenic patients: a morphometric postmortem study. American Journal of Psychiatry, 57, 3439.CrossRefGoogle Scholar
Vogeley, K. V., Tepest, R., Pfeiffer, U., et al (2001) Right frontal hypergyria differentiation in affected and unaffected siblings from families multiply affected with schizophrenia: a morphometric MRI study. American Journal of Psychiatry, 158, 494496.CrossRefGoogle ScholarPubMed
Welker, W. (1990) Why does cerebral cortex fissure and fold? A review of determinants of gyn and sulci. In Cerebral Cortex, vol. 8b: Comparative Structure and Evolution of Cerebral Cortex. Part 2 (eds Jones, E. G. & Peters, A.), pp. 3136. New York: Plenum Press.CrossRefGoogle Scholar
Wilson, W., Mathew, R., Turkington, T., et al (2000) Brain morphological changes and early marijuana use: a magnetic resonance and positron emission tomography study. Journal of Addictive Disorders, 19, 122.CrossRefGoogle ScholarPubMed
Wright, I. C., Ellison, Z. R., Sharma, T., et al (1999) Mapping of grey matter changes in schizophrenia. Schizophrenia Research, 35, 114.CrossRefGoogle ScholarPubMed
Yücel, M., Stuart, G. W., Maruff, P., et al (2001) Hemispheric and gender-related differences in gross morphology of the anterior cingulate/paracingulate cortex in normal volunteers: an IRM morphometric study. Cerebral Cortex, 11, 1725.CrossRefGoogle Scholar
Yücel, M., Stuart, G. W., Maruff, P., et al (2002a) Paracingulate morphologic differences in males with established schizophrenia: a magnetic resonance imaging morphometric study. Biological Psychiatry, 52, 1523.CrossRefGoogle ScholarPubMed
Yücel, M., Pantelis, C., Stuart, G. W., et al (2002b) Anterior cingulate activation during Stroop task performance: a PET to MRI coregistration study of individual patients with schizophrenia. American Journal of Psychiatry, 159, 251254.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1 Magnetic resonance images of the cingulate sulcus (black arrow) and paracingulate sulcus (white arrow): T1-weighted sagittal views showing the distinct paracingulate sulcus patterns evaluated in this study; (a) absent, (b) present, (c) prominent.

Figure 1

Table 1 Hemispheric distribution of the morphological patterns of the paracingulate sulcus in healthy men and men with schizophrenia. Values are percentages of cases presenting distinct patterns of paracingulate sulcus morphology in both left and right hemispheres

Submit a response

eLetters

No eLetters have been published for this article.