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Change in GFR over time in the Oxford renal cohort study

Change in GFR over time in the Oxford renal cohort study
Change in GFR over time in the Oxford renal cohort study
Background: Decline in kidney function can result in adverse health outcomes. The OxREN study has detailed baseline assessments from 884 participants ≥60 years. Aim: To determine the proportion of participants with decline in estimated glomerular filtration rate (eGFR), identify determinants of decline and determine proportions with chronic kidney disease (CKD) remission. Design and setting: Observational cohort study in UK primary care. Methods: Data were used from baseline and annual follow-up assessments to monitor change in kidney function. Rapid eGFR decline was defined as eGFR decrease >5 ml/min/1.73m2/year, improvement as eGFR increase >5ml/min/1.73m2/year and remission in those with CKD at baseline and eGFR>60 ml/min/1.73m2 during follow-up. Cox proportional hazard models were used to identify factors associated with eGFR decline. Results: In 686 participants with a median follow-up of 2.1 years, 164 (24%) evidenced rapid GFR decline, 185 (27%) experienced eGFR improvement and 82 of 394 (21%) meeting CKD stage 1-4 at baseline experienced remission. In the multivariable analysis, smoking status, higher systolic blood pressure and being known to have CKD at cohort entry were associated with rapid GFR decline. Those with CKD stage 3 at baseline were less likely to exhibit GFR decline compared with normal kidney function. Conclusions: This study established that 24% of people evidenced rapid GFR decline whereas 21% evidenced remission of CKD. People at risk of rapid GFR decline may benefit from closer monitoring and appropriate treatment to minimise risks of adverse outcomes, though only a small proportion meet the NICE criteria for referral to secondary care.
0960-1643
Hirst, Jennifer A
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Taal, Maarten W.
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Fraser, Simon
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Ordonez-Mena, Jose M.
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O'Callaghan, Chris
bdd99260-83bd-4ac1-9126-4f4c28372b40
McManus, R
d513fe52-aa42-422e-96d8-ae488a137e34
Taylor, CJ
008b4656-6e4f-4ca6-8e43-a6fcb83b98ae
Yang, Y
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Ogburn, Emma
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Hobbs, F.D.R.
ed141f5b-6bb8-49d5-ba3f-833ff8176556
Hirst, Jennifer A
29a62463-4d10-4617-b3cc-6cab2deab9e9
Taal, Maarten W.
10eeea62-a2fc-43b6-b5af-359e75c501ea
Fraser, Simon
135884b6-8737-4e8a-a98c-5d803ac7a2dc
Ordonez-Mena, Jose M.
44068755-83c7-4c44-9528-8441939dbe70
O'Callaghan, Chris
bdd99260-83bd-4ac1-9126-4f4c28372b40
McManus, R
d513fe52-aa42-422e-96d8-ae488a137e34
Taylor, CJ
008b4656-6e4f-4ca6-8e43-a6fcb83b98ae
Yang, Y
a279150b-c956-4e2a-8916-559dd3291d18
Ogburn, Emma
845b3de0-0ca0-46e5-acce-7c3ad58e1958
Hobbs, F.D.R.
ed141f5b-6bb8-49d5-ba3f-833ff8176556

Hirst, Jennifer A, Taal, Maarten W., Fraser, Simon, Ordonez-Mena, Jose M., O'Callaghan, Chris, McManus, R, Taylor, CJ, Yang, Y, Ogburn, Emma and Hobbs, F.D.R. (2021) Change in GFR over time in the Oxford renal cohort study. British Journal of General Practice. (doi:10.3399/BJGP.2021.0477).

Record type: Article

Abstract

Background: Decline in kidney function can result in adverse health outcomes. The OxREN study has detailed baseline assessments from 884 participants ≥60 years. Aim: To determine the proportion of participants with decline in estimated glomerular filtration rate (eGFR), identify determinants of decline and determine proportions with chronic kidney disease (CKD) remission. Design and setting: Observational cohort study in UK primary care. Methods: Data were used from baseline and annual follow-up assessments to monitor change in kidney function. Rapid eGFR decline was defined as eGFR decrease >5 ml/min/1.73m2/year, improvement as eGFR increase >5ml/min/1.73m2/year and remission in those with CKD at baseline and eGFR>60 ml/min/1.73m2 during follow-up. Cox proportional hazard models were used to identify factors associated with eGFR decline. Results: In 686 participants with a median follow-up of 2.1 years, 164 (24%) evidenced rapid GFR decline, 185 (27%) experienced eGFR improvement and 82 of 394 (21%) meeting CKD stage 1-4 at baseline experienced remission. In the multivariable analysis, smoking status, higher systolic blood pressure and being known to have CKD at cohort entry were associated with rapid GFR decline. Those with CKD stage 3 at baseline were less likely to exhibit GFR decline compared with normal kidney function. Conclusions: This study established that 24% of people evidenced rapid GFR decline whereas 21% evidenced remission of CKD. People at risk of rapid GFR decline may benefit from closer monitoring and appropriate treatment to minimise risks of adverse outcomes, though only a small proportion meet the NICE criteria for referral to secondary care.

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Accepted version BJGP_OxRen -progression of CKD - Accepted Manuscript
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Submitted date: 1 November 2021
Accepted/In Press date: 3 November 2021
Published date: 23 December 2021
Additional Information: This is the full-length article (published online 22 Feb 2022) of an abridged version published in print. Cite this version as: Br J Gen Pract 2022; DOI: https://doi.org/10.3399/BJGP.2021.0477 Funding The research was funded/supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, or the Department of Health and Social Care. Jennifer A Hirst and José M Ordóñez Mena are funded by the NIHR BRC, Oxford. Clare J Taylor is funded by an NIHR Academic Clinical Lectureship. FD Richard Hobbs acknowledges part- support from the NIHR Applied Research Collaboration Oxford Thames Valley, and the NIHR Oxford Biomedical Research Centre (OUHT BRC). Richard J McManus acknowledges part-support from the NIHR Collaboration for Leadership in Applied Research in Health and Care Oxford.

Identifiers

Local EPrints ID: 453312
URI: http://eprints.soton.ac.uk/id/eprint/453312
ISSN: 0960-1643
PURE UUID: 799753eb-ef1c-4c9e-ae26-53e903c603b0
ORCID for Simon Fraser: ORCID iD orcid.org/0000-0002-4172-4406

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Date deposited: 12 Jan 2022 17:40
Last modified: 17 Mar 2024 07:02

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Contributors

Author: Jennifer A Hirst
Author: Maarten W. Taal
Author: Simon Fraser ORCID iD
Author: Jose M. Ordonez-Mena
Author: Chris O'Callaghan
Author: R McManus
Author: CJ Taylor
Author: Y Yang
Author: Emma Ogburn
Author: F.D.R. Hobbs

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