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Ethnic differences in 25-year risk of incident chronic kidney disease among people with type 2 diabetes in New Zealand

Orr-Walker, BJ; Yu, D; Wang, Z; Cai, Y; Osuagwu, UL; Pickering, K; Baker, J; Cutfield, R; Sundborn, G; Jayanatha, K; Zhao, Z; Simmons, D

Ethnic differences in 25-year risk of incident chronic kidney disease among people with type 2 diabetes in New Zealand Thumbnail


Authors

BJ Orr-Walker

Z Wang

Y Cai

UL Osuagwu

K Pickering

J Baker

R Cutfield

G Sundborn

K Jayanatha

Z Zhao

D Simmons



Abstract

INTRODUCTION: Insights into ethnic differences in the natural history of chronic kidney disease (CKD) among people with type 2 diabetes mellitus (T2DM) might inform clinical strategies to address disparities in hospitalization and mortality. Risks of CKD II-V stages over a 25-year period between New Zealand Europeans (NZEs), Maori and Pasifika, and with T2DM in Auckland, New Zealand (NZ) were compared. RESEARCH DESIGN AND METHODS: As a primary care audit program in Auckland, the Diabetes Care Support Service was linked with national registration databases. People with existing CKD II-V were ruled out. To balance potential confounders, we applied a tapered matching method . 'Quasi-trial'-matched cohorts were set up separately between Maori and NZE and between Pasifika and NZE. Ethnic population differences in risk of any and each stage of CKD over 1994-2018 were examined by weighted Cox regression model. RESULTS: The HRs for developing any CKD, CKD stages II-V for Maori (n=2215) versus NZE (n=2028) were 1.18 (95% CI 0.99 to 1.41), 1.10 (95% CI 0.91 to 1.32), 1.70 (95% CI 1.19 to 2.43), 3.93 (95% CI 2.16 to 7.14), and 3.74 (95% CI 1.74 to 8.05), respectively. Compared with NZE (n=2474), the HRs for developing any CKD, CKD stages II-V for Pasifika (n=3101) were 1.31 (95% CI 1.09 to 1.57), 1.26 (95% CI 1.05 to 1.52), 1.71 (95% CI 1.14 to 2.57), 3.75 (95% CI 1.40 to 10.05), and 4.96 (95% CI 1.56 to 15.75), respectively. CONCLUSIONS: Among people with T2DM in NZ, significant ethnic differences exist in the risk of progressing to each stage of CKD (stage V in particular). Mechanism studies underlying these differences, as well as the need for identification of biomarkers to predict the early onset renal lesion, are warranted.

Journal Article Type Article
Acceptance Date Oct 14, 2022
Publication Date Dec 15, 2022
Publicly Available Date May 30, 2023
Journal BMJ Open Diabetes Research & Care
Publisher BMJ Publishing Group
DOI https://doi.org/10.1136/bmjdrc-2022-003077
Keywords Type 2 Diabetes; Ethnic Groups; Kidney Failure; Chronic; Cohort Studies
Publisher URL https://drc.bmj.com/content/10/6/e003077
Additional Information © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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