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Twentieth Anniversary of Leptin discovery and the Approval of Myalept by FDA

机译:瘦素发现二十周年和FDA批准Myalept

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Leptin is a 16 kDa hormone that is mainly expressed in adipose tissues (1). The major target of leptin is hypothalamus and it suppresses food intake and energy consumption, consequently diminishing adipose deposits and body weight (2, 3). The OB gene was isolated by Friedman in 1994 (4). Based on the suggestion of Roger Guillemin, Friedman named this new hormone "leptin" from the Greek lepto meaning thin (5, 6). Since leptin discovery, numerous studies have been conducted on its physiological effects and its function in pathological conditions. Most of studies on leptin concentrated on its metabolic actions (7), receptors (8) and further broad functions such as immunity modulation (9) and memory processing (10). Considering such a vast range of functions, it is clear that patients with lack of leptin physiologically need pharmacological interventions. At this moment, we are in the twentieth year of leptin discovery. Finally, FDA approved a drug named Myalept (metreleptin for injection) on February 2014 to treat rare metabolic disease caused by leptin deficiency. Congenital generalized lipodystrophy is a disorder with partial lack of fat tissues (11). The trial for the safety and effectiveness of Myalept demonstrated decrease in HbA1c, fasting blood glucose, and triglycerides (11). Nevertheless, there are some limitations to the usage of Myalept in HIV-related lipodystrophy and some metabolic disorders (11). Moreover, it may increase the risk of lymphoma by producing anti-metreleptin antibodies neutralizing endogenous leptin. Considering these concerns, Myalept is available only through a limited profile under a Risk Evaluation and Mitigation Strategy (REMS). Myalept is contraindicated in patients with general obesity not related to congenital leptin deficiency (12). Even though, Myalept has very limited indications for use in general population, it is considered a milestone towards the discovery of novel treatments for Leptin deficiencies and disorders. Future investigations are necessary for the discovery of unknown aspects of Myalept therapy and production of new leptin-based agents for treatment of a wide spectrum of diseases.
机译:瘦素是一种16 kDa的激素,主要在脂肪组织中表达(1)。瘦素的主要靶点是下丘脑,它抑制食物摄入和能量消耗,从而减少脂肪沉积和体重(2,3)。 OB基因是由Friedman在1994年分离的(4)。根据罗杰·吉列明(Roger Guillemin)的建议,弗里德曼(Friedman)将这种新的激素命名为希腊瘦素中的瘦素(leptin)(5,6)。自从发现瘦素以来,就其生理作用及其在病理条件下的功能进行了大量研究。关于瘦蛋白的大多数研究都集中在其代谢作用(7),受体(8)以及其他广泛功能上,如免疫调节(9)和记忆加工(10)。考虑到如此广泛的功能,很明显生理上缺乏瘦素的患者需要药理干预。目前,我们处于瘦素发现的二十年。最终,FDA于2014年2月批准了一种名为Myalept(注射用美曲汀)的药物,用于治疗因瘦素缺乏引起的罕见代谢疾病。先天性全身性脂肪营养不良是一种部分缺乏脂肪组织的疾病(11)。 Myalept的安全性和有效性试验证明HbA1c降低,空腹血糖和甘油三酸酯降低(11)。但是,在与HIV相关的脂肪营养不良和某些代谢性疾病中,使用Myalept仍存在一些局限性(11)。此外,它可能会通过产生中和内源性瘦素的抗metreleptin抗体而增加淋巴瘤的风险。考虑到这些问题,在风险评估和缓解策略(REMS)下,只能通过有限的配置文件来获取Myalept。与一般性肥胖无关的先天性瘦素缺乏症患者禁用Myalept(12)。即使Myalept在一般人群中使用的适应症非常有限,它仍被认为是发现针对瘦素缺乏症和疾病的新疗法的里程碑。对于发现Myalept治疗的未知方面以及生产用于治疗多种疾病的新的基于瘦蛋白的药物,未来的研究是必要的。

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