Diabetologia

, Volume 39, Issue 3, pp 344–348 | Cite as

The impact of reversal of hypoxia by revascularization on the peripheral nerve function of diabetic patients

  • A. Veves
  • V. M. Donaghue
  • M. R. Sarnow
  • J. M. Giurini
  • D. R. Campbell
  • F. W. LoGerfo
Originals

Summary

Hypoxia is considered to be one of the main aetiopathogenic factors of diabetic neuropathy. We have examined the effects of the reversal of hypoxia, achieved by revascularization, on peripheral nerve function in diabetic patients with or without clinical neuropathy. Fifty-six patients [mean age 62 (range 30–74) years, 44 (79%) males, 15 (27%) with insulin-dependent diabetes of 20 years (range 1–57) duration, and creatinine level 92.8±30.9 Μmol/l (mean ± SD)] were tested pre-operatively while 30 (54%) were re-examined at least 6 weeks post-operatively. At baseline the leg scheduled for operation showed worse measurements compared to the control leg when tested for Semmes-Weinstein monofilaments, peroneal motor conduction velocity (PMCV) (33.7±7.18 vs 35.7±6.09 m · s−1, p<0.05) and transcutaneous oxygen tension (37.4±24.6 vs 52.0±21.5 mm Hg, p<0.0001) while no differences were found in the vibration perception threshold and leg temperature. When baseline and post-operative measurements were later compared in the operated leg, no differences were noticed in the vibration perception threshold, PMCV and Semmes-Weinstein monofilaments but the transcutaneous oxygen tension increased significantly (32.7±27.1 vs 64.6±14.5 mm Hg, p<0.001). No differences were noticed in any of the above parameters in the contralateral leg. No correlations were found between changes in transcutaneous oxygen tension and PMCV values measured at baseline and at the follow-up visit in either leg. Similar results were found when patients were stratified according to severity of neuropathy, ischaemia and the level of the bypass. We conclude that although there is greater impairment of nerve function in the more ischaemic leg, reversal of hypoxia does not result in any significant improvement of the nerve function measurements.

Keywords

Hypoxia revascularization peripheral neuropathy 

Abbreviations

NDS

Neuropathy disability score

NSS

neuropathy symptom score

TcPO2

transcutaneous oxygen tension

PNCV

peroneal nerve conduction velocity

VPT

vibration perception threshold

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Boulton AJM (1993) Pathogenesis of diabetic neuropathy. In: Home PD, Marshall SM, Alberti KGMM, Krall LP (eds) The diabetes annual 7. Elsevier, Amsterdam, pp 192–210Google Scholar
  2. 2.
    Greene DA, Lattimer SA, Sima AAF (1987) Sorbitol, phosphoinositides, and sodium-potassium-ATPase in the pathogenesis of diabetic complications. N Engl J Med 316: 599–606Google Scholar
  3. 3.
    Dyck PJ, Hansen S, Karnes J et al. (1985) Capillary number and percentage closed in human diabetic sural nerve. Proc Natl Acad Sci USA 82: 2513–2517Google Scholar
  4. 4.
    Dyck PJ, Lais A, Karnes JL, O'Brien P, Rizza R (1986) Fiber loss is primary and multifocal in sural nerves in diabetic polyneuropathy. Ann Neurol 19: 425–429Google Scholar
  5. 5.
    Malik RA, Veves A, Masson EA et al. (1992) Endoneurial capillary abnormalities in early human diabetic neuropathy. J Neurol Neurosurg Psychiatry 55: 557–561Google Scholar
  6. 6.
    Appenzeller O, Parks RD, MacGee J (1968) Peripheral neuropathy in chronic disease of the respiratory tract. Am J Med 44: 873–880Google Scholar
  7. 7.
    Malik RA, Masson EA, Sharma AK et al. (1990) Hypoxic neuropathy: relevance to human diabetic neuropathy. Diabetologia 33: 311–318Google Scholar
  8. 8.
    Young MJ, Veves A, Walker MG, Boulton AJM (1992) Correlations between nerve function and tissue oxygenation in diabetic patients: further clues to the aetiology of diabetic neuropathy? Diabetologia 35: 1146–1150Google Scholar
  9. 9.
    LoGerfo FW, Coffman JD (1984) Vascular and microvascular disease of the foot in diabetes. N Engl J Med 311: 1615–1619Google Scholar
  10. 10.
    Consensus statement (1988) Report and recommendations of the San Antonio conference on diabetic neuropathy. Diabetes 37: 1000–1004Google Scholar
  11. 11.
    Wiles PG, Pearce SM, Rice PJS, Mitchell JMO (1991) Vibration perception threshold: influence of age, height, sex, and smoking and calculation of accurate centile values. Diabet Med 8: 157–161Google Scholar
  12. 12.
    Kumar S, Fernando DJS, Veves A, Knowles EA, Young MJ, Boulton AJM (1991) Semmes-Weinstein monofilaments: a simple, effective and inexpensive screening device for identifying diabetic patients at risk of foot ulceration. Diabetes Res Clin Pract 13: 63–67Google Scholar
  13. 13.
    Kimura J (1984) Nerve conduction studies and electromyography. In: Dyck PJ, Thomas PK, Lambert EH, Bunge R (eds) Peripheral neuropathy. WB Saunders, Philadelphia, pp 919–966Google Scholar
  14. 14.
    Dyck PJ (1989) Hypoxic neuropathy: does hypoxia play a role in diabetic neuropathy? Neurology 39: 111–118Google Scholar
  15. 15.
    Newrick PG, Wilson AJ, Jacubowski J, Boulton AJM, Ward JD (1986) Sural nerve oxygen tension in human diabetes. BMJ 293: 1053–1054Google Scholar
  16. 16.
    Malik RA, Tesfaye S, Thompson SD et al. (1993) Endoneurial localisation of microvascular damage in human diabetic neuropathy. Diabetologia 36: 454–459Google Scholar
  17. 17.
    Tesfaye S, Malik RA, Ward JD (1984) Vascular factors in diabetic neuropathy. Diabetologia 37: 847–854Google Scholar
  18. 18.
    Young MJ, Veves A, Smith JV, Walker MG, Boulton AJM (1995) Restoring lower limb blood flow improves conduction velocity in diabetic patients. Diabetologia 38: 1051–1054Google Scholar
  19. 19.
    Kennedy WR, Navarro X, Goetz FC, Sutherland DER, Navarian JS (1990) Effects of pancreatic transplantation on diabetic neuropathy. N Engl J Med 322: 1031–1037Google Scholar
  20. 20.
    Ward JD, Fisher DJ, Barnes CG, Jessop JD (1971) Improvement in nerve conduction following treatment in newly diagnosed diabetics. Lancet 1: 428–430Google Scholar
  21. 21.
    Hunter GC, Song GW, Nayak NN, Zapotowski D, Guernsey JM (1988) Peripheral nerve conduction abnormalities in lower extremity ischaemia: the effects of revascularisation. J Surg Res 45: 96–103Google Scholar
  22. 22.
    Dyck PJ, Kratz KM, Lehman KA et al. (1991) The Rochester diabetic neuropathy study: design, criteria for types of neuropathy, selection bias, and reproducibility of neuropathic tests. Neurology 41: 799–807Google Scholar
  23. 23.
    Veves A, Malik RA, Lye RH et al. (1991) Correlations between sural nerve histology and electrophysiology and quantitative sensory tests in mild diabetic neuropathy. Diabet Med 8: 917–921Google Scholar
  24. 24.
    Dyck PJ, Karnes JL, Daube J, O'Brien P, Service FJ (1985) Clinical and neuropathological criteria for the diagnosis and staging of diabetic neuropathy. Brain 108: 861–880Google Scholar
  25. 25.
    Malik RA, Newrick PG, Sharma AK et al. (1989) Microangiopathy in human diabetic neuropathy: relationship between capillary abnormalities and the severity of neuropathy. Diabetologia 32: 92–102Google Scholar
  26. 26.
    Proceedings of a consensus development conference on standardized measures in diabetic neuropathy (1992) Muscle and Nerve 15: 1143–1170Google Scholar

Copyright information

© Springer-Verlag 1996

Authors and Affiliations

  • A. Veves
    • 1
  • V. M. Donaghue
    • 2
  • M. R. Sarnow
    • 2
  • J. M. Giurini
    • 2
  • D. R. Campbell
    • 3
  • F. W. LoGerfo
    • 3
  1. 1.Deaconess-Joslin Foot Center, Department of MedicineHarvard Medical SchoolBostonUSA
  2. 2.Deaconess-Joslin Foot Center, Division of Podiatry, Department of SurgeryHarvard Medical SchoolBostonUSA
  3. 3.Deaconess-Joslin Foot Center, Division of Vascular Surgery, Department of SurgeryHarvard Medical SchoolBostonUSA

Personalised recommendations