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Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study

BACKGROUND: The presence of microalbuminuria can be associated with overt nephropathy and cardiovascular disease in patients with type 1 diabetes (T1D). We aimed to determine the incidence and evaluate the baseline predictors for the development of microalbuminuria in patients with T1D. METHODS: Thi...

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Autores principales: Cobas, Roberta A, Santos, Bráulio, da Silva, Pedro CB, Neves, Ricardo, Gomes, Marilia B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177769/
https://www.ncbi.nlm.nih.gov/pubmed/21871097
http://dx.doi.org/10.1186/1758-5996-3-21
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author Cobas, Roberta A
Santos, Bráulio
da Silva, Pedro CB
Neves, Ricardo
Gomes, Marilia B
author_facet Cobas, Roberta A
Santos, Bráulio
da Silva, Pedro CB
Neves, Ricardo
Gomes, Marilia B
author_sort Cobas, Roberta A
collection PubMed
description BACKGROUND: The presence of microalbuminuria can be associated with overt nephropathy and cardiovascular disease in patients with type 1 diabetes (T1D). We aimed to determine the incidence and evaluate the baseline predictors for the development of microalbuminuria in patients with T1D. METHODS: This study is a longitudinal cohort study of 122 normoalbuminuric patients with T1D who were receiving routine clinical care at baseline. A detailed medical history was taken, and a physical examination was performed at baseline. All of the patients were regularly examined for diabetes-associated complications. An analysis of predictors was performed using the Cox regression. RESULTS: Over 6.81 (3.59-9.75) years of follow-up, 50 (41%) of the patients developed microalbuminuria. The incidence density was 6.79/100 people per year (95% CI 5.04-8.95), and the microalbuminuria developed after 5.9 (2.44-7.76) and 11 (5-15) years of follow-up and diabetes duration, respectively. After an individual Cox regression, the baseline variables associated with the development of microalbuminuria were age, age at diagnosis, duration of diabetes, systolic and diastolic blood pressure, fasting glycemia, body mass index (BMI), total cholesterol and triglycerides levels, cholesterol/HDL ratio and a family history of type 2 diabetes.After a multivariate Cox regression, the only independent factors associated with the development of microalbuminuria were BMI [HR 1.12 (1.03-1.21)] and cholesterol/HDL ratio [HR 1.32 (1.05-1.67)]. CONCLUSIONS: A higher BMI and cholesterol/HDL ratio increased the risk of developing microalbuminuria in young patients with T1D after a short follow-up. Both risk factors are modifiable and should be identified early and followed closely.
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spelling pubmed-31777692011-09-22 Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study Cobas, Roberta A Santos, Bráulio da Silva, Pedro CB Neves, Ricardo Gomes, Marilia B Diabetol Metab Syndr Research BACKGROUND: The presence of microalbuminuria can be associated with overt nephropathy and cardiovascular disease in patients with type 1 diabetes (T1D). We aimed to determine the incidence and evaluate the baseline predictors for the development of microalbuminuria in patients with T1D. METHODS: This study is a longitudinal cohort study of 122 normoalbuminuric patients with T1D who were receiving routine clinical care at baseline. A detailed medical history was taken, and a physical examination was performed at baseline. All of the patients were regularly examined for diabetes-associated complications. An analysis of predictors was performed using the Cox regression. RESULTS: Over 6.81 (3.59-9.75) years of follow-up, 50 (41%) of the patients developed microalbuminuria. The incidence density was 6.79/100 people per year (95% CI 5.04-8.95), and the microalbuminuria developed after 5.9 (2.44-7.76) and 11 (5-15) years of follow-up and diabetes duration, respectively. After an individual Cox regression, the baseline variables associated with the development of microalbuminuria were age, age at diagnosis, duration of diabetes, systolic and diastolic blood pressure, fasting glycemia, body mass index (BMI), total cholesterol and triglycerides levels, cholesterol/HDL ratio and a family history of type 2 diabetes.After a multivariate Cox regression, the only independent factors associated with the development of microalbuminuria were BMI [HR 1.12 (1.03-1.21)] and cholesterol/HDL ratio [HR 1.32 (1.05-1.67)]. CONCLUSIONS: A higher BMI and cholesterol/HDL ratio increased the risk of developing microalbuminuria in young patients with T1D after a short follow-up. Both risk factors are modifiable and should be identified early and followed closely. BioMed Central 2011-08-26 /pmc/articles/PMC3177769/ /pubmed/21871097 http://dx.doi.org/10.1186/1758-5996-3-21 Text en Copyright ©2011 Cobas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cobas, Roberta A
Santos, Bráulio
da Silva, Pedro CB
Neves, Ricardo
Gomes, Marilia B
Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title_full Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title_fullStr Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title_full_unstemmed Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title_short Progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
title_sort progression to microalbuminuria in patients with type 1 diabetes: a seven-year prospective study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177769/
https://www.ncbi.nlm.nih.gov/pubmed/21871097
http://dx.doi.org/10.1186/1758-5996-3-21
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