Structural Abnormalities in Bipolar Euthymia: A Multicontrast Molecular Diffusion Imaging Study

• Published in: Biological psychiatry (1969) 2014-08, Vol.76 (3), p.239-248
• Main Authors: Canales-Rodríguez, Erick Jorge, Pomarol-Clotet, Edith, Radua, Joaquim, Sarró, Salvador, Alonso-Lana, Silvia, Del Mar Bonnín, Caterina, Goikolea, José Manuel, Maristany, Teresa, García-Álvarez, Roberto, Vieta, Eduard, McKenna, Peter, Salvador, Raymond
• Format: Article
• Language: English
• Subjects: Adult; Adult and adolescent clinical studies; Biological and medical sciences; Bipolar disorder; Bipolar Disorder - pathology; Bipolar disorders; Brain - pathology; Diffusion Magnetic Resonance Imaging; diffusion tensor imaging (DTI); euthymia; Female; high angular resolution diffusion imaging (HARDI); Humans; magnetic resonance imaging (MRI); Male; Medical sciences; Miscellaneous; Mood disorders; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; White Matter - pathology; whole-brain statistical analysis
• ISSN: 0006-3223; 1873-2402
• DOI: 10.1016/j.biopsych.2013.09.027

Background Evidence from decades of magnetic resonance imaging (MRI) research in bipolar disorder has been summarized in meta-analyses of various MRI modalities. Notably, although structural MRI studies suggest gray matter reductions are restricted to specific cortical regions, functional MRI has also shown involvement of subcortical dysfunction. Such disparity in results is open to discussion and requires further exploration with additional MRI modalities. Methods We applied whole-brain high angular resolution molecular diffusion imaging to compare different properties of the water diffusion process in brain tissues, using different contrasts. Specifically, we looked at fractional anisotropy, mean diffusivity, probability of return to the origin, and generalized fractional anisotropy in a sample of 40 euthymic patients with bipolar disorder and 40 well-matched healthy control subjects. Results Convergent abnormalities were detected by contrasts in various tissue types. Apart from alterations in white matter (in corpus callosum, cingulum bundle, corona radiata, and superior fronto-occipital fasciculus) and cortical gray matter (in medial frontal cortex, left insula, Heschl’s gyrus, and cerebellum), three of the contrasts (fractional anisotropy, mean diffusivity, and generalized fractional anisotropy) revealed abnormalities in subcortical structures, including the hippocampus, the thalamus and the caudate nucleus. Conclusions Our findings point to a wider pattern of axonal pathology in bipolar disorder than previously thought. Although findings related to cortical gray matter are consistent with structural meta-analyses, subcortical abnormalities suggest a cytoarchitectonic basis for previously reported subcortical dysfunction. Diffusion results could be interpreted in terms of loss of tissue volume and/or altered membrane permeability, agreeing with both hypotheses of mitochondrial malfunction and neuroinflammation.