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Anthranilic Acid: A Potential Biomarker and Treatment Target for Schizophrenia
Gregory Oxenkrug1, Marieke van der Hart2, Julien Roeser2
1Department of Psychiatry, Tufts University, USA.
Schizophrenia may involve the tryptophan-kynurenine pathway, with elevated serum anthranilic acid (AA) and decreased 3-hydroxykynurenine (3-HK) found in patients. These findings suggest AA as a potential biomarker and therapeutic target.
Area of Science:
- Neuroscience
- Biochemistry
- Psychiatry
Background:
- The tryptophan-kynurenine (Trp-Kyn) pathway is implicated in schizophrenia pathogenesis.
- Kynurenic acid (KYNA) overproduction is a leading hypothesis, potentially linked to reduced 3-hydroxykynurenine (3-HK).
- The role of anthranilic acid (AA), another Trp-Kyn metabolite, remains less understood in schizophrenia.
Purpose of the Study:
- To investigate serum concentrations of anthranilic acid (AA) in schizophrenia patients compared to controls.
- To assess the relationship between AA, 3-hydroxykynurenine (3-HK), and schizophrenia.
- To explore the potential of AA as a biomarker and therapeutic target in schizophrenia.
Main Methods:
- Serum samples from schizophrenia patients and control subjects were analyzed.
- High-performance liquid chromatography-mass spectrometry (HPLC-MS) was used for quantification.
- Concentrations of anthranilic acid (AA) and 3-hydroxykynurenine (3-HK) were measured.
Main Results:
- Schizophrenia patients exhibited a 2-fold increase in serum AA concentrations.
- A 3-fold decrease in serum 3-HK concentrations was observed in schizophrenia patients.
- These findings indicate a dysregulated Trp-Kyn pathway in schizophrenia.
Conclusions:
- Elevated AA and reduced 3-HK suggest a potential role for AA in schizophrenia mechanisms, possibly via autoimmune pathways.
- AA may serve as a biomarker for a subgroup of schizophrenia patients with autoimmune involvement.
- Further research is warranted to validate AA as a biomarker and therapeutic target in schizophrenia.
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