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Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy
BACKGROUND: Diabetic nephropathy, a major complication of diabetes, is characterized by progressive renal injury and increased cardiovascular mortality. An increased urinary albumin excretion due dysfunction of the glomerular barrier is an early sign of diabetic nephropathy. An increased urinary exc...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729477/ https://www.ncbi.nlm.nih.gov/pubmed/19653885 http://dx.doi.org/10.1186/1741-7015-7-39 |
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author | Tofik, Rafid Torffvit, Ole Rippe, Bengt Bakoush, Omran |
author_facet | Tofik, Rafid Torffvit, Ole Rippe, Bengt Bakoush, Omran |
author_sort | Tofik, Rafid |
collection | PubMed |
description | BACKGROUND: Diabetic nephropathy, a major complication of diabetes, is characterized by progressive renal injury and increased cardiovascular mortality. An increased urinary albumin excretion due dysfunction of the glomerular barrier is an early sign of diabetic nephropathy. An increased urinary excretion of higher molecular weight proteins such as IgM appears with progression of glomerular injury. We aim here to study the prognostic significance of urine IgM excretion in patients with type 1 diabetes mellitus (type 1 diabetic nephropathy). METHODS: This is an observational study of 139 patients with type1 diabetes mellitus (79 males and 60 females) under routine care at the diabetic outpatient clinic at the Lund University Hospital. The median follow-up time was 18 years (1 to 22) years. Urine albumin and urine IgM concentration were measured at time of recruitment. RESULTS: Overall 32 (14 male and 18 female) patients died in a cardiovascular event and 20 (11 male and 9 female) patients reached end-stage renal disease. Univariate analysis indicated that patient survival and renal survival were inversely associated with urine albumin excretion (RR = 2.9 and 5.8, respectively) and urine IgM excretion (RR = 4.6 and 5.7, respectively). Stratified analysis demonstrated that in patients with different degrees of albuminuria, the cardiovascular mortality rate and the incidence of end-stage renal disease was approximately three times higher in patients with increased urine IgM excretion. CONCLUSION: An increase in urinary IgM excretion in patients with type 1 diabetes is associated with an increased risk for cardiovascular mortality and renal failure, regardless of the degree of albuminuria. |
format | Text |
id | pubmed-2729477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27294772009-08-20 Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy Tofik, Rafid Torffvit, Ole Rippe, Bengt Bakoush, Omran BMC Med Research Article BACKGROUND: Diabetic nephropathy, a major complication of diabetes, is characterized by progressive renal injury and increased cardiovascular mortality. An increased urinary albumin excretion due dysfunction of the glomerular barrier is an early sign of diabetic nephropathy. An increased urinary excretion of higher molecular weight proteins such as IgM appears with progression of glomerular injury. We aim here to study the prognostic significance of urine IgM excretion in patients with type 1 diabetes mellitus (type 1 diabetic nephropathy). METHODS: This is an observational study of 139 patients with type1 diabetes mellitus (79 males and 60 females) under routine care at the diabetic outpatient clinic at the Lund University Hospital. The median follow-up time was 18 years (1 to 22) years. Urine albumin and urine IgM concentration were measured at time of recruitment. RESULTS: Overall 32 (14 male and 18 female) patients died in a cardiovascular event and 20 (11 male and 9 female) patients reached end-stage renal disease. Univariate analysis indicated that patient survival and renal survival were inversely associated with urine albumin excretion (RR = 2.9 and 5.8, respectively) and urine IgM excretion (RR = 4.6 and 5.7, respectively). Stratified analysis demonstrated that in patients with different degrees of albuminuria, the cardiovascular mortality rate and the incidence of end-stage renal disease was approximately three times higher in patients with increased urine IgM excretion. CONCLUSION: An increase in urinary IgM excretion in patients with type 1 diabetes is associated with an increased risk for cardiovascular mortality and renal failure, regardless of the degree of albuminuria. BioMed Central 2009-08-04 /pmc/articles/PMC2729477/ /pubmed/19653885 http://dx.doi.org/10.1186/1741-7015-7-39 Text en Copyright © 2009 Tofik 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 Article Tofik, Rafid Torffvit, Ole Rippe, Bengt Bakoush, Omran Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title | Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title_full | Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title_fullStr | Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title_full_unstemmed | Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title_short | Increased urine IgM excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
title_sort | increased urine igm excretion predicts cardiovascular events in patients with type 1 diabetes nephropathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729477/ https://www.ncbi.nlm.nih.gov/pubmed/19653885 http://dx.doi.org/10.1186/1741-7015-7-39 |
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