Wamelink M M, Smith D E, Jansen E E, Verhoeven N M, Struys E A, Jakobs C
Metabolic Unit, Department of Clinical Chemistry, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
J Inherit Metab Dis. 2007 Oct;30(5):735-42. doi: 10.1007/s10545-007-0590-2. Epub 2007 Jun 27.
Transaldolase deficiency, a recently discovered disorder of carbohydrate metabolism with multisystem involvement, has been diagnosed in 6 patients. Affected patients have abnormal concentrations of polyols in body fluids and in all patients we have previously found increased amounts of a seven-carbon chain carbohydrate which we suspected of being sedoheptulose. We report development of a liquid chromatography-tandem mass spectrometry method for quantitation of the seven-carbon carbohydrates sedoheptulose and mannoheptulose in urine. Additionally, other seven-carbon chain carbohydrates were characterized in urine, including sedoheptitol, perseitol and sedoheptulose 7-phosphate. Transaldolase-deficient patients had significantly increased urinary sedoheptulose and sedoheptulose 7-phosphate, associated with subtle elevations of mannoheptulose, sedoheptitol and perseitol. Our findings reveal novel urinary biomarkers for identification of transaldolase deficiency.
转醛醇酶缺乏症是一种最近发现的累及多系统的碳水化合物代谢紊乱疾病,已在6例患者中得到诊断。受影响患者体液中的多元醇浓度异常,并且在所有患者中,我们之前都发现一种七碳链碳水化合物的含量增加,我们怀疑其为景天庚酮糖。我们报告了一种用于定量尿液中七碳碳水化合物景天庚酮糖和甘露庚酮糖的液相色谱-串联质谱法的开发。此外,还对尿液中的其他七碳链碳水化合物进行了表征,包括景天庚醇、鳄梨糖醇和景天庚酮糖7-磷酸。转醛醇酶缺乏症患者的尿景天庚酮糖和景天庚酮糖7-磷酸显著增加,同时甘露庚酮糖、景天庚醇和鳄梨糖醇略有升高。我们的研究结果揭示了用于识别转醛醇酶缺乏症的新型尿液生物标志物。