• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

改良阿特金斯饮食可导致线粒体肌病患者出现亚急性选择性破碎红纤维溶解。

Modified Atkins diet induces subacute selective ragged-red-fiber lysis in mitochondrial myopathy patients.

作者信息

Ahola Sofia, Auranen Mari, Isohanni Pirjo, Niemisalo Satu, Urho Niina, Buzkova Jana, Velagapudi Vidya, Lundbom Nina, Hakkarainen Antti, Muurinen Tiina, Piirilä Päivi, Pietiläinen Kirsi H, Suomalainen Anu

机构信息

Research Program of Molecular Neurology, Biomedicum Helsinki University of Helsinki, Helsinki, Finland.

Clinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

出版信息

EMBO Mol Med. 2016 Nov 2;8(11):1234-1247. doi: 10.15252/emmm.201606592. Print 2016 Nov.

DOI:10.15252/emmm.201606592
PMID:27647878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5090657/
Abstract

Mitochondrial myopathy (MM) with progressive external ophthalmoplegia (PEO) is a common manifestation of mitochondrial disease in adulthood, for which there is no curative therapy. In mice with MM, ketogenic diet significantly delayed progression of the disease. We asked in this pilot study what effects high-fat, low-carbohydrate "modified Atkins" diet (mAD) had for PEO/MM patients and control subjects and followed up the effects by clinical, morphological, transcriptomic, and metabolomic analyses. All of our five patients, irrespective of genotype, showed a subacute response after 1.5-2 weeks of diet, with progressive muscle pain and leakage of muscle enzymes, leading to premature discontinuation of the diet. Analysis of muscle ultrastructure revealed selective fiber damage, especially in the ragged-red-fibers (RRFs), a MM hallmark. Two years of follow-up showed improvement of muscle strength, suggesting activation of muscle regeneration. Our results indicate that (i) nutrition can modify mitochondrial disease progression, (ii) dietary counseling should be part of MM care, (iii) short mAD is a tool to induce targeted RRF lysis, and (iv) mAD, a common weight-loss method, may induce muscle damage in a population subgroup.

摘要

伴有进行性眼外肌麻痹(PEO)的线粒体肌病(MM)是成年期线粒体疾病的常见表现,目前尚无治愈性疗法。在患有MM的小鼠中,生酮饮食可显著延缓疾病进展。在这项初步研究中,我们探究了高脂肪、低碳水化合物的“改良阿特金斯”饮食(mAD)对PEO/MM患者和对照受试者的影响,并通过临床、形态学、转录组学和代谢组学分析对这些影响进行了随访。我们的五名患者,无论基因型如何,在饮食1.5 - 2周后均出现亚急性反应,伴有进行性肌肉疼痛和肌肉酶泄漏,导致饮食提前中断。肌肉超微结构分析显示存在选择性纤维损伤,尤其是在破碎红纤维(RRFs)中,这是MM的一个标志。两年的随访显示肌肉力量有所改善,提示肌肉再生被激活。我们的结果表明:(i)营养可改变线粒体疾病的进展;(ii)饮食咨询应成为MM护理的一部分;(iii)短期mAD是诱导靶向RRF溶解的一种手段;(iv)mAD作为一种常见的减肥方法,可能会在一部分人群中诱发肌肉损伤。

相似文献

1
Modified Atkins diet induces subacute selective ragged-red-fiber lysis in mitochondrial myopathy patients.改良阿特金斯饮食可导致线粒体肌病患者出现亚急性选择性破碎红纤维溶解。
EMBO Mol Med. 2016 Nov 2;8(11):1234-1247. doi: 10.15252/emmm.201606592. Print 2016 Nov.
2
Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.线粒体疾病的诊断:60例伴有破碎红纤维患者的临床及组织学研究
Neurol India. 2004 Sep;52(3):353-8.
3
A pilot study of the modified Atkins diet for Sturge-Weber syndrome.Sturge-Weber 综合征改良 Atkins 饮食的初步研究。
Epilepsy Res. 2010 Dec;92(2-3):240-3. doi: 10.1016/j.eplepsyres.2010.09.008. Epub 2010 Oct 8.
4
Kearns-Sayre syndrome. A case report.卡恩斯-塞尔综合征。病例报告。
Turk J Pediatr. 1998 Apr-Jun;40(2):255-9.
5
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.卡恩斯-塞尔综合征的肌病理学进展:一项形态学随访研究。
Acta Neuropathol. 1993;85(6):679-81. doi: 10.1007/BF00334681.
6
Glycogen storage disease type III: modified Atkins diet improves myopathy.III型糖原贮积病:改良阿特金斯饮食改善肌病。
Orphanet J Rare Dis. 2014 Nov 28;9:196. doi: 10.1186/s13023-014-0196-3.
7
Establishing an Adult Epilepsy Diet Center: Experience, efficacy and challenges.建立成人癫痫饮食中心:经验、疗效与挑战。
Epilepsy Behav. 2016 May;58:61-8. doi: 10.1016/j.yebeh.2016.02.038. Epub 2016 Apr 6.
8
The modified Atkins diet.改良阿特金斯饮食法。
Epilepsia. 2008 Nov;49 Suppl 8:37-41. doi: 10.1111/j.1528-1167.2008.01831.x.
9
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.伴有破碎红纤维的慢性进行性眼外肌麻痹:43例患者的临床、形态学及遗传学研究
Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s.
10
[31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings].线粒体肌病的31P-核磁共振波谱分析:异常能量代谢与肌肉活检结果之间的关系
Rinsho Shinkeigaku. 1989 Feb;29(2):167-71.

引用本文的文献

1
Therapies for Mitochondrial Disease: Past, Present, and Future.线粒体疾病的治疗:过去、现在与未来
J Inherit Metab Dis. 2025 Jul;48(4):e70065. doi: 10.1002/jimd.70065.
2
Advances in Management of Mitochondrial Myopathies.线粒体肌病的管理进展
Int J Mol Sci. 2025 Jun 5;26(11):5411. doi: 10.3390/ijms26115411.
3
How to treat a "sweetheart" in mitochondrial cardiomyopathy.如何治疗线粒体心肌病中的“心上人”。

本文引用的文献

1
Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism.线粒体 DNA 复制缺陷扰乱细胞内 dNTP 池并重塑一碳代谢。
Cell Metab. 2016 Apr 12;23(4):635-48. doi: 10.1016/j.cmet.2016.01.019. Epub 2016 Feb 25.
2
Diets high in protein or saturated fat do not affect insulin sensitivity or plasma concentrations of lipids and lipoproteins in overweight and obese adults.高蛋白或饱和脂肪饮食不会影响超重和肥胖成年人的胰岛素敏感性或血脂及脂蛋白的血浆浓度。
J Nutr. 2014 Nov;144(11):1753-9. doi: 10.3945/jn.114.197624. Epub 2014 Sep 3.
3
Low carbohydrate versus isoenergetic balanced diets for reducing weight and cardiovascular risk: a systematic review and meta-analysis.
EMBO Mol Med. 2024 Jun;16(6):1226-1227. doi: 10.1038/s44321-024-00070-w. Epub 2024 May 9.
4
Efficacy and Safety of Ketogenic Diet Treatment in Pediatric Patients with Mitochondrial Disease. ketogenic 饮食治疗儿童线粒体疾病患者的疗效和安全性。
Nutrients. 2024 Mar 13;16(6):812. doi: 10.3390/nu16060812.
5
Optimized Nutrition in Mitochondrial Disease Correlates to Improved Muscle Fatigue, Strength, and Quality of Life.优化线粒体疾病的营养状况与改善肌肉疲劳、力量和生活质量相关。
Neurotherapeutics. 2023 Oct;20(6):1723-1745. doi: 10.1007/s13311-023-01418-9. Epub 2023 Sep 18.
6
Ketogenic diets and Ketone suplementation: A strategy for therapeutic intervention.生酮饮食与酮补充剂:一种治疗干预策略。
Front Nutr. 2022 Nov 15;9:947567. doi: 10.3389/fnut.2022.947567. eCollection 2022.
7
The Finnish genetic heritage in 2022 - from diagnosis to translational research.2022 年的芬兰基因遗传 - 从诊断到转化研究。
Dis Model Mech. 2022 Oct 1;15(10). doi: 10.1242/dmm.049490. Epub 2022 Oct 26.
8
Nutritional Interventions for Patients with Mitochondrial POLG-Related Diseases: A Systematic Review on Efficacy and Safety.线粒体 POLG 相关疾病患者的营养干预:疗效和安全性的系统评价。
Int J Mol Sci. 2022 Sep 13;23(18):10658. doi: 10.3390/ijms231810658.
9
Mosaic dysfunction of mitophagy in mitochondrial muscle disease.线粒体肌病中 mitophagy 的镶嵌功能障碍。
Cell Metab. 2022 Feb 1;34(2):197-208.e5. doi: 10.1016/j.cmet.2021.12.017. Epub 2022 Jan 13.
10
Differential ketogenic diet-induced shift in CSF lipid/carbohydrate metabolome of pediatric epilepsy patients with optimal vs. no anticonvulsant response: a pilot study.不同生酮饮食对有最佳抗惊厥反应与无抗惊厥反应的小儿癫痫患者脑脊液脂质/碳水化合物代谢组的影响:一项初步研究。
Nutr Metab (Lond). 2021 Mar 1;18(1):23. doi: 10.1186/s12986-020-00524-1.
低碳水化合物饮食与等能量均衡饮食对减轻体重和降低心血管风险的影响:一项系统评价和荟萃分析
PLoS One. 2014 Jul 9;9(7):e100652. doi: 10.1371/journal.pone.0100652. eCollection 2014.
4
Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3.烟酰胺核糖苷,一种维生素 B3,可有效治疗线粒体肌病。
EMBO Mol Med. 2014 Jun;6(6):721-31. doi: 10.1002/emmm.201403943.
5
The modified atkins diet in refractory epilepsy.改良阿特金斯饮食疗法治疗难治性癫痫
Epilepsy Res Treat. 2014;2014:404202. doi: 10.1155/2014/404202. Epub 2014 Jan 30.
6
Beyond weight loss: a review of the therapeutic uses of very-low-carbohydrate (ketogenic) diets.超越减肥:极低碳水化合物(生酮)饮食的治疗用途综述。
Eur J Clin Nutr. 2013 Aug;67(8):789-96. doi: 10.1038/ejcn.2013.116. Epub 2013 Jun 26.
7
Interplay between lipids and branched-chain amino acids in development of insulin resistance.脂质和支链氨基酸在胰岛素抵抗发展中的相互作用。
Cell Metab. 2012 May 2;15(5):606-14. doi: 10.1016/j.cmet.2012.01.024.
8
Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.常染色体隐性遗传进行性眼外肌麻痹伴多个线粒体 DNA 缺失中的胸苷激酶 2 突变。
Hum Mol Genet. 2012 Jan 1;21(1):66-75. doi: 10.1093/hmg/ddr438. Epub 2011 Sep 21.
9
Mechanisms of mitochondrial diseases.线粒体疾病的发病机制。
Ann Med. 2012 Feb;44(1):41-59. doi: 10.3109/07853890.2011.598547. Epub 2011 Aug 2.
10
Metabolite profiles and the risk of developing diabetes.代谢产物谱与糖尿病发病风险。
Nat Med. 2011 Apr;17(4):448-53. doi: 10.1038/nm.2307. Epub 2011 Mar 20.