Biomolecules (Mar 2020)

Variations in Circulating Active MMP-9 Levels During Renal Replacement Therapy

  • Elena Rodríguez-Sánchez,
  • José Alberto Navarro-García,
  • Jennifer Aceves-Ripoll,
  • Judith Abarca-Zabalía,
  • Andrea Susmozas-Sánchez,
  • Teresa Bada-Bosch,
  • Eduardo Hernández,
  • Evangelina Mérida-Herrero,
  • Amado Andrés,
  • Manuel Praga,
  • Mario Fernández-Ruiz,
  • José María Aguado,
  • Julián Segura,
  • Luis Miguel Ruilope,
  • Gema Ruiz-Hurtado

DOI
https://doi.org/10.3390/biom10040505
Journal volume & issue
Vol. 10, no. 4
p. 505

Abstract

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Renal replacement therapy (RRT) is complicated by a chronic state of inflammation and a high mortality risk. However, different RRT modalities can have a selective impact on markers of inflammation and oxidative stress. We evaluated the levels of active matrix metalloproteinase (MMP)-9 in patients undergoing two types of dialysis (high-flux dialysis (HFD) and on-line hemodiafiltration (OL-HDF)) and in kidney transplantation (KT) recipients. Active MMP-9 was measured by zymography and ELISA before (pre-) and after (post-) one dialysis session, and at baseline and follow-up (7 and 14 days, and 1, 3, 6, and 12 months) after KT. Active MMP-9 decreased post-dialysis only in HFD patients, while the levels in OL-HDF patients were already lower before dialysis. Active MMP-9 increased at 7 and 14 days post-KT and was restored to baseline levels three months post-KT, coinciding with an improvement in renal function and plasma creatinine. Active MMP-9 correlated with pulse pressure as an indicator of arterial stiffness both in dialysis patients and KT recipients. In conclusion, active MMP-9 is better controlled in OL-HDF than in HFD and is restored to baseline levels along with stabilization of renal parameters after KT. Active MMP-9 might act as a biomarker of arterial stiffness in RRT.

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