Sir: Obsessing and dwelling (or ruminating) are often
used interchangeably to describe types of worrying within the context of anxiety
and depressive disorders. However, they are probably different constructs, which
may involve two distinctly different brain neurotransmitter systems. It is plausible
that nature teleologically designed two distinct reflective systems: one to
process real events that have happened and another to predict future harmful
events. Obsessing refers to worrying about things yet to happen or are only
hypothetical and usually unlikely to happen. Dwelling or ruminating refers to
worry or concern or preoccupation with things that have already happened or
are realistic concerns. The importance of this distinction lies in its predictive
value with respect to response to antidepressants with differing receptor specificity.
I have observed that excessive obsessing is more responsive to serotonergic
agents. Conversely dwelling / ruminating responds best to medications that have
at least some noradrenergic effects. Patients suffering from both obsessing
and ruminating may do better on a dual acting medication or combination of medications.
The following brief case examples help to illustrate this.
Case report. BM is a 20 y/o male who had been treated successfully for classic
and severe obsessive-compulsive disorder with fluoxetine 80mg (This theoretically
provided mostly serotonergic effects but some noradrenergic effects due to the
high dose). He was changed to escitalapram 40mg (presumably devoid of noradreneric
effects) because of side effects. He did well initially for a few months but
he began to ruminate excessively about premature hair loss. This at first seemed
like a return of his obsessing, but he indeed had significant male pattern balding
over the prior few years. Since this was a realistic rumination about something
that has happened, buproprion SR 150mg (a non-serotonergic, primarily noradrenergic
medication) was added with a resultant robust reduction in this symptom.
Case report. JYis a 50 y/o woman who presented with depression, overeating,
crying and emotional blunting. She had been on citalapram 20mg which “pooped-out”
after several months. A change to escitalopram 10mg gave some improvement but
her mood was still down. An initial elicitation of symptoms revealed emotional
blunting, fatigue at the end of the day and well controlled anxiety. This symptom
pattern would have led me to consider augmentation with a noradrenergic agent.
However, more careful questioning noted that her depression was focused on her
worrying about her future in view of her unhappy marriage and her self described
irrational thoughts of divorcing her husband. Rather than augmenting the escitalopram,
I increased it to 20mg with dramatic improvement in mood and fatigue. The marital
situation was unchanged but she was not worrying as much about her future. Instead
she was agreeing to begin psychotherapy to work on realistic future goals and
her unrealistically negative view of her husband.
Case report. GO was a 55 y/o woman presenting with panic and depression as well
as arthritis and heart disease. Prior trials of paroxetine and escitalopram
produced fatigue and worsening of depression. A trial of buproprion XL gave
dramatic improvement in mood and anxiety. More careful questioning of her panic
revealed that she did not have classic fear of dying or loss of control, but
was dwelling on the realistic loss of function due to her medical problems.
These “panic” attacks had a more gradual onset and lasted up to
two hours.
Stahl proposed that serotonin might mediate symptoms of anxiety and obsessing,
while norepinephine (NE) might mediate energy, concentration and drive. However,
anxiety has been successfully treated in some patients by SSRI’s, SNRI’s
and in some cases just noradrenergic agents. I am proposing subdividing the
worrying component of anxiety symptoms into two types that have predictive value
in medication choice. This hypothesis would predict that patients who ruminate
about real, past traumas or losses would respond preferentially to a medication
that has some significant noradrenergic effect. On the other hand, patients
who are fearful about imagined or hypothetical things that may happen to them
or obsess unrealistically about their futures will need a serotonergic agent.
Patients with OCD and panic obsess about calamities that will befall them if
they don’t take some irrational or excessive precaution. These patients
respond well to SSRI’s. Buproprion, a noradrenergic medication, has been
effective in treating excessive grief associated with a real loss. Clearly there
are patients who have both symptoms and they will need dual acting medications.
Patients with ruminations share some features with patients with ADHD in their
difficulty concentrating enough to solve a real problem. The ruminative patient
can’t seem to organize their thinking and work out a logical solution.
ADHD has been traditionally treated with NE medications such as stimulants,
desipramine or atomoxetine. In obsessing there is a hyper focusing, albeit on
irrelevant or irrational items. The obsessive patient is hyper organized to
the extent of fantasizing too many scenarios that are illogical. Obsessive compulsive
disorder usually calls for treatment with a serotonergic agent.
This predictive hypothesis may not hold for patients who have bipolar disorder
or psychosis. In fact when it doesn’t seem to apply, I look more carefully
for a bipolar spectrum disorder. This is a testable hypothesis and I encourage
research to test its validity.
Baldwin et.al., proposed that anxiety and depression may exist on a continuum
with disturbances in serotonin and norepinephrine. It is conceivable that some
of the debate over the superiority of dual acting (SNRIs) versus single acting
(SSRIs, NRI) may be confounded by the failure to separate these two types of
worry when rating patients symptoms of anxiety and depression. Patients with
only obsessive worry may find a medication with some NE effect less calming
than a pure SSRI. Whereas patients with some dwelling anxiety may need an SNRI
for more complete remission of symptoms. The fact that some SSRI’s may
be less selective than others may also have obscured this distinction.
Sincerely,
Neil R. Liebowitz, M.D.
Connecticut Anxiety & Depression Treatment Center
Assistant Clinical Professor of Psychiatry
University of Connecticut, Farmington, CT USA
All pages copyright ©Priory Lodge Education Ltd 1994-2005.
First Published June 2005