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Updated: Jul 30, 2025

In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease
Published on: December 20, 2017
Is just enzyme replacement therapy enough for Fabry disease treatment? Have we missed a trick?
Hakan Ozer1, Ismail Baloglu1, Ali Topkac2
1Nephrology Department, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey.
Background And Aim:
In Fabry disease (FD), primary factors such as glycosphingolipid deposition that initiate kidney damage and secondary factors that advance kidney damage to fibrosis are different. Periostin is a molecule of proven importance in renal inflammation and fibrosis. It was previously shown that periostin plays an essential role in the process leading to renal fibrosis and its expression is increased in many kidney diseases. In the present study, we aimed to reveal the relationship between periostin and Fabry nephropathy.
Material-Method:
This cross-sectional study included 18 FD patients (10 males, 8 females) with enzyme replacement therapy (ERT) indications and 22 healthy control patients of similar age and gender. At the time of diagnosis, plasma alpha-galactosidase A (α-gal-A) and globotriaosylsphingosine (lyso-Gb3), proteinuria, and kidney function tests of all FD patients before ERT were scanned from the hospital system. Periostin was studied from serum samples collected and stored before ERT. Parameters related to serum periostin levels in Fabry disease were investigated.
Results:
In FD patients, serum periostin was negatively correlated with age of first symptom and GFR; and positively correlated with proteinuria and lyso-Gb3. In regression analysis, we found that serum periostin was the only independent determinant of proteinuria in patients with Fabry disease. The serum periostin levels were significantly lower in patients with low proteinuria, and the serum periostin levels were correlated with proteinuria.
Discussion:
Periostin may be a valuable marker of Fabry nephropathy and proteinuria. Periostin seems to be one of the molecules that may have an important role in the management of the fibrotic process in Fabry nephropathy. We think that the role of periostin among these mechanisms is worth investigating. In addition to standard ERTs, periostin-reducing therapies may contribute to better kidney survival in Fabry disease. Progressive fibrosis processes caused by periostin in patients with Fabry disease are still a hidden issue waiting to be clarified. Progressive fibrosis processes caused by periostin in Fabry patients are still a hidden issue waiting to be clarified.
Insights
Periostin may serve as a key biomarker for Fabry nephropathy and proteinuria. Targeting periostin could potentially improve kidney survival in Fabry disease patients undergoing enzyme replacement therapy.
Area of Science:
- Nephrology
- Biochemistry
- Genetics
Background:
- Fabry disease (FD) involves glycosphingolipid deposition leading to kidney damage and fibrosis.
- Periostin is implicated in renal inflammation and fibrosis, with elevated expression in various kidney diseases.
- The role of periostin in Fabry nephropathy requires further elucidation.
Purpose of the Study:
- To investigate the relationship between serum periostin levels and Fabry nephropathy.
- To determine if periostin is a determinant of proteinuria in FD patients.
Main Methods:
- A cross-sectional study involving 18 FD patients and 22 healthy controls.
- Analysis of serum periostin, plasma alpha-galactosidase A (α-gal-A), globotriaosylsphingosine (lyso-Gb3), proteinuria, and kidney function tests.
- Correlation and regression analyses were performed on pre-treatment samples.
Main Results:
- Serum periostin levels in FD patients were negatively correlated with age of first symptom and GFR.
- Serum periostin positively correlated with proteinuria and lyso-Gb3 levels.
- Serum periostin was identified as the sole independent determinant of proteinuria in FD patients.
Conclusions:
- Periostin may be a valuable biomarker for assessing Fabry nephropathy and proteinuria.
- Periostin-targeting therapies could potentially enhance kidney survival in FD.
- Further research is warranted to clarify periostin's role in FD-associated fibrosis.
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