Abstract
Aim: Efficacy and safety of benfotiamine in treatment of diabetic polyneuropathy.
Methods: Double blind, placebo-controlled, phase-III-study. 181 patients were screened. 165
patients with symmetrical, distal diabetic polyneuropathy were randomised to one of
three treatment groups entering the wash-out phase and 133/124 patients were analysed
in the ITT/PP analysis: Benfotiamine 600 mg per day (n=47/43), benfotiamine 300 mg
per day (n=45/42) or placebo (n=41/39).
Results: After 6 weeks of treatment, the primary outcome parameter NSS (Neuropathy Symptom
Score) differed significantly between the treatment groups (p=0.033) in the PP (per
protocol) population. In the ITT (intention to treat) population, the improvement
of NSS was slightly above significance (p=0.055). The TSS (Total Symptom Score) showed
no significant differences after 6 weeks of treatment. The improvement was more pronounced
at the higher benfotiamine dose and increased with treatment duration. In the TSS,
best results were obtained for the symptom “pain”. Treatment was well tolerated in
all groups.
Conclusion: Benfotiamine may extend the treatment option for patients with diabetic polyneuropathy
based on causal influence on impaired glucose metabolism. Further studies should confirm
the positive experiences.
Key words
diabetic polyneuropathy - benfotiamine - advanced glycation end products - glucose
metabolism
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Correspondence
Prof. Dr. H. Stracke
University Hospital Giessen and Marburg GmbH
Medical Clinic and Policlinic III
Rodthohl 6
35392 Giessen
Germany
Phone: +49/641/994 27 54
Fax: +49/641/994 27 69
Email: Hilmar.Stracke@innere.med.uni-giessen.de