Circadian variation in QT dispersion determined from a 12-lead Holter recording: a methodological study of an age- and sex-stratified group of healthy subjects

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Circadian variation in QT dispersion determined from a 12-lead Holter recording : a methodological study of an age- and sex-stratified group of healthy subjects. / Hansen, S; Rasmussen, Verner; Larsen, Klaus; Torp-Pedersen, Christian; Jensen, Gorm Boje; Hansen, Stig; Torp-Pedersen, Christian.

In: Annals of Noninvasive Electrocardiology (Online), Vol. 12, No. 3, 2007, p. 185-96.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, S, Rasmussen, V, Larsen, K, Torp-Pedersen, C, Jensen, GB, Hansen, S & Torp-Pedersen, C 2007, 'Circadian variation in QT dispersion determined from a 12-lead Holter recording: a methodological study of an age- and sex-stratified group of healthy subjects', Annals of Noninvasive Electrocardiology (Online), vol. 12, no. 3, pp. 185-96. https://doi.org/10.1111/j.1542-474X.2007.00160.x

APA

Hansen, S., Rasmussen, V., Larsen, K., Torp-Pedersen, C., Jensen, G. B., Hansen, S., & Torp-Pedersen, C. (2007). Circadian variation in QT dispersion determined from a 12-lead Holter recording: a methodological study of an age- and sex-stratified group of healthy subjects. Annals of Noninvasive Electrocardiology (Online), 12(3), 185-96. https://doi.org/10.1111/j.1542-474X.2007.00160.x

Vancouver

Hansen S, Rasmussen V, Larsen K, Torp-Pedersen C, Jensen GB, Hansen S et al. Circadian variation in QT dispersion determined from a 12-lead Holter recording: a methodological study of an age- and sex-stratified group of healthy subjects. Annals of Noninvasive Electrocardiology (Online). 2007;12(3):185-96. https://doi.org/10.1111/j.1542-474X.2007.00160.x

Author

Hansen, S ; Rasmussen, Verner ; Larsen, Klaus ; Torp-Pedersen, Christian ; Jensen, Gorm Boje ; Hansen, Stig ; Torp-Pedersen, Christian. / Circadian variation in QT dispersion determined from a 12-lead Holter recording : a methodological study of an age- and sex-stratified group of healthy subjects. In: Annals of Noninvasive Electrocardiology (Online). 2007 ; Vol. 12, No. 3. pp. 185-96.

Bibtex

@article{e937bb3d028d4c7995909427c54d23bf,
title = "Circadian variation in QT dispersion determined from a 12-lead Holter recording: a methodological study of an age- and sex-stratified group of healthy subjects",
abstract = "Background: QT dispersion is considered to reflect inhomogeneity of myocardial repolarization. Method: The circadian variation of QT interval dispersion was examined in 95 healthy subjects using 24-hour Holter monitoring. Three different methods of lead selection were applied: all 12 leads (QTdisp 12), only precordial leads (QTdisp 6), and the pair of leads selected at 3 a.m. in which the longest and shortest QT intervals were found in each individual subject (QTdisp 2). Results: A preliminary methodological study including measurements from every minute in 10 subjects revealed no significant circadian variation using mean values of QTdisp 12, QTdisp 6, or QTdisp 2 obtained every hour, every 2, or every 4 hours, except in QTdisp 6, which demonstrated a significant circadian variation (P < 0.01) in 1-hour measurements. Analysis of all 95 subjects using measurements obtained every 4 hours revealed a significant circadian variation in QTdisp 12 and QTdisp 6 (P < 0.0001), whereas no circadian variation was seen in QTdisp 2. A subdivision into 10-year age groups revealed that subjects at age >50 years had a significant circadian variation in QTdisp 12 and QTdisp 6, but not in QTdisp 2. Only in males a significant circadian variation was seen in QTdisp 12 (P < 0.0001), whereas QTdisp 6 demonstrated a circadian variation both in females (P < 0.001) and in males (P < 0.0001). Conclusions: Selection of leads is of crucial importance for repetitive measurements of QT dispersion. Circadian variation was detected in subjects over 50 years of age, when all 12 or only the 6 precordial leads were taken into account.",
author = "S Hansen and Verner Rasmussen and Klaus Larsen and Christian Torp-Pedersen and Jensen, {Gorm Boje} and Stig Hansen and Christian Torp-Pedersen",
year = "2007",
doi = "http://dx.doi.org/10.1111/j.1542-474X.2007.00160.x",
language = "English",
volume = "12",
pages = "185--96",
journal = "Annals of Noninvasive Electrocardiology",
issn = "1542-474X",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Circadian variation in QT dispersion determined from a 12-lead Holter recording

T2 - a methodological study of an age- and sex-stratified group of healthy subjects

AU - Hansen, S

AU - Rasmussen, Verner

AU - Larsen, Klaus

AU - Torp-Pedersen, Christian

AU - Jensen, Gorm Boje

AU - Hansen, Stig

AU - Torp-Pedersen, Christian

PY - 2007

Y1 - 2007

N2 - Background: QT dispersion is considered to reflect inhomogeneity of myocardial repolarization. Method: The circadian variation of QT interval dispersion was examined in 95 healthy subjects using 24-hour Holter monitoring. Three different methods of lead selection were applied: all 12 leads (QTdisp 12), only precordial leads (QTdisp 6), and the pair of leads selected at 3 a.m. in which the longest and shortest QT intervals were found in each individual subject (QTdisp 2). Results: A preliminary methodological study including measurements from every minute in 10 subjects revealed no significant circadian variation using mean values of QTdisp 12, QTdisp 6, or QTdisp 2 obtained every hour, every 2, or every 4 hours, except in QTdisp 6, which demonstrated a significant circadian variation (P < 0.01) in 1-hour measurements. Analysis of all 95 subjects using measurements obtained every 4 hours revealed a significant circadian variation in QTdisp 12 and QTdisp 6 (P < 0.0001), whereas no circadian variation was seen in QTdisp 2. A subdivision into 10-year age groups revealed that subjects at age >50 years had a significant circadian variation in QTdisp 12 and QTdisp 6, but not in QTdisp 2. Only in males a significant circadian variation was seen in QTdisp 12 (P < 0.0001), whereas QTdisp 6 demonstrated a circadian variation both in females (P < 0.001) and in males (P < 0.0001). Conclusions: Selection of leads is of crucial importance for repetitive measurements of QT dispersion. Circadian variation was detected in subjects over 50 years of age, when all 12 or only the 6 precordial leads were taken into account.

AB - Background: QT dispersion is considered to reflect inhomogeneity of myocardial repolarization. Method: The circadian variation of QT interval dispersion was examined in 95 healthy subjects using 24-hour Holter monitoring. Three different methods of lead selection were applied: all 12 leads (QTdisp 12), only precordial leads (QTdisp 6), and the pair of leads selected at 3 a.m. in which the longest and shortest QT intervals were found in each individual subject (QTdisp 2). Results: A preliminary methodological study including measurements from every minute in 10 subjects revealed no significant circadian variation using mean values of QTdisp 12, QTdisp 6, or QTdisp 2 obtained every hour, every 2, or every 4 hours, except in QTdisp 6, which demonstrated a significant circadian variation (P < 0.01) in 1-hour measurements. Analysis of all 95 subjects using measurements obtained every 4 hours revealed a significant circadian variation in QTdisp 12 and QTdisp 6 (P < 0.0001), whereas no circadian variation was seen in QTdisp 2. A subdivision into 10-year age groups revealed that subjects at age >50 years had a significant circadian variation in QTdisp 12 and QTdisp 6, but not in QTdisp 2. Only in males a significant circadian variation was seen in QTdisp 12 (P < 0.0001), whereas QTdisp 6 demonstrated a circadian variation both in females (P < 0.001) and in males (P < 0.0001). Conclusions: Selection of leads is of crucial importance for repetitive measurements of QT dispersion. Circadian variation was detected in subjects over 50 years of age, when all 12 or only the 6 precordial leads were taken into account.

U2 - http://dx.doi.org/10.1111/j.1542-474X.2007.00160.x

DO - http://dx.doi.org/10.1111/j.1542-474X.2007.00160.x

M3 - Journal article

VL - 12

SP - 185

EP - 196

JO - Annals of Noninvasive Electrocardiology

JF - Annals of Noninvasive Electrocardiology

SN - 1542-474X

IS - 3

ER -

ID: 34142129