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神经肌肉疾病的营养方面

Nutritional aspects of neuromuscular diseases.

作者信息

McCrory M A, Wright N C, Kilmer D D

机构信息

Energy Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts, USA.

出版信息

Phys Med Rehabil Clin N Am. 1998 Feb;9(1):127-43.

PMID:9894137
Abstract

Evidence suggests that individuals with DMD have reduced skeletal development, including decreased linear growth and bone mineral density, compared to normal subjects. Despite their reduced muscle mass, a high percentage of DMD patients are overweight. Body composition measurements can assist with monitoring changes in fat mass and skeletal muscle mass as the disease progresses. Weight management in overweight DMD patients is indicated because excess adiposity burdens mobility and breathing, but only one study in two DMD patients has documented that weight reduction can be done safely. In the latter stages of the disease most DMD subjects become underweight because of an acceleration in skeletal muscle protein degradation relative to its synthesis. Studies of energy, protein and branched chain amino acid supplementation in DMD have yielded promising but inconclusive results, and more well-designed studies are needed in this area. Although there is currently no cure for DMD, studies on the role of nutritional therapy in increasing the quality of life in these patients are urgently needed. Studies in adults with various SP-NMDs indicate a reduction in fat-free mass and an increase in fat mass relative to controls. The newly developed method of air displacement plethysmography for measuring body composition is ideally suited for SP-NMD subjects because it requires very little effort and the measurement procedure is relatively fast. Dual energy x-ray absorptiometry technology has been proposed for distinguishing myogenic from neurogenic SP-NMDs from calculation of the fat-to-lean soft tissue ratio, which is higher in patients with myogenic muscular atrophy. Studies on the energy metabolism of ambulatory SP-NMD subjects indicate that their basal metabolic rate is either similar to or slightly lower than controls, but 24-hour energy expenditure is about 25% lower than controls. This reduction in 24-hour energy expenditure is due to a reduction in physical activity in SP-NMD. Studies examining the roles of energy expenditure, physical activity, and diet in the development of adiposity and risk for secondary chronic diseases in SP-NMD subjects are currently underway.

摘要

有证据表明,与正常受试者相比,杜氏肌营养不良症(DMD)患者的骨骼发育减缓,包括线性生长和骨矿物质密度降低。尽管DMD患者的肌肉量减少,但仍有很大比例的患者超重。随着疾病进展,身体成分测量有助于监测脂肪量和骨骼肌量的变化。超重的DMD患者需要进行体重管理,因为过多的肥胖会给活动能力和呼吸带来负担,但在两项针对DMD患者的研究中,仅有一项记录了安全减重的可行性。在疾病后期,大多数DMD患者体重过轻,因为骨骼肌蛋白降解相对于合成加速。关于在DMD患者中补充能量、蛋白质和支链氨基酸的研究取得了有前景但尚无定论的结果,该领域需要更多精心设计的研究。尽管目前尚无治愈DMD的方法,但迫切需要开展关于营养疗法在提高这些患者生活质量方面作用的研究。对患有各种散发性神经肌肉病(SP-NMD)的成年人的研究表明,与对照组相比,他们的去脂体重减少,脂肪量增加。新开发的用于测量身体成分的空气置换体积描记法非常适合SP-NMD受试者,因为它所需的努力很少,测量过程相对较快。有人提出采用双能X线吸收测定技术,通过计算脂肪与瘦软组织的比例来区分肌源性和神经源性SP-NMD,该比例在肌源性肌肉萎缩患者中较高。对能够行走的SP-NMD受试者能量代谢的研究表明,他们的基础代谢率与对照组相似或略低于对照组,但24小时能量消耗比对照组低约25%。24小时能量消耗的降低是由于SP-NMD患者身体活动减少所致。目前正在进行研究,以探讨能量消耗、身体活动和饮食在SP-NMD受试者肥胖发展和继发性慢性病风险中的作用。

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