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.

Nefrologia
|May 13, 2023
PubMed
Abstract

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.