Cited by 333Autism Spectrum Disorder ResearchChild Nutrition and Feeding IssuesLanguage Development and Disorders

Evaluation of the Diagnostic Stability of the Early Autism Spectrum Disorder Phenotype in the General Population Starting at 12 Months

Open access
Pierce, Karen, Gazestani, Vahid H., Bacon, Elizabeth, Barnes, Cynthia Carter, Cha, Debra, Nalabolu, Srinivasa, Lopez, Linda, Moore, Adrienne +2 more·2019·JAMA Pediatrics

Abstract

Importance: Universal early screening for autism spectrum disorder (ASD) in primary care is becoming increasingly common and is believed to be a pivotal step toward early treatment. However, the diagnostic stability of ASD in large cohorts from the general population, particularly in those younger than 18 months, is unknown. Changes in the phenotypic expression of ASD across early development compared with toddlers with other delays are also unknown. Objectives: To examine the diagnostic stability of ASD in a large cohort of toddlers starting at 12 months of age and to compare this stability with that of toddlers with other disorders, such as developmental delay. Design, Setting, and Participants: In this prospective cohort study performed from January 1, 2006, to December 31, 2018, a total of 2241 toddlers were referred from the general population through a universal screening program in primary care or community referral. Eligible toddlers received their first diagnostic evaluation between 12 and 36 months of age and had at least 1 subsequent evaluation. Exposures: Diagnosis was denoted after each evaluation visit as ASD, ASD features, language delay, developmental delay, other developmental issue, typical sibling of an ASD proband, or typical development. Main Outcomes and Measures: Diagnostic stability coefficients were calculated within 2-month age bands, and logistic regression models were used to explore the associations of sex, age, diagnosis at first visit, and interval between first and last diagnosis with stability. Toddlers with a non-ASD diagnosis at their first visit diagnosed with ASD at their last were designated as having late-identified ASD. Results: Among the 1269 toddlers included in the study (918 [72.3%] male; median age at first evaluation, 17.6 months [interquartile range, 14.0-24.4 months]; median age at final evaluation, 36.2 months [interquartile range, 33.4-40.9 months]), the overall diagnostic stability for ASD was 0.84 (95% CI, 0.80-0.87), which was higher than any other diagnostic group. Only 7 toddlers (1.8%) initially considered to have ASD transitioned into a final diagnosis of typical development. Diagnostic stability of ASD within the youngest age band (12-13 months) was lowest at 0.50 (95% CI, 0.32-0.69) but increased to 0.79 by 14 months and 0.83 by 16 months (age bands of 12 vs 14 and 16 months; odds ratio, 4.25; 95% CI, 1.59-11.74). A total of 105 toddlers (23.8%) were not designated as having ASD at their first visit but were identified at a later visit. Conclusions and Relevance: The findings suggest that an ASD diagnosis becomes stable starting at 14 months of age and overall is more stable than other diagnostic categories, including language or developmental delay. After a toddler is identified as having ASD, there may be a low chance that he or she will test within typical levels at 3 years of age. This finding opens the opportunity to test the impact of very early-age treatment of ASD.

AI snapshot

Written from the paper’s full text.

TL;DR

In a general-population cohort of 1269 toddlers evaluated longitudinally from 12 to 36 months, an ASD diagnosis was more stable than other diagnoses, with overall stability of 0.84. Stability was weakest at 12–13 months (0.50) and improved by 14 months (0.79) and 16 months (0.83), while late-identified ASD occurred in 23.8% of toddlers ultimately diagnosed with ASD.

Key findings

  • Overall diagnostic stability was 0.84 (95% CI, 0.80–0.87) for ASD and 0.79 (95% CI, 0.74–0.83) for typical development (TD); ASD vs TD stability did not differ significantly (OR, 0.86; 95% CI, 0.57–1.29). ASD was significantly more stable than ASD features (OR, 0.11; 95% CI, 0.03–0.32), developmental delay (DD; OR, 0.15; 95% CI, 0.09–0.25), language delay (LD; OR, 0.04; 95% CI, 0.03–0.06), and other diagnoses (OR, 0.16; 95% CI, 0.09–0.28).
  • ASD stability was weakest at 12–13 months (0.50; 95% CI, 0.32–0.69), increasing to 0.79 by 14 months and 0.83 by 16 months (12 vs 14/16 months OR, 4.25; 95% CI, 1.59–11.74). When toddlers with ASD features were counted as ASD, stability rose to 0.70 at 12 months, 0.85 at 14 months, and 0.94 at 16 months.
  • Of 400 toddlers initially designated as having ASD, 336 retained the diagnosis at final visit; only 7 (1.8%) transitioned to TD, and 5 of those 7 were initially evaluated at 12–13 months. The most common transition was from an initial diagnosis of LD or DD to ASD.
  • Among toddlers ultimately diagnosed with ASD, 66 (15.9%) were early-age persistent, 270 (61.2%) middle-age persistent, and 105 (23.8%) late-identified. Late-identified toddlers had better first-visit scores than the other ASD groups (Cohen d range, 0.44–2.35) but worse scores than TD toddlers (Cohen d range, 1.43–1.84); 39 late-identified toddlers (37%) fell within the ADOS toddler-module concern cutoff but were designated non-ASD by practitioner judgment.

Methods

  • A total of 2241 toddlers aged 12–36 months were referred to a University of California, San Diego autism expert evaluation center through the Get SET Early program or community referral; 1269 were longitudinally evaluated 2 or more times with an interval of 6 months or longer and were the focus. Approximately 75% came from Get SET Early and 25% from community referral. Median age at first evaluation was 17.6 months, median age at final evaluation was 36.2 months, and mean number of diagnostic visits was 2.7.
  • Licensed psychologists performed diagnostic and psychometric testing, including ADOS-2, Mullen Scales of Early Learning, and Vineland Adaptive Behavior Scales. Toddlers were designated as having ASD, ASD features, developmental delay, language delay, other issue, TD, or typical sibling of an ASD proband.
  • Stability coefficients were calculated as the proportion retaining the same diagnosis from first to last visit within 2-month age bands. Logistic regression included sex, age at first diagnosis, interval between first and last diagnosis, and diagnostic group at first visit; age was binned as younger than 14 months, 14–17.99 months, 18–23.99 months, and 24 months or older. Analyses were performed in R.

Limitations

  • The paper states that practitioners making final diagnoses were not masked to previous diagnoses because DSM-5 procedures and criteria require consideration of historical information regarding ASD symptoms; this could have biased psychologists toward increased diagnostic stability, although the relatively weak stability in other delay groups was cited as counterevidence.
  • The paper notes that lower ASD stability at 12 months likely reflects limitations in the diagnostic tools used at that age, including the ADOS-2 and DSM.
  • The study was not designed to determine whether early treatments affected the speed with which toddlers with language delay caught up by final diagnosis age.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1001/jamapediatrics.2019.0624

Cites

44 of 44 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Claims the paper makes

0 of 38 cited sources checked · 0 supported · 0 flagged

  • Findingown data

    No clinical differences were found between the early and middle diagnosis groups.

    “No clinical differences were found between the early and middle diagnosis groups (Figure 4).”
    Quote in the paperSubstantial claim
  • Findingown data

    In our cohort, 84% of toddlers initially diagnosed with ASD at their first visit retained this diagnosis at 3 to 4 years of age.

    “In our cohort, 84% of toddlers initially diagnosed with ASD at their first visit retained this diagnosis at 3 to 4 years of age.”
    Quote in the paperSubstantial claim
  • Findingown data

    The transition from an initial diagnosis of LD or developmental delay to ASD was the most common transition type.

    “The transition from an initial diagnosis of LD or developmental delay to ASD was the most common transition type.”
    Quote in the paperNot a substantial claim
  • Findingown data

    Overall stability was 0.84 (95% CI, 0.80-0.87) for an ASD diagnosis.

    “Overall stability was 0.84 (95% CI, 0.80-0.87) for an ASD diagnosis and 0.79 (95% CI, 0.74-0.83) for a TD diagnosis (Figure 2A).”
    Quote in the paperSubstantial claim
    • Rests on an assumption: The final diagnostic evaluation at the last visit provides a valid reference standard for true ASD diagnostic status.
    • Rests on an assumption: The lack of masking of psychologists to previous diagnoses did not materially bias the diagnostic stability estimates.
  • Findingown data

    When toddlers with ASD features were considered to have ASD, stability coefficients increased to 0.94 (95% CI, 0.81-0.99) at 16 months of age.

    “When toddlers with ASD features were considered to have ASD, the stability coefficients increased to 0.70 (95% CI, 0.52-0.85) at 12 months of age, 0.85 (95% CI, 0.71-0.94) at 14 months of age, and 0.94 (95% CI, 0.81-0.99) at 16 months of age.”
    Quote in the paperSubstantial claim
    • Rests on an assumption: The final diagnostic evaluation at the last visit provides a valid reference standard for true ASD diagnostic status.
    • Rests on an assumption: The lack of masking of psychologists to previous diagnoses did not materially bias the diagnostic stability estimates.
  • Classified as probably not a substantial claim. 23
  • May combine two claims. 9
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Findingnone given

    Evidence counter to the point that review biased psychologists is the relatively weak diagnostic stability found in other delay groups.

    “Evidence counter to this point is the relatively weak diagnostic stability found in other delay groups.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingown data

    Although overall stability of an ASD diagnosis was high, examination of the data within 2-month age bands revealed that stability was selectively low at 12 months, with a stability coefficient of 0.50.

    “Although the overall stability of an ASD diagnosis was high, examination of the data within 2-month age bands revealed that stability was selectively low at 12 months, with a stability coefficient of 0.50.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    When toddlers with ASD features were included in the calculation at 12, 14, and 16 months of age, stability coefficients increased to 0.70 at 12 months, 0.85 at 14 months, and 0.94 at 16 months.

    “When toddlers with ASD features were included in the calculation at 12, 14, and 16 months of age, stability coefficients increased to 0.70 at 12 months, 0.85 at 14 months, and 0.94 at 16 months.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    For ASD, 66 toddlers (15.9%) were classified into the early-age diagnosis group, 270 (61.2%) into the middle-age diagnosis group, and 105 (23.8%) into the late-identified group.

    “For ASD, 66 toddlers (15.9%) were classified into the early-age diagnosis group, 270 (61.2%) into the middle-age diagnosis group, and 105 (23.8%) into the late-identified group.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Premisenone given

    It is unclear whether stability estimates from infant sibling designs would be found within a general population cohort.

    “First, it is unclear whether stability estimates from infant sibling designs would be found within a general population cohort.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Premisecitation

    In one infant sibling study, only 69% of siblings first diagnosed as having ASD at 24 months retained that diagnosis at a final diagnostic age (27 of 39).

    “but only 69% of siblings first diagnosed as having ASD at 24 months did so (ie, 27 of 39 retained diagnosis).17”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [17] Ozonoff S, Young GS, Landa RJ, Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study. J Child Psychol Psychiatry. 2015; 56(9): 988- 998. doi: 10.1111/jcpp.12421 25921776 PMC4532646

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    In one infant sibling study, 93% of siblings first diagnosed as having ASD at 18 months retained that diagnosis at a final diagnostic age of 36 months.

    “One of these studies reported that 93% of siblings first diagnosed as having ASD at 18 months retained that diagnosis at a final diagnostic age of 36 months,17”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [17] Ozonoff S, Young GS, Landa RJ, Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study. J Child Psychol Psychiatry. 2015; 56(9): 988- 998. doi: 10.1111/jcpp.12421 25921776 PMC4532646

      Not checked in the free run.

  • Classified as probably not a substantial claim. May combine two claims.

    Premisenone given

    Clinic-referred studies are small, usually containing 50 to 100 participants.

    “Third, clinic-referred studies are small, usually containing 50 to 100 participants, and may generate less stable results.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Premisenone given

    The stability of an ASD diagnosis at the toddler stage (around the first birthday) is unknown.

    “yet the stability of an ASD diagnosis at this pivotal age is unknown.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Premisecitation

    Most studies examining the diagnostic stability of ASD before 3 years of age have involved slightly older, clinic-referred cohorts, usually at approximately 2 years of age.

    “A previous report17 stated that most studies examining the diagnostic stability of ASD before 3 years of age have involved slightly older, clinic-referred cohorts, usually at approximately 2 years of age.”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [17] Ozonoff S, Young GS, Landa RJ, Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study. J Child Psychol Psychiatry. 2015; 56(9): 988- 998. doi: 10.1111/jcpp.12421 25921776 PMC4532646

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    Early signs of ASD can sometimes be detected using parent report screens as early as 12 or 18 months of age.

    “Although several studies have shown that early signs of ASD can sometimes be detected using parent report screens as early as 126,7,8 or 18 months of age,9,10”
    Quote in the paperSubstantial claim0 of 3 sources checked
    • cites [6] Pierce K, Carter C, Weinfeld M, Detecting, studying, and treating autism early: the one-year well-baby check-up approach. J Pediatr. 2011; 159(3): 458- 465, e451-e456. 21524759 PMC3157595 source

      Not checked in the free run.

    • cites [7] Wetherby AM, Brosnan-Maddox S, Peace V, Newton L Validation of the Infant-Toddler Checklist as a broadband screener for autism spectrum disorders from 9 to 24 months of age. Autism. 2008; 12(5): 487- 511. doi: 10.1177/1362361308094501 18805944 PMC2663025 source

      Not checked in the free run.

    • cites [8] Turner-Brown LM, Baranek GT, Reznick JS, Watson LR, Crais ER The First Year Inventory: a longitudinal follow-up of 12-month-old to 3-year-old children. Autism. 2013; 17(5): 527- 540. doi: 10.1177/1362361312439633 22781058 PMC3470769 source

      Not checked in the free run.

  • May combine two claims.

    Premisecitation

    The toddler stage is the earliest age that ASD can be detected and treatment started.

    “The toddler stage is also the earliest age that ASD can be detected and treatment started,6,16 yet the stability of an ASD diagnosis at this pivotal age is unknown.”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [6] Pierce K, Carter C, Weinfeld M, Detecting, studying, and treating autism early: the one-year well-baby check-up approach. J Pediatr. 2011; 159(3): 458- 465, e451-e456. 21524759 PMC3157595

      Not checked in the free run.

    • cites [16] Baranek GT, Watson LR, Turner-Brown L, Preliminary efficacy of adapted responsive teaching for infants at risk of autism spectrum disorder in a community sample. Autism Res Treat. 2015; 2015: 386951. 25648749 PMC4306223

      Not checked in the free run.

  • May combine two claims.

    Premisecitation

    Autism spectrum disorder is a common disorder that begins in prenatal life.

    “Autism spectrum disorder is a common disorder that begins in prenatal life.2”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [2] Courchesne E, Pramparo T, Gazestani V, Lombardo MV, Pierce K, Lewis NE The ASD living biology: from cell proliferation to clinical phenotype. Mol Psychiatry. 2019; 24(1): 88- 107. doi: 10.1038/s41380-018-0056-y 29934544 PMC6309606 source

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    50% to 80% of toddlers eventually diagnosed as having ASD at 3 years of age were not identified as having ASD by expert clinicians at 18 months of age.

    “the recent finding from infant sibling studies17,18 that 50% to 80% of toddlers eventually diagnosed as having ASD at 3 years of age were not identified as having ASD by expert clinicians at 18 months of age.”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [17] Ozonoff S, Young GS, Landa RJ, Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study. J Child Psychol Psychiatry. 2015; 56(9): 988- 998. doi: 10.1111/jcpp.12421 25921776 PMC4532646

      Not checked in the free run.

    • cites [18] Zwaigenbaum L, Bryson SE, Brian J, Stability of diagnostic assessment for autism spectrum disorder between 18 and 36 months in a high-risk cohort. Autism Res. 2016; 9(7): 790- 800. doi: 10.1002/aur.1585 26613202

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Psychologists were not masked to previous diagnoses during longitudinal test visits.

    “Psychologists were not masked to previous diagnoses during longitudinal test visits.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Premisecitation

    Children with ASD are detected and treated nationally at approximately 4 years of age.

    “Children with ASD are detected and treated nationally at approximately 4 years of age.1”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [1] Baio J, Wiggins L, Christensen DL, Prevalence of autism spectrum disorder among children aged 8 years: Autism and Developmental Disabilities Monitoring Network, 11 sites, United States, 2014. MMWR Surveill Summ. 2018; 67(6): 1- 23. doi: 10.15585/mmwr.ss6706a1 29701730 PMC5919599 source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    It is possible that review of historical information could have biased psychologists in favor of increased diagnostic stability.

    “Although unlikely, it is possible that review of this information could have biased psychologists in favor of increased diagnostic stability.”
    Quote in the paperNot a substantial claim
    • Rests on an assumption: DSM-5 procedures and criteria require consideration of historical information regarding ASD symptoms.
  • Classified as probably not a substantial claim.

    Premisecitation

    Early treatment may be more beneficial than treatment started at older ages.

    “which research suggests may be more beneficial than treatment started at older ages.26,27,28”
    Quote in the paperSubstantial claim0 of 3 sources checked
    • cites [26] Anderson DK, Liang JW, Lord C Predicting young adult outcome among more and less cognitively able individuals with autism spectrum disorders. J Child Psychol Psychiatry. 2014; 55(5): 485- 494. doi: 10.1111/jcpp.12178 24313878 PMC5819743 source

      Not checked in the free run.

    • cites [27] MacDonald R, Parry-Cruwys D, Dupere S, Ahearn W Assessing progress and outcome of early intensive behavioral intervention for toddlers with autism. Res Dev Disabil. 2014; 35(12): 3632- 3644. doi: 10.1016/j.ridd.2014.08.036 25241118 source

      Not checked in the free run.

    • cites [28] Rogers SJ, Vismara L, Wagner AL, McCormick C, Young G, Ozonoff S Autism treatment in the first year of life: a pilot study of infant start, a parent-implemented intervention for symptomatic infants. J Autism Dev Disord. 2014; 44(12): 2981- 2995. doi: 10.1007/s10803-014-2202-y 25212413 PMC4951093 source

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  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    Transient LD cases have been commonly noted in the literature.

    “Such transient LD cases have been commonly noted in the literature.25”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [25] Dale PS, Price TS, Bishop DV, Plomin R Outcomes of early language delay, I: predicting persistent and transient language difficulties at 3 and 4 years. J Speech Lang Hear Res. 2003; 46(3): 544- 560. doi: 10.1044/1092-4388(2003/044) 14696985 source

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  • Probably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).

    Premisecitation

    In many places in the United States, experience in early ASD development is severely lacking.

    “In many places in the United States, such experience is severely lacking.37”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [37] Martinez M, Thomas KC, Williams CS, Family experiences with the diagnosis of autism spectrum disorder: system barriers and facilitators of efficient diagnosis. J Autism Dev Disord. 2018; 48(7): 2368- 2378. doi: 10.1007/s10803-018-3493-1 29453706

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    ASD is a dimensional rather than categorical disorder.

    “This finding is likely related to the possibility that ASD is a dimensional rather than categorical disorder38,39”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites [38] Elton A, Di Martino A, Hazlett HC, Gao W Neural connectivity evidence for a categorical-dimensional hybrid model of autism spectrum disorder. Biol Psychiatry. 2016; 80(2): 120- 128. doi: 10.1016/j.biopsych.2015.10.020 26707088 PMC4853295 source

      Not checked in the free run.

    • cites [39] Kapur S, Phillips AG, Insel TR Why has it taken so long for biological psychiatry to develop clinical tests and what to do about it? Mol Psychiatry. 2012; 17(12): 1174- 1179. doi: 10.1038/mp.2012.105 22869033 source

      Not checked in the free run.

  • May combine two claims.

    Premisecitation

    Most screening studies validate diagnoses only once, usually at approximately the age of screening, leaving unclear the degree to which an initial diagnosis persists at later ages.

    “yet most screening studies9,10,41,42 validate diagnoses only once, usually at approximately the age of screening, leaving unclear the degree to which an initial diagnosis persists at later ages.”
    Quote in the paperSubstantial claim0 of 4 sources checked
    • cites [9] Chlebowski C, Robins DL, Barton ML, Fein D Large-scale use of the modified checklist for autism in low-risk toddlers. Pediatrics. 2013; 131(4): e1121- e1127. doi: 10.1542/peds.2012-1525 23530174 PMC3608483 source

      Not checked in the free run.

    • cites [10] Robins DL, Casagrande K, Barton M, Chen CM, Dumont-Mathieu T, Fein D Validation of the modified checklist for autism in toddlers, revised with follow-up (M-CHAT-R/F). Pediatrics. 2014; 133(1): 37- 45. doi: 10.1542/peds.2013-1813 24366990 PMC3876182 source

      Not checked in the free run.

    • cites [41] Charman T, Baird G, Simonoff E, Testing two screening instruments for autism spectrum disorder in UK community child health services. Dev Med Child Neurol. 2016; 58(4): 369- 375. doi: 10.1111/dmcn.12874 26303216 source

      Not checked in the free run.

    • cites [42] Hardy S, Haisley L, Manning C, Fein D Can screening with the Ages and Stages Questionnaire detect autism? J Dev Behav Pediatr. 2015; 36(7): 536- 543. doi: 10.1097/DBP.0000000000000201 26348972 PMC4563819 source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    The study was not designed to determine whether early treatments affected the speed with which toddlers caught up by final diagnosis age.

    “Our study was not designed to determine whether such early treatments affected the speed with which toddlers caught up by the time they reached final diagnosis age.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Study design and conductnone given

    This was not a screening study and the cohort contained approximately 25% community-referred cases.

    “Although this was not a screening study and the cohort contained approximately 25% community-referred cases”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted).

    Premisecitation

    Late-onset ASD cases may be attributable to weaknesses inherent in standardized diagnostic tools at early ages, rather than a lack of observable ASD symptoms per se.

    “A newer study,20 however, suggests that such so-called late-onset cases may be attributable to weaknesses inherent in standardized diagnostic tools at early ages, rather than a lack of observable ASD symptoms per se.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [20] Bacon EC, Courchesne E, Barnes CC, Rethinking the idea of late autism spectrum disorder onset. Dev Psychopathol. 2018; 30(2): 553- 569. doi: 10.1017/S0954579417001067 28803559 PMC10515446 source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    The ADOS-2 is not valid for use with toddlers who have a nonverbal mental age younger than 12 months.

    “Research from the ADOS-2 developers cautions that it is not valid for use with toddlers who have a nonverbal mental age younger than 12 months,24”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [24] Luyster R, Gotham K, Guthrie W, The Autism Diagnostic Observation Schedule-toddler module: a new module of a standardized diagnostic measure for autism spectrum disorders. J Autism Dev Disord. 2009; 39(9): 1305- 1320. doi: 10.1007/s10803-009-0746-z 19415479 PMC2893552

      Not checked in the free run.

  • Classified as probably not a substantial claim.

    Premisecitation

    Early screening starting at 18 months is recommended by the American Academy of Pediatrics.

    “particularly when early screening starting at 18 months is recommended by the American Academy of Pediatrics,40”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites [40] Johnson CP, Myers SM; American Academy of Pediatrics Council on Children With Disabilities Identification and evaluation of children with autism spectrum disorders. Pediatrics. 2007; 120(5): 1183- 1215. doi: 10.1542/peds.2007-2361 17967920

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  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    This finding is consistent with an infant sibling study that reported lower-than-expected language scores on the Mullen Scales of Early Learning test within their late-identified group.

    “This finding is consistent with an infant sibling study17 that reported lower-than-expected language scores on the Mullen Scales of Early Learning test within their late-identified group.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [17] Ozonoff S, Young GS, Landa RJ, Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study. J Child Psychol Psychiatry. 2015; 56(9): 988- 998. doi: 10.1111/jcpp.12421 25921776 PMC4532646

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    Stability coefficients were recalculated after removing toddlers whose nonverbal mental age was younger than 12 months or who were not ambulatory, due to caution from ADOS developers.

    “Given caution from the ADOS developers regarding use of the ADOS with toddlers with nonverbal mental ages younger than 12 months and those who are not ambulatory,24 stability coefficients were also recalculated after removing such cases.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [24] Luyster R, Gotham K, Guthrie W, The Autism Diagnostic Observation Schedule-toddler module: a new module of a standardized diagnostic measure for autism spectrum disorders. J Autism Dev Disord. 2009; 39(9): 1305- 1320. doi: 10.1007/s10803-009-0746-z 19415479 PMC2893552

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    There is a demand for early detection, intervention, and services, and marked effort and funding have gone into discovery of methods for early-age universal screening, detection, and diagnosis.

    “Because of this, there is a demand for early detection, intervention, and services,5 and,in response, marked effort and funding have gone into discovery of methods for early-age universal screening, detection, and diagnosis.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites [5] Pierce K, Courchesne E, Bacon E To screen or not to screen universally for autism is not the question: why the task force got it wrong. J Pediatr. 2016; 176: 182- 194. doi: 10.1016/j.jpeds.2016.06.004 27421956 PMC5679123

      Not checked in the free run.

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  • The paper relies on this without support.

    The 1269 toddlers longitudinally evaluated are representative of the general population of toddlers.

    “A total of 2241 toddlers 12 to 36 months of age were referred for a diagnostic evaluation to an autism expert evaluation center created at University of California, San Diego.”
    “A total of 1269 of the 2241 toddlers were longitudinally evaluated 2 or more times and were the focus of this study.”
  • The paper relies on this without support.

    The final diagnostic evaluation at the last visit provides a valid reference standard for true ASD diagnostic status.

    “A toddler was designated as having 1 of the following: ASD, ASD features, developmental delay, language delay (LD), other issue, TD, or typical sibling of an ASD proband.”
    “Stability coefficients were first calculated within 2-month age bands by determining the proportion of toddlers with a particular diagnosis at their first diagnostic visit who retained that same diagnosis at their last visit.”
  • The paper relies on this without support.

    The lack of masking of psychologists to previous diagnoses did not materially bias the diagnostic stability estimates.

    “Psychologists were not masked to previous diagnoses during longitudinal test visits.”
  • The paper relies on this without support.

    The human brain has an enormous capacity to resculpt and remodel, particularly during the first postnatal years.

    “The human brain has an enormous capacity to resculpt and remodel, particularly during the first postnatal years.”
  • The paper relies on this without support.

    DSM-5 procedures and criteria require consideration of historical information regarding ASD symptoms.

    “This lack of masking was because DSM-5 procedures and criteria require consideration of historical information regarding ASD symptoms.”
5 of 5

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

  • Incorrect percentage for the early-age ASD group

    Minor

    The three ASD identification groups contain 66, 270, and 105 toddlers, totaling 441. The early-age group is therefore 15.0% of that total, not 15.9%.

    Reported 15.9 · recomputed 14.965986

  • Incorrect percentage for males in the TD group

    Minor

    The TD group contains 439 toddlers, so 278 males represent 63.3%, not 65.6%.

    Reported 65.6 · recomputed 63.32574

2 of 2

Cites

Flagged first, then by citations

2 of the 46 references couldn’t be matched to a known paper.

Research works printed but not linked: 1

  1. Sparrow, 2005, Vineland-II Scales of Adaptive Behavior: Survey Form Manual

Cited by

Sorted by citations

Authors
Pierce, K., Gazestani, V. H., Bacon, E., Barnes, C. C., Cha, D., Nalabolu, S., Lopez, L., Moore, A., Pence-Stophaeros, S., & Courchesne, E.
Affiliations
  • University of California San Diego (US)
  • Department of Neurosciences, University of California, San Diego, La Jolla
Corresponding author
Pierce, Karen
Venue
JAMA Pediatrics
Published
2019-06-01
Volume
173
Issue
6
Pages
578
ISSN
  • 1072-4710 (ISSN-L)
  • 2168-6203
OpenAlex
W2941892929
Cited by
333
References
46
Citations by year
2026: 27 · 2025: 39 · 2024: 43 · 2023: 49 · 2022: 65 · 2021: 66 · 2020: 32 · 2019: 11
FWCI
25.27
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Archives of Pediatrics and Adolescent Medicine (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01mh110558-05)
  • National Institute of Mental Health (R01MH104446, R01-MH110558, R01MH036840, P50MH081755)
  • National Institute on Deafness and Other Communication Disorders (R01DC016385)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
  • Health Sciences › Medicine › Psychiatry and Mental health › Child Nutrition and Feeding Issues
  • Social Sciences › Psychology › Developmental and Educational Psychology › Language Development and Disorders
Keywords
autism spectrum disorder, diagnostic stability, toddlers, primary care, developmental delay, language delay, sex differences, age differences, typical development
MeSH terms
Autism Spectrum Disorder, Developmental Disabilities, Child, Preschool, Female, Follow-Up Studies, Humans, Infant, Male, Mass Screening, Phenotype, Primary Health Care, Prospective Studies, Psychiatric Status Rating Scales, Referral and Consultation, Logistic Models, Early Diagnosis

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-07.

Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-07.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

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