Skip to main content
Translational Psychiatry logoLink to Translational Psychiatry
. 2019 Nov 28;9:320. doi: 10.1038/s41398-019-0661-9

The Penrose Effect and its acceleration by the war on drugs: a crisis of untranslated neuroscience and untreated addiction and mental illness

Gregory G Grecco 1,2, R Andrew Chambers 3,4,
PMCID: PMC6882902  PMID: 31780638

Abstract

In 1939, British psychiatrist Lionel Penrose described an inverse relationship between mental health treatment infrastructure and criminal incarcerations. This relationship, later termed the ‘Penrose Effect’, has proven remarkably predictive of modern trends which have manifested as reciprocal components, referred to as ‘deinstitutionalization’ and ‘mass incarceration’. In this review, we consider how a third dynamic—the criminalization of addiction via the ‘War on Drugs’, although unanticipated by Penrose, has likely amplified the Penrose Effect over the last 30 years, with devastating social, economic, and healthcare consequences. We discuss how synergy been the Penrose Effect and the War on Drugs has been mediated by, and reflects, a fundamental neurobiological connection between the brain diseases of mental illness and addiction. This neuroscience of dual diagnosis, also not anticipated by Penrose, is still not being adequately translated into improving clinical training, practice, or research, to treat patients across the mental illness-addictions comorbidity spectrum. This failure in translation, and the ongoing fragmentation and collapse of behavioral healthcare, has worsened the epidemic of untreated mental illness and addictions, while driving unsustainable government investment into mass incarceration and high-cost medical care that profits too exclusively on injuries and multi-organ diseases resulting from untreated addictions. Reversing the fragmentation and decline of behavioral healthcare with decisive action to co-integrate mental health and addiction training, care, and research—may be key to ending criminalization of mental illness and addiction, and refocusing the healthcare system on keeping the population healthy at the lowest possible cost.

Subject terms: Addiction, Neuroscience

Introduction

Mental illness, addictions, and their comorbid variants (termed ‘dual diagnoses’) are poorly addressed by the U.S. healthcare system due to relatively low insurance reimbursement, declining treatment infrastructure, and insufficient professional training—allowing these brain diseases to produce an increasingly large burden of secondary medical, economic, and social consequences13. For Americans under 50, suicide and overdoses involving addictive drugs are now both ranked in the top four leading proximal causes of death4,5. As root cause pathologies that eventually generate many other secondary organ injuries, cardiovascular diseases, cancers and infections, undertreated addictions collectively represent the largest public health threat and cause of early death in the U.S68.

Toward unraveling the origins and complexities of this healthcare crisis, at the core of which persists an increasingly deficient behavioral healthcare system, this review explores the synergistic effects of three long-standing, interactive phenomena1: the ‘Penrose Effect’2; the ‘War on Drugs’3; and a failure in translation of the Neuroscience of Dual Diagnosis (i.e. the science that describes the biological connections between addictions and mental illness). Explaining these trends and their interactive dynamics, requires a weaving together of historical, sociological, and neuroscientific perspectives, that may inform a strategy for re-building behavioral healthcare as a core rather than marginal domain of the healthcare system. This rebuilding, involving a more complete, mainstream integration of addiction and mental health services, professional training and research, may be crucial for decisively reducing the twin challenges of mass incarceration and the modern behavioral healthcare crisis.

The Penrose Effect

In 1939, Lionel Penrose published his seminal theory that in industrialized nations, a decline of mental health treatment infrastructure is linked with reciprocal increases in incarcerations9 (Fig. 1). His analysis included cross-sectional data from 18 European countries, showing an inverse relationship between national volumes of psychiatric beds and numbers of prisoners and crime measures9. This theory, subsequently termed the “Penrose Effect”10, “Penrose Hypothesis”11, or “Penrose Law”12, has been increasingly referred to in modern studies examining the unintended consequences of deinstitutionalization13.

Fig. 1. The Penrose Effect describes the inverse relationship between mental health treatment infrastructure and prison populations.

Fig. 1

Dotted arrows indicate one pathway underlying the Penrose Effect in which removal of mental health treatment resources leads to the criminalization of untreated mental illness resulting in increased numbers of individuals with mental illness in correctional facilities.

Beginning in the late 1960s, large-scale deinstitutionalization commenced with depopulating and closure of long-term inpatient psychiatric hospitals with plans to expand outpatient community mental health services14,15. The movement was driven by several agendas: to cut costs, to improve civil rights and social integration for patients, and (in what has proven to be an over-optimistic appraisal of the therapeutic power of pharmaceuticals) to take advantage of a growing repertoire of psychiatric medications to promote healing aside from psychotherapies and environmental settings1416.

Problems with long-term psychiatric institutions were widely publicized following the Rosenhan Experiment, which highlighted the powerlessness, dehumanization, and isolation of patients17. Stanford psychologist David Rosenhan and seven other “pseudopatients” feigned auditory hallucinations to gain admissions into psychiatric wards, with plans to stop reporting symptoms immediately after entering. The pseudopatients were subsequently administered numerous psychotropic medications and were stuck for an average of 19 days in these institutions. Rosenhan concluded that community-based health approaches should be pursued due to the counter-therapeutic environment of institutionalization17. However, there was little evidence at the time to suggest community-based health services would be built to compensate for declining inpatient psychiatric services, or that they would be less expensive14,15,18. Unfortunately, deinstitutionalization was poorly organized and conducted without adequate build-up of supportive housing, social services, or outpatient-community mental health infrastructure19,20. Thus, deinstitutionalization has not only created unprecedented waves of homelessness, but it has, consistent with the Penrose Effect, forced the criminal justice system to assume the role of mental healthcare, as untreated, unsheltered individuals were relabeled as “criminals”2124.

As deinstitutionalization has progressed, evidence for the Penrose Effect has accumulated internationally including Argentina, Bolivia, Brazil, Chile, Paraguay, and Uruguay20, Norway25, Hungary26, Ireland27, Finland28, England, Spain, Sweden, Germany, the Netherlands29,30, Australia31, and the U.S.3235. Mundt et al. provides a notable demonstration of a direct association between deinstitutionalization and increasing prison populations in six of the most populous countries in South America from 1991 to 2012.20 Even after controlling for variance in macroeconomic changes across these countries, the numbers of psychiatric hospital beds had greatly reduced where and when prison populations increased20.

Although both cross-sectional and longitudinal data have been replicated in support of the Penrose Effect, controversy remains about what mechanisms are driving it, and/or whether it is an artifact of other phenomena, such as changes in income inequality, unemployment, macro-economies, social welfare programs, and/or changes in national healthcare systems11,13,14,19,36. Nevertheless, the existence of multiple forces contributing to the inverse relationship between mental health treatment infrastructure and prison populations does not preclude the existence of the Penrose Effect, nor its consequences; it only suggests the Penrose Effect is a complex phenomenon.

One dynamic that may underpin the Penrose Effect is increased labeling and categorization of behaviors, resulting from untreated and unsheltered mental illness, as minor forms of criminal activity, which would lead to greater incarceration rates for mentally ill people. The average number of state psychiatric hospital beds (U.S.) has dropped from 339 per 100,000 in 1955 to ~14 per 100,000 in 2010 leaving 3.2 million individuals with serious mental illness to reside in the community22,37,38. Mental illness rates and severity in U.S. prisons rose steeply during this time. In 1870, <1% of prisoners had a serious mental illness, yet today, that number is around 20% by conservative estimates22,39. By 2012, there were nearly 10 times the number of persons with a mental illness in prisons than in psychiatric hospitals39. In nearly every U.S. state, a correctional facility holds more inmates with a mental illness than the largest state psychiatric hospital39.

Although antisocial traits and diagnoses are present within mentally ill populations, this form of mental illness only represents a small fraction of patients, and does not represent the diversity of many other serious mental disorders for which incarceration has replaced access to appropriate treatment services and professionals22,37. Without easy access to expert psychiatric treatment and supportive, supervised housing, individuals with mental illness navigate a society that has placed the criminal justice system in front of, or between them and treatment40,41. Consequently, a substantial population of mentally ill now reside in correctional facilities40.

Remarkably, this state of affairs is not new. Despite advances in psychiatric neuroscience, and the destigmatizing effects this science was hoped to bring, the U.S. seems to have regressed significantly to a more primitive approach that was the norm before the U.S. Civil War, in which punishment was the first line approach for many patients. In the 1840s, Dorothea Dix and other advocates began to challenge state legislatures regarding the inhumane treatment of mentally ill people in prisons; this activism later spearheaded the building of a national mental healthcare infrastructure and hospital system that aimed to put treatment in front of punishment42,43.

The War on Drugs

The policy of addressing compulsive drug use (i.e. addiction) as a crime in the modern era is commonly referred to as “the War on Drugs” (Fig. 2). The War on Drugs massively increased drug enforcement spending, the scope of federal drug task forces44,45, and drug-related arrests46,47. Although Prohibition in the 1920s can be viewed as a failed, alcohol-specific prequel to the War on Drugs48,49, the modern War on non-alcohol intoxicants was formally launched by President Nixon in the early 1970s44. Since this time, the U.S. government, through bipartisan decisions, has expended more than $1 trillion on the War on Drugs at roughly $51 billion annually, which is about 50 times the annual research budget on addiction supported by the National Institute on Drug Abuse46. Subsequent “tough on crime” policies produced substantial increases in state, local, and federal police funding between 1992 and 200844,45. This growth in the size and power of the criminal justice system, has been accompanied by growing concerns about its militarization, suppression of civil rights, and conduct operating outside of constitutional law45,5052. For example, the civil forfeiture of assets in drug-related cases has permitted law enforcement agencies to seize around $7 billion in assets between 1985 and 1999 without due process rights50,52.

Fig. 2. The War on Drugs describes a variety of legal policies that attempt to solve addiction via criminal-justice and punitive actions rather than biomedical-treatment approaches.

Fig. 2

The War on Drugs has been shown to be a key driver in penal system expansion. The dotted arrows indicate a pathway by which the criminalization of behavior related to untreated addiction has led to increased prison populations resulting from drug-related offenses.

The War on Drugs has been enacted as a criminal-legal approach to addiction in sharp contrast to biomedical approaches, fundraising, and destigmatizing efforts that have also been labeled as “Wars” on other diseases. For example, the “War on Cancer” was also declared in the 1970s under the Nixon administration but as an entirely biomedical approach to find cures53,54. Few would argue that the War on Cancer has been “won”; however, significant strides in our understanding of cancer biology have led to dozens of innovations in early detection and cancer therapies53,54. Conversely, the War on Drugs has not encouraged progress in treatment delivery or development and has failed to reduce drug supply, drug-related crime, or addiction disease rates and death46,52,5557. In fact, the War on Drugs has been shown to promote barriers to treatment and to increase drug-related violence globally46,47,55. Likewise, viewing addiction as a criminal behavior has resulted in increased stigmatization, facilitated discriminatory racial policies, and is linked with increased overdoses and the transmission rates of HIV, hepatitis, and tuberculosis46,47,5658.

Another widely recognized consequence of the War on Drugs is the increased incarceration rate46,47. The number of arrests for drug possession between 1982 and 2007 rose from ~500,000 to 1.5 million, with arrests for all other offenses (excluding assaults) declining during the same timeframe44,45. This incarceration rate has allowed the U.S. to become the world’s leader in per capita incarcerations; although making up just 5% of the world’s population, it contains 25% of the world’s entire prison population44,45,59,60.

Comparable to how labeling mental illness-related behavior as a crime may drive the Penrose Effect, the War on Drugs has perpetuated beliefs, held by the public, including members and stakeholders of the healthcare industry, that addiction is a moral and criminal problem, and not a biomedical problem. Although the U.S. biomedical research system has accumulated overwhelming scientific proof that addiction is a highly prevalent brain disease and a leading root cause of premature illness, injury and death, the healthcare system ironically remains extremely ill-equipped to adequately diagnose and treat it68,61,62. Beyond this incapacity, the lack of professional awareness and training about addictive diseases among physicians has allowed the U.S. healthcare system to directly contribute to the single largest outbreak of serious addiction (and related illness and death) in U.S. history—through the iatrogenic opioid epidemic63. Although the opioid epidemic may have finally increased awareness of addiction as a treatable brain disease, the building of widely accessible treatment services and physician expertise needed to address the epidemic has proven elusive64,65. The road to parity of quality care for mental illness and addictions (that is on par with treatment of medical disease of body organs) remains largely blocked by profound shortages of behavioral health professionals and infrastructure, as well as entrenched stigma and financial incentives that benefit from keeping addiction framed as a criminal-legal issue rather than a biomedical problem40,61,66.

The addiction–mental illness connection: the science of dual diagnosis

Addictions and mental illnesses are tightly inter-connected diseases both within individual brains6770 and on population levels7174 (Fig. 3). The biological causal connection is involuntary and general across many types of addictions and mental illnesses. This causal connection is also bidirectional: having either illness category increases the risk of acquiring the other, and having either also worsens the severity of the other67,75. This bi-directionality of causality is sufficient to explain both the dense epidemiological overlap between these illnesses and the fact that dual diagnosis patients face greater degrees of virtually all quantifiable illness consequences compared to their single disease counterparts, including poorer psychosocial functioning, additional medical comorbidities and service utilization, increased risk for homelessness, suicide, overdose, and premature death in general40,76,77.

Fig. 3. The addiction–mental illness connection.

Fig. 3

Mental illness and addiction are highly comorbid diseases that have been demonstrated to be deeply interconnected through alterations in shared neural circuity and neurobiology, genetic risks, and environmental-developmental risk factors. The biological-causal relationship is also bidirectional: having either mental illness or addiction involuntarily/biologically increases the likelihood and severity of acquiring the other.

The involuntary causal nature of the mental illness–addiction connection is born out in both animal and human research. Animal models of mental illness show abnormal short and long-term motor and motivational reactions to addictive drug exposures whether they are self-administered or delivered by researchers78,79. In humans, the risk of acquiring addiction, illness severity, and resistance to treatment is not related to an individual’s choice or reasons for initially trying a drug, or their capacity to express a desire to quit using; rather, addiction risk and illness burden is increased with greater mental illness severity76,80,81.

An important clue about the mental illness–addiction connection is that this relationship is not specific to any one addictive drug type, or intoxicating profile. For example, it is constructive to compare nicotine and opioids, which have very different psychoactive properties, but are nevertheless both highly addictive, and very deadly as addictions. Half of all cigarettes smoked in the U.S. are consumed by only about 15% of the population—those with some form of mental illness82. Likewise, about half of all prescribed opioids in the U.S. are used by a similar fraction of the total population—those with mental illness83. Even prior to the modern opioid epidemic, large population-sample studies spanning decades have consistently replicated the observation that substance disorders are elevated 2–8-fold above the general population across all of the major mental illnesses including psychotic disorders, bipolar disorder, major depression, dysthymia, and personality disorders72,74,82,8486. And again, this connection, within each of these diagnostic categories, is not drug specific. Rather it is general to addiction risk that spans many drug types. Thus addictions involving nicotine, opioids, alcohol, stimulants, and cannabinoids are all elevated across a wide range of different forms of mental illness72,73,8790. As a reflection of this phenomena, multiple addictions also routinely occur together with mental illnesses in both individuals and across whole clinical populations91. These ‘high-order’ dual diagnosis illnesses have been replicated in animal modeling, reflecting the way mental illness biologically increases addiction risk simultaneously across different addictive drugs even with differing intoxication profiles70.

Only recently has the biological connection between mental illness and addiction been recognized or understood as a bidirectional causal problem. While it has been known for decades that alcohol and drug use can induce psychiatric symptoms in otherwise healthy people, or worsen mental illness, it has been less clear if and how the opposite happens, that is, how mental illness itself alters the progression of addiction disease. However, animal modeling and human neuroimaging evidence accumulating since the 1990s has made it clear that mental illness and addiction are inextricably linked on anatomical and pathophysiological levels. Abnormal neurocircuitry present in mental illness, even before drug exposure, changes thresholds for becoming addicted and increases the speed of disease progression and illness severity67,76,79,92. This reality, being quite general to many combinations of addictions and mental illness, likely reflects a fundamental design motif (and vulnerability) of the mammalian brain. All of the major limbic neural networks, including the prefrontal cortex, hippocampal formation and amygdala—which are each implicated across the major forms of mental illness—densely project via glutamatergic connections into the key motivational center of the brain, where addiction disease is primarily centered—the nucleus accumbens (or ventral striatum)67,93. This design allows all of the higher order neural networks of the brain (that represent and adapt contextual memory, emotion, social-attachment, and decision-making functions) to converge in the nucleus accumbens, where they contribute to the neural representations and computations that generate motivation92. Such an architecture optimizes the brain’s capacity to integrate past experiences and current cognitive states to best prioritize, sequence, select, and adapt motivated behavior for long-term success and survival. But, when one or more of these distributed limbic input territories to the nucleus accumbens are structurally and functionally impaired—as in mental illness—the function of the nucleus accumbens itself is altered. This causes the acute and long-term neuroplastic effects of dopamine neurotransmission that is pathologically evoked by addictive drug use, to have a much more profound, long lasting, and devastating effect on motivated behavior68,79,94,95.

Beyond this core frontal-cortical/temporal-limbic/ventral-striatal circuity, additional cortical and deep brain regions are increasingly implicated as neuroanatomical zones where addiction and mental illness pathologies are directly tied into one another. For example, recent studies have implicated the lateral septum96, the habenula97, and the insula98 in functions that integrate cognitive, emotional, motivational, and appetitive control systems. Thus across a broad swath of primary cortical-striatal and accessory limbic networks of the brain, mental illness, and addiction vulnerability are wired into one another and are mechanistically unified to such an extent that in many cases it is biophysically impossible to have one without increasing vulnerability to the other. Hence addiction vulnerability is a biologically intrinsic symptom of mental illness that pervades different types of psychiatric diagnoses.

Consistent with this integrated neurocircuit understanding of dual diagnosis, we are now gaining more insight into how both genetic and environmental/developmental risk elements contribute to this core neurocircuit vulnerability that gives rise to both mental illness and addictions69,99102. For example, twin studies and large genome-wide association studies have identified shared genetic risks for alcohol addiction and a range of mental illnesses that are frequently comorbid with addictions including schizophrenia, attention-deficit hyperactive disorder, and major depression103,104. Similarly, childhood neglect, abuse and trauma, which collectively represent the major non-genetic (i.e. environmental) root cause of adult psychopathology, are also robust risk factors for acquiring addiction71,105107. With this evidence, it is becoming clear that adverse childhood experiences and genetic determinants work in concert during pre-adult neurodevelopment, within the same cortical-striatal-limbic brain systems, to produce both mental illness and addiction vulnerability108.

The science of dual diagnosis: a failure in translation

Although mental illness and addiction share common etiological factors, have overlapping neuroanatomies and neurodevelopmental trajectories, show bidirectional causality and a tight epidemiological overlap (such that dual diagnosis patients represent the majority of all behavioral health patients) these patients are often referred to as ‘system misfits’ because of a lack of access to integrative treatment services40,109,110. The highly fragmented behavioral healthcare system has been built and operates in contradiction to this science: Federally sponsored psychiatric research (e.g. NIDA and NIAAA vs. NIMH), professional training, treatment teams and infrastructures, cultures of care, and insurance reimbursement remain largely divided by a line that separates the addiction vs. mental health-treatment fields108,111. Only 18% of addiction treatment programs and 9% of mental health-treatment programs are considered dual diagnosis capable111, while many cultural and structural barriers to mental health–addiction integration persist despite decades of effort to create a national system of integrated dual diagnosis treatment109112.

The failure to translate the science of dual diagnosis into driving the integration of clinical training and treatment delivery—so that mental illnesses, addictions, and their bidirectional causal dynamics can be diagnosed and treated by one healthcare team as comprehensively and efficiently as possible108,112 has had significant public health and social consequences. The iatrogenic opioid epidemic has revealed the consequences of low medical professional awareness of addiction, and disregard for the risk for addiction in persons with mental illness, contributing to the over prescription of high dose/chronic opioids specifically to people with mental illness and addictive disorders113,114. This targeting of vulnerable brains with opioid overprescribing, termed by Sullivan et al. as “Adverse Selection”, has occurred alongside declines in behavioral health expertise, workforce, and treatment access and an intensification of the War on Drugs115.

Dual diagnosis and acceleration of the penrose effect by the war on drugs

As reviewed thus far, mental illness and addiction are brain diseases that, via the Penrose Effect and the War on Drugs, have been marginalized by the healthcare system, but absorbed by the legal system as reflecting criminal behavior21,22,58,61,66. At the same time, however, the neuroscience of dual diagnosis has characterized mental illness and addiction as bi-directionally causative and tightly interlinked brain diseases68,79,99,106,108. A key implication of this neuroscience is that the Penrose Effect and the War on Drugs are not merely parallel social processes, but are interlinked and mutually reinforcing. With a decline of mental health-treatment infrastructure, we expect more people incarcerated for behaviors resulting from untreated mental illness. Simultaneously, because these populations are also biologically, involuntarily predisposed to acquiring addictions, then increasing numbers of people with mental illness living without access to good mental health services likely increases the numbers of patients who are acquiring addictions, and demonstrating behavioral consequences of untreated addiction, that are also criminalized by the War on Drugs. Then, as the Penrose Effect is accelerated by the War on Drugs, there is an ever greater transfer of resources, workforce development, public funds, and infrastructure away from treating either illness class as healthcare issues, and instead, toward enforcement, prosecution, conviction, and mass incarceration of untreated patients. These trends would thus intertwine to create a feed-forward amplification of untreated addictions and mental illness to crisis proportions, even to the extent where advances in the neuroscience of these disorders remain largely untranslated by an increasingly deficient and fragmented behavioral healthcare system (Fig. 4).

Fig. 4. Acceleration of the Penrose Effect by the War on Drugs.

Fig. 4

Through the fundamental neurobiological and clinical connections between addiction and mental illness, the criminalization of individuals with addiction promoted by the War on Drugs leads to an acceleration of the Penrose Effect. This ultimately hastens the decline and fragmentation of behavioral healthcare, while producing explosive growth of the U.S. penal system, even as neuroscience that is advancing our understanding addictions and mental illnesses as brain diseases, remains increasingly disconnected and unapplied to behavioral health care.

Recent studies suggest a synergy between the Penrose Effect and the War on Drugs has occurred in the U.S. and internationally, in which mentally ill people are not merely transferring out of treatment beds and into incarceration beds in 1:1 ratios. To the extent that mentally ill people, due to their addiction comorbidities, have been intensively subject to harsh drug penalties and the criminalization of addiction, we might expect a much more disproportionate exchange between treatment and penal capacities. Thus, in a multinational South American study examining the Penrose Effect from 1990 to 2012, for every one mental health treatment bed that disappeared, five more individuals ended up in prison, where, like in the U.S., very high prevalence rates of mental illness and addiction disorders have been identified20.

A national U.S. survey showed that individuals with a dual diagnosis were nearly 7.5 times more likely to be arrested in the last 12 months, compared to healthy individuals, with only 1.8 or 5.3 fold increases in arrests in persons with only a mental illness or an addiction116. In a Seattle study, substance use seems to directly mediate the relationship between a recent reduction in psychiatric beds and an increase in jail detention for those with mental illness32. Accordingly, a lack of substance disorder treatment throughout mental healthcare is an important risk factor for incarceration of patients with dual diagnosis77. Among individuals with a mental illness, co-occurring substance use increases behaviors that are criminalized (purchasing, dealing) leading to arrests and incarcerations to such an extent that having a dual diagnosis has become a normalized characteristic of prison populations117,118.

These observations suggest that deinstitutionalization and the War on Drugs may have intersected to accelerate the Penrose Effect, though multiple dynamics, at the core of which is a fundamental epidemiological and neurobiological linkage between mental illness and addiction. While Penrose may have had keen insight into the inverse relationship between psychiatric beds and prison populations 80 years ago, he was unaware both of the neurobiology of drug addiction and its biological link with mental illness, which have only been described in the last 30 years. Thus, he could not have predicted the impact the War on Drugs might later have, to not only accelerate the incarceration of mentally ill people (via their comorbid association with addiction), but the degree to which the resulting growth of the penal system might actually interdict the development and deployment of science-based treatments, and contribute adversely to the degradation of the behavioral healthcare system itself60,119.

The war and drugs as harm amplification

Aside from the channeling of public funds (and public regard) away from behavioral healthcare, into criminal justice approaches for addressing behaviors resulting from untreated mental illness and addictions60, there is evidence that the War on Drugs may directly worsen mental illness via a process that can be termed as ‘Harm Amplification’ (Fig. 5). Many treatments in mainstream medical care, particularly for conditions that are difficult to cure quickly or directly, pursue ‘Harm-Reduction’ strategies, where the therapeutic intervention seeks to limit the negative overall functional impact and/or spread of the injury or disease to other body organs. A cast on a broken arm, insulin for diabetes, and opioid maintenance treatments for opioid addiction are all evidence-based and highly effective Harm-Reduction interventions. Oppositely, the core strategy of the War on Drugs, through punishing drug use and closely related behavior, represents Harm Amplification, where various primary and secondary damages associated with having the disease are deliberately compounded by the criminal justice system (e.g. via public humiliation, financial penalties, and incarceration), in hopes that this will motivate effort in the individual to abandon their addiction.

Fig. 5. Harm amplification.

Fig. 5

The mass criminalization of addiction and mental illness has created a large population of individuals with these diseases in a massively overgrown penal system. This enlargement represents a barrier to treatment access for mental illness and addiction for both un-incarcerated and incarcerated patients alike, through reinforcing stigma and financial diversion away from treatment into criminalization. For imprisoned patients, the penal system may exacerbate symptomology and harm treatment access in either disease domain via isolation/confinement practices, victimization by other prisoners, disrupting family attachments, hampering reentry into the community, and impairing access to health insurance, employment and housing from months and years after incarceration.

Beyond the removal of mentally ill/addicted patients from access to mental health and addiction care more generally available at higher standards outside of jails and prisons39,58,60,120122, incarceration settings frequently tend to rely on behavioral control interventions that encompass isolation techniques60, which are well known to exacerbate brain abnormalities and behaviors that are present in mental illness and addiction79,123. Additionally, mentally ill patients face greater psychological and physical victimization in prison and disproportionate rates of solitary confinement, symptom worsening, and higher rates of suicide in prison39,60,120,124,125.

Dual diagnosis patients may be particularly adversely affected by incarceration in terms of long-term outcomes126,127. While lack of adequate addiction treatment is a major risk factor for re-arrest following release58,60 individuals with dual diagnosis post-incarceration have a higher risk for significant injuries (including drug-related and self-harm) compared to their single disease counterparts77,126,128. Finally, the long-term and ‘collateral consequences’ of criminalization of mental illness and addiction are significant. Life post-incarceration often includes problems with reestablishing family bonds, extended unemployment, lack of housing and access to health insurance, all of which are essential for patients (and a well-functioning behavioral health system needed to serve them)129,130. In the absence of a strong outpatient system and physician workforce that can provide integrated/longitudinal mental health and addiction care, a large portion of individuals with mental illness and addiction are stuck in repeated cycles between emergency rooms and correctional facilities without adequate care39,58,60,77,120,124. In turn, these patients and their brain diseases are viewed, even by the healthcare system and the insurance industry, as recidivistic, undeserving of healthcare resources, and essentially criminal. These trends have contributed to a healthcare system that has been negligent of addiction as a disease that is pathophysiologically connected with mental illness. The seeds of the modern iatrogenic opioid epidemic were thus planted, leading to unprecedented levels of opioid addiction, mortality, and criminal-legal consequences for addictions, especially in mentally ill people63,114,131.

Conclusion

Eighty years ago, Penrose warned that reducing mental health treatment infrastructure would result in increased prison populations. Dr. Penrose died just prior to the advent of the War on Drugs which has likely functioned as an unexpected accelerant of the Penrose Effect in the modern era. Underpinning this acceleration, there exits fundamental neurobiological, and epidemiological connections between addictions and mental illness, as characterized by a broad base of scientific evidence that is still not being adequately translated to inform integrated behavioral healthcare training, service delivery, and treatment research. The associated decline and fragmentation of behavioral healthcare, occurring despite major advances in our neuroscientific understanding of addictions and mental illness as brain diseases, is not only a public health calamity, but jeopardizes the future of psychiatric neuroscience itself, as this science continues to show that it cannot be effectively translated to clinical care, or, if there is no longer a functional behavioral health system to translate to.

While having focused on the Penrose Effect as being accelerated by the War on Drugs, it is also likely that the reverse is simultaneously true: The War on Drugs and associated consequences are probably also amplified by the Penrose Effect. Increased incarceration of those with untreated addiction would be exacerbated by a lack of treatment resources for mental illness, and the even greater paucity of integrated treatment services of addictions in mentally ill people. In this way, a bidirectional amplification of the Penrose Effect and the War on Drugs, happening on the sociological-population scale parallels the bidirectional causal connection and amplification that exists between mental illness and addictions within the brains of millions of individuals. The synergistic criminalization of addiction and mental illness, coupled with a failure in translating the neuroscience of dual diagnosis to building a strong national system of integrated dual diagnosis care, represents a critical failure of the U.S. healthcare system. Large scale signs of this failure continue to emerge both in terms of the iatrogenic opioid epidemic, and the recent decline in the life expectancy for all Americans, which is the first such decline in the era of modern medicine. This decline is remarkable not only for being unique among advanced nations, but also for principally reflecting increased mortality due to untreated addictions and mental illness132135.

From this big picture perspective, we can also infer that mass incarceration and the modern healthcare crisis may also be interlinked and even mutually reinforcing, as mediated by the Penrose-War on Drugs Effect. Given the depth and scope of expensive-to-treat injuries and chronic medical diseases of the body that the U.S. healthcare system is incentivized to treat (that frequently result from untreated addictions), the American people pay for a healthcare system that performs about as well as Cuba’s, but at 14 times the cost136. Yet, ultimate responsibility for solving this health crisis, must fall on the healthcare system itself and not the criminal justice system, which is equipped with professionals trained to carry out justice, enforce laws, and punish crime, not to provide healthcare21,23.

This big picture perspective may provide guidance for a new national strategy needed to restore the cost-effectiveness of U.S. healthcare and to decisively end mass-incarceration. Reversing the Penrose Effect, ending the War on Drugs (as a criminal-legal strategy), and treating addictions and mental illness before they transform into extremely expensive, lethal injuries, multi-organ diseases, and/or prosecutable behavior, will require a non-superficial rebuilding of the behavioral health workforce and infrastructure. The neuroscience of dual diagnosis should be expanded and advanced as a major (rather than largely excluded) NIH research domain as contributed to from across the NIAAA, NIDA, and NIMH portfolios. This would better align their research missions with addressing mental illness-addictions comorbidity as the mainstream public health crisis that it actually represents, allowing greater progress in the development of new integrative and more parsimoniously effective preventative and treatment measures for dual diagnosis conditions. Moreover, the science of dual diagnosis available to us already, which so clearly highlights the fallacy of segregating mental health from addiction expertise and services, needs to be practically and fully translated into a new system of clinics (and closely linked inpatient units) that fully integrate the diagnosis and treatment of mental illnesses and addictions, as provided by cross-trained physicians, nurses, and therapists108,112. This should occur along with removing the responsibility placed on the criminal justice system for paying for, dictating standards of care for, and providing addiction and mental health treatment. If occurring in parallel with efforts to achieve full parity of insurance coverage for behavioral health on par with medical care, in a way that completely separates insurance coverage and standards of care from criminal-legal history, or incarceration status, the U.S. might truly arrive at having the most advanced and cost effective healthcare system in the world.

Acknowledgements

This work was supported in part by T32-CM077229 (National Institute of General Medical Sciences (NIGMS) (G.G.C.) and NIAAA-1RC2AA019366 and R01 AA020396 (NIAAA) (R.A.C. as co-investigator).

Conflict of interest

Neither author has financial or commercial interests that pertain to the work of authorship or content of this manuscript. R.A.C. has had advisory contracts with Indigobio (Indianapolis-based Bioanalytics Technology and Software company) and Proniras (Pharmaceutical Orphan drug Research Firm) and serves as a consultant to the U.S. DOJ, DEA.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Patel V, et al. The Lancet Commission on global mental health and sustainable development. Lancet. 2018;392:1553–1598. doi: 10.1016/S0140-6736(18)31612-X. [DOI] [PubMed] [Google Scholar]
  • 2.Roehrig C. Mental disorders top the list of the most costly conditions in the United States: $201 billion. Health Aff. 2016;35:1130–1135. doi: 10.1377/hlthaff.2015.1659. [DOI] [PubMed] [Google Scholar]
  • 3.Dieleman JL, et al. US spending on personal health care and public health, 1996–2013. JAMA. 2016;316:2627–2646. doi: 10.1001/jama.2016.16885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Hedegaard, H., Curtin, S. C. & Warner, M. Suicide Mortality in the United States, 1999–2017. NCHS Data Brief, no. 330 (National Center for Health Statistics, Hyattsville, MD, 2018). [PubMed]
  • 5.CDC. Opioid Overdose: Understanding the Epidemic Centers for Disease Control and Prevention (2018).
  • 6.Peacock A, et al. Global statistics on alcohol, tobacco and illicit drug use: 2017 status report. Addiction. 2018;113:1905–1926. doi: 10.1111/add.14234. [DOI] [PubMed] [Google Scholar]
  • 7.McGinnis JM, Foege WH. Actual causes of death in the United States. JAMA. 1993;270:2207–2212. doi: 10.1001/jama.1993.03510180077038. [DOI] [PubMed] [Google Scholar]
  • 8.Mokdad AH, Marks JS, Stroup DF, Gerberding JL. Actual causes of death in the United States, 2000. JAMA. 2004;291:1238–1245. doi: 10.1001/jama.291.10.1238. [DOI] [PubMed] [Google Scholar]
  • 9.Penrose LS. Mental disease and crime: outline of a comparative study of European statistics. Br. J. Med. Psychol. 1939;18:1–15. doi: 10.1111/j.2044-8341.1939.tb00704.x. [DOI] [Google Scholar]
  • 10.Conacher GN. Psychiatric hospital downsizing and the Penrose effect. J. Nerv. Ment. Dis. 1996;184:708–710. doi: 10.1097/00005053-199611000-00010. [DOI] [PubMed] [Google Scholar]
  • 11.Large MM, Nielssen O. The Penrose hypothesis in 2004: patient and prisoner numbers are positively correlated in low-and-middle income countries but are unrelated in high-income countries. Psychol. Psychother. 2009;82(Part 1):113–119. doi: 10.1348/147608308X320099. [DOI] [PubMed] [Google Scholar]
  • 12.Gunn J. Future directions for treatment in forensic psychiatry. Br. J. Psychiatry. 2000;176:332–338. doi: 10.1192/bjp.176.4.332. [DOI] [PubMed] [Google Scholar]
  • 13.Blüml V, Waldhör T, Kapusta ND, Vyssoki B. Psychiatric hospital bed numbers and prison population sizes in 26 European countries: a critical reconsideration of the penrose hypothesis. PLoS ONE. 2015;10:e0142163. doi: 10.1371/journal.pone.0142163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Mundt Adrian P., Frančišković Tanja, Gurovich Isaac, Heinz Andreas, Ignatyev Yuriy, Ismayilov Fouad, Kalapos Miklós Péter, Krasnov Valery, Mihai Adriana, Mir Jan, Padruchny Dzianis, Potočan Matej, Raboch Jiří, Taube Māris, Welbel Marta, Priebe Stefan. Changes in the Provision of Institutionalized Mental Health Care in Post-Communist Countries. PLoS ONE. 2012;7(6):e38490. doi: 10.1371/journal.pone.0038490. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lamb HR, Bachrach LL. Some perspectives on deinstitutionalization. Psychiatr. Serv. 2001;52:1039–1045. doi: 10.1176/appi.ps.52.8.1039. [DOI] [PubMed] [Google Scholar]
  • 16.Lamb HR. Lessons learned from deinstitutionalisation in the US. Br. J. Psychiatry. 1993;162:587–592. doi: 10.1192/bjp.162.5.587. [DOI] [PubMed] [Google Scholar]
  • 17.Rosenhan DL. On being sane in insane places. Science. 1973;179:250–258. doi: 10.1126/science.179.4070.250. [DOI] [PubMed] [Google Scholar]
  • 18.Hamden A, Newton R, McCauley-Elsom K, Cross W. Is deinstitutionalization working in our community? Int. J. Ment. Health Nurs. 2011;20:274–283. doi: 10.1111/j.1447-0349.2010.00726.x. [DOI] [PubMed] [Google Scholar]
  • 19.Winkler P, et al. Deinstitutionalised patients, homelessness and imprisonment: systematic review. Br. J. Psychiatry. 2016;208:421–428. doi: 10.1192/bjp.bp.114.161943. [DOI] [PubMed] [Google Scholar]
  • 20.Mundt AP, et al. Psychiatric hospital beds and prison populations in South America since 1990: does the Penrose hypothesis apply? JAMA Psychiatry. 2015;72:112–118. doi: 10.1001/jamapsychiatry.2014.2433. [DOI] [PubMed] [Google Scholar]
  • 21.Kuehn BM. Criminal justice becomes front line for mental health care. JAMA. 2014;311:1953–1954. doi: 10.1001/jama.2014.4578. [DOI] [PubMed] [Google Scholar]
  • 22.Lamb HR, Weinberger LE. The shift of psychiatric inpatient care from hospitals to jails and prisons. J. Am. Acad. Psychiatry Law Online. 2005;33:529–534. [PubMed] [Google Scholar]
  • 23.Lamb HR, Weinberger LE, DeCuir WJ., Jr The police and mental health. Psychiatr. Serv. 2002;53:1266–1271. doi: 10.1176/appi.ps.53.10.1266. [DOI] [PubMed] [Google Scholar]
  • 24.Markowitz FE. Psychiatric hospital capacity, homelessness, and crime and arrest rates. Criminology. 2006;44:45–72. doi: 10.1111/j.1745-9125.2006.00042.x. [DOI] [Google Scholar]
  • 25.Hartvig P, Kjelsberg E. Penrose’s Law revisited: The relationship between mental institution beds, prison population and crime rate. Nord. J. Psychiatry. 2009;63:51–56. doi: 10.1080/08039480802298697. [DOI] [PubMed] [Google Scholar]
  • 26.Kalapos MP. Our social dilemma: prison or psychiatric hospital? Is the Penrose thesis valid for Hungary at the turn of the millennium? Orv. Hetil. 2007;148:1895–1898. doi: 10.1556/OH.2007.28154. [DOI] [PubMed] [Google Scholar]
  • 27.Kelly BD. Penrose’s Law in Ireland: an ecological analysis of psychiatric inpatients and prisoners. Ir. Med. J. 2007;100:373–374. [PubMed] [Google Scholar]
  • 28.Jüriloo A, Pesonen L, Lauerma H. Knocking on prison’s door: a 10-fold rise in the number of psychotic prisoners in Finland during the years 2005–2016. Nord. J. Psychiatry. 2017;71:543–548. doi: 10.1080/08039488.2017.1351579. [DOI] [PubMed] [Google Scholar]
  • 29.Priebe S, et al. Mental health care institutions in nine European countries, 2002 to 2006. Psychiatr. Serv. 2008;59:570–573. doi: 10.1176/ps.2008.59.5.570. [DOI] [PubMed] [Google Scholar]
  • 30.Priebe S, et al. Reinstitutionalisation in mental health care: comparison of data on service provision from six European countries. BMJ. 2005;330:123–126. doi: 10.1136/bmj.38296.611215.AE. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Biles D, Mulligan G. Mad or bad?—The enduring dilemma. Br. J. Criminol. 1973;13:275–279. doi: 10.1093/oxfordjournals.bjc.a046465. [DOI] [Google Scholar]
  • 32.Yoon J, Domino ME, Norton EC, Cuddeback GS, Morrissey JP. The impact of changes in psychiatric bed supply on jail use by persons with severe mental illness. J. Ment. Health Policy Econ. 2013;16:81–92. [PubMed] [Google Scholar]
  • 33.Raphael, S. The deinstitutionalization of the mentally ill and growth in the US prison populations: 1971 to 1996. Unpublished manuscript. (2000).
  • 34.Palermo GB, Smith MB, Liska FJ. Jails versus mental hospitals: a social dilemma. Int. J. Offender Ther. Comp. Criminol. 1991;35:97–106. doi: 10.1177/0306624X9103500202. [DOI] [Google Scholar]
  • 35.Steadman HJ, Monahan J, Duffee B, Hartstone E. The impact of state mental hospital deinstitutionalization on United States prison populations, 1968–1978. J. Crim. Law Criminol. 1984;75:474. doi: 10.2307/1143164. [DOI] [Google Scholar]
  • 36.Ceccherini-Nelli A, Priebe S. Economic factors and psychiatric hospital beds–an analysis of historical trends. Int. J. Soc. Econ. 2007;34:788–810. doi: 10.1108/03068290710826396. [DOI] [Google Scholar]
  • 37.Lamb HR, Weinberger LE. Some perspectives on criminalization. J. Am. Acad. Psychiatry Law. 2013;41:287–293. [PubMed] [Google Scholar]
  • 38.Torrey EF. Deinstitutionalization and the rise of violence. CNS Spectr. 2015;20:207–214. doi: 10.1017/S1092852914000753. [DOI] [PubMed] [Google Scholar]
  • 39.Torrey, E. F. et al. The treatment of persons with mental illness in prisons and jails: a state survey (Treatment Advocacy Center, 2014).
  • 40.Hartwell S. Triple stigma: Persons with mental illness and substance abuse problems in the criminal justice system. Crim. Justice Policy Rev. 2004;15:84–99. doi: 10.1177/0887403403255064. [DOI] [Google Scholar]
  • 41.Corrigan PW, Watson AC. Understanding the impact of stigma on people with mental illness. World Psychiatry. 2002;1:16. [PMC free article] [PubMed] [Google Scholar]
  • 42.Rubinow DR. Out of sight, out of mind: mental illness behind bars. Am. J. Psychiatry. 2014;171:1041–1044. doi: 10.1176/appi.ajp.2014.14060712. [DOI] [PubMed] [Google Scholar]
  • 43.Parry MS. Dorothea Dix (1802–1887) Am. J. Public Health. 2006;96:624–625. doi: 10.2105/AJPH.2005.079152. [DOI] [Google Scholar]
  • 44.Lynch M. Theorizing the role of the ‘War on Drugs’ in US punishment. Theor. Criminol. 2012;16:175–199. doi: 10.1177/1362480612441700. [DOI] [Google Scholar]
  • 45.Cooper HL. War on drugs policing and police brutality. Subst. Use Misuse. 2015;50:1188–1194. doi: 10.3109/10826084.2015.1007669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Coyne, C. J. & Hall, A. Four Decades and Counting: The Continued Failure of the War on Drugs Cato Institute Policy Analysis No. 811 (2017).
  • 47.Csete J, et al. Public health and international drug policy. Lancet. 2016;387:1427–1480. doi: 10.1016/S0140-6736(16)00619-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Hall W. What are the policy lessons of National Alcohol Prohibition in the United States, 1920–1933? Addiction. 2010;105:1164–1173. doi: 10.1111/j.1360-0443.2010.02926.x. [DOI] [PubMed] [Google Scholar]
  • 49.Thornton M. Cato Institute Policy Analysis no. 157: Alcohol Prohibition was a Failure (Cato Institute, 1991).
  • 50.Wagner, P. & Rabuy, B. Following the money of mass incarceration. Prison Policy Initiative (2017).
  • 51.Balko, R. Overkill: the rise of paramilitary police raids in America (2006).
  • 52.Jensen EL, Gerber J, Mosher C. Social consequences of the war on drugs: the legacy of failed policy. Crim. Justice Policy Rev. 2004;15:100–121. doi: 10.1177/0887403403255315. [DOI] [Google Scholar]
  • 53.Hanahan D. Rethinking the war on cancer. Lancet. 2014;383:558–563. doi: 10.1016/S0140-6736(13)62226-6. [DOI] [PubMed] [Google Scholar]
  • 54.Rehemtulla A. The war on cancer rages on. Neoplasia. 2009;11:1252–1263. doi: 10.1593/neo.91866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Werb D, et al. Effect of drug law enforcement on drug market violence: a systematic review. Int. J. Drug Policy. 2011;22:87–94. doi: 10.1016/j.drugpo.2011.02.002. [DOI] [PubMed] [Google Scholar]
  • 56.Wood E, et al. Vienna Declaration: a call for evidence-based drug policies. Lancet. 2010;376:310–312. doi: 10.1016/S0140-6736(10)60958-0. [DOI] [PubMed] [Google Scholar]
  • 57.Wood E, Werb D, Marshall BD, Montaner JS, Kerr T. The war on drugs: a devastating public-policy disaster. Lancet. 2009;373:989–990. doi: 10.1016/S0140-6736(09)60455-4. [DOI] [PubMed] [Google Scholar]
  • 58.Chandler RK, Fletcher BW, Volkow ND. Treating drug abuse and addiction in the criminal justice system: improving public health and safety. JAMA. 2009;301:183–190. doi: 10.1001/jama.2008.976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Pfaff JF. The war on drugs and prison growth: limited importance, limited legislative options. Harv. J. Legis. 2015;52:173. [Google Scholar]
  • 60.Collins, J. Ending the Drug Wars: Report of the LSE Expert Group on the Economics of Drug Policy (London School of Economics, London, 2014).
  • 61.Els C. Addiction is a mental disorder, best managed in a (public) mental health setting—but our system is failing us. Can. J. Psychiatry. 2007;52:167–169. doi: 10.1177/070674370705200305. [DOI] [PubMed] [Google Scholar]
  • 62.Chambers R. Andrew. The Addiction Psychiatrist as Dual Diagnosis Physician: A Profession in Great Need and Greatly Needed. Journal of Dual Diagnosis. 2013;9(3):260–266. doi: 10.1080/15504263.2013.807072. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Greene MS, Chambers RA. Pseudoaddiction: fact or fiction? An investigation of the medical literature. Curr. Addict. Rep. 2015;2:310–317. doi: 10.1007/s40429-015-0074-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Barry CL, Goldman HH, Huskamp HA. Federal parity in the evolving mental health and addiction care landscape. Health Aff. 2016;35:1009–1016. doi: 10.1377/hlthaff.2015.1653. [DOI] [PubMed] [Google Scholar]
  • 65.Friedman SA, et al. The Mental Health Parity and Addiction Equity Act evaluation study: impact on mental health financial requirements among commercial “carve‐in” plans. Health Serv. Res. 2018;53:366–388. doi: 10.1111/1475-6773.12614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Wakeman SE, Pham-Kanter G, Donelan K. Attitudes, practices, and preparedness to care for patients with substance use disorder: results from a survey of general internists. Subst. Abus. 2016;37:635–641. doi: 10.1080/08897077.2016.1187240. [DOI] [PubMed] [Google Scholar]
  • 67.Chambers RA, Krystal JH, Self DW. A neurobiological basis for substance abuse comorbidity in schizophrenia. Biol. Psychiatry. 2001;50:71–83. doi: 10.1016/S0006-3223(01)01134-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Hartwell KJ, Tolliver BK, Brady KT. Biologic commonalities between mental illness and addiction. Prim. Psychiatry. 2009;16:33–39. [PMC free article] [PubMed] [Google Scholar]
  • 69.Gandal MJ, et al. Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap. Science. 2018;359:693–697. doi: 10.1126/science.aad6469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Sentir, A. M., Bell, R. L., Engleman, E. A. & Chambers, R. A. Polysubstance addiction vulnerability in mental illness: concurrent alcohol and nicotine self‐administration in the neurodevelopmental hippocampal lesion rat model of schizophrenia. Addict. Biol. 1–20 (2018). [DOI] [PubMed]
  • 71.Felitti VJ, et al. Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults: The Adverse Childhood Experiences (ACE) Study. Am. J. Preventive Med. 1998;14:245–258. doi: 10.1016/S0749-3797(98)00017-8. [DOI] [PubMed] [Google Scholar]
  • 72.Hasin DS, et al. Epidemiology of adult DSM-5 major depressive disorder and its specifiers in the United States. JAMA Psychiatry. 2018;75:336–346. doi: 10.1001/jamapsychiatry.2017.4602. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Grant BF, et al. Epidemiology of DSM-5 alcohol use disorder: results from the national epidemiologic survey on alcohol and related conditions III. JAMA Psychiatry. 2015;72:757–766. doi: 10.1001/jamapsychiatry.2015.0584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Grant BF, et al. Epidemiology of DSM-5 drug use disorder: results from the national epidemiologic survey on alcohol and related conditions-III. JAMA Psychiatry. 2016;73:39–47. doi: 10.1001/jamapsychiatry.2015.2132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Mueser KT, Drake RE, Wallach MA. Dual diagnosis: a review of etiological theories. Addict. Behav. 1998;23:717–734. doi: 10.1016/S0306-4603(98)00073-2. [DOI] [PubMed] [Google Scholar]
  • 76.Ross S, Peselow E. Co-occurring psychotic and addictive disorders: neurobiology and diagnosis. Clin. Neuropharmacol. 2012;35:235–243. doi: 10.1097/WNF.0b013e318261e193. [DOI] [PubMed] [Google Scholar]
  • 77.Luciano A, et al. Predictors of incarceration among urban adults with co-occurring severe mental illness and a substance use disorder. Psychiatr. Serv. 2014;65:1325–1331. doi: 10.1176/appi.ps.201300408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Chambers RA. Animal modeling and neurocircuitry of dual diagnosis. J. Dual Diagnosis. 2007;3:19–29. doi: 10.1300/J374v03n02_04. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Chambers RA. Adult hippocampal neurogenesis in the pathogenesis of addiction and dual diagnosis disorders. Drug Alcohol Depend. 2013;130:1–12. doi: 10.1016/j.drugalcdep.2012.12.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Dixon L. Dual diagnosis of substance abuse in schizophrenia: prevalence and impact on outcomes. Schizophrenia Res. 1999;35:s93–s100. doi: 10.1016/S0920-9964(98)00161-3. [DOI] [PubMed] [Google Scholar]
  • 81.Buckley PF. Prevalence and consequences of the dual diagnosis of substance abuse and severe mental illness. J. Clin. Psychiatry. 2006;67(Suppl. 7):5–9. [PubMed] [Google Scholar]
  • 82.Lasser K, et al. Smoking and mental illness: a population-based prevalence study. JAMA. 2000;284:2606–2610. doi: 10.1001/jama.284.20.2606. [DOI] [PubMed] [Google Scholar]
  • 83.Davis MA, Lin LA, Liu H, Sites BD. Prescription opioid use among adults with mental health disorders in the United States. J. Am. Board Fam. Med. 2017;30:407–417. doi: 10.3122/jabfm.2017.04.170112. [DOI] [PubMed] [Google Scholar]
  • 84.Regier DA, et al. Comorbidity of mental disorders with alcohol and other drugs of abuse. J. Am. Med. Assoc. 1990;264:2511–2518. doi: 10.1001/jama.1990.03450190043026. [DOI] [PubMed] [Google Scholar]
  • 85.Kessler RC. The epidemiology of dual diagnosis. Biol. Psychiatry. 2004;56:730–737. doi: 10.1016/j.biopsych.2004.06.034. [DOI] [PubMed] [Google Scholar]
  • 86.Hunt, G. E., Large, M. M., Cleary, M., Lai, H. M. X. & Saunders, J. B. Prevalence of comorbid substance use in schizophrenia spectrum disorders in community and clinical settings, 1990–2017: systematic review and meta-analysis. Drug Alcohol Depend. 234–258 (2018). [DOI] [PubMed]
  • 87.Grant BF, et al. Prevalence and co-occurrence of substance use disorders and independent mood and anxiety disorders: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Arch. Gen. Psychiatry. 2004;61:807–816. doi: 10.1001/archpsyc.61.8.807. [DOI] [PubMed] [Google Scholar]
  • 88.Grant BF, Hasin DS, Chou SP, Stinson FS, Dawson DA. Nicotine dependence and psychiatric disorders in the United States: results from the National Epidemiologic Survey on alcohol and related conditions. Arch. Gen. Psychiatry. 2004;61:1107–1115. doi: 10.1001/archpsyc.61.11.1107. [DOI] [PubMed] [Google Scholar]
  • 89.Boscarino JA, et al. Risk factors for drug dependence among out-patients on opioid therapy in a large US health-care system. Addiction. 2010;105:1776–1782. doi: 10.1111/j.1360-0443.2010.03052.x. [DOI] [PubMed] [Google Scholar]
  • 90.Katz C, El-Gabalawy R, Keyes KM, Martins SS, Sareen J. Risk factors for incident nonmedical prescription opioid use and abuse and dependence: results from a longitudinal nationally representative sample. Drug Alcohol Depend. 2013;132:107–113. doi: 10.1016/j.drugalcdep.2013.01.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Hackman DT, et al. Prescription drug monitoring program inquiry in psychiatric assessment: detection of high rates of opioid prescribing to a dual diagnosis population. J. Clin. Psychiatry. 2014;75:750–756. doi: 10.4088/JCP.14m09020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Chambers RA, Bickel WK, Potenza MN. A scale-free systems theroy of motivation and addiction. Neurosci. Biobehav. Rev. 2007;31:1017–1045. doi: 10.1016/j.neubiorev.2007.04.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Pennartz CMA, Groenewegen HJ, Lopez, da Silva FH. The nucleus accumbens as a complex of functionally distinct neuronal ensembles: an integration of behavioral, electrophysiological and anatomical data. Prog. Neurobiol. 1994;42:719–761. doi: 10.1016/0301-0082(94)90025-6. [DOI] [PubMed] [Google Scholar]
  • 94.Chambers RA, et al. Cortical–striatal gene expression in neonatal hippocampal lesion (NVHL)‐amplified cocaine sensitization. Genes Brain Behav. 2013;12:564–575. doi: 10.1111/gbb.12051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Chambers RA, Sentir AM, Conroy SK, Truitt WA, Shekhar A. Cortical–striatal integration of cocaine history and prefrontal dysfunction in animal modeling of dual diagnosis. Biol. Psychiatry. 2010;67:788–792. doi: 10.1016/j.biopsych.2009.09.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Sheehan TP, Chambers RA, Russell DS. Regulation of affect by the lateral septum: implications for neuropsychiatry. Brain Res. Brain Res. Rev. 2004;46:71–117. doi: 10.1016/j.brainresrev.2004.04.009. [DOI] [PubMed] [Google Scholar]
  • 97.Boulos LJ, Darcq E, Kieffer BL. Translating the Habenula—from rodents to humans. Biol. Psychiatry. 2017;81:296–305. doi: 10.1016/j.biopsych.2016.06.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Gasquoine PG. Contributions of the insula to cognition and emotion. Neuropsychol. Rev. 2014;24:77–87. doi: 10.1007/s11065-014-9246-9. [DOI] [PubMed] [Google Scholar]
  • 99.Carey CE, et al. Associations between polygenic risk for psychiatric disorders and substance involvement. Front. Genet. 2016;7:149. doi: 10.3389/fgene.2016.00149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Kendler KS, Prescott CA, Myers J, Neale MC. The structure of genetic and environmental risk factors for common psychiatric and substance use disorders in men and women. Arch. Gen. Psychiatry. 2003;60:929–937. doi: 10.1001/archpsyc.60.9.929. [DOI] [PubMed] [Google Scholar]
  • 101.Olvera R, et al. Common genetic influences on depression, alcohol, and substance use disorders in Mexican‐American families. Am. J. Med. Genet. Part B. 2011;156:561–568. doi: 10.1002/ajmg.b.31196. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Carmiol N, et al. Shared genetic factors influence risk for bipolar disorder and alcohol use disorders. Eur. Psychiatry. 2014;29:282–287. doi: 10.1016/j.eurpsy.2013.10.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Prescott CA, Aggen SH, Kendler KS. Sex-specific genetic influences on the comorbidity of alcoholism and major depression in a population-based sample of US twins. Arch. Gen. Psychiatry. 2000;57:803–811. doi: 10.1001/archpsyc.57.8.803. [DOI] [PubMed] [Google Scholar]
  • 104.Walters R. K., et al. Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience21, 1656–1669 (2018). [DOI] [PMC free article] [PubMed]
  • 105.Kessler RC, et al. Childhood adversities and adult psychopathology in the WHO World Mental Health Surveys. Br. J. Psychiatry. 2010;197:378–385. doi: 10.1192/bjp.bp.110.080499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Van Dam NT, Rando K, Potenza MN, Tuit K, Sinha R. Childhood maltreatment, altered limbic neurobiology, and substance use relapse severity via trauma-specific reductions in limbic gray matter volume. JAMA Psychiatry. 2014;71:917–925. doi: 10.1001/jamapsychiatry.2014.680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Zarse, E. M. et al. The adverse childhood experiences questionnaire: two decades of research on childhood trauma as a primary cause of adult mental illness, addiction, and medical diseases. Cogent Med. 1–24 (2019).
  • 108.Chambers R. A. The 2 × 4 Model: A Neuroscience-Based Blueprint for the Modern Integrated Addiction and Mental Health Treatment System 1st edn (Routledge: CRC Press, New York, NY, 2017).
  • 109.Kelly TM, Daley DC. Integrated treatment of substance use and psychiatric disorders. Soc Work. Public Health. 2013;28:388–406. doi: 10.1080/19371918.2013.774673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.O Brien CP, et al. Priority actions to improve the care of persons with co-occurring substance abuse and other mental disorders: a call to action. Biol. Psychiatry. 2004;56:703–713. doi: 10.1016/j.biopsych.2004.10.002. [DOI] [PubMed] [Google Scholar]
  • 111.McGovern MP, Lambert-Harris C, Gotham HJ, Claus RE, Xie H. Dual diagnosis capability in mental health and addiction treatment services: an assessment of programs across multiple state systems. Adm. Policy Ment. Health. 2014;41:205–214. doi: 10.1007/s10488-012-0449-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Drake RE, Wallach MA. Dual diagnosis: 15 years of progress. Psychiatr. Serv. 2000;51:1126–1129. doi: 10.1176/appi.ps.51.9.1126. [DOI] [PubMed] [Google Scholar]
  • 113.Halbert BT, Davis RB, Wee CC. Disproportionate longer-term opioid use among U.S. adults with mood disorders. Pain. 2016;157:2452–2457. doi: 10.1097/j.pain.0000000000000650. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.Sullivan MD. Depression effects on long-term prescription opioid use, abuse, and addiction. Clin. J. Pain. 2018;34:878–884. doi: 10.1097/AJP.0000000000000603. [DOI] [PubMed] [Google Scholar]
  • 115.Winkelman TNA, Chang VW, Binswanger IA. Health, polysubstance use, and criminal justice involvement among adults with varying levels of opioid use. JAMA Netw. Open. 2018;1:e180558. doi: 10.1001/jamanetworkopen.2018.0558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Prince JD, Wald C. Risk of criminal justice system involvement among people with co-occurring severe mental illness and substance use disorder. Int. J. Law Psychiatry. 2018;58:1–8. doi: 10.1016/j.ijlp.2018.02.002. [DOI] [PubMed] [Google Scholar]
  • 117.Wallace C, Mullen PE, Burgess P. Criminal offending in schizophrenia over a 25-year period marked by deinstitutionalization and increasing prevalence of comorbid substance use disorders. Am. J. Psychiatry. 2004;161:716–727. doi: 10.1176/appi.ajp.161.4.716. [DOI] [PubMed] [Google Scholar]
  • 118.Swartz JA, Lurigio AJ. Serious mental illness and arrest: the generalized mediating effect of substance use. Crime Delinquency. 2007;53:581–604. doi: 10.1177/0011128706288054. [DOI] [Google Scholar]
  • 119.Wagner, P. & Rabuy, B. Mass Incarceration: The Whole Pie 2016. Prison Policy Initiative. 119, 1–23 (2017).
  • 120.Peters, R. H., Wexler, H. K. & Lurigio A. J. Co-occurring substance use and mental disorders in the criminal justice system: a new frontier of clinical practice and research. Psychiatr. Rehabil. J. 38, 1–6 (2015). [DOI] [PubMed]
  • 121.Rich JD, et al. Methadone continuation versus forced withdrawal on incarceration in a combined US prison and jail: a randomised, open-label trial. Lancet. 2015;386:350–359. doi: 10.1016/S0140-6736(14)62338-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122.Wakeman SE, Rich JD. Addiction treatment within U.S. Correctional facilities: bridging the gap between current practice and evidence-based care. J. Addict. Dis. 2015;34:220–225. doi: 10.1080/10550887.2015.1059217. [DOI] [PubMed] [Google Scholar]
  • 123.Stranahan AM, Khalil D, Gould E. Social isolation delays the positive effects of running on adult neurogenesis. Nat. Neurosci. 2006;9:526–533. doi: 10.1038/nn1668. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Al-Rousan T, Rubenstein L, Sieleni B, Deol H, Wallace RB. Inside the nation’s largest mental health institution: a prevalence study in a state prison system. BMC Public Health. 2017;17:342. doi: 10.1186/s12889-017-4257-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Rich JD, Wakeman SE, Dickman SL. Medicine and the epidemic of incarceration in the United States. N. Engl. J. Med. 2011;364:2081. doi: 10.1056/NEJMp1102385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Young JT, et al. Dual diagnosis of mental illness and substance use disorder and injury in adults recently released from prison: a prospective cohort study. The Lancet. Public Health. 2018;3:e237–e248. doi: 10.1016/S2468-2667(18)30052-5. [DOI] [PubMed] [Google Scholar]
  • 127.Gottfried ED, Christopher SC. Mental disorders among criminal offenders: a review of the literature. J. Correct. Health Care. 2017;23:336–346. doi: 10.1177/1078345817716180. [DOI] [PubMed] [Google Scholar]
  • 128.McNiel DE, Binder RL, Robinson JC. Incarceration associated with homelessness, mental disorder, and co-occurring substance abuse. Psychiatr. Serv. 2005;56:840–846. doi: 10.1176/appi.ps.56.7.840. [DOI] [PubMed] [Google Scholar]
  • 129.Council, N. R. in (eds Travis, J., Western, B. & Redburn, S.) The Growth of Incarceration in the United States: Exploring Causes and Consequences, 464 (The National Academies Press, Washington, DC, 2014).
  • 130.Massoglia M, Warner C. The consequences of incarceration: Challenges for scientifically informed and policy-relevant research. Criminol. Pub Pol’y. 2011;10:851. doi: 10.1111/j.1745-9133.2011.00754.x. [DOI] [Google Scholar]
  • 131.Amari E, Rehm J, Goldner E, Fischer B. Nonmedical prescription opioid use and mental health and pain comorbidities: a narrative review. Can. J. Psychiatry. 2011;56:495–502. doi: 10.1177/070674371105600808. [DOI] [PubMed] [Google Scholar]
  • 132.Hedegaard, H., Miniño, A. M. & Warner, M. Drug overdose deaths in the United States, 1999–2017. NCHS Data Brief, 329 (National Center for Health Statistics, Hyattsville, MD, 2018).
  • 133.Murphy S. L., Xu J., Kochanek K. D. & Arias, E. Mortality in the United States, 2017. NCHS Data Brief, 328 (National Center for Health Statistics, Hyattsville, MD, 2018). [PubMed]
  • 134.Dowell D, et al. Contribution of opioid-involved poisoning to the change in life expectancy in the United States, 2000–2015. JAMA. 2017;318:1065–1067. doi: 10.1001/jama.2017.9308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Kochanek KD, Arias E, Bastian BA. Statistics NCfH. The effect of changes in selected age-specific causes of death on non-Hispanic white life expectancy between 2000 and 2014. Heart Dis. 2017;1:0.581. [PubMed] [Google Scholar]
  • 136.Johnston S. Claiborne. Academic Medical Centers. JAMA. 2019;322(3):203. doi: 10.1001/jama.2019.6834. [DOI] [PubMed] [Google Scholar]

Articles from Translational Psychiatry are provided here courtesy of Nature Publishing Group

RESOURCES