TY - JOUR
T1 - The long-term effects of antipsychotic medication on clinical course in schizophrenia
AU - Goff, Donald C.
AU - Falkai, Peter
AU - Fleischhacker, W. Wolfgang
AU - Girgis, Ragy R.
AU - Kahn, Rene M.
AU - Uchida, Hiroyuki
AU - Zhao, Jingping
AU - Lieberman, Jeffrey A.
N1 - Funding Information:
Dr. Goff has received research support from Avanir Pharmaceuticals, NIMH, and the Stanley Medical Research Institute. Dr. Falkai has received speaking fees from Janssen, Lilly, Otsuka, and Servier and has received honoraria for serving on advisory boards for Janssen, Otsuka, and Servier. Dr. Fleischhacker has received research support from Boehringer-Ingelheim, Janssen, Lundbeck, and Otsuka; he has received honoraria for serving as a consultant to and/or on advisory boards for Allergan, Dainippon Sumitomo, Gedeon Richter, Janssen, Lundbeck, Otsuka, Takeda, and Teva; and he has received speaker’s fees and travel support from AOP Orphan, Dainippon Sumitomo, Gedeon Richter, Janssen, Lundbeck,Pfizer,Otsuka,andTeva.Dr.Girgisreceivesresearchsupportfrom Allergan,BioAdvantex,Genentech, and Otsuka. Dr. Kahn has received consulting fees from Alkermes, Forrest, Forum, Gedeon-Richter, Janssen-Cilag, Minerva Neurosciences, and Sunovion and speaker’s fees from Janssen-Cilag and Lilly. Dr. Uchida has received grants from Astellas Pharmaceutical, Dainippon-Sumitomo Pharma, Eisai, Eli Lilly, Meiji-Seika Pharmaceutical, Mochida Pharmaceutical, Novartis, OtsukaPharmaceutical,andShionogi;speaker’shonorariafromDainippon- Sumitomo Pharma, Eli Lilly, Janssen Pharmaceutical, Meiji-Seika Pharma, MSD, Otsuka Pharmaceutical, Pfizer, Shionogi, and Yoshitomi Yakuhin; and advisorypanelpaymentsfromDainippon-SumitomoPharma.Dr.Lieberman has received support administered through his institution in the form of funding or medication supplies for investigator-initiated research from Denovo, Genentech, Pfizer, Sunovion, and Taisho and for company sponsored phase II, III, and IV studies from Alkermes and Allergan, and is a consultant to or member of the advisory board of Intracellular Therapies, Lilly, Pierre Fabre, and Psychogenics. He neither accepts nor receives any personal financial remuneration for consulting, speaking, or research ac-tivitiesfromanypharmaceutical,biotechnology,ormedicaldevicecompany. He has received honoraria for serving on an advisory board for Clintara, a clinical research organization, and holds a patent from Repligen that yields no royalties. Dr. Zhao reports no financial relationships with commercial interests. ReceivedSept.9,2016;revisionsreceivedDec.16,2016, andFeb.13,2017; accepted Feb. 23, 2017; published online May 5, 2017.
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Concerns have been raised that treatment with antipsychotic medication might adversely affect long-term outcomes for people with schizophrenia. The evidence cited for these concerns includes the association of antipsychotic treatment with brain volume reduction and with dopamine receptor sensitization, which might make patients vulnerable to relapse and illness progression. An international group of experts was convened to examine findings from clinical and basic research relevant to these concerns. Little evidence was found to support a negative long-term effect of initial or maintenance antipsychotic treatment on outcomes, compared with withholding treatment. Randomized controlled trials strongly support the efficacy of antipsychotics for the acute treatment of psychosis and prevention of relapse; correlational evidence suggests that early intervention and reduced duration of untreated psychosis might improve longer-term outcomes. Strategies for treatment discontinuation or alternative non-pharmacologic treatment approaches maybenefit a subgroup of patients but may be associated with incremental risk of relapse and require further study, including the development of biomarkers that will enable a precision medicine approach to individualized treatment.
AB - Concerns have been raised that treatment with antipsychotic medication might adversely affect long-term outcomes for people with schizophrenia. The evidence cited for these concerns includes the association of antipsychotic treatment with brain volume reduction and with dopamine receptor sensitization, which might make patients vulnerable to relapse and illness progression. An international group of experts was convened to examine findings from clinical and basic research relevant to these concerns. Little evidence was found to support a negative long-term effect of initial or maintenance antipsychotic treatment on outcomes, compared with withholding treatment. Randomized controlled trials strongly support the efficacy of antipsychotics for the acute treatment of psychosis and prevention of relapse; correlational evidence suggests that early intervention and reduced duration of untreated psychosis might improve longer-term outcomes. Strategies for treatment discontinuation or alternative non-pharmacologic treatment approaches maybenefit a subgroup of patients but may be associated with incremental risk of relapse and require further study, including the development of biomarkers that will enable a precision medicine approach to individualized treatment.
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U2 - 10.1176/appi.ajp.2017.16091016
DO - 10.1176/appi.ajp.2017.16091016
M3 - Review article
C2 - 28472900
AN - SCOPUS:85021782269
SN - 0002-953X
VL - 174
SP - 840
EP - 849
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 9
ER -