期刊文献+

线粒体病的营养干预

Nutritional intervention in mitochondrial diseases
原文传递
导出
摘要 线粒体病是一组罕见的多系统疾病,目前尚无有效的治疗方法,多学科的对症支持十分必要。线粒体病患者营养摄入不足,营养不良又可继发线粒体功能障碍并加重病情。营养评估及保证营养摄入是所有治疗的基础,此外,营养补充剂、生酮饮食等还可以改善或稳定疾病症状。因此,线粒体病医学专家和临床营养师应共同努力,提高患者的生活质量。 Mitochondrial diseases are a group of rare multisys-tem disorders. There are no effective therapies and multidisciplinary symptomatic support is necessary. Patients with mitochondrial diseases have an inadequate nutrition intake,and malnutrition may cause secondary mitochondrial dysfunction and aggravate the disease. Evaluating the nutritional status and providing an adequate nutrition should be at the basis of any medical interventions. Moreover,nutritional supplements,ketogenic diet,etc. may improve,or stabilize,disease signs and symptoms. For this reason,medical experts in mitochondrial diseases and clinical nutritionists should work together to improve the quality of life of the patients.
作者 杨文利 闫洁 方方 YANG Wen-li;YAN Jie;FANG Fang(Department of Clinical Nutrition,Bejing Childrens Hospital,Capital Medical University,National Center for Children's Health,Bejing100045,China;不详)
出处 《中国实用儿科杂志》 CSCD 北大核心 2022年第10期743-748,共6页 Chinese Journal of Practical Pediatrics
关键词 线粒体病 营养干预 营养补充剂 生酮饮食 mitochondrial diseases nutritional intervention nutritional supplements ketogenic diet
  • 相关文献

参考文献5

二级参考文献18

  • 1Qian-Yun Cai,Zhong-Jie Zhou,Rong Luo,Jing Gan,Shi-Ping Li,De-Zhi Mu,Chao-Min Wan.Safety and tolerability of the ketogenic diet used for the treatment of refractory childhood epilepsy: a systematic review of published prospective studies[J].World Journal of Pediatrics,2017,13(6):528-536. 被引量:10
  • 2GrahamBH. Diagnostic challenges of mitochondrial disorders: complexities of two genomes[J]. Methods Mol Biol,2012,837:35–46.
  • 3ScagliaF, NorthropJL. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke–like episodes (MELAS) syndrome: a review of treatment options[J]. CNS Drugs,2006,20(6):443–464.
  • 4MeyersonC, Van StavernG, McclellandC. Leber hereditary optic neuropathy: current perspectives[J]. Clin Ophthalmol,2015,9:1165–1176.
  • 5ThorburnDR, RahmanS. Mitochondrial DNA–Associated Leigh Syndrome and NARP[M]. 1993, Last Update: April 17, 2014.Seattle:University of Washington, 2014.
  • 6WongLJ. Next generation molecular diagnosis of mitochondrial disorders[J]. Mitochondrion,2013,13(4):379–387.
  • 7CalvoSE, ComptonAG, HershmanSG, et al. Molecular diagnosis of infantile mitochondrial disease with targeted next–generation sequencing[J]. Sci Transl Med,2012,4(118):110r–118.
  • 8VastaV, MerrittJN, SanetoRP, et al. Next–generation sequencing for mitochondrial diseases: a wide diagnostic spectrum[J]. Pediatr Int,2012,54(5):585–601.
  • 9LieberDS, CalvoSE, ShanahanK, et al. Targeted exome sequencing of suspected mitochondrial disorders[J]. Neurology,2013,80(19):1762–1770.
  • 10WortmannSB, KoolenDA, SmeitinkJA, et al. Whole exome sequencing of suspected mitochondrial patients in clinical practice[J]. J Inherit Metab Dis,2015,38(3):437–443.

共引文献42

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部