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Record W4406363145 · doi:10.1101/2025.01.12.24318239

The natural history of CDKL5 deficiency disorder into adulthood

2025· preprint· en· W4406363145 on OpenAlexaff
Ángel Aledo‐Serrano, David Lewis‐Smith, Helen Leonard, Allan Bayat, Mohammed Junaid, Eveline Hagebeuk, Christina Fenger, Juliana Laze, Alessandra Rossi, Marina Trivisano, Beatriz González‐Giráldez, Julio Lama, Ilona Krey, Konrad Platzer, Elise Brischoux‐Boucher, Catherine Sarret, Lysa Boissé Lomax, Caterina Zanus, Luciana Musante, Paola Costa, Patrick B. Moloney, Norman Delanty, Angelo Russo, Bitten Schönewolf‐Greulich, Anne‐Marie Bisgaard, C. Berger, Elena Freri, Satoru Takahashi, Pia Zacher, Julien Jung, Scott Demarest, Eric D. Marsh, Alan K. Percy, Jeffrey L. Neul, Heather E. Olson, Lindsay C. Swanson, Stefano Meletti, Maria Cristina Cioclu, Quratulain Zulfiqar Ali, Ana Suller, Álvaro Beltrán‐Corbellini, António Gil‐Nagel, Xiaoming Zhang, Roberto Previtali, Anne F. Højte, Nicola Specchio, Jenny Downs, Gaëtan Lesca, Guido Rubboli, Danielle M. Andrade, Elena Gardella, Elia Pestana‐Knight, Orrin Devinsky, Tim A. Benke, Ingo Helbig, Rhys H. Thomas, Rikke S. Møller

Bibliographic record

VenuemedRxiv · 2025
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetics and Neurodevelopmental Disorders
Canadian institutionsWestern UniversityOntario Brain InstituteUniversity Health NetworkQueen's University
FundersNational Institute of Child Health and Human DevelopmentIntellectual and Developmental Disabilities Research CenterDeutsche ForschungsgemeinschaftLouLou FoundationWellcome TrustUniversity of PennsylvaniaEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentHartwell FoundationChildren's Hospital of Philadelphia
KeywordsNatural historyNatural (archaeology)PsychologyMedicineDevelopmental psychologyHistoryInternal medicine

Abstract

fetched live from OpenAlex

deficiency disorder (CDD) is limited to the results of cross-sectional analysis of largely pediatric cohorts. Assessment of outcomes in adulthood is critical for clinical decision-making and future precision medicine approaches but is challenging because of the diagnostic gap and duration of follow-up that would be required for prospective studies. We aimed to delineate the natural history retrospectively from adulthood. We analyzed clinical data about an international cohort of 67 adults with CDD. We analyzed demographic, phenotypic, CDKL5 Developmental Score (CDS), and treatment data, and tested associations with genetic factors, sex, and a positive or negative history of neonatal seizures, as an early predictor of prognosis. All but one of 67 adults (55 females, median age of 24 years at last follow-up) had epilepsy, typically beginning with epileptic spasms or tonic seizures before 4 months of age. Focal-onset and non-motor seizures emerged later. Fewer than a third had been documented as having bilateral tonic-clonic seizures or status epilepticus. Seizures often improved with age, but 73% had never experienced more than 6 months of seizure-freedom. Clobazam, sodium valproate, and lamotrigine were the most frequently prescribed antiseizure medications, but no specific treatment demonstrated superiority. Common comorbidities included movement disorders, visual impairment, sleep disorders, constipation, and scoliosis. All participants had intellectual disability, 75% had not acquired speech and 45% had regressed developmentally. 16% never achieved any CDS skill, but most attained at least three, and 28% attained six or all seven. By adulthood, half of those who had achieved any CDS skill retained all their CDS skills. The skills most frequently lost were independent walking and standing. Those with a history of neonatal seizures tended to attain fewer CDS skills and were more likely to have abnormal muscle tone in adulthood, atrioventricular conduction delay, and potential complications of their illness and treatment. Individuals carrying missense variants attained more CDS skills than those with other variants and were more likely to lose skills in adulthood and develop anxiety, possibly reflecting the limited neurodevelopment of those with non-missense variants, who manifested a more multisystemic disorder. In summary, retrospective data from adulthood elucidates the evolution of symptoms, variation in developmental outcomes, and the treatment landscape in CDKL5 deficiency disorder. Presence a non-missense variants or a history of neonatal seizures indicates a more complex disorder and lower developmental trajectory. Our findings will inform management decisions, prognostication, and the design of clinical trials in CDKL5 Deficiency Disorder.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.227
Teacher spread0.221 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2025
Admission routes1
Has abstractyes

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