Evidence map›Paper›PMID 42290996›Full record

ArticleFrontiers in psychiatry2026

Identifying dyslexia-consistent reading profiles in mild intellectual disability: cluster-derived severity gradients and severity-calibrated classification rules.

Bartosz M Radtke, Paweł Jurek, Michał Olech, Ariadna Łada-Maśko, Urszula Sajewicz-Radtke

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06215092 (Perinatal, Cognitive and Social-emotional Correlates of Neurodevelopmental Disorders and Learning Difficulties in Children and Adolescents, From a Biopsychosocial Perspective.), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06215092 completednot on this map

Perinatal, Cognitive and Social-emotional Correlates of Neurodevelopmental Disorders and Learning Difficulties in Children and Adolescents, From a Biopsychosocial Perspective.

TypeobservationalSponsorBartosz M. RadtkeRan2022 to 2025Enrolled500ConditionsPerinatal Condition, Neurodevelopmental Disorders, Social Functioning, Child DevelopmentArmsPsychological assessment
3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Bartosz M RadtkeLaboratory of Psychological and Educational Tests, Gdańsk, Poland.
Paweł JurekInstitute of Psychology, University of Gdańsk, Gdańsk, Poland.
Michał OlechDepartment of Psychology, Medical University of Gdańsk, Gdańsk, Poland.
Ariadna Łada-MaśkoInstitute of Psychology, University of Gdańsk, Gdańsk, Poland.
Urszula Sajewicz-RadtkeLaboratory of Psychological and Educational Tests, Gdańsk, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Translating dyslexia constructs to mild intellectual disability (MID) is challenging because population-based cut-offs may label broadly expected low attainment as 'specific'. This study combined person-centered profiling with explicit, ICD-11-guided, severity-calibrated classification rules to quantify when and why over-identification occurs in MID. Methods: Nationwide diagnostic data from 446 students with MID were analyzed using age-normed sten scores from the SB6/18 battery (decoding, reading fluency, reading comprehension, phonetic coding, rapid automatized naming [RAN]). We conducted hierarchical clustering with bootstrap stability and compared six rule-based groupings that systematically varied severity thresholds and inclusion of phonological/RAN indicators. Results: A robust two-cluster solution reflected a dominant severity gradient across reading and related markers. Broad criteria classified 88% of the sample, including many higher-performing cases. Introducing an extreme-severity anchor reduced prevalence (37%) and concentrated classified cases within the lower-performing profile. Notably, when very low decoding (sten = 1) was required, adding phonological/RAN criteria yielded little further classification gain under this rule structure. Conclusions: Dyslexia-consistent profiles can be delineated within mild ID, but prevalence and subgroup coherence depend critically on severity operationalization. Word-level reading-especially decoding and fluency-provides the most robust basis for subgroup identification; phonological/RAN indicators showed limited incremental classification value within the present rule structure. Clinical trial registration: https://clinicaltrials.gov/, identifier NCT06215092.

Indexed as

decodingdevelopmental learning disorderintellectual disabilityphonological processingRANreading fluency

Identifiers

PMID42290996
PMCPMC13260349

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.