Mahzari Moeber, Arnaout Amel, Freedman Mark S
1Division of Endocrinology and Metabolism,Ottawa,Ontario,Canada.
2Division of Neurology,Department of Medicine,University of Ottawa,Ottawa,Ontario,Canada.
Can J Neurol Sci. 2015 Sep;42(5):284-91. doi: 10.1017/cjn.2015.48. Epub 2015 May 20.
Alemtuzumab, an anti-CD52 monoclonal antibody, was recently approved for treatment of MS in Canada, having shown to significantly reduce relapses and disability in patients, particularly those who relapsed despite first line treatment. Offsetting its benefit however, is the development of novel secondary autoimmune disease, particularly affecting the thyroid gland in up to 36% of patients. The incidence of Alemtuzumab induced thyroid dysfunction (AITD) will likely rise as alemtuzumab becomes more widely used for treating MS. We review the clinical and investigational cues that help delineate the aetiology and management of thyrotoxicosis and hypothyroidism in ATID. AITD can be easily managed and we present a simple approach for its evaluation and management by neurologists that should be implemented prior to considering a referral to an internist or endocrinologist for further opinion or treatment.
阿仑单抗是一种抗CD52单克隆抗体,最近在加拿大被批准用于治疗多发性硬化症(MS),已证明可显著减少患者的复发和残疾,尤其是那些尽管接受了一线治疗仍复发的患者。然而,抵消其益处的是新型继发性自身免疫性疾病的发生,特别是在高达36%的患者中影响甲状腺。随着阿仑单抗越来越广泛地用于治疗MS,阿仑单抗诱导的甲状腺功能障碍(AITD)的发生率可能会上升。我们回顾了有助于阐明AITD中甲状腺毒症和甲状腺功能减退的病因及管理的临床和研究线索。AITD易于管理,我们提出了一种由神经科医生对其进行评估和管理的简单方法,该方法应在考虑转诊至内科医生或内分泌科医生以获取进一步意见或治疗之前实施。