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http://io9.com/the-most-popular-antidepressants-are-based-on-a-theory-1686163236
One in ten Americans takes an anti-depressant drug like Zoloft or Prozac. But these drugs are designed based on a theory that's already been roundly disproven: the "chemical imbalance" theory of depression. Why haven't our drugs kept up with the science of depression?
Image Credit: Tom Varco | CC BY-SA 3.0
The number of people taking antidepressants has increased by over 400% since the early '90s. In a certain light, this could be perceived as a success for public health; it is clear, for example, that tens of millions of people have found antidepressants to be effective. What's less clear is why these medications work, but decades of research on the subject suggest that an explanation parroted in ad campaigns and physicians' offices alike – that depression boils down to a "chemical imbalance" – is wrong.
This is the story of how pharmaceutical companies and psychiatrists convinced the public that depression was the result of a simple chemical imbalance – and how scientists, patients, and psychiatrists are working to piece together the more complicated truth.
Better Thinking (And Feeling) Through Chemistry
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
Flickr user spike55151. CC BY-NC-SA 2.0
Psychiatry in the 1950s was a field in transition. Mental disorders were often believed to be the direct result of social circumstance, and many psychiatrists relied on talk therapy to treat their patients. The few drug therapies that did exist were rarely well-suited for treating particular maladies. Morphine and opium were sometimes used to treat depression, while insulin shock therapy was used to render uncooperative schizophrenic patients comatose.
By the end of the 1950s, Thorazine, a new psychiatric drug, had become the treatment of choice for schizophrenia. Thorazine simplified the problem of safely keeping aggressive patients calm and docile, and was seen as far less cruel than putting those patients in a coma.
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
During the 1960s, researchers confirmed that neurotransmitters, like dopamine or serotonin, served as the chemical signals that allowed neurons to communicate, underpinning much of the brain's function. Thorazine was soon found to inhibit dopamine receptors in mice, blocking the normal effects of dopamine, and potentially explaining its sedating effects in humans.
Drugs similar to Thorazine were then developed on the premise that excessive dopamine in the brain could be responsible for certain aspects of schizophrenia. These drugs quickly demonstrated that the chemical manipulation of neurotransmitters could be effective in treating mental disorders.
Psychiatry had lagged behind other medical fields for decades, in large part because it lacked treatments tailored to treat specific conditions. Thorazine helped accelerate the acceptance of biological psychiatry, which focused on the biological basis of mental disorders. Biological psychiatry also provided a welcome opportunity for psychiatrists to work directly with pharmaceutical companies to develop targeted, drug-based treatments for mental disorders. Change was in the air.
Framing Low Serotonin As The Culprit Behind Depression
Psychiatrists in the mid-20th century were also keen to develop drug therapies for more common mental disorders, like depression. Case reports had documented mood changes in patients being treated with various drugs for non-psychiatric illnesses. Iproniazid, used to treat tuberculosis, seemed to improve patients' moods, while reserpine, originally used to manage high blood pressure, appeared to mimic depression. Just why either of these drugs influenced mood remained anyone's bet.
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
Thorazine's documented effects on dopamine receptors raised the possibility that iproniazid and reserpine might be influencing mood via their effects on some neurotransmitter. Remarkably, this appeared to be the case. Iproniazid increased serotonin levels in the brain, while reserpine decreased serotonin levels. Other drugs which had similarly shown promise as anti-depressants in the 1950s, like imipramine, were also shown to raise serotonin levels.
These examples suggested that low serotonin might be responsible for depression's symptoms, and that boosting serotonin's levels might alleviate these symptoms. In other words, they indicated that depression could be due to a chemical imbalance in the brain, and that this imbalance could be corrected through the targeted use of proper drugs.
Based on rodent studies, researchers could reasonably surmise that the drugs would increase serotonin levels. What they couldn't assume was that a boost in serotonin levels would be of benefit to people suffering from depression. And yet, at least for some patients, the therapeutic effects of these drugs were undeniable. But these early anti-depressants caused severe side effects, and psychiatrists were skeptical that patients would agree to take them. Pharmaceutical companies saw a major (and, potentially, majorly lucrative) opportunity: A drug that could increase serotonin levels without causing severe side effects could revolutionize the treatment of depression.
These companies began hunting for new chemicals that met these criteria.
SSRIs Top The Charts, To The Tune Of The Chemical Imbalance Theory
In the early 1970s, pharmaceutical chemists struck gold with the invention of drugs like fluoxetine (Prozac) and sertraline (Zoloft). These compounds were part of a new class of anti-depressants, called selective serotonin reuptake inhibitors (SSRIs), that raised serotonin levels by preventing neurons from recycling serotonin that had already been released. Promisingly, SSRIs were about as good at treating depression as their predecessors, but they caused milder side-effects.
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
Left: Prozac prevents serotonin from being reabsorbed, increasing its concentration in the synapse. Wikimedia Commons/vtvu. CC BY-SA 3.0
It took about twenty years for the first SSRIs to pass through clinical trials and receive FDA approval. Psychiatrists and drug companies alike were happy to trumpet a biological explanation for depression (low serotonin), and an appropriate, relatively safe remedy (SSRIs).
"Why am I depressed, and what can I do about it?" a patient might ask. "Well, there's research indicating that depression is related to low levels of serotonin," a psychiatrist might reply. "And here's a pill that will increase your serotonin levels, and alleviate your depression."
Television commercials soon parroted the same ideas. (It's worth noting that the U.S. and New Zealand are the only Western countries in the world that allow pharmaceutical companies to advertise to the general public). In 1997, the FDA shifted its rules and made it easier for companies to run infomercials about pharmaceutical drugs. Ads like the one below, for Zoloft, suggested to TV viewers that they might be suffering from depression and not even realize it.
The ad, like many pharmaceutical commercials, was careful not to make absolute claims about Zoloft's effectiveness. Instead, it prefaced a definitive statement (that Zoloft works to correct an imbalance) with an inconclusive one (i.e. that while its cause is unknown, depression may be related to an imbalance of natural chemicals). But couched in this careful language was an implication, that psychiatrists not only had a good idea of how depression worked, but had figured out how to treat it.
The effects of this and other direct-to-consumer marketing campaigns soon became starkly evident: By 2006, anti-depressants in the U.S. represented the most popular category of prescription drug.
Chances are, though, that you might know a few people who have struggled to cope with depression, in spite of seeking treatment. Not every depressed patient can be helped by anti-depressants that are said to "correct" a supposed serotonin deficit.
The Myth Of The Chemical Imbalance Theory
The chemical imbalance theory may have spurred chemists to invent modern anti-depressants, but the task of proving that low serotonin is to blame for depression – and that boosting serotonin levels is the key to its treatment – has turned out to be impossible.
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
To start, it is impossible to directly measure brain serotonin levels in humans. You can't sample human brain tissue without also destroying it. A crude work-around involves measuring levels of a serotonin metabolite, 5-HIAA, in cerebrospinal fluid (CSF), which can only be obtained with a spinal tap. A handful of studies from the 1980s (like this one) found slightly decreased 5-HIAA in the CSF of depressed and suicidal patients, while later studies have produced conflicting results on whether SSRIs lower or raise CSF levels of 5-HIAA. These studies are all circumstantial with regards to actual serotonin levels, though, and the fact remains there is no direct evidence of a chemical imbalance underlying depression.
The corollary to the chemical imbalance theory, which implies that raising brain serotonin levels alleviates depression, has also been hard to prove. In fact, the serotonin-depleting drug reserpine was itself shown to be an effective anti-depressant in the 1950s, the same decade in which other studies claimed that reserpine caused depression-like symptoms. At the time, few psychiatrists acknowledged these conflicting reports, as the studies muddled a beautiful, though incorrect, theory. Tianeptine is another drug that decreases serotonin levels while also serving as a bona-fide anti-depressant. Tianeptine does just the opposite of SSRIs – it enhances serotonin reuptake. Wellbutrin is a third anti-depressant that doesn't increase serotonin levels. You get the picture.
If you prefer your data to be derived more accurately, but less relevantly, from rodents, you might consider a recent meta-analysis carried out by psychologist Paul Andrews (McMaster University, Ontario) and colleagues. This meta-analysis revealed that, in rodents, elevated serotonin was usually associated with depression. While Andrews argues that depression is therefore a disorder of too much serotonin, it's clear from decades of conflicting literature that any chemical imbalance theory, serotonin low or high, will be exceedingly difficult to prove.
Though the dubious chemical imbalance theory provided psychiatry with dozens of somewhat-worthwhile anti-depressants, depression still afflicts many of us. Ditching the chemical imbalance theory, and possibly weaning society off SSRIs, will not be easy for the millions of Americans who currently depend on them. Any changes, we can expect, will be slow – but the time has come to move beyond the chemical imbalance theory of depression.
Bringing The Public Up To Speed With 50 Years Of Brain Science
To spur psychiatry forward, we need an improved public understanding of depression, and new forms of treatments. To learn more about the former , I contacted Jeffrey Lacasse – an assistant professor in the College of Social Work at Florida State University who specializes in mental health and psychiatric medications – and neuroanatomist Jonathan Leo of Lincoln Memorial University in Tennessee. In 2007, Lacasse and Leo published research on the media's propagation of the chemical imbalance theory. In their investigation, the researchers followed up on every mention of the chemical imbalance theory they could find over a one-year span, turning up zero hard evidence to substantiate the theory in the process. I wanted to know the extent to which the public dialogue about depression has shifted since their investigation was published.
In a joint e-mail, Lacasse and Leo told me that the public portrayal of the chemical imbalance theory has dropped off noticeably in the past few years. Though TV commercials promoted SSRIs using the chemical imbalance theory in the early 2000s, "we noticed these advertisements came to a screeching halt around 2006-07," they said. It's not entirely clear why these advertisements disappeared, but the researchers speculate it's because the underlying science had failed to corroborate the theory, and finally come to the attention of advertising execs who had knowingly skipped their homework.
The Most Popular Antidepressants Are Based On A Theory We Know Is Wrong
Flickr user pasukaru76. CC BY 2.0.
But Lacasse and Leo say depressed patients are still routinely told by their GPs and psychiatrists that they have a chemical imbalance, in spite of criticisms from prominent academic psychiatrists like Ronald Pies, who "states that no knowledgable, well-trained clinician would say such a thing."
"If patients search the internet on these issues," Lacasse and Leo say, "we would expect them to be very confused."
The two researchers are concerned "that the story most patients have been hearing from their clinicians for the past 25 years simply has never lined up with the actual scientific data," raising the question of whether patients have had the opportunity to give fully-informed consent.
There is no question that antidepressants can be very beneficial for some people. But the effectiveness of these medications has been shown to vary widely. As noted in a meta-analysis of antidepressant drug effects published January 2010 in The Journal of the American Medical Association:
The magnitude of benefit of antidepressant medication compared with placebo increases with severity of depression symptoms and may be minimal or nonexistent, on average, in patients with mild or moderate symptoms. For patients with very severe depression, the benefit of medications over placebo is substantial.
Some psychiatrists vehemently disagree with the way journalists and other psychiatrists have pushed back against the chemical imbalance theory, and anti-depressants in general, noting that these therapies are effective, even if we don't fully understand why they work.
For what it's worth, the sudden cessation of televised versions of the chemical imbalance theory still perplexes Lacasse and Leo, who are continuing to study how the public portrayal of depression influences patients. Thankfully, the chemical imbalance theory now seems to exist solely in the lay audience's mind, and potentially in the offices of less-than-responsible psychiatrists. It seems there exists opportunity for change.
The Science Of Depression Advances – With Luck, Psychiatry Will Follow
To get a sense of where an expert in depression felt the study and treatment of depression was heading, I contacted Poul Videbech, a professor of psychiatry at Aarhus University Hospital in Denmark. He was frank with his assessment of the field: " The truth is, the chemical imbalance theory has been immensely fruitful, as it has inspired us to develop new drugs," he said.
"At the same time," he adds, "it has probably been wrong, or at very least partially wrong. Depression – which is several disease entities – is much more complicated than this simplistic theory assumes. "
Videbech says depression's wide range of symptoms can be linked to myriad overlapping factors, from genetic vulnerability, to deficiency of certain neurotransmitters (chemical imbalance theory - lite), to disruptions in circadian rhythms, to factors that can alter the survival and growth of neurons. The birth of new neurons, for example, is a hallmark of a healthy brain; a prominent new theory about how SSRIs work has connected elevated serotonin levels to the elevated birth of neurons. But the science still has a ways to go.
" It is also obvious that psychological stress and so-called early lifetime stress can cause depression," he says. That's not to say that depression's social underpinnings are distinct from its biological ones, Videbech adds. "The dichotomy of depressions being either 'biological' or 'psychological' disorders," he says, "is thus false, and not justified by scientific literature."
This dichotomy, he says, is upheld in large part by lay people, who may think that treatment with anti-depressants implies a biological origin for the disease. "It is a major pedagogical task for doctors (and journalists) to eradicate these old fashioned beliefs. They are so beautifully simple to explain," says Videbech, "but nevertheless wrong."
Videbech also mentioned several new therapies that could gain traction in coming years. Ketamine, for example, shows promise, but must be given at regular intervals; transcranial magnetic stimulation, in which magnets are used to non-invasively manipulate brain activity, and wake therapy, in which patients are kept awake for prolonged periods, are two other options backed by reams of scientific evidence. In the future, we may even see psychedelics return to the psychiatric clinic; a number of psychedelic compounds – including psilocybin, the hallucinogen found in magic mushrooms – have shown promise as antidepressants in recent years, a fact that has led many to call for an end to bans on psychoactive drug research.
Psychiatry has been slow to actively correct the myth of the chemical imbalance theory of depression, and SSRIs remain the therapy of choice for millions of patients, but scientists and psychiatrists seem eager to improve our understanding of depression and its treatment. Big Pharma may have led the public to believe that drugs alone could cure a singular cause of depression, but evidence-based reasoning and experimentation stand to put us back on track.
Update: This piece originally stated that "studies have shown that much of {'antidepressants'} effect is likely due to placebo." In fact, meta analyses have concluded that the magnitude of benefit of antidepressant medication compared with placebo tends to increase with severity of depression symptoms. The piece has been revised to clarify this point.
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