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Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study

OBJECTIVE: Although low HDL cholesterol (HDL-C) is an established risk factor for atherosclerosis, data on HDL-C and the risk of microvascular disease are limited. We tested the association between HDL-C and microvascular disease in a cohort of patients with type 2 diabetes. RESEARCH DESIGN AND METH...

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Autores principales: Morton, Jamie, Zoungas, Sophia, Li, Qiang, Patel, Anushka A., Chalmers, John, Woodward, Mark, Celermajer, David S., Beulens, Joline W.J., Stolk, Ronald P., Glasziou, Paul, Ng, Martin K.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476889/
https://www.ncbi.nlm.nih.gov/pubmed/22891258
http://dx.doi.org/10.2337/dc12-0306
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author Morton, Jamie
Zoungas, Sophia
Li, Qiang
Patel, Anushka A.
Chalmers, John
Woodward, Mark
Celermajer, David S.
Beulens, Joline W.J.
Stolk, Ronald P.
Glasziou, Paul
Ng, Martin K.C.
author_facet Morton, Jamie
Zoungas, Sophia
Li, Qiang
Patel, Anushka A.
Chalmers, John
Woodward, Mark
Celermajer, David S.
Beulens, Joline W.J.
Stolk, Ronald P.
Glasziou, Paul
Ng, Martin K.C.
author_sort Morton, Jamie
collection PubMed
description OBJECTIVE: Although low HDL cholesterol (HDL-C) is an established risk factor for atherosclerosis, data on HDL-C and the risk of microvascular disease are limited. We tested the association between HDL-C and microvascular disease in a cohort of patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: A total of 11,140 patients with type 2 diabetes and at least one additional vascular risk factor were followed a median of 5 years. Cox proportional hazards models were used to assess the association between baseline HDL-C and the development of new or worsening microvascular disease, defined prospectively as a composite of renal and retinal events. RESULTS: The mean baseline HDL-C level was 1.3 mmol/L (SD 0.45 mmol/L [range 0.1–4.0]). During follow-up, 32% of patients developed new or worsening microvascular disease, with 28% experiencing a renal event and 6% a retinal event. Compared with patients in the highest third, those in the lowest third had a 17% higher risk of microvascular disease (adjusted hazard ratio 1.17 [95% CI 1.06–1.28], P = 0.001) after adjustment for potential confounders and regression dilution. This was driven by a 19% higher risk of renal events (1.19 [1.08–1.32], P = 0.0005). There was no association between thirds of HDL-C and retinal events (1.01 [0.82–1.25], P = 0.9). CONCLUSIONS: In patients with type 2 diabetes, HDL-C level is an independent risk factor for the development of microvascular disease affecting the kidney but not the retina.
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spelling pubmed-34768892013-11-01 Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study Morton, Jamie Zoungas, Sophia Li, Qiang Patel, Anushka A. Chalmers, John Woodward, Mark Celermajer, David S. Beulens, Joline W.J. Stolk, Ronald P. Glasziou, Paul Ng, Martin K.C. Diabetes Care Original Research OBJECTIVE: Although low HDL cholesterol (HDL-C) is an established risk factor for atherosclerosis, data on HDL-C and the risk of microvascular disease are limited. We tested the association between HDL-C and microvascular disease in a cohort of patients with type 2 diabetes. RESEARCH DESIGN AND METHODS: A total of 11,140 patients with type 2 diabetes and at least one additional vascular risk factor were followed a median of 5 years. Cox proportional hazards models were used to assess the association between baseline HDL-C and the development of new or worsening microvascular disease, defined prospectively as a composite of renal and retinal events. RESULTS: The mean baseline HDL-C level was 1.3 mmol/L (SD 0.45 mmol/L [range 0.1–4.0]). During follow-up, 32% of patients developed new or worsening microvascular disease, with 28% experiencing a renal event and 6% a retinal event. Compared with patients in the highest third, those in the lowest third had a 17% higher risk of microvascular disease (adjusted hazard ratio 1.17 [95% CI 1.06–1.28], P = 0.001) after adjustment for potential confounders and regression dilution. This was driven by a 19% higher risk of renal events (1.19 [1.08–1.32], P = 0.0005). There was no association between thirds of HDL-C and retinal events (1.01 [0.82–1.25], P = 0.9). CONCLUSIONS: In patients with type 2 diabetes, HDL-C level is an independent risk factor for the development of microvascular disease affecting the kidney but not the retina. American Diabetes Association 2012-11 2012-10-13 /pmc/articles/PMC3476889/ /pubmed/22891258 http://dx.doi.org/10.2337/dc12-0306 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Morton, Jamie
Zoungas, Sophia
Li, Qiang
Patel, Anushka A.
Chalmers, John
Woodward, Mark
Celermajer, David S.
Beulens, Joline W.J.
Stolk, Ronald P.
Glasziou, Paul
Ng, Martin K.C.
Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title_full Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title_fullStr Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title_full_unstemmed Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title_short Low HDL Cholesterol and the Risk of Diabetic Nephropathy and Retinopathy: Results of the ADVANCE study
title_sort low hdl cholesterol and the risk of diabetic nephropathy and retinopathy: results of the advance study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476889/
https://www.ncbi.nlm.nih.gov/pubmed/22891258
http://dx.doi.org/10.2337/dc12-0306
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