Subunit and whole molecule specificity of the anti-bovine casein immune response in recent onset psychosis and schizophrenia
Received 19 October 2009; received in revised form 16 December 2009; accepted 21 December 2009. published online 14 January 2010.
Abstract
Previous studies show increased antibody levels to bovine casein in some individuals with schizophrenia. The immunogenicity of specific domains of bovine casein varies among people with milk sensitivities and thus could vary among different neuropsychiatric disorders. Using ELISAs and immunoblotting, we characterized IgG class antibody specificity to whole bovine casein and to the αs, β, and κ subunits in individuals with recent onset psychosis (n=95), long-term schizophrenia (n=103), and non-psychiatric controls (n=65). In both patient groups, we found elevated IgG to casein proteins, particularly to whole casein and the αs subunit (p≤0.0001). Odds ratios of casein seroprevalence for recent onset psychosis (age-, gender-, race-, smoking-adjusted) were significant for whole casein (8.13, p≤0.0001), and the αs (7.89, p≤0.0001), β (5.23, p≤0.001) and κ (5.70, p≤0.0001) subunits. Odds ratios for long-term schizophrenia were significant for whole casein (7.85, p≤0.0001), and the αs (4.78, p≤0.003) and κ (4.92, p≤0.004) subunits. Within the recent onset group, odds ratios were particularly significant for a subgroup of people with psychotic disorders that included major depressive disorders (8.22–16.48, p≤0.0001). In a different recent onset subgroup (schizophrenia-spectrum disorders), PANSS scores for negative symptoms were correlated with casein antibody levels for the αs and κ subunits (p≤0.001–0.01). Immunoblotting patterns also exhibited group specificity, with κ predominant in recent onset and αs in schizophrenia (Fisher's Exact Test, p≤0.001). The elevated IgG and unique patterns of antibody specificity to bovine casein among diagnostic groups provide a rationale for clinical trials to evaluate efficacies of dietary modifications in individuals with neuropsychiatric diseases.
aStanley Division of Developmental Neurovirology, Department of Pediatrics, Johns Hopkins University School of Medicine, 600 N. Wolfe Street, Blalock 1105, Baltimore, MD 21287-4933, United States
bStanley Research Program, Sheppard Pratt Health System, Baltimore, Maryland, United States
cINRA – Agrocampus Ouest, UMR 1253, Science et Technologie du Lait et de l'Oeuf, Rennes, France
dBiomolecular Detection (BD), RIKILT-Institute of Food Safety, Wageningen UR, Netherlands