A low TSH profile predicts olanzapine-induced weight gain and relief by adjunctive topiramate in healthy male volunteers

被引:11
作者
Evers, Simon S. [2 ]
van Vliet, Andre [1 ]
van Vugt, Barbara [1 ]
Scheurink, Anton J. W. [2 ]
van Dijk, Gertjan [2 ,3 ]
机构
[1] PRA Hlth Sci, Zuidlaren, Netherlands
[2] Univ Groningen, Groningen Inst Evolutionary Life Sci Neurobiol, Dept Behav Neurosci, Groningen, Netherlands
[3] Univ Groningen, ESRIG Ctr Isotope Anal, Groningen, Netherlands
关键词
Olanzapine; Topiramate; Body weight; Thyroid stimulating hormone; Thermoregulation; Food intake; HOMEOSTASIS MODEL ASSESSMENT; LABELED WATER ANALYSIS; THYROID-HORMONE; TRIGLYCERIDE LEVELS; INSULIN-RESISTANCE; ENERGY-EXPENDITURE; METABOLIC SYNDROME; RECEPTOR DENSITY; DOUBLE-BLIND; SCHIZOPHRENIA;
D O I
10.1016/j.psyneuen.2015.12.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Second generation antipsychotics, like olanzapine (OLZ), have become the first line drug treatment for patients with schizophrenia. However, OLZ treatment is often associated with body weight (BW) gain and metabolic derangements. Therefore, the search for prospective markers for OLZ's negative side effects as well as adjunctive treatments to inhibit these has been of major interest. The aim of this study was to investigate in healthy male volunteers (age: 36 +/- 11 years; BW: 841 +/- 12 kg; BMI = 25.5 +/- 2.5) whether adjunctive topiramate (TPM) administration opposes OLZ-induced weight gain over the course of 14 days treatment. In addition, we investigated behavioral, endocrine and metabolic characteristics as underlying and potentially predictive factors for weight regulation and/or metabolic derangements associated with OLZ and TPM treatment. While adjunctive TPM indeed reduced OLZ-induced weight gain (P < 0.05, Mann-Whitney U), behavioral/metabolic/endocrine characteristics of OLZ treatment were not affected by TPM. Using multiple regression analysis, BW gain was the key factor explaining metabolic disturbances (e.g., plasma insulin LDL interaction: P < 0.01, R-2 = .320), and cumulative food intake during treatment was the best denominator of BW gain (P < 0.01, R-2 = .534). Neither TPM treatment, nor its circulating levels, contributed to variation observed in Delta BW. In a second multiple regression analysis, we observed that a low baseline thyrotropin profile (TSHAUC) before the start of drug treatment was associated with an increase in Delta BW over the course of drug treatment (P < 0.05, R-2 = .195). Adding TSHAUC as covariate revealed that adjunctive TPM treatment did attenuate OLZ induced BW gain (P < 0.05, ANCOVA). Further exploration of the circulating thyroid hormones revealed that individuals with a low plasma TSH profile were also those that were most sensitive to adjunctive TPM treatment blocking OLZ-induced Delta BW gain. Others have shown that OLZ-induced BW gain is associated with improvement in brief psychiatric rating scores (BPRS); adjunctive TPM treatment may be a solution specifically for those subjects susceptible to OLZ-induced rapid weight gain who on a therapeutic level benefit most of OLZ treatment. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:101 / 110
页数:10
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