Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A)

被引:33
|
作者
Liu, Hao-Chuan [1 ,2 ]
Lin, Hsiang-Yu [3 ,4 ,5 ,6 ]
Yang, Chia-Feng [1 ]
Liao, Hsuan-Chieh [3 ,7 ]
Hsu, Ting-Rong [1 ,3 ]
Lo, Chiao-Wei [8 ]
Chang, Fu-Pang [9 ]
Huang, Chun-Kai [1 ]
Lu, Yung-Hsiu [1 ,2 ,3 ]
Lin, Shuan-Pei [4 ,5 ,6 ]
Yu, Wen-Chung [2 ,10 ,11 ]
Niu, Dau-Ming [1 ,2 ,3 ]
机构
[1] Taipei Vet Gen Hosp, Dept Pediat, Taipei 112, Taiwan
[2] Taiwan Clin Trial Consortium Fabry Dis, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[4] Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan
[5] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[6] Mackay Jr Coll Med Nursing & Management, Taipei, Taiwan
[7] Chinese Fdn Hlth, Neonatal Screening Ctr, Taipei, Taiwan
[8] Cathay Gen Hosp, Dept Pediat, Taipei, Taiwan
[9] Taipei Vet Gen Hosp, Dept Pathol & Lab Med, Taipei, Taiwan
[10] Taipei Vet Gen Hosp, Dept Med, Div Cardiol, Taipei 112, Taiwan
[11] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
Biomarker; Fabry disease; Globotriaosylsphingosine; IVS4+919G > A mutation; Outcome; PLASMA GLOBOTRIAOSYLSPHINGOSINE; DISEASE; PREVALENCE; BIOMARKER; VARIANT; ADULTS;
D O I
10.1186/s13023-014-0111-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: In Taiwan, DNA-based newborn screening showed a surprisingly high incidence (1/875 in males and 1/399 in females) of a cardiac Fabry mutation (IVS4 + 919G > A). However, the natural course, long-term treatment outcomes and suitable biomarkers for monitoring the therapeutic outcomes of these patients are largely unknown. Methods: Fabry disease (FD) patients who had received enzyme replacement therapy (ERT) for more than 1 year were enrolled in this study from December 2008 to April 2013. Periodic echocardiography and serum globotriaosylsphingosine (lyso-Gb3) analysis were carried out. Before and after ERT, left ventricular mass index (LVMI) and serum lyso-Gb3 level were compared and the correlation between the change of LVMI and the change of serum lyso-Gb3 were also analyzed. Results: Thirty-six patients, in four patient groups, were enrolled: (1) 16 males with IVS4 + 919G > A mutation; (2) 7 females with IVS4 + 919G > A mutation; (3) 2 males with classical mutations; and (4) 11 females with classical mutations. The follow-up period was 13-46 months. There were significant LVMI reductions after ERT in all four groups after excluding confounding factors. However, interestingly, serum lyso-Gb3 decreased significantly in the early period after ERT in all groups, but increased gradually after an average of 11.1 months after ERT in late-onset male and female Fabry groups, even when their LVMI still decreased or remained stable. Furthermore, there was no correlation between the change of serum lyso-Gb3 and the change of LVMI in both classical and IVS4 + 919G > A FD patients. Conclusion: Although lyso-Gb3 has a high diagnostic sensitivity in late-onset Fabry patients and has a good response to ERT during the early stages, it might not be a reliable marker for monitoring the long-term therapeutic outcomes of ERT for late-onset Fabry patients with the Chinese hotspot mutation (IVS4 + 919G > A).
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页数:9
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