Evidence map›Paper›PMID 32386968›Full record

ArticleKidney international2020

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

Vicky Brocklebank, Gurinder Kumar, Alexander J Howie, Jayanthi Chandar, David V Milford, Janet Craze, Jonathan Evans, Eric Finlay, Michael Freundlich, Daniel P Gale and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Kidney international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Complement System Inhibitors in Nephrology: An Update-Narrative Review.International journal of molecular sciences · 2025
    Review
  9. Post-transplant Thrombotic Microangiopathy.Journal of the American Society of Nephrology : JASN · 2025
    Review
  10. Article
  11. Late Onset Thrombotic Microangiopathy in Kidney Transplants; Poor Outcome Despite Eculizumab Treatment.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  12. Review
  13. Article
  14. Review
  15. The Role of Genetic Testing in Adult CKD.Journal of the American Society of Nephrology : JASN · 2024
    Article
  16. Observational
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 17 institutions in 4 countries.

Vicky BrocklebankNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Gurinder KumarDivision of Paediatric Nephrology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Alexander J HowieBirmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
Jayanthi ChandarDivision of Pediatric Nephrology, University of Miami, Miami, Florida, USA.
David V MilfordBirmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
Janet CrazeDepartment of General Paediatrics, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Jonathan EvansChildren's Renal and Urology Unit, Nottingham Children's Hospital, Nottingham University Hospitals NHS Foundation Trust, Nottingham, UK.
Eric FinlayLeeds Teaching Hospitals NHS Trust, Leeds, UK.
Michael FreundlichDivision of Pediatric Nephrology, University of Miami, Miami, Florida, USA.
Daniel P GaleDepartment of Renal Medicine, University College London, UK.
Carol InwardDepartment of Paediatric Nephrology, Bristol Royal Hospital For Children, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
Martin MrazDepartment of Paediatric Nephrology, Bristol Royal Hospital For Children, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
Caroline JonesDepartment of Paediatric Nephrology, Alder Hey Children's Hospital NHS Trust, Liverpool, UK.
William WongDepartment of Paediatric Nephrology, Starship Children's Hospital, Grafton, Auckland, New Zealand.
Stephen D MarksDepartment of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
John ConnollyCentre for Nephrology, Royal Free Hospital, University College London, London, UK.
Bronte M CornerComplement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Kate Smith-JacksonNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Patrick R WalshNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Kevin J MarchbankNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Claire L HarrisNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Valerie WilsonNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Edwin K S WongNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Michal MalinaNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Great North Children's Hospital, Sir James Spence Institute, Royal Victoria Infirmary, Newcastle, UK.
Sally JohnsonNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Great North Children's Hospital, Sir James Spence Institute, Royal Victoria Infirmary, Newcastle, UK.
Neil S SheerinNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
David KavanaghNational Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK. Electronic address: david.kavanagh@newcastle.ac.uk.
Newcastle upon Tyne Hospitals NHS Foundation Trust · GBNewcastle University · GBBirmingham Women’s and Children’s NHS Foundation Trust · GBUniversity of Miami · USBristol Royal Hospital for Children · GBGreat North Children's Hospital · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBLeeds Teaching Hospitals NHS Trust · GBNottingham University Hospitals NHS Trust · GBOxford University Hospitals NHS Trust · GBRoyal Victoria Infirmary · GBShaikh Khalifa Medical City · AEStarship Children's Health · NZThe Royal Free Hospital · GBUniversity College London · GBUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Liverpool · GB

Funding

Medical Research Council MR/K023519/1Medical Research Council MR/R000913/1Medical Research Council MR/R001359/1Wellcome Trust
6 · The paper itself

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.

Indexed as

Atypical Hemolytic Uremic SyndromeDiacylglycerol KinaseChild, PreschoolHumansProspective StudiesRetrospective StudiesUnited KingdomDiacylglycerol Kinaseatypical hemolytic uremic syndromediacylglycerol kinase εmembranoproliferative glomerulonephritisthrombotic microangiopathy

Identifiers

PMID32386968
PMCPMC7242908
OpenAlexW3007235995

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.