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Elevation of circulating TNF receptors 1 and 2 increases the risk of end-stage renal disease in American Indians with type 2 diabetes
In Caucasians with type 2 diabetes, circulating TNF receptors 1 (TNFR1) and 2 (TNFR2) predict end-stage renal disease (ESRD). Here we examined this relationship in a longitudinal cohort study of American Indians with type 2 diabetes with measured glomerular filtration rate (mGFR, iothalamate) and ur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382420/ https://www.ncbi.nlm.nih.gov/pubmed/25272234 http://dx.doi.org/10.1038/ki.2014.330 |
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author | PAVKOV, MEDA E. NELSON, ROBERT G. KNOWLER, WILLIAM C. CHENG, YILING KROLEWSKI, ANDRZEJ S. NIEWCZAS, MONIKA A. |
author_facet | PAVKOV, MEDA E. NELSON, ROBERT G. KNOWLER, WILLIAM C. CHENG, YILING KROLEWSKI, ANDRZEJ S. NIEWCZAS, MONIKA A. |
author_sort | PAVKOV, MEDA E. |
collection | PubMed |
description | In Caucasians with type 2 diabetes, circulating TNF receptors 1 (TNFR1) and 2 (TNFR2) predict end-stage renal disease (ESRD). Here we examined this relationship in a longitudinal cohort study of American Indians with type 2 diabetes with measured glomerular filtration rate (mGFR, iothalamate) and urinary albumin-to-creatinine ratio. ESRD was defined as dialysis, kidney transplant, or death attributed to diabetic kidney disease. Age-gender-adjusted incidence rates and incidence rate ratios of ESRD were computed by Mantel-Haenszel stratification. The hazard ratio of ESRD was assessed per interquartile range increase in the distribution of each TNFR after adjusting for baseline age, gender, mean blood pressure, HbA1c, albumin-to-creatinine ratio, and mGFR. Among the 193 participants, 62 developed ESRD and 25 died without ESRD during a median follow-up of 9.5 years. The age-gender-adjusted incidence rate ratio of ESRD was higher among participants in the highest vs. lowest quartile for TNFR1 (6.6, 95% CI 3.3–13.3) or TNFR2 (8.8, 95% CI 4.3–18.0). In the fully adjusted model, the risk of ESRD per interquartile range increase was 1.6 times (95% CI 1.1–2.2) as high for TNFR1 and 1.7 times (95% CI 1.2–2.3) as high for TNFR2. Thus, elevated serum concentrations of TNFR1 or TNFR2 are associated with increased risk of ESRD in American Indians with type 2 diabetes after accounting for traditional risk factors including albumin-to-creatinine ratio and mGFR |
format | Online Article Text |
id | pubmed-4382420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43824202015-10-01 Elevation of circulating TNF receptors 1 and 2 increases the risk of end-stage renal disease in American Indians with type 2 diabetes PAVKOV, MEDA E. NELSON, ROBERT G. KNOWLER, WILLIAM C. CHENG, YILING KROLEWSKI, ANDRZEJ S. NIEWCZAS, MONIKA A. Kidney Int Article In Caucasians with type 2 diabetes, circulating TNF receptors 1 (TNFR1) and 2 (TNFR2) predict end-stage renal disease (ESRD). Here we examined this relationship in a longitudinal cohort study of American Indians with type 2 diabetes with measured glomerular filtration rate (mGFR, iothalamate) and urinary albumin-to-creatinine ratio. ESRD was defined as dialysis, kidney transplant, or death attributed to diabetic kidney disease. Age-gender-adjusted incidence rates and incidence rate ratios of ESRD were computed by Mantel-Haenszel stratification. The hazard ratio of ESRD was assessed per interquartile range increase in the distribution of each TNFR after adjusting for baseline age, gender, mean blood pressure, HbA1c, albumin-to-creatinine ratio, and mGFR. Among the 193 participants, 62 developed ESRD and 25 died without ESRD during a median follow-up of 9.5 years. The age-gender-adjusted incidence rate ratio of ESRD was higher among participants in the highest vs. lowest quartile for TNFR1 (6.6, 95% CI 3.3–13.3) or TNFR2 (8.8, 95% CI 4.3–18.0). In the fully adjusted model, the risk of ESRD per interquartile range increase was 1.6 times (95% CI 1.1–2.2) as high for TNFR1 and 1.7 times (95% CI 1.2–2.3) as high for TNFR2. Thus, elevated serum concentrations of TNFR1 or TNFR2 are associated with increased risk of ESRD in American Indians with type 2 diabetes after accounting for traditional risk factors including albumin-to-creatinine ratio and mGFR 2014-10-01 2015-04 /pmc/articles/PMC4382420/ /pubmed/25272234 http://dx.doi.org/10.1038/ki.2014.330 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article PAVKOV, MEDA E. NELSON, ROBERT G. KNOWLER, WILLIAM C. CHENG, YILING KROLEWSKI, ANDRZEJ S. NIEWCZAS, MONIKA A. Elevation of circulating TNF receptors 1 and 2 increases the risk of end-stage renal disease in American Indians with type 2 diabetes |
title | Elevation of circulating TNF receptors 1 and 2 increases the risk of
end-stage renal disease in American Indians with type 2 diabetes |
title_full | Elevation of circulating TNF receptors 1 and 2 increases the risk of
end-stage renal disease in American Indians with type 2 diabetes |
title_fullStr | Elevation of circulating TNF receptors 1 and 2 increases the risk of
end-stage renal disease in American Indians with type 2 diabetes |
title_full_unstemmed | Elevation of circulating TNF receptors 1 and 2 increases the risk of
end-stage renal disease in American Indians with type 2 diabetes |
title_short | Elevation of circulating TNF receptors 1 and 2 increases the risk of
end-stage renal disease in American Indians with type 2 diabetes |
title_sort | elevation of circulating tnf receptors 1 and 2 increases the risk of
end-stage renal disease in american indians with type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382420/ https://www.ncbi.nlm.nih.gov/pubmed/25272234 http://dx.doi.org/10.1038/ki.2014.330 |
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