Efficacy of pyruvate therapy in patients with mitochondrial disease: A semi-quantitative clinical evaluation study

被引:34
作者
Fujii, Tatsuya [1 ]
Nozaki, Fumihito [1 ]
Saito, Keiko [1 ]
Hayashi, Anri [1 ]
Nishigaki, Yutaka [2 ]
Murayama, Kei [3 ]
Tanaka, Masashi [2 ]
Koga, Yasutoshi [4 ]
Hiejima, Ikuko [1 ]
Kumada, Tomohiro [1 ]
机构
[1] Shiga Med Ctr Children, Dept Pediat, Moriyama, Shiga 5240022, Japan
[2] Tokyo Metropolitan Inst Gerontol, Dept Genom Longev & Hlth, Itabashi Ku, Tokyo 1730015, Japan
[3] Chiba Childrens Hosp, Dept Metab, Midori Ku, Chiba 2660007, Japan
[4] Kurume Univ, Grad Sch Med, Dept Pediat & Child Hlth, Kurume, Fukuoka 8300011, Japan
关键词
Pyruvate; Therapy; Mitochondria disease; NAD(+); Lactate-to-pyruvate ratio; GROSS MOTOR FUNCTION; LEIGH-SYNDROME; CHILDREN; MELAS;
D O I
10.1016/j.ymgme.2014.04.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Disorders of oxidative phosphorylation (OXPHOS) cause an increase in the NADH/NAD(+) ratio, which impairs the glycolysis pathway. Treatment with pyruvate is expected to decrease the ratio and thereby restore glycolysis. There are some case reports on the efficacy of pyruvate treatment for mitochondrial diseases. However, few of these reports assessed their results using a standardized scale. Methods: We monitored 4 bedridden patients with OXPHOS disorders who continued therapies of 0.5-1.0 g/kg/day of sodium pyruvate for more than 12 months. The efficacies of these treatments were evaluated with the Newcastle Pediatric Mitochondrial Disease Scale and the Gross Motor Function Measure with 88 items. Results: The ages of the patients at the treatment initiation ranged from 8-100 months. Of the 4 patients, 3 exhibited improvements within 1-3 months from the initiation of treatment. Among these 3 patients, one maintained the improvement for over 2 years. The remaining 2 regressed 3-6 months after the initiation of treatment. The blood lactate/pyruvate ratios did not correlate with the efficacy of treatment. Conclusion: Pyruvate was effective even in bedridden patients with OXPHOS disorders, at least in the short term. Clinical trials with more patients and less severe disabilities are necessary to evaluate the long-term efficacy of this treatment. Biomarkers other than lactate and pyruvate need to be identified to biochemically monitor the efficacy of this treatment. (C) 2014 Elsevier Inc All rights reserved.
引用
收藏
页码:133 / 138
页数:6
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