Your browser doesn't support javascript.
loading
Developing a cluster-based approach for deciphering complexity in individuals with neurodevelopmental differences.
Cuppens, Tania; Kaur, Manpreet; Kumar, Ajay A; Shatto, Julie; Ng, Andy Cheuk-Him; Leclercq, Mickael; Reformat, Marek Z; Droit, Arnaud; Dunham, Ian; Bolduc, François V.
Afiliação
  • Cuppens T; Département de Médecine Moléculaire de L'Université Laval, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
  • Kaur M; Department of Pediatric Neurology, University of Alberta, Edmonton, AB, Canada.
  • Kumar AA; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, United Kingdom.
  • Shatto J; Department of Pediatric Neurology, University of Alberta, Edmonton, AB, Canada.
  • Ng AC; Department of Pediatric Neurology, University of Alberta, Edmonton, AB, Canada.
  • Leclercq M; Département de Médecine Moléculaire de L'Université Laval, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
  • Reformat MZ; Department of Electrical and Computer Engineering, University of Alberta, Edmonton, AB, Canada.
  • Droit A; Département de Médecine Moléculaire de L'Université Laval, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
  • Dunham I; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, United Kingdom.
  • Bolduc FV; Department of Pediatric Neurology, University of Alberta, Edmonton, AB, Canada.
Front Pediatr ; 11: 1171920, 2023.
Article em En | MEDLINE | ID: mdl-37790694
ABSTRACT

Objective:

Individuals with neurodevelopmental disorders such as global developmental delay (GDD) present both genotypic and phenotypic heterogeneity. This diversity has hampered developing of targeted interventions given the relative rarity of each individual genetic etiology. Novel approaches to clinical trials where distinct, but related diseases can be treated by a common drug, known as basket trials, which have shown benefits in oncology but have yet to be used in GDD. Nonetheless, it remains unclear how individuals with GDD could be clustered. Here, we assess two different approaches agglomerative and divisive clustering.

Methods:

Using the largest cohort of individuals with GDD, which is the Deciphering Developmental Disorders (DDD), characterized using a systematic approach, we extracted genotypic and phenotypic information from 6,588 individuals with GDD. We then used a k-means clustering (divisive) and hierarchical agglomerative clustering (HAC) to identify subgroups of individuals. Next, we extracted gene network and molecular function information with regard to the clusters identified by each approach.

Results:

HAC based on phenotypes identified in individuals with GDD revealed 16 clusters, each presenting with one dominant phenotype displayed by most individuals in the cluster, along with other minor phenotypes. Among the most common phenotypes reported were delayed speech, absent speech, and seizure. Interestingly, each phenotypic cluster molecularly included several (3-12) gene sub-networks of more closely related genes with diverse molecular function. k-means clustering also segregated individuals harboring those phenotypes, but the genetic pathways identified were different from the ones identified from HAC.

Conclusion:

Our study illustrates how divisive (k-means) and agglomerative clustering can be used in order to group individuals with GDD for future basket trials. Moreover, the result of our analysis suggests that phenotypic clusters should be subdivided into molecular sub-networks for an increased likelihood of successful treatment. Finally, a combination of both agglomerative and divisive clustering may be required for developing of a comprehensive treatment.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2023 Tipo de documento: Article