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How Economic Factors Influence the Prevalence, Assessment, and Treatment of Mental Illness
Michelle Barton
December 5, 2016
Psychology 461: Psychological Assessment
Dr. Jason Doiron
University of Prince Edward Island
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Mental illness is commonly understood as an individual, and increasingly physiological,
problem. It is rarely situated in a political, economic or historical context. Nancy Scheper-
Hughes describes this as “a technical practice for ‘rationalizing’ human misery and for
containing it to safe quarters, keeping it ‘in its place,’ and so cutting off its potential for
generating an active critique” (Scheper-Hughes, 1994). The body is perceived as the site of dis-
ease, but Scheper-Hughes argues that the body can also offer a critique of “social dis-ease” and
that illness “can contain the elements necessary for critique and liberation.” Unfortunately, the
current trend in clinical psychology is to focus intensely on individual behaviours, symptoms,
and neurobiological causes. How the practice of psychology and psychiatry might be
transformed by researchers and clinicians paying as much attention to the broader social
context of mental illness as they give to individual behaviours and symptoms is yet to be seen.
This paper seeks to explore some of the economic factors contributing to this narrowing
of the assessment process in mental illness. It will also explore how financial interests are
contributing to the definition and “invention” of mental illnesses and influencing treatment
options. As we will see, when those responsible for defining mental illnesses also have a
financial stake in those definitions, the public is left in a very vulnerable position.
The Challenge of Defining Abnormality
One of the challenges in defining psychiatric disorders is that there are no natural
boundaries between what is normal and what is abnormal. There are no objective tests for
verifying or falsifying mental illnesses. What is considered appropriate behaviour in one setting
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may be considered inappropriate or pathological in another. Ultimately, what qualifies as a
disorder is heavily influenced by social norms and cultural practices.
Psychologists and psychiatrists often use psychological tests to measure how much of a
specific construct—such as depression or ADHD—an individual is experiencing. On norm-
referenced tests an individual’s score is interpreted in reference to a norm group that is
representative of the population for whom the test is intended. The distribution of scores
received by the norm group determines what is considered normal and what is considered
atypical.
But what happens if the majority of the population, the norm group, is dysfunctional? In
this case, creating group “norms” would serve to normalize pathological traits. The Scottish
psychiatrist R.D. Laing famously theorized that alienation—the condition of being “out of one’s
mind”—is the condition of the normal man. He goes on to say that “the ‘normally’ alienated
person, by reason of the fact that he acts more or less like everyone else, is taken to be sane”
(Laing, 1967). On the extreme end, the consequences of a socially reinforced pathology may be
evident in the brutal and often lethal acts by delinquent gangs, war, genocide, and ethnic
cleansing. However, when such behaviour is sanctioned by the majority of the population, or by
those with the greatest amount of power and influence, it is not considered pathological.
According to critical social theory, abnormality and deviance is defined by the people and
institutions in power.
More recently and in a similar vein, British psychologist Ian Parker criticized psychology
for normalizing conditions of social alienation and working to reproduce existing conditions and
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power relations (Parker, 2007). Not only is the individual enmeshed within a social-political
framework, but so too are the psychological constructs and clinical practices by which the
individual is assessed and treated. Ignoring social alienation and the structural violence that
harms or disadvantages individuals leads to assessment procedures that identify and treat
consequences rather than causes. In the past, it was the religious authorities who had the most
influence on how the mentally ill were perceived and treated. The current power structure that
dominates mental health research and clinical practices is capitalism. Economic inequality
impacts the prevalence of mental illness, and financial interests guide the direction and
outcomes of research as well as assessment practices, diagnostic parameters, and treatment
options.
Mental Illness and Economic Inequality
There is evidence that many mental illnesses—such as schizophrenia—correlate
positively with a lower socio-economic status. One reasonable explanation for the social-class
gradient is the social drift hypothesis, which posits that people with the greatest risk of
developing mental illness drift into low-status occupations and poorer neighbourhoods. Early
research into schizophrenia certainly appears to support this theory (Goldberg & Morrison,
1963). More recent research has focused on the increased stress associated with lower-class
living as a risk factor for developing schizophrenia (Berry& Cirulli, 2016).
Interestingly, in developing nations the prevalence of schizophrenia is higher among
upper-class, better-educated individuals (Warner & de Girolamo, 1995). This suggests class-
related differences may be related to the development of schizophrenia in ways that are not
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yet fully understood. A 2004 World Health Organization survey of mental illness shows that the
prevalence of DSM-IV disorders is highest in industrialized countries with significant income
inequality. Countries with higher standards of living coupled with lower levels of income
inequality due to strong social policy had the lowest rates of mental illness (World Health
Organization, 2004).
How mental illness affects and is affected by socio-economic factors is poorly
understood and seldom addressed. Despite a general awareness that socio-economic status
influences mental health, clinicians place little to no importance on a person’s financial income,
personal history, social capital, level of education, or experience of stigmatization, when
assessing and treating mental illness. The nature of the illness is conceptualized as essentially
individual and the treatment of choice is predominantly pharmacological.
The Bio-Bio-Bio Model
In 2005, Steven S. Sharfstein, the then-president of the American Psychiatric Association
(APA), addressed the “extraordinary presence of the pharmaceutical industry throughout the
scientific programs and on the exhibit floor” during the APA’s annual meeting (Sharfstein, 2005).
He acknowledged that the interests of Big Pharma and psychiatry are often not aligned, and
that there is much concern regarding the over-medicalization of mental disorders. Even more
troubling, the influence of Big Pharma has contributed to a reduction of the biopsychosocial
model to a bio-bio-bio model, in which psychiatric conditions are considered to be biological in
nature and broader social and personal realities are ignored. Michel Foucault described this
dehumanizing separation of the individual’s body from a total personhood as “the medical
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gaze” (Foucault, 1973). This practice of depersonalization and the narrowing of inquiry to
biological and behavioural determinants situates the problem within the individual’s body and
contributes to the overuse of medications. The person is regarded as being maladjusted or
anatomically defective, while the social, political and economic structures that shaped the
problem remain hidden.
The quality of hiddenness is not limited to the individual with the problem; it is also a
part of the current neoliberal capitalist system of healthcare that forces healthcare
professionals to work at a frantic pace and favour the quick-fix of pharmaceuticals. Taking
adequate time to understand their patients and addressing the multiple and complex root
causes of dysfunction would potentially put their job or clinic in jeopardy. In a recent Canadian
study, clinicians identified professional time constraints as the most significant barrier to
providing psychotherapy (Hadjipavlou, Hernandez, & Ogrodniczuk, 2015). Consequently, well-
meaning clinicians inadvertently blame their patients for their suffering by focusing on genetic
or lifestyle factors without assessing the broader social context in which these vulnerabilities
and behaviours develop. The simplicity and efficiency of assigning diagnostic labels and writing
prescriptions has stripped mental illness of its social, political, historical, and economic context.
Using Checklists to Classify Disorders
To quickly and efficiently assess psychological constructs, checklists and questionnaires
have become increasingly more popular. They are often meant to provide a simple, brief way to
screen for disorders but they are also increasingly used as diagnostic proxy. These types of
assessments limit the scope of assessment and further reduce an illness to a cluster of
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symptoms and behaviours stripping away any contextual factors that may be contributing to
the construct in question. There is also an increased risk of over- or under-diagnosing of
disorders depending on the test-taker’s attitude and interpretation of the test items. Although
checklists and questionnaires can serve as beneficial screening or supplementary tools,
clinicians should guard themselves against the increasingly streamlined process of assessing
and diagnosing mental illness. According to the Canadian Mental Health Association (CMHA),
one in five Canadians will be diagnosed with a mental illness in their lifetime (“Fast Facts About
Mental Illness,” 2016). With such a high percentage of individuals being diagnosed with mental
illness the reliability and the validity of the DSM has come into question.
The Ever-Increasing Number of Mental Disorders
In 1883 Emil Kräpelin (1856–1926), a German psychiatrist, published a classification
system for psychological disorders, paving the way for the first Diagnostic and Statistical
Manual (DSM) published by the American Psychiatric Association (APA) in 1952. The DSM-I
listed 106 disorders which were referred to as “reactions.” Each subsequent edition of the DSM
had an increasing number of disorders. The DSM-IV, published in 1994, described 297
disorders. Due to criticism about the ever-increasing number of disorders, the DSM-5 did not
increase the total number of disorders. However, it did add new diagnoses. The DSM-5
achieved the appearance of having fewer disorders while increasing the number of diagnosable
conditions by reclassifying previous listed disorders as “subtypes” of another disorder.
In addition to concern regarding the quantity of disorders being defined, there is also a
growing concern about the inclusion and medicalization of ordinary personality traits, such as
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shyness, which was introduced in the DSM-5. In his 1872 discourse on blushing, Charles Darwin
considered shyness an adaptive trait. Unfortunately, the present-day American ethos devalues
shyness in favour of the quick-wit, confidence, and leadership qualities associated with
extraversion. How labeling shyness as a mental disorder will come to be utilized in clinical
practice and what impact it will have on the individual is yet to be seen, but it certainly spurred
an important conversation about psychiatry’s scientific claims-making and what psychologist
Arthur Houts describes as the “social invention” of disorders (Houts, 2002).
A Financial Conflict of Interest
The “social invention” of disorders is a critical issue for psychology considering the close
relationship between those who write the DSM and the pharmaceutical industry. Sixty-nine
percent of the DSM-5 task force and 56% of panel members had financial ties to the
pharmaceutical industry (Cosgrove & Krimsky, 20012). This represents a 21% increase over the
number of DSM-IV task members with such ties. The panels that had the most conflicts of
interest were also the panels for which pharmaceuticals are the first-line of intervention. One
hundred percent of the Sleep/Wake Disorders panel members had financial ties to the
pharmaceutical industry as did 83% of those on the panel for Psychotic Disorders and 67% of
the Mood Disorders panel.
Although the current APA disclosure policy does not require panel members to identify
the specific nature of their financial ties, independent research by Cosgrove & Krimsky
identified at least 21 of the 141 panel members as members of drug companies’ speakers
bureaus or advisory boards. Additionally, APA’s disclosure policy does not require panel
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members to disclose unrestricted research grants they receive from industry. These grants are
not considered a financial conflict of interest. However, Cosgrove & Kimsky argue that these
grants may create an “obligation to reciprocate” or invoke a bias. Currently, panel members can
receive US 10,000 per year from industry and have up to US 50,000 invested in stock holdings in
pharmaceutical companies. Psychiatrists not involved in the DSM have been known to receive
as much as millions of dollars in speaking and consulting fees from pharmaceutical companies
for the promotion of their product (Angell, 2009).
In addition to having representatives involved in DSM revisions, the pharmaceutical
industry also spends billions of dollars to promote their products in the media—such as drug
commercials and the “Stop the Stigma of Mental Illness” campaign that was launched by the
National Alliance on Mental Illness (NAMI) but sponsored by Big Pharma—and lobbying the
government to influence legislation. According to the Centre for Public Integrity, the industry
spent more than $880 million lobbying and campaigning in the US from 2006 to 2015 (“Pharma
Lobbying,” 2016), more than any other industry and eight times the amount spent by the
formidable gun lobbyists. Additionally, millions of dollars are donated every year to federal
candidates and political parties.
Pharmaceutical companies also invest heavily in psychiatric research, providing the
capital required to conduct clinical trials. This type of sponsorship has increased significantly in
recent decades raising the question of funding bias and leading to a close examination of the
relationship between the drug industry and clinical research. One study examined the drug
outcomes of 542 clinical studies and compared their sponsorship source (Kelly et al., 2006).
Seventy-eight percent of studies sponsored by drug manufactures resulted in a favourable
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outcome. This was significantly higher than the 48% of favourable outcomes in studies without
industry sponsorship and the 28% of favourable outcomes in studies sponsored by a
competitor. This is a major concern, as these biases not only influence medical literature but
also inform evidence-based medicine (De Vries & Lemmens, 2006). In addition to the strong
bias in favour of industry funded research, the limited amount of public funding for non-
pharmaceutical psychological treatment research further reduces the body of innovative
psychological science.
These conflicts of interests between private enterprise and public health jeopardize the
integrity of academic and practical psychology and psychiatry. The financial muscle of the
pharmaceutical industry has established a stronghold on the profession that cannot be
eliminated without significant reforms. Until the profession demonstrates a willingness to wean
itself from industry money, pharmaceutical companies will remain actively involved in both
defining mental disorders and funding research to promote pharmacotherapy.
Conclusion
There exists within society power structures that seek monetary gain from those who
suffer with mental illness. These structures have a vested interest in how mental illness is
researched, diagnosed, and treated. They also have a vested interest in not investigating the
socio-political and economic factors that contribute to social alienation and subsequent illness.
These factors remain hidden while the biological factors that can be addressed with
pharmacological treatment are overemphasized.
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A thorough mental assessment should be rooted in the biopsychosocial model of health,
one that addresses social determinants of health as well as biological and psychological factors,
which, arguably, occur downstream. For researchers, identifying the relationships between
social worlds and private suffering could lead to social policy changes and even a paradigm shift
within the field of psychology. Rather than locating the illness within the individual and trying to
“fix” him or her, the individual illness may be understood as a symptom of a broader social
disorder that is affecting vast numbers of the population with various expressions.
By ignoring or paying lip-service to the social conditions that lead to our alienation and
subsequent disorders, and by trusting that psychological research and treatments are unbiased
and apolitical, we are blindly and uncritically supporting those who have a financial interest in
keeping us ill.
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