Imperlini Esther, Santorelli Lucia, Orrù Stefania, Scolamiero Emanuela, Ruoppolo Margherita, Caterino Marianna
IRCCS SDN, 80143 Naples, Italy.
CEINGE Biotecnologie Avanzate s.c.a.r.l., 80145 Naples, Italy.
Biomed Res Int. 2016;2016:9210408. doi: 10.1155/2016/9210408. Epub 2016 Jun 14.
Organic acidemias (OAs) are inherited metabolic disorders caused by deficiency of enzymatic activities in the catabolism of amino acids, carbohydrates, or lipids. These disorders result in the accumulation of mono-, di-, or tricarboxylic acids, generally referred to as organic acids. The OA outcomes can involve different organs and/or systems. Some OA disorders are easily managed if promptly diagnosed and treated, whereas, in others cases, such as propionate metabolism-related OAs (propionic acidemia, PA; methylmalonic acidemia, MMA), neither diet, vitamin therapy, nor liver transplantation appears to prevent multiorgan impairment. Here, we review the recent developments in dissecting molecular bases of OAs by using integration of mass spectrometry- (MS-) based metabolomic and proteomic strategies. MS-based techniques have facilitated the rapid and economical evaluation of a broad spectrum of metabolites in various body fluids, also collected in small samples, like dried blood spots. This approach has enabled the timely diagnosis of OAs, thereby facilitating early therapeutic intervention. Besides providing an overview of MS-based approaches most frequently used to study the molecular mechanisms underlying OA pathophysiology, we discuss the principal challenges of metabolomic and proteomic applications to OAs.
有机酸血症(OAs)是由氨基酸、碳水化合物或脂质分解代谢中酶活性缺乏引起的遗传性代谢紊乱。这些紊乱导致单羧酸、二羧酸或三羧酸的积累,通常称为有机酸。有机酸血症的后果可累及不同的器官和/或系统。一些有机酸血症疾病如果能及时诊断和治疗,很容易得到控制,而在其他情况下,如与丙酸代谢相关的有机酸血症(丙酸血症,PA;甲基丙二酸血症,MMA),饮食、维生素治疗或肝移植似乎都无法预防多器官损害。在此,我们综述了通过整合基于质谱(MS)的代谢组学和蛋白质组学策略剖析有机酸血症分子基础的最新进展。基于质谱的技术有助于快速、经济地评估各种体液中的多种代谢物,这些体液也可从小样本(如干血斑)中采集。这种方法能够及时诊断有机酸血症,从而便于早期治疗干预。除了概述最常用于研究有机酸血症病理生理学分子机制的基于质谱的方法外,我们还讨论了代谢组学和蛋白质组学应用于有机酸血症的主要挑战。