TY - JOUR
T1 - The clozapine to norclozapine ratio
T2 - a narrative review of the clinical utility to minimize metabolic risk and enhance clozapine efficacy
AU - Costa-Dookhan, Kenya A
AU - Agarwal, Sri Mahavir
AU - Chintoh, Araba
AU - Tran, Veronica N
AU - Stogios, Nicolette
AU - Ebdrup, Bjørn H
AU - Sockalingam, Sanjeev
AU - Rajji, Tarek K
AU - Remington, Gary J
AU - Siskind, Dan
AU - Hahn, Margaret K
PY - 2020/1/2
Y1 - 2020/1/2
N2 - Introduction: Clozapine remains the most effective antipsychotic for treatment-refractory schizophrenia. However, ~40% of the patients respond insufficiently to clozapine. Clozapine's effects, both beneficial and adverse, have been proposed to be partially attributable to its main metabolite, N-desmethylclozapine (NDMC). However, the relation of the clozapine to norclozapine ratio (CLZ:NDMC; optimally defined as ~2) to clinical response and metabolic outcomes is not clear.Areas covered: This narrative review comprehensively examines the clinical utility of the CLZ:NDMC ratio to reduce metabolic risk and increase treatment efficacy. The association of the CLZ:NDMC ratio with changes in psychopathology, cognitive functioning, and cardiometabolic burden will be explored, as well as adjunctive treatments and their effects.Expert opinion: The literature suggests a positive association between the CLZ:NDMC ratio and better cardiometabolic outcomes. Conversely, the CLZ:NDMC ratio appears inversely associated with better cognitive functioning but less consistently with other psychiatric domains. The CLZ:NDMC ratio may be useful for predicting and monitoring cardiometabolic adverse effects and optimizing potential cognitive benefits of clozapine. Future studies are required to replicate these findings, which if substantiated, would encourage examination of adjunctive treatments aiming to alter the CLZ:NDMC ratio to best meet the needs of the individual patient, thereby broadening clozapine's clinical utility.
AB - Introduction: Clozapine remains the most effective antipsychotic for treatment-refractory schizophrenia. However, ~40% of the patients respond insufficiently to clozapine. Clozapine's effects, both beneficial and adverse, have been proposed to be partially attributable to its main metabolite, N-desmethylclozapine (NDMC). However, the relation of the clozapine to norclozapine ratio (CLZ:NDMC; optimally defined as ~2) to clinical response and metabolic outcomes is not clear.Areas covered: This narrative review comprehensively examines the clinical utility of the CLZ:NDMC ratio to reduce metabolic risk and increase treatment efficacy. The association of the CLZ:NDMC ratio with changes in psychopathology, cognitive functioning, and cardiometabolic burden will be explored, as well as adjunctive treatments and their effects.Expert opinion: The literature suggests a positive association between the CLZ:NDMC ratio and better cardiometabolic outcomes. Conversely, the CLZ:NDMC ratio appears inversely associated with better cognitive functioning but less consistently with other psychiatric domains. The CLZ:NDMC ratio may be useful for predicting and monitoring cardiometabolic adverse effects and optimizing potential cognitive benefits of clozapine. Future studies are required to replicate these findings, which if substantiated, would encourage examination of adjunctive treatments aiming to alter the CLZ:NDMC ratio to best meet the needs of the individual patient, thereby broadening clozapine's clinical utility.
KW - Antipsychotic Agents/administration & dosage
KW - Clozapine/administration & dosage
KW - Cognition/drug effects
KW - Drug Monitoring/methods
KW - Humans
KW - Schizophrenia/drug therapy
KW - cognition
KW - Treatment-refractory schizophrenia
KW - metabolic adverse effects
KW - psychopathology
KW - clozapine
KW - norclozapine
KW - diabetes
KW - obesity
UR - http://www.scopus.com/inward/record.url?scp=85075938881&partnerID=8YFLogxK
U2 - 10.1080/14740338.2020.1698545
DO - 10.1080/14740338.2020.1698545
M3 - Review
C2 - 31770500
SN - 1474-0338
VL - 19
SP - 43
EP - 57
JO - Expert Opinion on Drug Safety
JF - Expert Opinion on Drug Safety
IS - 1
ER -