Abstract
Assessment of heart rate variability (HRV) and cardiac ectopic beats is a clinically relevant topic. The present exploratory observational study aimed to inspect the relationships of lifestyle, dietary patterns, and anthropometrics with HRV, premature ventricular complexes (PVCs), and supraventricular premature complexes (SVPCs). A cross-sectional study enrolling subjects undergoing Holter monitoring was performed. Sociodemographic and clinical characteristics, body composition (full-body bio-impedentiometry), dietary patterns (validated food frequency questionnaire and 24 h dietary recall), and quality of life were assessed. Generalized additive models were estimated to evaluate the relationships between outcomes of interest and variables collected. The study enrolled 121 consecutive patients undergoing 24 h Holter monitoring. Upon univariable analysis, HRV was found to have an inverse association with mass of body fat (MBF) (p-value 0.015), while doing physical activity was associated with a significantly higher HRV (p-value 0.036). Upon multivariable analysis, fruit consumption in the 24 h dietary recall was found to be directly associated with HRV (p-value 0.044). The present findings might be useful for improving the management of patients attending cardiac rhythm labs, and to tailor ad hoc prevention strategies (modification of lifestyle and eating habits) based on Holter parameters.
Keywords: heart rate variability, premature ventricular complexes, supraventricular premature complexes, dietary patterns, lifestyle
1. Introduction
Globally, the leading cause of death is cardiovascular diseases (CVDs); their prevalence is incessantly progressing in both developed and developing nations [1]. Although factors such as age, sex, and family history are considered crucial, some established factors are modifiable: hypertension, use of tobacco, diabetes mellitus, physical inactivity, unhealthy diet, cholesterol and lipids, and stress, among others [2]. Risk factors are often observed in clusters, so that even if just one risk factor such as hypertension is detected in a person, a search for coexisting risk factors such as smoking, central adiposity, hyperlipidemia, and diabetes mellitus becomes obligatory, because these risk factors occurring together can increase the risk of CVDs in a multiplicative rather than in an additive manner [3]. Though the prognosis of cardiovascular disease has improved because of better medical care, research on prognostic factors remains central. Heart rate variability (HRV) assessment is a clinically relevant topic, since even small alterations can predict severe, life-threatening, cardiac arrhythmias and cardiovascular events [4]. In recent decades, HRV has been extensively studied as a surrogate marker of autonomic function. Studies have been conducted both in healthy subjects and in those with underlying conditions affecting the cardiovascular system (e.g., previous myocardial infarction, congestive heart failure) [5]. Abnormal HRV (reduced) has been reported for patients suffering from myocardial infarction and diabetic neuropathy [5]. Although it has been shown that reduced HRV is a significant predictor of mortality and cardiovascular events, especially in patients with underlying cardiovascular diseases [6], it is still not entirely clear if reduced HRV represents the result of such diseases or the factor affecting the onset of such conditions.
Together with HRV, the role of cardiac ectopic beats (supraventricular premature complexes (SVPCs) and premature ventricular complexes (PVCs)) has been widely studied in the literature. More attention has been paid to PVCs, since PVCs is considered generally harmless but possibly a predictor of severe malignant cardiac arrhythmias (e.g., ventricular fibrillation).
Given the prognostic relevance of HRV and PVCs, it is crucial to understand the lifestyle factors and mechanisms associated with such parameters. In recent years, a role of anthropometrics, dietary patterns, and lifestyle in affecting cardiac ectopic beats and HRV has been suggested; however, evidence remains limited and unclear. In addition, there is a growing body of literature about the central role of some nutrients in the prevention of cardiac arrhythmias [7], especially fatal arrhythmias (ventricular arrhythmias), but little evidence is available regarding the protective effects of dietary patterns and lifestyle on PVCs and HRV.
Results from randomized controlled trials suggest that the supplementation of omega-3 polyunsaturated fatty acids (PUFA) may reduce the number of PVCs per day [8], also decreasing their severity [9]. Moreover, omega-3 PUFAs have also been hypothesized to be linked to HRV, supporting their protective role in subjects at high risk for arrhythmic events [10] and sudden cardiac death (SCD) [11]. Together with substances that may play a role in preventing PVCs, some food contents may act as triggers. Some studies have suggested that alcohol and caffeine consumption may be linked to cardiac performance. Evidence indicates the existence of an association between different doses of alcohol consumption with HRV [12] and cardiac ectopic beats [13], while the role of caffeine is still disputed.
Not only the type of food intake, but also meal frequency has been suggested to affect cardiovascular risk profile; it has been suggested that having late dinner may be a proxy for atrial arrhythmias [14], but evidence in the field is still scarce.
Together with dietary patterns, anthropometrics and lifestyle have also been hypothesized to affect HRV and cardiac ectopic beats. Physical activity has been demonstrated to be a relevant factor in improving HRV [15]. Regarding anthropometrics, obesity and being overweight represent a predictor of cardiac functions’ impairment. A higher number of PVCs and reduced HRV have been documented in obese subjects [16]. Additionally, a recent research study identified the waist-to-hip ratio, a marker of visceral adiposity, to be associated with HRV [17].
Although studies have suggested the existence of an association between lifestyle, HRV, and cardiac ectopic beats, the underlying mechanisms are not yet clear and evidence is limited and controversial. More specifically, data regarding PVCs and HRV are lacking, despite the prognostic relevance of PVCs and HRV in clinical practice.
The present exploratory observational study aimed to inspect relationships of dietary patterns, anthropometrics and lifestyle, with HRV, PVCs, and SVPCs. In particular, it aimed at analyzing if any difference exists in the role played by such factors on outcomes of interest in patients undergoing Holter monitoring.
2. Materials and Methods
This study was a cross-sectional exploratory investigation conducted at the Department of Cardiac, Thoracic, Vascular Sciences and Public Health of the University of Padova, Azienda Ospedaliera di Padova. It enrolled patients referred to the outpatient clinic for 24 h Holter monitoring, from May to July 2016.
To be enrolled in the study, patients were required to meet the following criteria: older than 18 years of age; ability to speak and understand the Italian language; and absence of cognitive impairment. Patients were asked to give written informed consent to participate in the study. The study was approved by the competent Institutional Review Board.
2.1. Holter Monitor
Patients were invited to wear a Holter monitor for 24 h and were provided with a diary in which to report activities and symptoms perceived during the 24 h Holter monitoring, with the final aim of finding potential associations between symptoms felt, reported in the diary, and modifications of heart activity documented by the Holter monitor.
Holter monitor data considered in this study were minimum and maximum heart rate, PVCs, SVPCs, and HRV (standard deviation of the N-N (SDNN) intervals in ms). For this study, PVCs, SVPCs, and HRV were considered as outcomes of interest.
2.2. Demographic Characteristics, Lifestyle, and Clinical Assessment
Demographic characteristics, lifestyle habits, and clinical history were collected through a purpose-designed questionnaire, administered by an interviewer, and available medical records.
Collected demographic characteristics were age, sex, educational level (categorized as “low”, “medium”, and “high”, corresponding to primary school, high school, and bachelor’s/master’s degree, respectively), and employment situation. Investigated lifestyle habits were tobacco smoking, physical activity, hours of sleep, and leisure activities. Clinical history focused on concomitant medications and comorbidities.
2.3. Health-Related Quality of Life (HRQoL)
Health-related quality of life was assessed using the EuroQol-5D 3 level version (EQ-5D-3L). EQ-5D is a self-administered questionnaire which consists of two parts: the EQ-5D descriptive system and the EQ visual analogue scale (EQ-VAS). EQ-5D focuses on five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Three levels are available for each dimension: “no problems”, “some problems”, and “severe or extreme problems”. Participants were asked to tick the option preferred for each dimension.
The EQ-VAS consists on a vertical visual analogue scale ranging from “best imaginable health state” to “worst imaginable health state”, corresponding respectively to 100 and 0 scores. Patients were asked to indicate in the scale the numeric value better describing their quality of life.
Psychometric properties, including reliability and construct validity, have been already assessed for the Italian version of EuroQol-5D [18].
2.4. Anthropometric Data
Patients underwent anthropometric assessment by trained dietitians. Weight, height, hip, waist and arm circumference were measured and body mass index (BMI) was computed dividing weight (in kilograms) by height squared (in meters). Tricep skinfold was measured using a Harpenden skinfold caliper.
Participants underwent body composition analysis using a D-1000-3 Full Body Analyzer (Heteren, Netherlands, Rice Lake®). The bioelectrical impedance analysis (BIA) measures body composition through the impedance of the human body, providing values of mass of body fat (MBF), lean body mass (LBM), total body water (TBW), intracellular water (ICW), body mass index (BMI), percentage of body fat (PBF), and segmental lean body mass of body parts (trunk, arms, and legs).
Patients with implantation of metallic material (e.g., stents) and/or of devices making electric signals (e.g., artificial heart), connection to electronic equipment with good conductivity, taking contraceptives, suspected to be pregnant, or susceptible to a small amount of electrical stimulation were excluded from the BIA assessment, according to the safety rules for the D-1000-3 Full Body Analyzer (Heteren, Netherlands, Rice Lake®).
2.5. Food Frequency Questionnaire (FFQ) and 24 h Dietary Recall
Patients’ eating habits were assessed using a brief version of the Turconi Food Frequency Questionnaire (FFQ). For the study, only two sections of the FFQ were administered, the one about the frequency of food consumption, and the one on eating habits. The first one consists of questions about the frequency of food consumption (daily, weekly, etc.) of food products from different food groups, including beverages. The section on eating habits consists of 14 questions that focus mainly on meal frequency, drinks, and food consumption during meals and outside mealtimes. A score is assigned to each question. The score ranged from 1 (less healthy habits) to 4 (more healthy habits). The total possible score of this second section is 56. Higher scores mean better eating habits. The questionnaire was previous validated in a sample of Italian adults [19].
The day after the Holter monitoring, 24 h dietary recall was collected, asking about food consumption during the 24 h of Holter monitoring. Food reported by patients at mealtimes was categorized using “What we Eat in America” (WWEIA) [20] food categories, an instrument proposed by the United States Department of Agriculture (USDA) to investigate food and beverage intake. The classification consists of three levels based on grouping similar foods and beverages based on nutrient content, without disaggregation into ingredients.
The choice of a U.S. classification tool was motivated by the fact that it was considered more suitable for the purpose of our study compared to that proposed from the European Food Safety Authority (EFSA), since that of EFSA is generally employed in total diet studies [21].
2.6. Analysis of Precision
Being an observational prospective study, it was designed to guarantee attainment of a desired target of precision in estimates. Relative precision was computed for mean difference in the number of meals (indicated below as X) during the 24 h dietary recall, between patients with and without cardiac ectopic beats (registered by Holter monitor), considering
the target difference in the number of meals between groups, defined as = 2;
the pooled standard error of the difference between groups, defined as ;
significance level set at 0.05.
Parameters above were derived from pre-existing clinical records. After having evaluated the patients’ distribution, an overall sample of 100 subjects, not balanced by the presence/absence of cardiac ectopic beats, was considered reasonable for the study. Under such assumptions, a relative precision of 4.43% of point estimate was expected.
2.7. Statistical Analysis
Categorical data were reported as relative and absolute frequencies, and continuous data as median and Quartiles I and III. Wilcoxon–Kruskal–Wallis tests were performed for continuous variables and Pearson chi-square tests for categorical ones.
For multiple-choice variables, multiple marginal independence (MMI) was tested, using nonparametric bootstrap resamples under the null hypothesis of independent sampling. A modified Pearson statistic was calculated for each resample (n = 2000).
PVCs and SVPCs were treated as semi-continuous data, since they presented a combination of both a point-mass at zero and a positively skewed distribution (as clearly shown in Figures S1 and S2, Supplementary Material). Such data are unsuitable for analysis using positively skewed distributions since distributions that are unbounded are likely to result in a poor fit [22]. To account for such a distribution, a generalized additive model, considering a zero adjusted gamma distribution (ZAGA) [23] for dependent variables, was estimated to evaluate the effect of independent variables on PVCs and SVPCs. More specifically, for both models, the probability that an outcome was non-zero was modeled via logistic regression. The distribution of the non-zero outcomes was modeled via gamma regression with a log-link for ZAGA. This type of non-negative data distribution is commonly found in data from many research fields, and, recently, this approach has also been applied in nutrition and dietary research [24].
HRV was modeled using a generalized additive model with gamma distribution considering the skewness of dependent variable (Figure S3, Supplementary Material).
Evaluation of the goodness of fit of the multivariable estimated models was performed using graphical inspection of theoretical and estimated residuals’ quantiles and via a Kernel density estimation of residual distribution.
P-values related to the effects of multiple testing were adjusted using the Benjamini and Hochberg procedure.
Computations were performed using R System 3.3.1 software [25] with rms, gamlss, and MRCV packages.
3. Results
One hundred and twenty-one consecutive patients attending the cardiac rhythm lab for 24 h Holter monitoring were enrolled in the study. The effects of single variables on PVCs, SVPCs, and HRV are reported in Table 1.
Table 1.
Descriptive statistics according to presence/absence of PVCs. Data are percentages (absolute numbers) for categorical variables, and Quartile I/median/Quartile III for continuous variables.
| Premature Ventricular Complexes: No (n = 26) | Premature Ventricular Complexes: Yes (n = 95) | Combined (n = 121) | p-Value | |
|---|---|---|---|---|
| Sociodemographic Characteristics and Lifestyle | ||||
| Age | 29.75/44.00/66.75 | 50.50/67.00/77.00 | 47.00/66.00/75.00 | 0.006 |
| Sex: Male | 38% (10) | 45% (43) | 44% (53) | 0.756 |
| Female | 62% (16) | 55% (52) | 56% (68) | |
| Educational level: Low | 38% (10) | 47% (45) | 45% (55) | 0.723 |
| Medium | 42% (11) | 29% (28) | 32% (39) | |
| High | 19% (5) | 23% (22) | 22% (27) | |
| Employment: No | 54% (14) | 67% (64) | 64% (78) | 0.496 |
| Yes | 46% (12) | 33% (31) | 36% (43) | |
| Cardiovascular comorbidities: No | 69% (18) | 35% (33) | 42% (51) | 0.06 |
| Yes | 31% (8) | 65% (62) | 58% (70) | |
| Concomitant medications. Ace inhibitors: Yes | 23% (6) | 41% (39) | 37% (45) | 0.496 |
| Diuretics: Yes | 19% (5) | 26% (25) | 25% (30) | |
| Potassium supplements: Yes | 0% (0) | 2% (2) | 2% (2) | |
| Flecainide: Yes | 4% (1) | 5% (5) | 5% (6) | |
| Class I antiarrhythmic agents: Yes | 4% (1) | 0% (0) | 1% (1) | |
| Class III antiarrhythmic agents: Yes | 0% (0) | 3% (3) | 2% (3) | |
| Digoxin: Yes | 0% (0) | 2% (2) | 2% (2) | |
| Nitrates: Yes | 0% (0) | 3% (3) | 2% (3) | |
| Calcium channel blockers: Yes | 8% (2) | 17% (16) | 15% (18) | |
| Beta blockers: Yes | 19% (5) | 39% (37) | 35% (42) | |
| Vasodilators: Yes | 0% (0) | 1% (1) | 1% (1) | |
| Platelets aggregation inhibitors: Yes | 19% (5) | 34% (32) | 31% (37) | |
| Anticoagulants: Yes | 8% (2) | 15% (14) | 13% (16) | |
| Cholesterol lowering medications: Yes | 19% (5) | 32% (30) | 29% (35) | |
| Insulin: Yes | 0% (0) | 4% (4) | 3% (4) | |
| Oral hypoglycemic agents: Yes | 4% (1) | 9% (9) | 8% (10) | |
| Smoking habit: No | 62% (16) | 58% (55) | 59% (71) | 0.285 |
| Past smoker | 12% (3) | 33% (31) | 28% (34) | |
| Current smoker | 27% (7) | 9% (9) | 13% (16) | |
| Cigarettes number (per day) | 7.00/10.00/20.00 | 5.00/ 8.00/15.00 | 4.75/ 9.00/20.00 | 0.756 |
| Physical activity: No | 50% (13) | 61% (58) | 59% (71) | 0.583 |
| Yes | 50% (13) | 39% (37) | 41% (50) | |
| Physical activity: number of weekly training sessions | 3/3/5 | 2/3/3 | 2/3/4 | 0.411 |
| Sleep hours | 6.0/6.5/7.0 | 5.0/6.5/7.0 | 5.0/6.5/7.0 | 0.883 |
| EQ5D VAS | 60.00/70.00/80.00 | 51.00/70.00/80.00 | 57.75/70.00/80.00 | 0.938 |
| Anthropometrics and BIA | ||||
| Lean body mass | 43.50/45.70/48.07 | 44.15/47.05/59.17 | 43.85/46.20/52.92 | 0.496 |
| Total body water | 31.35/32.90/34.60 | 31.80/33.90/42.57 | 31.57/33.25/38.10 | 0.496 |
| Extracellular water | 12.10/12.90/14.05 | 12.77/13.95/17.22 | 12.57/13.75/15.52 | 0.375 |
| Mass of body fat | 10.87/18.50/24.10 | 16.52/20.25/21.95 | 14.85/19.75/22.37 | 0.748 |
| Percent of body fat | 17.70/30.75/34.60 | 22.15/29.35/31.80 | 21.60/29.65/33.85 | 0.951 |
| BMI | 21.75/23.58/27.62 | 22.52/24.77/27.59 | 22.28/24.66/27.67 | 0.723 |
| Skinfold thickness | 11.57/18.43/26.08 | 11.67/18.30/23.17 | 11.57/18.30/23.91 | 0.82 |
| Waist | 81.12/ 90.00/ 98.75 | 87.00/ 95.00/103.00 | 86.00/ 95.00/103.00 | 0.496 |
| Hip | 94.0/100.5/106.0 | 98.0/103.0/108.0 | 96.0/102.0/107.5 | 0.583 |
| Food Frequency Questionnaire | ||||
| Score of eating habits section | 39.50/44.00/48.75 | 42.00/46.00/48.50 | 42.00/45.00/49.00 | 0.602 |
| Daily milk/yogurt: No | 35% (9) | 27% (26) | 29% (35) | 0.723 |
| Yes | 65% (17) | 73% (69) | 71% (86) | |
| If yes, how many? 1–2 | 100% (17) | 94% (65) | 95% (82) | 0.583 |
| 3–4 | 0% (0) | 6% (4) | 5% (4) | |
| If no, weekly milk/yogurt: at least once a week | 22% (2) | 35% (9) | 31% (11) | 0.735 |
| Less than once a week | 78% (7) | 65% (17) | 69% (24) | |
| Daily grains: No | 27% (7) | 19% (18) | 21% (25) | 0.639 |
| Yes | 73% (19) | 81% (77) | 79% (96) | |
| If yes, how many? 1–2 | 100% (19) | 99% (76) | 99% (95) | 0.789 |
| 3–4 | 0% (0) | 1% (1) | 1% (1) | |
| If no, weekly grains: 1–2 | 14% (1) | 25% (5) | 22% (6) | 0.496 |
| 3–4 | 86% (6) | 45% (9) | 56% (15) | |
| >4 | 0% (0) | 30% (6) | 22% (6) | |
| Daily fruits and vegetables: No | 31% (8) | 12% (11) | 16% (19) | 0.285 |
| Yes | 69% (18) | 88% (84) | 84% (102) | |
| If yes, how many? 1–2 | 61% (11) | 76% (64) | 74% (75) | 0.496 |
| 3–4 | 39% (7) | 20% (17) | 24% (24) | |
| >4 | 0% (0) | 4% (3) | 3% (3) | |
| Weekly servings of meat: at least once a week | 65% (17) | 76% (72) | 74% (89) | |
| At least once a day | 15% (4) | 11% (10) | 12% (14) | |
| Less than once a week | 19% (5) | 14% (13) | 15% (18) | |
| Weekly servings of fish: 1–2 | 46% (12) | 59% (56) | 56% (68) | 0.781 |
| 3–4 | 19% (5) | 13% (12) | 14% (17) | |
| >4 | 0% (0) | 1% (1) | 1% (1) | |
| every 10–15 days | 15% (4) | 17% (16) | 17% (20) | |
| never | 19% (5) | 11% (10) | 12% (15) | |
| Weekly servings of eggs: at least once a week | 73% (19) | 82% (78) | 80% (97) | |
| Less than once a week | 27% (7) | 18% (17) | 20% (24) | |
| Weekly servings of cheese: 1–2 | 35% (9) | 42% (40) | 40% (49) | 0.883 |
| 3–4 | 23% (6) | 25% (24) | 25% (30) | |
| >4 | 19% (5) | 19% (18) | 19% (23) | |
| every 10–15 days | 12% (3) | 5% (5) | 7% (8) | |
| never | 12% (3) | 8% (8) | 9% (11) | |
| Weekly servings of cured meat: 1–2 | 15% (4) | 48% (46) | 41% (50) | 0.375 |
| 3–4 | 19% (5) | 9% (9) | 12% (14) | |
| >4 | 12% (3) | 6% (6) | 7% (9) | |
| every 10–15 days | 31% (8) | 21% (20) | 23% (28) | |
| never | 23% (6) | 15% (14) | 17% (20) | |
| Weekly servings of legumes: 1–2 | 31% (8) | 52% (49) | 47% (57) | 0.411 |
| 3–4 | 31% (8) | 17% (16) | 20% (24) | |
| >4 | 8% (2) | 2% (2) | 3% (4) | |
| every 10-15 days | 12% (3) | 20% (19) | 18% (22) | |
| never | 19% (5) | 9% (9) | 12% (14) | |
| Weekly servings of cakes: 1–2 | 11% (2) | 29% (25) | 26% (27) | 0.411 |
| 3–4 | 16% (3) | 9% (8) | 10% (11) | |
| 1 per day | 58% (11) | 28% (24) | 33% (35) | |
| 2 per day | 11% (2) | 12% (10) | 11% (12) | |
| every 10–15 days | 5% (1) | 14% (12) | 12% (13) | |
| never | 0% (0) | 8% (7) | 7% (7) | |
| Weekly servings of French fries: 1–2 | 12% (3) | 9% (9) | 10% (12) | 0.95 |
| 3–4 | 0% (0) | 1% (1) | 1% (1) | |
| every 10–15 days | 27% (7) | 24% (23) | 25% (30) | |
| never | 62% (16) | 65% (62) | 64% (78) | |
| How often do you eat fast food per week? (weekly) 1–2 | 0% (0) | 2% (2) | 2% (2) | 0.496 |
| every 10–15 days | 12% (3) | 3% (3) | 5% (6) | |
| never | 88% (23) | 95% (90) | 93% (113) | |
| How often do you eat at a pizzeria? (weekly) 1–2 | 32% (8) | 23% (22) | 25% (30) | 0.411 |
| 3–4 | 48% (12) | 33% (31) | 36% (43) | |
| every 10-15 days | 20% (5) | 44% (42) | 39% (47) | |
| Do you drink wine: No | 62% (16) | 42% (40) | 46% (56) | 0.411 |
| Yes | 38% (10) | 58% (55) | 54% (65) | |
| If yes, how many? (weekly) 1–2 | 10% (1) | 16% (9) | 15% (10) | 0.639 |
| 3–4 | 20% (2) | 11% (6) | 12% (8) | |
| every 10–15 days | 40% (4) | 20% (11) | 23% (15) | |
| every day | 30% (3) | 53% (29) | 49% (32) | |
| Do you drink beer? No | 58% (15) | 72% (68) | 69% (83) | 0.496 |
| Yes | 42% (11) | 28% (27) | 31% (38) | |
| If yes, how many? (weekly): 1–2 | 45% (5) | 41% (11) | 42% (16) | 0.938 |
| 3–4 | 9% (1) | 4% (1) | 5% (2) | |
| every 10–15 days | 36% (4) | 44% (12) | 42% (16) | |
| every day | 9% (1) | 11% (3) | 11% (4) | |
| Do you drink other alcoholic beverages? No | 80% (20) | 79% (74) | 79% (94) | 0.938 |
| Yes | 20% (5) | 21% (20) | 21% (25) | |
| If yes, how many? (weekly): 1–2 | 20% (1) | 50% (10) | 44% (11) | 0.723 |
| 3–4 | 0% (0) | 5% (1) | 4% (1) | |
| every 10–15 days | 60% (3) | 40% (8) | 44% (11) | |
| every day | 20% (1) | 5% (1) | 8% (2) | |
| Do you drink spirits? No | 96% (25) | 96% (91) | 96% (116) | 0.95 |
| Yes | 4% (1) | 4% (4) | 4% (5) | |
| 24 h Dietary Recall | ||||
| Number of meals in the 24 h recall | 3/4/5 | 3/4/5 | 3/4/5 | 0.583 |
| Alcoholic beverages | 1.00/2.00/2.75 | 0.00/1.00/2.00 | 0.00/1.00/2.00 | 0.561 |
| Non-alcoholic beverages | 0/0/1 | 0/1/1 | 0/0/1 | 0.411 |
| Condiments and sauces | 0/1/1 | 0/1/1 | 0/1/1 | 0.781 |
| Fats and oils | 0.0/0.5/1.0 | 0.0/1.0/2.0 | 0.0/1.0/2.0 | 0.496 |
| Fruit | 0/1/2 | 1/2/2 | 1/1/2 | 0.375 |
| Grain products | 0/1/2 | 0/1/1 | 0/1/2 | 0.82 |
| Milk and dairy | 0/1/2 | 0/1/1 | 0/1/2 | 0.82 |
| Mixed dishes | 0.0/0.5/1.0 | 0.0/0.0/1.0 | 0.0/0.0/1.0 | 0.288 |
| Potatoes: No | 88% (23) | 95% (90) | 93% (113) | 0.561 |
| Yes | 12% (3) | 5% (5) | 7% (8) | |
| Protein food | 0/1/1 | 0/1/1 | 0/1/1 | 0.883 |
| Snacks and sweets | 0/1/2 | 0/1/1 | 0/1/2 | 0.496 |
| Sugars | 0.00/1.00/1.75 | 0.00/1.00/2.00 | 0.00/1.00/2.00 | 0.781 |
| Vegetables | 0/1/2 | 0/1/2 | 0/1/2 | 0.938 |
| Water | 0/2/2 | 0/1/2 | 0/1/2 | 0.496 |
3.1. Demographic and Lifestyle
Ninety-five patients had at least 1 PVCs (reported by the 24 h Holter monitoring), with a median of 78 PVCs (13–746, Quartiles I-III). Sociodemographic characteristics and lifestyle in presence/absence of PVCs are reported in Table 1. Subjects with PVCs were significantly older (median age of 67 vs. 44, p 0.006) compared to those who did not suffer from it (Table 1).
Subjects’ characteristics according to presence/absence of SVPCs are reported in Supplementary material (Table S1). Briefly, 109 subjects out of 121 presented with at least one SVPCs (median of 39, 9-224 Quartiles I-III). No statistical differences were found in sociodemographic characteristics and lifestyle in the presence/absence of SVPCs.
Regarding Holter parameters, no significant differences were reported, except for the number of SVPCs (PVCs subjects had a higher number of SVPCs compared to non-PVCs subjects, p-value < 0.001) (Table 2).
Table 2.
Holter monitor variables according to presence/absence of PVCs. Data are Quartile I/median/Quartile III.
| Premature Ventricular Complexes: No (n = 26) | Premature Ventricular Complexes: Yes (n = 95) | Combined (n = 121) | p-Value | |
|---|---|---|---|---|
| Heart beats | 85404.0/100830.0/112876.0 | 84779.0/94147.0/105342.5 | 85075.5/95447.5/106228.8 | 0.442 |
| Mean heart rate | 67.0/72.0/78.0 | 61.5/69.0/76.0 | 62.0/70.0/77.0 | 0.442 |
| Heart rate: Minimum | 45.00/48.00/54.00 | s41.50/48.00/54.50 | 42.75/48.00/54.25 | 0.959 |
| Heart rate: Maximum | 102.0/115.0/121.0 | 97.5/116.0/133.0 | 98.0/116.0/132.0 | 0.959 |
| Heart rate variability | 115.0/139.9/174.0 | 103.1/135.3/173.2 | 103.7/137.0/174.6 | 0.959 |
| Supraventricular Premature complexes | 0.00/7.50/38.75 | 13.50/54.00/326.00 | 9.00/39.00/224.00 | <0.001 |
Regarding the univariable analysis (Table 3), data showed that doing physical activity was associated with a significantly higher HRV (p-value 0.036), but not with PVCs and SVPCs. Higher age and the presence of cardiovascular comorbidities were shown to result in a significantly higher likelihood of SVPCs (both p-value < 0.001).
Table 3.
Results of univariable analyses for premature ventricular complexes, supraventricular premature complexes, and heart rate variability. Exp estimate represents E[(Y+1); X]/ E [Y; X] indicating the relative variation in the expected number of arrhythmic events consequently to a unit increase of each considered X variable.
| Premature Ventricular Complexes | Supraventricular Premature Complexes | Heart Rate Variability | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Estimate (Standard Error) | Exp. Estimate | p-Value | Estimate (Standard Error) | Exp. Estimate | p-Value | Estimate (Standard Error) | Exp. Estimate | p-Value | |
| Sociodemographic characteristics and lifestyle | |||||||||
| Age | 0.021 (0.011) | 1.021 | 0.112 | 0.06 (0.009) | 1.062 | <0.001 | −0.002 (0.002) | 0.998 | 0.253 |
| Sex: female vs. male | −0.618 (0.386) | 0.539 | 0.336 | −0.3 (0.342) | 0.741 | 0.462 | −0.053 (0.072) | 0.948 | 0.462 |
| Educational level: medium vs. low | −0.108 (0.452) | 0.898 | 0.82 | −0.088 (0.386) | 0.916 | 0.82 | 0.057 (0.082) | 1.059 | 0.82 |
| Educational level: high vs. low | −0.682 (0.488) | 0.506 | 0.248 | −1.038 (0.438) | 0.354 | 0.057 | −0.023 (0.094) | 0.977 | 0.803 |
| Employment: Yes vs. No | −1.567 (0.398) | 0.209 | <0.001 | −0.226 (0.354) | 0.798 | 0.524 | 0.059 (0.075) | 1.061 | 0.524 |
| Cardiovascular Comorbidities: Yes vs. No | 0.527 (0.405) | 1.694 | 0.294 | 1.723 (0.321) | 5.604 | <0.001 | −0.016 (0.072) | 0.985 | 0.831 |
| Tobacco smoking: Past smoker vs. Never smoked | 0.46 (0.421) | 1.585 | 0.414 | −0.576 (0.382) | 0.562 | 0.402 | 0.043 (0.081) | 1.044 | 0.601 |
| Tobacco smoking: Current smoker vs. Never smoker | −0.7 (0.673) | 0.496 | 0.45 | −1.197 (0.515) | 0.302 | 0.066 | −0.067 (0.106) | 0.935 | 0.53 |
| How many cigarettes/day | −0.048 (0.053) | 0.953 | 0.609 | −0.033 (0.039) | 0.967 | 0.609 | −0.004 (0.009) | 0.996 | 0.657 |
| Physical activity: Yes vs. No | 0.258 (0.397) | 1.294 | 0.517 | −0.315 (0.347) | 0.73 | 0.517 | 0.181 (0.07) | 1.199 | 0.036 |
| specify frequency per week | 0.161 (0.16) | 1.175 | 0.477 | −0.043 (0.157) | 0.958 | 0.786 | 0.032 (0.024) | 1.032 | 0.477 |
| Hours slept during the night | −0.084 (0.132) | 0.92 | 0.527 | −0.208 (0.113) | 0.812 | 0.115 | 0.042 (0.024) | 1.043 | 0.115 |
| EQ5D VAS | −0.006 (0.009) | 0.994 | 0.735 | −0.003 (0.008) | 0.997 | 0.735 | 0.002 (0.002) | 1.002 | 0.735 |
| Anthropometrics and BIA | |||||||||
| Lean body mass | 0.052 (0.026) | 1.054 | 0.076 | 0.003 (0.028) | 1.003 | 0.923 | 0.012 (0.005) | 1.012 | 0.076 |
| Total body water | 0.073 (0.036) | 1.076 | 0.076 | 0.004 (0.039) | 1.004 | 0.925 | 0.016 (0.007) | 1.016 | 0.076 |
| Extracellular water | 0.186 (0.085) | 1.205 | 0.098 | 0.062 (0.092) | 1.064 | 0.505 | 0.032 (0.017) | 1.033 | 0.098 |
| Mass of body fat | 0.142 (0.053) | 1.153 | 0.015 | 0.075 (0.046) | 1.078 | 0.113 | −0.023 (0.008) | 0.977 | 0.015 |
| Percentage of body fat | 0.035 (0.047) | 1.035 | 0.468 | 0.045 (0.041) | 1.046 | 0.42 | −0.024 (0.007) | 0.977 | 0.003 |
| BMI | 0.063 (0.05) | 1.065 | 0.315 | 0.008 (0.043) | 1.008 | 0.85 | −0.016 (0.009) | 0.984 | 0.216 |
| Skinfold thickness | −0.007 (0.023) | 0.993 | 0.754 | −0.011 (0.021) | 0.989 | 0.754 | −0.007 (0.004) | 0.993 | 0.333 |
| Waist circumference | 0.038 (0.015) | 1.038 | 0.024 | 0.051 (0.013) | 1.052 | <0.001 | −0.004 (0.003) | 0.996 | 0.203 |
| Hip circumference | 0.025 (0.018) | 1.025 | 0.449 | 0.014 (0.016) | 1.015 | 0.449 | −0.002 (0.003) | 0.998 | 0.449 |
| Food Frequency Questionnaire | |||||||||
| Score of eating habits section | −0.016 (0.037) | 0.984 | 0.67 | 0.023 (0.031) | 1.023 | 0.67 | 0.005 (0.006) | 1.005 | 0.67 |
| Daily milk/yogurt: Yes vs. No | 0.146 (0.434) | 1.157 | 0.738 | −0.254 (0.38) | 0.776 | 0.738 | −0.068 (0.077) | 0.934 | 0.738 |
| If yes. daily servings: 3–4 vs. 1–2 | −2.007 (0.956) | 0.134 | 0.117 | 0.208 (0.873) | 1.231 | 0.882 | 0.03 (0.203) | 1.031 | 0.882 |
| If no. weekly servings: less than once a week vs. at least once a week | −0.327 (0.788) | 0.721 | 0.681 | −1.372 (0.745) | 0.254 | 0.222 | 0.085 (0.147) | 1.088 | 0.681 |
| Daily pasta/bread/rice/potatoes. Yes vs. No | −0.468 (0.493) | 0.626 | 0.518 | −0.651 (0.413) | 0.521 | 0.351 | 0.012 (0.091) | 1.012 | 0.893 |
| If yes. daily servings: 3–4 vs. 1–2 | −3.255 (1.878) | 0.039 | 0.129 | −4.427 (1.667) | 0.012 | 0.027 | 0.489 (0.346) | 1.631 | 0.161 |
| If no. weekly servings: 3–4 vs. 1–2 | 1.124 (1.026) | 3.077 | 0.712 | −0.36 (0.965) | 0.697 | 0.712 | 0.127 (0.214) | 1.135 | 0.712 |
| If no. weekly servings: >4 vs. 1-2 | 1.817 (1.114) | 6.15 | 0.174 | −2.44 (1.184) | 0.087 | 0.15 | 0.193 (0.251) | 1.213 | 0.452 |
| Daily Fruits and vegetables: Yes vs. No | −0.419 (0.605) | 0.658 | 0.609 | 0.988 (0.475) | 2.685 | 0.12 | 0.055 (0.106) | 1.056 | 0.609 |
| If yes. daily servings: 3–4 vs. 1–2 | 0.227 (0.487) | 1.255 | 0.642 | −0.614 (0.412) | 0.541 | 0.42 | −0.077 (0.082) | 0.926 | 0.528 |
| If yes. daily servings: >4 vs. 1–2 | −1.977 (1.053) | 0.139 | 0.096 | −1.229 (1.227) | 0.292 | 0.319 | 0.506 (0.199) | 1.658 | 0.039 |
| Weekly meat: at least once a day vs. at least once a week | −0.107 (0.637) | 0.899 | 0.867 | 0.664 (0.545) | 1.943 | 0.675 | −0.065 (0.107) | 0.937 | 0.816 |
| Weekly meat: less than once a week vs. at least once a week | −0.141 (0.569) | 0.868 | 0.804 | 0.321 (0.495) | 1.379 | 0.777 | −0.139 (0.098) | 0.87 | 0.483 |
| Weekly fish: 3–4 vs. 1–2 | 0.383 (0.589) | 1.467 | 0.517 | −2.498 (0.471) | 0.082 | <0.001 | −0.069 (0.098) | 0.933 | 0.517 |
| Weekly fish: >4 vs. 1–2 | −2.492 (1.869) | 0.083 | 0.277 | −1.295 (1.698) | 0.274 | 0.447 | −0.553 (0.349) | 0.575 | 0.277 |
| Weekly fish: every 10–15 days vs. 1–2 | −1.003 (0.525) | 0.367 | 0.151 | −0.686 (0.45) | 0.503 | 0.151 | −0.15 (0.103) | 0.861 | 0.151 |
| Weekly fish: never vs. 1–2 | −0.798 (0.636) | 0.45 | 0.212 | −0.735 (0.55) | 0.48 | 0.212 | 0.149 (0.103) | 1.161 | 0.212 |
| Weekly eggs: less than once a week vs. at least once a week | 0.419 (0.504) | 1.52 | 0.597 | −0.237 (0.447) | 0.789 | 0.597 | 0.056 (0.086) | 1.058 | 0.597 |
| Weekly cheese: 3–4 vs. 1–2 | 1.316 (0.462) | 3.729 | 0.015 | −0.421 (0.417) | 0.656 | 0.471 | −0.065 (0.09) | 0.937 | 0.471 |
| Weekly cheese: >4 vs. 1–2 | 1.707 (0.508) | 5.514 | 0.003 | −0.7 (0.461) | 0.497 | 0.198 | −0.086 (0.101) | 0.917 | 0.394 |
| Weekly cheese: every 10–15 days vs. 1–2 | 0.461 (0.848) | 1.585 | 0.971 | −0.026 (0.705) | 0.975 | 0.971 | 0.035 (0.146) | 1.035 | 0.971 |
| Weekly cheese: never vs. 1–2 | −0.509 (0.693) | 0.601 | 0.696 | −2.164 (0.607) | 0.115 | 0.003 | 0.023 (0.131) | 1.023 | 0.863 |
| Weekly cured meat: 3–4 vs. 1–2 | −0.058 (0.687) | 0.943 | 0.932 | −2.451 (0.543) | 0.086 | <0.001 | −0.113 (0.129) | 0.893 | 0.573 |
| Weekly cured meat: >4 vs. 1–2 | −0.142 (0.818) | 0.868 | 0.863 | −1.349 (0.642) | 0.259 | 0.114 | 0.032 (0.135) | 1.032 | 0.863 |
| Weekly cured meat: every 10–15 days vs. 1–2 | 0.261 (0.505) | 1.298 | 0.607 | −0.925 (0.41) | 0.396 | 0.078 | −0.105 (0.091) | 0.901 | 0.381 |
| Weekly cured meat: never vs. 1–2 | 0.29 (0.575) | 1.337 | 0.615 | −1.31 (0.486) | 0.27 | 0.024 | 0.123 (0.097) | 1.131 | 0.312 |
| Weekly legumes: 3–4 vs. 1–2 | −1.586 (0.524) | 0.205 | 0.009 | 0.199 (0.454) | 1.22 | 0.934 | 0.008 (0.099) | 1.008 | 0.934 |
| Weekly legumes: >4 vs. 1–2 | −2.396 (1.313) | 0.091 | 0.213 | −1.121 (1.043) | 0.326 | 0.428 | −0.065 (0.212) | 0.937 | 0.759 |
| Weekly legumes: every 10–15 days vs. 1–2 | −0.361 (0.492) | 0.697 | 0.465 | 0.614 (0.462) | 1.848 | 0.465 | 0.073 (0.097) | 1.076 | 0.465 |
| Weekly legumes: never vs. 1–2 | 0.759 (0.66) | 2.136 | 0.759 | −0.076 (0.545) | 0.927 | 0.936 | −0.009 (0.115) | 0.991 | 0.936 |
| Weekly cakes: 3–4 vs. 1–2 | 0.404 (0.756) | 1.498 | 0.647 | −0.451 (0.649) | 0.637 | 0.647 | −0.059 (0.127) | 0.943 | 0.647 |
| Weekly cakes: every day vs. 1–2 | 0.118 (0.532) | 1.125 | 0.825 | −0.256 (0.469) | 0.774 | 0.825 | 0.109 (0.093) | 1.115 | 0.726 |
| Weekly cakes: 2 per day vs. 1–2 | −0.684 (0.696) | 0.504 | 0.492 | −0.94 (0.649) | 0.391 | 0.453 | 0.062 (0.115) | 1.064 | 0.591 |
| Weekly cakes: every 10–12 days vs. 1–2 | −0.433 (0.653) | 0.649 | 0.764 | −0.127 (0.609) | 0.881 | 0.835 | −0.117 (0.127) | 0.89 | 0.764 |
| Weekly cakes: never vs. 1–2 | −0.913 (0.795) | 0.401 | 0.381 | 0.232 (0.744) | 1.262 | 0.755 | −0.224 (0.148) | 0.799 | 0.381 |
| Weekly French fries: 3–4 vs. 1–2 | −7.757 (1.829) | 0.0004 | <0.001 | −3.289 (1.814) | 0.037 | 0.108 | −0.271 (0.374) | 0.762 | 0.471 |
| Weekly French fries: every 10–15 days vs. 1–2 | −3.085 (0.682) | 0.046 | <0.001 | 1.34 (0.608) | 3.82 | 0.045 | 0.056 (0.132) | 1.058 | 0.672 |
| Weekly French fries: never vs. 1–2 | −0.673 (0.619) | 0.51 | 0.419 | 0.996 (0.544) | 2.708 | 0.21 | 0.041 (0.122) | 1.042 | 0.736 |
| Weekly fast food: every 10–15 days vs. 1–2 | −2.86 (1.705) | 0.057 | 0.288 | −0.272 (1.491) | 0.762 | 0.856 | 0.34 (0.309) | 1.404 | 0.411 |
| Weekly fast food: never vs. 1–2 | −1.546 (1.336) | 0.213 | 0.294 | 3.395 (1.23) | 29.8 | 0.021 | 0.269 (0.255) | 1.308 | 0.294 |
| Weekly pizzeria: every 10–15 days vs. 1–2 | −0.075 (0.526) | 0.928 | 0.887 | −0.129 (0.451) | 0.879 | 0.887 | −0.139 (0.091) | 0.87 | 0.396 |
| Weekly pizzeria: never vs. 1–2 | −0.288 (0.496) | 0.75 | 0.844 | 0.05 (0.437) | 1.051 | 0.909 | −0.247 (0.09) | 0.781 | 0.021 |
| Wine Yes vs. No | −0.297 (0.392) | 0.743 | 0.675 | −0.102 (0.343) | 0.903 | 0.766 | −0.061 (0.072) | 0.941 | 0.675 |
| Weekly wine: 3–4 vs. 1–2 | 1.368 (0.907) | 3.926 | 0.137 | −1.511 (0.781) | 0.221 | 0.129 | −0.362 (0.207) | 0.696 | 0.129 |
| weekly wine: every 10–15 days vs. 1–2 | 0.71 (0.773) | 2.035 | 0.543 | 1.106 (0.682) | 3.022 | 0.33 | −0.086 (0.15) | 0.918 | 0.57 |
| weekly wine: never vs. 1–2 | 0.83 (0.656) | 2.293 | 0.211 | 1.55 (0.601) | 4.711 | 0.036 | −0.259 (0.135) | 0.772 | 0.09 |
| Beer. Yes vs. No | 0.251 (0.429) | 1.286 | 0.779 | −1.165 (0.352) | 0.312 | 0.003 | −0.022 (0.078) | 0.978 | 0.779 |
| Weekly beer: 3–4 vs. 1–2 | 0.664 (1.996) | 1.942 | 0.742 | −2.33 (1.07) | 0.097 | 0.093 | −0.48 (0.246) | 0.619 | 0.093 |
| weekly beer: every 10–15 days vs. 1–2 | 0.716 (0.798) | 2046 | 0.376 | 2.108 (0.519) | 8.232 | <0.001 | −0.144 (0.131) | 0.866 | 0.376 |
| weekly beer: never vs. 1–2 | −3.584 (1.245) | 0.028 | 0.021 | −1.596 (0.8) | 0.203 | 0.081 | 0.006 (0.187) | 1.006 | 0.973 |
| Other aperitifs and | −0.358 (0.477) | 0.699 | 0.454 | −1.656 (0.395) | 0.191 | <0.001 | 0.107 (0.094) | 1.113 | 0.386 |
| alcoholic drinks. Yes vs. No | |||||||||
| Weekly other aperitifs and | 0.347 (1.759) | 1.415 | 0.845 | −2.221 (1.583) | 0.109 | 0.525 | −0.214 (0.296) | 0.808 | 0.726 |
| alcoholic drinks: 3–4 vs. 1–2 | |||||||||
| Weekly aperitifs and | −2.024 (0.795) | 0.132 | 0.057 | 0.769 (0.662) | 2.158 | 0.388 | −0.107 (0.148) | 0.898 | 0.482 |
| alcoholic drinks: every 10–15 days vs. 1–2 | |||||||||
| Weekly aperitifs and | −1.755 (1.759) | 0.173 | 0.495 | −2.093 (1.165) | 0.123 | 0.261 | 0.02 (0.224) | 1.02 | 0.931 |
| alcoholic drinks: never vs. 1–2 | |||||||||
| Spirits Yes vs. No | 0.491 (0.964) | 1.634 | 0.612 | 1.121 (0.806) | 3.067 | 0.25 | 0.303 (0.18) | 1.353 | 0.25 |
| 24h Dietary Recall | |||||||||
| Number of meals in the 24h recall | −0.069 (0.119) | 0.934 | 0.793 | 0.028 (0.107) | 1.028 | 0.793 | 0.013 (0.021) | 1.013 | 0.793 |
| Alcoholic beverages | 0.41 (0.297) | 1.507 | 0.507 | −0.26 (0.272) | 0.771 | 0.512 | −0.027 (0.057) | 0.973 | 0.63 |
| Non−alcoholic beverages | 0.032 (0.164) | 1.032 | 0.995 | 0.001 (0.149) | 1.001 | 0.995 | 0.041 (0.029) | 1.042 | 0.471 |
| Condiments and sauces | −0.175 (0.318) | 0.84 | 0.584 | 0.66 (0.281) | 1.934 | 0.063 | 0.052 (0.064) | 1.053 | 0.584 |
| Fats and oils | −0.072 (0.262) | 0.931 | 0.784 | −0.421 (0.226) | 0.657 | 0.195 | 0.052 (0.048) | 1.053 | 0.43 |
| Fruit | 0.238 (0.205) | 1.268 | 0.372 | 0.409 (0.176) | 1.505 | 0.066 | 0.026 (0.036) | 1.026 | 0.471 |
| Grain products | −0.038 (0.165) | 0.962 | 0.817 | 0.039 (0.147) | 1.04 | 0.817 | 0.007 (0.03) | 1.007 | 0.817 |
| Milk and dairy | 0.135 (0.239) | 1.144 | 0.861 | 0.028 (0.193) | 1.029 | 0.884 | 0.035 (0.042) | 1.036 | 0.861 |
| Mixed dishes | 0.526 (0.325) | 1.692 | 0.327 | 0.291 (0.274) | 1.338 | 0.436 | 0.014 (0.054) | 1.014 | 0.791 |
| Potatoes: Yes vs. No | 0.14 (0.868) | 1.15 | 0.872 | −0.314 (0.651) | 0.731 | 0.872 | −0.383 (0.136) | 0.682 | 0.018 |
| Protein food | 0.112 (0.251) | 1.119 | 0.808 | −0.222 (0.233) | 0.801 | 0.808 | 0.012 (0.048) | 1.012 | 0.808 |
| Snacks and sweets | 0.204 (0.225) | 1.226 | 0.366 | 0.265 (0.183) | 1.304 | 0.225 | 0.079 (0.041) | 1.082 | 0.171 |
| Sugars | 0.095 (0.192) | 1.1 | 0.709 | 0.297 (0.168) | 1.346 | 0.237 | 0.013 (0.035) | 1.013 | 0.709 |
| Vegetables | 0.003 (0.236) | 1.003 | 0.991 | −0.508 (0.195) | 0.602 | 0.03 | −0.001 (0.041) | 0.999 | 0.991 |
| Water | −0.263 (0.187) | 0.769 | 0.243 | −0.277 (0.157) | 0.758 | 0.243 | −0.03 (0.034) | 0.971 | 0.376 |
In the multivariable analysis (Table 4), age appeared to be associated with PVCs (p-value 0.005) and SVPCs appeared to be associated with age and sex (respectively, p-value < 0.001 and p-value 0.004).
Table 4.
Multivariable analysis for premature ventricular complexes, supraventricular premature complexes, and heart rate variability. Estimates are changes in PVCs for a unit increase of each of the predictors, Exp (Estimate) represents E[(Y+1); X]/ E [Y; X] indicating the relative variation in the expected number of arrhythmic events consequently to a unit increase of each considered X variable.
| Estimate | Exp (Estimate) | Standard Error | p-Value | |
|---|---|---|---|---|
| Heart Rate Variability | ||||
| Age | −0.0005 | 0.9994 | 0.002 | 0.827 |
| Sex: Female vs. Male | 0.022 | 1.023 | 0.082 | 0.780 |
| Sleep hours | 0.058 | 1.059 | 0.027 | 0.034 |
| BMI | −0.017 | 0.983 | 0.009 | 0.083 |
| Fruit (24 h recall) | 0.087 | 1.091 | 0.042 | 0.044 |
| Premature Ventricular Complexes | ||||
| Age | 0.06 | 1.062 | 0.011 | 0.005 |
| Sex: Female vs. Male | −1.489 | 0.226 | 0.743 | 0.055 |
| Fruit (24 h recall) | −0.893 | 0.409 | 0.375 | 0.024 |
| Grain-based products (24 h recall) | 1.24677 | 3.479 | 0.352 | 0.001 |
| Snacks and sweets | 0.68307 | 1.979 | 0.352 | 0.063 |
| Sugars | 0.86821 | 2.383 | 0.327 | 0.013 |
| Mass of body fat | 0.232 | 1.26 | 0.052 | <0.001 |
| Supraventricular Premature Complexes | ||||
| Age | 0.049 | 1.050 | 1.039 | <0.001 |
| Sex: Female vs. Male | −0.909 | 0.403 | 0.308 | 0.004 |
| Sleep hours | −0.299 | 0.741 | 0.108 | 0.006 |
| Cardiovascular comorbidities: Yes vs. No | 1.893 | 6.638 | 0.332 | <0.001 |
| Condiments and sauces | 0.661 | 1.937 | 0.254 | 0.01 |
| Protein food | −0.764 | 0.466 | 0.215 | <0.001 |
Univariable and multivariable analyses for PVCs, SVPCs, and HRV are reported in Table 3 and Table 4, respectively.
3.2. Anthropometrics
No statistical differences in presence/absence of PVCs and SVPCs were found for anthropometrics (Table 1 and Table S1, respectively).
Regarding results of univariable analyses (Table 3), HRV was found to be in a direct (but nonsignificant, p-value 0.076) association with LBM. Conversely, it was found to be in an inverse association with MBF (p-value 0.015). Both LBM and MBF appeared to not affect SVPCs, while MBF appeared to be directly associated with PVCs (p-value 0.015). No statistical significance of BMI on outcomes was observed, whereas waist circumference was found to be directly associated with higher likelihood of both PVCs and SVPCs (p-value 0.024 and <0.001, respectively). In the multivariable analysis (Table 4), higher BMI was associated with lower HRV (although not significantly, p-value 0.083).
3.3. Dietary Pattern
No statistical differences in presence/absence of PVCs and SVPCs were found for dietary pattern (Table 1 and Table S1, respectively). Regarding 24 h dietary recall, no significant effects of single variables were observed, with only a few exceptions (e.g., consumption of condiments and sauces during the 24 h of Holter monitoring appeared to result in a higher risk of SVPCs; p-value 0.063, barely significant). Similar results were obtained from the analysis of the frequency of food consumption (assessed through the Turconi FFQ) (Table 3).
Upon multivariable analysis (Table 4), fruit consumption during the 24 h dietary recall was found to be directly associated with HRV (p-value 0.044). Regarding PVCs, results showed that it was significantly directly associated with higher intake of grain-based products (p-value 0.001) and consumption of snacks and sugars (p-value 0.063 and 0.013, respectively), whereas fruit intake was found to be significantly and inversely associated with PVCs (p-value 0.024). Consumption of condiments and sauces raised the likelihood of SVPCs (p-value 0.01), while protein food consumption was significantly and inversely proportional to SVPCs (p-value < 0.001).
4. Discussion
Results of our exploratory observational study suggest that lifestyle, eating habits, and body adiposity are significantly associated with cardiac ectopic beats and HRV.
Consistently with previous findings [26], the results of our study pointed out the close relationship between body composition and the outcomes of interest. The univariable analysis showed that waist circumference was significantly associated with both PVCs and SVPCs, in accordance with the growing body of literature which supports the relevant role played by the waist and hip circumference in cardiac risk predictive models [27]. Conversely to what is documented in the literature [28], our study showed no significant results regarding the effect of BMI on cardiac ectopic beats. In contrast from BMI, MBF resulted to be significantly directly associated to PVCs. This is consistent with evidence reported in the literature; a recent review documented the role of adipose tissue on cardiac arrhythmias, and in particular on ventricular rhythm disorders [29].
Regarding food intake, we found out that higher fruit consumption had a significant impact on the improvement of HRV and in reduced occurrence of PVCs. Despite the limited availability of evidence regarding potential associations between fruit intake and HRV and ectopic beats, the beneficial role of fruit in improving cardiac autonomic function has been documented [30].
Upon multivariable analysis, age was found to be associated with SVPCs and PVCs, but not with HRV; this finding is only partially consistent with literature in the field [31]. Regarding dietary patterns, our study showed a significant association between higher intake of snacks and sweets, sugars, and grain products with PVCs. To our knowledge, this is the first study in which the consumption of such food products has been investigated regarding its linkage to cardiac ectopic beats and HRV. Despite the lack of evidence regarding cardiac rhythm, studies have reported the potential risk of refined carbohydrates and simple sugars in facilitating weight gain [32], thus increasing cardiovascular risk. To reduce such risk, evidence suggests limiting the consumption of refined grains and to prefer low energy carbohydrates, such as whole grain cereals, fruit, vegetables, and legumes.
Regarding the consumption of protein, the present study suggested that protein intake was inversely associated with SVPCs. However, no specifications were made as to protein type (animal vs. plant). In the literature, limited evidence is available regarding the association between protein food and cardiac electrical activity, since previous studies have concentrated mainly on fish intake and cardiac rhythm, not on another type of protein food. Results of such studies suggested a beneficial role of omega-3 PUFA in fish against cardiac arrhythmias [33].
Together with dietary intake, lifestyle habits also appeared to be significantly associated with outcomes of interest. Consistently with recent publications, our study showed that physical activity was significantly associated with higher HRV (by reducing sympathetic activation [15]). Sleep hours also resulted in a significant relationship with HRV and SVPCs; sleep hours had a direct relationship with HRV and an inverse relationship with SVPCs. The effect on HRV is physiological, since it is well known that longer sleep time results in higher HRV, while poor sleeping or sleep deprivation can adversely affect HRV [34]. Conversely, no significant effects of sleep hours on PVCs were observed, whereas recent research has pointed out higher PVCs as a consequence of sleep disruption in hospitalized patients [35].
Some differences between this study and previous findings may be due to different data collection methods, especially regarding the 24 h recall. Generally, previous studies employed only FFQ to estimate the effect of food consumption on cardiac rhythm.
Despite the fact that this was an exploratory study and significant results should be researched further by independent labs in a more targeted research design, these findings provide new insights to improve the management of patients attending cardiac rhythm labs.
Holter monitoring is a clinical investigation that helps medical doctors to assess cardiac function, especially if a standard electrocardiogram does not give enough information about heart electrical activity. This instrumental examination generally falls under a set of clinical tests intended to be used for differential diagnosis. As a result, data from the Holter monitor are often underused, especially in the research context. Conversely, the findings of the present study provide new insights into the usefulness of such clinical examination. If lifestyle and dietary patterns influence the onset (and/or the severity) of cardiac rhythm disorders, clearly, Holter monitor parameters may support clinicians in the development of ad hoc strategies (modification of lifestyle and eating habits) based on Holter parameters to improve cardiac electrical function, reducing the risk of more severe, life-threating, cardiac arrhythmias.
5. Conclusions
Results of our study suggested that lifestyle, eating habits, and anthropometrics were significantly associated with cardiac ectopic beats and HRV.
To our knowledge, this is the first study to point out the association of such heterogeneous factors, from food intake to lifestyle habits and anthropometrics, on cardiac rhythm outcomes, providing new insight to the topic. Given the clinical relevance of HRV, SVPCs, and PVCs on morbidity and mortality, it may be useful to implement research in this field to improve clinical management (including both drugs and lifestyles prescriptions) of patients with such cardiac rhythm disorders, that, even small, may be relevant prognostic factors for more severe cardiac arrhythmias, especially in subjects with underlying cardiovascular diseases.
Supplementary Materials
The following are available online at https://www.mdpi.com/2077-0383/9/4/1121/s1, Figure S1: Distribution of Premature Ventricular Complexes, Figure S2: Distribution of Supraventricular Premature Complexes, Figure S3: Distribution of Heart Rate Variability, Table S1: Descriptive characteristic of subjects according with presence/absence of SVPCs.
Author Contributions
Conceptualization, S.I. and D.G.; Formal analysis, D.A.; Investigation, E.R. and C.B.; Methodology, F.F., R.V. and G.L.; Writing—Original draft, G.L.; Writing—review & editing, C.E.G., E.C. and L.V. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Conflicts of Interest
The authors declare no conflict of interest.
References
- 1.Balakumar P., Maung-U K., Jagadeesh G. Prevalence and prevention of cardiovascular disease and diabetes mellitus. Pharmacol. Res. 2016;113:600–609. doi: 10.1016/j.phrs.2016.09.040. [DOI] [PubMed] [Google Scholar]
- 2.Payne R.A. Cardiovascular risk. Br. J. Clin. Pharmacol. 2012;74:396–410. doi: 10.1111/j.1365-2125.2012.04219.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Pais P., Kamath D.Y., Sigamani A., Xavier D. Pathophysiology and Pharmacotherapy of Cardiovascular Disease. Springer; Berlin, Germany: 2015. Prevention of Cardiovascular Disease: The Polypill Concept; pp. 613–632. [Google Scholar]
- 4.Maheshwari A., Norby F.L., Soliman E.Z., Adabag S., Whitsel E.A., Alonso A., Chen L.Y. Low heart rate variability in a 2-minute electrocardiogram recording is associated with an increased risk of sudden cardiac death in the general population: The atherosclerosis risk in communities study. PLoS ONE. 2016;11:e0161648. doi: 10.1371/journal.pone.0161648. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Huikuri H.V., Stein P.K. Heart rate variability in risk stratification of cardiac patients. Prog. Cardiovasc. Dis. 2013;56:153–159. doi: 10.1016/j.pcad.2013.07.003. [DOI] [PubMed] [Google Scholar]
- 6.Sacha J. Interaction between heart rate and heart rate variability. Ann. Noninvasive Electrocardiol. 2014;19:207–216. doi: 10.1111/anec.12148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Jain A., Aggarwal K., Zhang P. Omega-3 fatty acids and cardiovascular disease. Eur. Rev. Med. Pharm. Sci. 2015;19:441–445. [PubMed] [Google Scholar]
- 8.Singer P., Wirth M. Can n-3 PUFA reduce cardiac arrhythmias? Results of a clinical trial. ProstaglandinsLeukot. Essent. Fat. Acids. 2004;71:153–159. doi: 10.1016/j.plefa.2004.03.003. [DOI] [PubMed] [Google Scholar]
- 9.Gogolashvili N., Litvinenko M., Pochikaeva T., Vavitova E., Polikarpov L., Novgorodtseva N. Possibilities of a preparation omega-3 polyunsaturated fatty acids in the treatment of patients with ventricular arrhythmias and myocardial infarction. Kardiologiia. 2010;51:28–31. [PubMed] [Google Scholar]
- 10.Christensen J.H. Omega-3 polyunsaturated fatty acids and heart rate variability. Front. Physiol. 2011;2:84. doi: 10.3389/fphys.2011.00084. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Christensen J.H. n-3 fatty acids and the risk of sudden cardiac death. Emphasis on heart rate variability. Dan. Med. Bull. 2003;50:347–367. [PubMed] [Google Scholar]
- 12.Karpyak V.M., Romanowicz M., Schmidt J.E., Lewis K.A., Bostwick J.M. Characteristics of Heart Rate Variability in Alcohol-Dependent Subjects and Nondependent Chronic Alcohol Users. Alcohol. Clin. Exp. Res. 2014;38:9–26. doi: 10.1111/acer.12270. [DOI] [PubMed] [Google Scholar]
- 13.Voskoboinik A., Prabhu S., Ling L.-H., Kalman J.M., Kistler P.M. Alcohol and Atrial Fibrillation: A Sobering Review. J. Am. Coll. Cardiol. 2016;68:2567–2576. doi: 10.1016/j.jacc.2016.08.074. [DOI] [PubMed] [Google Scholar]
- 14.Nakajima K., Suwa K., Oda E. Atrial fibrillation may be prevalent in individuals who report late-night dinner eating and concomitant breakfast skipping, a complex abnormal eating behavior around sleep. Int. J. Cardiol. 2014;177:1124–1126. doi: 10.1016/j.ijcard.2014.08.058. [DOI] [PubMed] [Google Scholar]
- 15.Fatisson J., Oswald V., Lalonde F. Influence diagram of physiological and environmental factors affecting heart rate variability: An extended literature overview. Heart Int. 2016;11:e32. doi: 10.5301/heartint.5000232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Plourde B., Sarrazin J.-F., Nault I., Poirier P. Sudden cardiac death and obesity. Expert Rev. Cardiovasc. Ther. 2014;12:1099–1110. doi: 10.1586/14779072.2014.952283. [DOI] [PubMed] [Google Scholar]
- 17.Yadav R.L., Yadav P.K., Yadav L.K., Agrawal K., Sah S.K., Islam M.N. Association between obesity and heart rate variability indices: An intuition toward cardiac autonomic alteration–a risk of CVD. DiabetesMetab. Syndr. Obes. Targets Ther. 2017;10:57. doi: 10.2147/DMSO.S123935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Balestroni G., Bertolotti G. EuroQol-5D (EQ-5D): An instrument for measuring quality of life. Monaldi Arch. Chest Dis. 2015;78:155–159. doi: 10.4081/monaldi.2012.121. [DOI] [PubMed] [Google Scholar]
- 19.Turconi G., Bazzano R., Roggi C., Cena H. Reliability and relative validity of a quantitative food-frequency questionnaire for use among adults in Italian population. Int. J. Food Sci. Nutr. 2010;61:846–862. doi: 10.3109/09637486.2010.495329. [DOI] [PubMed] [Google Scholar]
- 20.U.S. Department of Agriculture, Agricultural Research Service What We Eat in America Food Categories 2013–2014. [(accessed on 28 December 2016)];2016 Available online: www.ars.usda.gov/nea/bhnrc/fsrg.
- 21.Akhandaf Y., Van Klaveren J., De Henauw S., Van Donkersgoed G., Van Gorcum T., Papadopoulos A., Sirot V., Kennedy M., Pinchen H., Ruprich J. Exposure assessment within a Total Diet Study: A comparison of the use of the pan-European classification system FoodEx-1 with national food classification systems. Food Chem. Toxicol. 2015;78:221–229. doi: 10.1016/j.fct.2015.01.019. [DOI] [PubMed] [Google Scholar]
- 22.Rigby R.A., Stasinopoulos D.M. Generalized additive models for location, scale and shape. J. R. Stat. Soc. Ser. C (Appl. Stat. ) 2005;54:507–554. doi: 10.1111/j.1467-9876.2005.00510.x. [DOI] [Google Scholar]
- 23.Stasinopoulos D.M., Rigby R.A. Generalized additive models for location scale and shape (GAMLSS) in R. J. Stat. Softw. 2007;23:1–46. doi: 10.18637/jss.v023.i07. [DOI] [Google Scholar]
- 24.Agogo G.O. A zero-augmented generalized gamma regression calibration to adjust for covariate measurement error: A case of an episodically consumed dietary intake. Biom. J. 2017;59:94–109. doi: 10.1002/bimj.201600043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Team R. R development core team. Ra Lang. Env. Stat. Comput. 2013;55:275–286. [Google Scholar]
- 26.Chow G.V., Marine J.E., Fleg J.L. Epidemiology of arrhythmias and conduction disorders in older adults. Clin. Geriatr. Med. 2012;28:539–553. doi: 10.1016/j.cger.2012.07.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Cameron A., Magliano D., Söderberg S. A systematic review of the impact of including both waist and hip circumference in risk models for cardiovascular diseases, diabetes and mortality. Obes. Rev. 2013;14:86–94. doi: 10.1111/j.1467-789X.2012.01051.x. [DOI] [PubMed] [Google Scholar]
- 28.Pathak R.K., Mahajan R., Lau D.H., Sanders P. The implications of obesity for cardiac arrhythmia mechanisms and management. Can. J. Cardiol. 2015;31:203–210. doi: 10.1016/j.cjca.2014.10.027. [DOI] [PubMed] [Google Scholar]
- 29.Samanta R., Pouliopoulos J., Thiagalingam A., Kovoor P. Role of adipose tissue in the pathogenesis of cardiac arrhythmias. Heart Rhythm. 2016;13:311–320. doi: 10.1016/j.hrthm.2015.08.016. [DOI] [PubMed] [Google Scholar]
- 30.Park S.K., Tucker K.L., O'neill M.S., Sparrow D., Vokonas P.S., Hu H., Schwartz J. Fruit, vegetable, and fish consumption and heart rate variability: The Veterans Administration Normative Aging Study. Am. J. Clin. Nutr. 2009;89:778–786. doi: 10.3945/ajcn.2008.26849. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Silvetti M.S., Drago F., Ragonese P. Heart rate variability in healthy children and adolescents is partially related to age and gender. Int. J. Cardiol. 2001;81:169–174. doi: 10.1016/S0167-5273(01)00537-X. [DOI] [PubMed] [Google Scholar]
- 32.Van Dam R., Seidell J. Carbohydrate intake and obesity. Eur. J. Clin. Nutr. 2007;61:S75–S99. doi: 10.1038/sj.ejcn.1602939. [DOI] [PubMed] [Google Scholar]
- 33.Reiffel J.A., McDonald A. Antiarrhythmic effects of omega-3 fatty acids. Am. J. Cardiol. 2006;98:50–60. doi: 10.1016/j.amjcard.2005.12.027. [DOI] [PubMed] [Google Scholar]
- 34.Stein P.K., Pu Y. Heart rate variability, sleep and sleep disorders. Sleep Med. Rev. 2012;16:47–66. doi: 10.1016/j.smrv.2011.02.005. [DOI] [PubMed] [Google Scholar]
- 35.Miner S.E.S., Pahal D., Nichols L., Darwood A., Nield L.E., Wulffhart Z. Sleep Disruption is Associated with Increased Ventricular Ectopy and Cardiac Arrest in Hospitalized Adults. Sleep. 2016;39:927. doi: 10.5665/sleep.5656. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
