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Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy.

Authors :
Brocklebank V
Kumar G
Howie AJ
Chandar J
Milford DV
Craze J
Evans J
Finlay E
Freundlich M
Gale DP
Inward C
Mraz M
Jones C
Wong W
Marks SD
Connolly J
Corner BM
Smith-Jackson K
Walsh PR
Marchbank KJ
Harris CL
Wilson V
Wong EKS
Malina M
Johnson S
Sheerin NS
Kavanagh D
Source :
Kidney international [Kidney Int] 2020 Jun; Vol. 97 (6), pp. 1260-1274. Date of Electronic Publication: 2020 Feb 28.
Publication Year :
2020

Abstract

Recessive mutations in diacylglycerol kinase epsilon (DGKE) display genetic pleiotropy, with pathological features reported as either thrombotic microangiopathy or membranoproliferative glomerulonephritis (MPGN), and clinical features of atypical hemolytic uremic syndrome (aHUS), nephrotic syndrome or both. Pathophysiological mechanisms and optimal management strategies have not yet been defined. In prospective and retrospective studies of aHUS referred to the United Kingdom National aHUS service and prospective studies of MPGN referred to the National Registry of Rare Kidney Diseases for MPGN we defined the incidence of DGKE aHUS as 0.009/million/year and so-called DGKE MPGN as 0.006/million/year, giving a combined incidence of 0.015/million/year. Here, we describe a cohort of sixteen individuals with DGKE nephropathy. One presented with isolated nephrotic syndrome. Analysis of pathological features reveals that DGKE mutations give an MPGN-like appearance to different extents, with but more often without changes in arterioles or arteries. In 15 patients presenting with aHUS, ten had concurrent substantial proteinuria. Identified triggering events were rare but coexistent developmental disorders were seen in six. Nine with aHUS experienced at least one relapse, although in only one did a relapse of aHUS occur after age five years. Persistent proteinuria was seen in the majority of cases. Only two individuals have reached end stage renal disease, 20 years after the initial presentation, and in one, renal transplantation was successfully undertaken without relapse. Six individuals received eculizumab. Relapses on treatment occurred in one individual. In four individuals eculizumab was withdrawn, with one spontaneously resolving aHUS relapse occurring. Thus we suggest that DGKE-mediated aHUS is eculizumab non-responsive and that in individuals who currently receive eculizumab therapy it can be safely withdrawn. This has important patient safety and economic implications.<br /> (Copyright © 2020 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1523-1755
Volume :
97
Issue :
6
Database :
MEDLINE
Journal :
Kidney international
Publication Type :
Academic Journal
Accession number :
32386968
Full Text :
https://doi.org/10.1016/j.kint.2020.01.045