AUTONOMIC AND PERIPHERAL-NERVE FUNCTION IN ADOLESCENTS WITH AND WITHOUT DIABETES

被引:61
作者
DONAGHUE, KC
BONNEY, M
SIMPSON, JM
SCHWINGSHANDL, J
FUNG, ATW
HOWARD, NJ
SILINK, M
机构
[1] Ray Williams Institute of Paediatric Endocrinology, Royal Alexandra Hospital for Children, Sydney
[2] Department of Public Health, University of Sydney, Sydney
关键词
AUTONOMIC NEUROPATHY; PERIPHERAL NEUROPATHY; ADOLESCENTS; DIABETES;
D O I
10.1111/j.1464-5491.1993.tb00142.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study reference ranges were established for autonomic and peripheral nerve tests in 122 non-diabetic adolescents. Regression analysis was used to evaluate the effect of age and gender on neurological function. Increasing age was associated with: less heart rate variability during deep breathing (p = 0.03), higher thermal threshold for cold at the wrist (p = 0.009), and higher vibration threshold at the toe (p = 0.001) and medial malleolus (p = 0.01). Male gender was associated with higher Valsalva ratio (p = 0.0004), higher thermal threshold for hot at the foot (p = 0.002), and higher vibration threshold at the malleolus (p = 0.03). The REFVAL programme was used to determine parametric or non-parametric reference limits: the 5 % limits for autonomic and 95 % limits for peripheral tests. One hundred and eighty-one adolescents with diabetes were studied under identical conditions and similar effects of age and gender were found. Twenty-eight percent of the group with diabetes had at least one abnormal autonomic test result out of four (expected 18.5 %); 24 % had at least one abnormal peripheral test result out of six (expected 26.5 %). Glycaemic control was associated with autonomic (p = 0.04) but not peripheral abnormalities. Using multiple regression analysis and adjusting for age and gender, there was no effect of diabetes duration or glycaemic control on neurological function.
引用
收藏
页码:664 / 671
页数:8
相关论文
共 23 条
[11]  
Young RJ, Ewing DJ, Clarke BF., Nerve function and metabolic control in teenage diabetics, Diabetes, 32, pp. 142-147, (1983)
[12]  
Heimans JJ, Bertelsmann FW, de Beaufort CE, Faber YA, Bruining GJ., Quantitative sensory examination in diabetic children: Assessment of thermal discrimination, Diabetic Med, 4, pp. 251-253, (1987)
[13]  
Ewing DJ, Clarke BF., Diagnosis and management of diabetic autonomic neuropathy, Br Med J, 285, pp. 916-918, (1982)
[14]  
Eross J., Kreutzmann D., Jimenez M., Keen R., Rogers S., Cowell C., Et al., Colorimetric measurement of glycosylated protein in whole blood, red blood cells, plasma and dried blood, Ann Clin Biochem, 21, pp. 477-483, (1984)
[15]  
Solberg HE., Statistical treatment of collected reference values and determination of reference limits, Reference values in Laboratory Medicine, pp. 193-205, (1981)
[16]  
Royston P., Constructing time‐specific reference ranges, Stat Med, 10, pp. 675-690, (1991)
[17]  
Kostraba JN, Dorman JS, Orchard TJ, Becker DJ, Ohki Y., Ellis D., Et al., Contribution of diabetes duration before puberty to development of microvascular complications in IDDM subjects, Diabetes Care, 12, pp. 686-693, (1989)
[18]  
Bertelsmann FW, Heimans JJ, Weber EJM, Van der Veen EA, Schouten JA., Thermal discrimination thresholds in normal subjects and in patients with diabetic neuropathy, J Neurol Neurosurg Psychiatry, 48, pp. 686-690, (1985)
[19]  
Factors in development of diabetic neuropathy: Baseline analysis of neuropathy in feasibility phase of diabetes control and complications trial (DCCT), Diabetes, 37, pp. 476-481, (1988)
[20]  
Young RJ, Macintyre CCA, Martyn CN, Prescott RJ, Ewing DJ, Smith AF, Et al., Progression of subclinical polyneuropathy in young patients with Type 1 (insulin‐dependent) diabetes: Associations with glycaemic control and microangiopathy (microvascular complications), Diabetologia, 29, pp. 156-161, (1986)