Europace Advance Access published online on January 18, 2008
Europace, doi:10.1093/europace/eum286
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ORIGINAL ARTICLE
Cardiac repolarization during hypoglycaemia and hypoxaemia in healthy males: impact of renin–angiotensin system activity
1 Endocrinology Section, Division of Internal Medicine I, Nordsjællands Hospital - Hillerød, Helsevej 2, Hillerød DK-3400, Denmark; 2 Department of Neuroanaesthesia, Copenhagen University Hospital, Copenhagen, Denmark; 3 Danish National Research Foundation Centre for Cardiac Arrhythmia, Department of Biomedical Sciences, The Panum Institute, University of Copenhagen, Copenhagen, Denmark; 4 Department of Cardiology P, Gentofte University Hospital, Copenhagen, Denmark; 5 Department of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands
Manuscript submitted 12 October 2007. Accepted after revision 5 December 2007.
* Corresponding author. Tel: +45 48296403; fax: +45 48294783. E-mail address: rsa{at}noh.regionh.dk
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
Aims: Activity in the renin–angiotensin system (RAS) may influence the susceptibility to cardiac arrhythmia. To study the effect of basal RAS activity on cardiac repolarization during myocardial stress induced by hypoglycaemia or hypoxaemia in healthy humans.
Methods and results: Ten subjects with high RAS activity and 10 subjects with low RAS activity were studied on three different occasions: (i) hypoglycaemia (nadir P-glucose 2.7 ± 0.5 mmol/L), (ii) hypoxaemia (nadir pO2 5.8 ± 0.5 kPa), and (iii) normoglycaemic normoxia (control day). QT parameters were registered by Holter monitoring. Hypoglycaemia and hypoxaemia induced QTc prolongation (P < 0.001, both stimuli). The QT/RR slope and the VR increased as a function of hypoglycaemia, but were unaffected by hypoxaemia. Low RAS activity was associated with a steeper QT/RR slope in the recovery phase after both stimuli: hypoglycaemia: P = 0.04; hypoxia: P = 0.03. RAS activity had no impact on QTc [P = 0.48 (hypoglycaemia) and P = 0.40 (hypoxaemia)] or any of the other outcome variables.
Conclusion: Basal RAS activity has significant impact on QT dynamics, but not the corrected QT interval, during recovery from hypoglycaemia and hypoxaemia. The impact, however, is modest and more subtle than initially expected. The clinical relevance is unclear.
Key Words: Renin–angiotensin system, Cardiac repolarization, QT, Hypoglycaemia, Hypoxaemia, Substrate deficiency
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
Renin–angiotensin system (RAS) activity seems to be an important factor in the pathogenesis of cardiac arrhythmia.1
Low RAS activity, either genetically determined or pharmacologically induced, may be associated with a reduced risk of ventricular arrhythmia.2 Thus, the D (deletion) allele of the angiotensin converting enzyme (ACE) I/D polymorphism (which confers high ACE activity)3 is related to an increased occurrence of reperfusion-induced ventricular arrhythmia after myocardial infarction1 and to QTc prolongation in end-stage renal disease.4 Furthermore, a meta-analysis shows that ACE inhibitor treatment after myocardial infarction reduces the risk of sudden cardiac death.2 This effect may partly be ascribed to a positive impact of ACE inhibitors on cardiac repolarization, since ACE inhibitor treatment reduces QTc in hypertensive patients5 and QT dispersion in patients with myocardial infarction.6 The QT interval and its dynamics are surrogate measures of repolarization known to carry independent prognostic information on risk of sudden cardiac death7–9 and development of ventricular tachyarrhythmia.10,11
RAS activity also influences physical capacity in endurance training12 and vulnerability to hypoglycaemia,13 a common and feared adverse effect to insulin therapy, which has been suggested to play a role in the pathogenesis of the ‘dead-in-bed’ syndrome observed among young patients with type 1 diabetes. Patients with high spontaneous RAS activity have an increased risk of severe hypoglycaemia13–16 suggesting a more pronounced general susceptibility to glucose deficiency. Hence, the RAS seems to be involved in cellular energy expenditure, and spontaneous RAS activity may therefore constitute a risk marker of cardiac arrhythmia during substrate depletion.
The primary aim of this study was to investigate, if basal RAS activity has impact on the QT interval and its dynamics during hypoglycaemia and hypoxaemia, thereby being a potential risk marker of ventricular arrhythmia in situations characterized by lack of glucose or oxygen. The secondary aim was to determine the effect of hypoglycaemia and hypoxaemia on QT dynamics.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
Population
A total of 303 healthy young men participated in a screening procedure involving a venous blood sample and a health screening questionnaire. Blood samples were analysed for ACE activity, angiotensinogen concentration and the AT2 (1675A/G) polymorphism—the three RAS parameters associated with risk of hypoglycaemia. Based on a scoring system, we selected 20 subjects (26 ± 4 years) differing in terms of high or low RAS activity. The high RAS activity group was characterized by ACE activity and angiotensinogen concentration in the highest quartile and the AT2 receptor genotype AA corresponding to low expression [maximum stimulation via the angiotensin II receptor subtype 1 (AT1 receptor)].17
The low RAS activity group was characterized by ACE activity and angiotensinogen concentration in the lowest quartile and the AT2 receptor genotype GG corresponding to high expression (minimum stimulation via the AT1 receptor).17
Design
The study was a single-blinded, randomized, counter-balanced, cross-over study. Each subject was studied on three different experimental occasions: at hypoglycaemia, at hypoxia and at a normoglycaemic, normoxaemic control day, separated by at least 3 weeks. The study complies with the declaration of Helsinki. All participants gave written consent to participate and the study was approved by the Regional Ethics Committee.
Experimental set-up
Subjects were studied after an overnight fast upon arrival to the laboratory at 8.00 a.m. A three channel digital Holter Monitor (DelMar Aria recorder, Delmar Avionics, Irvine, CA, USA) was mounted. Two cannulae for blood sampling were placed in the antecubital vein and in the radial artery of the non-dominant arm. Baseline blood samples were drawn at time 15 and 45 min. Hereafter hypoglycaemia, hypoxaemia, or euglycaemia/normoxia (control) was induced. The stimulus period lasted 60 min. Blood samples were obtained at 100 (only plasma glucose), 115, 130 (only plasma glucose), and time 145 min. Samples at the recovery phase were drawn at 215 min. A flow diagram showing the study timeline is provided in Figure 1.
|
Hypoglycaemia
Hypoglycaemia was induced by subcutaneously administered fast-acting human insulin (Actrapid; Novo Nordisk, Bagsvaerd, Denmark; 0.2 U/kg administered twice—a dosage scheme which resulted in stable hypoglycaemia within the target range [plasma glucose 2.5–2.9 mmol/L] in pilot studies) with the aim of standardizing the dose of insulin. Euglycaemia was restored by ingestion of a small meal consisting of 400 mL of apple juice and a slice of brown bread (55 gm).
Hypoxaemia
Hypoxaemia was induced by spontaneous breathing of a gas mixture containing 12% oxygen administered via a soft facial mask. This oxygen content is well tolerated by healthy subjects, and mild dyspnoea was the only side effect experienced by the participants. During the study, oxygen saturation and plasma glucose were measured regularly using a pulse oximeter (N-180, Nellcor; Tyco Healthcare, Pleasanton, CA, USA) and bed-side plasma glucose measurements (HemoCue, HemoCue AB, Angelholm, Sweden), respectively. To keep participants from knowing the kind of stimulus on a particular day, atmospheric air was delivered on a facial mask during hypoglycaemia and placebo injections were given during hypoxaemia. On the control day, the subjects were subjected to two placebo injections without active insulin and atmospheric air via the mask as well.
QT parameters
QT intervals were calculated from Holter recordings obtained with modified chest leads V2, V3, and V5 for three 30-min periods each study day: baseline (15–45 min), hypoglycaemia/hypoxaemia/control (115–145 min), and recovery (215–245 min). Semiautomatic QT analysis was performed in the lead with the best defined T-wave using a modified Laguna algorithm to identify the end of the T-wave.18 Mean values of all accepted RR intervals and QT parameters were calculated for the three periods and the QT interval was corrected for differences in heart rate (HR) according to Bazett’s (QTc=QT/RR1/2) and Fridericia’s formulas (QTf=QT/RR1/3).
The adaptation of the QT interval to changes in the heart rate was assessed as the slope and the intercept of the linear regression line obtained by analysing pairs of QT interval length and the immediately preceding RR interval. SDQT and SDNN were defined as the standard deviations of all accepted QT intervals and RR intervals, respectively. The variability ratio (VR) was defined as SDQT/SDNN and reflects the variation in QT not explained by heart rate variability.8
Laboratory analyses
All biochemical analyses were performed blinded to the other results. Angiotensinogen was determined as the maximal quantity of angiotensin I generated during incubation of plasma in the presence of excess recombinant human renin as described previously.19 Serum ACE activity was determined by a commercial kinetics-based assay (Sigma Diagnostics, St Louis, MO, USA). DNA was extracted from peripheral blood leukocytes using a standard salting-out method. The ACE I/D variant and the AT2 receptor 1675G/A polymorphism were determined by polymerase chain reaction. Blood for measurements of adrenaline was sampled into chilled tubes containing 100 µL EDTA glutathione and heparin, centrifuged, drawn off by pipette and frozen (–80°C) within half an hour. Analyses were done using HPLC with fluorimetric detection.20 Glucose, potassium, and blood gases were analysed immediately by the local laboratory [plasma glucose concentrations were measured enzymatically (COBAS INTEGRA, Roche, Basel, Switzerland), pO2 by amperometry, pH by potentiometry (both ABL, Radiometer, Broenshoej, Denmark) and plasma potassium using a standard ion-selective electrode].
|
Statistics |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
Test for normality was done using Kolmogorov–Schmirnov’s model. To reduce the amount of statistical analyses performed, and thereby minimizing the risk of mass significance, mean values for the baseline period and the stimulus period were calculated and included in the statistical models. An unpaired T-test was used to compare baseline values in the two groups. To evaluate both the impact of the RAS group and the intervention (hypoglycaemia or hypoxaemia vs. placebo) on the outcome variables, a mixed linear model (ANCOVA) was applied. Hypoglycaemia and hypoxaemia data were analysed separately. ‘RAS group’ and ‘intervention’ were defined as fixed factors and ‘number of participant’ as a random factor. To correct for potential minor group differences in baseline values (and to eliminate the risk of outcome variables increases/decreases regressing towards the mean), the baseline value of the particular variable being investigated was included in the model as a covariate. The mixed model was applied on data obtained in the stimulus period and the recovery period, respectively. Correlations were evaluated using Pearson’s correlation coefficient. A level of significance <5% (P < 0.05; two-sided) was considered significant. Statistical analyses were performed using SPSS (version 13.0). Values are given as mean ± 1 SEM unless otherwise mentioned.
|
Results |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
The distribution of the ACE I/D genotypes were as follows: Low RAS activity, 4/6/0 (II/ID/DD); high RAS activity, 0/4/6 (II/ID/DD).
No parameters differed between RAS groups at baseline (Table 1 and Figure 2).
|
|
Hypoglycaemia
The hypoglycaemic stimulus was similar in both RAS groups with mean plasma glucose in 60 min lasting stimulus period of 2.8 ± 0.3 mmol/L and nadir plasma glucose of 2.7 ± 0.5 mmol/L.
Hypoglycaemia induced QTc (Figure 3) and QTf prolongation [18 ± 2 ms (aggregate mean of both groups)], whereas the dynamic QT parameters reacted ambiguously (Tables 1 and 2). The VR increased significantly. Plasma adrenaline increased by 1500%, P < 0.001 (Figure 2) and plasma potassium decreased by 20% (nadir: 3.4 mmol/L), P < 0.05. Neither plasma glucose, nor plasma adrenaline, nor plasma potassium concentrations were directly correlated to the QT prolongation.
|
|
RAS group had no impact on any of the outcome variables in the hypoglycaemic period.
During recovery, QTc and QTf were still prolonged and VR was still increased (Tables 1 and 2). The RR interval decreased and the QT/RR slope increased significantly (Figure 4). Plasma adrenaline (Figure 2) and plasma potassium tended to normalize in the recovery phase, but did not reach baseline levels.
|
Low RAS activity was significantly associated with a steeper QT/RR slope when compared with the high RAS group, whereas no other outcome variables were influenced by RAS group.
Hypoxaemia
The hypoxaemic stimulus lasted 60 min and was similar in both groups with mean pO2 of 5.9 ± 0.6 kPa and nadir pO2 of 5.8 ± 0.5 kPa. A small but significant increase in pH from 7.40 to 7.42 was observed (P < 0.05) during the hypoxaemic period.
QTc (Figure 3) and QTf prolonged, the RR interval, SDQT, and SDNN decreased, whereas VR was unaltered (Tables 1 and 3). Plasma adrenaline increased slightly but significantly from 33 to 53 pmol/L (aggregate means of both groups), P < 0.05 (Figure 2), whereas plasma potassium was unchanged. Plasma adrenaline was positively correlated to the QTc during hypoxia (R2 = 0.38, P < 0.005), whereas the correlation with QTf did not reach statistical significance. The hypoxaemic stimulus was not correlated to the QT prolongation.
|
RAS activity had no significant impact on any outcome variables during hypoxaemia, although the QT/RR slope tended to be steeper in the low RAS group (P = 0.08).
During recovery, QTc and QTf returned to baseline (Tables 1 and 3), whereas the effect of hypoxaemia on the RR interval, SDQT, and SDNN extended into this phase. Plasma adrenaline declined to baseline levels (Figure 2).
Low RAS activity was significantly associated with a steeper QT/RR slope when compared with the high RAS group. No other outcome variables were influenced by RAS group.
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
Hypoglycaemia/hypoxaemia and QT parameters
In the present study, hypoglycaemia induced QTc/QTf prolongation, which is in accordance with previous studies.21
The effect of hypoglycaemia on QT dynamics is unclear. In the present study, we found a significantly increased slope in the recovery phase of hypoglycaemia when compared with baseline. The variability ratio, VR, also increased in response to hypoglycaemia. These changes in QT dynamics may reflect alterations in the QT heart rate dependency, which are potentially harmful, as increases in slope and VR predicts sudden cardiac death in patients with heart failure and myocardial infarction.8,9,22 The impact of hypoglycaemia on QT dynamics may therefore be of relevance for the increased mortality rates seen among young patients with type 1 diabetes,23 who regularly experience hypoglycaemic episodes.24 The ‘dead-in-bed syndrome’ describes unexplained over-night death in a young patient with type 1 diabetes without late complications,25 and is suggested to involve hypoglycaemia-induced ventricular arrhythmias.26 The altered QT dynamics observed during hypoglycaemia tentatively supports this hypothesis. The slope is altered in patients with diabetes in general27—but this phenomenon seems to be related to autonomic neuropathy.28
The QT prolongation in response to hypoglycaemia is believed to be induced primarily by raised adrenaline levels, but also by insulin- and adrenaline-induced hypokalaemia. Adrenaline affects L-type Ca2+ channels,29 but do also increase Tpeak–Tend,30 which provides an index of transmural dispersion of repolarization (TDR).31 The idea is that the peak of the T-wave reflects the time of largest transmural dispersion, i.e. when the epicardium is fully repolarized and the endocardium still is depolarized. Hence, Tpeak–Tend is a window of vulnerability, where a transmural arrhythmogenic substrate exists. Increases in TDR seem to facilitate propagation of early afterdepolarizations,32 which again provide the substrate for the development of Torsade de Pointes.30 Hence, analysing Tpeak–Tend would have been another way of quantifying risk of arrhythmia in the present study. However, transmural dispersion is not the solely gradient in the ventricles. Action potentials are shorter in the right ventricle than in the left ventricle33 and furthermore, an apicobasal gradient also exists.34 The T-wave is therefore much more complex than transmural dispersion can explain.35
Hypokalaemia inhibits the human ether-a-go-go-related gene (HERG) K+ channel directly, and thereby reduces the rapid delayed rectifier potassium current (IKr).36 IKr is an important repolarizing current, and reductions in IKr can lead to QT prolongation.37 In correspondence with this, hypokalaemia is a known risk factor for arrhythmogenesis in congenital and acquired long QT syndromes.38,39 Insulin itself may also have the capacity to change the QT interval,40 just as hypoglycaemia also may affect repolarization directly by blocking the HERG K+ channel.41 In the present study, neither the highly significant rise in plasma adrenaline, nor the fall in plasma potassium, was correlated to QTc/QTf prolongation. The unexpected lack of correlation between potassium concentrations during hypokalaemia and QT prolongation probably has several explanations. First of all, the hypokalaemic stimulus was mild with a nadir plasma potassium concentration just below the reference range (3.5–4.5 mmol/L). Second of all, the participants were all healthy young men, who are known to have a large repolarization reserve when compared with women and patients with organic heart disease.38,39
Hypoglycaemia-induced changes in QT dynamics may also involve adrenaline and potassium. Adrenaline has been shown to affect QT heart rate dependence indirectly. For instance, Extramiana et al.42 showed that treatment with a beta blocking agent reduced the diurnal QT/RR slope in healthy subjects. In the present study, the slope increased after, and not during, hypoglycaemia, which may be explained by a protracted effect of adrenaline.
QTc/QTf also prolonged during hypoxaemia. Previous studies have found hypoxaemia to induce QTc prolongation43 and others have found no effect.44 The mechanism(s) behind the potential QT prolonging effect of hypoxaemia is largely unknown. The adrenaline levels, albeit only discretely increased, were positively correlated to QTc during hypoxaemia. This might indicate that adrenaline is involved in the QT prolonging response—possibly through an interplay with oxygen, which also by itself seems to affect the cardiac myocyte ion channels by inhibiting the slow component of the delayed rectifier K+ current (IKs).45 Acidosis is a potential complication to severe hypoxaemia, known to decrease IKr currents.46 In the present study, the hypoxaemic stimulus was only moderate, and pH increased vaguely as a function of hypoxaemia-induced hyperventilation (respiratory alkalosis).
QT dynamics were ambiguously influenced by hypoxaemia. The variation in QT intervals (SDQT) was reduced during recovery probably as a function of an increased heart rate. The VR and slope were unaffected, which is in conflict with a previous study using 11% oxygen that showed an increased slope in response to hypoxaemia.43 The differing results observed for hypoglycaemia and hypoxaemia were not unexpected, and may very well reflect different cellular response mechanisms. Alternatively, the magnitude of the two quite different stimuli did not correspond to each other, and the cardiac impact was of different extent.
Renin–angiotensin system activity and QT parameters
Basal RAS activity affected the QT/RR slope during recovery from both hypoglycaemia and hypoxaemia. Low RAS activity was significantly associated with a steeper slope when compared with high RAS activity. Since our definition of low basal RAS activity at some points is comparable with ACE inhibitor treatment, and since high RAS activity seems to be associated with a cellular vulnerability to hypoglycaemia,13–16 we expected low basal RAS activity to be related to an electrophysiological advantage when compared with high basal RAS activity. As a steep slope is associated with an increased risk of sudden death and ventricular arrhythmia in patients with myocardial infarction and congestive heart failure,9,10 low RAS activity was expected to be associated with a flatter slope than high RAS activity. In the present study, the opposite was observed. The finding could of course represent a statistical coincidence, but it does, nevertheless, lead to several considerations. Among these are, whether low basal RAS activity, in contrast to the initial hypothesis, constitutes a risk of arrhythmia during substrate depletion. Another is, whether a steeper slope, within the normal area, may actually be associated with a protective antiarrhythmic effect compared to a flatter slope. Previous results from a small study tentatively support the last claim.47 Here, the authors found the slope to be significantly steeper in normal subjects compared with patients resuscitated from ventricular fibrillation.
In contrast to the QT/RR slope, QTc and QTf were not associated with basal RAS activity. The fact that the participants were healthy may have influenced the result, as the QT shortening effect of ACE inhibitors,5 and the association between the ACE D-allele and QT prolongation,4 were described in the presence of structural cardiac disease. Consistent with this Jeron et al.48 found that the association between the D-allele and increased QT dispersion in patients with myocardial infarction could not be retrieved in the healthy siblings of the subjects.
The results of the present study underline the complexity of the RAS. On a long-term basis, the ACE activity seems to be positively correlated to the QT interval. On a short-term basis, however, the effects of angiotensin II and ACE inhibitors may be completely different. Thus, angiotensin II reduces action potential duration by increasing the delayed rectifier potassium current,49 just as in vitro studies found ACE inhibitors to increase action potential duration,50 thereby partly mimicking class 3 antiarrhytmic agents.
In conclusion, basal RAS activity has impact on QT dynamics in the recovery phases of both hypoglycaemia and hypoxaemia. Unexpectedly, low basal RAS activity is associated with a steeper QT/RR slope when compared with high basal RAS activity. The finding may be relevant for patients with insulin-treated diabetes or pulmonary disease, even though the difference was small, and the clinical consequence questionable. QTc and QTf were unaffected by RAS activity.
Hypoglycaemia, but not hypoxaemia, induces increases in QT/RR slope and variability ratio—a finding of potential relevance for young patients with insulin-treated diabetes, who experience hypoglycaemia on a regular basis. The different responses for hypoglycaemia and hypoxaemia may indicate different cellular responses.
|
Funding |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
The Foundation of Harald Jensen and wife, The Foundation of Olga Bryde Nielsen, The Danish Pharmacy Foundation of 1991, The Foundation of Region 3 and The Research Foundation of Frederiksborg Amt.
|
Acknowledgements |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
We thank research nurses Pernille Banck and Tove Larsen, Endocrinology Section, Division of Internal Medicine I, Hillerød Hospital, for skilful technical assistance during the experiments. Also thanks to associate professor Lene Theil Skovgaard, Department of Biostatistics, University of Copenhagen, for statistical guidance and assistance and to MD, DMSc Hugh Montgomery, MD, DMSc Børge Nordestgaard and technician Hanne Dam for helping with genotyping.
Conflict of interest: none declared.
|
References |
|---|
|
TopAbstractIntroductionMethodsStatisticsResultsDiscussionFundingAcknowledgementsReferences |
|---|
[1] Takezako T, Zhang B, Serikawa T, Fan P, Nomoto J, Saku K. The D allele of the angiotensin-converting enzyme gene and reperfusion-induced ventricular arrhythmias in patients with acute myocardial infarction. Jpn Circ J (2001) 65:603–9.[CrossRef][Medline]
[2] Domanski MJ, Exner DV, Borkowf CB, Geller NL, Rosenberg Y, Pfeffer MA. Effect of angiotensin converting enzyme inhibition on sudden cardiac death in patients following acute myocardial infarction. A meta-analysis of randomized clinical trials. J Am Coll Cardiol (1999) 33:598–604.
[3] Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest (1990) 86:1343–6.[Web of Science][Medline]
[4] Raizada V, Skipper B, Luo W, Garza L, Hines CW, Harford AA, et al. Renin–angiotensin polymorphisms and QTc interval prolongation in end-stage renal disease. Kidney Int (2005) 68:1186–9.[CrossRef][Web of Science][Medline]
[5] Gonzalez-Juanatey JR, Garcia-Acuna JM, Pose A, Varela A, Calvo C, Cabezas-Cerrato J, et al. Reduction of QT and QTc dispersion during long-term treatment of systemic hypertension with enalapril. Am J Cardiol (1998) 81:170–4.[CrossRef][Web of Science][Medline]
[6] Spargias KS, Lindsay SJ, Hall AS, Cowan JC, Ball SG. Ramipril reduces QT dispersion in patients with acute myocardial infarction and heart failure. Am J Cardiol (1999) 83:969–71. A10.[CrossRef][Web of Science][Medline]
[7] Straus SM, Kors JA, De Bruin ML, van der Hooft CS, Hofman A, Heeringa J, et al. Prolonged QTc interval and risk of sudden cardiac death in a population of older adults. J Am Coll Cardiol (2006) 47:362–7.
[8] Jensen BT, Abildstrom SZ, Larroude CE, Agner E, Torp-Pedersen C, Nyvad O, et al. QT dynamics in risk stratification after myocardial infarction. Heart Rhythm (2005) 2:357–64.[CrossRef][Web of Science][Medline]
[9] Pathak A, Curnier D, Fourcade J, Roncalli J, Stein PK, Hermant P, et al. QT dynamicity: a prognostic factor for sudden cardiac death in chronic heart failure. Eur J Heart Fail (2005) 7:269–75.
[10] Extramiana F, Neyroud N, Huikuri HV, Koistinen MJ, Coumel P, Maison-Blanche P. QT interval and arrhythmic risk assessment after myocardial infarction. Am J Cardiol (1999) 83:266–9.[CrossRef][Web of Science][Medline]
[11] Lankipalli RS, Zhu T, Guo D, Yan GX. Mechanisms underlying arrhythmogenesis in long QT syndrome. J Electrocardiol (2005) 38:69–73.[Web of Science][Medline]
[12] Montgomery HE, Marshall R, Hemingway H, Myerson S, Clarkson P, Dollery C, et al. Human gene for physical performance. Nature (1998) 393:221–2.[CrossRef][Medline]
[13] Pedersen-Bjergaard U, Agerholm-Larsen B, Pramming S, Hougaard P, Thorsteinsson B. Prediction of severe hypoglycaemia by angiotensin-converting enzyme activity and genotype in type 1 diabetes. Diabetologia (2003) 46:89–96.[Web of Science][Medline]
[14] Nordfeldt S, Samuelsson U. Serum ACE predicts severe hypoglycemia in children and adolescents with type 1 diabetes. Diabetes Care (2003) 26:274–8.
[15] Pedersen-Bjergaard U, Dhamrait S, Montgomery H, Pramming S, Thorsteinsson B. Angiotensin II receptor polymorphims and occurence of severe hypoglycemia in type 1 diabetes. (Abstract). Diabetes (2003) 52(Suppl. 1):A29.[CrossRef]
[16] Pedersen-Bjergaard U, Sethi AA, Frandsen E, Hougaard P, Pramming S, Thorsteinsson B. Synergistic effect of plasma angiotensinogen and ACE-activity on risk of severe hypoglycaemia in type 1 diabetes. (Abstract). Diabetologia (2002) 45:A78.
[17] Warnecke C, Mugrauer P, Surder D, Erdmann J, Schubert C, Regitz-Zagrosek V. Intronic ANG II type 2 receptor gene polymorphism 1675 G/A modulates receptor protein expression but not mRNA splicing. Am J Physiol Regul Integr Comp Physiol (2005) 289:R1729–35.
[18] Laguna P, Thakor NV, Caminal P, Jane R, Yoon HR, Bayes de LA, et al. New algorithm for QT interval analysis in 24-hour Holter ECG: performance and applications. Med Biol Eng Comput (1990) 28:67–73.[CrossRef][Web of Science][Medline]
[19] Derkx FH, Steunkel C, Schalekamp MP, Visser W, Huisveld IH, Schalekamp MA. Immunoreactive renin, prorenin, and enzymatically active renin in plasma during pregnancy and in women taking oral contraceptives. J Clin Endocrinol Metab (1986) 63:1008–15.
[20] van der Hoorn FA, Boomsma F, Man in ‘t Veld AJ, Schalekamp MA. Determination of catecholamines in human plasma by high-performance liquid chromatography: comparison between a new method with fluorescence detection and an established method with electrochemical detection. J Chromatogr (1989) 487:17–28.[Web of Science][Medline]
[21] Robinson RT, Harris ND, Ireland RH, Lee S, Newman C, Heller SR. Mechanisms of abnormal cardiac repolarization during insulin-induced hypoglycemia. Diabetes (2003) 52:1469–74.
[22] Chevalier P, Burri H, Adeleine P, Kirkorian G, Lopez M, Leizorovicz A, et al. QT dynamicity and sudden death after myocardial infarction: results of a long-term follow-up study. J Cardiovasc Electrophysiol (2003) 14:227–33.[Web of Science][Medline]
[23] Waernbaum I, Blohme G, Ostman J, Sundkvist G, Eriksson JW, Arnqvist HJ, et al. Excess mortality in incident cases of diabetes mellitus aged 15 to 34 years at diagnosis: a population-based study (DISS) in Sweden. Diabetologia (2006) 49:653–9.[CrossRef][Web of Science][Medline]
[24] Pedersen-Bjergaard U, Pramming S, Heller SR, Wallace TM, Rasmussen AK, Jorgensen HV, et al. Severe hypoglycaemia in 1076 adult patients with type 1 diabetes: influence of risk markers and selection. Diabetes Metab Res Rev (2004) 20:479–86.[CrossRef][Web of Science][Medline]
[25] Tattersall RB, Gill GV. Unexplained deaths of type 1 diabetic patients. Diabet med (1991) 8:49–58.[Web of Science][Medline]
[26] Marques JL, George E, Peacey SR, Harris ND, Macdonald IA, Cochrane T, et al. Altered ventricular repolarization during hypoglycaemia in patients with diabetes. Diabet med (1997) 14:648–54.[CrossRef][Web of Science][Medline]
[27] Lieb W. Impact of diabetes on QT dynamicity in patients with and without myocardial infarction: the KORA family heart study. Pacing Clin Electrophysiol (2007) 30:S183–7.[Medline]
[28] Valensi PE, Johnson NB, Maison-Blanche P, Extramania F, Motte G, Coumel P. Influence of cardiac autonomic neuropathy on heart rate dependence of ventricular repolarization in diabetic patients. Diabetes Care (2002) 25:918–23.
[29] Yue DT, Herzig S, Marban E. Beta-adrenergic stimulation of calcium channels occurs by potentiation of high-activity gating modes. Proc Natl Acad Sci USA (1990) 87:753–7.
[30] Shimizu W, Antzelevitch C. Cellular basis for the ECG features of the LQT1 form of the long-QT syndrome: effects of beta-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and torsade de pointes. Circulation (1998) 98:2314–22.
[31] Yan GX, Antzelevitch C. Cellular basis for the normal T wave and the electrocardiographic manifestations of the long-QT syndrome. Circulation (1998) 98:1928–36.
[32] Yan GX, Wu Y, Liu T, Wang J, Marinchak RA, Kowey PR. Phase 2 early afterdepolarization as a trigger of polymorphic ventricular tachycardia in acquired long-QT syndrome: direct evidence from intracellular recordings in the intact left ventricular wall. Circulation (2001) 103:2851–6.
[33] Watanabe T, Delbridge LM, Bustamante JO, McDonald TF. Heterogeneity of the action potential in isolated rat ventricular myocytes and tissue. Circ Res (1983) 52:280–90.
[34] Clark RB, Bouchard RA, Salinas-Stefanon E, Sanchez-Chapula J, Giles WR. Heterogeneity of action potential waveforms and potassium currents in rat ventricle. Cardiovasc Res (1993) 27:1795–9.
[35] Kanters JK, Graff C, Andersen MP, Hardahl T, Toft E, Christiansen M, et al. Long QT syndrome genotyping by electrocardiography: fact, fiction, or something in between? J Electrocardiol (2006) 39:S119–S122.[CrossRef][Web of Science][Medline]
[36] Numaguchi H, Johnson JP Jr, Petersen CI, Balser JR. A sensitive mechanism for cation modulation of potassium current. Nat Neurosci (2000) 3:429–30.[CrossRef][Web of Science][Medline]
[37] Roden DM. Drug-induced prolongation of the QT interval. N Engl J Med (2004) 350:1013–22.
[38] Zeltser D, Justo D, Halkin A, Prokhorov V, Heller K, Viskin S. Torsade de pointes due to noncardiac drugs: most patients have easily identifiable risk factors. Medicine (Baltimore) (2003) 82:282–90.[CrossRef][Medline]
[39] Camm AJ, Janse MJ, Roden DM, Rosen MR, Cinca J, Cobbe SM. Congenital and acquired long QT syndrome. Eur Heart J (2000) 21:1232–7.
[40] Aulbach F, Simm A, Maier S, Langenfeld H, Walter U, Kersting U, et al. Insulin stimulates the L-type Ca2+ current in rat cardiac myocytes. Cardiovasc Res (1999) 42:113–20.
[41] Zhang Y, Han H, Wang J, Wang H, Yang B, Wang Z. Impairment of human ether-a-go-go-related gene (HERG) K+ channel function by hypoglycemia and hyperglycemia. Similar phenotypes but different mechanisms. J Biol Chem (2003) 278:10417–26.
[42] Extramiana F, Maison-Blanche P, Tavernier R, Jordaens L, Leenhardt A, Coumel P. Cardiac effects of chronic oral beta-blockade: lack of agreement between heart rate and QT interval changes. Ann Noninvasive Electrocardiol (2002) 7:379–88.[CrossRef][Web of Science][Medline]
[43] Roche F, Reynaud C, Pichot V, Duverney D, Costes F, Garet M, et al. Effect of acute hypoxia on QT rate dependence and corrected QT interval in healthy subjects. Am J Cardiol (2003) 91:916–9.[CrossRef][Web of Science][Medline]
[44] Kiely DG, Cargill RI, Grove A, Struthers AD, Lipworth BJ. Abnormal myocardial repolarisation in response to hypoxaemia and fenoterol. Thorax (1995) 50:1062–6.
[45] Hool LC. Acute hypoxia differentially regulates K(+) channels. Implications with respect to cardiac arrhythmia. Eur Biophys J (2005) 34:369–76.[CrossRef][Web of Science][Medline]
[46] Lin C, Cvetanovic I, Ke X, Ranade V, Somberg J. A mechanism for the potential proarrhythmic effect of acidosis, bradycardia, and hypokalemia on the blockade of human ether-a-go-go-related gene (HERG) channels. Am J Ther (2005) 12:328–36.[CrossRef][Medline]
[47] Tavernier R, Jordaens L, Haerynck F, Derycke E, Clement DL. Changes in the QT interval and its adaptation to rate, assessed with continuous electrocardiographic recordings in patients with ventricular fibrillation, as compared to normal individuals without arrhythmias. Eur Heart J (1997) 18:994–9.
[48] Jeron A, Hengstenberg C, Engel S, Lowel H, Riegger GA, Schunkert H, et al. The D-allele of the ACE polymorphism is related to increased QT dispersion in 609 patients after myocardial infarction. Eur Heart J (2001) 22:663–8.
[49] Zankov DP, Omatsu-Kanbe M, Isono T, Toyoda F, Ding WG, Matsuura H, et al. Angiotensin II potentiates the slow component of delayed rectifier K+ current via the AT1 receptor in guinea pig atrial myocytes. Circulation (2006) 113:1278–86.
[50] Gilat E, Girouard SD, Pastore JM, Laurita KR, Rosenbaum DS. Angiotensin-converting enzyme inhibition produces electrophysiologic but not antiarrhythmic effects in the intact heart. J Cardiovasc Pharmacol (1998) 31:734–40.[CrossRef][Web of Science][Medline]
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  R. Due-Andersen, T. Hoi-Hansen, C. E. Larroude, N. V. Olsen, J. K. Kanters, F. Boomsma, U. Pedersen-Bjergaard, and B. Thorsteinsson Cardiac repolarization during hypoglycaemia in type 1 diabetes: impact of basal renin-angiotensin system activity Europace, July 1, 2008; 10(7): 860 - 867. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||