C-Peptide Replacement Therapy and Sensory Nerve Function in Type 1 Diabetic Neuropathy
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- Karin Ekberg
- Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
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- Tom Brismar
- Clinical Neuroscience, Section of Clinical Neurophysiology, Karolinska Institutet, Stockholm, Sweden
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- Bo-Lennart Johansson
- Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
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- Per Lindström
- Section of Neurology, Karolinska Institutet, Stockholm, Sweden
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- Lisa Juntti-Berggren
- Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
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- Anders Norrby
- Medicine at Lundby Hospital, Gothenburg, Sweden
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- Christian Berne
- Section of Medicine, Uppsala University Hospital, Uppsala, Sweden
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- Hans J. Arnqvist
- Section of Medicine, Linköping University Hospital, Linköping, Sweden
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- Jan Bolinder
- Section of Medicine, Karolinska Institutet, Stockholm, Sweden
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- John Wahren
- Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
書誌事項
- 公開日
- 2007-01-01
- DOI
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- 10.2337/dc06-1274
- 公開者
- American Diabetes Association
この論文をさがす
説明
<jats:p>OBJECTIVE—C-peptide replacement in animals results in amelioration of diabetes-induced functional and structural abnormalities in peripheral nerves. The present study was undertaken to examine whether C-peptide administration to patients with type 1 diabetes and peripheral neuropathy improves sensory nerve function.</jats:p> <jats:p>RESEARCH DESIGN AND METHODS—This was an exploratory, double-blinded, randomized, and placebo-controlled study with three study groups that was carried out at five centers in Sweden. C-peptide was given as a replacement dose (1.5 mg/day, divided into four subcutaneous doses) or a dose three times higher (4.5 mg/day) during 6 months. Neurological examination and neurophysiological measurements were performed before and after 6 months of treatment with C-peptide or placebo.</jats:p> <jats:p>RESULTS—The age of the 139 patients who completed the protocol was 44.2 ± 0.6 (mean ± SE) years and their duration of diabetes was 30.6 ± 0.8 years. Clinical neurological impairment (NIA) (score >7 points) of the lower extremities was present in 86% of the patients at baseline. Sensory nerve conduction velocity (SCV) was 2.6 ± 0.08 SD below body height–corrected normal values at baseline and improved similarly within the two C-peptide groups (P < 0.007). The number of patients responding with a SCV peak potential improvement >1.0 m/s was greater in C-peptide–treated patients than in those receiving placebo (P < 0.03). In the least severely affected patients (SCV < 2.5 SD below normal at baseline, n = 70) SCV improved by 1.0 m/s (P < 0.014 vs. placebo). NIA score and vibration perception both improved within the C-peptide–treated groups (P < 0.011 and P < 0.002). A1C levels (7.6 ± 0.1% at baseline) decreased slightly but similarly in C-peptide–and placebo-treated patients during the study.</jats:p> <jats:p>CONCLUSIONS—C-peptide treatment for 6 months improves sensory nerve function in early-stage type 1 diabetic neuropathy.</jats:p>
収録刊行物
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- Diabetes Care
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Diabetes Care 30 (1), 71-76, 2007-01-01
American Diabetes Association