Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-20T04:11:41.928Z Has data issue: false hasContentIssue false

Diffusion imaging studies of white matter integrity in bipolar disorder

Published online by Cambridge University Press:  04 April 2011

M. Bellani*
Affiliation:
Section of Psychiatry and Clinical Psychology, Department of Public Health and Community Medicine, Inter-University Center for Behavioural Neurosciences (ICBN), University of Verona, Verona, Italy
P. Brambilla
Affiliation:
DISM, Inter-University Center for Behavioural Neurosciences (ICBN), University of Udine, Udine, Italy IRCCS “E. Medea” Scientific Institute, Udine, Italy
*
*Address for correspondence: Dr M. Bellani, Section of Psychiatry and Clinical Psychology, Department of Public Health and Community Medicine, University of Verona, Piazzale L.A. Scuro 10, 37134 Verona, Italy. (Email: [email protected]; [email protected])
Rights & Permissions [Opens in a new window]

Abstract

Diffusion tensor imaging (DTI) is a neuroimaging technique with a potential to elucidate white matter integrity. Recently, it has been used in the field of psychiatry to further understand the pathophysiology of major diseases, including bipolar disorder (BD). This review sought to focus on existing DTI findings on white matter organization in BD.

Type
Neurobiology of Psychosis
Copyright
Copyright © Cambridge University Press 2011

In the last decade, several efforts have been made in order to detect possible biomarkers of bipolar disorder (BD) and recent advances in neuroimaging research have pointed out the putative role of white matter (Arnone et al. Reference Arnone, McIntosh, Chandra and Ebmeier2008; Doron & Gazzaniga Reference Doron and Gazzaniga2008). In this regard, structural magnetic resonance imaging (MRI) studies described diffuse cortical and callosal white matter pathology in BD patients (Adler et al. Reference Adler, Del Bello and Strakowski2006; Kempton et al. Reference Kempton, Geddes, Ettinger, Williams and Grasby2008; Vita et al. Reference Vita, De Peri and Sacchetti2009), suggesting the presence of altered intra- and inter-hemispheric connectivity (Atmaca et al. Reference Atmaca, Ozdemir and Yildirim2007; Bellani et al. Reference Bellani, Marzi and Brambilla2009aReference Bellani, Yeh, Tansella, Balestrieri, Soares and Brambillab). A relatively recent application of MRI is the diffusion tensor imaging (DTI), a non-invasive imaging technique that measures the motion of water molecules in brain tissue and provides information about the microstructural coherence of white matter (Basser & Jones Reference Basser and Jones2002). Water diffusion within the neural tissue is impeded by a myelin sheath, axonal density and thickness, and cellular structures. The degree of water molecule diffusion can be quantified by the apparent diffusion coefficient (ADC), and the fibre tract directionality can be evaluated indirectly by fractional anisotropy (FA; Beaulieu, Reference Beaulieu2002). ADC and FA may be considered as good markers of white matter microstructure organization. In particular, low FA values indicate probable damage to axonal membrane, de-/dys-myelination or reduced amount of intra-axonal structures, whereas high ADC measures are found when water diffusion is unimpeded, e.g. in ventricles or demyelinated white matter (Beaulieu & Allen, Reference Beaulieu and Allen1994). Several DTI data on BD have been published so far, showing some white matter abnormalities (Brambilla et al. Reference Brambilla, Bellani, Yeh, Soares and Tansella2009a). Most studies (see Table 1) reported reduced FA and/or elevated ADC values compared to healthy controls involving specific brain regions such as prefrontal, parietal, temporal and occipital lobes, internal capsule, uncinate fasciculus, superior longitudinal fasciculus and corpus callosum (for extensive review see Bellani et al. Reference Bellani, Marzi and Brambilla2009ab; Heng et al. Reference Heng, Song and Sim2010). However, the effect of mood states on white matter integrity is often not taken into account (Adler et al. Reference Adler, Holland, Schmithorst, Wilke, Weiss, Pan and Strakowski2004; Bruno et al. Reference Bruno, Cercignani and Ron2008; Mahon et al. Reference Mahon, Wu, Malhotra, Burdick, De Rosse, Ardekani and Szeszko2009) or patients with different clinical states are just studied together (Beyer et al. Reference Beyer, Taylor, MacFall, Kuchibhatla, Payne, Provenzale, Cassidy and Krishnan2005; Versace et al. Reference Versace, Almeida, Hassel, Walsh, Novelli, Klein, Kupfer and Phillips2008; Wang et al. Reference Wang, Kalmar, Edmiston, Chepenik, Bhagwagar, Spencer, Pittman, Jackowski, Papademetris, Constable and Blumberg2008a, Reference Wang, Jackowski, Kalmar, Chepenik, Tie, Qiu, Gong, Pittman, Jones, Shah, Spencer, Papademetris, Constable and Blumbergb; Barnea-Goraly et al. Reference Barnea-Goraly, Chang, Karchemskiy, Howe and Reiss2009). In this regard, patients suffering from different bipolar episode may be characterized by specific DTI ‘signature’. Anyway, till date, few studies have been conducted on patients with homogeneous mood state. In euthymia, FA is usually increased in the genu of corpus callosum, internal capsule, anterior thalamic radiation and uncinate fasciculus (Haznedar et al. Reference Haznedar, Roversi, Pallanti, Baldini-Rossi, Schnur, Licalzi, Tang, Hof, Hollander and Buchsbaum2005; Yurgelun-Todd et al. Reference Yurgelun-Todd, Silveri, Gruber, Rohan and Pimentel2007; Sussmann et al. Reference Sussmann, Lymer, McKirdy, Moorhead, Maniega, Job, Hall, Bastin, Johnstone, Lawrie and McIntosh2009; Wessa et al. Reference Wessa, Houenou, Leboyer, Chanraud, Poupon, Martinot and Paillère-Martinot2009; Zanetti et al. Reference Zanetti, Jackowski, Versace, Almeida, Hassel, Duran, Busatto, Kupfer and Phillips2009), whereas in bipolar depression lower FA has been shown in the genu of the corpus callosum and in corona radiata (Regenold et al. Reference Regenold, D'Agostino, Ramesh, Hasnain, Roys and Gullapalli2006; Chaddock et al. Reference Chaddock, Barker, Marshall, Schulze, Hall, Fern, Walshe, Bramon, Chitnis, Murray and McDonald2009; Benedetti et al. Reference Benedetti, Yeh, Bellani, Radaelli, Nicoletti, Poletti, Falini, Dallaspezia, Colombo, Scotti, Smeraldi, Soares and Brambilla2011). Not surprisingly, in mixed samples higher and lower FA values were found in different brain regions (Beyer et al. Reference Beyer, Taylor, MacFall, Kuchibhatla, Payne, Provenzale, Cassidy and Krishnan2005; Wang et al. Reference Wang, Kalmar, Edmiston, Chepenik, Bhagwagar, Spencer, Pittman, Jackowski, Papademetris, Constable and Blumberg2008a, Reference Wang, Jackowski, Kalmar, Chepenik, Tie, Qiu, Gong, Pittman, Jones, Shah, Spencer, Papademetris, Constable and Blumbergb; Barnea-Goraly et al. Reference Barnea-Goraly, Chang, Karchemskiy, Howe and Reiss2009).

Table 1. DTI studies in bipolar disorder

ADC, apparent diffusion coefficient; FA, fractional anisotropy; BD, bipolar disorder; HC, healthy controls.

The impact of mood stabilizers on white matter connectivity in BD should also be considered, particularly lithium and quetiapine, which have been suggested to potentially induce myelination processes (Bearden et al. Reference Bearden, Thompson, Dutton, Frey, Peluso, Nicoletti, Dierschke, Hayashi, Klunder, Glahn, Brambilla, Sassi, Mallinger and Soares2008; Zhang et al. Reference Zhang, Xu, Jiang, Xiao, Yan, He, Wang, Bi, Li, Kong and Li2008; Brambilla et al. Reference Brambilla, Bellani, Yeh and Soares2009b; Tondo & Baldessarini, Reference Tondo and Baldessarini2009). However, a recent DTI study did not find any lithium effect on DTI measures in patients suffering from BD (Benedetti et al. Reference Benedetti, Yeh, Bellani, Radaelli, Nicoletti, Poletti, Falini, Dallaspezia, Colombo, Scotti, Smeraldi, Soares and Brambilla2011).

In summary, the DTI literature on BD suggests loss of white matter network connectivity as a possible phenomenon of the disease, particularly including altered fronto-occipital, superior longitudinal fasciculus and callosal connections (Wang et al. Reference Wang, Kalmar, Edmiston, Chepenik, Bhagwagar, Spencer, Pittman, Jackowski, Papademetris, Constable and Blumberg2008a; Barnea-Goraly et al. Reference Barnea-Goraly, Chang, Karchemskiy, Howe and Reiss2009; Chaddock et al. Reference Chaddock, Barker, Marshall, Schulze, Hall, Fern, Walshe, Bramon, Chitnis, Murray and McDonald2009). However, diffusion-imaging studies in BD are mostly limited by heterogeneity and relatively small size of the samples. Moreover, the impact of some clinical variables on white matter coherence such as mood states and mood stabilizer administration still needs to be fully elucidated. In this perspective, future DTI studies are expected to further investigate whether abnormal white matter may represent a trait or a mood state biomarker of BD, potentially being preserved by psychotropic drugs such as lithium.

Footnotes

This Section of Epidemiology and Psychiatric Sciences regularly appears in each issue of the Journal to describe relevant studies investigating the relationship between neurobiology and psychosocial psychiatry in major psychoses. The aim of these Editorials is to provide a better understanding of the neural basis of psychopathology and clinical features of these disorders, in order to raise new perspectives in every-day clinical practice.

Paolo Brambilla, Section Editor and Michele Tansella, Editor EPS

References

Adler, CM, Del Bello, MP, Strakowski, SM (2006). Brain network dysfunction in bipolar disorder. CNS Spectrum 11, 312320.CrossRefGoogle ScholarPubMed
Adler, CM, Holland, SK, Schmithorst, V, Wilke, M, Weiss, KL, Pan, H, Strakowski, SM (2004). Abnormal frontal white matter tracts in bipolar disorder, a diffusion tensor imaging study. Bipolar Disorders 6, 197203.CrossRefGoogle ScholarPubMed
Arnone, D, McIntosh, AM, Chandra, P, Ebmeier, KP (2008). Meta-analysis of magnetic resonance imaging studies of the corpus callosum in bipolar disorder. Acta Psychiatrica Scandinavica 118, 357362.CrossRefGoogle ScholarPubMed
Atmaca, M, Ozdemir, H, Yildirim, H (2007). Corpus callosum areas in first episode patients with bipolar disorder. Psychological Medicine 37, 699704.CrossRefGoogle ScholarPubMed
Barnea-Goraly, N, Chang, K.D, Karchemskiy, A, Howe, ME, Reiss, AL (2009). Limbic and corpus callosum aberrations in adolescents with bipolar disorder: a tract-based spatial statistics analysis. Biological Psychiatry 66, 238244.CrossRefGoogle ScholarPubMed
Basser, PJ, Jones, DK (2002). Diffusion-tensor MRI, theory, experimental design and data analysis, a technical review. NMR Biomedicine 15, 456467.CrossRefGoogle ScholarPubMed
Bearden, CE, Thompson, PM, Dutton, RA, Frey, BN, Peluso, MA, Nicoletti, M, Dierschke, N, Hayashi, KM, Klunder, AD, Glahn, DC, Brambilla, P, Sassi, RB, Mallinger, AG, Soares, JC (2008). Three-dimensional mapping of hippocampal anatomy in unmedicated and lithium-treated patients with bipolar disorder. Neuropsychopharmacology 33, 12291238.CrossRefGoogle ScholarPubMed
Beaulieu, C (2002). The basis of anisotropic water diffusion in the nervous system, a technical review. NMR Biomedicine 15, 43544355.CrossRefGoogle ScholarPubMed
Beaulieu, C, Allen, PS (1994). Determinants of anisotropic water diffusion in nerves. Magnetic Resonance Medicine 31, 394400.CrossRefGoogle ScholarPubMed
Bellani, M, Marzi, CA, Brambilla, P (2009 a). Interhemispheric communication in schizophrenia. Epidemiologia e Psichiatria Sociale 18, 1922.CrossRefGoogle ScholarPubMed
Bellani, M, Yeh, PH, Tansella, M, Balestrieri, M, Soares, JC, Brambilla, P (2009 b). DTI studies of corpus callosum in bipolar disorder. Biochemical Society Transactions 37, 10961098.CrossRefGoogle ScholarPubMed
Benedetti, F, Yeh, PH, Bellani, M, Radaelli, D, Nicoletti, MA, Poletti, S, Falini, A, Dallaspezia, S, Colombo, C, Scotti, G, Smeraldi, E, Soares, JC, Brambilla, P (2011). Disruption of white matter integrity in bipolar depression as a possible structural marker of illness. Biological Psychiatry 69, 299300.CrossRefGoogle ScholarPubMed
Beyer, JL, Taylor, WD, MacFall, JR, Kuchibhatla, M, Payne, ME, Provenzale, JM, Cassidy, F, Krishnan, KR (2005). Cortical white matter microstructural abnormalities in bipolar disorder. Neuropsychopharmacology 30, 22252229.CrossRefGoogle ScholarPubMed
Brambilla, P, Bellani, M, Yeh, PH, Soares, JC (2009 b). Myelination in bipolar patients and the effects of mood stabilizers on brain anatomy. Current Pharmacological Design 15, 26322636.CrossRefGoogle ScholarPubMed
Brambilla, P, Bellani, M, Yeh, PH, Soares, JC, Tansella, M (2009 a). White matter connectivity in bipolar disorder. International Review Psychiatry 21, 380386.CrossRefGoogle ScholarPubMed
Bruno, S, Cercignani, M, Ron, MA (2008). White matter abnormalities in bipolar disorder: a voxel-based diffusion tensor imaging study. Bipolar Disorders 10, 460468.CrossRefGoogle ScholarPubMed
Chaddock, CA, Barker, GJ, Marshall, N, Schulze, K, Hall, MH, Fern, A, Walshe, M, Bramon, E, Chitnis, XA, Murray, R, McDonald, C (2009). White matter microstructural impairments and genetic liability to familial bipolar disorder. British Journal of Psychiatry 194, 527534.CrossRefGoogle Scholar
Doron, KW, Gazzaniga, MS (2008). Neuroimaging techniques offer new perspectives on callosal transfer and interhemispheric communication. Cortex 44, 10231029.CrossRefGoogle ScholarPubMed
Haznedar, MM, Roversi, F, Pallanti, S, Baldini-Rossi, N, Schnur, DB, Licalzi, EM, Tang, C, Hof, PR, Hollander, E, Buchsbaum, MS (2005). Fronto-thalamo-striatal gray and white matter volumes and anisotropy of their connections in bipolar spectrum illnesses. Biological Psychiatry 57, 733742.CrossRefGoogle ScholarPubMed
Heng, S, Song, AW, Sim, K (2010). White matter abnormalities in bipolar disorders: insights from diffusion tensor imaging studies. Journal of Neural Transmission 117, 639654.CrossRefGoogle ScholarPubMed
Kempton, MJ, Geddes, JR, Ettinger, U, Williams, SC, Grasby, PM (2008). Meta-analysis, database, and meta-regression of 98 structural imaging studies in bipolar disorder. Archives of General Psychiatry 65, 10171032.CrossRefGoogle ScholarPubMed
Mahon, K, Wu, J, Malhotra, AK, Burdick, KE, De Rosse, P, Ardekani, BA, Szeszko, PR (2009). A voxel-based diffusion tensor imaging study of white matter in bipolar disorder. Neuropsychopharmacology 34, 15901600.CrossRefGoogle ScholarPubMed
Regenold, WT, D'Agostino, CA, Ramesh, N, Hasnain, M, Roys, S, Gullapalli, RP (2006). Diffusion-weighted magnetic resonance imaging of white matter in bipolar disorder, a pilot study. Bipolar Disorders 8, 188195.CrossRefGoogle ScholarPubMed
Sussmann, JE, Lymer, GK, McKirdy, J, Moorhead, TW, Maniega, SM, Job, D, Hall, J, Bastin, ME, Johnstone, EC, Lawrie, SM, McIntosh, AM (2009). White matter abnormalities in bipolar disorder and schizophrenia detected using diffusion tensor magnetic resonance imaging. Bipolar Disorders 11, 1118.CrossRefGoogle ScholarPubMed
Tondo, L, Baldessarini, RJ (2009). Long-term lithium treatment in the prevention of suicidal behavior in bipolar disorder patients. Epidemiologia e Psichiatria Sociale 18, 179183.CrossRefGoogle ScholarPubMed
Versace, A, Almeida, JR, Hassel, S, Walsh, ND, Novelli, M, Klein, CR, Kupfer, DJ, Phillips, ML (2008). Elevated left and reduced right orbitomedial prefrontal fractional anisotropy in adults with bipolar disorder revealed by tract-based spatial statistics. Archives of General Psychiatry 65, 10411052.CrossRefGoogle ScholarPubMed
Vita, A, De Peri, L, Sacchetti, E (2009). Gray matter, white matter, brain, and intracranial volumes in first-episode bipolar disorder, a meta-analysis of magnetic resonance imaging studies. Bipolar Disorders 11, 807814.CrossRefGoogle ScholarPubMed
Wang, F, Jackowski, M, Kalmar, JH, Chepenik, LG, Tie, K, Qiu, M, Gong, G, Pittman, BP, Jones, MM, Shah, MP, Spencer, L, Papademetris, X, Constable, RT, Blumberg, HP (2008 b). Abnormal anterior cingulum integrity in bipolar disorder determined through diffusion tensor imaging. British Journal of Psychiatry 193, 126129.CrossRefGoogle ScholarPubMed
Wang, F, Kalmar, JH, Edmiston, E, Chepenik, LG, Bhagwagar, Z, Spencer, L, Pittman, B, Jackowski, M, Papademetris, X, Constable, RT, Blumberg, HP (2008 a). Abnormal corpus callosum integrity in bipolar disorder: a diffusion tensor imaging study. Biological Psychiatry 64, 730733.CrossRefGoogle ScholarPubMed
Wessa, M, Houenou, J, Leboyer, M, Chanraud, S, Poupon, C, Martinot, JL, Paillère-Martinot, ML (2009). Microstructural white matter changes in euthymic bipolar patients: a whole-brain diffusion tensor imaging study. Bipolar Disorders 11, 504514.CrossRefGoogle ScholarPubMed
Yurgelun-Todd, DA, Silveri, MM, Gruber, SA, Rohan, ML, Pimentel, PJ (2007). White matter abnormalities observed in bipolar disorder, a diffusion tensor imaging study. Bipolar Disorders 9, 504512.CrossRefGoogle ScholarPubMed
Zanetti, MV, Jackowski, MP, Versace, A, Almeida, JR, Hassel, S, Duran, FL, Busatto, GF, Kupfer, DJ, Phillips, ML (2009). State-dependent microstructural white matter changes in bipolar I depression. European Archives of Psychiatry and Clinical Neuroscience 259, 316328.CrossRefGoogle ScholarPubMed
Zhang, Y, Xu, H, Jiang, W, Xiao, L, Yan, B, He, J, Wang, Y, Bi, X, Li, X, Kong, J, Li, XM (2008). Quetiapine alleviates the cuprizone-induced white matter pathology in the brain of C57BL/6 mouse. Schizophrenia Research 106, 182189.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. DTI studies in bipolar disorder