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Data Show That Modest Lifestyle Changes Can Help Control, Reverse Weight Gain Associated with Antipsychotics

INDIANAPOLIS, May 22, 2002 (BW HealthWire) -- Patients can control and even reverse treatment-related weight gain by making simple lifestyle changes, according to data presented today at the 155th annual American Psychiatric Association (APA) meeting in Philadelphia, PA. These results support a growing body of evidence showing that this patient population can often effectively implement weight management strategies.

"Managing weight gain is a challenge for many Americans, especially those with severe and persistent mental illness, who often lack healthy lifestyle habits or have limited income," said Franca Centorrino, MD, director, Bipolar and Psychotic Disorders Outpatient Services, McLean Hospital, Harvard Medical School. "By designing our program specifically for the needs of people with mental illness, we have shown that with the right counseling and choices, patients can manage weight gain."

Simple Lifestyle Modifications Lead to Weight Loss

Dr. Centorrino presented results of her study, which showed patients who participated in a weight management program experienced a decrease in body mass index (BMI) and weight as well as general cardiac health benefits.

The 24-week study examined the benefits of lifestyle interventions in 17 subjects with a diagnosis of schizophrenia or schizoaffective disorder. When they entered the study, patients were taking olanzapine (n=4), risperidone (n=2), clozapine (n=10) or ziprasidone (n=1). Baseline body mass index (BMI) averaged 36.6 (231.4 pounds) and each patient had gained at least 10 pounds while on antipsychotic therapy.

The group participated in weekly dietary counseling and twice-weekly group exercise, which included using a treadmill, step machine, bike or rowing machine. Options for subjects on limited budgets included walking, recreational games and strength training at home. Changes in weight and appetite were monitored weekly. Mental status, quality of life and side effects were assessed monthly.

Ninety-four percent of subjects had an average decrease in BMI of 2.1 points and on average lost 13.1 pounds. Patients taking olanzapine showed the greatest reduction in BMI and weight loss (3.8, 24.5 lbs., respectively), followed by patients taking risperidone (2.0, 11.4 lbs.), clozapine (1.6, 10.1 lbs.), and ziprasidone (.27, 1.8 lbs.).

The lifestyle interventions also resulted in overall health benefits, as patients lowered their resting heart rate, blood pressure, cholesterol and triglycerides by the end of the study.

"Dependably managing schizophrenia with appropriate medication should be the first priority for physicians and their patients. Once their symptoms and lives are under control, patients can then implement simple lifestyle changes to help manage weight gain, and stay on the treatment that works best for them," said Dr. Centorrino. Her research was supported by a grant from Eli Lilly and Company.

Interventions Have Long-Term Benefits

Additional data presented here today show that people with severe mental illness can adhere to lifestyle changes over the long-term, maintaining and even improving weight loss.

"Our program was successful because patients were very satisfied with the program and found it easy to follow," said Betty Vreeland, MSN, RN, advanced practice nurse at the University of Medicine & Dentistry of New Jersey. "Ninety-eight percent of patients said they felt better in general, now eat healthier, exercise more and have found better ways to cope with stress and would even recommend it to a friend."

The 6-month study examined the effects of intensive weight interventions in 31 patients with schizophrenia and schizoaffective disorder. Patients were taking olanzapine (n= 14), risperidone (n=9), clozapine (n=6) and quetiapine (n=2) upon entering the study and each patient had gained at least five pounds during antipsychotic therapy. Weight interventions consisted of nutrition, exercise and behavioral counseling divided into two phases. In the first 12-week phase, patients in the intervention group attended two group sessions (including principles of physical fitness, nutrition counseling, and an aerobic walking activity) and one weekly individual session to assess goals. Family members and case managers were invited to attend sessions, and subjects were encouraged to engage in exercise at home. Subjects then participated in a less intensive 12-week program that reinforced the nutritional and physical counseling and continued the exercise component.

A non-intervention group maintained their psychiatric treatment without participating in any weight intervention activities.

Patients in the intervention group experienced a mean weight loss of 6.6 pounds, which equaled three percent of their baseline weight. Their average BMI decreased by 3.2 percent from 34.4 to 33.2. Intervention patients also reported that they had improved their lifestyle habits and had greater nutrition knowledge by the end of the study.

Patients in the non-intervention group, however, gained weight by the end of the study. They experienced a mean weight gain of 7.6 pounds, which equaled 3.7 percent of their baseline weight. Their average BMI increased by 4.5 percent from 33.4 to 34.9. Changes in weight and BMI were statistically significant compared to the non-intervention group.

"Physicians are often concerned that patients with severe mental illness will have difficulty managing the weight gain associated with antipsychotics," said Vreeland. "This study shows that incorporating weight counseling into a treatment program can make a difference in helping patients manage their weight and remain on appropriate medication."

Olanzapine Background

Olanzapine is currently indicated for the treatment of schizophrenia, the short-term treatment of acute manic episodes associated with bipolar disorder and for the long-term therapy and maintenance of treatment response of schizophrenia. Olanzapine is the first atypical antipsychotic to prove its long-term effectiveness in patients with schizophrenia. Since olanzapine was introduced in 1996, it has been prescribed to more than eight million people worldwide.

In the original schizophrenia registration trials, olanzapine was generally well tolerated. However, as with all medications, olanzapine was associated with some side effects. In the original six-week, acute-phase schizophrenia trials, the most common treatment-emergent adverse event associated with olanzapine was somnolence. Other common events were dizziness, weight gain, constipation, akathisia (restlessness) and postural hypotension. Modest elevations of prolactin were also seen, although mean changes from baseline to endpoint were not statistically significantly different between olanzapine and placebo. A small number of patients experienced asymptomatic elevations of hepatic transaminase; none of these patients developed jaundice or drug-induced hepatitis.

In short-term (3- and 4-week) acute bipolar mania trials, the most common treatment-emergent adverse event associated with olanzapine was somnolence. Other common events were dry mouth, dizziness, asthenia, constipation, dyspepsia, increased appetite and tremor.


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