Seroquel Study Gives Hope For Beating Depression In Bipolar Disorder
(June 4, 2006) -- Keeping the
manic-depressive
illness Bipolar Disorder under control may become simpler in future if
psychiatrists implement new research findings from the BOLDER II study
presented during the American Psychiatry Association's 159th annual meeting
20-25 May 2006.
Currently patients have to take
three or four different drugs to control symptoms of
mania and
depression, keep moods on an even keel and to try and prevent relapse.
Now, there is a prospect of one drug - the
atypical antispsychotic, quetiapine (Seroquel)) - being able to do the
job of four, controlling symptoms at both ends of the spectrum and resolving
feelings of anxiety without causing serious side effects.
Results of the randomised double-blind placebo-controlled BOLDER II
study, involving 509 patients with bipolar depression, show quetiapine
significantly and rapidly reduced symptoms of depression and
anxiety
within the first week of therapy compared to placebo and continued to
relieve symptoms over the course of the 8-week study.
BOLDER II was conducted to repeat an earlier study, BOLDER 1. Both
studies included patients with bipolar disorder types I or II reflecting
disease of varying symptom severity. In each trial two doses of quetiapine
(300 and 600mg) were tested against placebo. Improvements in depressive
symptoms were measured on the Montgomery Asberg Depression Rating Scale (MADRS)
scale. Anxiety was measured on the Hamilton Anxiety (HAM-A) rating scale
while quality of life, energy levels and overall improvement were also
measured on appropriate scales.
BOLDER II lead investigator Dr Michael Thase of University of Pittsburgh
said: “The findings are remarkable because such a close replication of
results in psychiatry is unusual.” In clinical trials investigating
depression there can be a large response to placebo making it hard to assess
the true extent of an active treatment's therapeutic effect, he explained.
“But In each of these two studies there was a clear-cut and early separation
of the curves showing response to quetiapine and placebo. Response to both
the 300mg and 600mg doses was almost identical.” Response to depression was
not associated with patients developing mania as a result of treatment, he
added.
Joseph Calabrese, Professor of Psychiatry at University Hospitals of
Cleveland, and a world leader in
treatment of bipolar disorder, commented:
“No other study in bipolar depression has shown such a large separation of
the curves showing response to active medication and placebo as was seen in
the BOLDER studies.”
Suicidal thoughts reduced
Robert Hirschfield, Professor of Psychiatry at University of Texas, who
conducted an analysis of bipolar II patients in the two BOLDER studies said:
“On every item in the rating scales, including the core symptoms of
depression - sadness and occurrence of suicidal thoughts - medication
outperformed placebo.” The effect on suicidal ideation gives hope that
treatment might reduce the high incidence of suicide in this condition, he
added. Over half of sufferers attempt suicide at some stage of their illness
and 10-15 per cent succeed.
Richard Weisler, Professor of Psychiatry of Duke University, North
Carolina who conducted an analysis of the bipolar 1 patients from both
studies said the effect size of quetiapine over placebo (0.8) was large and
robust. “This is some of the best data seen so far in bipolar depression” he
commented. “ If quetiapine is approved for bipolar depression it will be a
wonderful new option in an area where an effective treatment is desperately
needed because the suicide rate is high.”
Quetiapine is already approved for the control of mania in bipolar
disorder. In December 2005, FDA approval was sought to treat bipolar
depression using quetiapine in the US. Studies still in progress in Europe
are also investigating the drug's efficacy both in acute bipolar depressive
episodes as well as in longer-term symptom control.
“My hunch is that since we know quetiapine works on both acute mania and
depression that it will turn out to be good at stabilising the disease
also,” suggested Professor Calabrese. If this hypothesis proves correct
patients may not need to take another medication to prevent relapses.
The BOLDER
studies showed the average weight gained by patients receiving quetiapine
was 1.3kg and 1.4 kg at eight weeks. This is low compared to weight-gain
typically seen with another atypical antipsychotic used in bipolar disorder.
The most common
side effect
of quetiapine therapy was dry mouth affecting
around 40 per cent. Daytime sedation and somnolence affected around 30 per
cent of patients. “Patients who experience these symptoms usually do so in
the first couple of weeks,” noted Prof Calabrese. “If they can be encouraged
to remain on treatment for more than two weeks they may find symptoms less
troublesome over time.” Most patients will put up with some side effects if
they feel the treatment is controlling their bipolar symptoms, he added.
Only 8 per cent of patients taking 300mg quetiapine, and 11 per cent taking
600mg abandoned treatment because of adverse effects and there was no
significant difference among treatment and placebo groups in the proportions
of patients completing the study.
Source: Medical News Today
Last updated: 6/06
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