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THERAPY OF ENDOCRINE DISEASE: Endocrine dilemma: management of Graves’ orbitopathy

机译:内分泌疾病的治疗:内分泌两难:Graves眼眶病的治疗

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Management of Graves’ orbitopathy (GO) must be based on the correct assessment of activity and severity of the disease. Activity is usually assessed with the Clinical Activity Score, whereas severity is classified according to a European Group On Graves' Orbitopathy (EUGOGO) consensus statement as mild, moderate-to-severe, and sight-threatening. Myopathic and chronic congestive forms are uncommon clinical presentations of GO. Restoration and maintenance of stable euthyroidism are recommended in the presence of GO. In moderate-to-severe disease, steroids have been widely employed and have shown to possess an anti-inflammatory activity, but about 20–30% of patients are not responsive and present recurrence. Some novel immunosuppressors have already been employed in clinical studies and have shown interesting results, although the lack of randomized and controlled trials suggests caution for their use in clinical practice. Potential targets for therapy in GO are the thyroid-stimulating hormone and the insulin-like growth factor 1 receptor on the fibroblasts, inflammatory cytokines, B and T cells, and the PIK3/mTORC1 signaling cascades for adipogenesis. A recent open study has shown that tocilizumab, an anti-sIL-6R antibody, inactivates GO. Consistent reports on the efficacy of rituximab have recently been challenged by randomized controlled trials. As the main goal of treatment is the well-being of the patient, the therapeutic strategy should be addressed to better suit the patient needs, more than improving one or more biological parameters. The increasing availability of new therapies will expand the therapeutic options for GO patients and allow the clinician to really personalize the treatment to better suit the patients’ personal needs.
机译:格雷夫斯眼眶病(GO)的治疗必须基于对疾病活动性和严重性的正确评估。活动通常使用临床活动评分进行评估,而严重程度则根据欧洲Graves眼眶病小组(EUGOGO)共识声明分为轻度,中度至重度和视力威胁。肌病和慢性充血形式是GO的罕见临床表现。建议在GO的存在下恢复和维持稳定的甲状腺功能亢进。在中度至重度疾病中,类固醇已被广泛使用,并显示出具有抗炎活性,但约20%至30%的患者无反应并复发。尽管缺乏随机和对照试验表明在临床实践中应谨慎使用,但一些新型的免疫抑制剂已用于临床研究并显示出有趣的结果。 GO中潜在的治疗靶标是成纤维细胞,炎性细胞因子,B和T细胞以及用于脂肪形成的PIK3 / mTORC1信号级联反应中的促甲状腺激素和胰岛素样生长因子1受体。最近的一项公开研究表明,抗sIL-6R抗体Tocilizumab使GO失活。关于利妥昔单抗疗效的一致报道最近受到随机对照试验的挑战。由于治疗的主要目标是患者的健康,因此应制定治疗策略以更好地适应患者的需求,而不是改善一种或多种生物学参数。新疗法的日益普及将为GO患者扩大治疗选择范围,并使临床医生能够真正个性化治疗方案,以更好地满足患者的个人需求。

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