C-Peptide Replacement Therapy and Sensory Nerve Function in Type 1 Diabetic Neuropathy

  • Karin Ekberg
    Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
  • Tom Brismar
    Clinical Neuroscience, Section of Clinical Neurophysiology, Karolinska Institutet, Stockholm, Sweden
  • Bo-Lennart Johansson
    Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
  • Per Lindström
    Section of Neurology, Karolinska Institutet, Stockholm, Sweden
  • Lisa Juntti-Berggren
    Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
  • Anders Norrby
    Medicine at Lundby Hospital, Gothenburg, Sweden
  • Christian Berne
    Section of Medicine, Uppsala University Hospital, Uppsala, Sweden
  • Hans J. Arnqvist
    Section of Medicine, Linköping University Hospital, Linköping, Sweden
  • Jan Bolinder
    Section of Medicine, Karolinska Institutet, Stockholm, Sweden
  • John Wahren
    Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

書誌事項

公開日
2007-01-01
DOI
  • 10.2337/dc06-1274
公開者
American Diabetes Association

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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 &gt;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 &lt; 0.007). The number of patients responding with a SCV peak potential improvement &gt;1.0 m/s was greater in C-peptide–treated patients than in those receiving placebo (P &lt; 0.03). In the least severely affected patients (SCV &lt; 2.5 SD below normal at baseline, n = 70) SCV improved by 1.0 m/s (P &lt; 0.014 vs. placebo). NIA score and vibration perception both improved within the C-peptide–treated groups (P &lt; 0.011 and P &lt; 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

  • Diabetes Care

    Diabetes Care 30 (1), 71-76, 2007-01-01

    American Diabetes Association

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