Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort
| Title: | Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort |
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| Authors: | Wong K; Pitcher D; Braddon F; Downward L; Steenkamp R; Masoud S; Annear N; Barratt J; Bingham C; Coward RJ; Chrysochou T; 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; Thomas K; Turner AN; Walsh SB; Waters A; Wilson P; Wong E; Sy KTL; Huang K; Ye J; Nitsch D; Saleem M; Bockenhauer D; Bramham K; Gale DP; Abat S; Adalat S; Agbonmwandolor J; Ahmad Z; Alejmi A; Almasarwah R; Asgari E; Ayers A; Baharani J; Balasubramaniam G; Kpodo FJ-B; Bansal T; Barratt A; Bates M; Bayne N; Bendle J; Benyon S; Bergmann C; Bhandari S; Boddana P; Bond S; Branson A; Brearey S; Brocklebank V; Budwal S; Byrne C; Cairns H; Camilleri B; Campbell G; Capell A; Carmody M; Carson M; Cathcart T; Catley C; Cesar K; Chan M; Chea H; Chess J; Cheung CK; Chick K-J; Chitalia N; Christian M; Clark K; Clayton C; Clissold R; Cockerill H; Coelho J; Colby E; Colclough V; Conway E; Cook HT; Cook W; Cooper T; Crosbie S; Cserep G; Date A; Davidson K; Davies A; Dhaun N; Dhaygude A; Diskin L; Dixit A; Doctolero EA; Dorey S; Downard L; Drayson M; Dreyer G; Dutt T; Etuk K; Evans D; Finch J; Flinter F; Fotheringham J; Francis L; Gallagher H; Garcia EL; Gavrila M; Gear S; Geddes C; Gilchrist M; Gittus M; Goggolidou P; Goldsmith C; Gooden P; Goodlife A; Goodwin P; Grammatikopoulos T; Gray B; Griffith M; Gumus S; Gupta S; Hamilton P; Harper L; Harris T; Haskell L; Hayward S; Hegde S; Hendry B; Hewins S; Hewitson N; Hillman K; Hiremath M; Howson A; Htet Z; Huish S; Hull R; Humphries A; Hunt DPJ; Hunter K; Hunter S; Ijeomah-Orji M; Inston N; Jayne D; Jenfa G; Jenkins A; Jones CA; Jones C; Jones A; Jones R; Kamesh L; Frankl FK; Karim M; Kaur A; Kearley K; Khwaja A; King G; Kislowska E; Klata E; Kokocinska M; Lambie M; Lawless L; Ledson T; Lennon R; Levine AP; Maggie Lai LW; Lipkin G; Lovitt G; Lyons P; Mabillard H; Mackintosh K; Mahdi K; Maher E; Marchbank KJ; Mark PB; Masunda B; Mavani Z; Mayfair J; McAdoo S; Mckinnell J; Melhem N; Meyrick S; Morgan P; Morgan A; Muhammad F; Murray S; Novobritskaya K; Ong AC; Oni L; Osmaston K; Padmanabhan N; Parkes S; Patrick J; Pattison J; Paul R; Percival R; Perkins SJ; Persu A; Petchey WG; Pickering MC; Plumb L; Plummer Z; Popoola J; Post F; Power A; Pratt G; Pusey C; Rabara R; Rabuya M; Raju T; Javier C; Roberts IS; Roufosse C; Rumjon A; Salama A; Sandford RN; Sandu KS; Sarween N; Sebire N; Selvaskandan H; Shah S; Sharma A; Sharples EJ; Sheerin N; Shetty H; Shroff R; Sinha M; Smith K; Smith L; Stott I; Stroud K; Swift P; Szklarzewicz J; Tam F; Tan K; Taylor R; Tischkowitz M; Tse Y; Turnbull A; Tyerman K; Usher M; Venkat-Raman G; Walker A; Watt A; Webster P; Wechalekar A; Welsh GI; West N; Wheeler D; Wiles K; Willcocks L; Williams A; Williams E; Williams K; Wilson DH; Wilson PD; Winyard P; Wood G; Woodward E; Woodward L; Woolf A; Wright D |
| Source: | Kidney International Reports, 2024 |
| Publisher Information: | Elsevier Inc. |
| Publication Year: | 2024 |
| Collection: | Newcastle University Library ePrints Service |
| Description: | © 2024. Introduction: The National Registry of Rare Kidney Diseases (RaDaR) collects data from people living with rare kidney diseases across the UK, and is the world's largest, rare kidney disease registry. We present the clinical demographics and renal function of 25,880 prevalent patients and sought evidence of bias in recruitment to RaDaR. Methods: RaDaR is linked with the UK Renal Registry (UKRR, with which all UK patients receiving kidney replacement therapy [KRT] are registered). We assessed ethnicity and socioeconomic status in the following: (i) prevalent RaDaR patients receiving KRT compared with patients with eligible rare disease diagnoses receiving KRT in the UKRR, (ii) patients recruited to RaDaR compared with all eligible unrecruited patients at 2 renal centers, and (iii) the age-stratified ethnicity distribution of RaDaR patients with autosomal dominant polycystic kidney disease (ADPKD) was compared to that of the English census. Results: We found evidence of disparities in ethnicity and social deprivation in recruitment to RaDaR; however, these were not consistent across comparisons. Compared with either adults recruited to RaDaR or the English population, children recruited to RaDaR were more likely to be of Asian ethnicity (17.3% vs. 7.5%, P-value < 0.0001) and live in more socially deprived areas (30.3% vs. 17.3% in the most deprived Index of Multiple Deprivation (IMD) quintile, P-value < 0.0001). Conclusion: We observed no evidence of systematic biases in recruitment of patients into RaDaR; however, the data provide empirical evidence of negative economic and social consequences (across all ethnicities) experienced by families with children affected by rare kidney diseases. |
| Document Type: | article in journal/newspaper |
| File Description: | application/pdf |
| Language: | unknown |
| Relation: | https://eprints.ncl.ac.uk/298986; https://eprints.ncl.ac.uk/fulltext.aspx?url=298986/B19C71D2-0CCE-4ED2-9632-CCADEE5EF5B1.pdf&pub_id=298986 |
| Availability: | https://eprints.ncl.ac.uk/298986 |
| Rights: | https://creativecommons.org/licenses/by/4.0/ |
| Accession Number: | edsbas.BFB5B049 |
| Database: | BASE |