Effect of olanzapine on body composition and energy expenditure in adults with first-episode psychosis

被引:123
作者
Graham, KA
Perkins, DO
Edwards, LJ
Barrier, RC
Lieberman, JA
Harp, JB
机构
[1] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Biostat, Chapel Hill, NC 27599 USA
关键词
D O I
10.1176/appi.ajp.162.1.118
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Weight gain is a commonly observed adverse effect of atypical antipsychotic medications, but associated changes in energy balance and body composition are not well defined. The authors report here the effect of olanzapine on body weight, body composition, resting energy expenditure, and substrate oxidation as well as leptin, insulin, glucose, and lipid levels in a group of outpatient volunteers with first-episode psychosis. Method: Nine adults (six men and three women) experiencing their first psychotic episode who had no previous history of antipsychotic drug therapy began a regimen of olanzapine and were studied within 7 weeks and approximately 12 weeks after olanzapine initiation. Results: After approximately 12 weeks of olanzapine therapy, the median increase in body weight was 4.7 kg, a significant increase of 7.3% from first observation. Body fat, measured by dual-energy x-ray absorptiometry, increased significantly, with a propensity for central fat deposition. Lean body mass and bone mineral content did not change. Resting energy expenditure, measured by indirect calorimetry, did not change. Respiratory quotient significantly increased 0.12 with olanzapine and was greatest in those who gained >5% of their initial weight. Fasting insulin, C-peptide, and triglyceride levels significantly increased, but there were no changes in glucose levels; total, high density lipoprotein, or low density lipoprotein cholesterol levels; or leptin levels. Conclusions: Olanzapine appears to have induced an increase in central body fat deposition, insulin, and triglyceride levels, suggesting the possible development of insulin resistance. The decrease in fat oxidation may be secondary or predispose patients to olanzapine-induced weight gain.
引用
收藏
页码:118 / 123
页数:6
相关论文
共 44 条
[1]   The distribution of body mass index among individuals with and without schizophrenia [J].
Allison, DB ;
Fontaine, KR ;
Heo, M ;
Mentore, JL ;
Cappelleri, JC ;
Chandler, LP ;
Weiden, PJ ;
Cheskin, LJ .
JOURNAL OF CLINICAL PSYCHIATRY, 1999, 60 (04) :215-220
[2]  
Allison DB, 1999, AM J PSYCHIAT, V156, P1686
[3]  
Allison DB, 2001, J CLIN PSYCHIAT, V62, P22
[4]   Factors influencing acute weight change in patients with schizophrenia treated with olanzapine, haloperidol, or risperidone [J].
Basson, BR ;
Kinon, BJ ;
Taylor, CC ;
Szymanski, KA ;
Gilmore, JA ;
Tollefson, GD .
JOURNAL OF CLINICAL PSYCHIATRY, 2001, 62 (04) :231-238
[5]   Weight changes during clozapine treatment [J].
Briffa, D ;
Meehan, T .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 1998, 32 (05) :718-721
[6]   RECOMBINANT MOUSE OB PROTEIN - EVIDENCE FOR A PERIPHERAL SIGNAL LINKING ADIPOSITY AND CENTRAL NEURAL NETWORKS [J].
CAMPFIELD, LA ;
SMITH, FJ ;
GUISEZ, Y ;
DEVOS, R ;
BURN, P .
SCIENCE, 1995, 269 (5223) :546-549
[7]   EVIDENCE AGAINST EITHER A PREMATURE STOP CODON OR THE ABSENCE OF OBESE GENE MESSENGER-RNA IN HUMAN OBESITY [J].
CONSIDINE, RV ;
CONSIDINE, EL ;
WILLIAMS, CJ ;
NYCE, MR ;
MAGOSIN, SA ;
BAUER, TL ;
ROSATO, EL ;
COLBERG, J ;
CARO, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2986-2988
[8]   The effects of olanzapine, risperidone, and haloperidol on plasma prolactin levels in patients with schizophrenia [J].
David, SR ;
Taylor, CC ;
Kinon, BJ ;
Breier, A .
CLINICAL THERAPEUTICS, 2000, 22 (09) :1085-1096
[9]   Low plasma leptin concentration and low rates of fat oxidation in weight-stable post-obese subjects [J].
Filozof, CM ;
Murúa, C ;
Sanchez, MP ;
Brailovsky, C ;
Perman, M ;
Gonzalez, CD ;
Ravussin, E .
OBESITY RESEARCH, 2000, 8 (03) :205-210
[10]   Clozapine and body mass change [J].
Frankenburg, FR ;
Zanarini, MC ;
Kando, J ;
Centorrino, F .
BIOLOGICAL PSYCHIATRY, 1998, 43 (07) :520-524