Pharmacogenetic Biomarkers of Clozapine-Induced Sialorrhoea: A Systematic Review
https://doi.org/10.30895/2312-7821-2025-517
Abstract
INTRODUCTION. Despite the proven clozapine effectiveness in patients with treatment resistant schizophrenia, its use can cause adverse drug reactions, including clozapine-induced sialorrhea (CIS). Data on CIS pathogenesis are limited. Identifying CIS pharmacogenetic predictors will make it possible to both predict adverse drug reactions prior to therapy and specify individual pathogenetic elements.
AIM. This review aimed to identify CIS predictors using systematic analysis of literature data.
DISCUSSION. Research was conducted independently by two co-authors using PubMed, Google Scholar, GeneCads, and PharmGKB databases. A total of six (6) studies were selected that examined 17 candidate genes. The ADRA2A and DRD4 genes were associated with CIS. Polymorphism rs1800544 of ADRA2A gene regulates the expression of alpha-2A adrenoreceptor (ADRA2A). Alpha-2-adrenoreceptors regulate salivation, thus clozapine antagonistic effect causes CIS. Polymorphism of 120-bp DRD4 will reduce expression of type 4 dopamine receptor (DRD4). In turn, this may result in CIS as clozapine increases the receptor blockade. However, the results contradicted other studies, presumably due to assessment of different polymorphisms in the above studies. Moreover, the analysed studies had a number of methodological limitations.
CONCLUSIONS. The performed systematic review made it possible to identify CIS pharmacogenetic predictors. However, large multicenter studies using a strong prospective design and considering these limitations are required in order to develop a pharmacogenetic panel with high predictive accuracy for CIS.
REGISTRATION. Systematic review protocol is included in the national systematic review register (PROSPERO), Registry No. CRD420251089235.
Keywords
About the Authors
A. G. KirovaRussian Federation
Anastasia G. Kirova
2/1/1 Barrikadnaya St., Moscow 125993
Yu. S. Bellevich
Russian Federation
Yuri S. Bellevich
2/1/1 Barrikadnaya St., Moscow 125993
D. N. Sosin
Russian Federation
Dmitriy N. Sosin, Cand. Sci. (Med.), Associate Professor
2/1/1 Barrikadnaya St., Moscow 125993;
2/1 Abrikosovsky Lane, Moscow 119435
S. N. Mosolov
Russian Federation
Sergey N. Mosolov, Dr. Sci. (Med.), Professor
2/1/1 Barrikadnaya St., Moscow 125993;
3 Poteshnaya St., Moscow 107076
D. A. Sychev
Russian Federation
Dmitry A. Sychev, Academician of the Russian Academy of Sciences, Dr. Sci. (Med.), Professor
2/1/1 Barrikadnaya St., Moscow 125993;
2/1 Abrikosovsky Lane, Moscow 119435
References
1. Owen MJ, Sawa A, Mortensen PB. Schizophrenia. The Lancet. 2016;388(10039):86–97. https://doi.org/10.1016/S0140-6736(15)01121-6
2. Orzelska-Górka J, Mikulska J, Wiszniewska A, Biała G. New atypical antipsychotics in the treatment of schizophrenia and depression. Int J Mol Sci. 2022;23(18):10624. https://doi.org/10.3390/ijms231810624
3. Lally J, MacCabe JH. Antipsychotic medication in schizophrenia: A review. Br Med Bull. 2015;114(1):169–79. https://doi.org/10.1093/bmb/ldv017
4. Mosolov SN, Tsukarzi EE. Psychopharmacotherapy of schizophrenia. In: Aleksandrovsky YuA, Neznanov NG, eds. Psychiatry: National guidelines. Moscow: GEOTAR-Media; 2018. P. 299–328 (In Russ.).
5. Mosolov SN, Tsukarzi EE, Alfimov PV. Algorithms of biological therapy for schizophrenia. Current Therapy of Mental Disorders. 2014;(1):27–36 (In Russ.). EDN: QEWBKY
6. Correll CU, Agid O, Crespo-Facorro B, et al. A Guideline and checklist for initiating and managing clozapine treatment in patients with treatment-resistant schizophrenia. CNS Drugs. 2022;36(7):659–79. https://doi.org/10.1007/s40263-022-00932-2
7. Mizuno Y, McCutcheon RA, Brugger SP, Howes OD. Heterogeneity and efficacy of antipsychotic treatment for schizophrenia with or without treatment resistance: A meta-analysis. Neuropsychopharmacology. 2020;45(4):622–31. https://doi.org/10.1038/s41386-019-0577-3
8. Khasanova AK, Kovrizhnykh IV, Mosolov SN. Antisuicidal effect of clozapine (prescribing algorithm and clinical monitoring). Current Therapy of Mental Disorders. 2023;(4):48–63 (In Russ.). https://doi.org/10.21265/PSYPH.2023.31.74.005
9. Aliforenko AE, Khasanov VA, Larchenko VV, et al. Comparative efficacy and tolerability of immediate-release clozapine (AZALEPTIN®) and extended-release clozapine (Azaleptin® retard) in patients with schizophrenia resistant to antipsychotic therapy. Current Therapy of Mental Disorders. 2025;(2):2–10 (In Russ.). https://doi.org/10.48612/psyph/tf4x-dnzt-934b
10. Citrome L, McEvoy JP, Saklad SR. Guide to the management of clozapine-related tolerability and safety concerns. Clin Schizophr Relat Psychoses. 2016;10(3):163–77. https://doi.org/10.3371/1935-1232.10.3.163
11. Sosin DN, Khasanova AK, Moshevitin SYu, Mosolov SN. Pharmacogenetics predictors of clozapine metabolic disturbances. Current Therapy of Mental Disorders. 2024;(4):30–40 (In Russ.). EDN: FCSIOX
12. Gürcan G, Atalay B, Deveci E. Clozapine-associated sialorrhea. J Clin Psychopharmacol. 2024;44(6):570–5. https://doi.org/10.1097/JCP.0000000000001917
13. Uzun Ö, Bolu A, Çelik C. Effect of N-acetylcysteine on clozapine-induced sialorrhea in schizophrenic patients: a case series. Int Clin Psychopharmacol. 2020;35(4):229–31. https://doi.org/10.1097/YIC.0000000000000297
14. Maher S, Cunningham A, O’Callaghan N, et al. Clozapine-induced hypersalivation: an estimate of prevalence, severity and impact on quality of life. Ther Adv Psychopharmacol. 2016;6(3):178–84. https://doi.org/10.1177/2045125316641019
15. Yellepeddi VK, Race JA, McFarland MM, Constance JE, Fanaeian E, Murphy NA. Effectiveness of atropine in managing sialorrhea: A systematic review and meta-analysis. Int J Clin Pharmacol Ther. 2024;62(6):267–77. https://doi.org/10.5414/CP204538
16. Leung JG, Nelson S, Barreto JN, Schiavo DN. Necrotizing pneumonia in the setting of elevated clozapine levels. J Clin Psychopharmacol. 2016;36(2):176–8. https://doi.org/10.1097/JCP.0000000000000470
17. Saenger RC, Finch TH, Francois D. Aspiration pneumonia due to clozapine-induced sialorrhea. Clin Schizophr Relat Psychoses. 2016;9(4):170–2. https://doi.org/10.3371/CSRP.SAFI.061213
18. de Leon J, Ruan CJ, Verdoux H, Wang C. Clozapine is strongly associated with the risk of pneumonia and inflammation. Gen Psychiatr. 2020;33(2):e100183. https://doi.org/10.1136/gpsych-2019-100183
19. Schoretsanitis G, Kane JM, Ruan CJ, et al. A comprehensive review of the clinical utility of and a combined analysis of the clozapine/ norclozapine ratio in therapeutic drug monitoring for adult patients. Expert Rev Clin Pharmacol. 2019;12(7):603–21. https://doi.org/10.1080/17512433.2019.1617695
20. Zorn SH, Jones SB, Ward KM, Liston DR. Clozapine is a potent and selective muscarinic M4 receptor agonist. Eur J Pharmacol. 1994;269(3):R1–2. https://doi.org/10.1016/0922-4106(94)90047-7
21. Nakamura T, Matsui M, Uchida K, et al. M3 muscarinic acetylcholine receptor plays a critical role in parasympathetic control of salivation in mice. J Physiol. 2004;558(2):561–75. https://doi.org/10.1113/jphysiol.2004.064626
22. Weiner DM, Meltzer HY, Veinbergs I, et al. The role of M1 muscari nic receptor agonism of N-desmethylclozapine in the unique cli nical effects of clozapine. Psychopharmacology (Berl). 2004;177(1–2):207–16. https://doi.org/10.1007/s00213-004-1940-5
23. Ishikawa S, Kobayashi M, Hashimoto N, et al. Association between N-desmethylclozapine and clozapine-induced sialorrhea: Involvement of increased nocturnal salivary secretion via muscarinic receptors by N-desmethylclozapine. J Pharmacol Exp Ther. 2020;375(2):376–84. https://doi.org/10.1124/jpet.120.000164
24. Duarte JD, Cavallari LH. Pharmacogenetics to guide cardiovascular drug therapy. Nat Rev Cardiol. 2021;18(9):649–65. https://doi.org/10.1038/s41569-021-00549-w
25. Müller DJ. Pharmacogenetics in psychiatry. Pharmacopsychiatry. 2020;53(4):153–4. https://doi.org/10.1055/a-1212-1101
26. Brown LC, Allen JD, Eyre HA, et al. Editorial: Precision psychiatry from a pharmacogenetics perspective. Front Psychiatry. 2023;14:1159000. https://doi.org/10.3389/fpsyt.2023.1159000
27. Islam F, Hain D, Lewis D, et al. Pharmacogenomics of Clozapine-induced agranulocytosis: a systematic review and meta-analysis. Pharmacogenomics J. 2022;22(4):230–40. https://doi.org/10.1038/s41397-022-00281-9
28. Tsai SJ, Wang YC, Yu WY, et al. Association analysis of polymorphism in the promoter region of the α2a-adrenoceptor gene with schizophrenia and clozapine response. Schizophr Res. 2001;49(1–2):53–8. https://doi.org/10.1016/s0920-9964(00)00127-4
29. Lario S, Calls J, Cases A, et al. MspI identifies a biallelic polymorphism in the promoter region of the alpha 2A-adrenergic receptor gene. Clin Genet. 1997;51(2):129–30. https://pubmed.ncbi.nlm.nih.gov/9112004
30. Rajkumar AP, Poonkuzhali B, Kuruvilla A, et al. Outcome definitions and clinical predictors influence pharmacogenetic associations between HTR3A gene polymorphisms and response to clozapine in patients with schizophrenia. Psychopharmacology (Berl). 2012;224(3):441–9. https://doi.org/10.1007/s00213-012-2773-2
31. Rajkumar AP, Poonkuzhali B, Kuruvilla A, et al. Association between CYP1A2 gene single nucleotide polymorphisms and clinical responses to clozapine in patients with treatment-resistant schizophrenia. Acta Neuropsychiatr. 2013;25(1):2–11. https://doi.org/10.1111/j.1601-5215.2012.00638.x
32. Rajagopal V, Sundaresan L, Rajkumar AP, et al. Genetic association between the DRD4 promoter polymorphism and clozapine-induced sialorrhea. Psychiatr Genet. 2014;24(6):273–6. https://doi.org/10.1097/YPG.0000000000000058
33. Solismaa A, Kampman O, Seppälä N, et al. Polymorphism in alpha 2A adrenergic receptor gene is associated with sialorrhea in schizophrenia patients on clozapine treatment. Human Psychopharmacol. 2014;29(4):336–41. https://doi.org/10.1002/hup.2408
34. Puolakka H, Solismaa A, Lyytikäinen LP, et al. Polymorphisms in ERBB4 and TACR1 associated with dry mouth in clozapine-treated patients. Acta Neuropsychiatr. 2024;36(4):218–23. https://doi.org/10.1017/neu.2024.9
35. Solmi M, Murru A, Pacchiarotti I, et al. Safety, tolerability, and risks associated with first- and second-generation antipsychotics: A state-of-the-art clinical review. Ther Clin Risk Manag. 2017;13:757–77. https://doi.org/10.2147/TCRM.S117321
36. Kirilochev OO. Complications of clozapine therapy: update of information. Current Therapy of Mental Disorders. 2023;(3):12–20 (In Russ.). https://doi.org/10.21265/PSYPH.2023.11.37.002
37. Kim BN, Kim JW, Cummins TDR, et al. Norepinephrine genes predict response time variability and methylphenidate-induced changes in neuropsychological function in attention deficit hyperactivity disorder. J Clin Psychopharmacol. 2013;33(3):356–62. https://doi.org/10.1097/JCP.0b013e31828f9fc3
38. Freudenreich O. Drug-induced sialorrhea. Drugs Today (Barc). 2005;41(6):411–8. https://doi.org/10.1358/dot.2005.41.6.893628
39. Praharaj SK, Arora M, Gandotra S. Clozapine-induced sialorrhea: pathophysiology and management strategies. Psychopharmacology (Berl). 2006;185(3):265–73. https://doi.org/10.1007/s00213-005-0248-4
40. Essali A, Rihawi A, Altujjar M, et al. Anticholinergic medication for non-clozapine neuroleptic-induced hypersalivation in people with schizophrenia. Cochrane Database Syst Rev. 2013;2013(12):CD009546. https://doi.org/10.1002/14651858.CD009546.pub2
41. D’Souza UM, Russ C, Tahir E, et al. Functional effects of a tandem duplication polymorphism in the 5'flanking region of the DRD4 gene. Biol Psychiatry. 2004;56(9):691–7. https://doi.org/10.1016/j.biopsych.2004.08.008
42. Burk BG, Donaldson V, Jackson CW, et al. Paliperidone-associated sialorrhea. J Clin Psychopharmacol. 2022;42(5):480–4. https://doi.org/10.1097/JCP.0000000000001588
43. Kulkarni RR. Low-dose amisulpride for debilitating clozapine-induced sialorrhea: Case series and review of literature. Indian J Psychol Med. 2015;37(4):446–8. https://doi.org/10.4103/0253-7176.168592
44. Praharaj SK, Jana AK, Sinha VK. Aripiprazole-induced sialorrhea. Prog Neuropsychopharmacol Biol Psychiatry. 2009;33(2):384–5. https://doi.org/10.1016/j.pnpbp.2008.12.016
45. Howes OD, Kapur S. A neurobiological hypothesis for the classification of schizophrenia: type A (hyperdopaminergic) and type B (normodopaminergic). Br J Psychiatry. 2014;205(1):1–3. https://doi.org/10.1192/bjp.bp.113.138578
46. Nucifora FC Jr, Woznica E, Lee BJ, et al. Treatment resistant schizophrenia: Clinical, biological, and therapeutic perspectives. Neurobiol Dis. 2019;131:104257. https://doi.org/10.1016/j.nbd.2018.08.016
47. Vita A, Minelli A, Barlati S, et al. Treatment-resistant schizophrenia: Genetic and neuroimaging correlates. Front Pharmacol. 2019;10:402. https://doi.org/10.3389/fphar.2019.00402
Supplementary files
Review
For citations:
Kirova A.G., Bellevich Yu.S., Sosin D.N., Mosolov S.N., Sychev D.A. Pharmacogenetic Biomarkers of Clozapine-Induced Sialorrhoea: A Systematic Review. Safety and Risk of Pharmacotherapy. (In Russ.) https://doi.org/10.30895/2312-7821-2025-517