Please use this identifier to cite or link to this item: http://docs.prosentient.com.au/prosentientjspui/handle/1/10595
Title: High Baseline Levels of Tumor Necrosis Factor Receptor 1 Are Associated With Progression of Kidney Disease in Indigenous Australians With Diabetes: The eGFR Follow-up Study.
Authors: Barr, Elizabeth L M
Barzi, Federica
Hughes, Jaquelyne T
Jerums, George
Hoy, Wendy E
O'Dea, Kerin
Jones, Graham R D
Lawton, Paul D
Brown, Alex D H
Thomas, Mark
Ekinci, Elif I
Sinha, Ashim
Cass, Alan
MacIsaac, Richard J
Maple-Brown, Louise J
Affiliation: Menzies School of Health Research, Darwin, Northern Territory, Australia elizabeth.barr@menzies.edu.au.. Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia.. Royal Darwin Hospital, Darwin, Northern Territory, Australia..
Department of Endocrinology, Austin Health, Melbourne, Victoria, Australia.. Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia..
The University of Queensland, Brisbane, Queensland, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia.. Nutrition and Population Health, University of South Australia, Adelaide, South Australia, Australia..
SydPath, St Vincent's Hospital Sydney, Sydney, New South Wales, Australia.. Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia..
Aboriginal Health, Sansom Institute for Health Research, University of South Australia, Adelaide, South Australia, Australia.. Indigenous Health, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia..
Royal Perth Hospital, Perth, Western Australia, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia.. Department of Endocrinology, Austin Health, Melbourne, Victoria, Australia.. Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia..
Diabetes and Endocrinology, Cairns Base Hospital, Cairns, Queensland, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia..
Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.. Department of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia..
Menzies School of Health Research, Darwin, Northern Territory, Australia.. Royal Darwin Hospital, Darwin, Northern Territory, Australia..
Issue Date: Apr-2018
Citation: Diabetes care 2018-04; 41(4): 739-747
Abstract: To examine the association between soluble tumor necrosis factor receptor 1 (sTNFR1) levels and kidney disease progression in Indigenous Australians at high risk of kidney disease. This longitudinal observational study examined participants aged ≥18 years recruited from >20 sites across diabetes and/or kidney function strata. Baseline measures included sTNFR1, serum creatinine, urine albumin-to-creatinine ratio (uACR), HbA1c, C-reactive protein (CRP), waist-to-hip ratio, systolic blood pressure, and medical history. Linear regression was used to estimate annual change in estimated glomerular filtration rate (eGFR) for increasing sTNFR1, and Cox proportional hazards were used to estimate the hazard ratio (HR) and 95% CI for developing a combined renal outcome (first of a ≥30% decline in eGFR with a follow-up eGFR <60 mL/min/1.73 m2, progression to renal replacement therapy, or renal death) for increasing sTNFR1. Over a median of 3 years, participants with diabetes (n = 194) in the highest compared with the lowest quartile of sTNFR1 experienced significantly greater eGFR decline (-4.22 mL/min/1.73 m2/year [95% CI -7.06 to -1.38]; P = 0.004), independent of baseline age, sex, eGFR, and uACR. The adjusted HR (95% CI) for participants with diabetes per doubling of sTNFR1 for the combined renal outcome (n = 32) was 3.8 (1.1-12.8; P = 0.03). No association between sTNFR1 and either renal outcome was observed for those without diabetes (n = 259). sTNFR1 is associated with greater kidney disease progression independent of albuminuria and eGFR in Indigenous Australians with diabetes. Further research is required to assess whether TNFR1 operates independently of other metabolic factors associated with kidney disease progression.
URI: http://docs.prosentient.com.au/prosentientjspui/handle/1/10595
DOI: 10.2337/dc17-1919
ORCID: http://orcid.org/0000-0003-4284-1716
http://orcid.org/0000-0003-2372-395X
http://orcid.org/0000-0001-8058-6977
Type: Journal Article
Appears in Collections:NT Health digital library

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