Genetic Autopsy and Sudden Death

N/AUnknownNCT02920203

Assistance Publique - Hôpitaux de Paris300 enrolled

Overview

The purpose of the study is to better identify hereditary cardiac causes of sudden unexpected death in young subjects through Next-Generation Sequencing of autopsy tissue

Monitoring : For index cases group, all the data will be monitored. For the relatives group, only the informed consent will be monitored Statistical analysis : * Evaluate the additional elucidation rate of unexpected sudden death * Evaluate causes obtained by Next Generation Sequencing (NGS) ( in comparison with conventional autopsy (macroscopic and / or microscopic) * Descriptive study of the causes of sudden unexpected death, identified hereditary cardiac causes percentages compared via various diagnostic approaches * Cost-effectiveness analysis Data Management : A database is created for the AGEMOS study with control of the discrepancies. All the index cases' data entered in the data base will be double checked

Study Type

OBSERVATIONAL

Enrollment

300

Conditions

Sudden Death

Interventions

Heart and spleen tissueGENETIC

genetic sequencing

Eligibility

Sex: ALLMin age: 2 YearsMax age: 40 Years

Medical Language ↔ Plain English

Index cases : Inclusion Criteria: * Subjects of more than 2 years old and less than 41 years old * Sudden unexpected death from natural and nontraumatic causes * Macroscopic autopsy performed within 72 hours after death and without signs of body decomposition * No extracardiac obvious causes, including toxicological analysis when available * No significant coronary cause after autopsy (such as tight coronary stenosis, congenital abnormality of the arteries, coronary vasculitis) * Informed consent of the close relation (family/reliable person) and / or legal representative Relatives : Inclusion Criteria: * To be a first degree relative (parents, sister, brother, child) of a deceased subject included in the AGEMOS study and accept to perform medical examination and transmit results of examination

Locations (1)

Raymond Poincaré hospital

Garches, France

RECRUITING

Outcomes

Primary Outcomes

Comparison of sudden death elucidation rate obtained by high throughput sequencing (NGS) versus conventional autopsy (macroscopic and / or microscopic)

Aim is to determine if elucidation rate of unexpected sudden death causes obtained by high throughput sequencing (NGS) is significantly better than conventional autopsy (macroscopic and / or microscopic) alone. Inclusion of a series of 100 consecutive and exhaustive cases (index cases) recruited by forensic institutes or pathology departements. Determine the rate of sudden death elucidation after NGS (after targeted capturing of 100 genes responsible for inherited cardiac diseases, including cardiomyopathy and electrical diseases) and comparison of sudden death elucidation rate obtained with conventional autopsy (macroscopic and microscopic) by chi 2 analysis.

Time frame: 27 months

Secondary Outcomes

Describe the epidemiology of causes of sudden death

Inclusion of a serie of consecutive and exhaustive subjects recruited by forensic institutes or pathology departements. Determination all the causes of death after conventional autopsy (unnatural, toxicological, non-cardiovascular, vascular, cardiological and coronary, cardiological and non-coronary causes such as cardiomyopathies \& myocarditis, no cause identified Descriptive analysis. All quantitative data will be analyzed with the average, standard deviation and median. Frequencies and Clopper-Pearson confidence interval of 95% will be provided

Time frame: 27 months

Comparison of elucidation rates of cause of sudden death including systematic cardiac screening in relatives

Aim is to determine the impact of systematic family cardiac screening in the understanding of sudden deaths Comparison of elucidation rates of cause of sudden death according to three methods: i) identification of a hereditary heart disease via the systematic cardiac screening performed in relative; ii) by the conventional autopsy; iii) by sequencing NGS analysis; Statistics: test of McNemar (mated series). The threshold for level of statistical significance is chosen at 5 %.

Time frame: 39 months

Central Contacts

Geoffroy Lorin de la Grandmaison, Pr

CONTACT

+33(0)1 47 10 76 90 g.lorin@aphp.fr

Philippe Charron, MD, PhD

CONTACT

+33 (0)1 42 16 13 47 philippe.charron@aphp.fr

Data from ClinicalTrials.gov

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