Scholarly article on topic 'A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes'

A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes Academic research paper on "Veterinary science"

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Pediatr Rheumatol
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Academic research paper on topic "A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes"

Rusmini et al. Pediatric Rheumatology 2015, 13(Suppl 1):O24 http://www.ped-rheum.com/content/13/S1/O24

RHEUMATOLOGY

ORAL PRESENTATION Open Access

A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes

M Rusmini1, S Federici2, F Caroli1, A Grossi1, M Baldi3, L Obici4, A Insalaco5, A Tommasini6, R Caorsi7, E Gallo8, AN Olivieri9, AV Marzano10, D Coviello3, R Ravazzolo1, A Martini11, M Gattorno2, I Ceccherini1*

From 8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases Dresden, Germany. 30 September - 3 October 2015

Introduction

Systemic autoinflammatory diseases (SAIDs) are a group of monogenic disorders characterized by inflammation which occurs in the absence of pathogenic auto-antibodies, auto-reactive T lymphocytes or other infective causes. More than 50% of SAID patients recruited to our Unit does not show any mutation at gene(s) tested by direct Sanger sequencing in the routine diagnosis. Clinical misdiagnosis, mutations in untested gene regions and genetic heterogeneity are possible explanations.

Objectives

To improve both the molecular diagnosis and genotype interpretation of SAIDs, we aimed at the development of a Next Generation Sequencing based protocol, designed for the simultaneous screening of ten genes known to be involved in a remarkable proportion of SAIDs. Different bio-informatics approaches were taken into consideration in order to define the best pipeline for variants detection.

Patients and methods

A panel of gene amplicons specific for the diseases under study was designed through the Ion AmpliSeq™ designer software. Fifty SAID patients, already genotyped for the respective causative gene(s), were massively sequenced for the coding portions of MEFV, MVK, TNFRSF1A, NLRP3, NLRP12, NOD2, PSTPIP1, IL1RN, LPIN2 and

11RCCS G Gaslini, UOC MedicalGenetics, Genoa, Italy

Full list of author information is available at the end of the article

Bio Med Central

PSMB8. Three different bio-informatics pipelines, Ion Reporter™, CLC Bio Genomics Workbench, and GATK-based in-house workflow, were compared

Results

The approach we propose here for NGS-based diagnosis of SAIDs, has resulted technically suitable, with a very high mean coverage (336X) and nearly full detection of variants. Besides expected mutation, we could also identify many unexpected variants that were all validated by Sanger sequencing and compared to assess true and false positive detection rates of the three workflows. Finally, the overall clinical picture of 34 patients were re-evaluated in the light of the new mutations found.

Conclusions

The present gene panel has resulted suitable for molecular diagnosis of SAIDs. Besides causative mutations, most patients have turned out to carry variants of unclear significance that will need further investigation. Moreover, genotype-phenotype correlation drawn in 34 patients has confirmed a remarkably difficult interpretation of NGS data in patients with an undefined or complex inflammatory phenotype. This supports the need of evidence-based and validated clinical criteria as crucial tools to be used concurrently with the genetic analysis for the final diagnosis and classification of SAIDs patients. In addition to setting a first approach to mutational detection in SAIDs, patients left without a

© 2015 Rusmini et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http:// creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/ zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Rusmini et al. Pediatric Rheumatology 2015, 13(Suppl 1):O24 http://www.ped-rheum.com/content/13/S1/O24

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clear diagnosis will be identified as candidate for the successive NGS analysis of the whole exome.

Authors' details

11RCCS G Gaslini, UOC MedicalGenetics, Genoa, Italy. 2IRCCS G Gaslini, UOC Pediatric Rheumatology, Genoa, Italy. 3Ospedale Galliera, Laboratory of Human Genetics, Genoa, Italy. 4IRCCS Policlinico S Matteo, Laboratorio Biotecnologie, Pavia, Italy. 5Bambin Gesu Childern's Hospital, Division of Rheumatology, Rome, Italy. 6IRCCS Burlo Garofolo, Department of Pediatrics, Trieste, Italy. 7IRCCS G Gaslini, Department of Pediatrics, Genoa, Italy. 8Universita di Torino, Dipartimento di Salute Pubblica e Pediatria, Torino, Italy. 9Second University of Naples, Women, Child and Generaland Specialistic Surgery, Naples, Italy. 10Universita degli studi di Milano, UO Dermatologia, Milan, Italy. 11IRCCS, UOC Pediatric Rheumatology, Genoa, Italy.

Published: 28 September 2015

doi:10.1186/1546-0096-13-S1-O24

Cite this article as: Rusmini et al.: A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes. Pediatric Rheumatology 2015 13(Suppl 1):O24.

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