Early effects of olanzapine on serum levels of ghrelin, adiponectin and leptin in patients with schizophrenia

被引:96
作者
Hosojima, H
Togo, T
Odawara, T
Hasegawa, K
Miura, S
Kato, Y
Kanai, A
Kase, A
Uchikado, H
Hirayasu, Y
机构
[1] Yokohama City Univ, Sch Med, Dept Psychiat, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[2] Yokohama Maioka Hosp, Yokohama, Kanagawa, Japan
[3] Yokohama City Univ, Med Ctr, Ctr Psychiat, Yokohama, Kanagawa 232, Japan
[4] Yokohama City Univ, Sch Med, Radioisotope Res Ctr, Yokohama, Kanagawa 232, Japan
关键词
olanzapine; schizophrenia; weight gain; diabetes; ghrelin; adiponectin; leptin;
D O I
10.1177/0269881105056647
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Although treatment with antipsychotics, particularly olanzapine and clozapine, has been implicated in weight gain and higher incidence of diabetes, the mechanism of these adverse reactions remains unclear. The purposes of this study were to explore the early effects of olanzapine on serum levels of ghretin, adiponectin and teptin, three recently identified hormones that play crucial rates in the regulation of energy balance and glucose metabolism. Thirteen patients with schizophrenia who had not received any medication in the 4 weeks prior to this study were included. The patients received olanzapine at an average dose of 14.5 mg/day. Serum Levels of ghretin, adiponectin, teptin and insulin, as well as weight and fasting glucose, were investigated at the baseline and at 4 weeks. Serum ghrelin levels had decreased (p = 0.03) and leptin had increased (p = 0.02), white adiponectin and insulin Levels had not significantly changed at Week 4 (p = 0.29 and p = 0.25, respectively). Weight had increased (p = 0.01), while fasting glucose had not significantly changed (p = 0.46). These findings suggest that ghrelin levels decrease and leptin levels increase after initiation of olanzapine therapy. Weight gain is also considered to be an early change, white change in insulin sensitivity is not an early change of treatment with olanzapine. Further Large-scale and Longitudinal studies are warranted to elucidate metabolic changes involving ghretin, adiponectin, leptin and insulin and their impact on weight and glucose metabolism during treatment with olanzapine and other antipsychotics.
引用
收藏
页码:75 / 79
页数:5
相关论文
共 35 条
[1]  
Allison DB, 1999, AM J PSYCHIAT, V156, P1686
[2]  
American Diabetes Association, 2004, Diabetes Care, V27 Suppl 1, pS5, DOI 10.2337/diacare.27.2007.S5
[3]   Serum leptin and triglyceride levels in patients on treatment with atypical antipsychotics [J].
Atmaca, M ;
Kuloglu, M ;
Tezcan, E ;
Ustundag, B .
JOURNAL OF CLINICAL PSYCHIATRY, 2003, 64 (05) :598-604
[4]   Serum leptin levels increase rapidly after initiation of clozapine therapy [J].
Bromel, T ;
Blum, WF ;
Ziegler, A ;
Schulz, E ;
Bender, M ;
Fleischhaker, C ;
Remschmidt, H ;
Krieg, JC ;
Hebebrand, J .
MOLECULAR PSYCHIATRY, 1998, 3 (01) :76-80
[5]  
COOPER DG, 2005, PSYCHOPHARMACOLOGY B
[6]   A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans [J].
Cummings, DE ;
Purnell, JQ ;
Frayo, RS ;
Schmidova, K ;
Wisse, BE ;
Weigle, DS .
DIABETES, 2001, 50 (08) :1714-1719
[7]   Effect of olanzapine on body composition and energy expenditure in adults with first-episode psychosis [J].
Graham, KA ;
Perkins, DO ;
Edwards, LJ ;
Barrier, RC ;
Lieberman, JA ;
Harp, JB .
AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (01) :118-123
[8]   Glucose metabolism in patients with schizophrenia treated with atypical antipsychotic agents - A frequently sampled intravenous glucose tolerance test and minimal model analysis [J].
Henderson, DC ;
Caglicro, E ;
Copeland, PM ;
Borba, CP ;
Evins, E ;
Hayden, D ;
Weber, MT ;
Anderson, J ;
Allison, DB ;
Daley, TB ;
Schoenfeld, D ;
Goff, DC .
ARCHIVES OF GENERAL PSYCHIATRY, 2005, 62 (01) :19-28
[9]   Effects of long-term treatment with antipsychotics on serum leptin levels [J].
Herrán, A ;
García-Unzueta, MT ;
Amado, JA ;
De la Maza, MT ;
Alvarez, C ;
Vázquez-Barquero, JL .
BRITISH JOURNAL OF PSYCHIATRY, 2001, 179 :59-62
[10]  
Janecková R, 2001, PHYSIOL RES, V50, P443