Prevention of Weight Gain and Dyslipidemia by Green Tea in Patients Initiating Therapy With Olanzapine

Medical University of South Carolina (MUSC)

Status

Withdrawn

Conditions

Schizophrenia

Bipolar Disorder

Treatments

Other: Placebo

Dietary Supplement: Green Tea

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00934908

Green Tea and Olanzapine

Details and patient eligibility

About

The purpose of this study is to determine if taking green tea capsules can help prevent weight gain in patients that start therapy with Zyprexa® (olanzapine).

Full description

Atypical antipsychotic (AA) medications are associated with obesity, diabetes mellitus, dyslipidemia, and cardiovascular disease.1 The prevalence of obesity in the AA medicated population ranges from 40-60%, compared to 30% of the general population. Treatments that are aimed at either reducing the burden of obesity in psychotic illness or preventing the weight gain and other metabolic changes associated with AA are needed. One potential therapy that has received inadequate clinical evaluation is Green tea (Camillia sinensis; GT). GT contains flavonoids including epigallocatechin gallate (EGCG), as well as caffeine, that have been documented to promote weight and fat loss in normal to overweight healthy subjects. Recently green tea was shown to significantly decrease plasma LDL and triglyceride concentrations and increase HDL concentrations in obese women. GT has never been evaluated for its potential to prevent weight gain or changes in plasma lipid concentrations in patients initiating therapy with AA. However, case reports of individuals indicate that treatment with a green tea extract may have efficacy in preventing weight gain in 4 patients that initiated treatment with quetiapine.

We hypothesize that intake of GT in the form of a dietary supplement will result in significantly less weight gain than supplementation with placebo in patients initiating therapy with Zyprexa®. We propose to conduct an 12-week double-blind, placebo-controlled pilot study of 48 out-patient volunteers to determine if twice daily supplementation with GT 1) attenuates weight and fat gain in patients initiating therapy with Zyprexa® and 2) attenuates changes in cardiovascular risk factors including plasma lipoprotein and triglyceride concentrations. The experiments will be performed on patients who initiate therapy with Zyprexa® with a BMI < 40kg/m2 that do not have dyslipidemia requiring pharmacologic intervention.

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Concurrently taking Zyprexa® for a psychiatric indication such as bipolar disorder or schizophrenia
Stable body weight (+ 5%) for at least 2 weeks prior to baseline visit
No weight loss program participation within past 3 months

Exclusion criteria

Treatment with an atypical Anti-psychotic treatment other than olanzapine with the past 6 months
BMI > 40 kg/m2
Use of any dietary supplements related to weight gain or weight loss within past 1 month
Use of any medication related to weight or plasma lipid concentration (other than hormonal contraceptives). This includes, but not limited to: antihypertensives, benzodiazepines statins, and psychostimulants.
Uncontrolled hypertension (SBP >140 or DBP > 90 mmHg)
Use of a hypertensive medication
Known active alcohol or substance abuse or consumption of > three alcoholic beverages/day.
Active cardiovascular disease