Hughes Andrew T, Milan Anna M, Davison Andrew S, Christensen Peter, Ross Gordon, Gallagher James A, Dutton John J, Ranganath Lakshminarayan R
Department of Clinical Biochemistry and Metabolic Medicine, Liverpool Clinical Laboratories, Royal Liverpool and Broadgreen University Hospital Trust, Liverpool, UK Bone and Joint Research Group, Musculoskeletal Biology, Sherrington Building, University of Liverpool, Liverpool, UK.
Department of Clinical Biochemistry and Metabolic Medicine, Liverpool Clinical Laboratories, Royal Liverpool and Broadgreen University Hospital Trust, Liverpool, UK Bone and Joint Research Group, Musculoskeletal Biology, Sherrington Building, University of Liverpool, Liverpool, UK
Ann Clin Biochem. 2015 Sep;52(Pt 5):597-605. doi: 10.1177/0004563215571969. Epub 2015 Jan 27.
Alkaptonuria is a rare debilitating autosomal recessive disorder of tyrosine metabolism, where deficiency of homogentisate 1,2-dioxygenase results in increased homogentisic acid. Homogentisic acid is deposited as an ochronotic pigment in connective tissues, especially cartilage, leading to a severe early onset form of osteoarthritis, increased renal and prostatic stone formation and hardening of heart vessels. Treatment with the orphan drug, nitisinone, an inhibitor of 4-hydroxyphenylpyruvate dioxygenase has been shown to reduce urinary excretion of homogentisic acid.
A reverse phase liquid chromatography tandem mass spectrometry method has been developed to simultaneously analyse serum homogentisic acid, tyrosine and nitisinone. Using matrix-matched calibration standards, two product ion transitions were identified for each compound (homogentisic acid, tyrosine, nitisinone) and their respective isotopically labelled internal standards ((13)C6-homogentisic acid, d2-tyrosine, (13)C6-nitisinone).
Intrabatch accuracy was 94-108% for homogentisic acid, 95-109% for tyrosine and 89-106% for nitisinone; interbatch accuracy (n = 20) was 88-108% for homogentisic acid, 91-104% for tyrosine and 88-103% for nitisinone. Precision, both intra- and interbatch were <12% for homogentisic acid and tyrosine, and <10% for nitisinone. Matrix effects observed with acidified serum were normalized by the internal standard (<10% coefficient of variation). Homogentisic acid, tyrosine and nitisinone proved stable after 24 h at room temp, three freeze-thaw cycles and 24 h at 4℃. The assay was linear to 500μmol/L homogentisic acid, 2000μmol/L tyrosine and 10μmol/L nitisinone; increased range was not required for clinical samples and no carryover was observed.
The method developed and validated shows good precision, accuracy and linearity appropriate for the monitoring of alkaptonuria patients, pre- and post-nitisinone therapy.
黑尿症是一种罕见的、使人衰弱的常染色体隐性酪氨酸代谢紊乱疾病,其中尿黑酸1,2 -双加氧酶缺乏导致尿黑酸增加。尿黑酸作为一种褐黄病色素沉积在结缔组织中,尤其是软骨,导致严重的早发性骨关节炎、肾和前列腺结石形成增加以及心血管硬化。已证明使用孤儿药尼替西农(一种4 -羟基苯丙酮酸双加氧酶抑制剂)治疗可减少尿黑酸的尿排泄。
已开发出一种反相液相色谱串联质谱法,用于同时分析血清中的尿黑酸、酪氨酸和尼替西农。使用基质匹配校准标准品,为每种化合物(尿黑酸、酪氨酸、尼替西农)及其各自的同位素标记内标((13)C6 -尿黑酸、d2 -酪氨酸、(13)C6 -尼替西农)鉴定了两个产物离子跃迁。
批内准确度对于尿黑酸为94 - 108%,对于酪氨酸为95 - 109%,对于尼替西农为89 - 106%;批间准确度(n = 20)对于尿黑酸为88 - 108%,对于酪氨酸为91 - 104%,对于尼替西农为88 - 103%。尿黑酸和酪氨酸的批内和批间精密度均<12%,尼替西农的批内和批间精密度<10%。用内标对酸化血清中观察到的基质效应进行了校正(变异系数<10%)。尿黑酸、酪氨酸和尼替西农在室温下24小时、三个冻融循环以及4℃下24小时后均证明稳定。该测定法对尿黑酸至500μmol/L、酪氨酸至2000μmol/L和尼替西农至10μmol/L呈线性;临床样本不需要增加范围,且未观察到残留。
所开发和验证的方法显示出良好的精密度、准确度和线性,适用于监测尼替西农治疗前后的黑尿症患者。