The Effects of Long-Term Oral Benfotiamine Supplementation on Peripheral Nerve Function and Inflammatory Markers in Patients With Type 1 Diabetes A 24-month, double-blind, randomized, placebo-controlled trial

被引:52
作者
Fraser, David A. [1 ]
Diep, Lien M.
Hovden, Inger Anette [2 ]
Nilsen, Kristian B. [2 ,3 ]
Sveen, Kari Anne [1 ]
Seljeflot, Ingebjorg [4 ,5 ,6 ]
Hanssen, Kristian F. [5 ]
机构
[1] Oslo Univ Hosp, Diabet Res Ctr, Oslo, Norway
[2] Oslo Univ Hosp Ulleval, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway
[3] Norwegian Univ Sci & Technol, Dept Neurosci, N-7034 Trondheim, Norway
[4] Oslo Univ Hosp, Dept Cardiol B, Ctr Clin Heart Res, Oslo, Norway
[5] Univ Oslo, Fac Med, Oslo, Norway
[6] Oslo Univ Hosp, Dept Endocrinol, Oslo, Norway
关键词
POLYNEUROPATHY; NEUROPATHY;
D O I
10.2337/dc11-1895
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-To study the effects of long-term oral benfotiamine supplementation on peripheral nerve function and soluble inflammatory markers in patients with type 1 diabetes. RESEARCH DESIGN AND METHODS-The study randomly assigned 67 patients with type 1 diabetes to receive 24-month benfotiamine (300 mg/day) or placebo supplementation. Peripheral nerve function and levels. of soluble inflammatory variables were assessed at baseline and at 24 months. RESULTS-Fifty-nine patients completed the study. Marked increases in whole-blood concentrations of thiamine and thiamine diphosphate were found in the benfotiamine group (both P < 0.001 vs. placebo). However, no significant differences in changes in peripheral nerve function or soluble inflammatory biomarkers were observed between the groups. CONCLUSIONS-Our findings suggest that high-dose benfotiamine (300 mg/day) supplementation over 24 months has no significant effects upon peripheral nerve function or soluble markers of inflammation in patients with type 1 diabetes.
引用
收藏
页码:1095 / 1097
页数:3
相关论文
共 9 条
[1]   Benfotiamine blocks three major pathways of hyperglycemic damage and prevents experimental diabetic retinopathy [J].
Hammes, HP ;
Du, XL ;
Edelstein, D ;
Taguchi, T ;
Matsumura, T ;
Ju, QD ;
Lin, JH ;
Bierhaus, A ;
Nawroth, P ;
Hannak, D ;
Neumaier, M ;
Bergfeld, R ;
Giardino, I ;
Brownlee, M .
NATURE MEDICINE, 2003, 9 (03) :294-299
[2]  
Haupt E, 2005, INT J CLIN PHARM TH, V43, P71
[3]   Optimal blood glucose control during 18 years preserves peripheral nerve function in patients with 30 years' duration of type 1 diabetes [J].
Larsen, JR ;
Sjoholm, H ;
Hanssen, KF ;
Sandvik, L ;
Berg, TJ ;
Dahl-Jorgensen, K .
DIABETES CARE, 2003, 26 (08) :2400-2404
[4]   Symptom scoring systems to diagnose distal polyneuropathy in diabetes: the Diabetic Neuropathy Symptom score [J].
Meijer, JWG ;
Smit, AJ ;
Sonderen, EV ;
Groothoff, JW ;
Eisma, WH ;
Links, TP .
DIABETIC MEDICINE, 2002, 19 (11) :962-965
[5]   Benfotiamine relieves inflammatory and neuropathic pain in rats [J].
Sánchez-Ramírez, GM ;
Caram-Salas, NL ;
Rocha-González, HI ;
Vidal-Cantú, GC ;
Medina-Santillán, R ;
Reyes-García, G ;
Granados-Soto, V .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 530 (1-2) :48-53
[6]  
Schreeb KH, 1997, EUR J CLIN PHARMACOL, V52, P319
[7]   Benfotiamine in Diabetic Polyneuropathy (BENDIP): Results of a Randomised, Double Blind, Placebo-controlled Clinical Study [J].
Stracke, H. ;
Gaus, W. ;
Achenbach, U. ;
Federlin, K. ;
Bretzel, R. G. .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2008, 116 (10) :600-605
[8]   A Benfotiamine-vitamin B combination in treatment of diabetic polyneuropathy [J].
Stracke, H ;
Lindemann, A ;
Federlin, K .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 1996, 104 (04) :311-316
[9]   A MULTICENTER STUDY OF THE PREVALENCE OF DIABETIC PERIPHERAL NEUROPATHY IN THE UNITED-KINGDOM HOSPITAL CLINIC POPULATION [J].
YOUNG, MJ ;
BOULTON, AJM ;
MACLEOD, AF ;
WILLIAMS, DRR ;
SONKSEN, PH .
DIABETOLOGIA, 1993, 36 (02) :150-154