Laboratorio de Nutrición Molecular, Unidad de Investigación Médica en Nutrición, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de México (CDMX), Mexico.
Laboratorio de Nutrición Molecular, Unidad de Investigación Médica en Nutrición, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de México (CDMX), Mexico.
Brain Dev. 2021 Jan;43(1):111-120. doi: 10.1016/j.braindev.2020.06.013. Epub 2020 Jul 9.
A small number of studies have confirmed the presence of oxidative damage in patients with Duchenne muscular dystrophy (DMD). Nevertheless, it is unknown if there a relationship of circulating markers of oxidative stress with a muscle injury.
We evaluated if oxidative damage and anti-oxidant markers are associated with muscle damage in DMD.
This cross-sectional study included 24 patients with DMD classified in ambulatory and non-ambulatory. Markers of muscle damage (creatine kinase [CK]), oxidative damage (malondialdehyde [MDA], and 8-isoprostane), anti-oxidant function (Thiol and mRNA of NRF2 and NF-κB) and nitric oxide (NO) were quantified in circulation.
Total NO, MDA, and 8-isoprostane concentrations were significantly (p < 0.05) higher, and thiol concentration was lower in non-ambulatory than ambulatory patients. A significant correlation (p < 0.05) between muscle injury (evaluated by Vignos scale) with CK (r = -0.382), NO (r = 0.444), MDA (r = 0.503), 8-isoprostanes (r = 0.435) and thiol (r = -0.430) was observed.
These findings suggest that non-ambulatory have high oxidative damage and low anti-oxidant function than ambulatory patients with DMD. Total nitric oxide and oxidative damage plasma markers increase, but the anti-oxidant marker thiol decreases with a muscle injury in boys with DMD. The findings of this study suggest that these markers could be considered as goods indicators of oxidative damage in longitudinal studies to evaluate the muscle injury during DMD progression. Additionally, these findings add new information about the pathophysiology of DMD.
少数研究证实了杜兴氏肌营养不良症(DMD)患者存在氧化损伤。然而,目前尚不清楚循环氧化应激标志物是否与肌肉损伤有关。
我们评估了 DMD 患者的氧化损伤和抗氧化标志物是否与肌肉损伤有关。
本横断面研究纳入了 24 名 DMD 患者,分为可走动和不可走动两类。在循环中定量检测肌肉损伤标志物(肌酸激酶 [CK])、氧化损伤标志物(丙二醛 [MDA]和 8-异前列腺素)、抗氧化功能标志物(巯基和 NRF2 和 NF-κB 的 mRNA)和一氧化氮(NO)。
不可走动患者的总 NO、MDA 和 8-异前列腺素浓度明显(p < 0.05)更高,巯基浓度更低。肌肉损伤(通过 Vignos 量表评估)与 CK(r = -0.382)、NO(r = 0.444)、MDA(r = 0.503)、8-异前列腺素(r = 0.435)和巯基(r = -0.430)呈显著相关性(p < 0.05)。
这些发现表明,不可走动的 DMD 患者的氧化损伤更高,抗氧化功能更低。总一氧化氮和氧化损伤的血浆标志物增加,但抗氧化标志物巯基随着 DMD 男孩的肌肉损伤而减少。本研究的结果表明,这些标志物可作为评估 DMD 进展过程中肌肉损伤的纵向研究中的良好氧化损伤指标。此外,这些发现为 DMD 的病理生理学提供了新的信息。