TY - JOUR
T1 - N-Acetylcysteine (NAC) in schizophrenia resistant to clozapine : a double-blind, randomized, placebo-controlled trial targeting negative symptoms
AU - Neill, Erica
AU - Rossell, Susan L.
AU - Yolland, Caitlin
AU - Meyer, Denny
AU - Galletly, Cherrie
AU - Harris, Anthony
AU - Siskind, Dan
AU - Berk, Michael
AU - Bozaoglu, Kiymet
AU - Dark, Frances
AU - Dean, Olivia M.
AU - Francis, Paul S.
AU - Liu, Dennis
AU - Phillipou, Andrea
AU - Sarris, Jerome
AU - Castle, David J.
PY - 2022
Y1 - 2022
N2 - BACKGROUND AND HYPOTHESIS: Clozapine is the most effective antipsychotic for treatment-resistant schizophrenia, yet a significant proportion of individuals on clozapine continue to experience disabling symptoms, despite being treated with an adequate dose. There is a need for adjunct treatments to augment clozapine, notably for negative and cognitive symptoms. One such potential agent is the glutathione precursor N-acetylcysteine (NAC). STUDY DESIGN: A randomized double-blind, multi-center, placebo-controlled trial for clozapine patients with enduring psychotic symptoms (n = 84) was undertaken to investigate the efficacy of adjunctive NAC (2 g daily) for negative symptoms, cognition and quality of life (QoL). Efficacy was assessed at 8, 24, and 52 weeks. STUDY RESULTS: NAC did not significantly improve negative symptoms (P = .62), overall cognition (P = .71) or quality of life (Manchester quality of life: P = .11; Assessment of quality of life: P = .57) at any time point over a 1-year period of treatment. There were no differences in reported side effects between the groups (P = .26). CONCLUSIONS: NAC did not significantly improve schizophrenia symptoms, cognition, or quality of life in treatment-resistant patients taking clozapine. This trial was registered with "Australian and New Zealand Clinical Trials" on the 30 May, 2016 (Registration Number: ACTRN12615001273572).
AB - BACKGROUND AND HYPOTHESIS: Clozapine is the most effective antipsychotic for treatment-resistant schizophrenia, yet a significant proportion of individuals on clozapine continue to experience disabling symptoms, despite being treated with an adequate dose. There is a need for adjunct treatments to augment clozapine, notably for negative and cognitive symptoms. One such potential agent is the glutathione precursor N-acetylcysteine (NAC). STUDY DESIGN: A randomized double-blind, multi-center, placebo-controlled trial for clozapine patients with enduring psychotic symptoms (n = 84) was undertaken to investigate the efficacy of adjunctive NAC (2 g daily) for negative symptoms, cognition and quality of life (QoL). Efficacy was assessed at 8, 24, and 52 weeks. STUDY RESULTS: NAC did not significantly improve negative symptoms (P = .62), overall cognition (P = .71) or quality of life (Manchester quality of life: P = .11; Assessment of quality of life: P = .57) at any time point over a 1-year period of treatment. There were no differences in reported side effects between the groups (P = .26). CONCLUSIONS: NAC did not significantly improve schizophrenia symptoms, cognition, or quality of life in treatment-resistant patients taking clozapine. This trial was registered with "Australian and New Zealand Clinical Trials" on the 30 May, 2016 (Registration Number: ACTRN12615001273572).
UR - https://hdl.handle.net/1959.7/uws:71929
U2 - 10.1093/schbul/sbac065
DO - 10.1093/schbul/sbac065
M3 - Article
SN - 1745-1701
SN - 0586-7614
VL - 48
SP - 1263
EP - 1272
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
IS - 6
ER -