Kidney Res Clin Pract 2019 Jun; 38(2): 250-252
Monitoring globotriaosylsphingosine in a Korean male patient with Fabry disease
Heejoon Jang , Kwon Wook Joo , Seung Seok Han
Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea
Correspondence to: Seung Seok Han
Department of Internal Medicine, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul 03080, Korea. E-mail:

Edited by Gheun-Ho Kim, Hanyang University College of Medicine, Seoul, Korea
Received: December 12, 2018; Revised: March 15, 2019; Accepted: March 18, 2019; Published online: June 30, 2019.
© The Korean Society of Nephrology. All rights reserved.

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Fabry disease is a lysosomal storage disease caused by α-galactosidase A (α-Gal A) deficiency, resulting in globotriaosylceramide (GL-3) accumulation within lysosomes and various clinical features, including kidney failure. GL-3 may be converted to deacylated globotriaosylceramide (globotriaosylsphingosine: lyso-GL-3) [1], but the exact source of lyso-GL-3 is under investigation. Treatment of Fabry disease consists of replacing the deficient enzyme with recombinant human α-Gal A, and experts recommend starting enzyme replacement therapy if a symptom or sign is noticed [2]. Recent studies proposed lyso-GL-3 as a better biomarker of treatment response than GL-3 [35]. In this study, we first report a case of Fabry disease in a Korean patient in whom lyso-GL-3 level was high and subsequently declined after enzyme replacement therapy. The present case may be helpful for physicians in clinical practice to trace plasma lyso-GL-3 before and after enzyme replacement therapy in Korean patients with Fabry disease.

A 29-year-old Korean man initially visited the rheumatology department with a complaint of chronic pain in his left lower leg. However, he was referred to the nephrology department because of decreased kidney function and proteinuria. The patient’s blood laboratory findings were as follows: blood urea nitrogen, 17 mg/dL; creatinine, 1.90 mg/dL; and estimated glomerular filtration rate (eGFR) using the Chronic Kidney Disease Epidemiology Collaboration equation [6], 47.0 mL/min/1.73 m2. His random urine protein-to-creatinine ratio was 3.1 g/g.

To determine the cause of azotemia and proteinuria, kidney biopsy was performed. Light microscopy revealed diffuse foamy changes in podocytes. Focal interstitial fibrosis, tubular atrophy with foam cell changes, and fibrointimal thickening in blood vessels were also observed (Fig. 1A, B). Electron microscopy revealed diffuse lipid deposits in all podocytes, glomerular endothelial cells, and mesangial cells. Electron-dense deposits were not present. The foot processes of podocytes were diffusely effaced (Fig. 1C, D). Immunofluorescence analysis revealed weak positivity for immunoglobulin G and M but negativity for other markers, such as immunoglobulin A, complement, and fibrinogen.

The patient’s non-renal features of Fabry disease were further investigated. Physical examination identified clusters of deep-red to purple papules on both thighs, which was diagnosed as angiokeratoma by skin biopsy (Fig. 1E). Echocardiography revealed hypertrophy of the basal septal wall (14 mm) but no other abnormal findings, such as the ejection fraction, systolic function, and regional wall motion. Brain magnetic resonance imaging uncovered a suspected ischemic lesion in the right posterolateral putamen (6 mm lesion with high signal intensity on a T2-weighted fluid-attenuated inversion recovery image and low signal intensity on a T1-weighted brain magnetic resonance image) (Fig. 1F, G). An ophthalmic examination was performed, but there was no abnormality in either cornea. The α-Gal A activity was measured using a fluorometric assay on white blood cells, and the activity was reduced to 3.3 nmol/hr/mg protein (reference, 35–100 nmol/hr/mg protein; 3.5% of activity). The α-Gal A activities of the patient’s younger brother and mother were also low. Direct sequencing analysis confirmed a hemizygous mutation in c.275A>G (p.Asp92Gly) (Fig. 1H). Based on these results, the patient was diagnosed with classical Fabry disease.

The patient was treated with 1.0 mg/kg recombinant agalsidase-β (Fabrazyme®; Sanofi Genzyme, Cambridge, USA) every other week and losartan 50 mg per day. The patient’s plasma GL-3 and lyso-GL-3 concentrations were measured at baseline and every 3 months. The baseline plasma GL-3 level was 10.9 μg/mL (reference, 3.9–9.9 μg/mL), and it decreased to 7.9 μg/mL after 9 months of treatment (Fig. 2A). The baseline plasma lyso-GL-3 level was 108 ng/mL (reference, ≤ 1.74 ng/mL), and its level declined to 24.8 ng/mL after 9 months of treatment (Fig. 2B). The patient’s eGFR level remained static throughout the follow-up period (Fig. 2C). The random urine protein-to-creatinine ratio was not aggravated during treatment (Fig. 2D).

This study was approved by the Institutional Review Board of Seoul National University Hospital (No. H-1802-065-922) and was conducted according to the Declaration of Helsinki. The patient provided informed consent.

Conflicts of interest

All authors have no conflicts of interest to declare.

Fig. 1. Renal and non-renal manifestations of Fabry disease. (A) Focal interstitial fibrosis (arrow) (H&E, ×400). (B) Diffuse foamy changes in podocytes (arrowheads) and fibrointimal thickening in blood vessels (arrow) (periodic acid-Schiff, ×400). (C) Zebra bodies in podocytes (electron microscopy, ×3,000). (D) Diffuse effacement in foot processes of podocytes (electron microscopy, ×8,000). (E) Angiokeratoma in the gluteal region. (F) T2-weighted fluid-attenuated inversion recovery brain magnetic resonance image: approximately 6-mm-high signal intensity in the right posterolateral putamen (arrow). (G) T1-weighted brain magnetic resonance image; approximately 6 mm slightly low signal intensity in the right posterolateral putamen (arrow). (H) Gene analysis findings.
Fig. 2. Treatment response. (A) Plasma globotriaosylceramide (GL-3). (B) Plasma deacylated globotriaosylceramide (globotriaosylsphingosine: lyso-GL-3). (C) Estimated glomerular filtration rate (eGFR). (D) Random urine protein-to-creatinine ratio (uPCR).
  1. Ferraz MJ, Kallemeijn WW, Mirzaian M, et al. Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidoses. Biochim Biophys Acta 2014;1841:811-825.
    Pubmed CrossRef
  2. Ortiz A, Germain DP, Desnick RJ, et al. Fabry disease revisited: management and treatment recommendations for adult patients. Mol Genet Metab 2018;123:416-427.
    Pubmed CrossRef
  3. Sakuraba H, Togawa T, Tsukimura T, Kato H. Plasma lyso-Gb3: a biomarker for monitoring fabry patients during enzyme replacement therapy. Clin Exp Nephrol 2018;22:843-849.
    Pubmed CrossRef
  4. Nowak A, Mechtler TP, Desnick RJ, Kasper DC. Plasma lysoGb3: a useful biomarker for the diagnosis and treatment of Fabry disease heterozygotes. Mol Genet Metab 2017;120:57-61.
    Pubmed CrossRef
  5. Togawa T, Kodama T, Suzuki T, et al. Plasma globotriaosylsphingosine as a biomarker of Fabry disease. Mol Genet Metab 2010;100:257-261.
    Pubmed CrossRef
  6. Levey AS, Stevens LA, Schmid CH, et al, CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration). A new equation to estimate glomerular filtration rate. Ann Intern Med 2009;150:604-612.
    Pubmed KoreaMed CrossRef


This Article

Cited By Articles
  • CrossRef (0)
  • PMC (0)
  • SCOPUS (0)

Social Network Service


Indexed/Covered by