Literature DB >> 35022790

Lifelong Effect of Therapy in Young Patients with the COL4A5 Alport Missense Variant p.(Gly624Asp): a Prospective Cohort Study.

Jan Boeckhaus1, Julia Hoefele2, Korbinian M Riedhammer2,3, Mato Nagel4, Bodo Beck5, Mira Choi6, Maik Gollasch7,8, Carsten Bergmann9,10, Joseph E Sonntag1, Victoria Troesch1, Johanna Stock1, Oliver Gross1.   

Abstract

BACKGROUND: Angiotensin-converting enzyme inhibitors (ACEis) have evolved as a first-line therapy for delaying end-stage renal failure (ESRF) in Alport syndrome. The present study tested the hypothesis of a superior nephroprotective potential of an early ACEi intervention, examining a cohort with the COL4A5 missense variant p.(Gly624Asp).
METHODS: In this observational cohort study (NCT02378805), 114 individuals with the identical gene-variant were explored for "age at ESRF" and "life-expectancy" in correlation with treatment as endpoints.
RESULTS: All 13 untreated hemizygous patients developed ESRF (mean age 48.9+/-13.7 years) as did three very late treated hemizygotes (51.7+/-4.2 years), with a mean life-expectancy of 59.2+/-9.6 years. All 28 earlier (eGFR 60 ml/min or higher) treated hemizygous patients were still alive and still had not reached ESRF. Therapy minimized the annual loss of their glomerular filtration rate, similar to the annual loss in healthy individuals. Out of 65 heterozygotes, 4 untreated individuals developed ESRF at an age of 53.3+/-20.7 years. None of the treated heterozygous females developed ESRF.
CONCLUSIONS: For the first time, this study shows that in Alport syndrome, early therapy in individuals with missense variants might have the potential to delay renal failure for their lifetime and thus to improve life-expectancy and quality of life without the need for renal replacement therapy. Some treated patients have reached retirement age with still-functioning kidneys whereas untreated relatives have already reached ESRF at the same or younger age. Thus, in children with glomerular hematuria, early testing for Alport-related gene variants could lead to timely nephroprotective intervention.
© The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.

Entities:  

Keywords:  Alport syndrome; chronic renal failure; nephroprotective therapy; renin-angiotensin system; type IV collagen disease

Year:  2022        PMID: 35022790     DOI: 10.1093/ndt/gfac006

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  1 in total

1.  The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.

Authors:  Jasmina Ćomić; Korbinian M Riedhammer; Roman Günthner; Christian W Schaaf; Patrick Richthammer; Hannes Simmendinger; Donald Kieffer; Riccardo Berutti; Velibor Tasic; Nora Abazi-Emini; Valbona Nushi-Stavileci; Jovana Putnik; Nataša Stajic; Adrian Lungu; Oliver Gross; Lutz Renders; Uwe Heemann; Matthias C Braunisch; Thomas Meitinger; Julia Hoefele
Journal:  Front Med (Lausanne)       Date:  2022-08-31
  1 in total

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