[No authors listed]
OBJECTIVES:Ghrelin regulates appetite and also plays important roles in cognition and may be involved in vulnerability to SCZ. METHODS:In this study, we measured mRNA expression of the ghrelin-related molecules, growth hormone secretagogue receptor 1a (GHS-R1a) and 1b (GHS-R1b), and the ghrelin activator, membrane bound O-acyltransferase 4 (MBOAT4). Peripheral leukocytes from Japanese patients with SCZ (nâ¯=â¯49; 23 males, 26 females; ageâ¯=â¯61.8â¯Â±â¯13.3 years) and controls (nâ¯=â¯50; 25 males, 25 females; ageâ¯=â¯62.0â¯Â±â¯14.3 years) were recruited according to their clinical information. We also studied the DNA methylation rates of these genes in DNA from leukocytes. RESULTS:The mRNA expression of GHS-R1a was significantly decreased in SCZ (SCZ vs. control: 0.35â¯Â±â¯0.081 vs. 1.00â¯Â±â¯0.059, respectively, pâ¯=â¯0.007), but expression levels of GHS-R1b and MBOAT4 were significantly increased in SCZ (SCZ vs. control: 2.02â¯Â±â¯0.91 vs. 1.00â¯Â±â¯0.32, pâ¯=â¯0.023, 1.37â¯Â±â¯0.21 vs. 1.00â¯Â±â¯0.11, respectively, pâ¯=â¯0.014). No differences in methylation rates for any genes were found. CONCLUSION:We conclude that opposite expression of GHS-R1a and GHS-R1b, and elevated MBOAT4 mRNA expression may reflect the mechanisms of SCZ.
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