首页> 外文期刊>American journal of psychiatry >Sustained weight loss after treatment with a glucagon-like Peptide-1 receptor agonist in an obese patient with schizophrenia and type 2 diabetes.
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Sustained weight loss after treatment with a glucagon-like Peptide-1 receptor agonist in an obese patient with schizophrenia and type 2 diabetes.

机译:在患有精神分裂症和2型糖尿病的肥胖患者中,使用胰高血糖素样肽1受体激动剂治疗后,体重持续减轻。

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To the Editor: Obesity, diabetes, and cardiovascular disease associated with antipsychotics represent major unresolved clinical issues that contribute to the increasing mortality gap between patients with schizophrenia and the general population (1). At best, current interventions against antipsychotic-induced weight gain (e.g., metformin) facilitate a weight loss of up to 3 kg, but the long-term stability of this weight reduction is questionable (2). Glucagon-like peptide-1 (GLP-1) receptor agonists efficiently reduce blood glucose levels and confer only a negligible risk of hypoglycemia. For these reasons, GLP receptor agonists are widely used in the treatment of type 2 diabetes. GLP-1 receptor agonists stimulate glucose-induced insulin secretion, inhibit glucagon secretion, and reduce gastrointestinal motility, which reduce appetite and food intake. Ultimately, this also leads to weight loss in patients without type 2 diabetes (3). Currently, Novo Nordisk is pursuing U.S. Food and Drug Administration approval for liraglutide for obesity.
机译:致编辑:肥胖,糖尿病和与抗精神病药有关的心血管疾病代表了尚未解决的主要临床问题,这些问题加剧了精神分裂症患者与普通人群之间的死亡率差距(1)。充其量,目前针对抗精神病药物引起的体重增加(例如二甲双胍)的干预措施可以使体重减轻多达3公斤,但这种减重的长期稳定性值得怀疑(2)。胰高血糖素样肽1(GLP-1)受体激动剂可有效降低血糖水平,并且低血糖的风险可忽略不计。由于这些原因,GLP受体激动剂被广泛用于2型糖尿病的治疗。 GLP-1受体激动剂刺激葡萄糖诱导的胰岛素分泌,抑制胰高血糖素分泌,并降低胃肠蠕动,从而降低食欲和食物摄入量。最终,这还会导致没有2型糖尿病的患者减轻体重(3)。目前,诺和诺德(Novo Nordisk)正在寻求美国食品药品监督管理局(FDA)批准使用利拉鲁肽治疗肥胖症。

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