Cargando…

Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation

The factor V Leiden (FVL) mutation is the most frequent genetic cause of venous thrombosis in Caucasians. However, protective effects have been suggested to balance the disadvantages. We have recently observed protective effects of FVL mutation on experimental diabetic nephropathy in mice as well as...

Descripción completa

Detalles Bibliográficos
Autores principales: Peter, Andreas, Fritsche, Andreas, Machicao, Fausto, Nawroth, Peter P., Häring, Hans-Ulrich, Isermann, Berend
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960766/
https://www.ncbi.nlm.nih.gov/pubmed/24729885
http://dx.doi.org/10.1155/2014/530830
_version_ 1782308193061306368
author Peter, Andreas
Fritsche, Andreas
Machicao, Fausto
Nawroth, Peter P.
Häring, Hans-Ulrich
Isermann, Berend
author_facet Peter, Andreas
Fritsche, Andreas
Machicao, Fausto
Nawroth, Peter P.
Häring, Hans-Ulrich
Isermann, Berend
author_sort Peter, Andreas
collection PubMed
description The factor V Leiden (FVL) mutation is the most frequent genetic cause of venous thrombosis in Caucasians. However, protective effects have been suggested to balance the disadvantages. We have recently observed protective effects of FVL mutation on experimental diabetic nephropathy in mice as well as an association with reduced albuminuria in two human cohorts of diabetic patients. In the present study we aimed to reevaluate these findings in an independent, larger cohort of 1905 Caucasians at risk of developing type 2 diabetes and extend possible associations to earlier disease stages of nephropathy. Carriers of FVL mutation had a significantly lower urine albumin excretion (P = 0.03) and tended to have lower plasma creatinine concentrations (P = 0.07). The difference in plasma creatinine concentrations was significant after adjustment for the influencing factors: age, gender, and lean body mass (P = 0.048). These observations at a very early “disease” stage are an important extension of previous findings and suggest that modification of glomerular dysfunction by FVL mutation is relevant during very early stages of diabetic nephropathy. This makes the underlying mechanism an interesting therapeutic target and raises the question whether FVL mutation may also exert protective effects in other glomerulopathies.
format Online
Article
Text
id pubmed-3960766
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-39607662014-04-13 Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation Peter, Andreas Fritsche, Andreas Machicao, Fausto Nawroth, Peter P. Häring, Hans-Ulrich Isermann, Berend ISRN Endocrinol Research Article The factor V Leiden (FVL) mutation is the most frequent genetic cause of venous thrombosis in Caucasians. However, protective effects have been suggested to balance the disadvantages. We have recently observed protective effects of FVL mutation on experimental diabetic nephropathy in mice as well as an association with reduced albuminuria in two human cohorts of diabetic patients. In the present study we aimed to reevaluate these findings in an independent, larger cohort of 1905 Caucasians at risk of developing type 2 diabetes and extend possible associations to earlier disease stages of nephropathy. Carriers of FVL mutation had a significantly lower urine albumin excretion (P = 0.03) and tended to have lower plasma creatinine concentrations (P = 0.07). The difference in plasma creatinine concentrations was significant after adjustment for the influencing factors: age, gender, and lean body mass (P = 0.048). These observations at a very early “disease” stage are an important extension of previous findings and suggest that modification of glomerular dysfunction by FVL mutation is relevant during very early stages of diabetic nephropathy. This makes the underlying mechanism an interesting therapeutic target and raises the question whether FVL mutation may also exert protective effects in other glomerulopathies. Hindawi Publishing Corporation 2014-03-04 /pmc/articles/PMC3960766/ /pubmed/24729885 http://dx.doi.org/10.1155/2014/530830 Text en Copyright © 2014 Andreas Peter et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peter, Andreas
Fritsche, Andreas
Machicao, Fausto
Nawroth, Peter P.
Häring, Hans-Ulrich
Isermann, Berend
Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title_full Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title_fullStr Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title_full_unstemmed Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title_short Lower Plasma Creatinine and Urine Albumin in Individuals at Increased Risk of Type 2 Diabetes with Factor V Leiden Mutation
title_sort lower plasma creatinine and urine albumin in individuals at increased risk of type 2 diabetes with factor v leiden mutation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960766/
https://www.ncbi.nlm.nih.gov/pubmed/24729885
http://dx.doi.org/10.1155/2014/530830
work_keys_str_mv AT peterandreas lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation
AT fritscheandreas lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation
AT machicaofausto lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation
AT nawrothpeterp lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation
AT haringhansulrich lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation
AT isermannberend lowerplasmacreatinineandurinealbumininindividualsatincreasedriskoftype2diabeteswithfactorvleidenmutation