1 detailed study records

Key findings from detailed records

Population: 82 people with type 2 diabetes and nephropathy, taking an ACE inhibitor or ARB. Findings: Thiamine status improved, but urinary albumin and KIM-1 did not decrease significantly.

KNOWLEDGE RECORD

Category
Metabolism and cellular function
Last Reviewed

Names and related search termsBenfotiamine / Benfotiamine / Vitamin B1 derivative

Study type: human intervention study.

Explore 10 papers by research question ↓

OUTCOME-SPECIFIC EVIDENCE

Scientific Evidence Profile

Assessment pending

An outcome-specific assessment has not yet been completed. This is not a finding that the ingredient is ineffective. The study records below remain available.

This profile concerns the stated outcome and population, not the ingredient as a whole. It is not a probability of benefit, a safety rating, a product efficacy rating or an indication of product adoption.

How we assess evidence

Ingredient Profile

What is it?
Benfotiamine is a synthetic derivative of thiamine, vitamin B1. The derivative and the vitamin have different molecular structures. [1]
Sources for this profile

Compound properties and formulation properties are different. These sources do not establish the efficacy of a finished supplement.

  1. PubChem — Benfotiamine (CID 3032771) Chemical identity reference. Maintained by NCBI, U.S. National Library of Medicine. Database record; not a clinical trial.

Profile sources checked:

Read the evidence in context
  • Evidence: what was measured in the stated population or experimental model.
  • Inference: an interpretation connecting findings; its applicability depends on the study conditions.
  • Hypothesis: a proposed explanation or effect that remains to be tested.

Research Evidence · Scientific Synthesis

Why It Matters #

Does improving thiamine status also improve markers of kidney damage? Check the detailed records for study conditions and use the literature map to compare other populations and outcomes.

What Was Studied #

82 people with type 2 diabetes and nephropathy, taking an ACE inhibitor or ARB. Randomized, double-blind, placebo-controlled trial. Outcomes: 24-hour urinary albumin excretion and KIM-1[1]

What Was Found #

Thiamine status improved, but urinary albumin and KIM-1 did not decrease significantly.[1]

What the Evidence Means #

A short-term, high-dose trial in patients receiving medication. It does not establish long-term use in healthy people or effects on other symptoms.[1]

Comparing similar populations, formulations, durations and outcomes helps identify where findings agree and where they differ.

What We Can Learn #

Distinguish a change in nutrient status from improvement in disease markers. Classification as a medicine may also vary by country.

What Remains Unknown #

Further questions include reproducibility across populations and formulations, and the long-term balance of benefits and harms. Use the literature map as a starting point for these questions.

LITERATURE MAP / 10 PAPERS

Compare papers by conditions and findings.

A literature map covering different populations, outcomes and formulations. Read alongside detailed records to avoid treating one trial as the conclusion for an entire ingredient.

Selected: 2026-09-21. Bibliographic information checked against Europe PMC / PubMed. Editorial selection considered major papers and a range of populations and questions. This is not a systematic search covering all recent research.

10 RECORDS

A dash marks fields outside the bibliographic record. Use detailed records to compare findings and design records to connect mechanisms.

Research comparison table
Paper and topicStudy conditionsFindings and scope
Metabolism and blood glucoseA double-blind, randomized, placebo-controlled clinical trial on benfotiamine treatment in patients with diabetic nephropathy.2010 Diabetes carePMID 20413516 #Study conditions

Randomized, double-blind, placebo-controlled trial

Population
The methods report enrollment of 43 participants per group. The reported analysis contains 82 adults with type 2 diabetes and nephropathy (39 benfotiamine, 43 placebo), receiving ACE inhibitors or ARBs.
Dose
Benfotiamine 900 mg/day
Duration
12 weeks
Outcomes
24-hour urinary albumin excretion and KIM-1
Findings and scope

Thiamine status improved, but urinary albumin and KIM-1 did not decrease significantly.

View findings and limitations

DOI

Authors

Alkhalaf A, Klooster A, van Oeveren W, Achenbach U, Kleefstra N, Slingerland RJ et al.

Benfotiamine prevents macro- and microvascular endothelial dysfunction and oxidative stress following a meal rich in advanced glycation end products in individuals with type 2 diabetes.2006 Diabetes carePMID 16936154 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Stirban A, Negrean M, Stratmann B, Gawlowski T, Horstmann T, Götting C et al.

Benfotiamine reduces genomic damage in peripheral lymphocytes of hemodialysis patients.2008 Naunyn-Schmiedeberg's archives of pharmacologyPMID 18509620 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Schupp N, Dette EM, Schmid U, Bahner U, Winkler M, Heidland A et al.

Pharmacokinetic study of benfotiamine and the bioavailability assessment compared to thiamine hydrochloride.2014 Journal of clinical pharmacologyPMID 24399744 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Xie F, Cheng Z, Li S, Liu X, Guo X, Yu P et al.

Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of Benfotiamine in Healthy Subjects.2021 Drug design, development and therapyPMID 33727798 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Sheng L, Cao W, Lin P, Chen W, Xu H, Zhong C et al.

Variability of skin autofluorescence measurement over 6 and 12 weeks and the influence of benfotiamine treatment.2013 Diabetes technology & therapeuticsPMID 23964994 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Stirban A, Pop A, Fischer A, Heckermann S, Tschoepe D

Benfotiamine in diabetic polyneuropathy (BENDIP): results of a randomised, double blind, placebo-controlled clinical study.2008 Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes AssociationPMID 18473286 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Stracke H, Gaus W, Achenbach U, Federlin K, Bretzel RG

Benfotiamine and Cognitive Decline in Alzheimer's Disease: Results of a Randomized Placebo-Controlled Phase IIa Clinical Trial.2020 Journal of Alzheimer's disease : JADPMID 33074237 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Gibson GE, Luchsinger JA, Cirio R, Chen H, Franchino-Elder J, Hirsch JA et al.

Benfotiamine in treatment of alcoholic polyneuropathy: an 8-week randomized controlled study (BAP I Study).1998 Alcohol and alcoholism (Oxford, Oxfordshire)PMID 9872352 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Woelk H, Lehrl S, Bitsch R, Köpcke W

Benfotiamine in the treatment of diabetic polyneuropathy--a three-week randomized, controlled pilot study (BEDIP study).2005 International journal of clinical pharmacology and therapeuticsPMID 15726875 #Study conditions

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Findings and scope

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Open original paper

DOI

Authors

Haupt E, Ledermann H, Köpcke W

The literature map is an index of research questions and references. Individual assessment of results, doses, funding and COI is limited to the detailed study records. Related reports from the same trial may be included; paper counts are not counts of independent trials.

Explore the research Study Records

Listed doses describe study conditions, not recommended intake.

Study RecordPMID 20413516

A double-blind, randomized, placebo-controlled clinical trial on benfotiamine treatment in patients with diabetic nephropathy.

Authors
Alkhalaf A, Klooster A, van Oeveren W, Achenbach U, Kleefstra N, Slingerland RJ, Mijnhout GS, Bilo HJ, Gans RO, Navis GJ, Bakker SJ.
Journal
Diabetes care
Publication year
2010
Study design
Randomized, double-blind, placebo-controlled trial
Participants
The methods report enrollment of 43 participants per group. The reported analysis contains 82 adults with type 2 diabetes and nephropathy (39 benfotiamine, 43 placebo), receiving ACE inhibitors or ARBs.
Dose and intervention
Benfotiamine 900 mg/day
Duration
12 weeks
Outcomes and their role in the study
24-hour urinary albumin excretion and KIM-1
Findings
Thiamine status improved, but urinary albumin and KIM-1 did not decrease significantly.
Limitations
A short, high-dose trial in medicated patients, not evidence for long-term use in healthy people. In the active group, 4 withdrew: 2 after newly diagnosed malignancy and 2 withdrawing consent with dizziness or urticaria; the report does not establish causation. Missing dropout data were not replaced.
Funding
Partly supported by the EU PREDICTIONS network and the medical research foundation in Zwolle. Wörwag Pharma prepared the study medication.
Conflict of Interest
U.A. was head of medical affairs at Wörwag Pharma and contributed to protocol and approval documents, but not recruitment, evaluation, data collection or analysis. The paper also states that no relevant potential conflicts were reported.
Scope of source review
Primary methods, analysis population, outcomes, withdrawals and disclosures checked on 2026-10-24.

Cite this page

LÍFSVARÐA. Benfotiamine: Does improving thiamine status also improve markers of kidney damage? Version 1.1 / Updated 2026-10-24

https://lifsvarda.com/knowledge/benfotiamine/

Edited by LÍFSVARÐA (product brand).Editorial policy

Sources and updates

  1. Alkhalaf A, Klooster A, van Oeveren W, Achenbach U, Kleefstra N, Slingerland RJ, Mijnhout GS, Bilo HJ, Gans RO, Navis GJ, Bakker SJ. (2010). A double-blind, randomized, placebo-controlled clinical trial on benfotiamine treatment in patients with diabetic nephropathy.Primary methods, analysis population, outcomes, withdrawals and disclosures checked on 2026-10-24.

First published: 2026-09-21 / Version 1.1. Updated 2026-09-23: Added a research comparison table and links to design records. Source notes identify the scope of verification when the full paper has not been reviewed. Research summaries and LÍFSVARÐA’s interpretation are distinguished.