Colonoscopy: body and psyche. Can psychiatry contribute to the quality of the examination?

Authors

DOI:

https://doi.org/10.12923/2353-8627/2023-0024

Keywords:

psychiatry, gastroenterology, colonoscopy, gut-brain axis

Abstract

Introduction: The relationship between a state of a body and mind is well known, although difficult to grasp. Its existence is reflected in subsequent editions of the classifications of mental disorders. One important and frequently performed medical procedure that significantly interferes with the patient's somatic state is colonoscopy. The aim of this study was to review the literature on the patient's psychological functioning in the context of colonoscopy.

Material and methods: A review of literature in PubMed and Scopus databases was conducted. Keywords used were: colonoscopy, psychiatry, mental disorders, psychogastroenterology, gut-brain axis, anxiety, depression, cognitive functions, pain perception, limiting the search scope to 2013-2023.

Discussion: The bidirectional relationship between psychological factors and a range of functional gastrointestinal disorders, contributed to the introduction of the term psychogastroenterology. One of its important areas is the research on the gut-brain axis. The interplay between the gut microbiome and mental functioning is apparent. Colonoscopy disrupts the composition of the intestinal microflora. However, despite its invasiveness, it is still often irreplaceable for the diagnosis and treatment of bowel diseases (including colorectal cancer). Higher adherence is needed, which could be achieved by improving patient comfort. An increased level of anxiety before the procedure and its negative impact on cognitive functioning is observed. Negative affect amplifies the experience of pain. Colonoscopy technique continues to be developed. A comprehensive description of the patient's psychological functioning in a colonoscopy situation is still lacking.

Conclusions: A comprehensive description of the patient's affective and cognitive determinants in the context of colonoscopy and the associated pain and discomfort would be advisable.

References

1. Kępiński A. Lęk. Warszawa: PZWL; 1977, s.42.

2. Basavarajappa C, Dahale AB, Desai G. Evolution of bodily distress disorders. Curr Opin Psychiatry. 2020;33(5):447-450. https://doi.org/10.1097/yco.0000000000000630

3. Löwe B, Levenson J, Depping M, Hüsing P, Kohlmann S, Lehmann M, et al. Somatic symptom disorder: a scoping review on the empirical evidence of a new diagnosis. Psychol Med. 2022 Mar;52(4):632-648. https://doi.org/10.1017/s0033291721004177

4. Gomez-Bernal F, Madva EN, Puckett J, Amonoo HL, Millstein RA, Huffman JC. Relationships between life stressors, health behaviors, and chronic medical conditions in mid-life adults: a narrative review. Psychosomatics. 2019;60(2):153-63. https://doi.org/10.1016/j.psym.2018.12.007

5. International Classification of Diseases, Eleventh Revision (ICD11), World Health Organization (WHO) 2019/2021.

6. Cao J, Ding L. Psychosomatic practice in gastroenterology: new insights and models from China. Psychother Psychosom 2019;88(6):321-326. https://doi.org/10.1159/000502780

7. Koloski N, Holtmann G, Talley N. Is there a causal link between psychological disorders and functional gastrointestinal disorders? Expert Rev Gastroenterol Hepatol. 2020;14(11):1047-1059. https://doi.org/10.1080/17474124.2020.1801414

8. Keefer L, Palsson OS, Pandolfino JE. Best practice update: incorporating psychogastroenterology into management of digestive disorders. Gastroenterology. 2018;154(5):1249-1257. https://doi.org/10.1053/j.gastro.2018.01.045

9. Helander HF, Fandriks L. Surface area of the digestive tract- revisited. Scand J. Gastroenterol. 2014;49(6):681-689.

10. Sender R, Fuchs S, Milo R. Revised estimates for the number of human and bacteria cells in the body. PLoS Biol. 2016;14(8):e1002533. https://doi.org/10.1371/journal.pbio.1002533

11. Senchukova MA. Microbiota of the gastrointestinal tract: Friend or foe? World J Gastroenterol. 2023;29(1):19-42. https://doi.org/10.3748/wjg.v29.i1.19

12. Rinninella E, Raoul P, Cintoni M, Franceschi F, Miggiano GAD, Gasbarrini A, et al. What is the healthy gut microbiota composition? A changing ecosystem across age, environment, diet, and diseases. Microorganisms. 2019;7(1):14. https://doi.org/10.3390/microorganisms7010014

13. Pascale A, Marchesi N, Marelli C, Coppola A, Luzi L, Govoni S, et al. Microbiota and metabolic diseases. Endocrine 2018;61(3):357-371. https://doi.org/10.1007/s12020-018-1605-5

14. Bonaz B, Bazin T, Pellissier S. The vagus nerve at the interface of the microbiota-gut-brain axis. Front Neurosci. 2018;12:49. https://doi.org/10.3389/fnins.2018.00049

15. Shaik L, Kashyap R, Thotamgari SR, Singh R, Khanna S. Gutbrain axis and its neuro-psychiatric effects: a narrative review. Cureus. 2020;12(10):e11131. https://doi.org/10.7759/cureus.11131

16. Cuesta CM, Guerri C, Ureña J, Pascual M. Role of microbiota-derived extracellular vesicles in gut-brain communication. Int J Mol Sci. 2021;22(8):4235. https://doi.org/10.3390/ijms22084235

17. van de Wouw M, Lyte JM, Boehme M, Sichetti M, Moloney G, Goodson MS, et al. The role of the microbiota in acute stressinduced myeloid immune cell trafficking. Brain, Behavior, and Immunity. 2020;84:209-217. https://doi.org/10.1016/j.bbi.2019.12.003

18. Naveed M, Zhou QG, Xu C, Taleb A, Meng F, Ahmed B, et al. Gutbrain axis: a matter of concern in neuropsychiatric disorders…! Prog NeuroPsychopharmacol Biol Psychiatry. 2021;104:110051. https://doi.org/10.1016/j.pnpbp.2020.110051

19. Simpson CA, Diaz-Arteche C, Eliby D, Schwartz OS, Simmons JG, Cowan CSM. The gut microbiota in anxiety and depression - a systematic review. Clin Psychol Rev. 2021;83:101943. https://doi.org/10.1016/j.cpr.2020.101943

20. Maiuolo J, Gliozzi M, Musolino V, Carresi C, Scarano F, Nucera S, et al. The contribution of gut microbiota-brain axis in the development of brain disorders. Front Neurosci. 2021;15:616883. https://doi.org/10.3389/fnins.2021.616883

21. Socała K, Doboszewska U, Szopa A, Serefko A, Włodarczyk M, Zielińska A, et al. The role of microbiota-gut-brain axis in neuropsychiatric and neurological disorders. Pharmacol Res. 2021;172:105840. https://doi.org/10.1016/j.phrs.2021.105840

22. Margolis KG, Cryan JF, Mayer EA. The microbiota-gut-brain axis: From motility to mood. Gastroenterology. 2021;160(5):1486-1501. https://doi.org/10.1053/j.gastro.2020.10.066

23. Sanada K, Nakajima S, Kurokawa S, Barcelo-Soler A, Ikuse D, Hirata A, et al. Gut microbiota and major depressive disorder: a systematic review and meta-analysis. J Affect Disord. 2020;266:1-13. https://doi.org/10.1016/j.jad.2020.01.102

24. Borkent J, Ioannou M, Laman JD, Haarman BC, Sommer IE. Role of the gut microbiome in three major psychiatric disorders. Psychol Med. 2022;52(7):1222-1242. https://doi.org/10.1017/s0033291722000897

25. Valles-Colomer M, Falony G, Darzi, Y, Tigchelaar EF, Wang J, Tito RY, et al. The neuroactive potential of the human gut microbiota in quality of life and depression. Nat Microbiol. 2019;4(4):623- 632. https://doi.org/10.1038/s41564-018-0337-x

26. Marx W, McGuinness AJ, Rocks T, Ruusunen A, Cleminson J, Walker AJ, et al. The kynurenine pathway in major depressive disorder, bipolar disorder, and schizophrenia: a meta-analysis of 101 studies. Mol. Psychiatry. 2021;26(8):4158-4178. https://doi.org/10.1038/s41380-020-00951-9

27. Morris G, Berk M, Carvalho A, Caso JR, Sanz Y, Walder K, et al. The role of the microbial metabolites including tryptophan catabolites and short chain fatty acids in the pathophysiology of immune-inflammatory and neuroimmune disease. Mol Neurobiol. 2016;54(6):4432-4451. https://doi.org/10.1007/s12035-016-0004-2

28. Hoban AE, Stilling RM, Ryan FJ, Shanahan F, Dinan TG, Claesson MJ, et al. Regulation of prefrontal cortex myelination by the microbiota. Transl Psychiatry. 2016;6(4):e774. https://doi.org/10.1038/tp.2016.42

29. Nguyen TT, Kosciolek T, Eyler LT, Knight R, Jeste DV. Overview and systematic review of studies of microbiome in schizophrenia and bipolar disorder. J Psychiatr Res. 2018;99:50-61. https://doi.org/10.1016/j.jpsychires.2018.01.013

30. Yang JC, Troutman R, Buri H, Gutta A, Situ J, Aja E, et al. Ileal Dysbiosis Is Associated with Increased Acoustic Startle in the 22q11.2 Microdeletion Mouse Model of Schizophrenia. Nutrients. 2023;15(16):3631. https://doi.org/10.3390/nu15163631

31. Zhu F, Guo R, Wang W, Ju Y, Wang Q, Ma Q, et al. Transplantation of microbiota from drug-free patients with schizophrenia causes schizophrenia-like abnormal behaviors and dysregulated kynurenine metabolism in mice. Mol Psychiatry. 2019;25(11):2905-2918. https://doi.org/10.1038/s41380-019-0475-4

32. Zheng P, Zeng B, Liu M, Chen J, Pan J, Han Y, et al. The gut microbiome from patients with schizophrenia modulates the glutamate-glutamine-GABA cycle and schizophrenia-relevant behaviors in mice. Sci Adv. 2019;5(2):eaau8317. https://doi.org/10.1126/sciadv.aay2759

33. Uno Y, Coyle JT. Glutamate hypothesis in schizophrenia. Psychiatry Clin Neurosci. 2019;73(5):204-215.

34. Khandaker GM, Cousins L, Deakin J, Lennox BR, Yolken R, Jones PB. Inflammation and immunity in schizophrenia: implications for pathophysiology and treatment. Lancet Psychiatry. 2015;2(3):258-270. https://doi.org/10.1016/s2215-0366(14)00122-9

35. Fond G, Lançon C, Korchia T, Auquier P, Boyer L. The role of inflammation in the treatment of schizophrenia. Front. Psychiatry. 2020;11:160. https://doi.org/10.3389/fpsyt.2020.00160

36. Karakuła-Juchnowicz H, Dzikowski M, Pelczarska A, Dzikowska I, Juchnowicz D. The brain-gut axis dysfunctions and hypersensitivity to food antigens in the etiopathogenesis of schizophrenia. Psychiatr Pol. 2016;50(4):747-760. https://doi.org/10.12740/pp/onlinefirst/45053

37. Nemani K, Hosseini Ghomi R, McCormick B, Fan X. Schizophrenia and the gut-brain axis. Prog Neuropsychopharmacology Biol Psychiatry. 2015;56:155-160. https://doi.org/10.1016/j.pnpbp.2014.08.018

38. Schwarz E, Maukonen J, Hyytiäinen T, Kieseppä T, Orešiè M, Sabunciyan S, et al. Analysis of microbiota in first episode psychosis identifies preliminary associations with symptom severity and treatment response. Schizophr Res. 2018;192:398-403. https://doi.org/10.1016/j.schres.2017.04.017

39. Bartoli F, Misiak B, Callovini T, Cavaleri D, Cioni RM, Crocamo C, et al. The kynurenine pathway in bipolar disorder: a metaanalysis on the peripheral blood levels of tryptophan and related metabolites. Mol Psychiatry. 2021;26(7):3419-3429. https://doi.org/10.1038/s41380-020-00913-1

40. Puricelli C, Rolla R, Gigliotti L, Boggio E, Beltrami E, Dianzani U, et al. The gut-brain-immune axis in autism spectrum disorders: a state-of-art report. Front Psychiatry. 2022;12:755171. https://doi.org/10.3389/fpsyt.2021.755171

41. Jang SH, Woo YS, Lee SY, Bahk WM. The brain-gut-microbiome axis in psychiatry. Int J Mol Sci. 2020;21(19):7122. https://doi.org/10.3390/ijms21197122

42. Rog A, Skonieczna-Żydecka K, Juchnowicz D, Padała O, Łoniewski I, Budzyńska B, et al. Gut microbiota and intestinal barrierrelated markers in patients with anorexia nervosa: systematic review. Psychiatr Pol. 2022;1-20. https://doi.org/10.12740/pp/onlinefirst/140069

43. Karakuła-Juchnowicz H, Pankowicz H, Juchnowicz D, Valverde Piedra JL, Małecka-Massalska T. Intestinal microbiota - a key to understanding the pathophysiology of anorexia nervosa? Psychiatr Pol. 2017;51(5):859-870. https://doi.org/10.12740/pp/65308

44. Wang Z, Wang Z, Lu T, Chen W, Yan W, Yuan K, et al. The microbiota-gut-brain axis in sleep disorders. Sleep Med Rev. 2022;65:101691. https://doi.org/10.1016/j.smrv.2022.101691

45. Wang SC, Chen YC, Chen SJ, Lee CH, Cheng CM. Alcohol addiction, gut microbiota, and alcoholism treatment: a review. Int J Mol Sci. 2020;21(17):6413.

46. Bastiaanssen TFS, Cowan CSM, Claesson MJ, Dinan TG, Cryan JF. Making Sense of … the Microbiome in Psychiatry. Int J Neuropsychopharmacol. 2019;22(1):37-52. https://doi.org/10.1093/ijnp/pyy067

47. Stopińska K, Radziwoń-Zaleska M, Domitrz I. The microbiotagut-brain axis as a key to neuropsychiatric disorders: a mini review. J Clin Med. 2021;10(20):4640. https://doi.org/10.3390/jcm10204640

48. Li S, Hua D, Wang Q, Yang L, Wang X, Luo A, et al. The role of bacteria and its derived metabolites in chronic pain and depression: recent findings and research progress. Int J Neuropsychopharmacol. 2020;23(1):26-41. https://doi.org/10.1093/ijnp/pyz061

49. Vancamelbeke M, Vermeire S. The Intestinal Barrier: A Fundamental Role in Health and Disease. Expert Rev Gastroenterol Hepatol. 2017;11(9):821-834. https://doi.org/10.1080/17474124.2017.1343143

50. Staudacher HM, Mikocka-Walus A, Ford AC. Common mental disorders in irritable bowel syndrome: pathophysiology, management, and considerations for future randomised controlled trials. Lancet Gastroenterol Hepatol. 2021;6(5):401-410. https://doi.org/10.1016/s2468-1253(20)30363-0

51. Suganya K, Koo B-S. Gut-brain axis: role of gut microbiota on neurological disorders and how probiotics/prebiotics beneficially modulate microbial and immune pathways to improve brain functions. Int. J. Mol. Sci. 2020;21(20):7551. https://doi.org/10.3390/ijms21207551

52. Goh KK, Liu Y-W, Kuo P.-H., Chung Y-CE, Lu M-L, Chen C-H. Effect of probiotics on depressive symptoms: a meta-analysis of human studies. Psychiatry Res. 2019;282:112568.

53. Drago L, Casini V, Pace F. Gut microbiota, dysbiosis and colon lavage. Dig Liver Dis. 2019;51(9):1209-1213. https://doi.org/10.1016/j.dld.2019.06.012

54. Meroni G, Pace F, Grossi E, Casini V, Drago L. Bacterial network community in fecal and endoluminal Microbiota after colonoscopy. New Microbiol. 2020;43(1):22-27.

55. Kim JH, Choi YJ, Kwon HJ, Jung K, Kim SE, Moon W, et al. Effect of gut microbiome on minor complications after a colonoscopy. Intest Res. 2021;19(3):341-348. https://doi.org/10.5217/ir.2020.00057

56. Di Leo M, Iannone A, Arena M, Losurdo G, Palamara MA, Iabichino G, et al. Novel frontiers of agents for bowel cleansing for colonoscopy. World J Gastroenterol. 2021;27(45):7748-7770. https://doi.org/10.3748/wjg.v27.i45.7748

57. Nagata N, Tohya M, Fukuda S, Suda W, Nishijima S, Takeuchi F, et al. Effects of bowel preparation on the human gut microbiome and metabolome. Sci Rep. 2019;9(1):4042. https://doi.org/10.1038/s41598-019-40182-9

58. Palleja A, Mikkelsen KH, Forslund SK, Kashani A, Allin KH, Nielsen T, et al. Recovery of gut microbiota of healthy adults following antibiotic exposure. Nat Microbiol. 2018;3(11):1255- 1265. https://doi.org/10.1038/s41564-018-0257-9

59. Kaminski MF, Robertson DJ, Senore C, Rex DK. Optimizing the quality of colorectal cancer screening worldwide. Gastroenterology. 2020;158(2):404-17. https://doi.org/10.1053/j.gastro.2019.11.026

60. Wu W, Huang J, Yang Y, Gu K, Luu HN, Tan S, et al. Adherence to colonoscopy in cascade screening of colorectal cancer: a systematic review and meta-analysis. J Gastroenterol Hepatol. 2022;37(4):620-631. https://doi.org/10.1111/jgh.15762

61. Saito Y, Oka S, Kawamura T, Shimoda R, Sekiguchi M, Tamai N, et al. Colonoscopy screening and surveillance guidelines. Dig Endosc. 2021;33(4):486-519. https://doi.org/10.1111/den.13972

62. Chandan S, Facciorusso A, Yarra P, Khan SR, Ramai D, Mohan BP, et al. Colonoscopy related adverse events in patients with abnormal stool-based tests: a systematic review of literature and meta-analysis of outcomes. Am J Gastroenterol 2022;117(3):381-393. https://doi.org/10.14309/ajg.0000000000001614

63. Kanth P, Inadomi JM. Screening and prevention of colorectal cancer. BMJ. 2021;374:n1855. https://doi.org/10.1136/bmj.n1855

64. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209-249. https://doi.org/10.3322/caac.21660

65. Li P, He X, Yang X, Du J, Wu W, Tu J. Patient education by smartphones for bowel preparation before colonoscopy. Gastrology and Hepatology. 2022;37(7):1349-1359. https://doi.org/10.1111/jgh.15849

66. Yang C, Sriranjan V, Abou-Setta AM, Poluha W, Walker JR, Singh, H. Anxiety associated with colonoscopy and flexible sigmoidoscopy: a systematic review. The American Journal of Gastroenterology. 2018;113(12):1810-1818. https://doi.org/10.1038/s41395-018-0398-8

67. Shafer LA, Walker JR, Waldman C, Yang C, Michaud V, Bernstein CN, et al. Factors associated with anxiety about colonoscopy: the preparation, the procedure, and the anticipated findings. Dig Dis Sci. 2018;63(3):610-8. https://doi.org/10.1007/s10620-018-4912-z

68. Park J, Moghaddam B. Impact of anxiety on prefrontal cortex encoding of cognitive flexibility. Neuroscience. 2017;345:193-202. https://doi.org/10.1016/j.neuroscience.2016.06.013

69. Ackland GL, Harrington J, Downie P, Holding JW, Singh-Ranger D, Griva K,et al. Dehydration induced by bowel preparation in older adults does not result in cognitive dysfunction. Anesth Analg. 2008;106(3):924-929. https://doi.org/10.1213/ane.0b013e3181615247

70. Wadsworth P, Blackburne H, Dixon L, Dobbs B, Eglinton T, Ing A. Does Bowel Preparation for Colonoscopy Affect Cognitive Function? Medicine (Baltimore). 2015;94(44):e1823. https://doi.org/10.1097/md.0000000000001823

71. Reumkens A, van der Zander Q, Winkens B, Bogie R, Bakker CM, Sanduleanu S, et al. Electrolyte disturbances after bowel preparation for colonoscopy: systematic review and metaanalysis. Dig Endosc. 2022;34(5):913-926. https://doi.org/10.1111/den.14237

72. Hsueh F-C, Chen C-M, Sun C-A, Chou Y-C, Hsiao S-M, Yang T. A Study on the effects of a health education intervention on anxiety and pain during colonoscopy procedures. J Nurs Res. 2016;24(2):181-9. https://doi.org/10.1097/jnr.0000000000000112

73. Xiao X, Zhang YQ. A new perspective on the anterior cingulate cortex and affective pain. Neurosci Biobehav Rev. 2018;90:200-211.

74. Fu L, Dai M, Liu J, Shi H, Pan J, Lan Y, et al. Study on the influence of assistant experience on the quality of colonoscopy: a pilot single-center study. Medicine (Baltimore), 2019;98(45):e17747. https://doi.org/10.1097/md.0000000000017747

75. Sapci I, Jia X, Wu J, Gorgun E, Liska D, Church J, et al. Does time of day matter for colonoscopy quality? A review of over 13,000 screening colonoscopies in a colorectal surgery unit. Am J Surg. 2022;223(3):500-502. https://doi.org/10.1016/j.amjsurg.2021.11.032

76. Ramai D, Singh J, Brooks OW, Barakat M, Mohan BP, Chandan S, et al. Comparison of left versus right lateral starting position on colonoscopy: a systematic review and metaanalysis of randomized controlled trials. Ann Gastroenterol. 2021;34(5):699-704. https://doi.org/10.20524/aog.2021.0639

77. Sorkpor SK, Johnson CM, Santa Maria DM, Miao H, Moore C, Ahn H. The effect of music listening on pain in adults undergoing colonoscopy: a systematic review and meta-analysis. J Perianesth Nurs. 2021;36(5):573-580.e1. https://doi.org/10.1016/j.jopan.2020.12.012

78. Shine R, Bui A, Burgess A. Quality indicators in colonoscopy: an evolving paradigm. ANZ J Surg. 2020;90(3):215-221. https://doi.org/10.1111/ans.15775

79. Seward E. Recent advances in colonoscopy. F1000Res. 2019;8:F1000 Faculty Rev-1028.

80. Joseph J, LePage EM, Cheney CP, Pawa R. Artificial intelligence in colonoscopy. World J Gastroenterol. 2021;27(29):4802-4817. https://doi.org/10.3748/wjg.v27.i29.4802

81. Khan R, Zheng E, Wani SB, Scaffidi MA, Jeyalingam T, Gimpaya N, et al. Colonoscopy competence assessment tools: a systematic review of validity evidence. Endoscopy. 2021;53(12):1235-1245. https://doi.org/10.1055/a-1352-7293

82. Rosvall A, Gershater MA, Kumlien C, Toth E. Patient-reported experience measures for colonoscopy: a systematic review and meta-ethnography. https://doi.org/10.3390/diagnostics12020242

Downloads

Published

2023-11-02