共 50 条
Positive Impact of Expert Reference Center Validation on Performance of Next-Generation Sequencing for Genetic Diagnosis of Autoinflammatory Diseases
被引:11
|作者:
Boursier, Guilaine
[1
]
Rittore, Cecile
[1
]
Georgin-Lavialle, Sophie
[2
]
Belot, Alexandre
[3
]
Galeotti, Caroline
[4
]
Hachulla, Eric
[5
]
Hentgen, Veronique
[6
]
Rossi-Semerano, Linda
[4
]
Sarrabay, Guillaume
[7
]
Touitou, Isabelle
[7
]
机构:
[1] Univ Montpellier, Dept Med Genet Rare Dis & Personalized Med, CHU Montpellier, Rare & Autoinflammatory Dis Unit, F-34295 Montpellier, France
[2] Univ Paris 06, Tenon Hosp, AP HP, Dept Internal Med,CEREMAIA, F-75970 Paris, France
[3] Univ Lyon, Paediat Nephrol, Rheumatol Dermatol Unit, HFME,Dermatol Unit,HCL,RAISE, F-69677 Bron, France
[4] Bicetre Hosp, AP HP, Dept Paediat Rheumatol, CEREMAIA, F-94275 Le Kremlin Bicetre, France
[5] Univ Lille, Dept Internal Med & Clin Immunol, CHU Lille, F-59037 Lille, France
[6] CH Versailles, Dept Gen Pediat, CEREMAIA, F-78157 Le Chesnay, France
[7] Univ Montpellier, Cellules Souches Plasticite Cellulaire Med Regene, Dept Med Genet Rare Dis & Personalized Med, CEREMAIA,CHU Montpellier,INSERM, F-34295 Montpellier, France
关键词:
autoinflammatory diseases;
multidisciplinary consultation;
next-generation sequencing;
FAMILIAL MEDITERRANEAN FEVER;
CRITERIA;
GUIDELINES;
D O I:
10.3390/jcm8101729
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Monogenic autoinflammatory diseases (AIDs) are caused by variants in genes that regulate innate immunity. The current diagnostic performance of targeted next-generation sequencing (NGS) for AIDs is low. We assessed whether pre-analytic advice from expert clinicians could help improve NGS performance from our 4 years of experience with the sequencing of a panel of 55 AIDs genes. The study included all patients who underwent routine NGS testing between September 2014 and January 2019 at the laboratory of autoinflammatory diseases (Montpellier, France). Before March 2018, all medical requests for testing were accepted. After this time, we required validation by a reference center before NGS: the positive advice could be obtained after a face-to-face consultation with the patient or presentation of the patient's case at a multidisciplinary staff meeting. Targeted NGS resulted in an overall 7% genetic confirmation, which is consistent with recent reports. The diagnostic performance before and after implementation of the new pre-requisite increased from 6% to 10% (p = 0.021). Our study demonstrated, for the first time, the beneficial effect of a two-step strategy (clinical expert advice, then genetic testing) for AIDs diagnosis and stressed the possible usefulness of the strategy in anticipation of the development of pan-genomic analyses in routine settings.
引用
收藏
页数:9
相关论文