Brown G K, Cromby C H, Manning N J, Pollitt R J
Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
J Inherit Metab Dis. 1987;10(4):367-75. doi: 10.1007/BF01799979.
In addition to the previously reported abnormalities, urine extracts from three cases of succinic semialdehyde dehydrogenase deficiency have shown consistently increased amounts of 2,4-dihydroxybutyric acid, and its lactone, and 3-hydroxypropionic acid, metabolites related to the alpha-oxidation of 4-hydroxybutyric acid. Threo- and erythro-4,5-dihydroxyhexanoic acids have also been identified for the first time and probably arise from the reaction of succinic semialdehyde with an intermediate in the pyruvate dehydrogenase pathway. Adipic acid excretion is also consistently raised, suggesting secondary interference with mitochondrial beta-oxidation. The presence of these metabolites could be a source of diagnostic confusion.
除先前报道的异常情况外,三例琥珀酸半醛脱氢酶缺乏症患者的尿液提取物显示,与4-羟基丁酸α-氧化相关的代谢产物2,4-二羟基丁酸及其内酯和3-羟基丙酸的含量持续增加。苏阿糖型和赤藓糖型4,5-二羟基己酸也首次被鉴定出来,可能是琥珀酸半醛与丙酮酸脱氢酶途径中的一种中间体反应产生的。己二酸排泄量也持续升高,提示对线粒体β-氧化存在继发性干扰。这些代谢产物的存在可能会造成诊断混淆。