| Causes, Treatment of Bipolar Disease Coupled with Drug Abuse Studied | |
Dual-diagnosis psychiatric patients suffer from both mental illness and drug
abuse or dependence, Nejtek explained. The UT Southwestern researcher is
studying bipolar disorder coupled with stimulant abuse.
"Bipolar disorder, which has alternating cycles of depression and mania and/or
extreme irritability, may well be associated with the highest rates of substance
abuse of any psychiatric illness," she said.
Nejtek, head of dual-diagnosis research, said bipolar patients have a rate of
substance abuse that is as high as 60 percent; cocaine abuse is reportedly as
high as 30 percent. Bipolar patients who are also substance abusers require
increased hospitalization and have poorer psychiatric recovery and treatment
response than patients who have bipolar disorder alone, she said.
Dr. Saundra Gilfillan, associate professor of psychiatry and medical director of
emergency psychiatry services at Parkland Memorial Hospital, said cases of
dual-diagnosis patients coming into the emergency room with severe anxiety have
reached new levels since the events of Sept. 11.
"This last year we have seen more dual-diagnosis patients coming into the psych
ER than ever before," she said. "Also, we have seen more teen-agers with either
psychiatric or behavior-related problems, besides drug and alcohol use, than
ever before."
Nejtek is overseeing two research projects involving dual-diagnosis psychiatric
patients. The Stanley Medical Research Institute recently awarded $833,500 to
study medications in bipolar patients who also abuse or are addicted to
stimulants such as cocaine, amphetamines and ecstasy. A second study, partially
funded by the Department of Psychiatry at UT Southwestern, will examine
stress-induced drug use to determine whether major stress triggers drug cravings
and initiates relapse or increased drug use.
The Stanley study will look at the effectiveness of two medications -- atypical
antipsychotic agents quetiapine and risperidone, which have not been tested on
dual-diagnosis patients in double-blind studies.
"The primary aim of the Stanley study is to compare psychiatric, drug-craving,
and cognitive decision-making processes between the two patient groups," Nejtek
said. "I will also look at the amount of time individuals in the two drug groups
continue to improve on their medications and participate in the research and
treatment programs."
Nejtek said conventional neuroleptics rather than atypical antipsychotics, are
commonly prescribed to treat dual-diagnosis patients; however, previous clinical
research indicates that neuroleptics actually increase depressive symptoms as
well as cause a significant increase in stimulant cravings. She also said
preclinical study results have shown that giving neuroleptics to rats increases
cocaine self-administration while giving atypical antipsychotics decreases
cocaine self-administration.
"Since bipolar patients often self-medicate to alleviate stress-induced anxiety
and manic and depressive symptoms with illicit drugs, antipsychotic medications
that may reduce anxiety and depression, while stabilizing manic episodes, may
also help reduce drug cravings and usage," Nejtek said.
The second study will examine stress-induced drug use to predict whether high
levels of the stress-associated natural hormone cortisol may be related to drug
relapse or to frequency of drug use. "This information is vital in our
understanding of how stimulant abuse in some bipolar patients may escalate to
stimulant dependence," Nejtek said.
Volunteers for the second study who do not suffer from bipolar disorder and are
not drug-dependent will come from an earlier stress research study conducted by
Nejtek. The study was the first to identify two distinct patterns of cortisol
release corresponding to events of high and low emotional impact. The adult
study showed a strong correlation between the amount of emotionally impacted
stress, individual cognition and cortisol salivary levels when subjects watched
videos of differing emotional impact.
For further information about participation in any of Nejtek's studies, call
214-645-8127 or 214-648-5555.
---UT Southwestern Medical Center at Dallas
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