Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-24T04:21:51.388Z Has data issue: false hasContentIssue false

Dispersion of the P wave as a test for cardiac autonomic function in diabetic children

Published online by Cambridge University Press:  01 December 2008

Ebru Y. Imamoglu*
Affiliation:
Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey
Funda Oztunc
Affiliation:
Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey
Ayse G. Eroglu
Affiliation:
Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey
Hasan Onal
Affiliation:
Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey
Alper Guzeltas
Affiliation:
Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey
*
Correspondence to: Ebru Y. Imamoglu, Department of Pediatrics, İstanbul University Cerrahpasa Medical Faculty, Fatih, Istanbul, Turkey. Tel: +505 385 36 80; Fax: +212 632 86 33; E-mail: [email protected]

Abstract

Objective

We aimed, in this study, to compare dispersion of the p wave in patients with type 1 diabetes to nondiabetic control subjects, and to investigate the relationship between the dispersion of the p wave and cardiac autonomic dysfunction in diabetic children.

Methods

We enrolled 49 patients with type 1 diabetes, and 32 age- and sex-matched healthy subjects, measuring the Valsalva ratio, resting heart rate, and orthostatic hypotension in all. The duration of the p wave was measured manually on a high-resolution computer screen. Dispersion, defined as the difference between maximum and minimum durations of the p waves, was also measured in the 12-lead electrocardiogram before and after the Valsalva maneuver.

Results

The mean age of the patients and their controls were 14.2 ± 4.8 years, and 12.7 ± 4.5 years, respectively. The mean duration of diabetes had been 6.2 ± 4.6 years. Maximal and minimal values for the duration of the p wave were significantly decreased in the diabetic children, with the dispersion itself significantly increased. Values for the dispersion in the diabetic subjects were similar before and after the Valsalva maneuver, whereas dispersion was found significantly increased after this maneuver in the controls. The differences in the Valsalva ratio, resting heart rate, and orthostatic hypotension between the groups, on the other hand, were not found to be statistically significant.

Conclusion

The noted increase in the dispersion of the p wave in diabetic children reveals the onset of cardiac electrophysiological heterogeneity before it is possible to detect parasympathetic and sympathetic dysfunction with other tests.

Type
Original Article
Copyright
Copyright © Cambridge University Press 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Barkai, L, Madacsy, L. Cardiovascular autonomic dysfunction in diabetes mellitus. Arch Dis Child 1995; 73: 515518.Google Scholar
2.Arildsen, H, May, O, Christiansen, EH, Damsgaard, EM. Increased QT dispersion in patients with insulin-dependent diabetes mellitus. Int J Cardiol 1999; 71: 235242.Google Scholar
3.Barkai, L, Madacsy, L, Kassay, L. Investigation of subclinical signs of autonomic neuropathy in the early stage of childhood diabetes. Horm Res 1990; 34: 5459.Google Scholar
4.Ewing, DJ, Campbell, IW, Clarke, BF. Assessment of cardiovascular effects in diabetic autonomic neuropathy and prognostic implications. Ann Intern Med 1980; 92: 308311.CrossRefGoogle ScholarPubMed
5.Mitchell, EA, Wealthall, SR, Elliott, RB. Tests for autonomic neuropathy in diabetic children. Aust Paediatr J 1985; 21: 105109.Google Scholar
6.Mitchell, EA, Wealthall, SR, Elliott, RB. Diabetic autonomic neuropathy in children: immediate heart-rate response to standing. Aust Paediatr J 1983; 19: 175177.Google Scholar
7.Pourmoghaddas, A, Hekmatnia, A. The relationship between QTc interval and cardiac autonomic neuropathy in diabetes mellitus. Mol Cell Biochem 2003; 249: 125128.Google Scholar
8.Risk, M, Bril, V, Broadbridge, C, Cohen, A. Heart rate variability measurement in diabetic neuropathy:review of methods. Diabetes Technol Ther 2001; 3: 6376.CrossRefGoogle ScholarPubMed
9.Robillon, JF, Sadoul, JL, Benmerabet, S, et al. Assessment of cardiac arrhythmic risk in diabetic patients using QT dispersion abnormalities. Diabetes Metab 1999; 25: 419423.Google Scholar
10.Cheema, AN, Ahmed, MW, Kadish, AH, Goldberger, JJ. Effects of autonomic stimulation and blockade on signal-averaged P wave duration. J Am Coll Cardiol 1995; 26: 497502.Google Scholar
11.Elisberg, EI, Goldberg, H, Snider, GL. Value of intraoral pressure as a measure of intrapleural pressure. J Appl Physiol 1951; 4: 171176.CrossRefGoogle ScholarPubMed
12.Waggoner, AD, Adyanthaya, AV, Quinones, MA, Alexander, JK. Left atrial enlargement. Echocardiographic assessment of electrocardiographic criteria. Circulation 1976; 54: 553557.Google Scholar
13.Dogan, A, Acar, G, Gedikli, O, et al. A comparison of P-wave duration and dispersion in patients with short-term and long-term atrial fibrillation. J Electrocardiol 2003; 36: 251255.Google Scholar
14.Kose, S, Kilic, A, Iyisoy, A, Kursaklioglu, H, Lenk, MK. P wave duration and P dispersionin healthy children. Turk J Pediatr 2003; 45: 133135.Google Scholar
15.Dilaveris, PE, Gialafos, EJ, Sideris, SK, et al. Simple electrocardiographic markers for the prediction of paroxysmal idiopathic atrial fibrillation. Am Heart J 1998; 135: 733738.CrossRefGoogle ScholarPubMed
16.Tukek, T, Akkaya, V, Demirel, S, et al. Effect of Valsalva maneuver on surface electrocardiographic P-wave dispersion in paroxysmal atrial fibrillation. Am J Cardiol 2000; 85: 896899; A10.Google Scholar
17.Clarke, BF, Ewing, DJ, Campbell, IW. Diabetic autonomic neuropathy. Diabetologia 1979; 17: 195212. Review.Google Scholar
18.Hosking, DJ, Bennett, T, Hampton, JR. Diabetic autonomic neuropathy. Diabetes 1978; 27: 10431055. Review.CrossRefGoogle ScholarPubMed
19.Baldwa, VS, Ewing, DJ. Heart rate response to Valsalva manoeuvre. Reproducibility in normals, and relation to variation in resting heart rate in diabetics. Br Heart J 1977; 39: 641644.CrossRefGoogle ScholarPubMed
20.Ewing, DJ, Campbell, IW, Burt, AA, Clarke, BF. Vascular reflexes in diabetic autonomic neuropathy. Lancet 1973; 2: 13541356.CrossRefGoogle ScholarPubMed
21.Lewin, AB. A simple test of cardiac function based upon the heart rate changes induced by the Valsalva manoeuvre. Am J Cardiol 1966; 18: 9099.Google Scholar
22.Spach, MS, Dolber, PC. Relating extracellular potentials and their derivatives to anisotropic propagation at a microscopic level in human cardiac muscle. Evidence for electrical uncoupling of side-to-side fiber connections with increasing age. Circ Res 1986; 58: 356371.CrossRefGoogle Scholar
23.Dilaveris, PE, Andrikopoulos, GK, Metaxas, G, et al. Effects of ischemia on P wave dispersion and maximum P wave duration during spontaneous anginal episodes. Pacing Clin Electrophysiol 1999; 22: 16401647.CrossRefGoogle Scholar
24.Andrikopoulos, GK, Dilaveris, PE, Richter, DJ, et al. Increased variance of P wave duration on the electrocardiogram distinguishes patients with idiopathic paroxysmal atrial fibrillation. Pacing Clin Electrophysiol 2000; 23: 11271132.Google Scholar