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高剂量维生素、辅酶Q和高脂饮食对线粒体疾病患儿的影响。

Effect of high-dose vitamins, coenzyme Q and high-fat diet in paediatric patients with mitochondrial diseases.

作者信息

Panetta J, Smith L J, Boneh A

机构信息

Metabolic Service, Royal Children's Hospital, Melbourne 3052, Victoria, Australia.

出版信息

J Inherit Metab Dis. 2004;27(4):487-98. doi: 10.1023/B:BOLI.0000037354.66587.38.

Abstract

We reviewed the medical records of all patients with confirmed mitochondrial diseases treated with any or all of thiamin, riboflavin, coenzyme Q, vitamin C (approximately 10 mg/kg per day) and a high-fat diet (50-60% of caloric intake) between 1997 and 2003. There were 15 patients (9 male): 10 had enzymatic deficiency and 10 had a molecular diagnosis. Age at diagnosis was 11 months to 17 years 10 months. Treatment was commenced at time of clinical diagnosis in 12 patients. Follow-up period was 3 days to 7 years (median 22 months). Improvement was reported in 9 patients, of whom 4 attained further developmental skills, but this was only temporary in 6 patients. Five patients died during the follow-up period (3 days to 7 years). Patients with the 3243A > G mutation showed no significant change in the course of their disease, except for fewer migraine attacks. Of the six patients who had seizures, one has had a significant reduction in the severity of the seizures and one has had no further seizures. Plasma lactate levels were noncontributory. We conclude that high-dose vitamin and cofactor treatment and, where applicable, high-fat diet, are well tolerated and possibly effective in the short term, but ineffective in the longer term.

摘要

我们回顾了1997年至2003年间所有确诊为线粒体疾病且接受过硫胺素、核黄素、辅酶Q、维生素C(约每日10毫克/千克)和高脂饮食(热量摄入的50 - 60%)中任何一种或全部治疗的患者的病历。共有15名患者(9名男性):10名有酶缺乏,10名有分子诊断。诊断时年龄为11个月至17岁10个月。12名患者在临床诊断时开始治疗。随访期为3天至7年(中位值22个月)。9名患者报告有改善,其中4名获得了进一步的发育技能,但6名患者只是暂时改善。5名患者在随访期内死亡(3天至7年)。携带3243A > G突变的患者,除偏头痛发作减少外,疾病进程无显著变化。6名有癫痫发作的患者中,1名癫痫发作严重程度显著降低,1名未再发作。血浆乳酸水平无参考价值。我们得出结论,高剂量维生素和辅助因子治疗以及在适用时的高脂饮食,耐受性良好,短期内可能有效,但长期无效。

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