|Year : 2013 | Volume
| Issue : 2 | Page : 92-97
Screening and assessment of cardiac autonomic neuropathy in long-standing type 2 diabetic women
Department of Cardiology, Mansoura Faculty of Medicine, Mansoura, Egypt
|Date of Submission||21-Dec-2012|
|Date of Acceptance||27-Jan-2013|
|Date of Web Publication||4-Jul-2014|
Department of Cardiology, Mansoura Faculty of Medicine, 35111 Mansoura
Source of Support: None, Conflict of Interest: None
Patients with long-standing diabetes mellitus undergoing surgical interventions are under considerable risk, hence posing a surgical challenge, as they may have cardiovascular and/or cardiac autonomic neuropathy (CAN). CAN is serious, often overlooked and underdiagnosed, with possible arrhythmias and silent ischemia that may be life threatening.
The aim of this study was to screen for one of the underdiagnosed high-risk problems by assessment of CAN in long-standing type 2 diabetic women undergoing stressful situations.
Patients and methods
Hundred type 2 diabetic women scheduled for major surgery were assessed by autonomic function tests. CAN was assessed by analyzing heart rate variations during three standard tests (deep breathing, lying to standing, and the valsalva maneuver). Sympathetic functions were assessed by checking orthostatic hypotension. The CAN score of each patient was analyzed. Continuous 24 h ECG monitoring was performed to evaluate arrhythmia, corrected QT (QTc), and QT dispersion (QTd). Transthoracic Doppler echocardiography, with a focus on left ventricular hypertrophy, diastolic, and systolic dysfunctions, was carried out. Patients were classified as having mild (with only one abnormal test) or severe CAN when two or more abnormal function tests were present. Exclusion criteria included any systemic illness that could affect the results of the study or the autonomic functions, smoking, hypertension, and patients with evident ischemia.
CAN was detected in 70% of the patients studied, and 70% of them had a severe case of CAN. Postural hypotension was detected in 34% of the patients studied. QTc prolongation and QTd were frequent. ECG and Doppler echocardiography changes of left ventricular hypertrophy were more prevalent among patients with CAN. Diabetics with CAN were significantly older, had a longer duration of diabetes mellitus, and higher HbA1-c, higher pulse pressure, triglyceride, uric acid, and urinary albumin excretion rate. They also had a significantly increased left ventricular mass index and diastolic dysfunction.
Middle-aged women with long-standing diabetes are vulnerable to CAN with postural hypotension and prolonged QTc intervals, QTd, and increased left ventricular mass index. Identification of CAN is crucial to prevent the hazards of cardiovascular insults during stressful situations, and cases with severe CAN may require coronary artery disease screening preoperatively.
Keywords: cardiac autonomic neuropathy, coronary artery disease, diabetes
|How to cite this article:|
Refaie W. Screening and assessment of cardiac autonomic neuropathy in long-standing type 2 diabetic women. Egypt J Intern Med 2013;25:92-7
|How to cite this URL:|
Refaie W. Screening and assessment of cardiac autonomic neuropathy in long-standing type 2 diabetic women. Egypt J Intern Med [serial online] 2013 [cited 2020 Feb 23];25:92-7. Available from: http://www.esim.eg.net/text.asp?2013/25/2/92/135867
| Introduction|| |
Autonomic neuropathy, although not rare, is one of the most insidious complications of diabetes mellitus (DM), especially if long standing and poorly controlled. Cardiac autonomic neuropathy (CAN) is often overlooked both in the diagnosis and the treatment simply because there is no widely accepted single approach to its diagnosis 1. CAN involves exercise intolerance, intraoperative cardiovascular (CV) liability, orthostatic syndromes, and silent myocardial ischemia 2–4. These clinical manifestations can result in life-threatening outcomes that unquestionably associate the presence of CAN with the increased risk of CV morbidity and mortality in DM.
In the Eurodiab prospective study (2001), CAN was among the strongest risk markers of future total and CV mortality exceeding the effect of traditional risk factors such as age, obesity, hypertension, dyslipidemia, inflammatory, and prothrombotic emerging cardiac risk factor 4,5. In a meta-analysis of 12 published studies, Vinik et al. 6 reported a constant association between CAN and silent myocardial ischemia and in the DIAD study, CAN was a stronger predictor of silent ischemia and subsequent cardiac events 7.
The corrected QT (QTc) interval and QT dispersion (QTd) have been considered as markers of cardiac autonomic dysfunction and have been shown to be independent predictors of CV mortality and all-cause mortality risk in patients with type 2 DM 4. Combined abnormality in heart rate variability (HRV) and the QT index was a strong predictor of mortality independent of conventional risk factors 8,9.
Action to Control Cardiovascular Risk in Diabetes (ACCORD trial 2010) in the presence of CAN at baseline was an independent contributor to the higher CV mortality risk in both the intensive and the standard glycemic arm treatment. Individuals with baseline CAN were two times more likely to die compared with individuals without CAN 10,11. Considerable attention has been paid to the CV aspect of autonomic dysfunction, especially with the view regarding the association of very tight glycemic control with increased mortality. The ACCORD trial 12 attributed increased mortality to hypoglycemia-induced arrhythmias 1.
There is no widely accepted single approach to the diagnosis of CAN; however, during the 1970s, Ewing et al. 13 recommended a number of simple bedside tests of short-term RR difference (the distance between 2 successive ventricular contractions on ECG recording) to detect CAN including changes in RR with deep breathing, RR response to standing that induce reflex tachycardia, followed by bradycardia and Valsalva ratio, which evaluates the cardiovagal function in response to a standard increase in intrathoracic pressure.
Orthostatic hypotension, with its many troublesome symptoms ranging from light headedness to near syncope, which may be associated with poor quality of life with a decrease in systolic blood pressure (SBP) of at least 20 mmHg and of at least 10 mmHg in diastolic blood pressure (DBP) during 3 min of standing and resolving with sitting or lying down, is characteristic of CAN 14,15.
The clinical symptoms of CAN may be late; however, subclinical CAN manifest as changes in HRV may be detected within 1 year of diagnosis of type 2 DM 16.
Pop-Busui et al. 17 reported that screening for CAN showed that it ranges from as low as 2.5% (Diabetes Control Complications Trial, 1974) to as high as 90% in long-standing DM and should be instituted at diagnosis of type 2 DM and after 5 years of diagnosis of type 1 18. Vinik and Ziegler 19 reported that detection of CAN is a must before exposing patients with long-standing DM to stressful situations and also before planning exercise. Diabetics must be tested with a cardiac stress test before undergoing an exercise program. Patients with CAN need to rely on their perceived exertion and not heart rate to avoid the hazardous levels of exercise intensity 19.
This study aimed at screening and assessment of cardiac autonomic dysfunction in middle-aged women with long-standing type 2 DM who would be exposed to stress in the form of major surgery.
| Patients and methods|| |
The patients studied included 106 women who were known to be diabetic and were on oral hypoglycemic agents (70 cases) and 36 cases who were on combined insulin and sulfonylurea. All were receiving metformin 1.7 g/day. Six patients did not complete the study for unknown reasons and only 100 patients completed the study. Their ages ranged from 40 to 60 years (mean 52.4±3.7 years). The patients studied had no polyps symptoms. The mean duration of DM was 10±2 years, ranging from 6 to 14 years. BMI ranged from 25.1 to 29.2 (mean 27.1±1.1).
All medications that could affect the results of the study or the autonomic functions were withhold during and 1 week preceding the clinical assessment of autonomic functions.
Examinations were performed in the morning at least 2 h after a light breakfast and no caffeine was allowed. The patients were asked about symptoms suggestive of autonomic neuropathy, postural hypotension, and myocardial ischemia.
Diabetic complications such as retinopathy were checked, with a focus on peripheral neuropathy and sudomotor neuropathy. Peripheral neuropathy and sudomotor neuropathy were detected clinically by monofilament and dryness of the feet. Clinical examination, especially heart rate, SBP, DBP, and pulse pressure, was performed. Autonomic parasympathetic dysfunction was assessed by HRV testing (heart rate, ECG, and RR intervals on resting, standing, respiration, and valsalva). HRV was calculated from the RR interval using short continuous ECG recording. Continuous 24-h ECG monitoring (Schiller/MT101, Holter, Switzerland) was also used to evaluate ischemia, arrhythmia, QTc intervals, and QTd. Cases with evident ischemia or arrhythmias were not included. The resting 12-lead ECG was also performed to determine beside HRV evidences of left ventricular hypertrophy (LVH) and/or ischemia. Prolongation of the QTc interval greater than 460 ms and QTd greater than 10 ms were considered as evidences of HRV. Flattening of the T wave and ST segment depression were considered as evidences of myocardial ischemia. Cases with angina ECG and Holter monitor evidences of ischemia were not included in the screening study.
Testing for sympathetic dysfunction by postural hypotension in a supine position and after standing for 3 min was carried out using the standard mercury sphygmomanometer. The measurement in the supine position was taken after at least 15 min of rest and the measurement in the standing position was taken in the third minute of standing.
Transthoracic Doppler echocardiography was performed, with a focus on left ventricular mass index, diastolic, and systolic dysfunctions.
Biochemical studies were carried out, with a focus on blood glucose, fasting, and post 75 g glucose challenge together with HbA1-c, serum creatinine, plasma cholesterol, triglyceride, serum uric acid, and 24 h urine albumin excretion.
The prevalence and severity of CAN were assessed according to the number of autonomic function tests of Ewing’s methodology, and the CAN score in each patient was analyzed.
Subclinical CAN cases or mild CAN with only one abnormal function test were compared with severe CAN cases (two or more abnormal autonomic functions).
The study protocol was approved by the scientific committee of the Mansoura Faculty of Medicine and informed consent was obtained.
Patients with systemic illness that could affect the results of the study or autonomic functions such as congestive heart failure, coronary artery disease, arrhythmia, renal, hepatic impairment, hepatitis C virus infection, severe anemia, thyroid dysfunction, smoking, concomitant treatment with anticholinergic agents, adrenergic antagonists, vasoconstrictive agents, and patients with blood pressure (BP) of at least 140/90 mmHg on two occasions 2 weeks apart were not included.
Statistical analysis was carried out using the statistical package for social science program, version 16 (SPSS Inc., Chicago, Illinois, USA). The qualitative data were presented as frequency and percentages. The quantitative data were examined using the Kolmogorov–Smirnov test to test for normal distribution of the data and, when parametric, were expressed as mean and SD. The Student t-test was used to test for differences in normally distributed quantitative data between the two groups. The Mann–Whitney U-test was used for comparison between two groups when data were not normally distributed. A P-value less than 0.05 was considered significant.
| Results|| |
The prevalence of CAN as assessed by signs of autonomic neuropathy including HRV tests of the expiration to inspiration ratio (E/I) standing to lying flat and valsalva maneuver was 70% (20 cases with single HRV testing, 26 cases with three HRV testing, and 24 cases with moderate CAN where two HRV tests were present).
Postural hypotension was detected in 34% of the studied cases and the mean pulse pressure was significantly elevated in diabetics with CAN compared with those without CAN (P<0.01).
Prolonged QTc (>460 ms) was found in 42% of all the studied cases and 60% of the CAN cases, and significantly increased QTd (>10 ms) was observed in the CAN group compared with the non-CAN group as evident from continuous 24 h ECG Holter monitoring.
Women with DM and CAN were significantly older, with a significantly longer duration of uncontrolled DM with insignificant differences in BMI.
There was no significant difference in the prevalence of CAN in relation to the method of controlling hyperglycemia (oral vs. combined oral hypoglycemic and insulin).
Symptoms suggestive of CAN in other systems, mainly urogenital, were evident in the CAN group (P<0.04). Peripheral neuritis detected by monofilament with dryness of their feet (P<0.01). SBP, DBP, and the mean pulse pressure were significantly higher in the CAN group (P<0.001).
Transthoracic echo Doppler indicated the presence of mild LVH (LV wall mass index ≥126 g/m2 in 70.01% of CAN vs. 33.3% in the non-CAN group, P<0.001) and a significant abnormal relaxation pattern (E/A<1) with preserved LV systolic functions.
Significantly higher BG level and HbA1-c were observed in the CAN group, with significant hypertriglyceridemia and elevation in uric acid in the CAN group. The urinary albumin excretion in the CAN was significantly elevated compared to that in the non-CAN group (P<0.01). Comparison of the studied parameters in relation to the severity of CAN showed insignificant changes apart from significantly older age, more postural hypotension, HbA1-c, serum creatinine, urine albumin excretion, and QTc. Signs of LVH and QTd indicated a borderline significant increase in severe CAN cases.
| Discussion|| |
The present screening study aimed to evaluate CAN in middle-aged women with long-standing diabetes who would be experiencing a stressful situation in the form of major surgery. Detection of CAN preoperatively is necessary as such patients are vulnerable to perioperative CV instability, with a greater decrease in heart rate and BP during induction of anesthesia and more severe hypothermia 3,19.
In the present study, the prevalence of CAN detected by the methods of Ewings et al. in the 1970s using HRV tests 13 was high (70%). As the determination of CAN is usually based on a battery of autonomic function tests and as the proceeding from a consensus conference (1992) 20, recommended three tests. The three tests were: inspiration/expiration ratio, standing to lying flat, Valsalva's maneuver for parasympathetic. Postural hypotension for sympathetic. In the present study, the gold standard clinical autonomic testing 21 was followed (expiration/inspiration ratio, standing to lying flat, and valsalva maneuver, and postural hypotension) [Table 1] and [Table 2].
|Table 1: Clinical findings in diabetes with CAN versus diabetics without CAN|
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|Table 2: Biochemical findings in diabetes with CAN versus diabetics without CAN|
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The prevalence of CAN ranged from 20 to 42% according to the method of detection of the HRV state, being the highest (30%) by the valsalva maneuver procedure and the lowest (20%) by the reduced E/I ratio and by standing to lying flat. The CAN score was calculated, where more than one-fourth (26%) had at least 3 positive tests and 24% had at least 2 positive. This is in agreement with the study of Katsilambros et al. 1, who found that autonomic neuropathy and CAN are not rare, but often overlooked.
The prevalence of CAN ranged from as low as 2.5% (DCCT) 17 to as high as 90% in long-standing DM and in 69% of patients with treatment-induced neuropathy 22. In the present study, the valsalva ratio was 30% and the E/I ratio was 20%. Our results are not in agreement with England et al. 23, who found that HRV with deep breathing is the most widely used test of cardiovagal parasympathetic dysfunction. CV sympathetic function was assessed by measuring the BP response to orthostatic changes 24,25 and was detected in 34% of the studied cases [Table 3].
The prevalence of CAN in the present study is higher than that of Ziegler et al. 26, who, using HRV tests, found that 34.3% of type 2 DM patients had abnormal functions. Similar to Cabezas-Cerrato et al. 27, the HR response to deep breathing in the present study was the least evident among the studied cases.
In the present study, the patients studied were all women; this could avoid sex-related difference in biochemical and hematological values 28,29. CAN was more prevalent in diabetics of longer duration, older age, those with more pulse pressure, higher serum triglycerides, and those with more elevated HbA1-c. Kodama et al. 30, in a meta-analysis study, described the association of pulse pressure as a CV risk in DM. Mäkimattila et al. 31 found that poor glycemic control was the most important independent predictor of a decrease in all measures of absolute power of HRV [Table 4].
|Table 4: ECG findings and transthoracic Doppler echocardiography in diabetics with CAN versus diabetics without CAN|
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Our findings are also in agreement with those of Voulgari et al. 21, who reported that in type 2 DM patients, CAN is independently associated with elevated BP, hyperglycemia, longer duration of diabetes, dyslipidemia, and the presence of microvascular complications 21,32. Katsilambros et al. 1 reported the association of high serum uric acid level and sudomotor dysfunction in patient with type 2 DM and CAN. In the present study, similarly, serum uric acid showed significant differences.
Symptoms of orthostatic intolerance and gastrointestinal function, urinary frequency, nocturia, and anhydrosis have been reported more frequently in diabetics with CAN. This is in agreement with Gibbons and Freeman 22, although in the present study, only the urogenital symptoms were significantly more frequent in the CAN group [Table 5].
|Table 5: Clinical, biochemical, and ECG findings of cases with subclinical mild CAN versus severe CAN cases|
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Peripheral neuropathy was present in 80% of the patients examined. This is in agreement with Vinik and Ziegler 19, Gandhi et al. 33, who found that combined indices of autonomic and peripheral neurological dysfunction are associated with earlier CAN detection 34,35. In the EURODIAB 24 prospective complication study, peripheral and autonomic neuropathy were among the strongest risk markers exceeding the effects of traditional risk factors.
Orthostatic hypotension was found in 34% of all the patients studied and in 60% of patients in the CAN group. Orthostatic symptomatology such as light headedness, dizziness, fatigability, and faintness on standing was very frequent (60%). However, no reported cases of clear or near syncope were reported. Orthostatic hypotension in CAN is secondary to efferent sympathetic vasomotor denervation, causing reduced vasoconstriction of the splanchnic and other peripheral beds 20.
In the present study, the resting heart rate in the CAN group was around 100 bpm, but was insignificantly rapid than in the non-CAN group. This is in agreement with the study of Pop-Busui et al. 17, who reported that increased resting heart rate is not a reliable diagnostic criterion for CAN in the absence of other signs.
In the present study, QTc prolongation and the more prevalent QTd are in agreement with Voulgari et al. 4. The QTc interval is considered as a marker of cardiac autonomic dysfunction and is significantly associated with LVH 4. The increase in the number of abnormal CAN function tests increases the risk further 36. Pappachan et al. 37 concluded that the QTc interval can be used to diagnose CAN and the combined abnormalities of HRV, QTc, and QTd were strong predictors of mortality independent of conventional risk factors 38,39.
Prolongation of the QTc interval was detected in 60% of the CAN cases. This is in agreement with the finding of Lombardi 40. LVH was significantly manifest in the CAN group in comparison with the non-CAN group.
In the present study, QTc interval prolongation (>440 ms) has been associated with increased age and duration of DM, SBP, DBP, mean pulse pressure, and severity of autonomic neuropathy. This is in accordance with the finding of Ewing et al. 41 and Veglio et al. 42.
Comparison of mild CAN cases and severe CAN cases showed some clinical, biochemical, electrocardiographic, and echocardiographic significant differences including older age, more postural hypotension, elevated HbA1-c, serum creatinine, urine 24 albumin excretion, and more frequent QTc prolongation, which may lead to greater CV risk.
| Conclusion|| |
CAN in women with type 2 DM is common. Detection of CAN irrespective of its scoring in patients with DM is important and can help exercise more precautions during their diabetic management. As patients with prolonged QT intervals are at a higher risk of sudden cardiac death, cases with severe CAN have to be screened for coronary artery disease preoperatively and special clinics for CAN may be warranted.
| References|| |
|1.||Katsilambros NL, Boulton AJ, Tentolouris N, Kokkinos A, Liatis S. Autonomic neuropathy in diabetes mellitus and obesity: an update. Exp Diabetes Res. 2011;2011:607309 |
|2.||Maser RE, Lenhard MJ. An overview of the effect of weight loss on cardiovascular autonomic function. Curr Diabetes Rev. 2007;3:204–211 |
|3.||Tesfaye S, Boulton AJM, Dyck PJ, Freeman R, Horowitz M, Kempler P, et al. Diabetic neuropathies: update on definitions, diagnostic criteria, estimation of severity and treatments. Diabetes Care. 2010;33:2285–2293 |
|4.||Voulgari C, Tentolouris N, Stefanadis C. The ECG vertigo in diabetes and cardiac autonomic neuropathy. Exp Diabetes Res. 2011;2011:687624 |
|5.||Soedamah-Muthu SS, Chaturvedi N, Witte DR, Stevens LK, Porta M, Fuller JH, et al. Relationship between risk factors and mortality in type 1 diabetic patients in Europe: The EURODIAB Prospective Complications Study (PCS). Diabetes Care. 2008;31:1360–1366 |
|6.||Vinik AI, Maser RE, Mitchell BD, Freeman R. Diabetic autonomic neuropathy. Diabetes Care. 2003;26:1553–1579 |
|7.||Young LH, Wackers FJT, Chyun DA, Davey JA, Barrett EJ, Taillefer R, et al. Cardiac outcomes after screening for asymptomatic coronary artery disease in patients with type 2 diabetes the DIAD study: a randomized controlled trial. JAMA. 2009;301:1547–1555 |
|8.||Rossing P, Breum L, Major-Pedersen A, Sato A, Winding H, Pietersen A, et al. Prolonged QTc interval predicts mortality in patients with Type 1 diabetes mellitus. Diabet Med. 2001;18:199–205 |
|9.||Stettler C, Bearth A, Allemann S, Zwahlen M, Zanchin L, Deplazes M, et al. QTc interval and resting heart rate as long-term predictors of mortality in type 1 and type 2 diabetes mellitus: a 23-year follow-up. Diabetologia. 2007;50:186–194 |
|10.||Ziegler D, Rathmann W, Meisinger C, Dickhaus T, Mielck A. Prevalence and risk factors of neuropathic pain in survivors of myocardial infarction with pre-diabetes and diabetes. The KORA Myocardial Infarction Registry. Eur J Pain. 2009;13:582–587 |
|11.||Calles-Escand´on J, Lovato LC, Simons-Morton DG, Kendall DM, Pop-Busui R, Cohen RM, et al. Effect of intensive compared with standard glycemia treatment strategies on mortality by baseline subgroup characteristics: The Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. Diabetes Care. 2010;33:721–727 |
|12.||Pop-Busui R, Evans GW, Gerstein HC, Fonseca V, Fleg JL, Hoogwerf BJ, et al. Effects of cardiac autonomic dysfunction on mortality risk in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. Diabetes Care. 2010;33:1578–1584 |
|13.||Ewing DJ, Campbell IW, Clarke BF. Assessment of cardiovascular effects in diabetic autonomic neuropathy and prognostic implications. Ann Intern Med. 1980;92(II):308–311 |
|14.||Low PA, Opfer-Gehrking TL, McPhee BR, Fealey RD, Benarroch EE, Willner CL, et al. Prospective evaluation of clinical characteristics of orthostatic hypotension. Mayo Clin Proc. 1995;70:617–622 |
|15.||Singer W, Opfer-Gehrking TL, McPhee BR, Hilz MJ, Bharucha AE, Low PA. Acetylcholinesterase inhibition: a novel approach in the treatment of neurogenic orthostatic hypotension. J Neurol Neurosurg Psychiatry. 2003;74:1294–1298 |
|16.||Pfeifer MA, Weinberg CR, Cook DL, Reenan A, Halter JB, Ensinck JW, et al. Autonomic neural dysfunction in recently diagnosed diabetic subjects. Diabetes Care. 1984;7:447–453 |
|17.||Pop-Busui R, Herman WH, Feldman EL, Low PA, Martin CL, Cleary PA, et al. DCCT and EDIC studies in type 1 diabetes: lessons for diabetic neuropathy regarding metabolic memory and natural history. Curr Diabetes Rep. 2010;10:276–282 |
|18.||Kennedy WR, Navarro X, Sutherland DE. Neuropathy profile of diabetic patients in a pancreas transplantation program. Neurology. 1995;45:773–780 |
|19.||Vinik AI, Ziegler D. Diabetic cardiovascular autonomic neuropathy. Circulation. 2007;115:387–397 |
|20.||Schatz IJ, Goetz CG, Koller WC, Qinn NP, Robertson D. Consensus statement on the definition of orthostatic hypotension, pure autonomic failure and multiple system atrophy. The Consensus Committee of the American Autonomic Society and the American Academy of Neurology. Neurology. 1996;46:1470 |
|21.||Voulgari C, Psallas M, Kokkinos A, Argiana V, Katsilambros N, Tentolouris N. The association between cardiac autonomic neuropathy with metabolic and other factors in subjects with type 1 and type 2 diabetes. J Diabetes Complications. 2011;25:159–167 |
|22.||Gibbons CH, Freeman R. Treatment-induced diabetic neuropathy: a reversible painful autonomic neuropathy. Ann Neurol. 2010;67:534–541 |
|23.||England JD, Gronseth GS, Franklin G, Carter GT, Kinsella LJ, Cohen JA, et al. Evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review). Muscle Nerve. 2009;39:116–125 |
|24.||Kempler P, Tesfaye S, Chaturvedi N, Stevens LK, Webb DJ, Eaton S, et al. Blood pressure response to standing in the diagnosis of autonomic neuropathy: The EURODIAB IDDM Complications Study. Arch Physiol Biochem. 2001;109:215–222 |
|25.||Freeman R. Assessment of cardiovascular autonomic function. Clin Neurophysiol. 2006;117:716–730 |
|26.||Ziegler D, Dannehl K, Muhlen H, Spuler M, Gries FA. Prevalence of cardiovascular autonomic dysfunction assessed by spectral analysis, vector analysis and standard tests of heart rate variation and blood pressure responses at various stages of diabetic neuropathy. Diabet Med. 1992;9:806–814 |
|27.||Cabezas-Cerrato J, Gonzalez-Quintela A, Perez-Rodriguez M, Calle A, Faure-Noguera E, Vazquez-Garcia JA. Combination of cardiorespiratory reflex parameters and heart rate variability power spectrum analysis for early diagnosis of diabetic cardiac autonomic neuropathy. Diabetes Metab. 2009;35:305–311 |
|28.||Giorno R, Clifford JH, Beverly S, Rossing RG. Hematology reference values. Analysis by different statistical technics and variations with age and sex. Am J Clin Pathol. 1980;74:765–770 |
|29.||Hale WE, Stewart RB, Marks RG. Haematological and biochemical laboratory values in an ambulatory elderly population: an analysis of the effects of age, sex and drugs. Age Ageing. 1983;12:275–284 |
|30.||Kodama S, Heianza Y, Yoshizawa S, Fujihara K, Tanaka S, Lida KT, et al. Association between pulse pressure and cardiovascular risk in diabetes mellitus: a meta analysis. Diabetologia. 2012;22(Suppl):S1–S538 |
|31.||Mäkimattila S, Schlenzka A, Mäntysaari M, Bergholm R, Summanen P, Saar P, et al. Predictors of abnormal cardiovascular autonomic function measured by frequency domain analysis of heart rate variability and conventional tests in patients with type 1 diabetes. Diabetes Care. 2000;23:1686–1693 |
|32.||Valensi P, Pariès J, Attali JR. Cardiac autonomic neuropathy in diabetic patients: influence of diabetes duration, obesity and microangiopathic complications – the French multicenter study. Metabolism. 2003;52:815–820 |
|33.||Gandhi RA, Marques JL, Selvarajah D, Emery CJ, Tesfaye S. Painful diabetic neuropathy is associated with greater autonomic dysfunction than painless diabetic neuropathy. Diabetes Care. 2010;33:1585–1590 |
|34.||Liatis S, Marinou K, Tentolouris N, Pagoni S, Katsilambros N. Usefulness of a new indicator test for the diagnosis of peripheral and autonomic neuropathy in patients with diabetes mellitus. Diabet Med. 2007;24:1375–1380 |
|35.||Tentolouris N, Voulgari C, Liatis S, Kokkinos A, Eleftheriadou I, Makrilakis K, et al. Moisture status of the skin of the feet assessed by the visual test neuropad correlates with foot ulceration in diabetes. Diabetes Care. 2010;33:1112–1114 |
|36.||Giunti S, Bruno G, Lillaz E, Gruden G, Lolli V, Chaturvedi N, et al. Incidence and risk factors of prolonged QTc interval in type 1 diabetes: The EURODIAB Prospective Complications Study. Diabetes Care. 2007;30:2057–2063 |
|37.||Pappachan JM, Sebastian J, Bino BC, Jayaprakash K, Vijayakumar K, Sujathan P, et al. Cardiac autonomic neuropathy in diabetes mellitus: prevalence, risk factors and utility of corrected QT interval in the ECG for its diagnosis. Postgrad Med J. 2008;84:205–210 |
|38.||Lykke JA, Tarnow L, Parving HH, Hilsted J. A combined abnormality in heart rate variation and QT corrected interval is a strong predictor of cardiovascular death in type 1 diabetes. Scand J Clin Lab Invest. 2008;68:654–659 |
|39.||Ziegler D, Zentai CP, Perz S, Rathmann W, Haastert B, Döring A, et al. Prediction of mortality using measures of cardiac autonomic dysfunction in the diabetic and nondiabetic population: The MONICA/KORA Augsburg Cohort Study. Diabetes Care. 2008;31:556–561 |
|40.||Lombardi F. Clinical implications of present physiological understanding of HRV components. Card Electrophysiol Rev. 2002;6:245–249 |
|41.||Ewing DJ, Boland O, Neilson JMM, Gho CG, Clarke BF. Autonomic neuropathy, QT interval lengthening and unexpected deaths in male diabetic patients. Diabetologia. 1991;34:182–185 |
|42.||Veglio M, Chinaglia A, Cavallo Perin P. The clinical utility of QT interval assessment in diabetes. Diabetes Nutr Metab. 2000;13:356–365 |
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]