Heldman D A, Grever M R, Speicher C E, Trewyn R W
J Lab Clin Med. 1983 May;101(5):783-92.
Urinary excretion of modified nucleosides was measured in 15 patients with Philadelphia chromosome-positive CML to determine the correlation with activity of this disease. Resolution and quantitation of seven nucleosides were accomplished with reversed-phase HPLC. Patients in the stable phase of CML had excretion levels one to two times normal, whereas patients in the blastic phase showed elevations up to 12 times normal. The nucleosides showing the most significant differences in excretion between stable phase and blastic phase were 1-methylinosine, pseudouridine, and N2,N2-dimethylguanosine (p less than 0.01, p less than 0.001, and p less than 0.01, respectively). Nucleoside excretion was also determined in patients with bacterial pneumonia and urinary tract infection for comparison. Serial nucleoside determinations were made in two patients with CML and found to correlate closely with disease activity. The degree of elevation and the correlation with disease activity suggest the potential value of urinary nucleoside quantitation in monitoring patients with CML; in particular, nucleoside excretion may be useful in detecting early blastic transformation.
检测了15例费城染色体阳性慢性粒细胞白血病(CML)患者的修饰核苷尿排泄情况,以确定其与该疾病活性的相关性。采用反相高效液相色谱法对7种核苷进行分离和定量。处于CML稳定期的患者排泄水平为正常的1至2倍,而处于原始细胞期的患者排泄水平升高至正常的12倍。在稳定期和原始细胞期之间排泄差异最为显著的核苷是1-甲基肌苷、假尿苷和N2,N2-二甲基鸟苷(p分别小于0.01、小于0.001和小于0.01)。还对细菌性肺炎和尿路感染患者的核苷排泄情况进行了检测以作比较。对2例CML患者进行了连续核苷测定,发现其与疾病活性密切相关。排泄升高的程度以及与疾病活性的相关性表明,尿核苷定量在监测CML患者方面具有潜在价值;特别是,核苷排泄可能有助于检测早期原始细胞转化。