Clinical Validation Study for EDIT-B Test: an Aid for Differential Diagnosis of Bipolar Disorder, Based on RNA Editing Blood Biomarkers

Sponsor
Alcediag (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05603819
Collaborator
Hospital Clinic of Barcelona (Other), Fundacion Clinic per a la Recerca Biomédica (Other), The Capital Region of Denmark (Other), GHU Paris Psychiatrie & Neurosciences (Other), Parc Sanitari Sant Joan de Déu (Other), Fundació Sant Joan de Déu (Other), Synlab Italie (Other)
436
4
30.1
109
3.6

Study Details

Study Description

Brief Summary

Differentiation between major depressive disorder (MDD) and bipolar disorder (BD) as soon as possible in the patient journey represents a major clinical issue. When the patient is in a depressive phase, the symptoms are similar between the two pathologies and the current clinical scales fail in distinguishing them. Physicians often report this difficulty and as a consequence, the mean time from onset to bipolar disorder diagnosis is currently 7.5 years. These diagnostic delays and misdiagnosis lead to damaging consequences for patients and their loved ones: worsening of symptoms, comorbidities, suicide risk and inadequate care resulting in severe impairment in social and occupational functioning. Faced with these high expectations for accurate diagnostic methods for an earlier management of psychiatric patients, the combination of relevant clinical features and biomarkers could stand for a solution, leading to a personalised approach in patients with mood disorders.

In a first clinical discovery study, a panel of RNA biomarkers in the blood of patients with a major depressive episode (MDE) has been identified, allowing to differentiate bipolar disorder from MDD (unipolar depression). These biomarkers are based on RNA modifications, namely RNA editing, that could be identified using molecular biology, NGS and artificial intelligence. This panel constitutes EDIT-B test, which is based on Alcediag's proprietary and patented biomarkers and algorithms.

The present study aims to validate the biomarker signatures proposed by Alcediag by measuring the association between the modifications of the RNA editing and major depressive disorder/ bipolar disorder diagnosis, in patients with a MDE in real-life setting pilot centres.

Condition or Disease Intervention/Treatment Phase
  • Device: EDIT-B

Study Design

Study Type:
Observational
Anticipated Enrollment :
436 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Clinical Validation Study for EDIT-B Test: an Aid for Differential Diagnosis of Bipolar Disorder, Based on RNA Editing Blood Biomarkers
Actual Study Start Date :
Jun 29, 2022
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Bipolar disorder

Patients with depression suffering from bipolar disorder.

Device: EDIT-B
To perform EDIT-B test, questionnaires and 2x0.5 mL whole blood are collected from each patient.

Major depressive disorder

Patients with depression suffering from major depressive disorder.

Device: EDIT-B
To perform EDIT-B test, questionnaires and 2x0.5 mL whole blood are collected from each patient.

Outcome Measures

Primary Outcome Measures

  1. Diagnostic performances of EDIT-B signatures on MDD vs. BD differentiation in patients with depression. [Specimen collection needed for evaluation of diagnostic performances: 1 day (= 1 visit).]

    The objective of this study is to estimate three EDIT-B signatures in term of their external validity. For this purpose, performances of the tests will be estimated by calculating for each signature its Sensitivity (i.e. the probability that a test will indicate 'bipolar disorders' among those with this disease), Specificity (i.e. the fraction of those without bipolar disorders who will have a negative test result) and its Accuracy to predict the diagnosis of bipolar disorders. In addition, Area under the ROC curves of each EDIT-B signature will be calculated. The categorisation of the type of disorder (MDD vs. BD) by experts will be based on the MINI considered as the gold standard for diagnosis. The performances of the tested signatures will be compared on a two-by-two basis by comparing sensitivities and specificity , using the methods based on Mac Nemar test proposed by Hawass. AUC-ROC of the 3 signatures will also be compared by DeLong method.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Signed informed consent.

  2. Male or female ≥ 18 and ≤ 80 years of age at inclusion.

  3. MADRS ≥ 20

  4. In- and out-patients can be recruited.

  5. Diagnosed with MDE with the MINI for DSM-5

  6. Currently treated for the MDE

  7. Diagnosed with MDD or BD with the MINI for DSM-5.

  8. For patients with BD: at least one manic or hypomanic episode

  9. For patients with MDD: at least one MDE

Exclusion Criteria:
  1. MDD patients with first degree family history of bipolar disorder

  2. YMRS > 12

  3. Pregnant women

  4. Unipolar or bipolar depression secondary to major central nervous system affections, including infections in the brain, tumours of the brain, stroke, Alzheimer's disease, Parkinson's disease, Multiple sclerosis, other major brain affections

  5. Schizo-affective patients

Abbrevations:

BD Bipolar Disorder DSM-5 Diagnostic and Statistical Manual of Mental disorders 5 MADRS Montgomery-Asberg Depression Rating Scale MDD Major Depressive Disorder MDE Major Depressive Episode MINI Mini-International Neuropsychiatric Interview YMRS Young Mania Rating Scale

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Capital Region of Denmark Copenhagen Denmark 2100
2 GHU Paris Psychiatrie & Neurosciences Paris France 75014
3 Parc Sanitari Sant Joan de Déu Sant Boi De Llobregat Barcelona Spain 08830
4 Hospital Clínic de Barcelona Barcelona Spain 08036

Sponsors and Collaborators

  • Alcediag
  • Hospital Clinic of Barcelona
  • Fundacion Clinic per a la Recerca Biomédica
  • The Capital Region of Denmark
  • GHU Paris Psychiatrie & Neurosciences
  • Parc Sanitari Sant Joan de Déu
  • Fundació Sant Joan de Déu
  • Synlab Italie

Investigators

  • Principal Investigator: Eduard Vieta, Hospital Clinic of Barcelona

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Alcediag
ClinicalTrials.gov Identifier:
NCT05603819
Other Study ID Numbers:
  • EDIT-B
First Posted:
Nov 3, 2022
Last Update Posted:
Nov 3, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 3, 2022