芬戈莫德治疗对多发性硬化患者谷丙转氨酶和天冬氨酸转氨酶水平的影响。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2020-06-15 eCollection Date: 2020-01-01
Saeid Sadeghi Joni, Masoumeh Cheshmavar, Pouria Shoureshi, Zohreh Zamani, Niusha Taoosi, Morteza Akbari, Mahdieh Afzali
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引用次数: 0

摘要

简介:多发性硬化症(MS)是一种慢性神经系统疾病,没有已知的原因和治疗方法。Fingolimod (FTY720)是一种最近被批准用于治疗多发性硬化症以及其他自身免疫性疾病的口服药物。然而,这种药物并非没有副作用。这些副作用的严重程度和普遍程度尚不完全清楚。患者停止服用芬戈莫德最常见的原因之一是肝酶增加,这表明可能出现炎症或肝细胞损伤。谷丙转氨酶(ALT)和天冬氨酸转氨酶(AST)是最常用的肝酶,被用作肝脏健康指标。目的:这项为期三个月的前瞻性队列研究选择了诊断为复发-缓解型MS (RRMS)且未服用芬戈莫口服治疗的患者。在基线时测定这些患者的ALT和AST水平,然后在服用FTY720三个月后测定这些肝酶是否改变。方法:36例RRMS患者完成本研究,为期3个月。在医生批准并完成AST/ALT血液测试后,他们开始服用0.5口服FTY720。确定了基线水平,然后在三个月后再次测量。结果:在该患者样本中,在一般队列中,只有ALT水平在芬戈莫德治疗后显著升高(P=0.00)。一般队列显示AST水平不显著升高。在男性和女性人群中,AST均未显著升高。ALT仅在男性中显著升高(P=0.00),在女性中无显著升高。结论:本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。虽然这些数据确实支持该药物在患者群体中平均增加ALT的说法,但重要的是要注意大多数这些患者没有真正的肝脏副作用。此外,先前的研究表明,停止服用芬戈莫德后,ALT和AST水平恢复正常,表明其作用是暂时的,对普通患者没有严重损害。
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Effects of fingolimod treatments on alanine transaminase and aspartate transaminase levels in patients with multiple sclerosis.

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.

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