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High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease

AIMS/HYPOTHESIS: To assess thiamine status by analysis of plasma, erythrocytes and urine in type 1 and type 2 diabetic patients and links to markers of vascular dysfunction. METHODS: Diabetic patients (26 type 1 and 48 type 2) with and without microalbuminuria and 20 normal healthy control volunteer...

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Autores principales: Thornalley, P. J., Babaei-Jadidi, R., Al Ali, H., Rabbani, N., Antonysunil, A., Larkin, J., Ahmed, A., Rayman, G., Bodmer, C. W.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1998885/
https://www.ncbi.nlm.nih.gov/pubmed/17676306
http://dx.doi.org/10.1007/s00125-007-0771-4
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author Thornalley, P. J.
Babaei-Jadidi, R.
Al Ali, H.
Rabbani, N.
Antonysunil, A.
Larkin, J.
Ahmed, A.
Rayman, G.
Bodmer, C. W.
author_facet Thornalley, P. J.
Babaei-Jadidi, R.
Al Ali, H.
Rabbani, N.
Antonysunil, A.
Larkin, J.
Ahmed, A.
Rayman, G.
Bodmer, C. W.
author_sort Thornalley, P. J.
collection PubMed
description AIMS/HYPOTHESIS: To assess thiamine status by analysis of plasma, erythrocytes and urine in type 1 and type 2 diabetic patients and links to markers of vascular dysfunction. METHODS: Diabetic patients (26 type 1 and 48 type 2) with and without microalbuminuria and 20 normal healthy control volunteers were recruited. Erythrocyte activity of transketolase, the concentrations of thiamine and related phosphorylated metabolites in plasma, erythrocytes and urine, and markers of metabolic control and vascular dysfunction were determined. RESULTS: Plasma thiamine concentration was decreased 76% in type 1 diabetic patients and 75% in type 2 diabetic patients: normal volunteers 64.1 (95% CI 58.5–69.7) nmol/l, type 1 diabetes 15.3 (95% CI 11.5–19.1) nmol/l, p < 0.001, and type 2 diabetes 16.3 (95% CI 13.0–9.6) nmol/l, p < 0.001. Renal clearance of thiamine was increased 24-fold in type 1 diabetic patients and 16-fold in type 2 diabetic patients. Plasma thiamine concentration correlated negatively with renal clearance of thiamine (r = −0.531, p < 0.001) and fractional excretion of thiamine (r = −0.616, p < 0.001). Erythrocyte transketolase activity correlated negatively with urinary albumin excretion (r = −0.232, p < 0.05). Thiamine transporter protein contents of erythrocyte membranes of type 1 and type 2 diabetic patients were increased. Plasma thiamine concentration and urinary excretion of thiamine correlated negatively with soluble vascular adhesion molecule-1 (r = −0.246, p < 0.05, and −0.311, p < 0.01, respectively). CONCLUSIONS/INTERPRETATION: Low plasma thiamine concentration is prevalent in patients with type 1 and type 2 diabetes, associated with increased thiamine clearance. The conventional assessment of thiamine status was masked by increased thiamine transporter content of erythrocytes.
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spelling pubmed-19988852007-10-02 High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease Thornalley, P. J. Babaei-Jadidi, R. Al Ali, H. Rabbani, N. Antonysunil, A. Larkin, J. Ahmed, A. Rayman, G. Bodmer, C. W. Diabetologia Article AIMS/HYPOTHESIS: To assess thiamine status by analysis of plasma, erythrocytes and urine in type 1 and type 2 diabetic patients and links to markers of vascular dysfunction. METHODS: Diabetic patients (26 type 1 and 48 type 2) with and without microalbuminuria and 20 normal healthy control volunteers were recruited. Erythrocyte activity of transketolase, the concentrations of thiamine and related phosphorylated metabolites in plasma, erythrocytes and urine, and markers of metabolic control and vascular dysfunction were determined. RESULTS: Plasma thiamine concentration was decreased 76% in type 1 diabetic patients and 75% in type 2 diabetic patients: normal volunteers 64.1 (95% CI 58.5–69.7) nmol/l, type 1 diabetes 15.3 (95% CI 11.5–19.1) nmol/l, p < 0.001, and type 2 diabetes 16.3 (95% CI 13.0–9.6) nmol/l, p < 0.001. Renal clearance of thiamine was increased 24-fold in type 1 diabetic patients and 16-fold in type 2 diabetic patients. Plasma thiamine concentration correlated negatively with renal clearance of thiamine (r = −0.531, p < 0.001) and fractional excretion of thiamine (r = −0.616, p < 0.001). Erythrocyte transketolase activity correlated negatively with urinary albumin excretion (r = −0.232, p < 0.05). Thiamine transporter protein contents of erythrocyte membranes of type 1 and type 2 diabetic patients were increased. Plasma thiamine concentration and urinary excretion of thiamine correlated negatively with soluble vascular adhesion molecule-1 (r = −0.246, p < 0.05, and −0.311, p < 0.01, respectively). CONCLUSIONS/INTERPRETATION: Low plasma thiamine concentration is prevalent in patients with type 1 and type 2 diabetes, associated with increased thiamine clearance. The conventional assessment of thiamine status was masked by increased thiamine transporter content of erythrocytes. Springer-Verlag 2007-08-04 2007-10 /pmc/articles/PMC1998885/ /pubmed/17676306 http://dx.doi.org/10.1007/s00125-007-0771-4 Text en © Springer-Verlag 2007
spellingShingle Article
Thornalley, P. J.
Babaei-Jadidi, R.
Al Ali, H.
Rabbani, N.
Antonysunil, A.
Larkin, J.
Ahmed, A.
Rayman, G.
Bodmer, C. W.
High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title_full High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title_fullStr High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title_full_unstemmed High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title_short High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
title_sort high prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1998885/
https://www.ncbi.nlm.nih.gov/pubmed/17676306
http://dx.doi.org/10.1007/s00125-007-0771-4
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