Posttraumatic
stress disorder (PTSD) is a condition that affects 8 million adults in the United
States, and 8% of the population will suffer from some form of PTSD throughout
their life. This disorder is characterized by consistent and often highly
distressing memories that cue some aspect of a traumatic event in the past. Prevalence
of PTSD is higher among women and combat veterans, with women are twice as likely
as men to experience PTSD throughout their lifetime. This disorder is more impactful
than simply having persistent uncomfortable flashbacks as most people might imagine.
PTSD causes high degrees of disability in normal daily activities among those
affected. These individuals are more likely to suffer from poor family relationships,
and are associated with lower income, and less occupational success according to
the DSM-5. Lastly, individuals diagnosed with PTSD are 80% more likely to
suffer from another mental disorder.
These data are supported in the article “Alcohol
use and craving among Veterans with mental health disorders and mild traumatic
brain injury” where Dr. Amy Herrold states that individuals suffering from PTSD
or depression are 3 to 4 times more likely to suffer from alcohol use disorder
(AUD). Dr. Herrold specializes in assessing potential treatments for cooccurring
conditions which are common with PTSD. She points out that these cooccurring
conditions such as a patient suffering from both PTSD and AUD makes it far more
difficult for the patient to recover, and intensifies the symptoms of both
disorder. Dr. Harold is investigating the use of transcranial magnetic
stimulation (TMS) to treat cases of cooccurring disorders such as PTSD, AUD,
and mild traumatic brain injury (mTBI). TMS has been shown to reduce symptoms
of AUD in patients with these cooccurring conditions, which indicates that it
could be a potential treatment option for these disorders.
While treatments aimed at modulating
the neural activity of circuits involved in the symptoms of these disorders are
becoming more popular, traditional methods of treating PTSD are pharmacological.
The most common medications to treat PTSD are selective serotonin or serotonin-norepinephrine
reuptake inhibitors (SSRIs/SNRIs) which are the go-to medication to treat depression
and anxiety related disorders. This is evidenced by the fact that 13% of the population
in the U.S. is on some sort of antidepressants. While these medications are effective
in treating major symptoms for anxiety and depressive disorders, they are now being
prescribed at lower rates due to concerns with major side effects that these
medications often bring on. However, new experimental treatment options show
promise, specifically as it relates to treating PTSD.
One
of these new treatment options is ketamine, which has shown to reduce the
negative symptoms of PTSD in a more targeted manner, and with greater effectiveness
that traditional SSRIs. Ketamine was originally used as an anesthetic and works
as an NDMA receptor antagonist. In normal conditions, this this receptor is
activated by glutamate, and has a general effect of increasing the excitability
of neurons. When ketamine acts to antagonize or reduce the excitatory effects
of glutamate in the brain, the general result is a slowing down of these neural
circuits. Understanding this mechanism is useful in the study of PTSD
treatments, since a potential hypothesis is that ketamine treatment can disrupt
fear conditioning in the hippocampus (the brain area most commonly associated
with memory) which is dependent on the activity of the NMDA receptor to encode a
situation that we perceive as harmful. In a human double-blind controlled study
of 41 patients, researchers found that ketamine was more effective than a
commonly prescribed benzodiazepine at reducing the severity of PTSD symptoms. Additionally,
several specific case studies corroborate that ketamine treatment was effective
in reducing PTSD symptoms when traditional SSRIs failed. One such example was
from a 23-year old veteran with PTSD, who had previously been prescribed SSRIs,
SNRIs, TCAs (tricyclic antidepressants), valproate, as well as numerous types
of psychotherapies without a consistent positive result. After a brief ketamine
treatment, he showed “an immediate drastic decrease in dysphoria that led to
improved functioning.”
While
this new experimental treatment shows promise, there are also areas of
scrutiny, mainly being that the treatment itself can sometimes cause “transient
dissociation.” While this has only been documented in rare cases, it is not a
minor side effect, and more research should be conducted into the efficacy of
the treatment, as well as the potential off-target effects such as dissociation
events that have been reported. However, no experimental medication comes without
its potential downsides. While ketamine might not be the treatment option best
suited for a majority of patients, it is at the very least opening the door to
exploring more potential options to treat this increasingly widespread mental
health disorder.
References
Liriano, Felix, et al.
“Ketamine as Treatment for Post-Traumatic Stress Disorder: a Review.” Drugs
in Context, vol. 8, 2019, pp. 1–7., doi:10.7573/dic.212305.
Herrold, Amya, et al.
“Transcranial Magnetic Stimulation: Potential Treatment for Co-Occurring
Alcohol, Traumatic Brain Injury and Posttraumatic Stress Disorders.” Neural
Regeneration Research, vol. 9, no. 19, 2014, p. 1712., doi:10.4103/1673-5374.143408.
Herrold, Amy A., et al.
“Alcohol Use and Craving among Veterans with Mental Health Disorders and Mild
Traumatic Brain Injury.” Journal of Rehabilitation Research and Development,
vol. 51, no. 9, 2014, pp. 1397–1410., doi:10.1682/jrrd.2013.07.0170.
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