Skip to main content

High prevalence of sarcopenia among binge drinking elderly women: a nationwide population-based study

Abstract

Background

Alcohol consumption is considered a risk factor for sarcopenia, but the association between alcohol consumption and the prevalence of sarcopenia has not been evaluated in detail. This study was to identify the relationship between alcohol drinking patterns and the prevalence of sarcopenia in the elderly Korean population.

Methods

The cross-sectional study was performed using data from the Korea National Health and Nutrition Examination Survey. Participants were excluded if they were under the age of 65, or if data was not available regarding skeletal muscle mass or dietary intake. After these exclusions, a total of 4020 participants (men: 1698; women: 2322) were analyzed in the present study. Sarcopenia is defined according to the criteria for the Asia Working Group for Sarcopenia (AWGS). Binge drinking was defined as consuming ≥5 standard alcoholic drinks (≥4 drinks for women) consecutively on one occasion. This data was subcategorized into two groups based on presence of binge drinking: Social drinking (≤1 time/month) and binge drinking (>1 time/month).

Results

Women binge drinkers with weekly or daily consumption had 2.8 times higher prevalence of sarcopenia than social drinkers (Odds Ratio [OR] = 2.84; 95% Confidence Interval [CI] = 1.12–7.29). However, there were no associations between binge drinkers and sarcopenia in men. After adjusting for age, body mass index (BMI), energy intake, moderate physical activity, and energy intake, women binge drinkers with weekly or daily alcohol consumption had 3.9 times higher prevalence of sarcopenia than social drinkers (OR = 3.88; 95% CI = 1.33–11.36).

Conclusions

The prevalence of sarcopenia in elderly women was related to binge drinking frequency and amounts of drinking after adjusting for covariates. Elderly Korean women who binge drink once or more per week may be associated with sarcopenia, as seen with the observed 3.9 times higher prevalence compared to social drinkers.

Peer Review reports

Background

Habitual alcohol consumption is detrimental to health, although some beneficial effects have been documented [1, 2]. As an estimated 3.8% of all deaths and 4.6% of disability-adjusted life years lost are being attributed to alcohol consumption and alcoholism, excessive alcohol consumption is known to be a significant public health problem [3]. For Korean adults, alcohol drinking is a very common component of the social culture, and according to a nationwide database, 81.6% of adult men and 52.4% of women were reported to be alcohol drinkers [4]. The high prevalence of alcohol consumption is a current major health problem and socioeconomic burden in Korea [5].

Sarcopenia is defined as a loss of muscle strength and mass, and it generally results from a complex bone-muscle interaction in relation to chronic disease and aging [6]. In the elderly, sarcopenia is considering an independent risk factor for falls, disability, morbidity, and mortality [7,8,9,10]. Among several candidate risk factors for sarcopenia, alcohol consumption is known to be one of the risk factors due to the relationship of loss of skeletal muscle mass and alcohol consumption in animal studies [6, 11].

In human studies, although the relationship between alcohol consumption and sarcopenia has been reported in the general population, the number of studies are not large enough and their results are still controversial [12,13,14]. In addition, the results of a recently reported meta-analysis did not support alcohol consumption as a risk factor for sarcopenia [15]. However, studies included in that meta-analysis were not designed considering the relationship between alcohol consumption and sarcopenia as the primary end point.

Therefore, the purpose of this study was to identify the relationship between alcohol drinking patterns and the prevalence of sarcopenia in the elderly Korean population.

Methods

Participants

This study was based on data from the 2008 to 2011 KNHANES, which was conducted by the Korea Ministry of Health and Welfare. KNHANES has been a nationwide representative cross-sectional survey for the Korean population with a clustered, multistage, stratified, and rolling sampling design. KNHANES consists of three sections: a health interview, a health examination, and a dietary survey. The survey data is collected via household interviews and by direct standardized physical examinations conducted in specially equipped mobile examination centers. The data was collected from 37,753 participants from survey years; 2008 (n = 9744), 2009 (n = 10,533), 2010 (n = 8958), and 2011 (n = 8518). Participants were excluded if they were under the age of 65, or if data was not available to evaluate skeletal muscle mass or dietary intake. After these exclusions, a total of 4020 participants (men: 1698; women: 2322) were analyzed for the present study (Fig. 1).

Fig. 1
figure 1

Selection process of study subjects, KNHANES IV, V (2008–2011)

Health examination survey

A health questionnaire was used to obtain information on age, gender, socioeconomic status, education status, smoking status (current, former, or never smoker), alcohol intake, moderate physical activity, and walking activity (yes or no). Moderate physical activity was defined as 5 or more days of moderately intense activity for at least 30 min per day. Walking physical activity was defined as 5 or more days of walking for at least 30 min per day. Body weight and height were measured in light clothing with no shoes, and body mass index (BMI) was calculated as weight (kg) divided by height squared (m2). Information regarding comorbidities, including: diabetes, chronic obstructive pulmonary disease (COPD), chronic renal failure (CRF), and malignancy as potential confounding factors were examined through the health interview survey.

Drinking variables

The total amount of pure alcohol consumed (in grams per day) was calculated using the average number of alcoholic beverages consumed and the frequency of alcohol consumption. The participants were divided into three groups depending on the amount of alcohol consumed per day (non-drinker, light-to-moderate drinker [1–30 g/day], and heavy drinker [>30 g/day]). In this study, one glass was equivalent to roughly 8 g of pure alcohol, which can be found in 220 mL of regular beer of about 4.5% alcohol, and 50 ml of distilled spirits (e.g. Korean soju) of about 19% alcohol. The amount of alcohol was computed as: [amount of drink (mL) × volume of alcohol (%) × density of ethanol at room temperature (0.8)]/100. With 8 g of pure alcohol per glass, less than four glasses were considered equal to less than 32 g of pure alcohol. The frequency of drinking was divided into three groups: (< 1 time/month), (≥ 1 time/month and ≤2–4 times a month), (≥2–3 times a week).

Binge drinking was defined as consuming ≥5 standard drinks (≥4 drinks for women) consecutively in one occasion, and the data was subcategorized into two groups based on presence of binge drinking: Social drinking (≤1 time/month) and binge drinking (>1 time/month).

Alcohol Use Disorders Identification Test (AUDIT) scores were also considered. The participants were grouped according to their AUDIT scores: abstinence or low-risk drinking (0–7 points), more than low-risk drinking (8–14 points), harmful and hazardous drinking (15–19 points), and alcohol dependence (>20 points) [16].

Measurements of appendicular skeletal muscle mass and definition of sarcopenia

Body composition in the KNHANES was measured by whole-body dual x-ray absorptiometry (DXA) (QDR 4500A, Hologic, Inc., Waltham, MA, USA). All subjects changed into paper gowns and were asked to remove all jewelry and other personal effects that could interfere with the DXA examination. To obtain accurate and reliable results, all data regarding body composition were gathered by educated and quality controlled sarcopenia examination surveyors [17]. Bone mineral content, fat mass, and lean soft-tissue mass were measured separately for each part of the body, including the arms and legs. The lean soft-tissue masses of the arms and legs were nearly equal to the skeletal muscle mass. As absolute muscle mass correlates with height, the skeletal muscle mass index was calculated by the following formula: (lean mass [kg]/height [m]2), which is directly analogous to body mass index (BMI = weight [kg]/height [m]2). Arm skeletal muscle mass index was defined as (arm lean mass [kg]/height [m]2). Leg skeletal muscle mass index was defined as (leg lean mass [kg] /height [m]2). Appendicular skeletal muscle mass index (SMI) was defined as the sum of the arm and leg SMIs. Sarcopenia was defined according to the criteria for the Asia Working Group for Sarcopenia (AWGS) (SMI of below 5.4 kg/m2 in women and below 7.0 kg/m2 in men) [18].

Dietary intake measurement

Dietary intake was assessed by trained staff using a complete 24-h recall method. Daily intake of energy and protein was calculated by referencing nutrient concentrations in foods according to the Korean Food Composition Table.

Statistical analysis

Complex sample analyses were used in this study to correct for the distributions of the cluster samples regarding the primary sampling unit, covariance and significance to correspond with those of the general Korean population. The target population for the sampling procedure in the Korean National Health and Nutrition Examination Survey was residents of Korea. However, residents of nursing homes, military facilities, and prisons were excluded. In order to improve the accuracy of the nationwide representative data, the sample design was carried out in a three-year cycle (according to the time of the year). Also, a survey of household members was conducted for the sample area and the number of residential households extracted through the sample design. We selected 20 households as the sample size. All analyses were carried out with the sample weights of KNHANES.

A rolling sampling survey refers to a survey in which independent rolling samples (n = F), not overlapping with the entire sample, are established and compared. In this case, each rolling sample should be extracted in the way that the probability distribution should be the sampling ratio of f = 1/F for the entire sample. Therefore, at the time of passing the F th cycle, the cumulative of the samples surveyed for all the time will organize a sample survey for the entire population.

In order to compare means between the non-sarcopenia group and the sarcopenia group, the Student’s t-test was used. To compare proportions, the chi-squared (χ2) test was used, and univariate analysis was performed. To differentiate interaction between chronic disease and binge drinking for sarcopenia, multivariable analysis including interaction term was conducted.

Variables that had a p value of <0.10 were included in the multivariate model. Multiple logistic regression analysis was conducted to calculate ORs and 95% CIs for the association between the frequency of binge drinking and the presence of sarcopenia after the adjustment of demographic variables (age, BMI, smoking status, moderate PA, and energy intake) served as covariates. All statistical tests were two-tailed, and statistical significance was defined as p < 0.05. The statistical calculation was performed using SPSS Statistics V.22 (SPSS, Chicago, IL, USA).

Results

Characteristics of elderly Korean population older than 65 years by presence of sarcopenia

In the elderly men, age (p = 0.006), chronic renal failure (p = 0.01), and malignancy (p < 0.001) were significantly higher in the sarcopenia group than the non-sarcopenia group. Although former cigarette smoking status was significantly higher in the sarcopenia group, current smoking status was significantly lower (p = 0.012). Waist circumference (p < 0.001) and moderate physical activity (p = 0.043) were significantly lower in the sarcopenia group than the non-sarcopenia group (Table 1).

Table 1 Characteristics of elderly Korean men older than 65 years by presence of sarcopenia

In the elderly women, age was significantly higher in the sarcopenia group than the non-sarcopenia group (p < 0.001). However, BMI (p < 0.001), waist circumference (p < 0.001), appendicular SMI (p < 0.001), energy intake (p < 0.001), and protein intake (p = 0.001) were significantly lower in the sarcopenia group than the non-sarcopenia group (Table 2).

Table 2 Characteristics of elderly Korean women older than 65 years by presence of sarcopenia

Pattern of alcohol consumption according to the prevalence of sarcopenia

Table 3 shows subject characteristics of alcohol consumption according to the prevalence of sarcopenia. For the elderly men, drinking quantity, binge drinking, and AUDIT scores, there were no significant differences between the sarcopenia and non-sarcopenia groups. However, drinking frequency was more frequent in the non-sarcopenia group than the sarcopenia group (p = 0.011).

Table 3 Patterns of alcohol consumption according to the prevalence of sarcopenia

In elderly women, the frequency of drinking and AUDIT scores revealed no significant differences between the sarcopenia and non-sarcopenia groups. Although the quantity of alcohol consumption in heavy drinkers was larger in the sarcopenia group than the non-sarcopenia group, the quantity of alcohol consumption in light-to-moderate drinkers was larger in the non-sarcopenia group than the sarcopenia group (p = 0.022). Also, binge drinking was more frequent in the sarcopenia group than the non-sarcopenia group (p = 0.024).

Univariate analysis of the variables for sarcopenia

In elderly men, age (p < 0.001), body mass index (p < 0.001), waist circumference (p < 0.001), former cigarette smoker (p = 0.011), moderate physical activity (p = 0.04), energy intake (p < 0.001) and protein intake (p < 0.001) were significantly affected by sarcopenia. For elderly women, age (p < 0.001), body mass index (p < 0.001), waist circumference (p < 0.001), moderate physical activity (p = 0.066), energy intake (p < 0.001) and protein intake (p = 0.001) were significantly affected by sarcopenia. Chronic renal failure, diabetes and smoking status with binge drinking in men and women were not significantly affected by sarcopenia as interaction term.

Odds ratios for sarcopenia according to alcohol drinking patterns in the elderly population

The odds ratios for the prevalence of sarcopenia according to alcohol drinking patterns are shown in Table 4. In the elderly men, after adjusting for age, body mass index, smoking status, moderate physical activity, and energy intake, odds ratios of sarcopenia according to alcohol drinking patterns displayed no statistically significant differences.

Table 4 Odds ratios (ORs) and 95% confidence intervals (CIs) for sarcopenia according to alcohol-drinking patterns in elderly population

For elderly women, for quantity of drinking, after adjusting for age, body mass index, moderate physical activity, and energy intake, odds ratios for the sarcopenia versus the non-sarcopenia were no statistically different. However, elderly women binge drinkers with a weekly or daily consumption had 2.8 times higher prevalence of sarcopenia than social drinkers (OR = 2.84; 95% CI = 1.12–7.29). After adjusting for age, body mass index, moderate physical activity, and energy intake, binge drinkers with weekly or daily consumption had 3.9 times higher prevalence of sarcopenia than social drinkers (OR = 3.88; 95% CI = 1.33–11.36).

Discussion

Although alcohol consumption has been proven to cause muscle atrophy in animal studies, the relationship between alcohol consumption and sarcopenia in humans is still controversial [19,20,21,22]. This nationwide cross-sectional study identified the relationship between sarcopenia and alcohol drinking pattern in elderly women. After adjusting for variables, it was found that among elderly women, binge drinkers with weekly or daily consumption had a 3.9 times higher prevalence of sarcopenia than social drinkers.

So far, several basic experimental animal studies have proven the relationship between alcohol consumption and sarcopenia. A few studies were performed to assess the net effect of alcohol consumption on the prevalence of sarcopenia. These studies reported that acute alcohol consumption decreased muscle protein synthesis and caused changes in skeletal muscles in female mice and rats [19, 20]. Human studies reported that heavy alcohol consumption in patients with alcoholic cirrhosis was related to acceleration of sarcopenia [23, 24]. However, these findings are not consistent with those of other human studies. The results of a meta-analysis to explore the relationship between sarcopenia and alcohol consumption did not support alcohol consumption as a risk factor for sarcopenia [15]. However, the recent meta-analysis study has several important limitations. Among the references of the study, there was no study that considered the relationship between sarcopenia and alcohol consumption as the primary end point. In addition, the study did not confirm the relationship between alcohol drinking pattern and sarcopenia [15]. This study was primarily designed to assess the relationship between sarcopenia and alcohol drinking pattern. In the current study, among elderly women, binge drinkers with weekly or daily consumption had a 3.9 times higher prevalence of sarcopenia than social drinkers (OR = 3.88; 95% CI = 1.33–11.36) after adjusting for age, body mass index, moderate physical activity, and energy intake and after considering interaction terms such as chronic renal failure, diabetes and smoking status.

Although we could not identify the relationship between alcohol consumption and sarcopenia among men, among elderly women, binge drinking was related to sarcopenia. Elderly women who binge drink are more vulnerable to the consequences of alcohol consumption than men, as proven in other studies [25,26,27,28]. The possible related mechanisms that might be involved are as follows: women have proportionately more body fat and a lower volume of body water compared with men of similar weight [29]. As a result, women have a higher concentration of alcohol because there is less volume of water to dilute the alcohol. In addition, elderly women have even less body water, a decreased tolerance for alcohol, and an even slower metabolism rate for alcohol [30]. Therefore, sarcopenia associated with the metabolic disorder may also be affected by gender differences in alcohol’s effects.

This study has several limitations. First, it could not evaluate the causality between alcohol consumption and low skeletal muscle mass. Prospectively designed studies are necessary to clarify this relationship. Second, we classified the subjects into three alcohol-drinking groups based on a self-reported questionnaire. The use of self-reported information on alcohol-drinking patterns could lead to misrepresentation of actual drinking styles. Third, self-reported alcohol intake, AUDIT scores, and smoking status may be underreported due to recall and social desirability biases. Finally, we adopted different cut-off levels of binge drinking in men and women. We that said, we could not adopt different cut-off levels of quantity of drinking in men and women. The reason of this limitation was that in the survey the quantity of drinking was not separately analyzed for men and women. In addition, the definitions of alcoholism according to DSM-V and WHO guidelines were not used to quantify the extent of drinking in men and women.

Conclusions

In conclusion, the prevalence of sarcopenia in elderly Korean women was related to binge drinking frequency and amount of drinking after adjusting for covariates. Korean women who binge drink once per week or more than one time per week have almost 4 times higher risk of sarcopenia than female social drinkers.

Abbreviations

ALP:

Alkaline phosphatase

AUDIT:

Alcohol Use Disorders Identification Test

AWGS:

Asia Working Group for Sarcopenia

BMI:

Body mass index

CI:

Confidence interval

COPD:

Chronic obstructive pulmonary disease

CRF:

Chronic renal failure

DXA:

Dual x-ray absorptiometry

KCDC:

Korea Centers for Disease Control and Prevention

KNHANES:

Korean National Health and Nutrition Examination Survey

ORs:

Odds ratios

PTH:

Parathyroid hormone

SMI:

Skeletal muscle mass index

References

  1. Boffetta P, Garfinkel L. Alcohol drinking and mortality among men enrolled in an American Cancer Society prospective study. Epidimiology. 1990;1:342–8.

    Article  CAS  Google Scholar 

  2. Kannel WB, Ellison RC. Alcohol and coronary heart disease: the evidence for a protective effect. Clin Chim Acta. 1996;246:59–76.

    Article  CAS  PubMed  Google Scholar 

  3. Rehm J, Mathers C, Popova S, Thavorncharoensap M, Teerawattananon Y, Patra J. Global burden of disease and injury and economic cost attributable to alcohol use and alcohol-use disorders. Lancet. 2009;373:2223–33.

    Article  PubMed  Google Scholar 

  4. Hong S-W, Linton JA, Shim J-Y, Kang H-T. High-risk drinking is associated with a higher risk of diabetes mellitus in Korean men, based on the 2010–2012 KNHANES. Alcohol. 2015;49:275–81.

    Article  PubMed  Google Scholar 

  5. Kim J, Chung W, Lee S, Park C. Estimating the socioeconomic costs of alcohol drinking among adolescents in Korea. J Prev Med Public Health. 2010;43:341–51.

    Article  PubMed  Google Scholar 

  6. Steiner JL, Lang CH. Alcohol impairs skeletal muscle protein synthesis and mTOR signaling in a time-dependent manner following electrically stimulated muscle contraction. J Appl Physiol. 2014;117:1170–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Vanitallie TB. Frailty in the elderly: contributions of sarcopenia and visceral protein depletion. Metabolism. 2003;52:22–6.

    Article  PubMed  Google Scholar 

  8. Lloyd BD, Williamson DA, Singh NA, Hansen RD, Diamond TH, Finnegan TP, et al. Recurrent and injurious falls in the year following hip fracture: a prospective study of incidence and risk factors from the sarcopenia and hip fracture study. J Gerontol A Biol Sci Med Sci. 2009;64:599–609.

    Article  PubMed  Google Scholar 

  9. Yoon H-K, Park C, Jang S, Jang S, Lee Y-K, Ha Y-C. Incidence and mortality following hip fracture in Korea. J Korean Med Sci. 2011;26:1087–92.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Frisoli A, Chaves PH, Ingham SJM, Fried LP. Severe osteopenia and osteoporosis, sarcopenia, and frailty status in community-dwelling older women: results from the women’s health and aging study (WHAS) II. Bone. 2011;48:952–7.

    Article  PubMed  Google Scholar 

  11. Adachi J, Asano M, Ueno Y, Niemelä O, Ohlendieck K, Peters TJ, et al. Alcoholic muscle disease and biomembrane perturbations (review). J Nutr Biochem. 2003;14:616–25.

    Article  CAS  PubMed  Google Scholar 

  12. Lau EM, Lynn HS, Woo JW, Kwok TC, Melton LJ. Prevalence of and risk factors for sarcopenia in elderly Chinese men and women. J Gerontol A Biol Sci Med Sci. 2005;60:213–6.

    Article  PubMed  Google Scholar 

  13. Castillo EM, Goodman-Gruen D, Kritz-Silverstein D, Morton DJ, Wingard DL, Barrett-Connor E. Sarcopenia in elderly men and women: the rancho Bernardo study. Am J Prev Med. 2003;25:226–31.

    Article  PubMed  Google Scholar 

  14. Kim S-H, Kim T-H, Hwang H-J. The relationship of physical activity (PA) and walking with sarcopenia in Korean males aged 60 years and older using the fourth Korean national health and nutrition examination survey (KNHANES IV-2, 3), 2008-2009. Arch Gerontol Geriatr. 2013;56:472–7.

    Article  PubMed  Google Scholar 

  15. Steffl M, Bohannon RW, Petr M, Kohlikova E, Holmerova I. Alcohol consumption as a risk factor for sarcopenia - a meta-analysis. BMC Geriatr. 2016;16:99.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Saunders JB, Aasland OG, Babor TF, de la Fuente JR, Grant M. Development of the alcohol use disorders identification test (AUDIT): WHO collaborative project on early detection of persons with harmful alcohol consumption--II. Addiction. 1993;88:791–804.

    Article  CAS  PubMed  Google Scholar 

  17. Lewiecki EM, Gordon CM, Baim S, Leonard MB, Bishop NJ, Bianchi M-L, et al. International society for clinical densitometry 2007 adult and pediatric official positions. Bone. 2008;43:1115–21.

    Article  PubMed  Google Scholar 

  18. Chen L-K, Liu L-K, Woo J, Assantachai P, Auyeung T-W, Bahyah KS, et al. Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia. J Am Med Dir Assoc. 2014;15:95–101.

    Article  PubMed  Google Scholar 

  19. Steiner JL, Kimball SR, Lang CH. Acute alcohol-induced decrease in muscle protein synthesis in female mice is REDD-1 and mTOR-independent. Alcohol Alcohol. 2016;51:242–50.

    Article  PubMed  Google Scholar 

  20. Lang CH, Frost RA, Vary TC. Acute alcohol intoxication increases REDD1 in skeletal muscle. Alcohol Clin Exp Res. 2008;32:796–805.

    Article  CAS  PubMed  Google Scholar 

  21. Korzick DH, Sharda DR, Pruznak AM, Lang CH. Aging accentuates alcohol-induced decrease in protein synthesis in gastrocnemius. Am J Physiol Regul Integr Comp Physiol. 2013;304:R887–98.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Maddalozzo GF, Turner RT, Edwards CHT, Howe KS, Widrick JJ, Rosen CJ, et al. Alcohol alters whole body composition, inhibits bone formation, and increases bone marrow adiposity in rats. Osteoporos Int. 2009;20:1529–38.

    Article  CAS  PubMed  Google Scholar 

  23. Song DS, Chang UI, Choi S, Jung YD, Han K, Ko S-H, et al. Heavy alcohol consumption with alcoholic liver disease accelerates sarcopenia in elderly Korean males: the Korean national health and nutrition examination survey 2008-2010. PLoS One. 2016;11:e0163222.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Thapaliya S, Runkana A, McMullen MR, Nagy LE, McDonald C, Naga Prasad SV, et al. Alcohol-induced autophagy contributes to loss in skeletal muscle mass. Autophagy. 2014;10:677–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Taylor JL, Dolhert N, Friedman L, Mumenthaler M, Yesavage JA. Alcohol elimination and simulator performance of male and female aviators: a preliminary report. Aviat Space Environ Med. 1996;67:407–13.

    CAS  PubMed  Google Scholar 

  26. Thomasson H. Alcohol elimination: faster in women? Alcohol Clin Exp Res. 2000;24:419–20.

    Article  CAS  PubMed  Google Scholar 

  27. Frezza M, di Padova C, Pozzato G, Terpin M, Baraona E, Lieber CS. High blood alcohol levels in women. The role of decreased gastric alcohol dehydrogenase activity and first-pass metabolism. N Engl J Med. 1990;322:95–9.

    Article  CAS  PubMed  Google Scholar 

  28. Li TK, Beard JD, Orr WE, Kwo PY, Ramchandani VA, Thomasson HR. Variation in ethanol pharmacokinetics and perceived gender and ethnic differences in alcohol elimination. Alcohol Clin Exp Res. 2000;24:415–6.

    Article  CAS  PubMed  Google Scholar 

  29. Frances RJ, Miller SI, Mack AH, editors. Clinical textbook of addictive disorders. 3rd ed. New York: Guilford Press; 2005.

    Google Scholar 

  30. Mumenthaler MS, Taylor JL, O'Hara R, Yesavage JA. Gender differences in moderate drinking effects. Alcohol Res Health. 1999;23(1):55–64.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank the Korea Centers for Disease Control and Prevention, who performed the KNHANES. And this research was supported by a grant from the Korean Health Technology R & D Project through the Korean Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HC15C1189).

In addition, we acknowledge the statistical assistance of So Yeon Ahn, associate professor of the department of medical research collaborating center, Seoul national university Bundang hospital.

Funding

This research was supported by a grant from the Korean Health Technology R & D Project through the Korean Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HC15C1189).

Availability of data and materials

Cross-sectional data from the Korea National Health and Nutrition Examination Survey by Korea Centers for Disease Control and Prevention and Korean Ministry of Health and Welfare. The data, therefore, is freely available at: https://knhanes.cdc.go.kr/knhanes/eng/index.do.

Authors’ contributions

The study was conceived and funding was obtained by Y-CH. All authors contributed to data collection, data management, and the development of the study protocol. The manuscript was drafted by J-IY and Y-CH. All authors finalized, provided critical review, and approved the final manuscript.

Competing interests

The authors declare that they have no competing interest.

Consent for publication

Not applicable.

Ethics approval and consent to participate

The protocol of this study for performing an analysis of the 2008–2011 Korean National Health and Nutrition Examination Survey (KNHANES) data was reviewed and approved by the Institutional Review Board (IRB) of Korea Centers for Disease Control and Prevention (KCDC) (Approval No. 2008–04EXP-01-C, 2009–01CON-03-C, 2010–02CON-21-C, and 2011–02CON-06-C). Informed consent was obtained from all participants when the 2008 KNHANES, 2009 KNHANES, 2010 KNHANES and 2011 KNHANES were conducted.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yong-Chan Ha.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yoo, JI., Ha, YC., Lee, YK. et al. High prevalence of sarcopenia among binge drinking elderly women: a nationwide population-based study. BMC Geriatr 17, 114 (2017). https://doi.org/10.1186/s12877-017-0507-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12877-017-0507-3

Keywords