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DOI 10.1016/j.ophtha.2014.06.006

Медицинская библиотека · Ophthalmology · 2014

Personalized diagnosis and management of congenital cataract by next-generation sequencing.

Gillespie Rachel L, O'Sullivan James, Ashworth Jane, Bhaskar Sanjeev, Williams Simon, Biswas Susmito, Kehdi Elias, Ramsden Simon C, Clayton-Smith Jill, Black Graeme C, Lloyd I Christopher

Оценочное исследованиеСтатьяПоддержка исследования: вне правительства СШАВалидационное исследованиеПеревод в очереди

Аннотация

PURPOSE: To assess the utility of integrating genomic data from next-generation sequencing and phenotypic data to enhance the diagnosis of bilateral congenital cataract (CC).

DESIGN

Evaluation of diagnostic technology.

PARTICIPANTS

Thirty-six individuals diagnosed with nonsyndromic or syndromic bilateral congenital cataract were selected for investigation through a single ophthalmic genetics clinic.

METHODS

Participants underwent a detailed ophthalmic examination, accompanied by dysmorphology assessment where appropriate. Lenticular, ocular, and systemic phenotypes were recorded. Mutations were detected using a custom-designed target enrichment that permitted parallel analysis of 115 genes associated with CC by high-throughput, next-generation DNA sequencing (NGS). Thirty-six patients and a known positive control were tested. Suspected pathogenic variants were confirmed by bidirectional Sanger sequencing in relevant probands and other affected family members.

MAIN OUTCOME MEASURES: Molecular genetic results and details of clinical phenotypes were identified.

RESULTS

Next-generation DNA sequencing technologies are able to determine the precise genetic cause of CC in 75% of individuals, and 85% patients with nonsyndromic CC were found to have likely pathogenic mutations, all of which occurred in highly conserved domains known to be vital for normal protein function. The pick-up rate in patients with syndromic CC also was high, with 63% having potential disease-causing mutations.

CONCLUSIONS

This analysis demonstrates the clinical utility of this test, providing examples where it altered clinical management, directed care pathways, and enabled more accurate genetic counseling. This comprehensive screen will extend access to genetic testing and lead to improved diagnostic and management outcomes through a stratified medicine approach. Establishing more robust genotype-phenotype correlations will advance knowledge of cataract-forming mechanisms.

Для цитирования: Gillespie Rachel L, O'Sullivan James, Ashworth Jane, Bhaskar Sanjeev, Williams Simon, Biswas Susmito, Kehdi Elias, Ramsden Simon C, Clayton-Smith Jill, Black Graeme C, Lloyd I Christopher. Personalized diagnosis and management of congenital cataract by next-generation sequencing.. Ophthalmology. 2014. DOI: 10.1016/j.ophtha.2014.06.006.

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