Prostaglandin E1 in lipid microspheres ameliorates diabetic peripheral neuropathy: clinical usefulness of Semmes-Weinstein monofilaments for evaluating diabetic sensory abnormality

被引:24
作者
Akahori, H [1 ]
Takamura, T [1 ]
Hayakawa, T [1 ]
Ando, H [1 ]
Yamashita, H [1 ]
Kobayashi, KI [1 ]
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Endocrinol & Metab, Kanazawa, Ishikawa 920, Japan
关键词
diabetic peripheral neuropathy; Lipo-PGE1; Semmes-Weinstein monofilaments;
D O I
10.1016/j.diabres.2003.10.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the effect of Prostaglandin E I in lipid microspheres (Lipo-PGE1) on diabetic peripheral neuropathy from view of symptoms, neurological examinations including sensory threshold evaluated with Semmes-Weinstein monofilaments (SWM). Type 2 diabetic patients with diabetic peripheral neuropathy were participated in this study. The patients were randomly assigned to two groups, 11 Lipo-PGE1-treated patients and 16 control patients. Lipo-PGE1 at a dose of 10 mg in 20 ml of saline was injected intravenously as a bolus once daily for 2 weeks. Before and, 1, 2 and 4 weeks after the start of treatment with Lipo-PGE1, sensory threshold was evaluated with Semmes-Weinstein monofilaments at total 18 touch sites on the feet. Administration of Lipo-PGE1 improved subjective symptoms especially in items of numbness and imperception. Such improvement in subjective symptoms correlated well with the improvement in Semmes-Weinstein monotilaments examination, whereas the improvement was not recognized in motor nerve conduction velocity (MCV), sensory nerve conduction velocity (SCV) and coefficient variation of R-R interval on ECG (CVR-R). The improvement lasted for at least 6 months. This study demonstrated that Lipo-PGE1 has long term amelioration effects on diabetic neuropathy especially in symptoms and sensory threshold, and that Semmes-Weinstein monofilaments examination is a simpler, more valid and quantitative tool for assessing the clinical effect of Lipo-PGE1 on diabetic peripheral neuropathy. (C) 2003 Published by Elsevier Ireland Ltd.
引用
收藏
页码:153 / 159
页数:7
相关论文
共 12 条
[1]  
AKIRA T, 1999, MED POSTGRAD, V37, P194
[2]  
HAU P, 2000, DIABETES CARE, V23, P606
[3]  
HOSHI K, 1986, DRUG EXP CLIN RES, V12, P681
[4]   Approved indications of lipo-PGE(1) in Japan [J].
Hoshi, K .
ADVANCED DRUG DELIVERY REVIEWS, 1996, 20 (2-3) :171-176
[5]   Apoptosis and impaired axonal regeneration of sensory neurons after nerve crush in diabetic rats [J].
Kogawa, S ;
Yasuda, H ;
Terada, M ;
Maeda, K ;
Kikkawa, R .
NEUROREPORT, 2000, 11 (04) :663-667
[6]  
LEROITH D, 2000, DIABETES MELLITUS FU, P910
[7]   Diabetic neuropathy examination - A hierarchical scoring system to diagnose distal polyneuropathy in diabetes [J].
Meijer, JWG ;
van Sonderen, E ;
Blaauwwiekel, EE ;
Smit, AJ ;
Groothoff, JW ;
Eisma, WH ;
Links, TP .
DIABETES CARE, 2000, 23 (06) :750-753
[8]  
MIZUSHIMA Y, 1985, DRUG EXP CLIN RES, V11, P595
[9]   4-g monofilament is clinically useful for detecting diabetic peripheral neuropathy [J].
Nagai, Y ;
Sugiyama, Y ;
Abe, T ;
Nomura, G .
DIABETES CARE, 2001, 24 (01) :183-184
[10]   Reversal of experimental diabetic neuropathy by VEGF gene transfer [J].
Schratzberger, P ;
Walter, DH ;
Rittig, K ;
Bahlmann, FH ;
Pola, R ;
Curry, C ;
Silver, M ;
Krainin, JG ;
Weinberg, DH ;
Ropper, AH ;
Isner, JM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (09) :1083-1092