Prevalence of depressive disorders in patients with multiple sclerosis with foci of demyelination

 

Authors

 

N.V. Zarubina

Federal State Budgetary Educational Institution of Higher Education “Yaroslavl State Medical University” of the Ministry of Health of the Russian Federation, Yaroslavl, Russian Federation

 

https://doi.org/10.26617/1810-3111-2024-2(123)-32-40

 

Journal: Siberian Herald of Psychiatry and Addiction Psychiatry. 2024; 2 (123):  32-40.

 

Abstract

Background. Depressive disorders in multiple sclerosis (MS) are largely due to the processes that occur during the development of this chronic autoimmune disease. Therefore, researchers are faced with the task of searching for MRI markers of MS progression. Objective: to identify foci of demyelination in multiple sclerosis and establish their association with depressive disorders. Material and Methods. The study involved patients with relapsing-remitting MS (n=203) (n=179 – 88.2%, mean age 38±10 years, average disease duration 8.23±6.57 years, mean age of onset 30.2±10.5 years) and secondary progressive (n=24 ‒ 11.8%, mean age 46±9 years, average disease duration 8.23±6.57 years, mean age of onset 33.33±8.02 years) during MS. Two groups were formed: group 1 – patients with multiple sclerosis without depression (n=90, 44.3%), group 2 – patients with multiple sclerosis and depression (n=113, 55.7%). According to ICD-10 criteria, a diagnosis was made: mood disorders (affective disorders) (F3). Results and Discussion. The first atrophic disorders in the brain of MS patients were documented 7 years after onset of MS. Depending on the location in the brain, statistically significant differences (p<0.001) in the foci of demyelination in the right and left hemispheres were revealed. In patients with MS and comorbid depression, subcortical foci of demyelination were found statistically significantly (p<0.05) more often in the occipital lobe of the right hemisphere, the temporal lobe of the left hemisphere, and the thalamus. In the secondary progressive course of MS, juxtacortical lesions were statistically significantly (p=0.038) more common. Based on MRI data, areas of the brain that had been significant for cognitive functioning and had been responsible for emotional regulation (emotional and personality disorders, including depressive disorders) were identified. An association between foci of demyelination and anxious, melancholic, asthenic, and apathetic forms of depression was revealed. Conclusion. Depressive disorders were associated with foci of demyelination with predominant lateralization periventricularly in the frontal lobe, subcortically in the temporal lobe, in the juxtacortical regions of the left hemisphere, in the infratentorial regions of the brain, in the cerebellum and thalamus. As the duration of MS increased, the types of depression changed. The timing of the onset of the first atrophic disorders in the brain of MS patients was established. MRI markers of anxious, melancholic, asthenic, and adynamic depression in patients with MS were determined. The immunopathogenesis of MS was associated with depressive disorders. The processes of the onset and the progression of MS were the etiological factor of depression. Timely diagnosis and adequate treatment of depression could achieve a positive effect in stopping exacerbations and slowing down the progression of MS.

 

Keywords: multiple sclerosis, depressive disorders, MRI diagnostics, brain lesions, foci of demyelination.

 

Article (pdf)

 

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For citation: Zarubina N.V. Prevalence of depressive disorders in patients with multiple sclerosis with foci of demyelination. Siberian Herald of Psychiatry and Addiction Psychiatry.2024; 2 (123): 32-40. https://doi.org/10.26617/1810-3111-2024-2(123)-32-40

REFERENCES

  1. Zhang WY, Hou YL. Prognostic value of magnetic resonance imaging in patients with clinically isolated syndrome conversion to multiple sclerosis: a meta-analysis. Neurol India. 2013 May-Jun;61(3):231-8. doi: 10.4103/0028-3886.115058. PMID: 23860140.
  2. Sombekke MH, Wattjes MP, Balk LJ, Nielsen JM, Vrenken H, Uitdehaag BM, Polman CH, Barkhof F. Spinal cord lesions in patients with clinically isolated syndrome: a powerful tool in diagnosis and prognosis. Neurology. 2013 Jan 1;80(1):69-75. doi: 10.1212/WNL.0b013e31827b1a67. Epub 2012 Dec 12. PMID: 23243070.
  3. Boiko AN, Gusev EI. Modern algorithms for the diagnosis and treatment of multiple sclerosis, based on an individual assessment of the patient’s condition. S.S. Korsakov Journal of Neurology and Psychiatry. Special Issues. 2017;117(2‑2):92‑106. https://doi:10.17116/jnevro20171172292-106 (in Russian).
  4. Malygin YaV. Features of anxiety and depressive disorders in patients with multiple sclerosis at various stages of the disease. S.S. Korsakov Journal of Neurology and Psychiatry. Special Issues. 2019;119 (2‑2):58‑63. https://doi.org/10.17116/jnevro20191192258 (in Russian).
  5. Bryukhov VV, Kulikova SN, Krotenkova IA, Krotenkova MV, Peresedova AV. MRI in the diagnosis of multiple sclerosis. Medical Imaging. 2014;2:10-21 (in Russian).
  6. Geurts JJ, Bö L, Pouwels PJ, Castelijns JA, Polman CH, Barkhof F. Cortical lesions in multiple sclerosis: combined postmortem MR imaging and histopathology. AJNR Am J Neuroradiol. 2005 Mar;26(3):572-7. PMID: 15760868; PMCID: PMC7976495.
  7. Gilmore CP, Bö L, Owens T, Lowe J, Esiri MM, Evangelou N. Spinal cord gray matter demyelination in multiple sclerosis-a novel pattern of residual plaque morphology. Brain Pathol. 2006 Jul;16(3):202-8. doi: 10.1111/j.1750-3639.2006.00018.x. PMID: 16911477; PMCID: PMC8095912.
  8. Kutzelnigg A, Lucchinetti CF, Stadelmann C, Brück W, Rauschka H, Bergmann M, Schmidbauer M, Parisi JE, Lassmann H. Cortical demyelination and diffuse white matter injury in multiple sclerosis. Brain. 2005 Nov;128(Pt 11):2705-12. doi: 10.1093/brain/awh641. Epub 2005 Oct 17. PMID: 16230320.
  9. Kutzelnigg A, Faber-Rod JC, Bauer J, Lucchinetti CF, Sorensen PS, Laursen H, Stadelmann C, Brück W, Rauschka H, Schmidbauer M, Lassmann H. Widespread demyelination in the cerebellar cortex in multiple sclerosis. Brain Pathol. 2007 Jan;17(1):38-44. doi: 10.1111/j.1750-3639.2006.00041.x. PMID: 17493036; PMCID: PMC8095596.
  10. Krotenkova IA, Bryukhov, Krotenkova MV. Atrophy of the central nervous system in multiple sclerosis: data from MRI morphometry. S.S. Korsakov Journal of Neurology and Psychiatry. 2014;114(10-2):50-56 (in Russian).
  11. Smulevich AB. Depression as a general medical problem: clinical and therapeutic issues. Psychiatry and Psychopharmacology. 2006;8(3):4-10 (in Russian).
  12. Feinstein A. Multiple sclerosis and depression. Mult Scler. 2011 Nov;17(11):1276-81. doi: 10.1177/1352458511417835. PMID: 22058085.
  13. Trufanov GE, Shamrey VK, Fokin AV, Boikov IV, Abritalin EYu, Efimtsev AYu, Tarumov DA, Korzenev AV. Neuroimaging of depressive disorders. St. Petersburg: ELBI Publishing House, 2015:128 (in Russian).
  14. Mayberg HS. Limbic-cortical dysregulation: a proposed model of depression. J Neuropsychiatry Clin Neurosci. 1997 Summer;9(3):471-81. doi: 10.1176/jnp.9.3.471. PMID: 9276848.
  15. Drevets WC, Price JL, Bardgett ME, Reich T, Todd RD, Raichle ME. Glucose metabolism in the amygdala in depression: relationship to diagnostic subtype and plasma cortisol levels. Pharmacol Biochem Behav. 2002 Mar;71(3):431-47. doi: 10.1016/s0091-3057(01)00687-6. PMID: 11830178.
  16. Amat J, Paul E, Zarza C, Watkins LR, Maier SF. Previous experience with behavioral control over stress blocks the behavioral and dorsal raphe nucleus activating effects of later uncontrollable stress: role of the ventral medial prefrontal cortex. J Neurosci. 2006 Dec 20;26(51):13264-72. doi: 10.1523/JNEUROSCI.3630-06.2006. PMID: 17182776; PMCID: PMC6675012.
  17. Zavalishin IA, Spirin NN, Boiko AN, Nikitin SS. Chronic neuroinfections. Moscow: Publishing House GEOTAR-Media, 2011:560 (in Russian).
  18. Yarilin AA. Regulatory T cells / Yarilin AA. Immunology: textbook. Moscow: Publishing House GEOTAR-Media, 2010:Chapter:512-517 (in Russian).
  19. Yarilin AA. Th-17 and other adaptive T cell subsets / Yarilin AA. Immunology: textbook. Moscow: Publishing House GEOTAR-Media, 2010:Chapter:190-218(in Russian).
  20. Koch M, Uyttenboogaart M, van Harten A, Heerings M, De Keyser J. Fatigue, depression and progression in multiple sclerosis. Mult Scler. 2008 Jul;14(6):815-22. doi: 10.1177/1352458508088937. Epub 2008 Jun 5. PMID: 18535019.
  21. Mohr DC, Hart SL, Julian L, Cox D, Pelletier D. Association between stressful life events and exacerbation in multiple sclerosis: a meta-analysis. BMJ. 2004 Mar 27;328(7442):731. doi: 10.1136/bmj.38041.724421.55. Epub 2004 Mar 19. PMID: 15033880; PMCID: PMC381319.
  22. Zarubina NV, Mozokina KS, Spirin NN. The relationship between depressive disorders and MRI images of patients with multiple sclerosis. Eurasian Union of Scientists. 2020;6-5(75):45-52 (in Russian).