PsyNIT: Estimating Prevalence of Inherited Disorders of Sulfur Amino Acids Metabolism in Patients With Psychotic Disorders.

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Recruiting
CT.gov ID
NCT05206292
Collaborator
(none)
600
1
1
30.6
19.6

Study Details

Study Description

Brief Summary

Screening for sulfur amino acid metabolism pathologies using a sulfitest in adult patients with psychotic disorder.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Sulfitest
N/A

Detailed Description

Psychotic disorder is a public health problem, with a cumulative incidence in the general population estimated at 3%. Although in most cases the origin is purely psychiatric, psychotic disorder can also represent a mode of entry into many organic pathologies. Among these, hereditary metabolic diseases, although rare in the general population, hold a special place, especially in view of their potentially treatable character. However, the identification of this type of disease within the mass of patients with psychotic disorders can be an extremely complex task, and has been the subject of scientific interest for many years.

Recently, at the Grenoble Alpes University Hospital, a new hereditary metabolic disease that causes psychotic disorders has been discovered. This disease was identified in a family of patients, most of whom had psychotic disorders, and all of whom had deep cystic leukoencephalopathy on MRI and a positive sulfitest. The discovery of this new hereditary metabolic disease raises the question of its prevalence in patients with psychotic disorders, and more generally of the prevalence of diseases of sulfur amino acid metabolism.

PsyNIT study therefore aims, using the sulfitest, to detect hereditary diseases of sulfur amino acid metabolism in a sample of patients with psychotic disorders without known organic etiology. The discovery of other patients would raise the question of screening more widely for this type of pathology, and would modify the management of the patients thus screened in terms of follow-up and possibly treatment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Adult patients with psychotic disorder without known organic cause.Adult patients with psychotic disorder without known organic cause.
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Estimating Prevalence of Inherited Disorders of Sulfur Amino Acids Metabolism in Patients With Psychotic Disorders.
Actual Study Start Date :
Mar 16, 2022
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Oct 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Patient cohort

There is only one patient arm. It corresponds to the cohort of included patients, all of whom had psychotic disorders with no known organic etiology.

Diagnostic Test: Sulfitest
Urine strip to detect the presence of sulfites in urine. Immediate result.

Outcome Measures

Primary Outcome Measures

  1. Number of positive sulfitests (compared to the number of patients included). [15 minutes]

    Sulfitest is considered positive if clearly colored.

Secondary Outcome Measures

  1. Sulfite concentration in urine (semi-quantitative scale). [15 minutes]

    Sulfite concentration is estimated by visual analysis of the urine dipstick test.

  2. Clinical characteristics of patients with a positive sulfitest. [15 minutes]

    Collection of clinical characteristics of patients with a positive sulfitest, by questioning or by analysis of the medical record.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female 18 years of age and older,

  • Followed for a psychotic disorder,

  • With no known organic etiology for the psychotic disorder,

  • Not having formulated its opposition to participation in the study (or his/her tutor/curator),

  • Affiliated with the social security system.

Exclusion Criteria:
  • Patients protected by law (minors, pregnant or breastfeeding women, deprived of liberty or hospitalized under constraint, under administrative or judicial supervision) except patients under tutorship or curatorship.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Grenoble Alpes Grenoble France 38043

Sponsors and Collaborators

  • University Hospital, Grenoble

Investigators

  • Principal Investigator: GĂ©rard Besson, University Hospital, Grenoble

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT05206292
Other Study ID Numbers:
  • 38RC21.0294
  • 2021-A01940-41
First Posted:
Jan 25, 2022
Last Update Posted:
May 12, 2022
Last Verified:
May 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
Keywords provided by University Hospital, Grenoble
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2022