Abstract |
Thiamine supplementation may prevent and reverse early-stage diabetic nephropathy. This probably occurs by correcting diabetes-linked increased clearance of thiamine, maintaining activity and expression of thiamine pyrophosphate-dependent enzymes that help counter the adverse effects of high glucose concentrations-particularly transketolase. Evidence from experimental and clinical studies suggests that metabolism and clearance of thiamine is disturbed in diabetes leading to tissue-specific thiamine deficiency in the kidney and other sites of development of vascular complications. Thiamine supplementation prevented the development of early-stage nephropathy in diabetic rats and reversed increased urinary albumin excretion in patients with type 2 diabetes and microalbuminuria in two recent clinical trials. The thiamine monophosphate prodrug, Benfotiamine, whilst preventing early-stage development of diabetic nephropathy experimentally, has failed to produce similar clinical effect. The probable explanations for this are discussed. Further definitive trials for prevention of progression of early-stage diabetic nephropathy by thiamine are now required.
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Authors | N Rabbani, P J Thornalley |
Journal | Diabetes, obesity & metabolism
(Diabetes Obes Metab)
Vol. 13
Issue 7
Pg. 577-83
(Jul 2011)
ISSN: 1463-1326 [Electronic] England |
PMID | 21342411
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Copyright | © 2011 Blackwell Publishing Ltd. |
Chemical References |
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Topics |
- Albuminuria
(complications, prevention & control)
- Animals
- Diabetes Mellitus, Experimental
(complications, drug therapy)
- Diabetes Mellitus, Type 2
(complications, drug therapy, prevention & control)
- Diabetic Nephropathies
(drug therapy, prevention & control)
- Dietary Supplements
- Humans
- Rats
- Thiamine
(pharmacokinetics, therapeutic use)
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