NIMH STUDY TO GUIDE TREATMENT CHOICES FOR SCHIZOPHRENIA

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Mental Health (NIMH) 
http://www.nimh.nih.gov/

FOR IMMEDIATE RELEASE: Monday, September 19, 2005 

CONTACT: Marilyn Weeks, 301-443-4536, NIMHpress@xxxxxxx

  
NIMH STUDY TO GUIDE TREATMENT CHOICES FOR SCHIZOPHRENIA 

A large study funded by NIH's National Institute of Mental Health (NIMH)
provides, for the first time, detailed information comparing the
effectiveness and side effects of five medications -- both new and older
medications -- that are currently used to treat people with schizophrenia.
Overall, the medications were comparably effective but were associated with
high rates of discontinuation due to intolerable side effects or failure to
adequately control symptoms. One new medication, olanzapine, was slightly
better than the other drugs but also was associated with significant
weight-gain and metabolic changes. Surprisingly, the older, less expensive
medication used in the study generally performed as well as the newer
medications. The study, which included more than 1,400 people, supplies
important new information that will help doctors and patients choose the
most appropriate medication according to the patients' individual needs. The
study results are published in the September 22 issue of the "New England
Journal of Medicine". 

"The study has vital public health implications because it provides doctors
and patients with much-needed information comparing medication treatment
options," said NIMH Director Thomas R. Insel, M.D. "It is the largest,
longest, and most comprehensive independent trial ever done to examine
existing therapies for this disease." 

Schizophrenia, which affects 3.2 million Americans, is a chronic, recurrent
mental illness, characterized by hallucinations, delusions, and disordered
thinking. The medications used to treat the disorder are called
antipsychotics. Previous studies have demonstrated that taking antipsychotic
medication is far more effective than taking no medicine, and that taking it
consistently is essential to the long-term treatment of this severe,
disabling disorder. Although the medications alone are not sufficient to
cure the disease, they are necessary to manage it. 

In the CATIE (Clinical Antipsychotic Trials of Intervention Effectiveness)
trial, researchers directly compared an older medication (perphenazine),
available since the 1950s, to four newer medications (olanzapine,
quetiapine, risperidone, and ziprasidone), introduced in the 1990s. The
purpose of the study was to learn whether there are differences among the
newer medications and whether the newer medications hold significant
advantages over the older medications; these newer medications known as
atypical antipsychotics, cost roughly 10 times as much as the older
medications. 

The size and scope of the trial, with more than 1,400 participants at 57
sites around the country, its 18-month duration, and its inclusion of a wide
range of patients in a variety of treatment settings ensure that the
findings are reliable and relevant to the 3.2 million Americans suffering
from schizophrenia. 

At the beginning of the study, patients were randomly assigned to receive
one of the five medications. Almost three quarters of patients switched from
their first medication to a different medication. The patients started on
olanzapine were less likely to be hospitalized for a psychotic relapse and
tended to stay on the medication longer than patients taking other
medications. However, patients on olanzapine also experienced substantially
more weight gain and metabolic changes associated with an increased risk of
diabetes than those study participants taking the other drugs. 

Contrary to expectations, movement side effects (rigidity, stiff movements,
tremor, and muscle restlessness) primarily associated with the older
medications, were not seen more frequently with perphenazine (the drug used
to represent the class of older medications) than with the newer drugs. The
older medication was as well tolerated as the newer drugs and was equally
effective as three of the newer medications. The advantages of olanzapine --
in symptom reduction and duration of treatment -- over the older medication
were modest and must be weighed against the increased side effects of
olanzapine. 

Thus, taken as a whole, the newer medications have no substantial advantage
over the older medication used in this study. An important issue still to be
considered is individual differences in patient response to these drugs. 

Several factors, such as adequacy of symptom relief, tolerability of side
effects, and treatment cost influence a person's willingness and ability to
stay on medication. 

"There is considerable variation in the therapeutic and side effects of
antipsychotic medications. Doctors and patients must carefully evaluate the
tradeoffs between efficacy and side effects in choosing an appropriate
medication. What works for one person may not work for another," said
Jeffrey Lieberman, M.D., CATIE's Principal Investigator and Chair of The
Department of Psychiatry, Columbia University and Director of the New York
State Psychiatric Institute. 

The CATIE study was led by Lieberman, and co-Principal Investigators Scott
Stroup, M.D. (University of North Carolina at Chapel Hill), and Joseph
McEvoy, M.D. (Duke University). CATIE was carried out by researchers at 57
sites across the country, including private and public mental health
clinics, Veteran's Health Administration Medical Centers, and University
Medical Centers, where people with schizophrenia received their usual care. 

This "New England Journal of Medicin" article is the first to report
outcomes from the CATIE schizophrenia trial, and addresses many of the
primary questions from the study. Future reports will address a multitude of
topics (e.g., cost-effectiveness of the medications, quality of life,
predictors of response) and will provide a more detailed picture of the
interaction between patient characteristics, medication, and outcomes. The
information from the CATIE study will inform new approaches for improving
outcomes in schizophrenia. 

CATIE is part of an overall NIMH effort to conduct "practical" clinical
trials that address public health issues important to those persons affected
by major mental illnesses in real world settings. 

The NIMH mission is to reduce the burden of mental illness and behavioral
disorders through research on mind, brain, and behavior. Additional
information about NIMH and schizophrenia can be found at its website,
www.nimh.nih.gov. 

NIMH is part of the National Institutes of Health (NIH), the Federal
Government's primary agency for biomedical and behavioral research. NIH is a
component of the U.S. Department of Health and Human Services.

The National Institutes of Health (NIH) -- "The Nation's Medical Research
Agency" -- includes 27 Institutes and Centers and is a component of the U.
S. Department of Health and Human Services. It is the primary Federal agency
for conducting and supporting basic, clinical, and translational medical
research, and investigates the causes, treatments, and cures for both common
and rare diseases. For more information about NIH and its programs, visit
http://www.nih.gov.
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/sep2005/nimh-19.htm.

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