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血浆溶血型Gb3:一种在酶替代疗法期间监测法布里病患者的生物标志物。

Plasma lyso-Gb3: a biomarker for monitoring fabry patients during enzyme replacement therapy.

作者信息

Sakuraba Hitoshi, Togawa Tadayasu, Tsukimura Takahiro, Kato Hiroshi

机构信息

Department of Clinical Genetics, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.

Department of Functional Bioanalysis, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.

出版信息

Clin Exp Nephrol. 2018 Aug;22(4):843-849. doi: 10.1007/s10157-017-1525-3. Epub 2017 Dec 29.

Abstract

BACKGROUND

Recently, globotriaosylsphingosine (lyso-Gb3) has attracted interest as a biomarker of Fabry disease. However, little is known regarding its utility for the evaluation of the therapeutic efficacy.

METHOD

We measured plasma lyso-Gb3 concentration in Japanese healthy subjects and Fabry patients by means of liquid chromatography-tandem mass spectrometry (LC-MS/MS). We determined the reference interval in Japanese (UMIN000016854), and examined the effect of enzyme replacement therapy (ERT) with recombinant α-galactosidase A (GLA) and the influence of antibodies against the enzyme on the plasma lyso-Gb3 level in Fabry patients (UMIN000017152).

RESULTS

The reference interval was determined to be 0.35-0.71 nmol/L, this being almost the same as the normal range in a non-Japanese population previously reported. The analysis revealed that the plasma lyso-Gb3 level was strikingly increased in classic Fabry males, and to a lesser extent in later-onset Fabry males and Fabry females. The elevation of the plasma lyso-Gb3 level was related to renal involvement in the Fabry females. ERT gave a rapid reduction in the elevated plasma lyso-Gb3 level in the classic Fabry males, and a gradual one or stabilization in most of the later-onset Fabry males and Fabry females. However, formation of antibodies against the recombinant GLA had a negative effect on the reduction of plasma lyso-Gb3.

CONCLUSIONS

Regular observation of plasma lyso-Gb3 and antibodies is useful for monitoring of Fabry patients during ERT.

摘要

背景

最近,球三糖基鞘氨醇(溶血型Gb3)作为法布里病的生物标志物引起了关注。然而,关于其在评估治疗效果方面的效用知之甚少。

方法

我们通过液相色谱 - 串联质谱法(LC-MS/MS)测量了日本健康受试者和法布里病患者血浆中的溶血型Gb3浓度。我们确定了日本人群的参考区间(UMIN000016854),并研究了重组α-半乳糖苷酶A(GLA)进行酶替代疗法(ERT)的效果以及酶抗体对法布里病患者血浆溶血型Gb3水平的影响(UMIN000017152)。

结果

参考区间确定为0.35 - 0.71 nmol/L,这与先前报道的非日本人群的正常范围几乎相同。分析显示,经典型法布里病男性的血浆溶血型Gb3水平显著升高,迟发型法布里病男性和法布里病女性的升高程度较小。血浆溶血型Gb3水平的升高与法布里病女性的肾脏受累有关。ERT使经典型法布里病男性升高的血浆溶血型Gb3水平迅速降低,使大多数迟发型法布里病男性和法布里病女性的水平逐渐降低或稳定。然而,针对重组GLA的抗体形成对血浆溶血型Gb3的降低有负面影响。

结论

定期观察血浆溶血型Gb3和抗体对于法布里病患者ERT期间的监测很有用。

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