Voxel-based morphometric analysis on the volume of gray matter in bipolar I disorder

Psychiatry Research - Neuroimaging

Volumn 191, Issue 2, 2011, Pages 92-97

  Li, Mingli ^a   Cui, Liqian ^a   Deng, Wei ^a   Ma, Xiaohong ^a   Huang, Chaohua ^a   Jiang, Lijun ^a   Wang, Yingcheng ^a   Collier, David A ^b   Gong, Qiyong ^a   Li, Tao ^a,b  

^a SICHUAN UNIVERSITY   (China)

^b KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Bipolar I disorder; Brain structure; Magnetic resonance imaging

Indexed keywords

ADULT; AGE; ARTICLE; BIPOLAR I DISORDER; BRAIN SIZE; CAUDATE NUCLEUS; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE DURATION; FEMALE; GENDER; GRAY MATTER; HUMAN; INFERIOR PARIETAL LOBULE; MALE; MIDDLE FRONTAL GYRUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; STATISTICAL ANALYSIS; SUPERIOR TEMPORAL GYRUS; VOXEL BASED MORPHOMETRY;

ADOLESCENT; ADULT; BIPOLAR DISORDER; BRAIN; BRAIN MAPPING; FEMALE; FUNCTIONAL LATERALITY; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; STATISTICS AS TOPIC; YOUNG ADULT;

EID: 78751701526     PISSN: 09254927     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pscychresns.2010.09.006     Document Type: Article

References (46)

1. Adler C.M., Levine A.D., DelBello M.P., Strakowski S.M. Changes in gray matter volume in patients with bipolar disorder. Biological Psychiatry 2005, 58:151-157.
2. Arnone D., Cavanagh J., Gerber D., Lawrie S.M., Ebmeier K.P., McIntosh A.M. Magnetic resonance imaging studies in bipolar disorder and schizophrenia: meta-analysis. The British Journal of Psychiatry 2009, 195:194-201.
3. Ashburner J., Friston K.J. Unified segmentation. Neuroimage 2005, 26:839-851.
4. Baumann B., Danos P., Krell D., Diekmann S., Leschinger A., Stauch R., Wurthmann C., Bernstein H.G., Bogerts B. Reduced volume of limbic system affiliated basal ganglia in mood disorders: preliminary data from a postmortem study. Journal of Neuropsychiatry and Clinical Neurosciences 1999, 11:71-78.
5. Berk M., Dodd S., Kauer-Sant'anna M., Malhi G.S., Bourin M., Kapczinski F., Norman T. Dopamine dysregulation syndrome: implications for a dopamine hypothesis of bipolar disorder. Acta Psychiatrica Scandinavica 2007, 116:41-49.
6. Beyer J.L., Kuchibhatla M., Payne M., Moo-Young M., Cassidy F., MacFall J., Krishnan K.R.R. Caudate volume measurement in older adults with bipolar disorder. International Journal of Geriatric Psychiatry 2004, 19:109-114.
7. Cecil K.M., DelBello M.P., Morey R., Strakowski S.M. Frontal lobe differences in bipolar disorder as determined by proton MR spectroscopy. Bipolar Disorders 2002, 4:357-365.
8. Chen X.H., Wen W., Malhi G.S., Ivanovski B., Sachdev P.S. Regional gray matter changes in bipolar disorder: a voxel-based morphometric study. Australian and New Zealand Journal of Psychiatry 2007, 41:327-336.
9. Dickstein D.P., Milham M.P., Nugent A.C., Drevets W.C., Charney D.S., Pine D.S., Leibenluft E. Frontotemporal alterations in pediatric bipolar disorder - results of a voxel-based morphometry study. Archives of General Psychiatry 2005, 62:734-741.
10. Ellison-Wright I., Bullmore E. Anatomy of bipolar disorder and schizophrenia: a meta-analysis. Schizophrenia Research 2010, 117:1-12.
11. Frazier J.A., Breeze J.L., Makris N., Giuliano A.S., Herbert M.R., Seidman L., Biederman J., Hodge S.M., Dieterich M.E., Gerstein E.D., Kennedy D.N., Rauch S.L., Cohen B.M., Caviness V.S. Cortical gray matter differences identified by structural magnetic resonance imaging in pediatric bipolar disorder. Bipolar Disorders 2005, 7:555-569.
12. Frye M.A., Thomas M.A., Yue K., Binesh N., Davanzo P., Ventura J., O'Neill J., Guze B., Curran J.G., Mintz J. Reduced concentrations of N-acetylaspartate (NAA) and the NAA-creatine ratio in the basal ganglia in bipolar disorder: a study using 3-Tesla proton magnetic resonance spectroscopy. Psychiatry Research: Neuroimaging 2007, 154:259-265.
13. Giuliani N.R., Calhoun V.D., Pearlson G.D., Francis A., Buchanan R.W. Voxel-based morphometry versus region of interest: a comparison of two methods for analyzing gray matter differences in schizophrenia. Schizophrenia Research 2005, 74:135-147.
14. Good C.D., Johnsrude I.S., Ashburner J., Henson R.N.A., Friston K.J., Frackowiak R.S.J. A voxel-based morphometric study of ageing in 465 normal adult human brain. Neuroimage 2001, 14:21-36.
15. Ha T.H., Ha K., Kim J.H., Choi J.E. Regional brain gray matter abnormalities in patients with bipolar II disorder: a comparison study with bipolar I patients and healthy controls. Neuroscience Letters 2009, 456:44-48.
16. Hauser P., Matochik J., Altshuler L.L., Denicoff K.D., Conrad A., Li X.M., Post R.M. MRI-based measurements of temporal lobe and ventricular structures in patients with bipolar I and bipolar II disorders. Journal of Affective Disorders 2000, 60:25-32.
17. Haznedar M.M., Roversi F., Pallanti S., Baldini-Rossi N., Schnur D.B., LiCalzi E.M., Tang C., Hof P.R., Hollander E., Buchsbaum M.S. Fronto-thalamo-striatal gray and white matter volumes and anisotropy of their connections in bipolar spectrum illnesses. Biological Psychiatry 2005, 57:733-742.
18. Kempton M.J., Geddes J.R., Ettinger U., Williams S.C.R., Grasby P.M. Meta-analysis, database, and meta-regression of 98 structural imaging studies in bipolar disorder. Archives of General Psychiatry 2008, 65:1017-1032.
19. Konarski J.Z., Mcintyre R.S., Kennedy S.H., Rafi-Tari S., Soczynska J.K., Ketter T.A. Volumetric neuroimaging investigations in mood disorders: bipolar disorder versus major depressive disorder. Bipolar Disorders 2008, 10:1-37.
20. Lopez-Larson M.P., DelBello M.P., Zimmerman M.E., Schwiers M.L., Strakowski S.M. Regional prefrontal gray and white matter abnormalities in bipolar disorder. Biological Psychiatry 2002, 52:93-100.
21. Lyoo I.K., Kim M.J., Stoll A.L., Demopulos C.M., Parow A.M., Dager S.R., Friedman S.D., Dunner D.L., Renshaw P.F. Frontal lobe gray matter density decreases in bipolar I disorder. Biological Psychiatry 2004, 55:648-651.
22. Malhi G.S., Lagopoulos J., Owen A.M., Ivanovski B., Shnier R., Sachdev P. Reduced activation to implicit affect induction in euthymic bipolar patients: an fMRI study. Journal of Affective Disorders 2007, 97:109-122.
23. McElroy S.L., Altshuler L.L., Suppes T., Keck P.E., Frye M.A., Denicoff K.D., Nolen W.A., Kupka R.W., Leverich G.S., Rochussen J.R., Rush A.J., Post R.M. Axis I psychiatric comorbidity and its relationship to historical illness variables in 288 patients with bipolar disorder. American Journal of Psychiatry 2001, 158:420-426.
24. Mitchell R.L.C., Elliott R., Barry M., Cruttenden A., Woodruff P.W.R. The neural response to emotional prosody, as revealed by functional magnetic resonance imaging. Neuropsychologia 2003, 41:1410-1421.
25. Mitchell R.L.C., Elliott R., Barry M., Cruttenden A., Woodruff P.W.R. Neural response to emotional prosody in schizophrenia and in bipolar affective disorder. British Journal of Psychiatry 2004, 184:223-230.
26. Molina V., Sanchez J., Sanz J., Reig S., Benito C., Leal I., Sarrarnea F., Rebolledo R., Palomo T., Desco M. Dorsolateral prefrontal N-acetyl-aspartate concentration in male patients with chronic schizophrenia and with chronic bipolar disorder. European Psychiatry 2007, 22:505-512.
27. Monkul E.S., Matsuo K., Nicoletti M.A., Dierschke N., Hatch J.P., Dalwani M., Brambilla P., Caetano S., Sassi R.B., Mallinger A.G., Soares J.C. Prefrontal gray matter increases in healthy individuals after lithium treatment: a voxel-based morphometry study. Neuroscience Letters 2007, 429:7-11.
28. Moorhead T.W.J., McKirdy J., Sussmann J.E.D., Hall J., Lawrie S.M., Johnstone E.C., McIntosh A.M. Progressive gray matter loss in patients with bipolar disorder. Biological Psychiatry 2007, 62:894-900.
29. Najt P., Nicoletti M., Chen H.H., Hatch J.P., Caetano S.C., Sassie R.B., Axelson D., Rambilla P., Keshavan M.S., Ryan N.D., Birmaher B., Soares J.C. Anatomical measurements of the orbitofrontal cortex in child and adolescent patients with bipolar disorder. Neuroscience Letters 2007, 413:183-186.
30. Nudmamud S., Reynolds L.M., Reynolds G.P. N-acetylaspartate and N-acetylaspartylglutamate deficits in superior temporal cortex in schizophrenia and bipolar disorder: a postmortem study. Biological Psychiatry 2003, 53:1138-1148.
31. Nugent A.C., Milham M.P., Bain E.E., Mah L., Cannon D.M., Marrett S., Zarate C.A., Pine D.S., Price J.L., Drevets W.C. Cortical abnormalities in bipolar disorder investigated with MRI and voxel-based morphometry. Neuroimage 2006, 30:485-497.
32. Port J.D., Unal S.S., Mrazek D.A., Marcus S.M. Metabolic alterations in medication-free patients with bipolar disorder: a 3T CSF-corrected magnetic resonance spectroscopic imaging study. Psychiatry Research: Neuroimaging 2008, 162:113-121.
33. Ridgway G., Omar R., Ourselin S., Hill D., Warren J., Fox N. Issues with threshold masking in voxel-based morphometry of atrophied brains. NeuroImage 2008, 44:99-111.
34. Rorden C., Brett M. Stereotaxic display of brain lesions. Behavioura. Neurology 2000, 12:191-200.
35. Rushworth M.F.S., Taylor P.C.J. TMS in the parietal cortex: updating representations for attention and action. Neuropsychologia 2006, 44:2700-2716.
36. Sanches M., Keshavan M.S., Brambilla P., Soares J.C. Neurodevelopmental basis of bipolar disorder: a critical appraisal. Progress in Neuro-Psychopharmacology & Biological Psychiatry 2008, 32:1617-1627.
37. Smith S.M. Fast robust automated brain extraction. Human Brain Mapping 2002, 17:143-155.
38. Strakowski S.M., DelBello M.P., Zimmerman M.E., Getz G.E., Mills N.P., Ret J., Shear P., Adler C.M. Ventricular and periventricular structural volumes in first- versus multiple-episode bipolar disorder. American Journal of Psychiatry 2002, 159:1841-1847.
39. Strakowski S.M., DelBello M.P., Adler C.M. The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings. Molecular Psychiatry 2005, 10:105-116.
40. van der Schot A.C., Vonk R., Brans R.G.H., van Haren N.E.M., Koolschijn P.C.M.P., Nuboer V., Schnack H.G., van Baal G.C.M., Boomsma D.I., Nolen W.A., Pol H.E.H., Kahn R.S. Influence of genes and environment on brain volumes in twin pairs concordant and discordant for bipolar disorder. Archives of General Psychiatry 2009, 66:142-151.
41. Vita A., De Peri L., Sacchetti E. Gray matter, white matter, brain, and intracranial volumes in first-episode bipolar disorder: a meta-analysis of magnetic resonance imaging studies. Bipolar Disorders 2009, 11:807-814.
42. Wada A., Yokoo H., Yanagita T., Kobayashi H. Lithium: potential therapeutics against acute brain injuries and chronic neurodegenerative diseases. Journal of Pharmacological Sciences 2005, 99:307-321.
43. Wilke M., Kowatch R.A., DelBello M.P., Mills N.P., Holland S.K. Voxel-based morphometry in adolescents with bipolar disorder: first results. Psychiatry Research: Neuroimaging 2004, 131:57-69.
44. Yildiz-Yesiloglu A., Ankerst D.P. Neurochemical alterations of the brain in bipolar disorder and t heir implications for pathophysiology: a systematic review of the in vivo proton magnetic resonance spectroscopy findings. Progress in Neuro-Psychopharmacology & Biological Psychiatry 2006, 30:969-995.
45. Yuan P.X., Gould T.D., Gray N.A., Bachmann R.F., Schloesser R.J., Lan M.J.K., Du J., Moore G.J., Manji H.K. Neurotrophic signaling cascades are major long-term targets for lithium: clinical implications. Clinical Neuroscience Research 2004, 4:137-153.
46. Yurgelun-Todd D.A., Gruber S.A., Kanayama G., Killgore W.D.S., Baird A.A., Young A.D. fMRI during affect discrimination in bipolar affective disorder. Bipolar Disorders 2000, 2:237-248.