Functional characteristics of the right ventral frontal/anterior insular cortex in the pathogenesis of delusions: a pilot study
https://doi.org/10.14412/2074-2711-2023-3-27-34
Abstract
Brain lesion studies demonstrated that the right ventral frontal/anterior insular cortex (r-VF/AI) and its functional connectivity (FC) can play an important role in belief evaluation and delusions of various content.
Objective: to test the hypothesis about the associations between the functional characteristics of this region and delusions in patients with mental disorders.
Material and methods. The sample included 16 patients with delusional disorder and paranoid schizophrenia. We analyzed the whole-brain FC of the r-VF/AI as well as the local coherence and amplitude of low-frequency fluctuations of BOLD signal in this region.
Results. The “Conviction” item of the Brown Assessment of Beliefs Scale was positively correlated with the FC between the region of interest and a cluster in the right occipital cortex (located predominantly in the occipital fusiform gyrus and the occipital pole and slightly extending to the lingual gyrus and inferior lateral occipital cortex). Local coherence and amplitude of low-frequency fluctuations in the region of interest were not associated with clinical characteristics related to delusions.
Conclusion. The correlations of delusional conviction with FC between the regions involved in belief evaluation and visual perception may reflect aberrant top-down/bottom-up or cyclic processes described within the Bayesian models of delusions.
About the Authors
Ya. R. PanikratovaRussian Federation
Yana Romanovna Panikratova
34, Kashirskoe Shosse, Moscow 115522
Competing Interests:
There are no conflicts of interest
E. G. Abdullina
Russian Federation
34, Kashirskoe Shosse, Moscow 115522
Competing Interests:
There are no conflicts of interest
I. S. Lebedeva
Russian Federation
34, Kashirskoe Shosse, Moscow 115522
Competing Interests:
There are no conflicts of interest
K. Yu. Dmitrenko
Russian Federation
2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
P. G. Yuzbashian
Russian Federation
2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
E. V. Ilyina
Russian Federation
2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
G. P. Kostyuk
Russian Federation
2/4, Bolshaya Pirogovskaya St., Moscow 119991; 2, Zagorodnoe Shosse, Moscow 117152
Competing Interests:
There are no conflicts of interest
A. V. Andrushchenko
Russian Federation
2, Zagorodnoe Shosse, Moscow 117152
Competing Interests:
There are no conflicts of interest
E. I. Voronova
Russian Federation
34, Kashirskoe Shosse, Moscow 115522; 2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
I. Yu. Dorozhenok
Russian Federation
34, Kashirskoe Shosse, Moscow 115522; 2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
D. V. Romanov
Russian Federation
34, Kashirskoe Shosse, Moscow 115522; 2/4, Bolshaya Pirogovskaya St., Moscow 119991
Competing Interests:
There are no conflicts of interest
References
1. Sadock BJ, Sadock VA, Ruiz P, eds. Kaplan and Sadock’s comprehensive textbook of psychiatry. 10th ed. Philadelphia: Wolters Kluwer; 2017.
2. Gao B, Wang Y, Liu W, et al. Spontaneous Activity Associated with Delusions of Schizophrenia in the Left Medial Superior Frontal Gyrus: A Resting-State fMRI Study. PLoS One. 2015;10(7):e0133766. doi: 10.1371/journal.pone.0133766
3. Vicens V, Radua J, Salvador R, et al. Structural and functional brain changes in delusional disorder. Br J Psychiatry. 2016;208(2):153-9. doi: 10.1192/bjp.bp.114.159087
4. Li T, Wang Q, Zhang J, et al. Brain-Wide Analysis of Functional Connectivity in First-Episode and Chronic Stages of Schizophrenia. Schizophr Bull. 2017;43(2):436-48. doi: 10.1093/schbul/sbw099
5. Ferri J, Ford JM, Roach BJ, et al. Restingstate thalamic dysconnectivity in schizophrenia and relationships with symptoms. Psychol Med. 2018;48(15):2492-9. doi: 10.1017/S003329171800003X
6. Chen X, Duan M, He H, et al. Functional abnormalities of the right posterior insula are related to the altered self-experience in schizophrenia. Psychiatry Res Neuroimaging. 2016;256:26-32. doi: 10.1016/j.pscychresns.2016.09.006
7. Orliac F, Naveau M, Joliot M, et al. Links among resting-state default-mode network, salience network, and symptomatology in schizophrenia. Schizophr Res. 2013;148(1-3):74-80. doi: 10.1016/j.schres.2013.05.007
8. Csukly G, Szabo A, Polgar P, et al. Fronto-thalamic structural and effective connectivity and delusions in schizophrenia: a combined DTI/DCM study. Psychol Med. 2021 Sep;51(12):2083-93. doi: 10.1017/S0033291720000859. Epub 2020 Apr 24.
9. Limongi R, Mackinley M, Dempster K, et al. Frontal-striatal connectivity and positive symptoms of schizophrenia: implications for the mechanistic basis of prefrontal rTMS. Eur Arch Psychiatry Clin Neurosci. 2021;271(1):3-15. doi: 10.1007/s00406-02001163-6
10. Arjmand S, Kohlmeier KA, Behzadi M, et al. Looking into a Deluded Brain through a Neuroimaging Lens. Neuroscientist. 2021;27(1):73-87. doi: 10.1177/1073858420936172
11. Joyce EM. Organic psychosis: The pathobiology and treatment of delusions. CNS Neurosci Ther. 2018;24(7):598-603. doi: 10.1111/cns.12973
12. Darby RR, Laganiere S, Pascual-Leone A, et al. Finding the imposter: brain connectivity of lesions causing delusional misidentifications. Brain. 2017;140(2):497-507. doi: 10.1093/brain/aww288
13. Gurin L, Blum S. Delusions and the Right Hemisphere: A Review of the Case for the Right Hemisphere as a Mediator of RealityBased Belief. J Neuropsychiatry Clin Neurosci. 2017;29(3):225-35. doi: 10.1176/appi.neuropsych.16060118
14. Perianez JA, Lubrini G, Garcia-Gutierrez A, Rios-Lago M. Construct Validity of the Stroop Color-Word Test: Influence of Speed of Visual Search, Verbal Fluency, Working Memory, Cognitive Flexibility, and Conflict Monitoring. Arch Clin Neuropsychol. 2021;36(1):99-111. doi: 10.1093/arclin/acaa034
15. Petrolini V. When emotion and cognition do (not) work together: Delusions as emotional and executive dysfunctions. Behav Brain Sci. 2015;38:e84. doi: 10.1017/S0140525X14000995
16. Rotarska-Jagiela A, van de Ven V, Oertel-Knochel V, et al. Resting-state functional network correlates of psychotic symptoms in schizophrenia. Schizophr Res. 2010;117(1):21-30. doi: 10.1016/j.schres.2010.01.001
17. Walker DA. JMASM9: Converting Kendall’s Tau For Correlational Or MetaAnalytic Analyses. J Modern Appl Stat Meth. 2003;2(2):525-30. doi: 10.22237/jmasm/1067646360
18. Faul F, Erdfelder E, Lang AG, Buchner A. G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007;39(2):175-91. doi: 10.3758/bf03193146
19. Kay SR, Fiszbein A, Opler LA. The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophr Bull. 1987;13(2):261-76. doi: 10.1093/schbul/13.2.261
20. Eisen JL, Phillips KA, Baer L, et al. The Brown Assessment of Beliefs Scale: reliability and validity. Am J Psychiatry. 1998;155(1):102-8. doi: 10.1176/ajp.155.1.102
21. Assanovich MV, Assanovich MA.Evaluation of psychometric properties and minimally clinically important differences of the Brown Assessment of Beliefs Scale (BABS) in schizophrenia. Psikhiatriya, psikhoterapiya i klinicheskaya psikhologiya = Psychiatry, Psychotherapy and Clinical Psychology. 2019;10(1):61-8 (In Russ.).
22. Keefe RS, Goldberg TE, Harvey PD, et al. The Brief Assessment of Cognition in Schizophrenia: reliability, sensitivity, and comparison with a standard neurocognitive battery. Schizophr Res. 2004;68(2-3):283-97. doi: 10.1016/j.schres.2003.09.011
23. Sarkisyan GR, Gurovich IYa, Keefe RS. Normative data for the Russian population and standardization of the Brief Assessment of Cognition in Schizophrenia (BACS) Scale. Sotsial’naya i klinicheskaya psikhiatriya = Social and Clinical Psychiatry. 2010;20(3):13-9 (In Russ.).
24. Stangeland H, Orgeta V, Bell V. Poststroke psychosis: a systematic review. J Neurol Neurosurg Psychiatry. 2018;89(8):879-85. doi: 10.1136/jnnp-2017-317327
25. Wang L, Mruczek RE, Arcaro MJ, Kastner S. Probabilistic Maps of Visual Topography in Human Cortex. Cereb Cortex. 2015;25(10):3911-31. doi: 10.1093/cercor/bhu277
26. Grill-Spector K, Malach R. The human visual cortex. Annu Rev Neurosci. 2004;27:649-77. doi: 10.1146/annurev.neuro.27.070203.144220
27. Nielsen KM, Nordgaard J, Henriksen MG. Delusional Perception Revisited. Psychopathology. 2022;55(6):325-34. doi: 10.1159/000524642. Epub 2022 May 19.
28. Abdel-Hamid M, Brune M. Neuropsychological aspects of delusional disorder. Curr Psychiatry Rep. 2008;10(3):229-34. doi: 10.1007/s11920-008-0038-x
29. DeCross SN, Farabaugh AH, Holmes AJ, et al. Increased amygdala-visual cortex connectivity in youth with persecutory ideation. Psychol Med. 2020;50(2):273-83. doi: 10.1017/S0033291718004221
30. Orliac F, Delamillieure P, Delcroix N, et al. Network modeling of resting state connectivity points towards the bottom up theories of schizophrenia. Psychiatry Res Neuroimaging. 2017;266:19-26. doi: 10.1016/j.pscychresns.2017.04.003
31. Maher BA. Delusional thinking and perceptual disorder. J Individ Psychol. 1974;30(1):98-113.
32. Hohwy J. Top-Down and Bottom-Up in Delusion Formation. Philosophy, Psychiatry, Psychology. 2004;11(1):65-70. doi: 10.1353/ppp.2004.0043
33. Williams D. Hierarchical Bayesian models of delusion. Conscious Cogn. 2018;61:129-47. doi: 10.1016/j.concog.2018.03.003
Review
For citations:
Panikratova Y.R., Abdullina E.G., Lebedeva I.S., Dmitrenko K.Yu., Yuzbashian P.G., Ilyina E.V., Kostyuk G.P., Andrushchenko A.V., Voronova E.I., Dorozhenok I.Yu., Romanov D.V. Functional characteristics of the right ventral frontal/anterior insular cortex in the pathogenesis of delusions: a pilot study. Neurology, Neuropsychiatry, Psychosomatics. 2023;15(3):27-34. (In Russ.) https://doi.org/10.14412/2074-2711-2023-3-27-34