Neuroimaging procedures and related acquisitions in bipolar disorder: state of the art
- PMID: 24572578
- DOI: 10.1708/1407.15619
Neuroimaging procedures and related acquisitions in bipolar disorder: state of the art
Abstract
Bipolar disorder (BD) is a chronic and disabling mood disorder, with significant suicide rates among psychiatric disorders. Although the pathophysiological bases of BD have not been fully elucidated yet, over the last two decades, neuroimaging research has documented specific neuroanatomic and functional abnormalities in bipolar patients. The present review was aimed to provide an updated and comprehensive overview about currently available evidence on main structural and functional alterations documented in BD by neuroimaging procedures, through a Medline research. Among the structural alterations, the most consistent ones seem to be at the level of frontal, temporal and insular cortices, amygdala and basal ganglia, having been ventriculomegaly reported as well. Magnetic resonance spectroscopy findings showed, in turn, biochemical alterations in several neurotransmitter systems. Functional neuroimaging data are quite heterogeneous with positron emission tomography and single photon emission computed tomography studies showing phase-specific abnormalities of blood flow and glucose metabolism, as well as modifications of serotonin transporter density and binding. Functional magnetic resonance imaging data documented impaired neural networks involved in emotional regulation, including anterior limbic, ventral and dorsal prefrontal regions. Taken as a whole, neuroimaging data are strongly advancing the understanding of the neural bases of BD as described in the present review.
Similar articles
-
[Neuroimaging of bipolar disorders].Fortschr Neurol Psychiatr. 2013 May;81 Suppl 1:S17-21. doi: 10.1055/s-0033-1335378. Epub 2013 May 16. Fortschr Neurol Psychiatr. 2013. PMID: 23681711 Review. German.
-
Cerebral blood flow, metabolic, receptor, and transporter changes in bipolar disorder: the role of PET and SPECT studies.Int Rev Psychiatry. 2009;21(4):323-35. doi: 10.1080/09540260902962131. Int Rev Psychiatry. 2009. PMID: 20374147 Review.
-
Cerebral blood flow in bipolar disorder: A systematic review.J Affect Disord. 2018 Dec 1;241:505-513. doi: 10.1016/j.jad.2018.08.040. Epub 2018 Aug 11. J Affect Disord. 2018. PMID: 30149339
-
Neuroimaging in bipolar disorder: what have we learned?Biol Psychiatry. 2000 Sep 15;48(6):505-17. doi: 10.1016/s0006-3223(00)00982-3. Biol Psychiatry. 2000. PMID: 11018223 Review.
-
New insights help define the pathophysiology of bipolar affective disorder: neuroimaging and neuropathology findings.Prog Neuropsychopharmacol Biol Psychiatry. 2004 Sep;28(6):943-60. doi: 10.1016/j.pnpbp.2004.05.040. Prog Neuropsychopharmacol Biol Psychiatry. 2004. PMID: 15380855 Review.
Cited by
-
Increased Asymmetric Perfusion of the Cerebral Cortices and Thalamus Indicates Individuals at Risk for Bipolar Disorder: A Family Cohort Single Photon Emission Computed Tomography Neuroimaging Study.Front Psychiatry. 2022 May 10;13:829561. doi: 10.3389/fpsyt.2022.829561. eCollection 2022. Front Psychiatry. 2022. PMID: 35619621 Free PMC article.
-
DTI and Myelin Plasticity in Bipolar Disorder: Integrating Neuroimaging and Neuropathological Findings.Front Psychiatry. 2016 Mar 1;7:21. doi: 10.3389/fpsyt.2016.00021. eCollection 2016. Front Psychiatry. 2016. PMID: 26973545 Free PMC article. Review.
-
Decreased Functional Connectivity in Insular Subregions in Depressive Episodes of Bipolar Disorder and Major Depressive Disorder.Front Neurosci. 2018 Nov 14;12:842. doi: 10.3389/fnins.2018.00842. eCollection 2018. Front Neurosci. 2018. PMID: 30487732 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical