Key result
Elevated antigliadin IgG in schizophrenia is linked to ~18% higher kynurenine levels and KYN-TRP ratios.
Why the study?
Are kynurenine and tryptophan levels altered in schizophrenia patients with elevated antigliadin IgG antibodies compared to those without?
Cross-Sectional (n=950)
Are kynurenine and tryptophan levels altered in schizophrenia patients with elevated antigliadin IgG antibodies compared to those without?
In patients with schizophrenia, elevated antigliadin IgG antibodies are associated with higher kynurenine levels and KYN-TRP ratio, linking nonceliac gluten sensitivity with the kynurenine pathway of tryptophan metabolism.
Answers are grounded in this paper and cite their sources.
Association in schizophrenia is hypothesis-generating; prospective studies needed to clarify causality and clinical relevance.
OBJECTIVE: Several studies have reported an association between nonceliac gluten sensitivity and schizophrenia. Immune and kynurenine (KYN) pathways have also been implicated in the pathophysiology of schizophrenia, and certain proinflammatory immune mediators may increase KYN and reduce tryptophan (TRP) levels. METHODS: We measured serum antigliadin immunoglobulin G (IgG), KYN, and TRP in 950 patients with schizophrenia. Patients with antibody level at the 90th percentile or higher of control participants (21.9% of all patients) were classified as having elevated antigliadin IgG. Independent t tests and linear regression models were used to compare TRP, KYN, and KYN-TRP ratio (indicator of TRP metabolism) between patients with and those without elevated antigliadin IgG. The correlation between antigliadin IgG and TRP, KYN, and the ratio was also evaluated in the patients. RESULTS: KYN and KYN-TRP ratio were higher in patients with elevated antigliadin IgG (geometric mean [standard deviation {SD}] = 2.65 [0.25] µmol/L versus 2.25 [0.23] µmol/L [p < .001] and 0.05 [0.26] versus 0.04 [0.25; p = .001] respectively), findings robust to adjustment for potential demographic and clinical confounders. Antigliadin IgG positively correlated with KYN and KYN-TRP ratio (r = 0.12, p < .001; r = 0.11, p = .002). TRP did not differ between the two groups and did not correlate with antigliadin IgG. CONCLUSIONS: Our results connect nonceliac gluten sensitivity with the KYN pathway of TRP metabolism in psychotic illness and hint toward potential individualized treatment targets.
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Okusaga et al. (2016) conducted a cross-sectional in Schizophrenia (n=950). Elevated antigliadin IgG vs. Without elevated antigliadin IgG was evaluated on Kynurenine (KYN) levels (p=< .001). Elevated antigliadin IgG in patients with schizophrenia was associated with higher kynurenine levels and KYN-TRP ratios compared to those without elevated antibodies.
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