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Noninvasive Evaluation of Neural Impairment in Subjects With Impaired Glucose Tolerance

  1. Zsuzsanna Putz, MD12,
  2. Ádám G Tabák, MD, PHD13,
  3. Nelli Tóth, MD1,
  4. Ildikó Istenes, MD1,
  5. Nóra Németh1,
  6. Rajiv A. Gandhi, MD4,
  7. Zsolt Hermányi, MD12,
  8. Katalin Keresztes, MD, PHD1,
  9. György Jermendy, MD, PHD, DSC2,
  10. Solomon Tesfaye, MD, FRCP4 and
  11. Péter Kempler, MD, PHD, DSC1
  1. 11st Department of Medicine, Semmelweis University, Budapest, Hungary
  2. 23rd Department of Internal Medicine, Bajcsy-Zsilinszky Hospital, Budapest, Hungary
  3. 3Department of Epidemiology and Public Health, University College London, London, UK
  4. 4Royal Hallamshire Hospital, Sheffield, U.K.
  1. Corresponding author: Zsuzsanna Putz, zsuzsannaputz{at}yahoo.com

Abstract

OBJECTIVE—To evaluate neural dysfunction in subjects with impaired glucose tolerance (IGT).

RESEARCH DESIGN AND METHODS—For this study, 46 subjects with IGT and 45 healthy volunteers underwent detailed neurological assessment. Cardiovascular autonomic function was assessed by standard cardiovascular reflex tests, and heart rate variability was characterized by the triangle index. Sensory nerve function was assessed using Neurometer (for current perception threshold) and Medoc devices. Peak plantar pressure was measured by dynamic pedobarography, and symptoms were graded using the neuropathy total symptom score.

RESULTS—Subjects with IGT had significantly greater abnormalities detected by four of five cardiovascular reflex tests and greater heart rate variability characterized by the triangle index. They had a higher frequency of both hyperesthesia and hypoesthesia as detected by current perception threshold testing at 5 Hz, as well as increased heat detection thresholds.

CONCLUSIONS—This study provides evidence that subclinical neural dysfunction is present in subjects with IGT and can be detected noninvasively. Cardiovascular autonomic neuropathy may contribute to increased cardiovascular risk in IGT subjects.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 3 October 2008.

    Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted September 17, 2008.
    • Received July 30, 2008.
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This Article

  1. Diabetes Care January 2009 vol. 32 no. 1 181-183
  1. Online-Only Appendix
  2. All Versions of this Article:
    1. dc08-1406v1
    2. 32/1/181 most recent
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