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Clinical validation of EDIT-B test for the diagnosis of bipolar disorder

INTRODUCTION: Bipolar disorder (BD) is a psychiatric disorder characterized by alternating episodes of high mood and low mood similar to depression. To differentiate BD patients from unipolar (UN) depressed patients remains a challenge and the clinical scales available failed to distinguish these 2...

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Autores principales: Abraham, J.-D., Salvetat, N., Guerra, P., Ferrari, M., Le Guen, P., Biglia, O., Henry, C., Kessing, L., Haro, J.M., Vieta, E., Weissmann, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565526/
http://dx.doi.org/10.1192/j.eurpsy.2022.1047
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author Abraham, J.-D.
Salvetat, N.
Guerra, P.
Ferrari, M.
Le Guen, P.
Biglia, O.
Henry, C.
Kessing, L.
Haro, J.M.
Vieta, E.
Weissmann, D.
author_facet Abraham, J.-D.
Salvetat, N.
Guerra, P.
Ferrari, M.
Le Guen, P.
Biglia, O.
Henry, C.
Kessing, L.
Haro, J.M.
Vieta, E.
Weissmann, D.
author_sort Abraham, J.-D.
collection PubMed
description INTRODUCTION: Bipolar disorder (BD) is a psychiatric disorder characterized by alternating episodes of high mood and low mood similar to depression. To differentiate BD patients from unipolar (UN) depressed patients remains a challenge and the clinical scales available failed to distinguish these 2 populations. ALCEDIAG developed EDIT-B, the first blood test able to make a differential diagnosis of BD. Based on RNA editing modifications measurement and AI, the test requires a simple blood draw and equipment available in most central laboratories. A first study on 160 UN and 95 BD patients allowed a differential diagnosis with an AUC of 0.935 and high specificity (Sp=84.6%) and sensitivity (Se=90.9%). A multicentric clinical study has been set up to validate these performances. OBJECTIVES: The objective of this project is to run a multicentric clinical study in Europe and assess the performances of the test. METHODS: The EDIT-B project, led by Alcediag, is supported by EIT-Health grant (European institute of Innovation and Technology) and gathers 4 clinical centers in 3 countries (France, Spain, Danemark), a CRO for the clinical study management (Aixial), a CRO for the development of a diagnostic kit (Veracyte), a diagnostic lab for molecular biology analyses (Synlab), and a regulatory company (PLG). RESULTS: At the end of the study, the EDIT-B performance will be confirmed and the test will be CE-marked. CONCLUSIONS: This test will address the needs of millions of patients suffering from misdiagnosis and therefore allow them to receive the correct treatment. DISCLOSURE: JDA, NS and DW are employees of Alcediag.
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spelling pubmed-95655262022-10-17 Clinical validation of EDIT-B test for the diagnosis of bipolar disorder Abraham, J.-D. Salvetat, N. Guerra, P. Ferrari, M. Le Guen, P. Biglia, O. Henry, C. Kessing, L. Haro, J.M. Vieta, E. Weissmann, D. Eur Psychiatry Abstract INTRODUCTION: Bipolar disorder (BD) is a psychiatric disorder characterized by alternating episodes of high mood and low mood similar to depression. To differentiate BD patients from unipolar (UN) depressed patients remains a challenge and the clinical scales available failed to distinguish these 2 populations. ALCEDIAG developed EDIT-B, the first blood test able to make a differential diagnosis of BD. Based on RNA editing modifications measurement and AI, the test requires a simple blood draw and equipment available in most central laboratories. A first study on 160 UN and 95 BD patients allowed a differential diagnosis with an AUC of 0.935 and high specificity (Sp=84.6%) and sensitivity (Se=90.9%). A multicentric clinical study has been set up to validate these performances. OBJECTIVES: The objective of this project is to run a multicentric clinical study in Europe and assess the performances of the test. METHODS: The EDIT-B project, led by Alcediag, is supported by EIT-Health grant (European institute of Innovation and Technology) and gathers 4 clinical centers in 3 countries (France, Spain, Danemark), a CRO for the clinical study management (Aixial), a CRO for the development of a diagnostic kit (Veracyte), a diagnostic lab for molecular biology analyses (Synlab), and a regulatory company (PLG). RESULTS: At the end of the study, the EDIT-B performance will be confirmed and the test will be CE-marked. CONCLUSIONS: This test will address the needs of millions of patients suffering from misdiagnosis and therefore allow them to receive the correct treatment. DISCLOSURE: JDA, NS and DW are employees of Alcediag. Cambridge University Press 2022-09-01 /pmc/articles/PMC9565526/ http://dx.doi.org/10.1192/j.eurpsy.2022.1047 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Abraham, J.-D.
Salvetat, N.
Guerra, P.
Ferrari, M.
Le Guen, P.
Biglia, O.
Henry, C.
Kessing, L.
Haro, J.M.
Vieta, E.
Weissmann, D.
Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title_full Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title_fullStr Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title_full_unstemmed Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title_short Clinical validation of EDIT-B test for the diagnosis of bipolar disorder
title_sort clinical validation of edit-b test for the diagnosis of bipolar disorder
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565526/
http://dx.doi.org/10.1192/j.eurpsy.2022.1047
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