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Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry

Yıl 2017, Cilt: 34 Sayı: 2, 99 - 110, 08.09.2017

Öz





Temporal lobe dysfunction leads to a model of the cognitive impairments in

schizophrenia. The aim of this study was to evaluate changes in grey and white

matter volume, cortical area and cortical thickness of the temporal lobe in

schizophrenic patients and to explore the functional significance of these changes

through correlation with clinical symptoms of patients as measured with the

positive and negative syndrome scale. 88 control subjects and 57 chronic schizophrenics

were participated in the study. Structural magnetic resonance imaging

was performed and the DICOM images were evaluated using automatic brain

segmentation software (BrainSuite). The volume and volume fraction of the region

of interest were evaluated. The mean volume of temporal lobe was smaller

in the schizophrenics (154.20±16.49 cm3) than that of controls (174.85±17.70

cm3), (p≤0.05). Mean volumes of the temporal grey and temporal white matter

in schizophrenics (110.41±12.25 cm3 and 43.81±4.96 cm3) were smaller

than that of controls (124.14±13.15 cm3 and 50.71±6.29 cm3), (p≤0.05). The

mean cortical area pial in schizophrenics (425.8±40.95 cm2) was smaller than

that of control (462.30±44.42 cm2), (p≤0.05), while no differences found between

schizophrenics and controls related to the thickness of the temporal lobe

(p>0.05). The male patients tend to have positive correlation between the volumes

and the positive symptoms. The present study suggests that patients with

schizophrenia have a generalized temporal deficit. Surface area of the temporal

lobe was smaller in the schizophrenics both for males and females. However,

the cortex was proportionally thinner in the male schizophrenics. Positive correlations

were observed between the volume and positive symptoms more in the

male patients. Finally, there was no asymmetry in the volume of temporal lobe.

Kaynakça

  • Andreasen, N.C., Nopoulos, P., Magnotta, V., Pierson, R., Ziebell, S., Ho, B.C., 2011. Progressive brain change in schizophrenia: A prospective longitudinal study of first-episode schizophrenia. Biol. Psychiatry. 70, 672-679. doi: 10.1016/j.biopsych.2011.05.017. Andreone, N., Tansella, M., Cerini, R., Versace, A., Rambaldelli, G., Perlini, C., Dusi, N., Pelizza, L., Balestrieri, M., Barbui, C., Nose, M., Gasparini, A., Brambilla, P., 2007. Cortical white-matter microstructure in schizophrenia. Diffusion imaging study. Br. J. Psychiatry: The journal of mental science. 191, 113-119. Aso, M., Suzuki, M., Kawasaki, Y., Matsui, M., Hagino, H., Kurokawa, K., Seto, H., Kurachi, M., 2001. Sylvian fissure and medial temporal lobe structures in patients with schizophrenia: A magnetic resonance imaging study. Psychiatry Clin. Neurosci. 55, 49-56. Cao, X.Y., Li, Z., Metcalfe, H.M., Yang, T.X., Tan, S.P., Wang, Y., Hong, X.H., Li, Z.J., Yu, X., Cheung, E.F., Neumann, D.L., Shum, D.H., Chan, R.C., 2013. The nature and extent of working memory dysfunction in schizophrenia. Psych. J. 2, 175-182. doi: 10.1002/pchj.30. Chavarria-Siles, I., White, T., de Leeuw, C., Goudriaan, A., Lips, E., Ehrlich, S., Turner, J.A., Calhoun, V.D., Gollub, R.L., Magnotta, V.A., Ho, B.C., Smit, A.B., Verheijen, M.H., Posthuma, D., 2015. Myelination-related genes are associated with decreased white matter integrity in schizophrenia. Eur. J. Hum. Genet. 24, 381-386. doi: 10.1038/ejhg.2015.120. da Silva, T.L., Ravindran, A.V., 2015. Contribution of sex hormones to gender differences in schizophrenia: A review. Asian J. Psychiatr. 18, 2-14. doi: 10.1016/j.ajp.2015.07.016. DeLisi, L.E., 2001. Speech disorder in schizophrenia: Review of the literature and exploration of its relation to the uniquely human capacity for language. Schizophr. Bull. 27, 481-496. Dogdas, B., Shattuck, D.W., Leahy, R.M., 2005. Segmentation of skull and scalp in 3-D human MRI using mathematical morphology. Hum. Brain Mapp. 26, 273-285. Elfaki, A., Elfaki, A., Osman, T., Sahin, B., Elsheikh, A., Mohamed, A., Hamdoun, A., Mohammed, A., 2013. Stereological evaluation of brain magnetic resonance images of schizophrenic patients. Image Analysis and Stereology. 32, 145-153. Flynn, S.W., Lang, D.J., Mackay, A.L., Goghari, V., Vavasour, I.M., Whittall, K.P., Smith, G.N., Arango, V., Mann, J.J., Dwork, A.J., Falkai, P., Honer, W.G., 2003. Abnormalities of myelination in schizophrenia detected in vivo with MRI, and post-mortem with analysis of oligodendrocyte proteins. Mol. Psychiatry. 8, 811-820. Green, M.F., Olivier, B., Crawley, J.N., Penn, D.L., Silverstein, S., 2005. Social cognition in schizophrenia: Recommendations from the measurement and treatment research to improve cognition in schizophrenia new approaches conference. Schizophr Bull. 31, 882-887. Gutierrez-Galve, L., Wheeler-Kingshott, C.A., Altmann, D.R., Price, G., Chu, E.M., Leeson, V.C., Lobo, A., Barker, G.J., Barnes, T.R., Joyce, E.M., Ron, M.A., 2010. Changes in the frontotemporal cortex and cognitive correlates in first-episode psychosis. Biol. Psychiatry. 68, 51-60. doi: 10.1016/j.biopsych.2010.03.019. Harrison, P.J., 2004. The hippocampus in schizophrenia: A review of the neuropathological evidence and its pathophysiological implications. Psychopharmacology. 174, 151-162. Havermans, R., Honig, A., Vuurman, E.F., Krabbendam, L., Wilmink, J., Lamers, T., Verheecke, C.J., Jolles, J., Romme, M.A., van Praag, H.M., 1999. A controlled study of temporal lobe structure volumes and P300 responses in schizophrenic patients with persistent auditory hallucinations. Schizophr. Res. 38, 151-158. Hayashi, N., Igarashi, Y., Yamashina, M., Suda, K., 2002. Is there a gender difference in a factorial structure of the positive and negative syndrome scale? A test by structural equation modeling. Psychopathology. 35, 28-35. Highley, J.R., McDonald, B., Walker, M.A., Esiri, M.M., Crow, T.J., 1999. Schizophrenia and temporal lobe asymmetry. A postmortem stereological study of tissue volume. British journal of psychiatry : The journal of mental science. 175, 127-134. Hugdahl, K., Loberg, E.M., Nygard, M., 2009. Left temporal lobe structural and functional abnormality underlying auditory hallucinations in schizophrenia. Front. Neurosci. 3, 34-45. doi: 10.3389/neuro.01.001.2009. Joshi, A.A., Shattuck, D.W., Thompson, P.M., Leahy, R.M., 2007. Surface-constrained volumetric brain registration using harmonic Journal of Experimental and Clinical Medicine 34 (2017) 99-110 109 mappings. IEEE Trans. Med. Imaging. 26, 1657-1669. Jung, W.H., Jang, J.H., Byun, M.S., An, S.K., Kwon, J.S., 2010. Structural brain alterations in individuals at ultra-high risk for psychosis: A review of magnetic resonance imaging studies and future directions. J. Korean Med. Sci. 25, 1700-1709. doi: 10.3346/jkms.2010.25.12.1700. Kiernan, J.A., 2012. Anatomy of the temporal lobe. Epilepsy Res. Treat. 2012, 176157. doi: 10.1155/2012/176157. Luders, E., Gaser, C., Jancke, L., Schlaug, G., 2004. A voxel-based approach to gray matter asymmetries. Neuroimage. 22, 656- 664. Modinos, G., Costafreda, S.G., van Tol, M.J., McGuire, P.K., Aleman, A., Allen, P., 2013. Neuroanatomy of auditory verbal hallucinations in schizophrenia: A quantitative meta-analysis of voxel-based morphometry studies. Cortex. 49, 1046-1055. doi: 10.1016/j.cortex.2012.01.009. Montoya, A., Lepage, M., Malla, A., 2005. Temporal lobe dysfunction in patients with first-episode schizophrenia. Salud. Mental. 28, 33-39. Morey, R.A., Selgrade, E.S., Wagner, H.R., Huettel, S.A., Wang, L., McCarthy, G., 2010. Scan-rescan reliability of subcortical brain volumes derived from automated segmentation. Hum. Brain Mapp. 31, 1751-1762. doi: 10.1002/hbm.20973. Najjar, S., Pearlman, D.M., 2015. Neuroinflammation and white matter pathology in schizophrenia: Systematic review. Schizophr. Res. 161, 102-112. doi: 10.1016/j.schres.2014.04.041. Neckelmann, G., Specht, K., Lund, A., Ersland, L., Smievoll, A.I., Neckelmann, D., Hugdahl, K., 2006. Mr morphometry analysis of grey matter volume reduction in schizophrenia: Association with hallucinations. Int. J. Neurosci. 116, 9-23. Oertel-Knochel, V., Knochel, C., Rotarska-Jagiela, A., Reinke, B., Prvulovic, D., Haenschel, C., Hampel, H., Linden, D.E., 2013. Association between psychotic symptoms and cortical thickness reduction across the schizophrenia spectrum. Cereb. Cortex. 23, 61-70. doi: 10.1093/cercor/bhr380. Okugawa, G., Sedvall, G.C., Agartz, I., 2002. Reduced grey and white matter volumes in the temporal lobe of male patients with chronic schizophrenia. Eur. Arch. Psychiatry Clin. Neurosci. 252, 120-123. Pantelis, C., Velakoulis, D., McGorry, P.D., Wood, S.J., Suckling, J., Phillips, L.J., Yung, A.R., Bullmore, E.T., Brewer, W., Soulsby, B., Desmond, P., McGuire, P.K., 2003. Neuroanatomical abnormalities before and after onset of psychosis: A cross-sectional and longitudinal MRI comparison. Lancet. 361, 281-288. Rabinowicz, E.F., Silipo, G., Goldman, R., Javitt, D.C., 2000. Auditory sensory dysfunction in schizophrenia: imprecision or distractibility? Arch. Gen. Psychiatry. 57, 1149-1155. Riecher-Rossler, A., Hafner, H., 2000. Gender aspects in schizophrenia: Bridging the border between social and biological psychiatry. Acta. Psychiatr. Scand. Suppl. 58-62. Rimol, L.M., Hartberg, C.B., Nesvag, R., Fennema-Notestine, C., Hagler, D.J., Jr., Pung, C.J., Jennings, R.G., Haukvik, U.K., Lange, E., Nakstad, P.H., Melle, I., Andreassen, O.A., Dale, A.M., Agartz, I., 2010. Cortical thickness and subcortical volumes in schizophrenia and bipolar disorder. Biol. Psychiatry. 68, 41-50. doi: 10.1016/j.biopsych.2010.03.036. Rimol, L.M., Nesvag, R., Hagler, D.J., Jr., Bergmann, O., Fennema-Notestine, C., Hartberg, C.B., Haukvik, U.K., Lange, E., Pung, C.J., Server, A., Melle, I., Andreassen, O.A., Agartz, I., Dale, A.M., 2012. Cortical volume, surface area, and thickness in schizophrenia and bipolar disorder. Biol. Psychiatry. 71, 552-560. doi: 10.1016/j.biopsych.2011.11.026. Rossi, A., Stratta, P., D’Albenzio, L., Tartaro, A., Schiazza, G., di Michele, V., Bolino, F., Casacchia, M., 1990. Reduced temporal lobe areas in schizophrenia: Preliminary evidences from a controlled multiplanar magnetic resonance imaging study. Biol. Psychiatry. 27, 61-68. Sahin, B., Elfaki, A., 2012. Estimation of the volume and volume fraction of brain and brain structures on radiological images. Neuroquantology. 10, 87-97. Shattuck, D.W., Leahy, R.M., 2002. BrainSuite: An automated cortical surface identification tool. Med. Image Anal. 6, 129-142. Shenton, M.E., Dickey, C.C., Frumin, M., McCarley, R.W., 2001. A review of MRI findings in schizophrenia. Schizophr. Res. 49, 1-52. Sigmundsson, T., Suckling, J., Maier, M., Williams, S., Bullmore, E., Greenwood, K., Fukuda, R., Ron, M., Toone, B., 2001. Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms. Am. J. Psychiatry. 158, 234-243. Takahashi, T., Suzuki, M., Zhou, S.Y., Tanino, R., Nakamura, K., Kawasaki, Y., Seto, H., Kurachi, M., 2010. A follow-up MRI study of the superior temporal subregions in schizotypal disorder and first-episode schizophrenia. Schizophr. Res.. 119, 65-74. doi: 10.1016/j.schres.2009.12.006. Takao, H., Abe, O., Yamasue, H., Aoki, S., Kasai, K., Ohtomo, K., 2010. Cerebral asymmetry in patients with schizophrenia: A voxel-based morphometry (VBM) and diffusion tensor imaging (DTI) study. J. Magn. Reson. Imaging. 31, 221-226. doi: 10.1002/jmri.22017. Unlu, E., Bagcioglu, E., Acay, M.B., Kacar, E., Turamanlar, O., Gonul, Y., Cevik, M., Akpinar, A., Coskun, K.S., 2014. Magnetic resonance imaging study of corpus callosum abnormalities in patients with different subtypes of schizophrenia. S. Afr. J. Psychiatry. 20, 146-152. Vita, A., De Peri, L., Deste, G., Sacchetti, E., 2012. Progressive loss of cortical gray matter in schizophrenia: A meta-analysis and meta-regression of longitudinal MRI studies. Transl. Psychiatry. 2, e190. doi: 10.1038/tp.2012.116. Williams, L.M., 2008. Voxel-based morphometry in schizophrenia: Implications for neurodevelopmental connectivity models, cognition and affect. Expert Rev. Neurother. 8, 1049-1065. doi: 10.1586/14737175.8.7.1049. Williams, M.R., Chaudhry, R., Perera, S., Pearce, R.K., Hirsch, S.R., Ansorge, O., Thom, M., Maier, M., 2013. Changes in cortical thickness in the frontal lobes in schizophrenia are a result of thinning of pyramidal cell layers. Eur. Arch. Psychiatry Clin. Elfaki et al. 110 Neurosci. 263, 25-39. doi: 10.1007/s00406-012-0325-8. World Medical Association, 2013. World Medical Association Declaration of Helsinki: Ethical principles for medical research involving human subjects. JAMA. 310, 2191-2194. Yang, Y., Nuechterlein, K.H., Phillips, O., Hamilton, L.S., Subotnik, K.L., Asarnow, R.F., Toga, A.W., Narr, K.L., 2010. The contributions of disease and genetic factors towards regional cortical thinning in schizophrenia: The UCLA family study. Schizophr. Res. 123, 116-125. doi: 10.1016/j.schres.2010.08.005. Zheng, P., 2009. Neuroactive steroid regulation of neurotransmitter release in the CNS: Action, mechanism and possible significance. Prog. Neurobiol. 89, 134-152.
Yıl 2017, Cilt: 34 Sayı: 2, 99 - 110, 08.09.2017

Öz

Kaynakça

  • Andreasen, N.C., Nopoulos, P., Magnotta, V., Pierson, R., Ziebell, S., Ho, B.C., 2011. Progressive brain change in schizophrenia: A prospective longitudinal study of first-episode schizophrenia. Biol. Psychiatry. 70, 672-679. doi: 10.1016/j.biopsych.2011.05.017. Andreone, N., Tansella, M., Cerini, R., Versace, A., Rambaldelli, G., Perlini, C., Dusi, N., Pelizza, L., Balestrieri, M., Barbui, C., Nose, M., Gasparini, A., Brambilla, P., 2007. Cortical white-matter microstructure in schizophrenia. Diffusion imaging study. Br. J. Psychiatry: The journal of mental science. 191, 113-119. Aso, M., Suzuki, M., Kawasaki, Y., Matsui, M., Hagino, H., Kurokawa, K., Seto, H., Kurachi, M., 2001. Sylvian fissure and medial temporal lobe structures in patients with schizophrenia: A magnetic resonance imaging study. Psychiatry Clin. Neurosci. 55, 49-56. Cao, X.Y., Li, Z., Metcalfe, H.M., Yang, T.X., Tan, S.P., Wang, Y., Hong, X.H., Li, Z.J., Yu, X., Cheung, E.F., Neumann, D.L., Shum, D.H., Chan, R.C., 2013. The nature and extent of working memory dysfunction in schizophrenia. Psych. J. 2, 175-182. doi: 10.1002/pchj.30. Chavarria-Siles, I., White, T., de Leeuw, C., Goudriaan, A., Lips, E., Ehrlich, S., Turner, J.A., Calhoun, V.D., Gollub, R.L., Magnotta, V.A., Ho, B.C., Smit, A.B., Verheijen, M.H., Posthuma, D., 2015. Myelination-related genes are associated with decreased white matter integrity in schizophrenia. Eur. J. Hum. Genet. 24, 381-386. doi: 10.1038/ejhg.2015.120. da Silva, T.L., Ravindran, A.V., 2015. Contribution of sex hormones to gender differences in schizophrenia: A review. Asian J. Psychiatr. 18, 2-14. doi: 10.1016/j.ajp.2015.07.016. DeLisi, L.E., 2001. Speech disorder in schizophrenia: Review of the literature and exploration of its relation to the uniquely human capacity for language. Schizophr. Bull. 27, 481-496. Dogdas, B., Shattuck, D.W., Leahy, R.M., 2005. Segmentation of skull and scalp in 3-D human MRI using mathematical morphology. Hum. Brain Mapp. 26, 273-285. Elfaki, A., Elfaki, A., Osman, T., Sahin, B., Elsheikh, A., Mohamed, A., Hamdoun, A., Mohammed, A., 2013. Stereological evaluation of brain magnetic resonance images of schizophrenic patients. Image Analysis and Stereology. 32, 145-153. Flynn, S.W., Lang, D.J., Mackay, A.L., Goghari, V., Vavasour, I.M., Whittall, K.P., Smith, G.N., Arango, V., Mann, J.J., Dwork, A.J., Falkai, P., Honer, W.G., 2003. Abnormalities of myelination in schizophrenia detected in vivo with MRI, and post-mortem with analysis of oligodendrocyte proteins. Mol. Psychiatry. 8, 811-820. Green, M.F., Olivier, B., Crawley, J.N., Penn, D.L., Silverstein, S., 2005. Social cognition in schizophrenia: Recommendations from the measurement and treatment research to improve cognition in schizophrenia new approaches conference. Schizophr Bull. 31, 882-887. Gutierrez-Galve, L., Wheeler-Kingshott, C.A., Altmann, D.R., Price, G., Chu, E.M., Leeson, V.C., Lobo, A., Barker, G.J., Barnes, T.R., Joyce, E.M., Ron, M.A., 2010. Changes in the frontotemporal cortex and cognitive correlates in first-episode psychosis. Biol. Psychiatry. 68, 51-60. doi: 10.1016/j.biopsych.2010.03.019. Harrison, P.J., 2004. The hippocampus in schizophrenia: A review of the neuropathological evidence and its pathophysiological implications. Psychopharmacology. 174, 151-162. Havermans, R., Honig, A., Vuurman, E.F., Krabbendam, L., Wilmink, J., Lamers, T., Verheecke, C.J., Jolles, J., Romme, M.A., van Praag, H.M., 1999. A controlled study of temporal lobe structure volumes and P300 responses in schizophrenic patients with persistent auditory hallucinations. Schizophr. Res. 38, 151-158. Hayashi, N., Igarashi, Y., Yamashina, M., Suda, K., 2002. Is there a gender difference in a factorial structure of the positive and negative syndrome scale? A test by structural equation modeling. Psychopathology. 35, 28-35. Highley, J.R., McDonald, B., Walker, M.A., Esiri, M.M., Crow, T.J., 1999. Schizophrenia and temporal lobe asymmetry. A postmortem stereological study of tissue volume. British journal of psychiatry : The journal of mental science. 175, 127-134. Hugdahl, K., Loberg, E.M., Nygard, M., 2009. Left temporal lobe structural and functional abnormality underlying auditory hallucinations in schizophrenia. Front. Neurosci. 3, 34-45. doi: 10.3389/neuro.01.001.2009. Joshi, A.A., Shattuck, D.W., Thompson, P.M., Leahy, R.M., 2007. Surface-constrained volumetric brain registration using harmonic Journal of Experimental and Clinical Medicine 34 (2017) 99-110 109 mappings. IEEE Trans. Med. Imaging. 26, 1657-1669. Jung, W.H., Jang, J.H., Byun, M.S., An, S.K., Kwon, J.S., 2010. Structural brain alterations in individuals at ultra-high risk for psychosis: A review of magnetic resonance imaging studies and future directions. J. Korean Med. Sci. 25, 1700-1709. doi: 10.3346/jkms.2010.25.12.1700. Kiernan, J.A., 2012. Anatomy of the temporal lobe. Epilepsy Res. Treat. 2012, 176157. doi: 10.1155/2012/176157. Luders, E., Gaser, C., Jancke, L., Schlaug, G., 2004. A voxel-based approach to gray matter asymmetries. Neuroimage. 22, 656- 664. Modinos, G., Costafreda, S.G., van Tol, M.J., McGuire, P.K., Aleman, A., Allen, P., 2013. Neuroanatomy of auditory verbal hallucinations in schizophrenia: A quantitative meta-analysis of voxel-based morphometry studies. Cortex. 49, 1046-1055. doi: 10.1016/j.cortex.2012.01.009. Montoya, A., Lepage, M., Malla, A., 2005. Temporal lobe dysfunction in patients with first-episode schizophrenia. Salud. Mental. 28, 33-39. Morey, R.A., Selgrade, E.S., Wagner, H.R., Huettel, S.A., Wang, L., McCarthy, G., 2010. Scan-rescan reliability of subcortical brain volumes derived from automated segmentation. Hum. Brain Mapp. 31, 1751-1762. doi: 10.1002/hbm.20973. Najjar, S., Pearlman, D.M., 2015. Neuroinflammation and white matter pathology in schizophrenia: Systematic review. Schizophr. Res. 161, 102-112. doi: 10.1016/j.schres.2014.04.041. Neckelmann, G., Specht, K., Lund, A., Ersland, L., Smievoll, A.I., Neckelmann, D., Hugdahl, K., 2006. Mr morphometry analysis of grey matter volume reduction in schizophrenia: Association with hallucinations. Int. J. Neurosci. 116, 9-23. Oertel-Knochel, V., Knochel, C., Rotarska-Jagiela, A., Reinke, B., Prvulovic, D., Haenschel, C., Hampel, H., Linden, D.E., 2013. Association between psychotic symptoms and cortical thickness reduction across the schizophrenia spectrum. Cereb. Cortex. 23, 61-70. doi: 10.1093/cercor/bhr380. Okugawa, G., Sedvall, G.C., Agartz, I., 2002. Reduced grey and white matter volumes in the temporal lobe of male patients with chronic schizophrenia. Eur. Arch. Psychiatry Clin. Neurosci. 252, 120-123. Pantelis, C., Velakoulis, D., McGorry, P.D., Wood, S.J., Suckling, J., Phillips, L.J., Yung, A.R., Bullmore, E.T., Brewer, W., Soulsby, B., Desmond, P., McGuire, P.K., 2003. Neuroanatomical abnormalities before and after onset of psychosis: A cross-sectional and longitudinal MRI comparison. Lancet. 361, 281-288. Rabinowicz, E.F., Silipo, G., Goldman, R., Javitt, D.C., 2000. Auditory sensory dysfunction in schizophrenia: imprecision or distractibility? Arch. Gen. Psychiatry. 57, 1149-1155. Riecher-Rossler, A., Hafner, H., 2000. Gender aspects in schizophrenia: Bridging the border between social and biological psychiatry. Acta. Psychiatr. Scand. Suppl. 58-62. Rimol, L.M., Hartberg, C.B., Nesvag, R., Fennema-Notestine, C., Hagler, D.J., Jr., Pung, C.J., Jennings, R.G., Haukvik, U.K., Lange, E., Nakstad, P.H., Melle, I., Andreassen, O.A., Dale, A.M., Agartz, I., 2010. Cortical thickness and subcortical volumes in schizophrenia and bipolar disorder. Biol. Psychiatry. 68, 41-50. doi: 10.1016/j.biopsych.2010.03.036. Rimol, L.M., Nesvag, R., Hagler, D.J., Jr., Bergmann, O., Fennema-Notestine, C., Hartberg, C.B., Haukvik, U.K., Lange, E., Pung, C.J., Server, A., Melle, I., Andreassen, O.A., Agartz, I., Dale, A.M., 2012. Cortical volume, surface area, and thickness in schizophrenia and bipolar disorder. Biol. Psychiatry. 71, 552-560. doi: 10.1016/j.biopsych.2011.11.026. Rossi, A., Stratta, P., D’Albenzio, L., Tartaro, A., Schiazza, G., di Michele, V., Bolino, F., Casacchia, M., 1990. Reduced temporal lobe areas in schizophrenia: Preliminary evidences from a controlled multiplanar magnetic resonance imaging study. Biol. Psychiatry. 27, 61-68. Sahin, B., Elfaki, A., 2012. Estimation of the volume and volume fraction of brain and brain structures on radiological images. Neuroquantology. 10, 87-97. Shattuck, D.W., Leahy, R.M., 2002. BrainSuite: An automated cortical surface identification tool. Med. Image Anal. 6, 129-142. Shenton, M.E., Dickey, C.C., Frumin, M., McCarley, R.W., 2001. A review of MRI findings in schizophrenia. Schizophr. Res. 49, 1-52. Sigmundsson, T., Suckling, J., Maier, M., Williams, S., Bullmore, E., Greenwood, K., Fukuda, R., Ron, M., Toone, B., 2001. Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms. Am. J. Psychiatry. 158, 234-243. Takahashi, T., Suzuki, M., Zhou, S.Y., Tanino, R., Nakamura, K., Kawasaki, Y., Seto, H., Kurachi, M., 2010. A follow-up MRI study of the superior temporal subregions in schizotypal disorder and first-episode schizophrenia. Schizophr. Res.. 119, 65-74. doi: 10.1016/j.schres.2009.12.006. Takao, H., Abe, O., Yamasue, H., Aoki, S., Kasai, K., Ohtomo, K., 2010. Cerebral asymmetry in patients with schizophrenia: A voxel-based morphometry (VBM) and diffusion tensor imaging (DTI) study. J. Magn. Reson. Imaging. 31, 221-226. doi: 10.1002/jmri.22017. Unlu, E., Bagcioglu, E., Acay, M.B., Kacar, E., Turamanlar, O., Gonul, Y., Cevik, M., Akpinar, A., Coskun, K.S., 2014. Magnetic resonance imaging study of corpus callosum abnormalities in patients with different subtypes of schizophrenia. S. Afr. J. Psychiatry. 20, 146-152. Vita, A., De Peri, L., Deste, G., Sacchetti, E., 2012. Progressive loss of cortical gray matter in schizophrenia: A meta-analysis and meta-regression of longitudinal MRI studies. Transl. Psychiatry. 2, e190. doi: 10.1038/tp.2012.116. Williams, L.M., 2008. Voxel-based morphometry in schizophrenia: Implications for neurodevelopmental connectivity models, cognition and affect. Expert Rev. Neurother. 8, 1049-1065. doi: 10.1586/14737175.8.7.1049. Williams, M.R., Chaudhry, R., Perera, S., Pearce, R.K., Hirsch, S.R., Ansorge, O., Thom, M., Maier, M., 2013. Changes in cortical thickness in the frontal lobes in schizophrenia are a result of thinning of pyramidal cell layers. Eur. Arch. Psychiatry Clin. Elfaki et al. 110 Neurosci. 263, 25-39. doi: 10.1007/s00406-012-0325-8. World Medical Association, 2013. World Medical Association Declaration of Helsinki: Ethical principles for medical research involving human subjects. JAMA. 310, 2191-2194. Yang, Y., Nuechterlein, K.H., Phillips, O., Hamilton, L.S., Subotnik, K.L., Asarnow, R.F., Toga, A.W., Narr, K.L., 2010. The contributions of disease and genetic factors towards regional cortical thinning in schizophrenia: The UCLA family study. Schizophr. Res. 123, 116-125. doi: 10.1016/j.schres.2010.08.005. Zheng, P., 2009. Neuroactive steroid regulation of neurotransmitter release in the CNS: Action, mechanism and possible significance. Prog. Neurobiol. 89, 134-152.
Toplam 1 adet kaynakça vardır.

Ayrıntılar

Bölüm Surgery Medical Sciences
Yazarlar

Amani Elfaki Bu kişi benim

Tahir Osman Ali Bu kişi benim

Abdelgani Elsheikh Bu kişi benim

Ibrahim Erkan Bu kişi benim

Meltem Acar Güdek Bu kişi benim

Murat Golpınar Bu kişi benim

Bunyamin Sahin Bu kişi benim

Yayımlanma Tarihi 8 Eylül 2017
Gönderilme Tarihi 7 Eylül 2017
Kabul Tarihi 17 Ekim 2016
Yayımlandığı Sayı Yıl 2017 Cilt: 34 Sayı: 2

Kaynak Göster

APA Elfaki, A., Ali, T. O., Elsheikh, A., Erkan, I., vd. (2017). Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry. Journal of Experimental and Clinical Medicine, 34(2), 99-110.
AMA Elfaki A, Ali TO, Elsheikh A, Erkan I, Güdek MA, Golpınar M, Sahin B. Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry. J. Exp. Clin. Med. Eylül 2017;34(2):99-110.
Chicago Elfaki, Amani, Tahir Osman Ali, Abdelgani Elsheikh, Ibrahim Erkan, Meltem Acar Güdek, Murat Golpınar, ve Bunyamin Sahin. “Morphological Changes of the Temporal Lobe Structures in Schizophrenia and Their Link to the Clinical Symptoms Regarding the Gender Difference and Asymmetry”. Journal of Experimental and Clinical Medicine 34, sy. 2 (Eylül 2017): 99-110.
EndNote Elfaki A, Ali TO, Elsheikh A, Erkan I, Güdek MA, Golpınar M, Sahin B (01 Eylül 2017) Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry. Journal of Experimental and Clinical Medicine 34 2 99–110.
IEEE A. Elfaki, “Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry”, J. Exp. Clin. Med., c. 34, sy. 2, ss. 99–110, 2017.
ISNAD Elfaki, Amani vd. “Morphological Changes of the Temporal Lobe Structures in Schizophrenia and Their Link to the Clinical Symptoms Regarding the Gender Difference and Asymmetry”. Journal of Experimental and Clinical Medicine 34/2 (Eylül 2017), 99-110.
JAMA Elfaki A, Ali TO, Elsheikh A, Erkan I, Güdek MA, Golpınar M, Sahin B. Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry. J. Exp. Clin. Med. 2017;34:99–110.
MLA Elfaki, Amani vd. “Morphological Changes of the Temporal Lobe Structures in Schizophrenia and Their Link to the Clinical Symptoms Regarding the Gender Difference and Asymmetry”. Journal of Experimental and Clinical Medicine, c. 34, sy. 2, 2017, ss. 99-110.
Vancouver Elfaki A, Ali TO, Elsheikh A, Erkan I, Güdek MA, Golpınar M, Sahin B. Morphological changes of the temporal lobe structures in schizophrenia and their link to the clinical symptoms regarding the gender difference and asymmetry. J. Exp. Clin. Med. 2017;34(2):99-110.