α-N-acetylgalactosaminidase in Methamphetamine Psychosis
Could α-N-acetylgalactosaminidase Levels Be Associated With the Presence of Psychotic Symptoms in Methamphetamine Use Disorder? A Cross-Sectional Observational Study
1 other identifier
observational
93
1 country
1
Brief Summary
This cross-sectional observational cohort study examined serum α-N-acetylgalactosaminidase levels in methamphetamine use disorder (MUD), methamphetamine-induced psychotic disorder (MP), and healthy control (HC) groups. The study aimed to determine whether decreased α-N-acetylgalactosaminidase levels are associated with psychotic symptoms in methamphetamine users.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2025
CompletedFirst Submitted
Initial submission to the registry
February 20, 2026
CompletedFirst Posted
Study publicly available on registry
February 25, 2026
CompletedFebruary 25, 2026
February 1, 2026
4 months
February 20, 2026
February 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
α-N-acetylgalactosaminidase
Serum α-N-acetylgalactosaminidase levels measured by ELISA (ng/mL).
At hospital admission (baseline)
Secondary Outcomes (2)
Aggregate Index of Systemic Inflammation (AISI)
At hospital admission (baseline)
Positive and Negative Syndrome Scale (PANSS) Score
At hospital admission (baseline)
Study Arms (3)
Methamphetamine Use Disorder
Adult participants (18-65 years) diagnosed with Methamphetamine Use Disorder according to DSM-5-TR criteria. Participants were evaluated at hospital admission (baseline). No intervention was assigned by the study protocol. Blood samples were collected for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count parameters. No psychometric scales were administered to this group. Sociodemographic and clinical data were recorded for all participants.
Methamphetamine-Induced Psychotic Disorder
Adult participants (18-65 years) diagnosed with Methamphetamine-Induced Psychotic Disorder according to DSM-5-TR criteria. Participants were evaluated at hospital admission (baseline). No intervention was assigned by the study protocol. Blood samples were collected for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count parameters. Psychotic symptom severity was assessed using the Positive and Negative Syndrome Scale (PANSS). Sociodemographic and clinical data were recorded for all participants.
Healthy Control
Healthy control adult participants (18-65 years) without any current or past psychiatric disorder. No intervention was administered as part of the research protocol. Participants underwent a baseline clinical evaluation and provided a single blood sample for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count inflammatory markers. Sociodemographic and clinical data were recorded for all participants.
Eligibility Criteria
The study population consisted of adult male inpatients aged 18-49 years who were admitted to Elazığ Mental Health and Diseases Hospital between May 1, 2025 and August 31, 2025. The MP group included consecutive inpatients diagnosed with methamphetamine-induced psychotic disorder and the MUD group included consecutive inpatients diagnosed with methamphetamine use disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR). Both patient groups consisted of active methamphetamine users and were hospitalized for clinical management at the time of assessment. Urine toxicology screening was performed at admission to confirm substance use status. The Healthy Control (HC) group consisted of adult male individuals without current or past psychiatric disorders and without substance use disorders, matched to patient groups in terms of age and body mass index. HCs had no significant medical illnesses.
You may qualify if:
- Diagnosis of MUD according to DSM-5-TR
- Medication-free for at least one month prior to admission
- Age ≥ 18 years and \<65 years
- Provided informed consent
- For Methamphetamine Use Disorder (MUD) Group:
You may not qualify if:
- Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Primary psychiatric disorders other than MUD
- Alcohol use disorder
- For Methamphetamine-Induced Psychotic Disorder (MP) Group:
- Diagnosis of MP according to DSM-5-TR
- Medication-free for at least one month prior to admission
- Age ≥ 18 years and \<65 years
- Provided informed consent
- +28 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Elazığ Mental Health and Diseases Hospital
Elâzığ, Elâzığ, 23200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mehmet Hamdi ÖRÜM, MD, Associate Professor
Elazığ Mental Health and Diseases Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor Mehmet Hamdi Örüm, MD, Psychiatrist
Study Record Dates
First Submitted
February 20, 2026
First Posted
February 25, 2026
Study Start
May 1, 2025
Primary Completion
August 31, 2025
Study Completion
August 31, 2025
Last Updated
February 25, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- Data will be available beginning 6 months after publication and will remain available for 5 years.
- Access Criteria
- Access will be granted to researchers who provide a methodologically sound proposal. Requests must be approved by the principal investigator and may require a data use agreement in accordance with institutional and ethical regulations.
Deidentified individual participant data (IPD) underlying the results reported in this study (including demographic variables, serum α-N-acetylgalactosaminidase levels, complete blood count parameters, and Positive and Negative Syndrome Scale (PANSS)) will be made available to qualified researchers upon reasonable request for academic purposes. Data will be shared after removal of all direct identifiers and in accordance with applicable ethical approvals and data protection regulations. Access to the data will require a methodologically sound research proposal and a data use agreement. Requests should be directed to the corresponding author.