Chronic Kidney Disease Clinical Trial
Official title:
Depressed Cardiac Autonomic Modulation in Patients With Chronic Kidney Disease Diagnosed by Spectral Analysis of Heart Rate Variability Upon Postural Stress
Background/Aims: To evaluate the sympathovagal balance in patients with chronic kidney disease (CKD) on conservative treatment. Methods: In a cross-sectional study, patients with CKD stages 3, 4 and 5 not yet on dialysis (CKD group) and age-matched healthy subjects (CON group) underwent continuous heart rate recording during two twenty-minute periods in the supine position (pre-inclined), followed by passive postural inclination at 70° (inclined period). Power spectral analysis of the heart rate variability was used to assess the normalized low frequency (LFnu), indicative of sympathetic activity, and the normalized high frequency (HFnu), indicative of parasympathetic activity. The LFnu/HFnu ratio represented sympathovagal balance.
Patients We evaluated 32 individuals (18 men and 14 women) with CKD at stages 3, 4 or 5 who
were not yet on dialysis. The individuals were recruited at the Interdisciplinary Nucleus
for Studies, Research and Treatment in Nephrology, Federal University of Juiz de Fora. All
patients had been followed by a nephrologist for at least 6 months before inclusion in the
study. Patients with severe cardiac disease, cancer, diabetes, collagen and demyelinating
diseases, left ventricular systolic dysfunction, or a history of stroke were excluded. The
control group consisted of 14 subjects with normal renal function who were non-diabetic,
normotensive and free of heart disease. The study was approved by the Ethics Committee of
the University Hospital of the Federal University of Juiz de Fora, document number 073/2007,
and all subjects signed an informed consent before being included in the protocol.
Study Design This was a cross-sectional study in which we evaluated ANS function in patients
with CKD under conservative treatment and compared the results to a control group. Power
spectral analysis of the HRV at rest and during a passive orthostatic stress was performed
in both groups.
Cardiovascular Evaluation The medical evaluation was performed by a cardiologist and
consisted of an interview and clinical examination. Blood pressure was measured at each 2
minutes intervals using a conventional sphygmomanometer. A conventional 12-lead
electrocardiogram (ECG) was performed with an electrocardiograph (model Apex 1000, TEB,
Brazil). To detect LVH, we used the Cornell criterion [9]. Ventricular geometry and function
were analyzed using a two-dimensional Doppler echocardiogram generated using a Philips
EnVisor C Ultrasound System (Philips Medical Systems-Ultrasound, MA, USA). Measurements and
indices of left ventricular function at rest were obtained through the two-dimensional and M
modes, using a 3.5 MHz linear transducer placed over the third or fourth intercostal space.
The diagnosis of LVH was based on the left ventricular mass index (LVMI), values for which
were considered normal up to 115 g/m2 for men and up to 95 g/m2 for women [10]. The data
were interpreted according to criteria established by the American Society of
Echocardiography [11].
Laboratory Evaluation The results of the following tests were obtained from the patients'
charts: glomerular filtration rate (eGFR; estimated from creatinine using the Modification
of Diet in Renal Disease equation) [12], urea, potassium, calcium, phosphorus, hemoglobin,
uric acid, parathyroid hormone (PTH), total cholesterol, HDL cholesterol, LDL cholesterol,
triglycerides, glucose and urinalysis. The diagnosis of CKD was based on the Kidney Disease
Outcomes Quality Initiative of the National Kidney Foundation (KDOQI/NKF) [13]: eGFR <60
ml/min/1.73 m2 and/or at least one marker of renal parenchymal damage (e.g., proteinuria),
present for a period of ≥3 months.
Analysis of Heart Rate Variability The HRV was measured at rest in the supine position and
during orthostatic stress. All subjects were instructed to fast for six hours and not to
smoke or drink caffeine for 12 hours prior to the test. All medications that could
potentially interfere with the cardiovascular response such as non-dihydropyridine calcium
channel blockers, beta-blockers, central sympatholytic, tricyclic antidepressants as well as
anti-arrhythmic drugs were withdrawn for at least five drug half-lives before the study. The
evaluation was conducted in the morning in a calm environment with low light on a tilting
table with seat belts and a platform for a footrest. The subjects underwent continuous HR
recording using a Holter system (Cardio Light, Brazil) during two 20 minute periods in the
supine position (pre-inclined), followed by passive postural inclination at 70° (inclined
period) [14,15]. To evaluate the spectral analysis of HRV, a fast Fourier transform was used
[16], obtained by means of Holter-specific software (Cardio Smart 550, Brazil), that allows
periodic signals, an average of 500 sequential R-R intervals, to be divided into various
bands of frequency response: ultra-low frequency (ULF: <0.0033 Hz), very low frequency (VLF:
0.0033 to 0.04 Hz), low frequency (LF: 0.04 to 0.15 Hz), and high frequency (HF: 0.15 to 0.4
Hz). The LF and HF components were used as markers of sympathetic and parasympathetic
activities, respectively, and the LF/HF ratio was used as a measure of the sympathovagal
balance. To minimize the effects of changes in ULF and VLF bands, the data were normalized
and the results expressed as normalized units (nu). The normalization was done by dividing
the power of a given component (LF or HF) by the total power spectrum; from this result, the
VLF component was subtracted, and this number was then multiplied by 100. Thus, the
variables used for the HRV analysis were LFnu, HFnu and the LFnu/HFnu ratio. The data were
interpreted following previously published guidelines [17]. The HRV was analyzed using the
highest total power expressed in msec², which was obtained after 10 minutes in the supine
position and during the first 5 minutes after tilting the table.
Statistical Analysis The variables are described as mean, standard deviation, percentage or
median. The descriptive statistics and normality of the data were tested by the Kolmogorov
Smirnov test. The laboratory data of the control and CKD groups at baseline were compared
using an independent sample T test, Chi-square test or Mann Whitney test depending on the
characteristics of the variable. Spectral analysis of heart rate variability was assessed
within groups in the pre-inclined and inclined periods by Kruskal Wallis or ANOVA (with post
Hoc test) for both the control group and for the CKD group divided into disease stages
three, four and five. The LFnu / HFnu ratio for the control and CKD groups was compared by
the Mann Whitney Test. To assess the correlation between CKD stages and biochemical
variables with the LFnu/HFnu ratio, Spearman's linear correlation coefficient was used. A p
value less than or equal to 0.05 was considered statistically significant. All analyses were
performed using SPSS 13.0 for Windows (SPSS Inc., Chicago, USA).
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Observational Model: Case-Crossover
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