Solis Java O, Singh Rani H
Sarah Lawrence College, Bronxville, NY, USA.
J Am Diet Assoc. 2002 Dec;102(12):1800-3. doi: 10.1016/s0002-8223(02)90386-x.
Standardization of the nutritional care for patients with fatty-acid oxidation disorders is lacking. A literature review and national survey of metabolic dietitians describes the range of therapeutic strategies currently employed in the U.S. to treat patients with fatty-acid oxidation disorders. Questionnaire responses provided by dietitians specializing in metabolic disorders evaluated practices used for treatment of fatty acid oxidation disorders, medium-chain acyl-CoA dehydrogenase deficiency (MCAD), very-long-chain acyl-CoA dehydrogenase deficiency (VLCAD), long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD), long-chain acyl-CoA dehydrogenase deficiency (LCAD), and Trifunctional Protein deficiency (TFP). This survey reveals a significant lack of evidence supporting the protocols in use. Recent advances in tandem mass spectrometry technology promises an increase in the number of identified patients with fatty-acid oxidation disorders, which reinforces the need for comprehensive, clinical research studies to determine optimal care for patients with these genetic disorders.
目前缺乏针对脂肪酸氧化障碍患者营养护理的标准化方案。一项文献综述以及针对代谢营养师的全国性调查描述了美国当前用于治疗脂肪酸氧化障碍患者的一系列治疗策略。专门从事代谢紊乱治疗的营养师提供的问卷调查回复评估了用于治疗脂肪酸氧化障碍、中链酰基辅酶A脱氢酶缺乏症(MCAD)、极长链酰基辅酶A脱氢酶缺乏症(VLCAD)、长链3-羟基酰基辅酶A脱氢酶缺乏症(LCHAD)、长链酰基辅酶A脱氢酶缺乏症(LCAD)和三功能蛋白缺乏症(TFP)的实践方法。这项调查显示,目前使用的方案严重缺乏证据支持。串联质谱技术的最新进展有望增加已确诊的脂肪酸氧化障碍患者数量,这进一步凸显了开展全面临床研究以确定这些遗传疾病患者最佳护理方案的必要性。