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Effects of fingolimod treatments on alanine transaminase and aspartate transaminase levels in patients with multiple sclerosis

机译:芬戈莫德治疗对多发性硬化症患者丙氨酸转氨酶和天冬氨酸转氨酶水平的影响

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摘要

Introduction: Multiple Sclerosis (MS) is a chronic neurological disorder with no known cause or cure. Fingolimod (FTY720) is an oral medication recently approved for the treatment of MS as well as other diseases with autoimmune aspects. However, the drug is not without side effects. The severity and prevalence of these side effects are not completely understood. One of the most common causes for the patient cessation of fingolimod is an increase in liver enzymes, indicating possible inflammation or damage to liver cells. Alanine transaminase (ALT) and aspartate transaminase (AST) are the most common liver enzymes used as indicators of hepatic health. Objectives: This three-month prospective cohort study selected patients who were diagnosed with relapsing-remitting MS (RRMS) and who were not taking fingolimod oral treatment. ALT and AST levels were determined for these patients at baseline and then after three months of taking FTY720 to determine if these liver enzymes were changed. Methods: 36 RRMS patients completed this study, which lasted three months. They were started on 0.5 oral FTY720 after approval from a physician and completion of an AST/ALT blood test. Baseline levels were determined and then taken again three months later. Statistical analysis of these values was performed using P<0.05 as a significance threshold. Results: In this sample of patients, only ALT levels were significantly increased after fingolimod treatment in the general cohort (P=0.00). The general cohort showed an insignificant increase in AST levels. In male and female populations separately, AST was not significantly increased. ALT was only significantly increased in men (P=0.00) and insignificantly increased in women. Conclusion: This study further confirms our concerns about fingolimod’s possible effects on the liver. While these numbers do support the claim that the drug does on average increase ALT in patient populations, it is important to note that most of these patients have no real hepatic side effects. In addition, previous studies have cited a return to normal ALT and AST levels after cessation of fingolimod, suggesting its effects are temporary and not severely damaged in the usual patient.
机译:简介:多发性硬化症(MS)是一种慢性神经病,尚无已知病因或治愈方法。芬戈莫德(FTY720)是最近被批准用于治疗MS以及其他具有自身免疫性疾病的口服药物。但是,该药并非没有副作用。这些副作用的严重程度和患病率尚未完全了解。患者停用芬戈莫德的最常见原因之一是肝酶增加,表明可能存在炎症或肝细胞受损。丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)是最常用作肝健康指标的肝酶。目的:这项为期三个月的前瞻性队列研究选择了被诊断患有复发缓解型MS(RRMS)且未接受芬戈莫德口服治疗的患者。在基线时确定这些患者的ALT和AST水平,然后在服用FTY720三个月后确定这些肝酶是否改变。方法:36名RRMS患者完成了这项研究,历时三个月。在获得医生批准并完成AST / ALT血液检查后,他们开始使用0.5口服FTY720。确定基线水平,然后在三个月后再次测量。使用P <0.05作为显着性阈值对这些值进行统计分析。结果:在该患者样本中,芬戈莫德治疗后,一般队列中仅ALT水平显着升高(P = 0.00)。一般队列显示AST水平无明显增加。在男性和女性人群中,AST均未显着增加。 ALT仅在男性中显着增加(P = 0.00),而在女性中则微不足道。结论:这项研究进一步证实了我们对芬戈莫德可能对肝脏产生影响的担忧。尽管这些数字确实支持了该药物确实在患者人群中增加ALT的说法,但重要的是要注意,这些患者中的大多数没有真正的肝副作用。此外,先前的研究表明芬戈莫德停药后ALT和AST水平恢复正常,这表明其作用是暂时的,在普通患者中并未受到严重损害。

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