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    O R I G I N A L P A P E R

    Comparison of ICD-10R, DSM-IV-TR and DSM-5 in an AdultAutism Spectrum Disorder Diagnostic Clinic

    C. Ellie Wilson Nicola Gillan Deborah Spain Dene Robertson

    Gedeon Roberts Clodagh M. Murphy Stefanos Maltezos Janneke Zinkstok

    Katie Johnston Christina Dardani Chris Ohlsen P. Quinton Deeley

    Michael Craig Maria A. Mendez Francesca Happe Declan G. M. Murphy

    Published online: 16 March 2013

    Springer Science+Business Media New York 2013

    Abstract An Autism Spectrum Disorder (ASD) diagnosis

    is often used to access services. We investigated whetherASD diagnostic outcome varied when DSM-5 was used

    compared to ICD-10R and DSM-IV-TR in a clinical

    sample of 150 intellectually able adults. Of those diagnosed

    with an ASD using ICD-10R, 56 % met DSM-5 ASD

    criteria. A further 19 % met DSM-5 (draft) criteria for

    Social Communication Disorder. Of those diagnosed with

    Autistic Disorder/Asperger Syndrome on DSM-IV-TR,

    78 % met DSM-5 ASD criteria. Sensitivity of DSM-5 was

    significantly increased by reducing the number of criteria

    required for a DSM-5 diagnosis, or by rating uncertain

    criteria as present, without sacrificing specificity.Reduced rates of ASD diagnosis may mean some ASD

    individuals will be unable to access clinical services.

    Keywords Autism Spectrum Disorder Diagnosis

    Prevalence DSM-5

    Introduction

    Autism Spectrum Disorder (ASD) is a neurodevelopmental

    disorder with a prevalence currently estimated at 1 in 80

    individuals (Pinborough-Zimmerman et al.2012). In recent

    years there has been a rise in reported rates of ASD. The

    reason for this is unclear, but changes in diagnostic practice

    are likely to have contributed (Fombonne 2005). Also, a

    formal diagnosis of an ASD is often used as a gatekeeper

    for services and support. Therefore changes in diagnostic

    practice may have important implicationsboth for clini-

    cal prevalence rates and for an individuals care options.

    An Autism Spectrum Disorder is diagnosed on the basis

    of three domains: impaired social interaction, abnormal

    communication, and restricted and repetitive behaviours

    and interests. Using current diagnostic criteria in the

    International Classification of Diseases (ICD-10R; World

    Health Organization 1993) and the Diagnostic and Statis-

    tical Manual (DSM-IV-TR; American Psychiatric Associ-

    ation 2000), ASD comes under the umbrella term of

    Pervasive Developmental Disorder (PDD) and an individ-

    ual may be defined as having one of four diagnostic sub-

    types according to the range of symptoms and the presence/

    absence of factors such as developmental language delay

    and intellectual disability (i.e., Asperger Syndrome,

    Childhood Autism/Autistic Disorder, Atypical Autism,

    Francesca Happe and Professor Declan Murphy are joint senior

    authors.

    Data from this manuscript were presented at the International Meeting

    for Autism Research, Toronto, Canada, May 2012.

    Francesca Happe is part of the DSM-5 workgroup on

    neurodevelopmental disorders.

    C. E. Wilson (&) N. Gillan D. Spain G. Roberts

    C. M. Murphy S. Maltezos J. Zinkstok C. Dardani

    P. Q. Deeley M. Craig M. A. Mendez D. G. M. Murphy

    Department of Forensic and Neurodevelopmental Science,

    Institute of Psychiatry, Kings College, London SE5 8AF, UK

    e-mail: [email protected]

    C. E. Wilson N. Gillan D. Spain D. Robertson

    G. Roberts C. M. Murphy S. Maltezos J. Zinkstok

    K. Johnston C. Ohlsen P. Q. Deeley M. Craig

    M. A. Mendez D. G. M. Murphy

    Behavioural Genetics Clinic, Maudsley Hospital, South London

    and Maudsley NHS Foundation Trust, London SE5 8AZ, UK

    F. Happe

    Department of Social Genetic Developmental and Psychiatry

    Centre, Institute of Psychiatry, Kings College,

    London SE5 8AF, UK

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    J Autism Dev Disord (2013) 43:25152525

    DOI 10.1007/s10803-013-1799-6

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    PDD-unspecified). There are, however, problems with

    current diagnostic algorithms. First, distinguishing the

    social and communication domains is somewhat arbi-

    trary since almost any example of communication is social

    and vice versa, and, several social and communication

    symptoms are covered by multiple criteria. For instance,

    behaviors indicative of poor socio-emotional reciprocity

    are currently covered in three criteriapoor emotionalreciprocity (social domain), lack of sharing enjoyment and

    interests (social domain), and poor reciprocal conversation

    (communication domain) (see Appendix1). Second, there

    is a lack of evidence for significant differences between

    ASD diagnostic subtypes (once IQ matched) in etiology,

    neuropsychological profile, treatment or outcome, and poor

    clinical agreement when diagnosing (Ozonoff 2012).

    Unclear guidance on how to define people who have

    symptoms of ASD but do not meet full criteria also con-

    tributes to disagreement between clinicians.

    To address these problems, the Neurodevelop-

    mental Disorders Workgroup, convened by the AmericanPsychiatric Association (APA), has proposed a number of

    significant changes to the diagnostic criteria for ASD

    (Happe 2011; Swedo et al. 2012). The social and com-

    munication impairment criteria will be combined into a

    single set, thus reducing the current triad of impairments

    to two domains. In the social and communication domain

    there will be three criteria, instead of the current total of

    eight, and each criteria will include several examples of

    behaviors from across the lifespan that might indicate the

    presence of that symptom. Next, the previously distinct

    diagnostic subtypes will be collapsed into a single category

    of Autism Spectrum Disorder. People who do not present

    with the full range of symptoms will no longer be eligible

    for an ASD diagnosis, since there is no atypical or not

    otherwise specified category (as in ICD-10R, DSM-IV-

    TR). Instead, a new diagnostic category called Social

    Communication Disorder (SCD) has been proposed. This is

    defined as being outside the autism spectrum, but will

    provide diagnostic coverage for those individuals with

    symptoms in the social-communication domain, but who

    have never displayed repetitive, restricted behaviours or

    interests. The intention is that the changes to the diagnostic

    algorithm will reduce the wide variability between indi-

    viduals on the autistic spectrum, by more clearly defining

    the symptoms required for diagnosis and by reducing the

    potential for clinicians to disagree.

    The effect of the proposed changes on diagnostic out-

    comes has been investigated in children and adolescents

    with several studies reporting that the specificity of the

    proposed DSM-5 criteria is good, but sensitivity is rela-

    tively poor, when judged against current ICD-10R or

    DSM-IV-TR criteria (Frazier et al. 2012; Matson et al.

    2012; Mattila et al. 2011; McPartland et al. 2012; Taheri

    and Perry 2012; Worley and Matson 2012). This high-

    lights a key concern of some: that the new criteria will fail

    to capture individuals currently receiving an ASD diag-

    nosis who are on the broader spectrum according to

    DSM-IV-TR or ICD-10R criteria (e.g., Pervasive Devel-

    opmental Disorder-not otherwise specified; PDD-NOS).

    As a consequence it is feared by some that these indi-

    viduals will be denied access to services. Reassuringly,however, a large study of children diagnosed within the

    PDD category according to DSM-IV-TR suggested that

    sensitivity of DSM-5 is very good (0.91) although sensi-

    tivity in this study was much lower (0.53) (Huerta et al.

    2012).

    The effect of the proposed changes for adults has

    received relatively little attention. This is of importance

    because ASD is a lifelong condition therefore most people

    with ASD are adults. Moreover, the number of individuals

    presenting for first diagnosis in adulthood is rapidly

    increasing: at the National ASD assessment service at the

    South London and Maudsley in the UK, the number ofASD assessments per month increased fourfold between

    2005 and 2010 (Murphy et al. 2011). Further, diagnosis is

    particularly challenging in this group because a develop-

    mental history is often unavailable and/or unreliable; and

    presentation is frequently complicated by additional

    mental health conditions (Carpenter2012). The only prior

    study that explored the agreement between current and

    proposed ASD criteria in adults included only individuals

    with (mostly profound) intellectual disability living in

    residential centers (Matson et al. 2012); they reported that

    approximately one third of the individuals who met DSM-

    IV-TR criteria no longer met them using the draft DSM-5.

    This study was a valuable first step. However, the

    majority of the ASD population does not have profound

    intellectual impairment (Baird et al. 2000) and such

    people are assessed within mental health or social/edu-

    cational services. Also, it is unknown what proportion of

    individuals would qualify for the new, alternative diag-

    nosis of SCD.

    Our primary aim, therefore, was to investigate how

    diagnostic outcomes of the DSM-5 algorithm differed from

    both ICD-10R and the DSM-IV-TR when applied in a

    clinical health service; and to compare all three algorithms

    to so-called gold-standard research diagnostic assessment

    tools (the Autism Diagnostic Interview-Revised (ADI-R;

    Lord et al. 1994) and Autism Diagnostic Observation

    Schedule (ADOS-G; Lord et al.2000). Our secondary aims

    were to investigate whether diagnostic outcomes were

    affected by participant characteristics (age, sex, IQ, pres-

    ence of additional mental health conditions), or alterations

    to the formulation of the proposed algorithm. Specifically,

    the impact of reducing the number of criteria required for a

    formal diagnosis was examined, and also the treatment of

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    criteria where the clinician was uncertain or had insuffi-

    cient information to code the item.

    Method

    Participants

    Participants included 158 individuals consecutively asses-

    sed for ASD in a specialist National tertiary ASD diag-

    nostic clinic for adults between January and May 2011. The

    clinic is situated within the South London and Maudsley

    NHS Foundation Trust. People are typically referred by

    their local family physician/general practitioner (GP) or

    consultant psychiatrist for a second opinion. In 8 cases

    diagnosis was inconclusive due to a history of acquired

    head injury or the presence of severe psychotic symptoms

    during assessment. Data from these cases were excluded

    from the study. The remaining 150 participants were aged

    1865 years, with a mean age of 31 years. There were 110males (mean age 32 years) and 40 females (mean age

    31 years). Seventy-three patients already had a diagnosis of

    a mental health condition (most commonly depression,

    anxiety, Obsessive Compulsive Disorder (OCD), or

    Attention Deficit Hyperactivity Disorder (ADHD)), and

    only 7 of these had previously been diagnosed with ASD.

    Measures

    The ADI-R and ADOS-G are gold-standard research

    diagnostic assessment tools for ASD. The ADI-R is a semi-

    structured interview with the parent or caregiver assessing

    ASD traits during childhood, and the ADOS-G is assess-

    ment completed with the patient assessing current traits of

    ASD. High levels of testretest reliability have been

    reported for both the ADI-R (in all domains, j[ 0.6; Hill

    et al. 2001), and the ADOS-G (in social and communica-

    tion domains, j[ 0.7; Lord et al. 2000). Well-validated

    self-rating questionnaires were used to assess levels of

    other mental health conditions. The Obsessive Compulsive

    Inventory-Revised (OCI-R; Foa et al. 2002) was used to

    assess traits of OCD, and has high internal consistency

    when used among patients with OCD (a = .83) and

    patients with other anxiety disorders (a = .88), (Abramo-

    witz and Deacon 2006). Symptoms of ADHD were asses-

    sed using the Barkleys Current and Childhood Symptom

    Scales (Barkley and Murphy 2005), which is a self- and

    informant-rated questionnaire used widely in clinical

    assessments for ADHD in adults (Barkley 2011). Finally,

    the Hospital Anxiety and Depression Scale (HADS; Zig-

    mond and Snaith1983) was used to assess levels of anxiety

    and depression, and has high levels of internal consistency

    when used in general population adult sample, (a = .90)

    (Lisspers et al.1997).

    Clinical Assessment

    Assessment included a detailed psychiatric assessment

    using ICD-10R research diagnostic criteria and, wherepossible (i.e., where parents were available, able and

    willing), an ADI-R. In the event that no parent was avail-

    able for the ADI-R the person seeking diagnosis was asked

    to undergo the ADOS-G. In some cases both assessment

    tools were required to gather enough relevant information.

    Seventy-one individuals were assessed using the ADI-R, 62

    were assessed with the ADOS-G, and 17 were assessed

    using both ADI-R and ADOS-G.

    All information obtained was compiled by the multi-

    disciplinary clinical teama consultant psychiatrist, junior

    doctor, and ADI-R/ADOS-G administrator (nurse or psy-

    chologist)who together decided whether each criterionon the ICD-10R algorithm was fulfilled (see Appendix1).

    If a patient met full ICD-10R criteria (a total of at least six

    symptoms must be presenteither currently or by his-

    torywith at least two from the first domain and one from

    each of the second and third domains) and the symptoms

    were noted before the age of 3, they were diagnosed with

    Childhood Autism (if they exhibited a language delay) or

    Asperger Syndrome (if there was no evidence of a lan-

    guage delay). In line with ICD-10R guidelines, if a patient

    exhibited some autistic symptoms but did not meet full

    ICD-10R diagnostic criteria they were diagnosed with

    Pervasive Developmental Disorder, unspecified (PDD-

    unspecified) or Atypical Autism. For the purposes of this

    study these two sub-threshold diagnostic groups were

    collapsed into a single PDD-unspecified group. In some

    cases it was not possible to decide confidently whether or

    not a symptom was present due to a lack of information, or

    because information obtained from patient and parent

    contradicted each other. In this event the criterion was

    coded as Unclear, and the team made the clinical diag-

    nostic decision based on the gestalt of the information

    received. Of the 150 consecutive assessments, 113 were

    diagnosed with an ASD using ICD-10R criteria. Of these,

    28 participants were subtyped as having Childhood Aut-

    ism, 48 Asperger Syndrome, and 37 PDD-unspecified.

    Additional mental health conditions were also diagnosed

    in accordance with the ICD-10R (with the exception of

    adult ADHD which, in keeping with UK guidelines, was

    assessed using DSM-IV-TR), and the supplementary self-

    report questionnaires were used to help inform assessment

    of OCD, ADHD, depression and anxiety (respectively, the

    OCI-R, Barkleys Current and Childhood Symptom Scales,

    and the HADS).

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    Where there was clinical suspicion that a participant

    might have intellectual disability (F70-73 in ICD-10R) or a

    significant lacuna in a neuropsychological function, they

    were referred for testing of general intellectual and exec-

    utive functioning. These participants (N = 35) were tested

    using the Weschler Abbreviated Intelligence Scale-III,

    (WAIS III; Wechsler 1997) which revealed a mean Per-

    formance IQ of 87 (SD = 16, range 55132) and a meanVerbal IQ of 95 (SD = 18, range 60133). Mean full-scale

    IQ could not be calculated in 16 participants due to large

    discrepancies between Performance IQ and Verbal IQ; in

    the remaining 19 mean full-scale IQ was 90 (SD= 17,

    range 53129) and only 2 participants had an IQ below 70.

    The remaining 115 participants, not referred for such

    testing, were estimated to be in the normal range of general

    intellectual function based on educational attainment,

    employment, and informant report.

    Procedure

    For each participant the diagnostic outcome (ASD/not

    ASD; ICD-10R subtype of ASD; ADI-R and ADOS-G

    scores; presence of additional mental health problems) was

    reviewed by the research team. Information from the

    ICD-10R algorithm was used to determine whether each

    criterion on the proposed DSM-5 algorithm would be sat-

    isfied, and this was supplemented by anonymized reports

    from the ADI-R, ADOS-G, and the psychiatric interview.

    Appendix2shows how information in the ICD-10R maps

    onto the DSM-5. Each criterion could be coded as Yes,

    No, or Unclear. A participant was considered to meet

    criteria for ASD on the DSM-5 only when all three criteria

    in A and at least 2 out of 4 criteria in B were coded as

    Yes, as suggested in the criteria last posted by APA. If a

    participant did not meet criteria for ASD on the DSM-5 it

    was determined whether they would meet criteria for the

    alternative diagnosis of Social Communication Disorder

    (SCD). Re-coding was completed by pairs of researchers,

    and for 40 sets of participant data the re-coding was

    reviewed at consensus meetings with the whole team (10

    researchers) to ensure agreement.

    Data were also re-coded to complete the DSM-IV-TR

    algorithm (demonstrated in Appendix 1), on which par-

    ticipants could be diagnosed as either ASD (Autistic

    Disorder/Asperger Syndrome) if they fulfilled at least six

    criteria, with at least 2 in domain A and 1 from each of

    domains B and C, or not ASD.

    Factors affecting agreement between ICD-10R, DSM-

    IV-TR and DSM-5 were also investigated. Participant

    characteristics (age, sex, IQ, additional mental health

    conditions) were compared between ASD positive and

    negative groups, and the effect of being assessed using the

    ADI-R, ADOS-G, or both, was also investigated. The

    effect of altering the DSM-5 algorithm was examined in

    two ways: by relaxing the number of criterion required for

    diagnosis, and by considering criteria that were coded as

    Unclear as either met or not met. To examine the effect of

    relaxing the number of criteria required for diagnosis the

    thresholds were reduced in Criteria A (from 3 to 2), or in

    Criteria B (from 2 to 1), or both. To examine the effect of

    including or excluding the Unclear items, the DSM-5algorithm was re-coded by considering Unclear items to

    be present. This was relevant because the DSM-5 allows

    criteria to be met by history, and allowing or disallowing

    the Unclear criteria is likely to be crucial in many adult

    cases where multiple informants are not available.

    It was hypothesized that, (a) prevalence of Childhood

    Autism or Asperger Syndrome diagnosed using ICD-10R

    criteria would be similar to that using DSM-IV-TR and

    DSM-5, (b) most participants diagnosed with ASD on the

    ICD-10R but not the DSM-5 would be diagnosed with

    SCD, and (c) altering the DSM-5 algorithm would have

    significant effects on the rate of positive DSM-5 ASDdiagnosis.

    Results

    Conclusions of Initial Diagnostic Assessments

    ICD-10R Versus DSM-5 (Table1)

    Of the 150 participants, 113 (75 %) met criteria for an ASD

    according to the ICD-10R (Childhood Autism, Asperger

    Syndrome or PDD-unspecified). In contrast, however,

    according to the DSM-5, only 63 (42 %) met ASD criteria:

    this was a highly significant decline, v2(1) = 35.6,

    p\ 0.001. A further 21 (14 %) participants met DSM-5

    criteria for SCD. Overall, therefore, of those individuals

    positive for ASD on ICD-10R, 74 % (84 of 113) met criteria

    for ASD or SCD on DSM-5. Nevertheless, the proportion of

    individuals with no diagnosis at all (ASD or SCD) remained

    significantly higher when applying the DSM-5 criteria

    instead of ICD-10R (v2(1) = 62.5,p\ 0.001). None of the

    participants that were ASD negative using ICD-10R met

    diagnostic criteria for ASD (or SCD) according to the

    DSM-5, thus specificity of the DSM-5 was 100 %.

    DSM-IV-TR Versus DSM-5 (Table1)

    The rate of ASD positive diagnosis using DSM-5 (42 %)

    was also significantly lower than the rate of Autistic Dis-

    order or Asperger Syndrome assessed using DSM-IV-TR

    (53 %), v2(1)[ 82.5, p\0.001. Additionally, two indi-

    viduals were diagnosed with ASD on the DSM-5, but not

    with Autistic Disorder or Asperger Syndrome on the

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    DSM-IV-TR, therefore specificity of the DSM-5 according

    to the DSM-IV-TR was 0.97.

    Agreement with ADI-R and ADOS-G Results (Table2)

    Agreement between diagnosis according to the ICD-10R/

    DSM-IV-TR/DSM-5 and outcomes of the ADI-R and

    ADOS-G was calculated where this information wasavailable. When measured against results of the ADI-R, the

    sensitivity of the ICD-10R and the DSM-IV-TR was higher

    than the DSM-5 (respectively 0.97, 0.97 and 0.79; both

    McNemarsp = 0.07), but their specificity was marginally

    lower. For the ADOS-G, sensitivity was also higher on the

    ICD-10R and the DSM-IV-TR than the DSM-5 (respec-

    tively 0.6, 0.7 and 0.5; McNemars p = 0.07/0.01) and

    specificity was very similar.

    Factors Affecting Agreement Between ICD-10R

    and DSM-5

    Participant Characteristics: Age, Gender, IQ, Diagnostic

    Subtype and Additional Mental Health Conditions

    Of the participants that were ASD positive using the ICD-

    10R, there were no differences with respect to age, gender

    or IQ (where available) for those individuals that were

    ASD positive versus negative on the DSM-5.

    There was, however, a significant difference in rate of

    DSM-5 ASD positive diagnosis between ICD-10R sub-

    types, v2(2) = 31.58, p\ 0.001. Significantly more par-

    ticipants diagnosed with ICD-10R Childhood Autism or

    Asperger Syndrome met DSM-5 criteria for ASD thanthose in the PDD-unspecified group (Table3, Column A).

    The difference between ICD-10R defined Childhood

    Autism and Asperger Syndrome was not significant,

    v2(1) = 1.64, p = 0.2.

    With respect to additional mental health conditions, a

    significant difference was only found for OCD: higher rates

    of OCD were found in the group that were ASD positive on

    the DSM-5 than those that were ASD positive only on the

    ICD-10R, v2(1) = 4.58, p = 0.03 (Fig. 1).

    Table 1 Outcome of initial assessment of 150 participants according

    to the ICD-10R, and outcome of data re-coded according to DSM-IV-

    TR and DSM-5: % (N)

    Above/below ASD

    threshold

    Diagnosis of below ASD

    threshold participants

    ASD full-

    threshold

    Below ASD

    threshold

    PDD-

    unspecified or

    SCD

    No

    diagnosis

    ICD-10R,

    % (N)

    51 (76) 50 (74) 25 (37) 25 (37)

    DSM-IV-TR,

    % (N)

    53 (80) 47 (70) N/A N/A

    DSM-5,

    % (N)

    42 (63) 58 (87) 14 (21) 44 (66)

    Table 2 Percentage of participants in each diagnostic group scoring above and below threshold on ADI-R and ADOS-G, and sensitivity and

    specificity of each diagnostic algorithm compared to ADI-R/ADOS-G. % (N)

    ADI-R below

    cut-off (%)aADI-R above

    cut-off (%)aADOS-G below

    cut-off (%)bADOS-G above

    cut-off (%)b

    ICD-10R: Below ASD threshold (not ASD/PDD

    unspecified)

    96 (27) 4 (1) 75 (35) 25 (15)

    ICD-10R: ASD (Asperger Syndrome/Childhood

    Autism)

    36 (17) 64 (30) 32 (12) 68 (25)

    ICD-10RSensitivity: 0.97*

    Specificity: 0.61

    Sensitivity: 0.63*

    Specificity: 0.74

    DSM-IV-TR: ASD negative 96 (27) 4 (1) 75 (36) 25 (12)

    DSM-IV-TR: ASD positive 36 (17) 64 (30) 28 (11) 71 (28)

    DSM-IV-TR Sensitivity: 0.97*Specificity: 0.61

    Sensitivity: 0.70**Specificity: 0.77

    DSM-5: ASD negative 83 (29) 17 (6) 64 (36) 36 (20)

    DSM-5: ASD positive 38 (15) 63 (25) 36 (11) 65 (20)

    DSM-5Sensitivity: 0.81

    Specificity: 0.66

    Sensitivity: 0.50

    Specificity: 0.77

    * Difference between ICD-10R/DSM-IV-TR and DSM-5: McNemars p\ 0.1

    ** Difference between ICD-10R/DSM-IV-TR and DSM-5: McNemars p\ 0.05a ADI-R cut-off scores: Social = 10; Communication = 8; Repetitive behaviors/interests = 3b DOS-G cut-off scores: Communication = 3; Social interaction = 6; Communication ? Social = 10

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    Finally, of the participants that were ASD positive

    using the ICD-10R, there was no significant effect of

    using different ASD assessment tools (ADI-R, ADOS-G,or both) on the outcome of the DSM-5, v2(2) = 4.20,

    p = 0.12.

    Effects of Relaxing the DSM-5 Algorithm (Table 3, Column

    C)

    For the 113 participants that were ASD positive on the

    ICD-10R, the sensitivity of the DSM-5 increased signifi-

    cantly (and specificity remained at 100 %) when thresholds

    for Criteria A or B, or both, were relaxed (all v2

    (1)[

    20.0,ps\ .001).

    Of the 80 participants that were ASD positive on the

    DSM-IV-TR, sensitivity of the DSM-5 increased to 99 %

    when thresholds A and B were both relaxed, however

    specificity was significantly reduced.

    Uncertainty on the DSM-5 Algorithm: ASD Diagnostic

    Outcome When Criteria Coded as Unclear Were

    Considered to Be Present

    Of the participants diagnosed with ASD on the ICD-10R,

    74 % received a diagnosis of ASD on the DSM-5 whencriteria that were Unclear were treated as Yes; this was

    a significant increase from 56 % when Unclear was coded

    as No (v2(1) = 51.46, p\ .001). Specificity remained at

    100 %.

    Discussion

    This is the first study to investigate how the DSM-5 cri-

    teria for ASD might perform in a specialist diagnostic

    clinic for adults without significant intellectual disabil-

    itywho form a large proportion of individuals withASD.

    Our findings suggest that the specificity of the DSM-5

    criteria, as compared to the currently used ICD-10R and

    DSM-IV-TR criteria, is good. However, sensitivity is rel-

    atively poor. For instance, 44 % of the participants that

    received a diagnosis of an ASD according to ICD-10R did

    not meet DSM-5 criteria. Similarly, 22 % of the individ-

    uals that met criteria for Asperger Syndrome or Autistic

    Disorder on DSM-IV-TR would not qualify for a DSM-5

    Table 3 Percentage of participants that would be diagnosed with:

    (A) ASD on DSM-5; (B) Social Communication Disorder (SCD) on

    DSM-5; (C) ASD on DSM-5 if number of criterion required in

    Criteria A was reduced from 3 to 2, and/or the number of criterion

    required in Criteria B was reduced from 2 to 1 % (N)

    A B C

    ICD 10R/DSM-IV-TR

    diagnosis

    DSM-5

    ASD

    DSM-5

    SCD

    DSM-5 ASD:

    relax A

    DSM-5 ASD:

    relax B

    DSM-5 ASD:

    relax A and B

    ICD-10R, % (N) Not ASD, (N=

    37) 0 0 0 0 0ASD, (N = 113) 56 (63) 19 (21) 69 (78)** 70 (79)** 87 (98)**

    Childhood autism, (N = 28) 82 (23) 11 (3) 86 (24) 93 (26) 96 (27)

    Asperger Syndrome, (N = 48) 69 (33) 15 (7) 83 (40)* 83 (40)* 98 (47)**

    PDD-unspecified, (N = 37) 19 (7) 30 (11) 38 (14)* 35 (13)* 65 (24)**

    DSM-IV-TR, % (N) Not ASD, (N=70) 3 (2) 13 (9) 14 (10)* 10 (7)* 27 (19)**

    ASD, (N = 80) 77 (61) 15 (12) 85 (68)* 90 (72)** 99 (79)**

    * Difference between full criteria and relaxed threshold: McNemars p\0.05

    ** Difference between full criteria and relaxed threshold: McNemars p\ 0.001

    Fig. 1 Percentage of participants in ICD-10R/DSM-5 diagnostic

    groups that met criteria for additional mental health conditions. GAD

    General Anxiety Disorder, OCD Obsessive Compulsive Disorder,

    ADHD Attention Deficit Hyperactivity Disorder, None: No addi-

    tional/alternative mental health condition. *p\ 0.05; **p\ 0.01

    2520 J Autism Dev Disord (2013) 43:25152525

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    diagnosis of ASD. This is consistent with the only previous

    study that investigated agreement between current and

    proposed ASD criteria in intellectually disabled adults with

    ASD (Matson et al. 2012), and is cause for concern since

    these individuals, who have genuine difficulties and are

    most likely on the spectrum, may not be able to access

    services available to the ASD population if the DSM-5 is

    used to define eligibility (i.e., if it is used as an entrycriteria).

    The decline in sensitivity was highlighted when per-

    formance of each diagnostic algorithm was measured

    against results of gold-standard assessment tools. Both

    the ICD-10R and DSM-IV-TR had a 97 % chance of

    reporting a true ASD positive diagnosis according to the

    outcome of the ADI-R, and this fell to 81 % when using the

    DSM-5a marginally significant decline. The chance of

    reporting a true negative, however, was slightly better

    when using the DSM-5 as compared to current diagnostic

    algorithms. Comparison with the ADOS-G revealed similar

    results, although there was a lower chance of true positivesacross all algorithms. It should be noted the ADI-R and

    ADOS-G were developed in order to align with the DSM-

    IV-TR, therefore the finding that the assessment tools fit

    better with current algorithms than with the DSM-5 is not

    entirely unexpected. Nevertheless, disagreement between

    diagnostic algorithms and gold-standard research assess-

    ment tools may lead to confusion in both research and

    clinical settings, therefore revisions of the assessment tools

    is likely to be required for use in adult populations.

    Given the evidence that a significant proportion of

    individuals currently considered to be on the autism spec-

    trum may not be included in the DSM-5 ASD category, it is

    important to clarify what factors are associated with the

    likelihood that an individual will meet criteria. Encourag-

    ingly, there was no evidence of an effect of age or sex on

    diagnostic outcome, suggesting no particular demographic

    is more or less likely to receive an ASD diagnosis. We also

    found no effect of IQ in the subset of participants for which

    this information was available. This subset was a fairly

    small group, therefore conclusions are drawn with caution,

    however the results show no indication that higher-func-

    tioning people are more likely to be missed by the proposed

    DSM-5 criteria than lower functioning peoplea concern

    which has been raised in recent studies with children

    (McPartland et al.2012).

    In the current study, the difference in rate of DSM-5

    ASD positive diagnosis between the ICD-10R subtypes of

    Childhood Autism and Asperger Syndrome was non-sig-

    nificant. This suggests that adults with an Asperger Syn-

    drome diagnosis will be at no greater risk of missing out on

    an ASD diagnosis when using DSM-5 than adults with

    Childhood Autism, and supports the DSM-5 proposal to

    combine these diagnoses into a single category. However,

    the third ICD-10R subtypePDD-unspecifiedhad a

    significantly lower rate of ASD diagnosis using DSM-5

    than both of the other two diagnostic subtypes. This is not

    necessarily cause for concern: people with a PDD-

    unspecified diagnosis did not actually meet full diagnostic

    criteria on the ICD-10R eitherinstead they showed sig-

    nificant ASD traits and were considered to be on the

    spectrum. What is perhaps of concern is that a quarter ofpeople with an ICD-10R ASD diagnosis would not qualify

    foreitherASD orSCD on the DSM-5, and the majority of

    those affected were of the PDD-unspecified subtype. This

    is the first study to report the proportion of people that

    would qualify for the new SCD diagnosis as currently

    drafted, but our results suggest this alternative category,

    which was intended to provide diagnostic coverage to

    many of those who will not qualify for the ASD diagnosis,

    may not solve the problem of the comparatively poor

    sensitivity of the DSM-5 relative to ICD-10R.

    The present data suggest that the sensitivity of the draft

    DSM-5 criteria, compared at least to ICD-10R and DSM-IV-TR, can be improved. Several authors have suggested

    that increased sensitivity without reduced specificity might

    be achieved by relaxing the proposed criteria (Frazier et al.

    2012; Kapp and Neeman 2012; McPartland et al. 2012).

    Our results supported this: it was found that relaxing

    thresholds in DSM-5 for social communication and social

    interaction (Criteria A), and/or repetitive patterns of

    behaviour, interests, and activities (Criteria B) allowed the

    inclusion of almost all people currently diagnosed with

    Childhood Autism or Asperger Syndrome, and the majority

    of those with PDD-unspecifiedwhile maintaining speci-

    ficity. Therefore relaxing one, or both, criteria will likely

    allow the inclusion of more people currently considered to

    be ASD using ICD-10R and DSM-IV-TR, without weak-

    ening the boundaries between ASD and non-ASD. In

    addition, clear guidance on how to deal with uncertainty in

    the DSM-5 classification system will be particularly

    important; the latest drafts of the DSM-5 criteria allow

    criteria to be met by history or current state, which may

    help where information is missing or uncertain. Rating

    criteria that were unclear as present versus absent had

    significant effects on the rates of DSM-5 ASD diagnosis.

    While this is the first study to examine the draft DSM-5

    criteria in adults with ASD who do not have intellectual

    disabilities, some limitations should be noted. Like other

    studies comparing existing criteria to the DSM-5 draft,

    existing clinical notes and instruments that were used pri-

    marily for allocating current (ICD-10R) diagnostic cate-

    gories were analyzed. It remains to be seen whether using

    the DSM-5 criteria in the clinic during assessment in a

    prospective fashion would result in different findings. For

    example, sensory sensitivities are not part of current clin-

    ical criteria and might be more thoroughly assessed in

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    future in clinics where DSM-5 criteria are adopted.

    Nonetheless one potentially useful feature of the present

    study, in contrast to many others, is the relatively large

    number of participants (25 %) who were assessed for ASD

    but found to be negative using current criteria. This

    allowed examination of specificity of the different diag-

    nostic measures. Finally, it should be noted, of course, that

    it remains unclear whether existing ICD-10R or DSM-IV-TR criteria should be considered the gold-standard

    against which new criteria are compared; in the absence of

    biomarkers, the exact definition of ASD and its boundaries

    remain a matter for debate.

    Conclusions

    The specificity of the DSM-5 criteria, as compared to the

    currently used ICD-10R and DSM-IV-TR criteria is good

    but sensitivity is relatively low. This may be improved

    (without adversely affecting specificity) by relaxingDSM-5 criteria and by careful consideration of missing or

    uncertain symptom information.

    Acknowledgments Funding was provided by the Medical Research

    Council (MRC, UK), the EU Autism Imaging Study (AIMS) network

    (Grant Agreement: 115300), and the National Institute for Health

    Research Biomedical Research Centre for Mental Health at Kings

    College London, Institute of Psychiatry and South London and

    Maudsley National Health Service Foundation Trust. The authors

    wish to thank all the participants involved in this study. Also the

    administrative support staff at the Behavioural Genetics Clinic:

    Frances Harwood, Pauline Domingo and Marie Simpson.

    Appendix 1

    ICD-10R algorithm, with corresponding DSM-IV-TR

    items provided alongside each criterion. Of the participants

    that were diagnosed with ASD on the ICD-10R, the pro-

    portion of participants that were coded Yes, No and

    Unclear for each item is given.

    ICD-10R Algorithm (Corresponding DSM-IV

    item provided for each criterion).

    ICD-10R: ASD

    positive group

    1 Qualitative abnormalities in reciprocal social

    interaction are manifest in at least two of the

    following areas:

    Yes No Unclear

    a. Failure adequately to use eye-to-eye gaze,

    facial expression, body posture, and gesture to

    regulate social interaction

    DSM-IV-TR: 1a: Marked impairment in the use of

    multiple nonverbal behaviours such as eye-to-

    eye gaze, facial expression, body postures, and

    gestures to regulate social interaction.

    78.8 13.3 8.0

    Appendix continued

    ICD-10R Algorithm (Corresponding DSM-IV

    item provided for each criterion).

    ICD-10R: ASD

    positive group

    b. Failure to develop (in a manner appropriate to

    mental age, and despite ample opportunities)

    peer relationships that involve a mutual sharing

    of interests, activities, and emotions

    DSM-IV-TR: 1b: Failure to develop peerrelationships appropriate to developmental

    level

    92.0 3.5 4.4

    c. Lack of socio-emotional reciprocity as shown

    by an impaired or deviant response to other

    peoples emotions; or lack of modulation of

    behaviour according to social context; or a

    weak integration of social, emotional, and

    communicative behaviours

    DSM-IV-TR: 1d: Lack of social or emotional

    reciprocity

    79.6 7.1 13.3

    d. Lack of spontaneous seeking to share

    enjoyment, interests, or achievements with

    other people (e.g. a lack of showing, bringing,

    or pointing out to other people objects of

    interest to the individual).

    DSM-IV-TR: 1c: a lack of spontaneous seeking to

    share enjoyment, interests, or achievements

    with other people (e.g., by a lack of showing,

    bringing, or pointing out objects of interest)

    38.1 24.8 37.2

    2. Are there restricted, repetitive patterns of

    behavior, interests, and activities, as manifested

    by at least one of the following:

    Yes No Unclear

    a. A delay in, or total lack of, development of

    spoken language that is not accompanied by an

    attempt to compensate through the use of

    gesture or mime as an alternative mode of

    communication (often preceded by a lack of

    communicative babbling);

    DSM-IV-TR: 2a: delay in, or total lack of, thedevelopment of spoken language(not

    accompanied by an attempt to compensate

    through alternative modes of communication

    such as gesture or mime)

    23.9 51.3 24.8

    b. Relative failure to initiate or sustain

    conversational interchange (at whatever level of

    language skills is present), in which there is

    reciprocal responsiveness to the

    communications of the other person

    DSM-IV-TR: 2b: in individuals with adequate

    speech, marked impairment in the ability to

    initiate or sustain a conversation with others

    94.7 0 5.3

    c. Stereotyped and repetitive use of language or

    idiosyncratic use of words or phrases

    DSM-IV-TR: 2c: stereotyped and repetitive use oflanguage or idiosyncratic language

    38.9 50.4 10.6

    d. lack of varied spontaneous make-believe or

    (when young) social imitative play

    DSM-IV-TR: 2d: lack of varied, spontaneous

    make-believe play or social imitative play

    appropriate to developmental level

    51.3 24.8 23.9

    3. Restricted, repetitive, and stereotyped patterns

    of behaviour, interests, and activities are

    manifest in at least one of the following areas:

    Yes No Unclear

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    Appendix continued

    ICD-10R Algorithm (Corresponding DSM-IV

    item provided for each criterion).

    ICD-10R: ASD

    positive group

    a. An encompassing preoccupation with one or

    more stereotyped and restricted patterns of

    interest that are abnormal in content or focus; or

    one or more interests that are abnormal in their

    intensity and circumscribed nature though notin their content or focus

    DSM-IV-TR: 3a: encompassing preoccupation

    with one or more stereotyped and restricted

    patterns of interest that is abnormal either in

    intensity or focus.

    66.4 20.4 13.3

    b. Apparently compulsive adherence to specific,

    non-functional routines or rituals

    DSM-IV-TR: 3b: apparently inflexible adherence

    to specific, nonfunctional routines or rituals

    56.6 25.7 17.7

    c. Stereotyped and repetitive motor mannerisms

    that involve either hand or finger flapping or

    twisting, or complex whole body movements

    DSM-IV-TR: 3c: stereotyped and repetitive motor

    mannerisms (e.g. hand or finger flapping or

    twisting, or complex whole-body movements)

    17.7 65.5 16.8

    d. Preoccupations with part-objects or non-

    functional elements of play materials (such as

    their odor, the feel of their surface, or the noise

    or vibration that they generate).

    DSM-IV-TR: 3d: persistent preoccupation with

    parts of objects

    27.4 50.4 22.1

    Appendix 2

    DSM-5 algorithm indicating the proportion of participants

    diagnosed with ASD on the ICD-10R that were coded

    Yes, No and Unclear for each item. Criteria from

    ICD-10R that contribute to each DSM-5 criterion are

    indicated, and underlined sections indicate sections not

    explicitly in ICD-10R criteria.

    DSM-5 Algorithm ICD-10R:

    ASD positive group

    Criteria from

    ICD-10R

    CRITERION A: Are

    there persistent deficits

    in social

    communication and

    social interaction across

    contexts, not accounted

    for by general

    developmental delays,

    and manifest by ALL

    THREE of the

    following:

    Yes No Unclear

    Appendix continued

    DSM-5 Algorithm ICD-10R:ASD

    positive group

    2b; 1c; 1d 1. Deficits in social-

    emotional reciprocity;

    ranging from abnormal

    social approach and

    failure of normal backand forth conversation/

    through reduced sharing

    of interests, emotions,

    and affect and response

    to total lack of initiation

    of social interaction?

    94.7 1.8 3.5

    1a; 2. Deficits in nonverbal

    communicative

    behaviors used for

    social interaction;

    ranging from poorly

    integrated- verbal and

    nonverbal

    communication,

    through abnormalities

    in eye contact and

    body-language, or

    deficits in

    understanding and use

    of nonverbal

    communication, to total

    lack of facial expression

    or gestures?

    80.5 13.3 6.2

    1b; 2d (but must

    be shared

    imaginative

    play)

    3. Deficits in developing

    and maintaining

    relationships,

    appropriate to

    developmental level

    (beyond those withcaregivers); ranging

    from difficulties

    adjusting behavior to

    suit different social

    contexts through

    difficulties in sharing

    imaginative play and in

    making friends to an

    apparent absence of

    interest in people?

    93.8 2.7 3.5

    CRITERION B: Are

    there restricted,

    repetitive patterns of

    behavior, interests, and

    activities, as manifestedby AT LEAST TWO of

    the following:

    Yes No Unclear

    2c; 3c; 3d 1. Stereotyped or

    repetitive speech, motor

    movements, or use of

    objects (such as, simple

    motor stereotypies and

    echolalia, repetitive use

    of objects, or

    idiosyncratic phrases)?

    54.9 33.6 11.5

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    Appendix continued

    DSM-5 Algorithm ICD-10R:ASD

    positive group

    2c; 3b 2. Excessive adherence to

    routines, ritualized

    patterns of verbal or

    nonverbal behavior, or

    excessive resistance tochange (such as,

    motoric rituals,

    insistence on same

    route or food, repetitive

    questioning, or extreme

    distress at small

    changes)?

    57.5 25.7 16.8

    3a; 3d 3. Highly restricted,

    fixated interests that is

    abnormal in intensity or

    focus (such as, strong

    attachment to or

    preoccupation with

    unusual objects,

    excessively

    circumscribed or

    perseverative interests)?

    66.4 22.1 11.5

    3d 4. Hyper- or hypo-

    reactivity to sensory

    input or unusual interest

    in sensory aspects of

    environment (such as,

    apparent indifference to

    pain/heat/cold, adverse

    response to specific

    sounds or textures,

    excessive smelling or

    touching of objects,

    fascination with lightsor spinning objects)?

    18.6 31.0 50.4

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