Glucagon-like peptide agonists for weight management in antipsychotic-induced weight gain: A systematic review and meta-analysis

被引:8
作者
Bak, Maarten [1 ,2 ]
Campforts, Bea [1 ]
Domen, Patrick [1 ,2 ]
van Amelsvoort, Therese [1 ,2 ]
Drukker, Marjan [1 ]
机构
[1] Maastricht Univ, Dept Psychiat & Neuropsychol, POB 616 Vijverdal, Maastricht NL-6200 MD, Netherlands
[2] Mondriaan Mental Hlth, Dept FACT & Transit Psychiat, Maastricht, Netherlands
关键词
anti-obesity medication; antipsychotics; GLP-1; agonist; meta-analysis; obesity; CLOZAPINE-ASSOCIATED OBESITY; RANDOMIZED CONTROLLED-TRIAL; METABOLIC SYNDROME; SCHIZOPHRENIA; OVERWEIGHT; GUIDELINES; PEOPLE; RISK; EXENATIDE; DISORDER;
D O I
10.1111/acps.13734
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Introduction: Managing body weight in patients with antipsychotic-induced weight gain (AIWG) is challenging. Besides lifestyle interventions, pharmacological interventions may contribute to weight loss. This systematic review and meta-analysis evaluated the effect on weight loss and adverse effects of glucagon-like peptide-1 (GLP-1) agonists in patients with AIWG. Materials and Methods: Following PRISMA guidelines, we performed a meta-analysis of blinded and open-label randomised controlled trials (RCTs), non-randomised controlled trials and cohort studies that evaluated treatment with GLP-1 in patients with AIWG, regardless of psychiatric diagnosis. PubMed, Embase, PsycINFO and Cochrane Library databases were searched. Primary outcome measures were changes in body weight and BMI. Secondary outcomes were changes in adverse effects and severity of psychopathology due to GLP-1 agonists. Results: Only data for exenatide and liraglutide could be included, that is, five RCTs and one cohort study. For exenatide the mean weight loss was -2.48 kg (95% Confidence Interval (CI) -5.12 to +0.64; p = 0.07), for liraglutide the mean weight loss was -4.70 kg (95% CI -4.85 to -4.56; p < 0.001). The mean change in BMI was -0.82 (95% CI -1.56 to -0.09; p = 0.03) in the exenatide groups and -1.52 (95% CI -1.83 to -1.22; p < 0.001) in the liraglutide groups. Exenatide and liraglutide did not adversely affect psychopathology. The most common adverse events were nausea, vomiting, and diarrhoea. Conclusion: The GLP-1 agonists exenatide and liraglutide are promising drugs for inducing weight loss in patients with AIWG. The adverse effects are acceptable, and the addition of GLP-1 does not increase the severity of psychopathology. However, more research is needed.
引用
收藏
页码:516 / 529
页数:14
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