Professional Documents
Culture Documents
BPD II
Cyclothymia
Mania
Required
No
No
Hypomania
Possible
Required
No
Major depression
Possible
Required
No
Mixed state
Possible
No
No
Criteria
Manic Episode:
Differential Diagnoses
Differential diagnosis
Mood disorder due to a
general medical
condition
Substance-induced
mood disorder
Consider if . . .
Major medical condition present
First episode at >50 years of age
Symptoms in context of intoxication
or withdrawal
History of treatment for depression
Hypomanic episode
Mixed episode
Manic Episode:
Differential Diagnoses (cont.)
Differential diagnosis
AD/HD
Consider if . . .
Early childhood mood disturbance onset
Chronic rather than episodic course
No clear onsets and offsets
No abnormally elevated mood
No psychotic features
Sleep disorder
Appetite change
Fatigue
Psychomotor
retardation
Psychological
Low self
esteem/guilt
Poor concentration/
indecisiveness
Thoughts of
death/SI
BPD I
BPD II
Prevalence
1.6%
0.5%
Ethnic/racial
differential
None
None
Gender
differential
M=F
FM (?)
Course
Familial
pattern
BPD I
Recurrent in
>90% of cases
First-degree
relatives have
increased rates of
BPD I, BPD II,
and MDD
BPD II
Hypomanic episodes
in BPD II immediately
precede or follow
MDEs in 60% to
70% of cases
First-degree relatives
may have increased
rates of BPD I, BPD
II, and MDD
Epidemiology
Peak age of onset: adolescence through early
20s
Onset of first manic episode after age 40 years is
red flag to consider substance use or general
medical condition
Seasonal variation
Depression more common in spring and autumn
Mania more common in summer
Diagnostic Dilemmas:
Unipolar Versus Bipolar
Unipolar
BPD I
BPD II
BPD NOS
No evidence of hypomania,
cyclothymia, hyperthymic personality,
or family history of BPD
1 manic episode
Recurrent major depression with
hypomania and/or cyclothymic
temperament
Recurrent major depression without
spontaneous hypomania but often
with hyperthymic temperament
and/or family history of BPD
Etiology
Heritability
Evidence for heritability is much stronger
for bipolar than for unipolar disorders
Specific genetic association has not been
consistently replicated
FAMILY STUDIES
The majority of individuals with bipolar disorder
have a positive family history of some type of
mood disorder
About 50% of all bipolar I patients have at least
one parent with a mood disorder
ADOPTION STUDIES
Prevalence of bipolar disorder in adopted away
offspring corresponds to rates in biological, but
not adoptive relatives
Cognitive Deficits
Working memory
Sustained attention
Abstract reasoning
Visuomotor skills
Verbal memory
Verbal fluency
Cognitive flexibility
General cognitive functioning
Potential Explanations
for Cognitive Deficits
Alcohol Use
Alcohol use occurs in 30-50% of cases
Impairs memory and executive functioning
Gorp et al (1998)
Compared BP only, BP + AD, Control
BP + AD > BP only for cognitive impairment
No difference between Control and BP only
Iatrogenic
Lithium
Memory and psychomotor functioning
Neuroleptics
Sustained attention
Visuomotor speed deficits
Benzodiazapines
Memory
Crews et al.
Performance on WCST negatively related to years of exposure
to antipsychotic drugs
Questions
Some evidence indicates that Lithium exerts a
neuroprotective effect on neuronal tissue
Are studies indicating adverse effects of lithium not
accounting for complex combinations of meds?
Mania
Opposite pattern
Decreased ventral and increased dorsal activity of the prefrontal cortex
Reductions in right hemisphere activity
Summary
Authors contend (Savitz et al, 2005) that
functional disturbances have a
neurodevelopmental and possibly genetic
etiology that may be exacerbated by mood
disturbances