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Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia
INTRODUCTION: Postprandial hyperglycemia is a major risk factor for the development of cardiovascular diseases (CVDs), and Most of the times it occurs in patients with normal glycemic control diagnosed by fasting blood glucose (FBG) and glycated hemoglobin levels. Urine albumin excretion (UAE) is an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015496/ https://www.ncbi.nlm.nih.gov/pubmed/28042215 http://dx.doi.org/10.4103/0974-2727.187925 |
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author | Shilpasree, Alagilawada S Patil, Vidya S Patil, Vijayetha P Ingleshwar, Deepti G |
author_facet | Shilpasree, Alagilawada S Patil, Vidya S Patil, Vijayetha P Ingleshwar, Deepti G |
author_sort | Shilpasree, Alagilawada S |
collection | PubMed |
description | INTRODUCTION: Postprandial hyperglycemia is a major risk factor for the development of cardiovascular diseases (CVDs), and Most of the times it occurs in patients with normal glycemic control diagnosed by fasting blood glucose (FBG) and glycated hemoglobin levels. Urine albumin excretion (UAE) is an independent predictor of CVD risk. AIM: To estimate UAE in isolated postprandial hyperglycemia (IPPHG) patients and to assess the relationship of UAE with FBG and postprandial blood glucose (PPBG) levels. SETTINGS AND DESIGN: A cross-sectional study was carried out in 318 patients with Type II diabetes in the age group 30–60 years for 6 months. MATERIALS AND METHODS: Patients were divided into five groups based on their FBG and PPBG values. UAE and lipid profile were measured in all the groups. STATISTICAL ANALYSIS: UAE and lipid profile in different groups were compared using ANOVA. Regression analysis was used to predict the variation of UAE with FBG, PPBG, and total cholesterol (TC). RESULTS: Patients with IPPHG had significantly higher albumin excretion compared to normoglycemia (NG) group [P < 0.0001]. In impaired glucose tolerance and isolated fasting hyperglycemia groups, it did not differ significantly from NG group [P = 0.206 and P = 0.173]. Lipid profile did not show any significant difference between the groups. On regression analysis, PPBG but not FBG or TC correlated positively with UAE. CONCLUSION: UAE is easy, less expensive, and Widely available method done on spot urine samples which predicts the acute glycemic changes and increased risk of developing CVDs in patients with IPPHG. |
format | Online Article Text |
id | pubmed-5015496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50154962017-01-01 Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia Shilpasree, Alagilawada S Patil, Vidya S Patil, Vijayetha P Ingleshwar, Deepti G J Lab Physicians Original Article INTRODUCTION: Postprandial hyperglycemia is a major risk factor for the development of cardiovascular diseases (CVDs), and Most of the times it occurs in patients with normal glycemic control diagnosed by fasting blood glucose (FBG) and glycated hemoglobin levels. Urine albumin excretion (UAE) is an independent predictor of CVD risk. AIM: To estimate UAE in isolated postprandial hyperglycemia (IPPHG) patients and to assess the relationship of UAE with FBG and postprandial blood glucose (PPBG) levels. SETTINGS AND DESIGN: A cross-sectional study was carried out in 318 patients with Type II diabetes in the age group 30–60 years for 6 months. MATERIALS AND METHODS: Patients were divided into five groups based on their FBG and PPBG values. UAE and lipid profile were measured in all the groups. STATISTICAL ANALYSIS: UAE and lipid profile in different groups were compared using ANOVA. Regression analysis was used to predict the variation of UAE with FBG, PPBG, and total cholesterol (TC). RESULTS: Patients with IPPHG had significantly higher albumin excretion compared to normoglycemia (NG) group [P < 0.0001]. In impaired glucose tolerance and isolated fasting hyperglycemia groups, it did not differ significantly from NG group [P = 0.206 and P = 0.173]. Lipid profile did not show any significant difference between the groups. On regression analysis, PPBG but not FBG or TC correlated positively with UAE. CONCLUSION: UAE is easy, less expensive, and Widely available method done on spot urine samples which predicts the acute glycemic changes and increased risk of developing CVDs in patients with IPPHG. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5015496/ /pubmed/28042215 http://dx.doi.org/10.4103/0974-2727.187925 Text en Copyright: © Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Shilpasree, Alagilawada S Patil, Vidya S Patil, Vijayetha P Ingleshwar, Deepti G Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title | Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title_full | Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title_fullStr | Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title_full_unstemmed | Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title_short | Urine Albumin Excretion as a Marker of Acute Glycemic Changes in Isolated Postprandial Hyperglycemia |
title_sort | urine albumin excretion as a marker of acute glycemic changes in isolated postprandial hyperglycemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015496/ https://www.ncbi.nlm.nih.gov/pubmed/28042215 http://dx.doi.org/10.4103/0974-2727.187925 |
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