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Microvascular and C-fibre function in Diabetic Charcot Neuro-arthropathy and Diabetic Peripheral Neuropathy

  1. Neil Baker, BSc DPodM1,
  2. Alistair Green, MRCP1,
  3. Singhan Krishnan, MRCP1 and
  4. Gerry Rayman, MD FRCP (Gerry.Rayman{at}ipswichhospital.nhs.uk)1
  1. 1Ipswich Diabetic Foot Unit and Diabetes Centre

    Abstract

    Objective: Sympathetic denervation and hyperaemia are implicated in the pathogenesis of Charcot neuro-arthropathy (CN) but also features of diabetic peripheral neuropathy (DPN). Differences in these physiological parameters were sought by determining C-fibre function (LDI flare) and maximum microvascular hyperaemia (MMH) in 13 subjects with diabetic CN (DCN), 10 diabetic neuropaths (DPN) and 10 healthy controls (HC). Additionally, unaffected limbs of the 9 DCN with unilateral charcot (UCN) were studied to determine whether any observed differences precede CN.

    Results: The LDIflare was reduced in DPN (1.41 ± 0.51, cm2±SD) and DCN groups (1.42 ± 0.37) compared to HC (5.24 ± 1.33), p<0.0001. MMH was higher in DCN (432 ± 88 PU±SD) than DPN (262 ± 71), p=0.001, though lower than HC (564 ± 112) p < 0.01.

    Conclusion: C-fibre function is equally impaired in neuropathic patients with and without CN, however a higher MMH distinguishes those with CN. Unaffected and affected limbs of those with unilateral CN have the same neuro-vascular abnormalities suggesting these precede rather than result from CN.

    Footnotes

      • Received June 5, 2007.
      • Accepted August 24, 2007.

    This Article

    1. Diabetes Care September 5, 2007
    1. All Versions of this Article:
      1. dc07-1063v1
      2. 30/12/3077 most recent
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