Associations with age and glomerular filtration rate in a referred population with chronic kidney disease: methods and baseline data from a UK multicentre cohort study (NURTuRE-CKD).


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
31 Oct 2023
Historique:
received: 12 02 2023
medline: 2 11 2023
pubmed: 26 5 2023
entrez: 25 5 2023
Statut: ppublish

Résumé

Chronic kidney disease (CKD) is common but heterogenous and is associated with multiple adverse outcomes. The National Unified Renal Translational Research Enterprise (NURTuRE)-CKD cohort was established to investigate risk factors for clinically important outcomes in persons with CKD referred to secondary care. Eligible participants with CKD stages G3-4 or stages G1-2 plus albuminuria >30 mg/mmol were enrolled from 16 nephrology centres in England, Scotland and Wales from 2017 to 2019. Baseline assessment included demographic data, routine laboratory data and research samples. Clinical outcomes are being collected over 15 years by the UK Renal Registry using established data linkage. Baseline data are presented with subgroup analysis by age, sex and estimated glomerular filtration rate (eGFR). A total of 2996 participants was enrolled. Median (interquartile range) age was 66 (54-74) years, eGFR 33.8 (24.0-46.6) mL/min/1.73 m2 and urine albumin to creatinine ratio 209 (33-926) mg/g; 58.5% were male. Of these participants, 1883 (69.1%) were in high-risk CKD categories. Primary renal diagnosis was CKD of unknown cause in 32.3%, glomerular disease in 23.4% and diabetic kidney disease in 11.5%. Older participants and those with lower eGFR had higher systolic blood pressure and were less likely to be treated with renin-angiotensin system inhibitors (RASi) but were more likely to receive a statin. Female participants were less likely to receive a RASi or statin. NURTuRE-CKD is a prospective cohort of persons who are at relatively high risk of adverse outcomes. Long-term follow-up and a large biorepository create opportunities for research to improve risk prediction and to investigate underlying mechanisms to inform new treatment development.

Sections du résumé

BACKGROUND BACKGROUND
Chronic kidney disease (CKD) is common but heterogenous and is associated with multiple adverse outcomes. The National Unified Renal Translational Research Enterprise (NURTuRE)-CKD cohort was established to investigate risk factors for clinically important outcomes in persons with CKD referred to secondary care.
METHODS METHODS
Eligible participants with CKD stages G3-4 or stages G1-2 plus albuminuria >30 mg/mmol were enrolled from 16 nephrology centres in England, Scotland and Wales from 2017 to 2019. Baseline assessment included demographic data, routine laboratory data and research samples. Clinical outcomes are being collected over 15 years by the UK Renal Registry using established data linkage. Baseline data are presented with subgroup analysis by age, sex and estimated glomerular filtration rate (eGFR).
RESULTS RESULTS
A total of 2996 participants was enrolled. Median (interquartile range) age was 66 (54-74) years, eGFR 33.8 (24.0-46.6) mL/min/1.73 m2 and urine albumin to creatinine ratio 209 (33-926) mg/g; 58.5% were male. Of these participants, 1883 (69.1%) were in high-risk CKD categories. Primary renal diagnosis was CKD of unknown cause in 32.3%, glomerular disease in 23.4% and diabetic kidney disease in 11.5%. Older participants and those with lower eGFR had higher systolic blood pressure and were less likely to be treated with renin-angiotensin system inhibitors (RASi) but were more likely to receive a statin. Female participants were less likely to receive a RASi or statin.
CONCLUSIONS CONCLUSIONS
NURTuRE-CKD is a prospective cohort of persons who are at relatively high risk of adverse outcomes. Long-term follow-up and a large biorepository create opportunities for research to improve risk prediction and to investigate underlying mechanisms to inform new treatment development.

Identifiants

pubmed: 37230953
pii: 7180015
doi: 10.1093/ndt/gfad110
pmc: PMC10615633
doi:

Substances chimiques

Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2617-2626

Subventions

Organisme : Medical Research Council
ID : MR/R013942/1
Pays : United Kingdom

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the ERA.

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Auteurs

Maarten W Taal (MW)

Centre for Kidney Research and Innovation, Academic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Renal Medicine, Royal Derby Hospital, University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.

Bethany Lucas (B)

Centre for Kidney Research and Innovation, Academic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Renal Medicine, Royal Derby Hospital, University Hospitals of Derby and Burton NHS Foundation Trust, Derby, UK.

Paul Roderick (P)

School of Primary Care, Population Sciences and Medical Education, Faculty of Medicine, University of Southampton, Southampton, UK.

Paul Cockwell (P)

Department of Renal Medicine, Queen Elizabeth Hospital, University Hospitals of Birmingham, Birmingham, UK.

David C Wheeler (DC)

University College London, London, UK.

Moin A Saleem (MA)

Bristol Renal and Children's Renal Unit, Bristol Medical School, University of Bristol, Bristol, UK.

Simon D S Fraser (SDS)

School of Primary Care, Population Sciences and Medical Education, Faculty of Medicine, University of Southampton, Southampton, UK.

Rosamonde E Banks (RE)

Leeds Institute of Medical Research at St James's, School of Medicine, University of Leeds, Leeds, UK.

Tim Johnson (T)

Experimental Renal Medicine, Human Metabolism and Oncology, The Medical School, University of Sheffield, Sheffield, UK.

Lorna J Hale (LJ)

UCB Pharma, Slough, UK.

Uwe Andag (U)

Evotec International GmbH, Göttingen, Germany.

Philipp Skroblin (P)

Evotec International GmbH, Göttingen, Germany.

Michaela Bayerlova (M)

Evotec International GmbH, Göttingen, Germany.

Robert Unwin (R)

AstraZeneca BioPharmaceuticals, Cambridge Biomedical Campus, Cambridge, UK.

Nicolas Vuilleumier (N)

Diagnostics Department, Laboratory Medicine Division, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

Rodolphe Dusaulcy (R)

Diagnostics Department, Laboratory Medicine Division, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

Fiona Robertson (F)

Centre for Kidney Research and Innovation, Academic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.

Elizabeth Colby (E)

Bristol Renal and Children's Renal Unit, Bristol Medical School, University of Bristol, Bristol, UK.

David Pitcher (D)

United Kingdom Renal Registry, Bristol, UK.

Fiona Braddon (F)

United Kingdom Renal Registry, Bristol, UK.

Melissa Benavente (M)

Centre for Kidney Research and Innovation, Academic Unit for Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.

Elaine Davies (E)

Kidney Research UK, Peterborough, UK.

Michael Nation (M)

Kidney Research UK, Peterborough, UK.

Philip A Kalra (PA)

Renal Services, Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust, Salford, UK.

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Classifications MeSH