Wang QingQing, Guo Lili, Strawser Cassandra J, Hauser Lauren A, Hwang Wei-Ting, Snyder Nathaniel W, Lynch David R, Mesaros Clementina, Blair Ian A
Penn/CHOP Center of Excellence in Friedreich's Ataxia, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Penn SRP Center and Center of Excellence in Environmental Toxicology Center, Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania Philadelphia, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2018 Feb 15;13(2):e0192779. doi: 10.1371/journal.pone.0192779. eCollection 2018.
Friedreich's ataxia (FA) is an autosomal recessive neurodegenerative disorder, which results primarily from reduced expression of the mitochondrial protein frataxin. FA has an estimated prevalence of one in 50,000 in the population, making it the most common hereditary ataxia. Paradoxically, mortality arises most frequently from cardiomyopathy and cardiac failure rather than from neurological effects. Decreased high-density lipoprotein (HDL) and apolipoprotein A-I (ApoA-l) levels in the general population are associated with an increased risk of mortality from cardiomyopathy and heart failure. However, the pathophysiology of heart disease in FA is non-vascular and there are conflicting data on HDL-cholesterol in FA. Two studies have shown a decrease in HDL-cholesterol compared with controls and two have shown there was no difference between FA and controls. One also showed that there was no difference in serum Apo-A-I levels in FA when compared with controls. Using a highly specific stable isotope dilution mass spectrometry-based assay, we demonstrated a 21.6% decrease in serum ApoA-I in FA patients (134.8 mg/dL, n = 95) compared with non-affected controls (172.1 mg/dL, n = 95). This is similar to the difference in serum ApoA-I levels between non-smokers and tobacco smokers. Knockdown of frataxin by > 70% in human hepatoma HepG2 cells caused a 20% reduction in secreted ApoA-I. Simvastatin, a 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor caused a 200% increase in HMG-CoA in the control HepG2 cells with a similar increase in the frataxin knockdown HepG2 cells, back to levels found in the control cells. There was a concomitant 20% increase in secreted ApoA-I to levels found in the control cells that were treated with simvastatin. This study provides compelling evidence that ApoA-I levels are reduced in FA patients compared with controls and suggest that statin treatment would normalize the ApoA-I levels.
弗里德赖希共济失调(FA)是一种常染色体隐性神经退行性疾病,主要由线粒体蛋白酵母氨酸还原酶表达减少所致。FA在人群中的估计患病率为五万分之一,是最常见的遗传性共济失调。矛盾的是,死亡最常源于心肌病和心力衰竭,而非神经学影响。普通人群中高密度脂蛋白(HDL)和载脂蛋白A-I(ApoA-I)水平降低与心肌病和心力衰竭导致的死亡风险增加相关。然而,FA中心脏病的病理生理学是非血管性的,且关于FA中HDL胆固醇的数据存在矛盾。两项研究显示与对照组相比HDL胆固醇降低,另外两项研究则显示FA与对照组之间无差异。一项研究还表明,FA患者血清Apo-A-I水平与对照组相比无差异。使用基于高特异性稳定同位素稀释质谱分析法,我们证明FA患者(n = 95,血清ApoA-I为134.8 mg/dL)与未受影响的对照组(n = 95,血清ApoA-I为172.1 mg/dL)相比,血清ApoA-I降低了21.6%。这与非吸烟者和吸烟者之间血清ApoA-I水平的差异相似。在人肝癌HepG2细胞中,酵母氨酸还原酶敲低> 70%导致分泌的ApoA-I减少20%。辛伐他汀是一种3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂,在对照HepG2细胞中使HMG-CoA增加了200%,在酵母氨酸还原酶敲低的HepG2细胞中也有类似增加,恢复到对照细胞中的水平。同时,分泌的ApoA-I增加了20%,达到用辛伐他汀处理的对照细胞中的水平。这项研究提供了令人信服的证据,表明FA患者的ApoA-I水平与对照组相比降低,并表明他汀类药物治疗可使ApoA-I水平正常化。