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Published on: October 20, 2016
CSF-methionine is elevated in psychotic patients
B Regland1, L Abrahamsson, K Blennow
1Institute of Clinical Neuroscience, Göteborg University, Sahlgrenska University Hospital, Mölndal, Sweden.
Patients with psychotic disorders often exhibit elevated methionine (MET) and homocysteine (HCY) levels in cerebrospinal fluid, indicating a disturbed one-carbon metabolism during acute phases.
Area of Science:
- Neuroscience
- Biochemistry
- Psychiatry
Background:
- One-carbon metabolism is crucial for various biological processes.
- Alterations in one-carbon metabolism have been implicated in neurological and psychiatric conditions.
Purpose of the Study:
- To investigate cerebrospinal fluid (CSF) levels of methionine (MET), homocysteine (HCY), and cystathionine in patients with psychotic disorders.
- To determine if these metabolites are altered compared to healthy controls and if factors like gender, age, or neuroleptic treatment influence these levels.
Main Methods:
- Cerebrospinal fluid (CSF) samples were collected from patients with psychotic disorders (n=36) and healthy controls (n=25).
- Levels of methionine (MET), homocysteine (HCY), and cystathionine were measured in the CSF of all participants.
Main Results:
- Patients with psychotic disorders showed significantly higher CSF methionine (MET) levels compared to healthy controls (p<0.00001).
- Ten patients had MET levels exceeding those of any control subject.
- Three young male patients exhibited markedly elevated CSF homocysteine (HCY) levels, far above control ranges.
- No significant gender differences were observed for any measured parameter.
- Elevated MET levels were present even in young, drug-naive patients, ruling out age and neuroleptic treatment as sole explanations.
Conclusions:
- Patients experiencing psychotic disorders, particularly during acute exacerbation, frequently display disruptions in one-carbon metabolism.
- Elevated CSF methionine and homocysteine may serve as potential biomarkers for disturbed one-carbon metabolism in psychotic disorders.
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