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The neuroendocrinology of childhood obesity.

机译:儿童肥胖的神经内分泌学。

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The regulation of energy balance is enormously complex, with numerous genetic, hormonal, neural and behavioral, and societal influences. Although the current epidemic of obesity clearly has its underpinnings in the changes in culture during the past half-century (see other articles in this issue), the role of the neuroendocrine system in the genesis of obesity, as described in this article, is physiologically and therapeutically unavoidable. An understanding of this system has suggested organic causes (and therapies) for some rare and not-so-rare forms of obesity. With so many inputs, it is not far-fetched to assume that dysfunction of other parts of this feedback system will be found to explain other forms of obesity in the future. What does this mean for obese children entering the pediatrician's office? Fortunately or unfortunately, diet and exercise are the mainstays of obesity therapy for children and adults. Most diet-exercise programs result in an acute 11-kg weight loss in adults; the question is whether it can be sustained without significant long-term behavioral modification. For instance, the European Sibutramine Trial of Obesity Reduction and Maintenance trial showed that 42% of treated subjects drop out; of those remaining, 77% of subjects lost more than 5% of initial body weight, but only 43% of those maintained more than 80% of this over 2 years. Could there be an organic component in those who do not respond? Of course, obesity pharmacotherapies sometimes have beneficial acute effects, but these drugs work for only as long as they are consumed; discontinuation tends to result in a "rebound" weight gain, suggesting that the cause of the obesity is still present. Furthermore, in 2001, there are no obesity drugs approved for children. A useful guiding principle is that children deserve at the minimum an initial medical evaluation, including birth weight, medical history, family history, dietary evaluation, and exercise assessment. Perhaps the most important feature that can distinguish "organic" from "behavioral" weight gain in childhood is the age of the "adiposity rebound." The Centers for Disease Control and Prevention now supplies BMI charts for boys and girls at www.cdc.gov/growthcharts. Plotting of the BMI versus age allows pediatricians to determine the age at which the BMI starts to increase (mean, 5.5 years). The earlier the adiposity rebound, the more likely the child will be obese as an adult, and the more likely that an organic cause can be determined. In such patients, thyroid levels and fasting insulin and leptin levels should be measured. An initial attempt at diet and exercise is essential; patients who do not respond with BMI stabilization should be investigated for a more ominous cause of their obesity. As the nosology of obesity improves, pediatricians will be able to increase the diagnostic efficiency and therapeutic success of this unfortunate, debilitating, and expensive epidemic.
机译:能量平衡的调节极其复杂,受到众多遗传,激素,神经和行为以及社会的影响。尽管当前的肥胖病流行在过去半个世纪的文化变化中显然有其基础(请参阅本期其他文章),但如本文所述,神经内分泌系统在肥胖症的发生中的作用是生理上的和治疗上不可避免的。对该系统的了解已提出一些罕见且不太罕见的肥胖症的有机病因(和疗法)。有了这么多的输入,假设将来会发现该反馈系统其他部分功能障碍来解释其他形式的肥胖症,并不是很难理解的。这对进入儿科医生办公室的肥胖儿童意味着什么?幸运的是,饮食和运动是儿童和成人肥胖疗法的主要手段。大多数饮食锻炼计划都会使成年人的体重减轻11公斤。问题是,如果没有重大的长期行为改变,是否可以维持下去。例如,欧洲减少肥胖和维持肥胖的西布曲明试验表明,有42%的被治疗者退出了研究;在剩下的这些人中,有77%的受试者的体重减轻了超过初始体重的5%,但只有43%的受试者在2年内保持了初始体重的80%以上。那些不响应的人是否有有机的组成部分?当然,肥胖症药物疗法有时会产生有益的急性作用,但这些药物仅在食用后才起作用。停药往往导致体重“反弹”,表明肥胖的原因仍然存在。此外,在2001年,没有批准用于儿童的减肥药。一个有用的指导原则是,儿童至少应接受初步医学评估,包括出生体重,病史,家族史,饮食评估和运动评估。可以区分儿童“有机”体重增加和“行为”体重增加的最重要特征可能是“肥胖反弹”的年龄。疾病控制与预防中心现在在www.cdc.gov/growthcharts上提供男孩和女孩的BMI图表。通过绘制BMI与年龄的关系图,儿科医生可以确定BMI开始增加的年龄(平均5.5岁)。肥胖反弹越早,儿童成年后肥胖的可能性就越大,并且更有可能确定器质性原因。在此类患者中,应测量甲状腺水平以及空腹胰岛素和瘦素水平。饮食和运动的初步尝试至关重要。对BMI稳定无反应的患者,应调查其肥胖的不祥原因。随着肥胖症的改善,儿科医生将能够增加这种不幸,使人衰弱和昂贵的流行病的诊断效率和治疗成功率。

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