Current trends in antithyroid drug treatment of Graves' disease

被引:14
作者
Okosieme, Onyebuchi E. [1 ,2 ]
Lazarus, John H. [1 ,2 ]
机构
[1] Cardiff Univ, Sch Med, Inst Mol & Expt Med, Thyroid Res Grp, Cardiff, S Glam, Wales
[2] Cwm Taf Univ Hlth Board, Prince Charles Hosp, Endocrine & Diabet Dept, Merthyr Tydfil CF47 9DT, M Glam, Wales
关键词
Hyperthyroidism; Graves' disease; antithyroid drugs; carbimazole; methimazole; propylthiouracil; THYROTROPIN RECEPTOR ANTIBODIES; AMERICAN THYROID ASSOCIATION; B-LYMPHOCYTE DEPLETION; TSH-RECEPTOR; POTASSIUM PERCHLORATE; PREOPERATIVE PREPARATION; CAMP PRODUCTION; HYPERTHYROIDISM; THERAPY; THYROTOXICOSIS;
D O I
10.1080/14656566.2016.1232388
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Graves' hyperthyroidism is associated with significant morbidity and mortality risk. The thionamides, methimazole, its pro-drug derivative carbimazole, and propylthiouracil, remain a cornerstone of management. Yet despite decades of use, optimal strategies for maximising treatment response and curtailing adverse effect risk remains uncertain. Areas covered: We reviewed the current literature on the evidence based medical management of Graves' disease. Specifically, we evaluated current approaches to the use of thionamides, adjunctive therapies, and potential novel agents for controlling Graves' hyperthyroidism. Expert opinion: Primary medical therapy is successful in less than 50% of cases and so careful selection of patients for medical treatment based on a combination of pathological and pragmatic considerations is essential. Carbimazole or methimazole is the treatment of choice in the non-pregnant population driven by its more favourable pharmacokinetic and adverse effect profile over propylthiouracil. In pregnancy the choice of treatment is less straightforward and an approach that minimises undue fetal exposure to all thionamides should be adopted. Additional data is needed on the value of adjunctive therapies including potassium perchlorate, iodides, glucocorticoids, lithium, and cholestyramine. Novel agents directed against pathogenetic targets including TSH receptor blocking monoclonal antibodies and small molecule antagonists may hold promise for the future.
引用
收藏
页码:2005 / 2017
页数:13
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