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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.

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    Author
    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
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    Publication date
    2024-03-13
    Subject
    Nephrology/Renal medicine
    
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    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.
    Citation
    Wong K, Pitcher D, Braddon F, Downward L, Steenkamp R, Annear N, Barratt J, Bingham C, Chrysochou C, Coward RJ, Game D, Griffin S, Hall M, Johnson S, Kanigicherla D, Karet Frankl F, Kavanagh D, Kerecuk L, Maher ER, Moochhala S, Pinney J, Sayer JA, Simms R, Sinha S, Srivastava S, Tam FWK, Turner AN, Walsh SB, Waters A, Wilson P, Wong E, Taylor CM, Nitsch D, Saleem M, Bockenhauer D, Bramham K, Gale DP; RaDaR consortium. Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort. Lancet. 2024 Mar 30;403(10433):1279-1289. doi: 10.1016/S0140-6736(23)02843-X. Epub 2024 Mar 13.
    Type
    Article
    Handle
    http://hdl.handle.net/20.500.14200/4417
    Additional Links
    http://www.sciencedirect.com/science/journal/01406736
    DOI
    10.1016/S0140-6736(23)02843-X
    PMID
    38492578
    Journal
    The Lancet
    Publisher
    Elsevier
    ae974a485f413a2113503eed53cd6c53
    10.1016/S0140-6736(23)02843-X
    Scopus Count
    Collections
    Renal

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