Assessment of brain structural changes in patients with opium dependence disorder on Methadone Maintenance Treatment, Opium Tincture Treatment and healthy individuals

Document Type : Research Paper

Authors

1 Associate professor of psychiatry, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

2 Assistant professor of psychiatry, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

3 Radiologist, Head of Radiology Department of Razavi Hospital, Mashhad, Iran

4 Assistant professor of medical physics, Medical Physics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

5 Associate professor of medical physics, Nuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

6 Assistant professor of radiology, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran

7 Radiologist, Mashhad University of Medical Sciences, Mashhad, Iran

Abstract

Introduction: Methadone maintenance and opium tincture treatments has been recommended as harm reduction strategies for opioid-dependent patients in Iran. However, the effects of long-term administration of methadone and opium tincture on the brain are not fully understood. In this study we investigated the effects of methadone and opium tincture maintenance treatments on the brain volumes of former opium addicts by magnetic resonance imaging (MRI) volumetry of brain compared to healthy participants. 
Materials and Methods: The present case-control study was performed in Mashhad, Iran in 2015-2017. Via convenient sampling method, 36 participants were selected and allocated in 3 equal groups (methadone maintenance treatment, opium tincture treatment, and normal control). The volumes of gray matter, frontal lobe, temporal lobe, cingulate gyrus, limbic system, amygdala, and hippocampus of all participants were assessed using MRI volumetry. Data analyzed by ANOVA, using SPSS software (ver. 16). 
Results: There were no significant statistical differences between mean volumes of any assessed region of the brain among three groups (P>0.05). 
Conclusion: Methadone maintenance treatment and opium tincture treatment have no hazardous effects on the volumes of gray matter, frontal lobe, temporal lobe, cingulate gyrus, limbic system, amygdala, and hippocampus of former opium addicts.

Keywords


  1. Aldemir E, Coskunol H, Kilic M, Sert I. Treatment of opioid dependence with buprenorphine/naloxone after liver transplantation: report of two cases. Transplant Proc 2016; 48(8): 2769-72.
  2. Amin-Esmaeili M, Rahimi-Movaghar A, Sharifi V, Hajebi A, Radgoodarzi R, Mojtabai R, et al. Epidemiology of illicit drug use disorders in Iran: prevalence, correlates, comorbidity and service utilization results from the Iranian Mental Health Survey. Addiction 2016; 111(10): 1836-47.
  3. Manchikanti L, Helm S, Fellows B, Janata JW, Pampati V, Grider JS, et al. Opioid epidemic in the United States. Pain Physician 2012; 15(3 Suppl): ES9-38.
  4. Bjork JM, Grant SJ, Hommer DW. Cross-sectional volumetric analysis of brain atrophy in alcohol dependence: effects of drinking history and comorbid substance use disorder. Am J Psychiatry 2003; 160(11): 2038-45.
  5. Agartz I, Brag S, Franck J, Hammarberg A, Okugawa G, Svinhufvud K, et al. MR volumetry during acute alcohol withdrawal and abstinence: a descriptive study. Alcohol Alcohol 2003; 38(1): 71-8.
  6. Pascual-Leone A, Dhuna A, Anderson DC. Cerebral atrophy in habitual cocaine abusers: a planimetric CT study. Neurology 1991; 41(1): 34-8.
  7. Pfefferbaum A, Sullivan EV, Rosenbloom MJ, Mathalon DH, Lim KO. A controlled study of cortical gray matter and ventricular changes in alcoholic men over a 5-year interval. Arch Gen Psychiatry 1998; 55(10): 905-12.
  8. Lyoo IK, Pollack MH, Silveri MM, Ahn KH, Diaz CI, Hwang J, et al. Prefrontal and temporal gray matter density decreases in opiate dependence. Psychopharmacology (Berl) 2006; 184(2): 139-44.
  9. Li W, Li Q, Wang Y, Zhu J, Ye J, Yan X, et al. Methadone-induced damage to white matter integrity in methadone maintenance patients: A longitudinal self-control DTI study. Sci Rep 2016; 6: 19662.
  10. Farrell M, Ward J, Mattick R, Hall W, Stimson GV, des Jarlais D, et al. Methadone maintenance treatment in opiate dependence: a review. BMJ 1994; 309(6960): 997-1001.
  11. Mokri A, Noroozi A. [Protocol on management of opioid dependence with methadone]. 3rd ed. [cited 2014].  Available from: https://treatment.sbmu.ac.ir/uploads/protokol.afuni93.pdf. (Persian)
  12. Mokri A. [Protocol on management of opioid dependence with opium tincture]. 2nd ed. [cited 2011].  Available from: http://darman.fums.ac.ir/upload/17/06/28/5-protechol%20tantoor.pdf. (Persian)
  13. van Osch MJP, Webb AG. Safety of ultra-high field MRI: what are the specific risks? Curr Radiol Rep 2014; 2: 61-8.
  14. Friston K, Ashburner J, Kiebel S, Nichol T, Penny W. Statistical parametric mapping. UK: Elsevier; 2007.
  15. Statistical parametric mapping. [cited Jan 21, 2016]. Available from: http://www.fil.ion.ucl.ac.uk/spm/. 
  16. WFU_PickAtlas. [cited Jan 21, 2016]. Available from: http://www.nitrc.org/projects/wfu_pickatlas/.
  17. Language and Categorization Laboratory. [cited Jan 21, 2016]. Available from: http://www. sbirc.ed.ac. uk/LCL/LCL_M1.html.
  18. Johnson RE, Chutuape MA, Strain EC, Walsh SL, Stitzer ML, Bigelow GE. A comparison of levomethadyl acetate, buprenorphine, and methadone for opioid dependence. N Engl J Med 2000; 343(18): 1290-7.
  19. Contet C, Kieffer BL, Befort K. Mu opioid receptor: A gateway to drug addiction. Curr Opin Neurobiol 2004; 14(3): 370-8.
  20. Pezawas LM, Fischer G, Diamant K, Schneider C, Schindler SD, Thurnher M, et al. Cerebral CT findings in male opioid-dependent patients: stereological, planimetric and linear measurements. Psychiatry Res 1998; 83(3): 139-47.
  21. Tanabe J, Tregellas JR, Dalwani M, Thompson L, Owens E, Crowley T, et al. Medial orbitofrontal cortex gray matter is reduced in abstinent substance-dependent individuals. Biol Psychiatry 2009; 65(2): 160-4.
  22. Sklair-Tavron L, Shi WX, Lane SB, Harris HW, Bunney BS, Nestler EJ. Chronic morphine induces visible changes in the morphology of mesolimbic dopamine neurons. Proc Natl Acad Sci U S A 1996; 93(20): 11202-7.
  23. Berhow MT, Russell DS, Terwilliger RZ, Beitner-Johnson D, Self DW, Lindsay RM, et al. Influence of neurotrophic factors on morphine- and cocaine-induced biochemical changes in the mesolimbic dopamine system. Neuroscience 1995; 68(4): 969-79.
  24. Mohammad Ghasemi F, Dezfolyan A, Mahmoudzadeh Sagheb HR, Shohani B. [Application of the stereology technique in evaluating the addictive effects of morphine on the cerebella cortex volume in male rat]. Journal of Sabzevar University of Medical Sciences 2000; 7(1): 3-13. (Persian)
  25. Shahramian I, Heidari Z. Volumetry of brain of rat following methadone and buprenorphine administration. International journal of pharmacology 2006; 2(2): 253-5.
  26. Linden DEJ. How psychotherapy changes the brain--the contribution of functional neuroimaging. Mol Psychiatry 2006; 11(6): 528-38.