有证据表明,长期治疗可预防丙酸通路遗传性疾病患者的组织氧化损伤。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Bianca Gomes Dos Reis, Graziela Schmitt Becker, Desiree Padilha Marchetti, Daniella de Moura Coelho, Angela Sitta, Moacir Wajner, Carmen Regla Vargas
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引用次数: 0

摘要

丙酸血症(PAcidemia)和甲基丙二酸血症(MMAcidemia)是一种遗传性疾病,临床特点是新生儿期代谢失调并伴有危及生命的脑病发作。充分和快速的治疗对患者的存活和预后至关重要。本研究显示,限制蛋白质饮食并补充左旋肉碱(LC)可降低这些疾病患者的死亡率和发病率,这可能是由于减少了主要代谢产物的积累,从而降低了其毒性。由于氧化应激被认为是 PAcidemia 和 MMAcidemia 中组织损伤的一个促成机制,而 LC 具有强大的抗氧化特性,因此我们在这项工作中的目标是研究由减少蛋白质摄入量和补充 LC 组成的长期疗法对这些疾病患者氧化损伤指标的影响。我们测量了未接受治疗或接受短期或长期治疗的患者尿液中分别反映脂质、蛋白质和 DNA/RNA 氧化损伤的异前列腺素、二酪氨酸和氧化鸟嘌呤物种,以及 NO 产物(硝酸盐和亚硝酸盐)的浓度。结果显示,与对照组相比,未接受治疗的患者体内异丙基酪氨酸、二酪氨酸和氧化鸟嘌呤含量明显增加,而 NO 含量则略有增加,但不明显。此外,这些指标的变化在短期治疗后有所减轻,在长期治疗后趋于正常。总之,这项研究的数据首次表明,对丙酸通路失调的患者进行长期治疗可以防止氧化损伤。不过,本研究中发现的氧化应激是否与患者的临床症状直接相关,还有待进一步阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence That Long-Term Treatment Prevents Tissue Oxidative Damage in Patients With Inherited Disorders of the Propionate Pathway.

Propionic and methylmalonic acidemias (PAcidemia and MMAcidemia, respectively) are genetic disorders clinically characterized by metabolic decompensation associated with life-threatening encephalopathic episodes in the neonatal period. Adequate and rapid therapeutic management is essential for patients' survival and prognosis. In this study, a restricted protein diet associated with L-carnitine (LC) supplementation was shown to decrease mortality and morbidity in patients affected by these disorders probably by decreasing the accumulation of the major metabolites and therefore their toxicity. Since oxidative stress was proposed as a contributing mechanism of tissue damage in PAcidemia and MMAcidemia and LC has potent antioxidant properties, our objective in this work was to investigate the effects of a long-term therapy consisting of reduced protein intake associated with LC supplementation on oxidative damage markers in patients affected by these diseases. We measured urinary isoprostanes, di-tyrosine, and oxidized guanine species, which reflect oxidative damage to lipids, proteins, and DNA/RNA, respectively, as well as the concentrations of NO products (nitrate plus nitrite) in patients untreated or submitted to short-term or a long-term treatment. Results revealed significant increases of isoprostanes, di-tyrosine, and oxidized guanine species, as well as a moderate nonsignificant increase of NO levels in the untreated patients, relatively to controls. Furthermore, these altered markers were attenuated after short-term treatment and normalized after prolonged treatment. In conclusion, data from this work show for the first time that long-standing treatment of patients with disorders of the propionate pathway can protect against oxidative damage. However, it remains to be elucidated whether oxidative stress identified in this study directly correlates with the clinical conditions of the affected patients.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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