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Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort.
Wong, Katie; Pitcher, David; Braddon, Fiona; Downward, Lewis; Steenkamp, Retha; Annear, Nicholas; Barratt, Jonathan; Bingham, Coralie; Chrysochou, Constantina; Coward, Richard J; Game, David; Griffin, Sian; Hall, Matt; Johnson, Sally; Kanigicherla, Durga; Karet Frankl, Fiona; Kavanagh, David; Kerecuk, Larissa; Maher, Eamonn R; Moochhala, Shabbir; Pinney, Jenny; Sayer, John A; Simms, Roslyn; Sinha, Smeeta; Srivastava, Shalabh; Tam, Frederick W K; Turner, Andrew Neil; Walsh, Stephen B; Waters, Aoife; Wilson, Patricia; Wong, Edwin; Taylor, Christopher Mark; Nitsch, Dorothea; Saleem, Moin; Bockenhauer, Detlef; Bramham, Kate; Gale, Daniel P.
Afiliação
  • Wong K; National Registry of Rare Kidney Diseases, Bristol, UK; Department of Renal Medicine, University College London, London, UK.
  • Pitcher D; National Registry of Rare Kidney Diseases, Bristol, UK.
  • Braddon F; National Registry of Rare Kidney Diseases, Bristol, UK.
  • Downward L; National Registry of Rare Kidney Diseases, Bristol, UK.
  • Steenkamp R; UK Renal Registry, Bristol, UK.
  • Annear N; Institute of Medical and Biomedical Education, St George's University of London, London, UK.
  • Barratt J; Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
  • Bingham C; University of Exeter Medical School, University of Exeter, Exeter, UK.
  • Chrysochou C; Division of Cardiovascular Sciences, University of Manchester, Manchester, UK.
  • Coward RJ; Translational Health Sciences, University of Bristol, Bristol, UK.
  • Game D; Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Griffin S; Department of Nephrology, University Hospital Wales, Cardiff, UK.
  • Hall M; Nottingham Renal and Transplant Unit, Nottingham University Hospitals NHS Foundation Trust, Nottingham, UK.
  • Johnson S; Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Kanigicherla D; Division of Cardiovascular Sciences, University of Manchester, Manchester, UK.
  • Karet Frankl F; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
  • Kavanagh D; National Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK; Complement Therapeutics Research Group, Newcastle University, Newcastle upon Tyne, UK; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne,
  • Kerecuk L; Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Maher ER; Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Moochhala S; Department of Renal Medicine, Royal Free London NHS Foundation Trust, London, UK.
  • Pinney J; Department of Renal Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Sayer JA; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Simms R; Academic Unit of Nephrology, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
  • Sinha S; Division of Cardiovascular Sciences, University of Manchester, Manchester, UK; Department of Renal Medicine, Northern Care Alliance NHS Foundation Trust, Manchester, UK.
  • Srivastava S; Department of Renal Medicine, South Tyneside and Sunderland NHS Foundation Trust, Sunderland, UK.
  • Tam FWK; Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, UK.
  • Turner AN; Medical Research Council Centre for Inflammation, Edinburgh University, Edinburgh, UK.
  • Walsh SB; Department of Renal Medicine, University College London, London, UK; Department of Renal Medicine, Royal Free London NHS Foundation Trust, London, UK.
  • Waters A; Department of Paediatrics and Child Health, University College Cork, Cork, Ireland.
  • Wilson P; Department of Renal Medicine, University College London, London, UK.
  • Wong E; National Renal Complement Therapeutics Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Taylor CM; Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Nitsch D; UK Renal Registry, Bristol, UK; London School of Hygiene and Tropical Medicine, London, UK.
  • Saleem M; Translational Health Sciences, University of Bristol, Bristol, UK.
  • Bockenhauer D; Department of Renal Medicine, University College London, London, UK; Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Bramham K; National Registry of Rare Kidney Diseases, Bristol, UK; King's Health Partners, King's College London, London, UK.
  • Gale DP; National Registry of Rare Kidney Diseases, Bristol, UK; Department of Renal Medicine, University College London, London, UK; Department of Renal Medicine, Royal Free London NHS Foundation Trust, London, UK. Electronic address: d.gale@ucl.ac.uk.
Lancet ; 403(10433): 1279-1289, 2024 Mar 30.
Article em En | MEDLINE | ID: mdl-38492578
ABSTRACT

BACKGROUND:

Individuals with rare kidney diseases account for 5-10% of people with chronic kidney disease, but constitute more than 25% of patients receiving kidney replacement therapy. The National Registry of Rare Kidney Diseases (RaDaR) gathers longitudinal data from patients with these conditions, which we used to study disease progression and outcomes of death and kidney failure.

METHODS:

People aged 0-96 years living with 28 types of rare kidney diseases were recruited from 108 UK renal care facilities. The primary outcomes were cumulative incidence of mortality and kidney failure in individuals with rare kidney diseases, which were calculated and compared with that of unselected patients with chronic kidney disease. Cumulative incidence and Kaplan-Meier survival estimates were calculated for the following

outcomes:

median age at kidney failure; median age at death; time from start of dialysis to death; and time from diagnosis to estimated glomerular filtration rate (eGFR) thresholds, allowing calculation of time from last eGFR of 75 mL/min per 1·73 m2 or more to first eGFR of less than 30 mL/min per 1·73 m2 (the therapeutic trial window).

FINDINGS:

Between Jan 18, 2010, and July 25, 2022, 27 285 participants were recruited to RaDaR. Median follow-up time from diagnosis was 9·6 years (IQR 5·9-16·7). RaDaR participants had significantly higher 5-year cumulative incidence of kidney failure than 2·81 million UK patients with all-cause chronic kidney disease (28% vs 1%; p<0·0001), but better survival rates (standardised mortality ratio 0·42 [95% CI 0·32-0·52]; p<0·0001). Median age at kidney failure, median age at death, time from start of dialysis to death, time from diagnosis to eGFR thresholds, and therapeutic trial window all varied substantially between rare diseases.

INTERPRETATION:

Patients with rare kidney diseases differ from the general population of individuals with chronic kidney disease they have higher 5-year rates of kidney failure but higher survival than other patients with chronic kidney disease stages 3-5, and so are over-represented in the cohort of patients requiring kidney replacement therapy. Addressing unmet therapeutic need for patients with rare kidney diseases could have a large beneficial effect on long-term kidney replacement therapy demand.

FUNDING:

RaDaR is funded by the Medical Research Council, Kidney Research UK, Kidney Care UK, and the Polycystic Kidney Disease Charity.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Insuficiência Renal Crônica / Falência Renal Crônica Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Insuficiência Renal Crônica / Falência Renal Crônica Idioma: En Ano de publicação: 2024 Tipo de documento: Article