TY - JOUR
T1 - Relationship between polydipsia and antipsychotics
T2 - A systematic review of clinical studies and case reports
AU - Kirino, So
AU - Sakuma, Mutsuki
AU - Misawa, Fuminari
AU - Fujii, Yasuo
AU - Uchida, Hiroyuki
AU - Mimura, Masaru
AU - Takeuchi, Hiroyoshi
N1 - Funding Information:
None. Dr. Kirino has received a speaker's honorarium from Novartis Pharma. Dr. Sakuma has no conflicts of interest. Dr. Misawa has received speaker's honoraria from Eli Lilly, Janssen, Novartis Pharma, Otsuka, Pfizer, and Sumitomo Dainippon Pharma. Dr. Fujii has received speaker's honoraria from Janssen and Otsuka. Dr. Uchida has received grants from Eisai, Meiji Seika Pharma, Otsuka, and Sumitomo Dainippon Pharma; speaker's honoraria from Eli Lilly, Meiji Seika Pharma, MSD, Otsuka, Pfizer, Sumitomo Dainippon Pharma, and Yoshitomiyakuhin; and advisory panel payments from Sumitomo Dainippon Pharma. Dr. Mimura has received speaker's honoraria from Daiichi Sankyo, Eisai, Eli Lilly, Fujifilm RI Pharma, Janssen, Mochida, MSD, Nippon Chemipher, Novartis Pharma, Ono, Otsuka, Pfizer, Sumitomo Dainippon Pharma, Takeda, Tsumura, and Yoshitomiyakuhin; and grants from Daiichi Sankyo, Eisai, Mitsubishi Tanabe Pharma, Pfizer, Shionogi, Takeda, and Tsumura. Dr. Takeuchi has received fellowship grants from the Canadian Institutes of Health Research (CIHR), Centre for Addiction and Mental Health (CAMH) Foundation, the Japanese Society of Clinical Neuropsychopharmacology, and Astellas Foundation for Research on Metabolic Disorders; speaker's honoraria from Meiji Seika Pharma, Mochida, Otsuka, Sumitomo Dainippon Pharma, and Yoshitomiyakuhin; and manuscript fees from Sumitomo Dainippon Pharma.
Funding Information:
Dr. Takeuchi has received fellowship grants from the Canadian Institutes of Health Research (CIHR), Centre for Addiction and Mental Health (CAMH) Foundation, the Japanese Society of Clinical Neuropsychopharmacology, and Astellas Foundation for Research on Metabolic Disorders; speaker's honoraria from Meiji Seika Pharma, Mochida, Otsuka, Sumitomo Dainippon Pharma, and Yoshitomiyakuhin; and manuscript fees from Sumitomo Dainippon Pharma.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2020/1/10
Y1 - 2020/1/10
N2 - Objective: This systematic review aimed to elucidate the relationship between polydipsia and antipsychotics. Methods: We systematically searched MEDLINE, Embase, and PsycINFO, and included clinical studies and case reports on polydipsia induced or improved by antipsychotics. Results: We identified 61 articles: 1 double-blind randomized controlled trial (RCT), 4 single-arm trials, 1 cross-sectional study, 3 case series, and 52 case reports. The double-blind RCT demonstrated no significant difference in improvement in polydipsia between olanzapine and haloperidol. Two single-arm trials showed that polydipsia improved during clozapine treatment, whereas the other 2 showed that risperidone did not improve polydipsia. The cross-sectional study showed the prevalence of hyponatremia with first-generation antipsychotics (FGAs: 26.1%) and second-generation antipsychotics (SGAs: 4.9%). Two case series reported that clozapine improved polydipsia; the other one indicated that patients with polydipsia who were treated with FGAs had schizophrenia (70.4%) and mental retardation (25.9%). Of 90 cases in the case reports, 67 (75.3%) were diagnosed with schizophrenia. Of 83 cases in which antipsychotic treatment started before the onset of polydipsia, 75 (90.3%) received FGAs, particularly haloperidol (n = 24, 28.9%), and 11 (13.3%) received risperidone. Among 40 cases in which polydipsia was improved following antipsychotic treatment, 36 (90.0%) received SGAs, primarily clozapine (n = 14, 35.0%). Conclusions: Although the causal relationship between polydipsia and antipsychotics remains unclear because of the paucity of high-quality studies, antipsychotics with high affinity to dopamine D2 receptors may be associated with an increased risk of polydipsia while clozapine may be effective for treating polydipsia.
AB - Objective: This systematic review aimed to elucidate the relationship between polydipsia and antipsychotics. Methods: We systematically searched MEDLINE, Embase, and PsycINFO, and included clinical studies and case reports on polydipsia induced or improved by antipsychotics. Results: We identified 61 articles: 1 double-blind randomized controlled trial (RCT), 4 single-arm trials, 1 cross-sectional study, 3 case series, and 52 case reports. The double-blind RCT demonstrated no significant difference in improvement in polydipsia between olanzapine and haloperidol. Two single-arm trials showed that polydipsia improved during clozapine treatment, whereas the other 2 showed that risperidone did not improve polydipsia. The cross-sectional study showed the prevalence of hyponatremia with first-generation antipsychotics (FGAs: 26.1%) and second-generation antipsychotics (SGAs: 4.9%). Two case series reported that clozapine improved polydipsia; the other one indicated that patients with polydipsia who were treated with FGAs had schizophrenia (70.4%) and mental retardation (25.9%). Of 90 cases in the case reports, 67 (75.3%) were diagnosed with schizophrenia. Of 83 cases in which antipsychotic treatment started before the onset of polydipsia, 75 (90.3%) received FGAs, particularly haloperidol (n = 24, 28.9%), and 11 (13.3%) received risperidone. Among 40 cases in which polydipsia was improved following antipsychotic treatment, 36 (90.0%) received SGAs, primarily clozapine (n = 14, 35.0%). Conclusions: Although the causal relationship between polydipsia and antipsychotics remains unclear because of the paucity of high-quality studies, antipsychotics with high affinity to dopamine D2 receptors may be associated with an increased risk of polydipsia while clozapine may be effective for treating polydipsia.
KW - Antipsychotics
KW - Clozapine
KW - Polydipsia
KW - Water intoxication
UR - http://www.scopus.com/inward/record.url?scp=85072038679&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85072038679&partnerID=8YFLogxK
U2 - 10.1016/j.pnpbp.2019.109756
DO - 10.1016/j.pnpbp.2019.109756
M3 - Review article
C2 - 31472167
AN - SCOPUS:85072038679
SN - 0278-5846
VL - 96
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
M1 - 109756
ER -