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使用柳氮磺胺吡啶治疗关节炎患者的叶酸、同型半胱氨酸状态及溶血情况

Folate and homocysteine status and haemolysis in patients treated with sulphasalazine for arthritis.

作者信息

Krogh Jensen M, Ekelund S, Svendsen L

机构信息

Department of Haematology and Internal Medicine, Aalborg Hospital, Denmark.

出版信息

Scand J Clin Lab Invest. 1996 Aug;56(5):421-9. doi: 10.3109/00365519609088797.

Abstract

In an attempt to estimate the frequency of folate deficiency and haemolysis in a group of 25 outpatients with arthritis treated with sulphasalazine (SASP), haematological measurements, including plasma total homocysteine (tHcy) which is a sensitive marker of folate deficiency, serum folate (S-folate), erythrocyte (RBC) folate, S-cobalamin and routine indices of haemolysis were performed. No patient had been taking folate-containing vitamins for at least 8 weeks prior to the study. Compared to a group of 72 healthy hospital staff, the median plasma tHcy was significantly higher in the patient group (8.8 mumol 1(-1) vs. 6.8 mumol 1(-1); p = 0.003). Five patients (20%) had plasma tHcy levels that exceeded the upper normal limit of plasma tHcy (median+2 SD of the reference group). Median S-folate was significantly lower in the patient group (6.0 nmol 1(-1) vs. 8.5 nmol 1(-1); p < 0.001), and 11 (44%) patients had depressed S-folate. Only three (12%) patients had RBC folate values below the reference interval. There was no difference in the levels of RBC folate between the two groups. A comparison of S-cobalamin levels in the two groups disclosed a significantly lower level in the patient group. However, no patient had cobalamin deficiency as assessed by S-cobalamin and S-methylmalonate measurements. Thus, it is unlikely that any patient had increased plasma tHcy due to cobalamin deficiency. Of 24 patients having a HbA1c measurement performed, 12 (50%) had decreased levels indicating chronic haemolysis. Only seven (28%) patients had reticulocytosis. HbA1c was positively correlated to haptoglobin levels (r = 0.77; p < 0.001) and negatively correlated to the percentage of reticulocytes (r = -0.50; p = 0.02). The percentage of reticulocytes was negatively correlated to haptoglobin levels (r = -0.42; p = 0.04). The chronic haemolysis of the patients' blood due to SASP might explain the similar RBC folate values in the two groups because of a relatively higher folate content of young erythrocytes. In conclusion, our results support previous findings of folate deficiency and haemolysis occurring in a considerable fraction of patients receiving treatment with SASP. Measurements of plasma tHcy suggest that a substantial number of patients may have folate deficiency at the tissue level.

摘要

为了估算一组25例接受柳氮磺胺吡啶(SASP)治疗的关节炎门诊患者中叶酸缺乏和溶血的发生率,进行了血液学检测,包括血浆总同型半胱氨酸(tHcy)(它是叶酸缺乏的敏感标志物)、血清叶酸(S - 叶酸)、红细胞(RBC)叶酸、S - 钴胺素以及溶血的常规指标。在研究前至少8周内,没有患者服用过含叶酸的维生素。与72名健康医院工作人员组成的对照组相比,患者组的血浆tHcy中位数显著更高(8.8 μmol/L vs. 6.8 μmol/L;p = 0.003)。5名患者(20%)的血浆tHcy水平超过了血浆tHcy的正常上限(参考组中位数 + 2个标准差)。患者组的S - 叶酸中位数显著更低(6.0 nmol/L vs. 8.5 nmol/L;p < 0.001),11名(44%)患者的S - 叶酸水平降低。只有3名(12%)患者的RBC叶酸值低于参考区间。两组之间的RBC叶酸水平没有差异。两组S - 钴胺素水平的比较显示患者组水平显著更低。然而,通过S - 钴胺素和S - 甲基丙二酸测量评估,没有患者存在钴胺素缺乏。因此,不太可能有任何患者因钴胺素缺乏而导致血浆tHcy升高。在进行糖化血红蛋白(HbA1c)检测的24名患者中,12名(50%)患者的水平降低,表明存在慢性溶血。只有7名(28%)患者有网织红细胞增多。HbA1c与触珠蛋白水平呈正相关(r = 0.77;p < 0.001),与网织红细胞百分比呈负相关(r = -0.50;p = 0.02)。网织红细胞百分比与触珠蛋白水平呈负相关(r = -0.42;p = 0.04)。SASP导致患者血液慢性溶血,这可能解释了两组RBC叶酸值相似的原因,因为年轻红细胞的叶酸含量相对较高。总之,我们的结果支持了之前的研究发现,即相当一部分接受SASP治疗的患者会出现叶酸缺乏和溶血。血浆tHcy的检测表明大量患者可能在组织水平存在叶酸缺乏。

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