|
Diabetes Care, Vol 12, Issue 9 649-652, Copyright © 1989 by American Diabetes Association
Meaningful degrees of prevention or improvement of nerve conduction in controlled clinical trials of diabetic neuropathy
PJ Dyck and PC O'Brien
Peripheral Neuropathy Research Laboratory, Mayo Clinic, Rochester, Minnesota 55905.
Use of nerve conduction in assessing therapy in preventing or ameliorating
neuropathy is desirable because abnormalities of nerve conduction are
associated with severity of neuropathic symptoms and deficits. Assuming
that a therapy is associated with a statistically significant improvement
of nerve conduction, what degree of nerve conduction change is clinically
meaningful? We suggest that in controlled clinical trials, a mean change of
2 points on the neurologic disability score is clinically detectable and
meaningful. Based on our previously published cross-sectional
epidemiological data, this corresponds to a change of motor nerve
conduction velocity of the average ulnar median and peroneal nerves of 2.9
m/s and peroneal nerve of 2.2 m/s. The corresponding changes of amplitude
were 1.2 and 0.7 mV, respectively. Smaller degrees of nerve conduction
change were found when only insulin-dependent patients were evaluated.

CiteULike Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. W. Albers, W. H. Herman, R. Pop-Busui, C. L. Martin, P. Cleary, B. Waberski, and for the Diabetes Control and Complications Trial (
Subclinical Neuropathy Among Diabetes Control and Complications Trial Participants Without Diagnosable Neuropathy at Trial Completion: Possible predictors of incident neuropathy?
Diabetes Care,
October 1, 2007;
30(10):
2613 - 2618.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J W Albers, D H Garabrant, S J Schweitzer, R P Garrison, R J Richardson, and S Berent
The effects of occupational exposure to chlorpyrifos on the peripheral nervous system: a prospective cohort study
Occup. Environ. Med.,
March 1, 2004;
61(3):
201 - 211.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. R. Sharma, J. Cross, O. Farronay, D. R. Ayyar, R. T. Shebert, and W. G. Bradley
Demyelinating Neuropathy in Diabetes Mellitus
Arch Neurol,
May 1, 2002;
59(5):
758 - 765.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. R. Cornblath, V. Chaudhry, K. Carter, D. Lee, M. Seysedadr, M. Miernicki, and T. Joh
Total neuropathy score: Validation and reliability study
Neurology,
November 1, 1999;
53(8):
1660 - 1660.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
C. M. Akbari, G. W. Gibbons, G. M. Habershaw, F. W. LoGerfo, and A. Veves
The Effect of Arterial Reconstruction on the Natural History of Diabetic Neuropathy
Arch Surg,
February 1, 1997;
132(2):
148 - 152.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Reichard, B.-Y. Nilsson, and U. Rosenqvist
The Effect of Long-Term Intensified Insulin Treatment on the Development of Microvascular Complications of Diabetes Mellitus
N. Engl. J. Med.,
July 29, 1993;
329(5):
304 - 309.
[Abstract]
[Full Text]
|
 |
|
Copyright © 1989 by the American Diabetes Association.
|
|
| |
|