Journal Abstracts
Nervenarzt. 2014 Sep;85(9):1166-70. doi:
10.1007/s00115-014-4083-x.
[New facts of long-term prophylaxis for bipolar affective
disorder].
[Article in German]
Bschor T1, Müller-Oerlinghausen B, Stoppe G, Hiemke C.
Lithium
and with restrictions, carbamazepine, valproic acid, lamotrigine, olanzapine,
aripiprazole and quetiapine, are approved in Germany for maintenance treatment
of bipolar disorder.
Lithium is the only drug that (I) proved to be effective
for the prevention of depressive as well as manic episodes in state-of-the-art
studies without an enriched design and that (II) is approved for the
maintenance treatment of bipolar disorders without restrictions. It (III) is also
the only drug which is recommended for maintenance treatment by the current
German S3 guidelines on bipolar disorders with the highest degree of
recommendation (A) and (IV) is the only drug with a well proven suicide
preventive effect. Hence, lithium is the mood stabilizer of first choice.
No patient should be
deprived of lithium without a specific reason. Side effects and risks are
manageable if both the physician and the patient are well informed.
For patients who do not respond
sufficiently to lithium, have contraindications or non-tolerable side effects,
other mood stabilizers should be used. Restrictions in their respective
approval as well as specific side effects and risks have to be taken into
account.
Because
maintenance treatment is a long-term treatment, particular concern should be
paid to drugs with the potential risk of a metabolic syndrome, particularly
atypical antipsychotics.
Harv Rev
Psychiatry. 2014 Nov-Dec;22(6):353-7. Factors associated
with lithium efficacy
in bipolar disorder.
Rybakowski
JK.
About
one-third of lithium-treated, bipolar patients are excellent lithium
responders; that is, lithium monotherapy totally
prevents further episodes of bipolar disorder for ten years and more. These
patients are clinically characterized by an episodic clinical course with
complete remission, a bipolar family history, low psychiatric comorbidity,
mania-depression episode sequences, a moderate number of episodes, and a low
number of hospitalizations in the pre-lithium period.
Recently,
it has been found that temperamental features of hypomania (a hyperthymic
temperament) and a lack of cognitive disorganization predict the best results
of lithium prophylaxis.
Lithium exerts a neuroprotective effect, in which
increased expression of brain-derived neurotrophic factor (BDNF) and inhibition
of the glycogen synthase kinase-3 (GSK-3) play an important role. The response
to lithium has been connected with the genotype of the BDNF gene and serum BDNF
levels. A better response to lithium is connected with the Met allele of the
BDNF Val/Met polymorphism, as is a hyperthymic temperament.
Excellent lithium responders have normal
cognitive functions and serum BDNF levels, even after long-term duration of the
illness. The preservation of cognitive functions in long-term lithium-treated
patients may be connected with the stimulation of the BDNF
system, with the resulting prevention of affective episodes exerting
deleterious cognitive effects, and possibly also with lithium's antiviral
effects.
A
number of candidate genes that are related to neurotransmitters, intracellular
signaling, neuroprotection, circadian rhythms, and other pathogenic mechanisms
of bipolar disorder were found to be associated with the lithium prophylactic
response. The Consortium on Lithium Genetics (ConLiGen) has recently performed
the first genome-wide association study on the lithium response in bipolar
disorder.