Abstract
The results of previous studies on the relation between alcohol consumption and heart failure (HF) have been inconsistent. This study aimed to evaluate the association between alcohol consumption and left ventricular ejection fraction (LVEF) in a general population.
A total of 10,824 adults were examined using a multistage cluster sampling method to select a representative sample of individuals who were at least 35-years old. The participants were asked to provide information about their alcohol consumption. Echocardiograms were obtained, and LVEF was calculated using modified Simpson's rule.
Of the 10,824 participants included in the present study, 46.1% were males, and the mean participant age was 54 years; age ranged from 35 to 93 years. The overall prevalence of LVEF< 0.50 and LVEF < 0.40 in the studied population was 11.6% and 2.9%, respectively. The prevalence of LVEF < 0.5 and LVEF < 0.04 was higher in both the moderate and heavy drinker groups than in the nondrinker group (P <0.05). Multivariate logistic regression analyses corrected according to the different levels of alcohol consumption showed that moderate and heavy drinkers had an –1.3-fold and 1.2-fold higher risk of LVEF <0.5, respectively, than nondrinkers (OR: 1.381, 95% CI: 1.115–1.711, P = 0.003 for moderate drinkers; OR: 1.246, 95% CI: 1.064–1.460, P = 0.006 for heavy drinkers). Heavy drinkers had an ∼1.5-fold higher risk of decreased LVEF < 0.4 than nondrinkers (OR: 1.482, 95% CI: 1.117–1.965, P = 0.006). Moderate drinkers did not show a risk of decreased LVEF < 0.4 that was significantly higher than that of nondrinkers (OR: 1.183, 95% CI: 0.774–1.808, P = 0.437).
According to these results, we concluded that increased alcohol consumption was associated with decreased LVEF compared with no alcohol consumption in this general population.
INTRODUCTION
The effect of alcohol on the heart is a controversial issue. Some studies have reported that alcohol intake can reduce the risk of coronary heart disease,1,2 whereas other studies have reported that alcohol use is associated with increased cardiac morbidity and mortality.3–5 The results of previous studies on alcohol consumption and heart failure (HF) have also been inconsistent. The Framingham Heart Study reported that alcohol consumption is not associated with an increased risk of congestive HF, even among heavy drinkers (>15 drinks/week in men and >8 drinks/week in women).6 The Olmsted County Heart Function Study concluded that in a community setting, light alcohol consumption (<1 drink a day) was associated with a reduced prevalence of moderate systolic dysfunction.7 The British Regional Heart Study concluded that there was no evidence that light to moderate drinking is beneficial for the prevention of HF in older men without a history of MI. However, heavier drinking (≥5 drinks/day) was associated with an increased risk of HF in susceptible men with underlying myocardial ischemia.8
The latest study indicates that HF has been an important cause of cardiac mortality globally, with increasing prevalence and incidence.9–11 Although left ventricular (LV) performance can be evaluated by multiple parameters, including LV dimensions, the LV mass index, regional wall motion abnormalities, diastolic dysfunction, and left ventricular ejection fraction (LVEF) are the most representative measures of LV systolic function.12,13 However, few studies have focused on the association between alcohol consumption and HF among the general population; clarifying this relationship will be useful for the management of individuals with HF from a clinical perspective. Thus, we performed this study based on a general population from rural China with the aim of examining the association between alcohol consumption and depressed LVEF.
Methods
Study Population
This study adopted a multistage, stratified, random cluster sampling scheme. From January 2012 to August 2013, a representative sample of individuals who were at 35 years or older was selected in order to examine the prevalence, incidence, and natural history of cardiovascular risk factors in Liaoning Province. This research was approved by the Ethics Committee of China Medical University (Shenyang, China). Procedures were performed in accordance with ethical standards. The detailed methods have been previously published.41,44,45 We used baseline data in this report, and only participants who had complete data sets for the variables analyzed were included, yielding a final sample size of 10,824 individuals (4989 males and 5835 females).
Data Collection and Definitions
Via an interview with a standardized questionnaire, the data were obtained on demographics, lifestyle, dietary habits, income, history of heart disease, and medication used over the past 2 weeks .Blood samples were obtained from all the subjects in the morning after at least 12 hours of fasting. Serum potassium and magnesium, as well as other routine blood biochemical indexes, were analyzed using an autoanalyzer (Olympus AU 640; Olympus Corp., Kobe, Japan). The detailed process have been presented elsewhere.14,46,47
Hypertension was defined as SBP ≥140 mm Hg, DBP ≥90 mm Hg and/or use of antihypertensive medications according to the JNC-7 report.15 And according to the World Health Organization (WHO) criteria, body mass index (BMI) values were categorized into different groups16: normal, overweight, and obese (for normal, BMI <25 kg/m2; for overweight, 25≤ BMI <30 kg/m2; and for obese, BMI ≥30 kg/m2). Participants with waist circumference (WC) ≥88 cm for females and WC ≥102 cm for males were defined as abdominal obesity.17 Dyslipidemia was determined by the National Cholesterol Education Program-Third Adult Treatment Panel (ATP III) criteria.18 FPG ≥7 mmol/L (126 mg/dL) and/or receiving treatment for diabetes was diagnosed as diabetes mellitus according to the following WHO criteria.19 Using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation, the glomerular filtration rate (GFR) was estimated.20,47 Reduced GFR was defined as an estimated GFR (eGFR) <60 mL/min/1.73 m2. In accordance with WHO criteria, anemia was defined as serum hemoglobin levels <12.0 g/dL (<120 g/L) for women and <13.0 g/dL (<130 g/L) for men21 Uric acid levels >422 μmol/L for men and >363 μmol/L for women was defined as hyperuricemia.22
Echocardiography Measurements
The transthoracic echocardiogram included M-mode, 2-dimensional, and color Doppler. Detailed measurements used in this study have been previously published.41,48 According to the guideline of American Society of Echocardiography,39 left ventricular internal dimensions (LVIDs), posterior wall thickness (PWT),as well as interventricular septal thickness (IVST) were obtained.40 Left ventricular volumes were obtained from the apical 4-chamber view and the left ventricular ejection fraction (LVEF) was computed using the modified Simpson's rule.23,24 We used thresholds of LVEF < 0.5 and LVEF < 0.4 to indicate decreased LVEF.25,26
Alcohol Consumption Assessment
Alcohol consumption was assessed during the interview using the questionnaire. The participants were asked to provide information regarding whether they regularly consumed alcohol, the average amount of alcohol they consumed per day, and the number of days per month that they consumed alcohol. The amount of pure alcohol consumed was calculated based on the reported frequency and amount of drinking. In China, the ethanol weight content differed among the beverages as follows: 5% in beer, 12.5% in red wine, and 45% in hard liquor. One drink was defined as an average of 15 g of ethanol.37 We used thresholds based on the definition of daily alcohol consumption from the National Institute on Alcohol Abuse and Alcoholism to categorize the participants based on their level of consumption as follows: nondrinkers (i.e., abstainers, or no alcohol consumption history), moderate drinkers (i.e., up to 1 drink/day for women and up to 2 drinks/day for men), and heavy drinkers (i.e., >1 drink/day for women and >2 drinks/day for men).38
Statistical Analysis
Descriptive statistics were calculated for all the variables; continuous variables are reported as the mean values and standard deviations, and categorical variables are reported as counts and percentages. Differences among the categories were evaluated using nonparametric tests or the χ2 test, as appropriate. Multivariate logistic regression analyses were used to identify correlates of decreased LVEF; the association strengths are expressed as odds ratios (ORs) and corresponding 95% confidence intervals (CIs). All the statistical analyses were performed using SPSS version 22.0 and P values <0.05 were considered statistically significant.
RESULTS
Basic Characteristics of the Study Population
Of the 10,824 participants included in the present study, 46.1% were males; the mean age was 54 years and ranged from 35 to 93 years. Of all the participants, 810 (7.5%) and 1820 (7.5%) were moderate and heavy drinkers, respectively. On average, the LVEF calculated using the modified Simpson's rule was 0.62 ± 0.10 among the included population. The overall prevalence of LVEF< 0.50 and LVEF < 0.40 in the included population was 11.6% and 2.9%, respectively. Table 1 shows the clinical characteristics and demographics of the study population according to the alcohol consumption level. The mean age of participants in the nondrinker, moderate, and heavy drinker groups was 53.75 ± 10.56, 54.20 ± 10.79, and 53.74 ± 10.30 years, respectively. No significant differences were found among the 3 groups in the demographic or and laboratory variables included in the table, except in FPG. The prevalence of comorbidities, history of stroke, history of heart disease, and diabetes was significant different among the 3 groups (all P < 0.001).
TABLE 1.
Baseline Characteristics of the Study Population According to Alcohol Consumption Groups (n = 10,824)

Mean Level of LVEF and Prevalence of Decreased LVEF With Different Levels of Alcohol Consumption
As shown in Table 2, the echocardiogram results for the left ventricle in different alcohol consumption groups showed that there were no significant differences in the left ventricular internal diastolic dimensions, interventricular septal thickness, posterior wall thickness, left ventricular internal systolic dimensions, left ventricular end-diastolic volume, and left ventricular end-systolic volume among the 3 alcohol consumption groups. However, there were significant differences in the stroke volume and the minor fraction of the left ventricle among the 3 groups. The mean level of LVEF of the nondrinker, moderate, and heavy drinker groups was 0.62 ± 0.10, 0.61 ± 0.10, and 0.62 ± 0.11,respectively. Compared with the nondrinker group, the mean LVEF was lower in both the moderate and heavy drinker groups (P = 0.007). We used thresholds of LVEF < 0.50 and <0.40 to indicate decreased LVEF. The prevalences of LVEF <0.50 among the nondrinker, moderate, and heavy drinker groups were 10.9%, 14.6%, and 13.1%, respectively (Figure 1). The prevalences of LVEF <0.50 were higher in both the moderate and heavy drinker groups than in the nondrinker group (P = 0.001), and the prevalences of LVEF <0.40 among the nondrinker, moderate, and heavy drinker groups were 2.7%, 3.2%, and 3.8%, respectively (Figure 2). The prevalence of LVEF <0.40 was higher in both the moderate and heavy drinker groups than in the nondrinker group (P = 0.021).
TABLE 2.
Left Ventricle Echocardiogram Results in Different Alcohol Consumption Groups

FIGURE 1.

Prevalence of LVEF < 0.50 in the different alcohol consumption groups. LVEF = left ventricular ejection fraction.
FIGURE 2.

Prevalence of LVEF < 0.40 in the different alcohol consumption groups. LVEF = left ventricular ejection fraction.
Association Between Alcohol Consumption and LVEF
Table 3 presents multivariate logistic regression analyses of the risk of decreased LVEF corrected according to the different levels of alcohol consumption. The analyses fully adjusted for the following factors: gender, age, height, abdominal obesity, race, education, diabetes, income, current smoking, activity level, decreased GFR, history of stroke, anemia, hyperuricemia, dyslipidemia, heart rate, history of heart disease, intake of medication over the past 2 weeks, diet score, and general obesity. After these adjustments, the data showed that the moderate and heavy drinkers had an ∼1.3-fold and 1.2-fold higher risk of LVEF <0.5, respectively, than nondrinkers (OR: 1.381, 95% CI: 1.115–1.711, P = 0.003 for moderate drinkers; OR: 1.246, 95% CI: 1.064–1.460, P = 0.006 for heavy drinkers), and heavy drinkers had an ∼1.5-fold higher risk of decreased LVEF <0.4 than nondrinkers (OR: 1.482, 95% CI: 1.117–1.965, P = 0.006). Moderate drinkers did not show a significantly higher risk of decreased LVEF <0.4 compared with nondrinkers (OR: 1.183, 95% CI: 0.774–1.808, P = 0.437).
TABLE 3.
Multivariate Logistic Regression Analyses for the Association Between Increased Alcohol Consumption and Decreased Left Ventricular Ejection Fraction

DISCUSSION
In the present study, we first evaluated the association between alcohol consumption and LVEF in a large Chinese population. We found that both moderate and heavy drinkers were at greater risk for LVEF than were nondrinkers. This is the first study to focus specifically on the relationship between alcohol consumption and LVEF in a general population in China.
Few studies have focused on the association between alcohol consumption and left ventricular ejection fraction in the general population. In a community-based, elderly population (76 ± 5 years and 60% women), higher alcohol intake was shown to be associated with lower left ventricular ejection fraction.27 In a population-based random sample of 2,042 adults (aged ≥45 years), a U-shaped relationship between alcohol consumption volume and LVEF was reported, and the lowest risk of moderate LV dysfunction (LVEF ≤ 40%) was observed in light drinkers (< 1 drink a day); however, no significant association was found between alcohol consumption and LV dysfunction (LVEF ≤5 0%).28 In the present study, both moderate and heavy alcohol consumption were associated with LVEF < 0.5. Heavy alcohol consumption was associated with both LVEF < 0.5 and LVEF < 0.4. The differences in the conclusions drawn among these studies may be due to differences in population characteristics. The present study is the first to utilize data from a rural population in China.
Based on these results, the idea that moderate alcohol consumption (≤1 drink a day for women and elderly and 1–2 drinks a day for men) is reasonable should be reconsidered.29 Moreover, LVEF is an important indicator of left ventricular systolic cardiac dysfunction.30 Our results suggest that individuals with HF should not consume moderate or excessive amounts of alcohol. However, long-term follow-up studies are needed to support this conclusion.
The mechanism of action of alcohol on the heart involves both ethanol and its metabolites, which induce reactive oxygen species generation, lipid peroxidation, inflammatory cytokine expression, organelle damage, and stress, as well as activate both the apoptotic and necrotic cell death pathways.31–33 For population-based studies, genetic and environmental factors should be considered. Studies have shown that the common homozygote of CHRM2 rs1824024 is significantly associated with alcohol dependence severity.34–36 Moreover, the echocardiogram results indicated that further studies on the relation between alcohol use and contractility of the myocardium should also be conducted.
Our study had some limitations. We analyzed the average daily alcohol consumption, but cumulative alcohol consumption was not analyzed in this study. This information will be included in the follow-up study, and the effect of cumulative alcohol consumption on LVEF could be different from the observations of this study. In addition, we did not statistically analyze whether the type of alcoholic drink consumed influenced LVEF. Several previous studies have suggested that wine intake had a relatively lower effect on cardiovascular disease.42,43 However, as shown in the supplementary table, nearly no wine consumption occurred within the studied population. This difference may be due to local customs and does not affect our results. In addition, our results were obtained using a cross-sectional design; thus, no cause-and-effect relationships could be established.
In conclusion, based on this general population from China, we found that increased alcohol consumption was associated with decreased LVEF compared with that of nondrinking individuals, and we recommend that the general population should consider refraining from drinking alcohol.
Footnotes
Abbreviations: BMI = body mass index, CVD = cardiovascular disease, DBP = diastolic blood pressure, FPG = fasting plasma glucose, GFR = glomerular filtration rate, HDL-C = high-density lipoprotein cholesterol, HF = heart failure, LDL-C = low-density lipoprotein cholesterol, LVEF = left ventricular ejection fraction, SBP = systolic blood pressure, TC = total cholesterol, TG = triglyceride, WC = waist circumference.
Funding: this study was supported by grants from the “Twelfth Five-Year” project funds (National Science and Technology Support Program of China, Grant No. 2012BAJ18B02) and the Natural Science Foundation of China (Grant No. 81373018).
The authors have no conflicts of interest to disclose.
REFERENCES
- 1.Jelinek MV, Santamaria JD, Best JD, et al. Reversing social disadvantage in secondary prevention of coronary heart disease. Int J Cardiol 2014; 171:346–350. [DOI] [PubMed] [Google Scholar]
- 2.Lima MC, Kerr-Côrrea F, Rehm J. Alcohol consumption pattern and coronary heart disease risk in metropolitan São Paulo: analyses of GENACIS Project. Rev Bras Epidemiol 2013; 16:49–57. [PubMed] [Google Scholar]
- 3.Almeida OP, McCaul K, Hankey GJ, et al. Excessive alcohol consumption increases mortality in later life: a genetic analysis of the health in men cohort study. Addict Biol 2015; 1–11. [DOI] [PubMed] [Google Scholar]
- 4.Bobak M, Malyutina S, Horvat P, et al. Alcohol, drinking pattern and all-cause, cardiovascular and alcohol-related mortality in Eastern Europe. Eur J Epidemiol 2015; 31:21–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Schuckit MA. Alcohol-use disorders. Lancet 2009; 373:492–501. [DOI] [PubMed] [Google Scholar]
- 6.Walsh CR, Larson MG, Evans JC, et al. Alcohol consumption and risk for congestive heart failure in the Framingham Heart Study. Ann Intern Med 2002; 136:181–191. [DOI] [PubMed] [Google Scholar]
- 7.Aguilar D, Skali H, Moyé LA, et al. Alcohol consumption and prognosis in patients with left ventricular systolic dysfunction after a myocardial infarction. J Am Coll Cardiol 2004; 43:2015–2021. [DOI] [PubMed] [Google Scholar]
- 8.Wannamethee SG, Whincup PH, Lennon L, et al. Alcohol consumption and risk of incident heart failure in older men: a prospective cohort study. Open Heart 2015; 2:e000266. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Farmakis D, Stafylas P, Giamouzis G, et al. The medical and socioeconomic burden of heart failure: a comparative delineation with cancer. Int J Cardiol 2015; 203:279–281. [DOI] [PubMed] [Google Scholar]
- 10.Böhm M, Tschöpe C, Wirtz JH, et al. Treatment of heart failure in real-world clinical practice: findings from the REFLECT-HF registry in patients with NYHA class II symptoms and a reduced ejection fraction. Clin Cardiol 2015; 38:200–207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Maison P, Desamericq G, Hemery F, et al. Relationship between recommended chronic heart failure treatments and mortality over 8 years in real-world conditions: a pharmacoepidemiological study. Eur J Clin Pharmacol 2013; 69:901–908. [DOI] [PubMed] [Google Scholar]
- 12.Sengupta PP, Korinek J, Belohlavek M, et al. Left ventricular structure and function: basic science for cardiac imaging. J Am Coll Cardiol 2006; 48:1988–2001. [DOI] [PubMed] [Google Scholar]
- 13.Vasan RS, Benjamin EJ, Larson MG, et al. Plasma natriuretic peptides for community screening for left ventricular hypertrophy and systolic dysfunction: the Framingham heart study. JAMA 2002; 288:1252–1259. [DOI] [PubMed] [Google Scholar]
- 14.Sun Z, Zheng L, Zhang X, et al. Ethnic differences in the incidence of hypertension among rural Chinese adults: results from Liaoning province. PloS One 2014; 9:e86867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Chobanian AV, Bakris GL, Black HR, et al. The Seventh Report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure: the JNC 7 report. JAMA 2003; 289:2560–2572. [DOI] [PubMed] [Google Scholar]
- 16.World Health Organization. Hypertension control: report of a WHO Expert Committee. World Health Organization technical report series. 1996;862:1–883. [PubMed]
- 17.Nishida C, Uauy R, Kumanyika S, et al. The joint WHO/FAO expert consultation on diet, nutrition and the prevention of chronic diseases: process, product and policy implications. Public health nutrition 2004; 7:245–250. [DOI] [PubMed] [Google Scholar]
- 18.Expert Panel on Detection E. Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA 2001; 285:2486–2489. [DOI] [PubMed] [Google Scholar]
- 19.World Health Organization (WHO). Definition and diagnosis of diabetes mellitus and intermediate hyperglycemia: report of a WHO/IDF consultation. Geneva: World Health Organization. 2006:1–41.
- 20.Levey AS, Stevens LA, Schmid CH, et al. A new equation to estimate glomerular filtration rate. Ann Int Med 2009; 150:604–612. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.World Health Organization. Worldwide Prevalence of Anaemia 1993–2005: WHO Global Database on Anaemia. 2008; Geneva: World Health Organization, 1–51. [Google Scholar]
- 22.Zhang L, Wang F, Wang L, et al. Prevalence of chronic kidney disease in China: a cross-sectional survey. Lancet 2012; 379:815–822. [DOI] [PubMed] [Google Scholar]
- 23.Devereux RB, Alonso DR, Lutas EM, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol 1986; 57:450–458. [DOI] [PubMed] [Google Scholar]
- 24.Schiller NB, Shah PM, Crawford M, et al. Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr 1989; 2:358–367. [DOI] [PubMed] [Google Scholar]
- 25.Reinstadler SJ, Baum A, Rommel KP, et al. ST-segment depression resolution predicts infarct size and reperfusion injury in ST-elevation myocardial infarction. Heart 2015; 101:1819–1825. [DOI] [PubMed] [Google Scholar]
- 26.Moss TJ, Krantz MJ, Zipse MM, et al. Left ventricular systolic function following alcohol septal ablation for symptomatic hypertrophic cardiomyopathy. Am J Cardiol 2014; 113:1401–1404. [DOI] [PubMed] [Google Scholar]
- 27.Gonçalves A, Jhund PS, Claggett B, et al. Relationship between alcohol consumption and cardiac structure and function in the elderly: the Atherosclerosis Risk In Communities Study. Circ Cardiovasc Imaging 2015; 8:ii:e002846. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Yousaf H, Rodeheffer RJ, Paterick TE, et al. Association between alcohol consumption and systolic ventricular function: a population-based study. Am Heart J 2014; 167:861–868. [DOI] [PubMed] [Google Scholar]
- 29.Martin-Moreno JM, Harris ME, Breda J, et al. Enhanced labelling on alcoholic drinks: reviewing the evidence to guide alcohol policy. Eur J Public Health 2013; 23:1082–1087. [DOI] [PubMed] [Google Scholar]
- 30.Kudo R, Yuui K, Kasuda S, et al. Effect of alcohol on vascular function]. Nihon Arukoru Yakubutsu Igakkai Zasshi 2015; 50:123–134. [PubMed] [Google Scholar]
- 31.Godfrey J, Jeanguenin L, Castro N, et al. Chronic voluntary ethanol consumption induces favorable ceramide profiles in selectively bred alcohol-preferring (P) rats. PLoS One 2015; 10:e0139012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Litwiejko-Pietryńczak E, Szkudlarek M, Niemcunowicz-Janica A, et al. Histological assessment of myocardium in lethal ethanol intoxication. Kardiol Pol 2015; 73:644–649. [PubMed] [Google Scholar]
- 33.Nesbitt GC, Mankad S, Oh JK. Strain imaging in echocardiography: methods and clinical applications. Int J Cardiovasc Imaging 2009; 25 suppl 1:9–22. [DOI] [PubMed] [Google Scholar]
- 34.Jung MH, Park BL, Lee BC, et al. Association of CHRM2 polymorphisms with severity of alcohol dependence. Genes Brain Behav 2011; 10:253–256. [DOI] [PubMed] [Google Scholar]
- 35.Luo X, Kranzler HR, Zuo L, et al. CHRM2 gene predisposes to alcohol dependence, drug dependence and affective disorders: results from an extended case-control structured association study. Hum Mol Genet 2005; 14:2421–2434. [DOI] [PubMed] [Google Scholar]
- 36.Wang JC, Hinrichs AL, Stock H, et al. Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndrome. Hum Mol Genet 2004; 13:1903–1911. [DOI] [PubMed] [Google Scholar]
- 37.Qiao Y, Shi R, Hou B, et al. Impact of alcohol consumption on substrate remodeling and ablation outcome of paroxysmal atrial fibrillation. J Am Heart Assoc 2015; 4:e002349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.US Department of Health and Human Services. The physicians’ guide to helping patients with alcohol problems. Rockville, MD: US Department of Health and Human Services, Public Heath Service, National Institute of Health (NIH), National Institute on Alcohol Abuse and Alcoholism (NIAAA). 1995;95:3769.
- 39.Sahn DJ, De Maria A, Kisslo J, et al. The Committee on M-mode Standardization of the American Society of Echocardiography: recommendations regarding quantitation in M-mode echocardiography: results of a survey of echocardiographic measurements. Circulation 1978; 58:1072–1083. [DOI] [PubMed] [Google Scholar]
- 40.Schiller NB, Shah PM, Crawford M. The American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms: recommendations for quantitation of the left ventricle by two-dimensional echocardiography. J Am Soc Echocardiogr 1989; 2:358–367. [DOI] [PubMed] [Google Scholar]
- 41.Zheng L, Li J, Sun Z, et al. Relationship of blood pressure with mortality and cardiovascular events among hypertensive patients aged ≥60 years in rural areas of China: a strobe-compliant study. Medicine 2015; 94:e1551. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Naissides M, Mamo JC, James AP, et al. The effect of chronic consumption of red wine on cardiovascular disease risk factors in postmenopausal women. Atherosclerosis 2006; 185:438–445. [DOI] [PubMed] [Google Scholar]
- 43.Artero A, Artero A, Tarín JJ, et al. The impact of moderate wine consumption on health. Maturitas 2015; 80:3–13. [DOI] [PubMed] [Google Scholar]
- 44.Yu S, Sun Z, Zheng L, et al. Prevalence of diabetes and impaired fasting glucose in hypertensive adults in rural China: far from leveling-off. Int J Environ Res Public Health 2015; 12:14764–14779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Sun GZ, Li Z, Guo L, et al. High prevalence of dyslipidemia and associated risk factors among rural Chinese adults. Lipids Health Dis 2014; 13:1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Guo X, Li Z, Guo L, et al. An update on overweight and obesity in rural Northeast China: from lifestyle risk factors to cardiometabolic comorbidities. BMC Public Health 2014; 14:1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Sun G, Ma M, Ye N, et al. Diabetes mellitus is an independent risk factor for atrial fibrillation in a general Chinese population. J Diabetes Invest 2016; 1–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Zhang N, Ye N, Chen Y, et al. The relationship between snoring and left ventricular hypertrophy of China: a cross-sectional study. BMC Cardiovasc Disord 2016; 16:1. [DOI] [PMC free article] [PubMed] [Google Scholar]
