Abnormal Left Ventricular Torsion and Cardiac Autonomic Dysfunction in Subjects with Type 1 Diabetes

Abstract

Objective

Left ventricular torsion is increased and cardiac energetics reduced in uncomplicated type 1 diabetes (T1DM). Our aim was to determine the relationships of these abnormalities to cardiovascular autonomic neuropathy (CAN) in subjects with T1DM.

Materials/Methods

A cross-sectional study was conducted in twenty subjects with T1DM free of known coronary heart disease attending an outpatient clinic. CAN was assessed using heart rate variability studies and the continuous wavelet transform method. Left ventricular function was determined by speckle tracking echocardiography. Magnetic resonance spectroscopy and stress magnetic resonance imaging was used to measure cardiac energetics and myocardial perfusion reserve index, respectively.

Results

Twenty subjects (age 35±8 years, diabetes duration 16±9 years, HbA1c 8.0±1.1%) were recruited. 40% subjects exhibited definite or borderline CAN. Log peak radial strain was significantly increased in subjects with CAN compared to those without (1.56±0.06 vs. 1.43±0.14 respectively, p=0.011). Data was adjusted for log duration of diabetes, and log left ventricular torsion correlated (r=0.593, p=0.01) with log low frequency-to-high frequency ratio during the Valsalva maneuver. Log isovolumic relaxation time correlated significantly with log Valsalva ratio and log pNN50 during deep breathing. However, CAN did not correlate with cardiac energetics or myocardial perfusion reserve index.

Conclusions

Spectral analysis of low frequency-to-high frequency ratio power during the Valsalva maneuver is associated with altered left ventricular torsion in subjects with T1DM. Parasympathetic dysfunction is closely associated with diastolic deficits. CAN is not however the principal cause of impaired cardiac energetics. The role of CAN in the development of cardiomyopathy warrants further evaluation.

Introduction

Cardiovascular autonomic neuropathy (CAN) is a common complication of diabetes that confers considerable morbidity and mortality [1–3]. In type 1 diabetes, cardiovascular mortality is usually due to coronary artery disease (CAD), heart failure or hypertension [4,5]. However, left ventricular (LV) dysfunction can occur without CAD or hypertension in diabetes [6], suggesting direct metabolic effects on the heart- metabolic heart disease [7]. Most reports have indicated that diastolic dysfunction pre cedes systolic dysfunction, but these findings may reflect the insensitivity of conventional systolic parameters [7]. Detection of early changes in the myocardium and identification of the contributing factors such as CAN is highly desirable to instigate preventative strategies.

LV twist, torsion, and strain provide information on regional and global cardiac tissue deformation [8]. Torsion reports the rotation of the apex with respect to the base along its long axis and is produced by contraction of the heart’s obliquely spiraling myofiber layers. A period of rapid untwisting recoil follows maximal torsion and occurs largely during isovolumic relaxation [9]. The counter clockwise rotation of the apex during systole normally precedes the clockwise rotation of the base. Impairment of the function of the subendocardial fibers results in a delay and slowing in apical rotation. This has the paradoxical effect of increasing twist and untwist by moving apical and basal rotation into synchrony. Increased LV torsion and strain may provide sensitive and timely information on the early phases of LV systolic dysfunction in diabetes. Tagged magnetic resonance imaging (MRI) has identified increased torsion in subjects with both type 1 and type 2 diabetes with normal ejection fractions [8,10]. Speckle tracking echocardiography (STE) is a novel angle-independent method of measuring LV strain and strain rates, which can measure LV rotation on grey scale two dimensional image [11,12]. We have previously used STE to demonstrate a significant increase in LV torsion in healthy subjects with type 1 diabetes compared to healthy controls [13] which correlated with the deficits of myocardial microvascular perfusion. This suggests a role for microvascular disease in the development of LV torsion.

Impaired cardiac energetic status may also play an important role in the development of heart failure [14]. We have previously demonstrated using magnetic resonance spectroscopy (MRS) that cardiac energetics are impaired in as ymptomatic type 1 diabetes, a finding which is unrelated to diabetes duration or coronary microvascular function [15].

In summary, increased LV torsion, impaired cardiac energetics and CAN often complicate type 1 diabetes. The aim of our study was therefore to determine the interrelationships of these functional and metabolic deficits.

Methods

Consecutive type 1 diabetes subjects who met the inclusion criteria and provided written informed consent were recruited from general diabetes clinics in the Heart of England NHS Foundation Trust and University Hospital Birmingham NHS Foundation Trust, Birmingham, UK. All investigations were undertaken in the University of Birmingham with approval from the Multicenter Regional Ethics Committee, Birmingham. LV torsion and LV torsion rate values for healthy controls with no history of diabetes were derived from data we have previously published, with baseline characteristics including age, gender, BMI, lipid profile and blood pressure included in table 1[13].

Table 1.

Baseline characteristics comparing study population with type 1 diabetes and historical non-diabetic controls¹³

Variable	Patients with T1DM	Historical Controls
Age (years)	34.8 ± 8	30 ± 8
Male/Female n, (%)	12 / 8 (60% / 40%)	22/10 (69% / 31%)
Duration of Diabetes (years)	16.1 ± 9.0	-
HBA1C (%)	8.0 ± 1.12	-
BMI (Kg/m2)	24.7 ± 3.2	25 ± 3.0
Cholesterol (mmol/l)	4.4 ± 0.8	4.9 ± 0.9
HDL (mmol/l)	1.7 ± 0.4	1.7 ± 0.6
Microalbuminuria (ACR ≥2.5 males, ≥3.5 females)	7 patients (35%)	-
Retinopathy (any stage)	13 patients (65%)	-
Systolic Blood Pressure	119 ± 15	112 ± 10
Diastolic Blood Pressure	77 ± 9	70 ± 10

Data are expressed as (mean ± 1standard deviation) if not otherwise specified.

Patients

We recruited 20 subjects with type 1 diabetes without evidence of CAD or heart failure based on history, 12 lead electrocardiogram, a normal ejection fraction (EF) on echocardiography and metabolic exercise testing. Subjects fasted overnight and blood samples were taken on the morning of the study. Subjects underwent exercise testing to rule out CAD and echocardiography, cardiac MRS and stress MRI as previously reported [13]. CAN was assessed on a separate visit and there were no episodes of hypoglycemia during the assessment of CAN.

Exercise Testing

Subjects underwent a symptom-limited e rect treadmill exercise testing to exclude CAD.

Echocardiography

Echocardiography was performed with a Vivid 7 (GE Vingmed) echocardiographic unit and a 2.5-MHz transducer. Standard echocardiographic views were obtained from parasternal and apical windows with the patient in left lateral decubitus position and breath held in end expiration. Left ventricular ejection fraction (EF) was calculated with Simpson’s rule. Other cardiac parameters assessed included isovolumic relaxation time (IVRT), the ratio of early to late diastolic filling (E/A ratio) measured at the mitral valve, peak radial strain and peak longitudinal strain, measured using speckle tracking. IVRT and E/A ratio are measures of diastolic dysfunction while radial strain and longitudinal strain reflect systolic function.

³¹ P Cardiac Magnetic Resonance Spectroscopy

In vivo myocardial energetics were measured using MRS at 3-Tesla Phillips Achieva scanner, as previously validated and described by our group [16]. A Java magnetic resonance user interface v3.0 (jMRUI) was used for analysis [17]. Phosphocreatine (PCr) and γ-adenosine triphosphate (γATP) peaks in the distal septum were used to determine the PCr/γATP ratio. Data were analyzed blinded to the participants’ clinical status. Cramér–Rao ratios were used to assess signal:noise ratio [16].

Stress MRI

Cardiac MRI was performed on a 3T Phillips Achieva MRI scanner as previously described [13]. Survey images were followed by first pass images after Gadolinium contrast injection (0.1ml/kg body weight, 4ml/sec). For perfusion images, a single shot Turbo Field Echo SENSE pulse sequence was used with three slices per heart beat. After a twenty minute gap, adenosine infusion was started at a rate of 140mcg/kg/min. At three minutes of infusion stress first pass images we re obtained following injection of further Gadolinium contrast (0.1ml/kg).

Cardiac Autonomic Neuropathy (CAN) assessment

Heart rate (HR) variability was analyzed using the continuous wavelet transform methods to generate numerical and graphical data, instead of conventional Fast Fourier Transform for frequency domain analysis (ANX-3.0 software, ANSAR Inc., Philadelphia, PA). The heartbeat intervals are recorded and the HR variability is plotted in the frequency domain to separate the high-frequency (Rfa, 0.15 to 0.4 Hz) from the low-frequency (Lfa, 0.04 to 0.15 Hz) components by spectral analysis.

ANALYSIS

Speckle Tracking Echocardiography (STE)

LV rotation was measured using a commercially available speckle tracking system in an ECHOPAC (version 4.2.0) workstation as we have described previously [13]. Of the 20 subjects in the study, 19 (95%) subjects had both adequate LV basal and apical images for speckle tracking to complete analysis of all LV rotational parameters.

Cardiac Autonomic Neuropathy (CAN)

The ANX-3.0 software was used to calculate Low Frequency Area (LFA, analogous to low frequency power) and Respiratory Frequency Area (RFA, analogous to high frequency power). The ratio of low frequency power (LF) to high frequency power (HF) is an estimate of the sympathetic/parasympathetic balance and was determined at baseline, deep breathing, Valsalva maneuver (VM) and standing. For the definition of CAN, standardized ratios were calculated during deep breathing [expiration inspiration (E/I) ratio], during VM (the Valsalva ratio), in response to standing (30/15 ratio) and postural drop in systolic blood pressure. Age specific normal values were derived from published data [1,18,19]. We defined 1 or ≥2 abnormal tests as being consistent with borderline or definite CAN, respectively, out of the three ratios and postural drop in systolic blood pressure. Time domain indices including sdNN (standard deviation of the RR interval from normal to normal beats), rmsSD (root mean square of successive differences) and pNN50 (proportion of differences in consecutive RR intervals of normal beats >50msec) were also calculated for each of the four stages of the test, and correlations with LV torsion, parameters of diastolic function, cardiac energetic as well as myocardial perfusion reserve index were done.

Statistics

SPSS 16.0 software (SPSS Inc, Chicago, USA) was used for analysis. Continuous variables are expressed as means ± standard deviation. The means of independent groups were compared using the independent t test. A p value of <0.05 was considered to indicate statistical significance. Data was checked for normality using the Shapiro-Wilk test. Non-normally distributed data was log transformed and Pearson correlation coefficient (r) was used to describe the relationship between log transformed variables.

Results

Baseline characteristics are described in Table 1. The mean age was 35 ± 8 years with 60% males, mean HbA1c of 8 ± 1.1%, and mean diabetes duration of 16 ± 9 years. 35% of subjects had retinopathy (background, pre-proliferative or proliferative) and 65% had microalbuminuria (albumin creatinine ratio [ACR] ≥ 2.5 for males, and ≥3.5 for females). 75% of the subjects in this study had retinopathy, microalbuminuria or both, while 25% of the subjects had no evidence of either. Baseline characteristics of historical non-diabetic controls[13] used to derive normal LV torsion values are also included in Table 1.

Cardiac Autonomic Neuropathy

E/I ratio was abnormal in 3 of the 20 patients (15%), the Valsalva ratio was abnormal in 7 of the 20 patients (35%), and the 30/15 ratio was abnormal in 2 of the 18 patients (11%). One patient had more than a 20 mmHg drop in systolic blood pressure on standing. Based on the above CAN tests, 4 subjects (20%) had 2 or more abnormalities and were classified as definite CAN, and 4 subjects (20%) had 1 abnormality and were classified as borderline CAN.

LV torsion and CAN

LV torsion was significantly increased in the subjects with type 1 diabetes compared to values in our data base of age matched healthy non-diabetic controls (NC) that we have previously reported (2.0 ± 0.7 °/cm vs. 1.4 ± 0.7 °/cm, p=0.01) [13]. There was a trend towards significant increase in LV torsion rate during systole compared to NC (13.7 ± 6.0 °/cm/sec vs.10.9 ± 4.8 °/cm/sec), p=0.07) [13].

Log peak radial strain was significantly increased in type 1 diabetes subjects with borderline and/or definite CAN compared to subjects without abnormalities of autonomic function 1.56 ± 0.06 vs 1.43 ± 0.14 respectively, (p=0.011). No other differences of LV function were however identified.

There was a significant positive correlation between log LF/HF ratio during the VM and log LV torsion (r=0.58, p=0.009),(figure 1). This correlation was still significant after adjusting for log duration of diabetes (r=0.593, p=0.01) (Table 2). The correlation between log LF/HF ratio during the VM and log LV torsion remained significant (r= 0.594, p= 0.019), even after adjusting for age, s ystolic and diastolic blood pressure in addition to log duration of diabetes. Analysis of the 15 subjects who had either retinopathy, microalbuminuria or both showed the correlation between log LF/HF ratio during the VM and log LV torsion remained similar (r=0.584, p=0.036) when adjusted for log duration of diabetes. Log LV torsion did not correlate with any of the other CAN tests.

Figure 1.

Scatterplot of Log LV Torsion and Log Valsalva Low Frequency/High Frequency ratio

Table 2.

Significant correlations of echocardiographic findings with parameters of heart rate variability, after adjusting for log duration of diabetes.

Correlation	Correlation coefficient (r)	Significance (p value)
Log LV Torsion (degrees/cm) with Log Valsalva LF/HF ratio	r= 0.593	p= 0.01
Log IVRT (msec) with Log Valsalva ratio	r= 0.502	p= 0.029
Log IVRT (msec) with Log Deep Breathing pNN50	r= 0.483	p= 0.042
Log E/A Ratio with Log Baseline pNN50	r= 0.564	p= 0.015
Log Radial Strain (%) with Log E/I ratio	r= −0.607	p= 0.006
Log Radial Strain (%) with Log Valsalva ratio	r= −0.509	p= 0.026
Log Longitudinal Strain (cm/sec) with Log Deep Breathing LF/HF ratio	r= −0.456	p= 0.05

Diastolic Function and CAN

Correlations of log transformed data were performed after adjustment for log duration of diabetes, and the significant correlations are presented in Table 2. Log IVRT was significantly positively correlated with log pNN50 during deep breathing, and with log E/I ratio. Log E/A ratio was significantly positively correlated with log pNN50 at baseline. Log radial strain was significantly negatively correlated with log E/I ratio and log Valsalva ratio, while log longitudinal strain was significantly negatively correlated with log LF/HF ratio during deep breathing.

Cardiac Energetics and CAN

Overall, the PCr/γATP ratio, a measure of cardiac energetics, was reduced in type 1 diabetes compared to our data base of healthy controls (1.6 ± 0.2 vs. 2.1 ± 0.5) p=0.003 [15]. Log PCr/γATP ratio was not different in subjects with borderline and/or definite CAN compared to those with normal autonomic function (0.19 ± 0.09 vs 0.19 ± 0.06). No correlation of log PCr/γATP ratio was detected with any of the time or frequency domains parameters of CAN. (data not shown).

Myocardial Perfusion Reserve Index (MPRI) and CAN

The MPRI was calculated using stress MRI, and log MPRI showed no correlation with any of the time or frequency domains parameters of CAN (data not shown).

Discussion

LV torsion which contributes significantly to energy-efficient ejection during systole [20] is increased in asymptomatic subjects with type 1 diabetes. The etiology of this deficit is poorly understood. We therefore explored the relationships of LV torsion and cardiac energetic deficits to CAN in these subjects. Log peak radial strain was significantly increased in subjects with CAN compared to subjects with normal autonomic function tests. Spectral analysis of LF/HF power during the VM (a measure of sympathovagal balance) was associated with altered LV torsion. This correlation remained significant after adjustment for log duration of diabetes, age, systolic and diastolic blood pressure. A similar correlation remained when only the 15 subjects with retinopathy, microalbuminuria or both were included. In contrast, parasympathetic dysfunction was more closely correlated with diastolic deficits in these subjects [21].

Spectral analysis of LF/HF power during VM has, to our knowledge, not previously been reported. During the VM, forced expiration and resultant increased intrathoracic pressure and reduced venous return subsequently stimulates the arterial baroreceptors to create a sympathetic drive in late phase II [22]. In phase IV, an increase in BP stimulates lung mechanoreceptors to elicit parasympathetic predominance resulting in bradycardia [22]. Therefore complex, co-ordinated changes in sympathetic and parasympathetic activity and balance are elicited during the VM which when expressed as log LF/HF power, correlate with increased log LV torsion. These data therefore implicate a role for altered autonomic balance in the development of abnormal LV systolic function.

We have previously reported using positron emission tomography (PET) and the sympathetic neurotransmitter analogue [¹¹C]meta-hydroxyephedrine ([¹¹C]HED) [23], that microvascular complications in type 1 diabetes are associated with increased cardiac sympathetic tone and adrenergic hyper-responsiveness. Increased LV torsion may therefore be the early consequence of cardiac sympathetic activation thereby leading to myocardial injury [23]. In more advanced CAN, there is heterogeneous LV sympathetic denervation [24]. LV torsion is greatest at the apex of the LV, thus regional LV sympathetic denervation may be mechanistically important. Future studies using HED-PET will need to directly characterize sympathetic innervation/LV function relationships.

Alternatively, sympathetic activation and consequent increased torsion may be compensatory for a subclinical reduction in LV long axis function and impaired early diastolic filling secondary to subendocardial ischemia and fibrosis. Longitudinal (long-axis) contraction of the LV is dependent on the integrity of longitudinal subendocardial myocardial fibers which are more susceptible to ischemia and fibrosis than circumferential fibers that are responsible for radial (short-axis) contraction [25]. In diabetes, increased radial contractility may compensate for reduced longitudinal contractility [26]. We have previously reported that LV torsion correlates with impaired MPRI in type 1 diabetes consistent with a role for myocardial ischemia [13]. However, this interpretation is complicated by evidence that sympathetic activation per se can impair myocardial perfusion in diabetes [23].

Our data demonstrated a robust correlation of CAN with a diverse spectrum of diastolic abnormalities. Diastolic dysfunction is an early marker of heart failure and has been demonstrated using radionuclide assessment as well as echocardiography in patients with diabetes, especially in those with CAN [27,28]. After maximal LV torsion occurs during systole, the heart experiences a clockwise recoil of twist (untwists) during the period of isovolumic relaxation of the LV. This release of restoring forces contributes to diastolic suction which is largely responsible for early LV diastolic filling. Increased LV torsion is associated with increased late peak LV untwisting rate and delayed time to late peak untwisting rate. Increased LV torsion is associated with ea rly relaxation abnormalities in the LV and the left atrial (LA) contribution to LV filling is increased [15]. We found a robust correlation of log transformed IVRT and the E/A ratio with multiple frequency and time domain parameters in our subjects consistent with a role for parasympathetic deficits in diastolic dysfunction.

We did not detect a correlation of cardiac energetics with any parameter of CAN in our subject population. In the diabetic heart, fatty acids (FFA) contribute to over 90% of the myocardial oxygen consumption [29]. However, fatty acids are inefficient as an energy source in terms of oxygen requirement, and may contribute to mitochondrial uncoupling, programmed cell death, fibrosis and arrhythmogenesis [30]. Sympathetic activation increases plasma FFA and can increase mitochondrial FFA uptake and oxidation [31]. The lack of correlation of CAN with cardiac energetics in our subjects is therefore somewhat surprising but may reflect either the small sample size particularly with regards to subjects with advanced CAN, or that CAN does not significantly further exacerbate the diabetes mediated perturbations of cardiac fatty acid and glucose metabolism.

A limitation of our study was the small sample size, which may limit our ability to detect significant correlations and the indirect nature of the cardiac sympathetic assessment. We are also aware that a history of frequent severe hypoglycemia or degree of antecedent long-term diabetes control can affect the development of complications in diabetes, and these data were not available in our study. However, our data are consistent with the construct that LF/HF ratio during the VM may deserve consideration as a potential screening test for LV torsion. Prospective studies in which direct characterization of cardiac sympathetic tone is compared to LV torsion are currently in progress.

In summary, spectral analysis of LF/HF power during the VM is associated with altered LV torsion in healthy subjects with type 1 diabetes. Parasympathetic dysfunction is closely associated with diastolic deficits. CAN is not however the principal cause of impaired cardiac energetics. The role of CAN in the development of cardiomyopathy warrants further evaluation.

Abbreviations

ACR

albumin creatinine ratio

BMI

body mass index

CAN

cardiovascular autonomic neuropathy

CAD

coronary artery disease

E/A ratio

ratio of early to late diastolic filling

E/I ratio

expiration inspiration ratio

EF

ejection fraction

FFA

free fatty acids

γATP

γ-adenosine triphosphate

HED

meta-hydroxyephedrine

HR

heart rate

Hz

hertz

IVRT

isovolumic relaxation time

jMRUI

Java magnetic resonance user interface

Lfa

low-frequency area

LA

left atrial

LV

left ventricular

MPRI

Myocardial Perfusion Reserve Index

MRI

magnetic resonance imaging

MRS

magnetic resonance spectroscopy

NC

non-diabetic controls

PCr

Phosphocreatine

PCr/γATP

ratio of the peaks of phosphocreatinine to γ-adenosine triphosphate

PET

positron emission tomography

pNN50

proportion of differences in consecutive RR intervals of normal beats >50msec

r

pearson correlation coefficient (r)

Rfa

respiratory frequency area

rmsSD

root mean square of successive differences

sdNN

standard deviation of the RR interval from normal to normal beats

STE

speckle tracking echocardiography

T

tesla

T1DM

type 1 diabetes

VM

Valsalva maneuver