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Association Study of the HTR2C, Leptin and Adiponectin Genes and Serum Marker Analyses in Clozapine Treated Long-Term Patients with Schizophrenia

Published online by Cambridge University Press:  15 April 2020

J.-P. Klemettilä*
Affiliation:
Department of Psychiatry, Pitkäniemi Hospital, Tampere University Hospital, 33380Pitkäniemi, Finland
O. Kampman
Affiliation:
School of Medicine, University of Tampere, 33014Tampere, Finland Department of Psychiatry, Seinäjoki Hospital District, 60220Seinäjoki, Finland
N. Seppälä
Affiliation:
Department of Psychiatry, Satakunta Hospital District, 28500Pori, Finland
M. Viikki
Affiliation:
School of Medicine, University of Tampere, 33014Tampere, Finland Tampere Mental Health Centre, Hallituskatu 8B, 33200Tampere, Finland
M. Hämäläinen
Affiliation:
The Immunopharmacology Research Group, School of Medicine, University of Tampere and Tampere University Hospital, 33014Tampere, Finland
E. Moilanen
Affiliation:
The Immunopharmacology Research Group, School of Medicine, University of Tampere and Tampere University Hospital, 33014Tampere, Finland
N. Mononen
Affiliation:
Fimlab Laboratories, Department of Clinical Chemistry, School of Medicine, University of Tampere, 33014Tampere, Finland
T. Lehtimäki
Affiliation:
Fimlab Laboratories, Department of Clinical Chemistry, School of Medicine, University of Tampere, 33014Tampere, Finland
E. Leinonen
Affiliation:
Department of Psychiatry, Pitkäniemi Hospital, Tampere University Hospital, 33380Pitkäniemi, Finland School of Medicine, University of Tampere, 33014Tampere, Finland
*
*Corresponding author. Department of Psychiatry, Pitkäniemi Hospital, Tampere University Hospital, 33380 Pitkäniemi, Finland. Tel.: +358 50 5928308. E-mail address:jari-pekka.klemettila@pshp.fi (J.-P. Klemettilä).
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Abstract

Clozapine treatment is associated with weight gain and cardio-metabolic consequences among patients with schizophrenia. Polymorphisms of leptin, serotonin receptor HTR2 C and adiponectin genes have been associated with antipsychotic-induced weight gain and metabolic comorbidity. However, the results of the studies so far are inconclusive. The aim of the present study was first to test for a possible role of serum leptin and adiponectin levels as a marker of weight gain in association with inflammatory cytokines/adipokines (IL-6, IL-1Ra, hs-CRP and adipsin), and second to study associations between SNPs LEP rs7799039 (-2548 A/G), ADIPOQ rs1501299 and HTR2 C rs1414334 and weight gain and levels of leptin and adiponectin, in 190 patients with schizophrenia on clozapine treatment, with retrospectively assessed weight change and cross-sectionally measured cytokine levels. A strong association was found between serum levels of leptin and weight gain and cytokines/adipokines related to metabolic comorbidity, especially among female patients (in women leptin vs. weight gain, IL-6 and IL-1Ra, P < 0.001; in men leptin vs. weight gain, P = 0.026, leptin vs. IL-1Ra, P < 0.001). In male patients low adiponectin level was a more specific marker of clozapine-induced weight gain (P = 0.037). The results of the present study do not support a major role of SNPs LEP rs7799039, ADIPOQ rs1501299 and HTR2 C rs1414334 in the regulation of weight gain or association of serum levels of leptin and adiponectin and corresponding studied SNPs in patients with schizophrenia on clozapine treatment.

Type
Original article
Copyright
Copyright © Elsevier Masson SAS 2014

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