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Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4

Type 2 diabetes (T2D)-associated end-stage kidney disease (ESKD) is a global burden, while the renoprotective effects of metformin remain controversial. In a population-based cohort (2002–2018) including 96,643 patients with T2D observed for 0.7 million person-years, we estimated the risk associatio...

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Autores principales: Yang, Aimin, Lau, Eric S. H., Wu, Hongjiang, Ma, Ronald C. W., Kong, Alice P. S., So, Wing Yee, Luk, Andrea O. Y., Fu, Amy W. C., Chan, Juliana C. N., Chow, Elaine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505840/
https://www.ncbi.nlm.nih.gov/pubmed/36145361
http://dx.doi.org/10.3390/ph15091140
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author Yang, Aimin
Lau, Eric S. H.
Wu, Hongjiang
Ma, Ronald C. W.
Kong, Alice P. S.
So, Wing Yee
Luk, Andrea O. Y.
Fu, Amy W. C.
Chan, Juliana C. N.
Chow, Elaine
author_facet Yang, Aimin
Lau, Eric S. H.
Wu, Hongjiang
Ma, Ronald C. W.
Kong, Alice P. S.
So, Wing Yee
Luk, Andrea O. Y.
Fu, Amy W. C.
Chan, Juliana C. N.
Chow, Elaine
author_sort Yang, Aimin
collection PubMed
description Type 2 diabetes (T2D)-associated end-stage kidney disease (ESKD) is a global burden, while the renoprotective effects of metformin remain controversial. In a population-based cohort (2002–2018) including 96,643 patients with T2D observed for 0.7 million person-years, we estimated the risk association of metformin and its dose-relationship with ESKD in a propensity-score overlap-weighting (PS-OW) cohort by eGFR categories. Amongst 96,643, 83,881 (86.8%) had eGFR-G1/G2 (≥60 mL/min/1.73 m(2)), 8762 (9.1%) had eGFR-G3a (≥45–60 mL/min/1.73 m(2)), 3051 (3.2%) had eGFR-G3b (≥30–45 mL/min/1.73 m(2)), and 949 (1.0%) had eGFR-G4 (≥15–30 mL/min/1.73 m(2)). The respective proportions of metformin users in these eGFR categories were 95.1%, 81.9%, 53.8%, and 20.8%. In the PS-OW cohort with 88,771 new-metformin and 7872 other oral glucose-lowering-drugs (OGLDs) users, the respective incidence rates of ESKD were 2.8 versus 22.4/1000 person-years. Metformin use associated with reduced risk of ESKD (hazard ratio (HR) = 0.43 [95% CI: 0.35–0.52] in eGFR-G1/G2, 0.64 [0.52–0.79] in eGFR-G3a, 0.67 [0.56–0.80] in eGFR-G3b, and 0.63 [0.48–0.83] in eGFR-G4). Metformin use was associated with reduced or neutral risk of major adverse cardiovascular events (MACE) (7.2 versus 16.0/1000 person-years) and all-cause mortality (14.6 versus 65.1/1000 person-years). Time-weighted mean daily metformin dose was 1000 mg in eGFR-G1/G2, 850 mg in eGFR-G3a, 650 mg in eGFR-G3b, and 500 mg in eGFR-G4. In a subcohort of 14,766 patients observed for 0.1 million person-years, the respective incidence rates of lactic acidosis and HR in metformin users and non-users were 42.5 versus 226.4 events/100,000 person-years (p = 0.03) for eGFR-G1/G2 (HR = 0.57, 0.25–1.30) and 54.5 versus 300.6 events/100,000 person-years (p = 0.01) for eGFR-G3/G4 (HR = 0.49, 0.19–1.30). These real-world data underscore the major benefits and low risk of lactic acidosis with metformin use down to an eGFR of 30 mL/min/1.73 m(2) and possibly even 15 mL/min/1.73 m(2), while reinforcing the importance of dose adjustment and frequent monitoring of eGFR.
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spelling pubmed-95058402022-09-24 Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4 Yang, Aimin Lau, Eric S. H. Wu, Hongjiang Ma, Ronald C. W. Kong, Alice P. S. So, Wing Yee Luk, Andrea O. Y. Fu, Amy W. C. Chan, Juliana C. N. Chow, Elaine Pharmaceuticals (Basel) Article Type 2 diabetes (T2D)-associated end-stage kidney disease (ESKD) is a global burden, while the renoprotective effects of metformin remain controversial. In a population-based cohort (2002–2018) including 96,643 patients with T2D observed for 0.7 million person-years, we estimated the risk association of metformin and its dose-relationship with ESKD in a propensity-score overlap-weighting (PS-OW) cohort by eGFR categories. Amongst 96,643, 83,881 (86.8%) had eGFR-G1/G2 (≥60 mL/min/1.73 m(2)), 8762 (9.1%) had eGFR-G3a (≥45–60 mL/min/1.73 m(2)), 3051 (3.2%) had eGFR-G3b (≥30–45 mL/min/1.73 m(2)), and 949 (1.0%) had eGFR-G4 (≥15–30 mL/min/1.73 m(2)). The respective proportions of metformin users in these eGFR categories were 95.1%, 81.9%, 53.8%, and 20.8%. In the PS-OW cohort with 88,771 new-metformin and 7872 other oral glucose-lowering-drugs (OGLDs) users, the respective incidence rates of ESKD were 2.8 versus 22.4/1000 person-years. Metformin use associated with reduced risk of ESKD (hazard ratio (HR) = 0.43 [95% CI: 0.35–0.52] in eGFR-G1/G2, 0.64 [0.52–0.79] in eGFR-G3a, 0.67 [0.56–0.80] in eGFR-G3b, and 0.63 [0.48–0.83] in eGFR-G4). Metformin use was associated with reduced or neutral risk of major adverse cardiovascular events (MACE) (7.2 versus 16.0/1000 person-years) and all-cause mortality (14.6 versus 65.1/1000 person-years). Time-weighted mean daily metformin dose was 1000 mg in eGFR-G1/G2, 850 mg in eGFR-G3a, 650 mg in eGFR-G3b, and 500 mg in eGFR-G4. In a subcohort of 14,766 patients observed for 0.1 million person-years, the respective incidence rates of lactic acidosis and HR in metformin users and non-users were 42.5 versus 226.4 events/100,000 person-years (p = 0.03) for eGFR-G1/G2 (HR = 0.57, 0.25–1.30) and 54.5 versus 300.6 events/100,000 person-years (p = 0.01) for eGFR-G3/G4 (HR = 0.49, 0.19–1.30). These real-world data underscore the major benefits and low risk of lactic acidosis with metformin use down to an eGFR of 30 mL/min/1.73 m(2) and possibly even 15 mL/min/1.73 m(2), while reinforcing the importance of dose adjustment and frequent monitoring of eGFR. MDPI 2022-09-13 /pmc/articles/PMC9505840/ /pubmed/36145361 http://dx.doi.org/10.3390/ph15091140 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Aimin
Lau, Eric S. H.
Wu, Hongjiang
Ma, Ronald C. W.
Kong, Alice P. S.
So, Wing Yee
Luk, Andrea O. Y.
Fu, Amy W. C.
Chan, Juliana C. N.
Chow, Elaine
Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title_full Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title_fullStr Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title_full_unstemmed Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title_short Attenuated Risk Association of End-Stage Kidney Disease with Metformin in Type 2 Diabetes with eGFR Categories 1–4
title_sort attenuated risk association of end-stage kidney disease with metformin in type 2 diabetes with egfr categories 1–4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505840/
https://www.ncbi.nlm.nih.gov/pubmed/36145361
http://dx.doi.org/10.3390/ph15091140
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