Department of Internal Medicine, Divisions of Nephrology and Cardiology, University Hospital Würzburg, Würzburg, Germany.
Department of Internal Medicine, Divisions of Nephrology and Cardiology, University Hospital Würzburg, Würzburg, Germany
Postgrad Med J. 2018 Dec;94(1118):709-713. doi: 10.1136/postgradmedj-2018-136056. Epub 2018 Dec 17.
Fabry disease is a rare inborn error of the enzyme α-galactosidase (α-Gal) and results in lysosomal substrate accumulation in tissues with a wide range of clinical presentations. The disease has attracted a lot of interest over the last years, in particular since enzyme replacement therapy (ERT) has become widely available in 2001. With rising awareness and rising numbers of (diagnosed) patients, physicians encounter new challenges. Over 900 α-Gal gene mutations are currently known, some with doubtful clinical significance, posing diagnostic and prognostic difficulties for the clinician and a lot of uncertainty for patients. Another challenge are patients who develop neutralising antibodies to ERT, which possibly leads to reduced therapy effectiveness. In this article, we summarise the latest developments in the science community regarding diagnostics and management of this rare lysosomal storage disorder and offer an outlook to future treatments.
法布瑞氏病是一种罕见的溶酶体α-半乳糖苷酶(α-Gal)遗传性缺陷疾病,可导致广泛临床表现的组织内溶酶体底物蓄积。自 2001 年以来,酶替代疗法(ERT)广泛应用,该病近年来受到了广泛关注。随着(确诊)患者数量的增加,医生面临着新的挑战。目前已知超过 900 种α-Gal 基因突变,其中一些具有可疑的临床意义,这给临床医生的诊断和预后带来了困难,也给患者带来了很大的不确定性。另一个挑战是对 ERT 产生中和抗体的患者,这可能导致治疗效果降低。本文总结了科学界在该罕见溶酶体贮积症的诊断和治疗方面的最新进展,并对未来的治疗方法进行了展望。