Toward more efficient diagnostic criteria sets and rules: The use of optimization approaches in addiction science☆
Introduction
Valid and reliable diagnostic criteria sets and rules (DCSRs) are fundamental to clinical research and practice. Current diagnostic standards, such as the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM–5; American Psychiatric Association [APA], 2013) utilize expert consensus informed by relevant literature to develop DCSRs of psychopathology (Frances & Widiger, 2012; Hasin et al., 2013). For example, in revising the DSM, the DSM-5 Substance-Related Disorders Workgroup (Hasin et al., 2013) tasked itself with answering questions such as: “Which if any diagnostic criteria can be dropped?” and “What should the diagnostic threshold be?” (Hasin et al., 2013). The ability to answer questions such as these is limited by the inherent subjectivity that permeates the consensus process (Frances & Widiger, 2012; Wakefield, 2015). However, statistical techniques can be used to empirically derive new DCSRs where the process is transparent and biases are made explicit.
The optimization procedure described here (Steinley et al., 2016, Steinley et al., 2016; Stevens et al., 2018), can empirically derive DCSRs based on a priori clinical correlates and outcomes that serve as optimization criteria (OptCrit). Raffo and colleagues (2018) have successfully demonstrated that a similar method could be used to create short-forms of diagnosis by optimizing the correlations between the full DSM-5 Alcohol Use Disorder (AUD) criteria set with diagnostic thresholds (i.e., the number of criteria in a set one must endorse to diagnose) of one or two. By optimizing on the basis of part-whole correlations, Raffo et al.'s approach is likely influenced by intrinsic correlated error, a limitation not shared with our current approach. Additionally, the Raffo et al., (2018) approach employed a post hoc evaluation of a fixed number of diagnostic thresholds subsequent to short-form derivation, in effect, evaluating only a restricted subset of possible criteria sets and diagnostic rules and thus not guaranteed to identify an optimal solution (OS). The current procedure, however, is optimizing on external criteria to derive novel diagnoses rather than creating a shortened form of the diagnostic sets. This approach uses complete enumeration to compare all possible criteria set sizes and diagnostic thresholds from a selected set of criteria. Table 1 illustrates complete enumeration on an 11 item criteria set varying the diagnostic threshold from 1 to 11, producing 11,264 DCSRs. Once completely enumerated, the distribution of all measures of separation produced can be used to identify where the diagnostic grouping (i.e., those diagnosing under the given rule versus those not diagnosed by the rule) are meaningfully distinguishable using some objective function, such as maximizing the effect size. Here, we extend our previous work (Steinley et al., 2016, Steinley et al., 2016; Stevens et al., 2018) by deriving a common DCSR across alcohol and cannabis in order to illustrate how this approach can be used to identify a single OS common to alcohol and other drugs of abuse (e.g., Budney, 2006). Although the focus of the current paper is to describe how optimal DCSRs can be derived, applications using the current approach can be found in optimizing the diagnosis of Alcohol Use Disorder (AUD; Boness et al., 2018), resulting in variable, equally performing diagnostic rules (i.e., set size of 9 with a diagnostic threshold of three or a set size of five with a diagnostic threshold of 2).
Section snippets
Method
Below we describe the process that one would go through in using complete enumeration to identify an optimal DCSR, with the application provided in Section 4. This includes both basic decisions about selection of datasets, OptCrit, and external validation approaches.
Dataset
Data were drawn from the National Epidemiological Survey on Alcoholism and Related Conditions- III (NESARC-III; Grant et al., 2009). NESARC-III, conducted from 2012 to 2013, was sponsored by the National Institute on Alcohol Abuse and Alcoholism (NIAAA). Multistage probability sampling (see Grant et al., 2015) was used to randomly select a nationally representative sample of United States citizens at least 18 years old. There were a total of 36,309 participants in the NESARC-III survey,
Demonstration
In this section, we provide a detailed, step-by-step example of optimizing diagnosis across AUD and CUD to develop a general SUD diagnosis at a moderate or above severity level (i.e., endorsing at least four of the 11 criteria) defined by the DSM-5.
Step 0: Data preparation and a priori decisions
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Diagnostic Criteria (DxCrit). The DxCrit used to develop an overall SUD diagnosis are the 11 DSM-5 AUD and CUD criteria. In total, 22 DxCrit (11 from each substance) were used.
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Optimization criterion
Selection of optimal sets
The identified moderate-severe optimal diagnostic rule included a set size of 4 with a diagnostic threshold of 2. The DxCrit of the derived general SUD rule are: 1) having a strong urge or craving for the substance (CR), 2) failure to fulfill major role obligations at work school or home (FF), 3) continued use of the substance despite social or interpersonal problems caused by the substance use (SI) and 4) physically hazardous use (HU).
Validation
Planned comparisons incorporating NESARC-III's complex
Conclusions
This paper provides a guide for a data-driven, empirical optimization procedure that can be used for diagnostic refinement. The results from the example, creating a diagnostic set to optimally diagnose AUD or CUD, demonstrated that large sets can be reduced to more efficient and manageable set sizes to decrease research, clinician, and patient burden during assessment. In the current case we identified 4 items: 1) having a strong urge or craving for the substance (CR), 2) failure to fulfill
Role of funding sources
Funding for this study was provided by the NIH grants T32AA013526, F31AA026177, R01 AA13397, K24 AA020840 and R01AA024133. This is a secondary analysis of the NESARC-III dataset that was conducted by the entramural branch of NIAAA. The authors were funded in part by NIH grants T32AA013526, F31AA026177, R01 AA13397, K24 AA020840 and R01AA024133. Consquently, NIAAA is responsible for the conduct of NEARC-III but the investigators were wholly responsible for the analyses, interpretation of the
Contributors
Authors Stevens and Steinley developed and performed the statistical techniques described in this manuscript. Stevens wrote the first draft of the manuscript and all other authors (McDowell, Boness, Trull, Martin, Steinley, and Sher) contributed to and have approved the final manuscript.
Conflict of interest
All authors declare that they have no conflicts of interest.
Acknowledgments
The present study was supported by the NIH grants T32AA013526, F31AA026177, R01 AA13397, K24 AA020840 and R01AA024133.
References (42)
- et al.
The role of cannabis use within a dimensional approach to cannabis use disorders
Drug & Alcohol Dependence
(2009) - et al.
A multidimensional assessment of the validity and utility of alcohol use disorder severity as determined by item response theory models
Drug and Alcohol Dependence
(2010) Future paths for integer programming and links to artificial intelligence
Computers & Operations Research
(1986)- et al.
The Alcohol Use Disorder and Associated Disabilities Interview Schedule-IV (AUDADIS-IV): reliability of alcohol consumption, tobacco use, family history of depression and psychiatric diagnostic modules in a general population sample
Drug and Alcohol Dependence
(2003) - et al.
Alcohol consumption indices of genetic risk for alcohol dependence
Biological Psychiatry
(2009) - et al.
The role of alcohol consumption in future classifications of alcohol use disorders
Drug and Alcohol Dependence
(2007) Diagnostic and statistical manual of mental disorders
(2013)- et al.
Gender differences in pharmacokinetics of alcohol
Alcoholism: Clinical and Experimental Research
(2001) - et al.
Liking, wanting, and the incentive-sensitization theory of addiction
American Psychologist
(2016) - et al.
What Is Addiction? How Can Animal and Human Research Be Used to Advance Research, Diagnosis, and Treatment of Alcohol and Other Substance Use Disorders?
Alcoholism: Clinical and Experimental Research
(2019)
Deriving alternative criteria sets for alcohol use disorders using statistical optimization: Results from the National Survey on Drug Use and Health
Experimental and clinical psychopharmacology
Are specific dependence criteria necessary for different substances: how can research on cannabis inform this issue?
Addiction
Psychiatric diagnosis: Lessons from the DSM-IV past and cautions for the DSM-5 future
Annual Review of Clinical Psychology
Epidemiology of DSM-5 alcohol use disorder: results from the National Epidemiologic Survey on Alcohol and Related Conditions III
JAMA Psychiatry
The National Epidemiologic Survey on Alcohol and Related Conditions (NESARC) Waves 1 and 2: review and summary of findings
Social Psychiatry and Psychiatric Epidemiology
DSM-5 criteria for substance use disorders: Recommendations and rationale
American Journal of Psychiatry
Adaptation in natural and artificial systems. An introductory analysis with application to biology, control, and artificial intelligence
Optimization by simulated annealing. World Scientific Lecture Notes in Physics Spin Glass Theory and Beyond
Limits of current approaches to diagnosis severity based on criterion counts: An example with DSM-5 alcohol use disorder
Clinical Psychological Science
How should we revise diagnostic criteria for substance use disorders in the DSM-V?
Journal of Abnormal Psychology
Truth or consequences in the diagnosis of substance use disorders
Addiction
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The present study was supported by the NIH grants T32AA013526, F31AA026177, R01AA13397, K24-AA020840 and R01AA024133.