Literature DB >> 35437944

Association between changes in facial flushing and hypertension across drinking behavior patterns in South Korean adults.

Yu Shin Park1,2, Soo Hyun Kang1,2, Eun-Cheol Park2,3, Suk-Yong Jang1,2.   

Abstract

Heavy alcohol drinking has been reported to be associated with hypertension. Moreover, when drinking alcohol, individuals may experience symptoms such as facial flushing. Therefore, this study aimed to examine the association between changes in facial flushing and hypertension across different drinking behavior patterns in South Korean adults. Data from the Korea Community Health Survey conducted in 2019 were used, and 118 129 (51 047 men and 67 082 women) participants were included. The participants were divided into five groups based on the change in facial flushing (non-drinking, non-flushing to non-flushing, flushing to flushing, non-flushing to flushing, flushing to non-flushing). The risk of hypertension in each facial flushing group was analyzed by multiple logistic regression. Men in the non-flushing to flushing group had a significantly higher association with hypertension than other groups (men: odds ratio (OR) 1.42, confidence interval (CI) 1.14-1.76). According to the level of alcohol use disorder, the non-flushing to flushing group showed a significantly increased odds of hypertension compared to all levels of drinking (men: mild drinking: OR 1.95, CI 1.40-2.71; moderate drinking: OR 2.02, CI 1.41-2.90; women: moderate drinking: OR 1.71, CI 1.16-2.52; heavy drinking: OR 1.90, CI 1.19-3.04). This study found a significant association between changes in facial flushing and hypertension among adults in South Korea. In particular, individuals who changed from non-flushing to flushing reactions had an increased association with hypertension than the other groups. Compared to people at the same drinking level, people with non-flushing to flushing reactions were highly associated with hypertension at moderate drinking level.
© 2022 The Authors. The Journal of Clinical Hypertension published by Wiley Periodicals LLC.

Entities:  

Keywords:  Asian flushing; alcohol use disorder; facial flushing; hypertension

Mesh:

Year:  2022        PMID: 35437944      PMCID: PMC9106078          DOI: 10.1111/jch.14475

Source DB:  PubMed          Journal:  J Clin Hypertens (Greenwich)        ISSN: 1524-6175            Impact factor:   2.885


INTRODUCTION

Hypertension is a commonly occurring and leading preventable risk factor for cardiovascular disease and a subject of great interest to researchers. The Global Burden of Disease study found that hypertension is at risk of placing an increasing economic burden on societies globally. , , In South Korea, neoplasms caused 158.2 deaths per 100 000 in 2019. In comparison, diseases of the circulatory system caused 117.8 deaths. These included cardiovascular diseases (60.4 deaths) and cerebrovascular diseases (40.2 deaths). It is well recognized that hypertension is associated with traditional risk factors such as age, body mass index (BMI), smoking, and family history. Additionally, drinking behavior, especially excessive or frequent drinking, is also a risk factor for hypertension. , When drinking alcohol, some people experience facial flushing or palpitations, shortness of breath, headache, and vomiting due to the accumulation of acetaldehyde. In particular, East Asian ethnic groups, such as Korean, Chinese, and Japanese populations, have a higher prevalence of ALDH2 polymorphism than the Western population. , Ethanol is metabolized by alcohol dehydrogenase (ADH) to acetaldehyde, which is eliminated by aldehyde dehydrogenase (ALDH). Alcohol dependence is associated with the isozymes ADH2*2 and ADH3*1, which oxidize alcohol rapidly and produce high amounts of acetaldehyde. Moreover, the ALDH2 polymorphism encodes an inactive subunit, , resulting in high acetaldehyde levels in the blood after alcohol intake. , A previous study suggested a greater association with hypertension in people who have alcohol‐related facial flushing than non‐flushers. Moreover, the risk of hypertension in facial flushers is markedly increased with excessive drinking. More research on specific genotypes associated with alcohol metabolism are necessary because the specific genotypes associated with alcohol metabolism are common in South Korean populations. To the best of our knowledge, no study has examined the association between facial flushing and hypertension changes. Therefore, we examined the association between change in facial flushing and hypertension across different drinking behavior patterns, such as alcohol use disorders, to fill this research gap. We focused both on the presence and absence of facial flushing as well as the occurrence or elimination of facial flushing with time in adults.

METHODS

We used data from the Korea Community Health Survey (KCHS) conducted by the Korea Center for Disease Control and Prevention (KCDC) in 2019. The KCHS is a cross‐sectional, nationally representative survey that has been conducted regularly since 2008 to gather regional data for planning, monitoring, and evaluating community health services. The data for providing country‐level health indicators is made using a large population‐based National Census Registry and a systematic, stratified, and multistage cluster sampling method. The weights allocated to each participant's data were calculated based on geographic and demographic distributions to generalize the entire population of Korea.

Participants

The 2019 survey included 229 099 individuals, and the analysis excluded individuals who were younger than 19 years of age (n = 2200) and pregnant (n = 641). In addition, we excluded individuals who had been undergoing anti‐hypertensive drug treatment were excluded (n = 62 286). Some anti‐hypertensive drugs cause facial flushing. , Finally, after excluding those with missing data (n = 45 843), 118 129 healthy participants were included in this study. Our study did not require approval from the Institutional Review Board or informed consent because the KCHS is a secondary dataset available in the public domain and does not contain private information.

Variables

The dependent variable of this study was the risk of hypertension. Blood pressure was measured thrice with intervals of 1 minute for stabilization, and the final blood pressure was the average of the three measurements. Hypertension was classified as systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg. We classified those who met the hypertension criteria and those who did not meet the hypertension criteria when measuring blood pressure, except for taking anti‐hypertensive drugs. Facial flushing reaction was the primary independent variable of interest. The following question assessed past facial flushing reaction: “In the past year or two, did you experience a quick facial flushing reaction when drinking a small glass of beer?” A current facial flushing reaction was assessed by asking the following question: “Do you currently experience a facial flushing reaction when drinking a small amount of beer?” The data on past and present facial flushing reactions were self‐reported. We divided the study population into five categories: people who have never drunk alcohol (ND, non‐drinking); people who never had facial flushing reaction (NN, non‐flushing→ non‐flushing); people who had facial flushing reaction in the past and present (FF, flushing→ flushing); people who had facial flushing reaction in the past but not in the present (FN, flushing→ non‐flushing); and people who did not have facial flushing reaction in the past but did in the present (NF, non‐flushing→ flushing). Furthermore, we analyzed each group stratified by variables such as alcohol use. We controlled for covariates such as sociodemographic and socioeconomic factors, health behaviors, and health conditions of the participants. The sociodemographic factors were age (19–29, 30–39, 40–49, 50–59, and ≥60 years) and sex (men and women). The socioeconomic factors were education level (below middle school, high school, and college or higher), region (city and rural areas), marital status (yes and no), occupation (white‐collar, pink collar, blue‐collar, and unemployed), and household income (high, middle high, middle‐low, and low). Health behavior factors included smoking status (non‐smoker, past smoker, and current smoker), BMI (non‐obese and obese), diagnosis of diabetes (yes and no), and physical activity assessed to walking practice rate (yes and no). In the female group, menopause status was added (yes and no). Additionally, we used the Alcohol Use Disorder Identification Test Score (AUDIT‐C) to assess the pattern of alcohol use. Cut‐off scores of AUDIT‐C for heavy alcohol drinking were 7 for men and 6 for women, and mild alcohol drinking were 3 for both men and women.

Statistical analysis

Independent variables were compared using the chi‐squared test to identify the association between changes in facial flushing and hypertension. After adjusting for sociodemographic, economic, and health‐related variables, we used a multiple logistic regression analysis to evaluate the association between the change of facial flushing and hypertension. The results were reported using odds ratios (ORs) and confidence intervals (CIs). Moreover, we performed a subgroup analysis stratified by sex and multiple logistic regression analysis was used to examine the associations with change in facial flushing in persons with hypertension according to the level of alcohol use disorder. Differences were considered significant at P‐values of <.05 as well as at P‐values for trends <.05. Data were analyzed using SAS 9.4 (SAS Institute Inc; Cary, North Carolina, USA) and a P value <.05 was considered to be statistically significant.

RESULTS

Table 1 shows the general characteristics of the participants. There were 51 047 men and 67 082 women in this study, and 11 234 (22%) men and 10 406 (15.5%) women had a risk of hypertension. Participants were grouped into five categories based on the change in facial flushing reaction. Of the men, 5798 (11.4%) reported they have never drunk alcohol, 29 044 (56.9%) reported non‐flushing to alcohol, 11 592 (22.7%) reported flushing in the past and present, 3711 (7.3%) reported facial flushing reaction in the past but not in the present, and 902 (1.8%) reported facial flushing reaction in the present but not in the past. Of the women, 18 060 (26.9%) reported they have never drunk alcohol, 32 616 (48.6%) reported non‐flushing to alcohol, 11 476 (17.1%) reported flushing in the past and present, 3958 (5.9%) reported facial flushing reaction in the past but not in the present, and 972 (1.4%) reported facial flushing reaction in the present but not in the past.
TABLE 1

General characteristics of the study population

Hypertension
MenWomen
TOTALYesNoTOTALYesNo
VariablesNo.%No.%No.% P No.%No.%No.% P
Total 118 12951,047100.011 23422.039 81378.067 082100.010 40615.556 67684.5
Facial flushing change
 non‐drinking579811.4114219.7465680.3<.000118 06026.9378921.014 27179.0<.0001
 non‐flushing →non‐flushing29 04456.9653022.522 51477.532 61648.6427113.128 34586.9
 flushing →flushing11 59222.7241420.8917879.211 47617.1156013.6991686.4
 non‐flushing →flushing9021.825528.364771.79721.420120.777179.3
 flushing →non‐flushing37117.389324.1281875.939585.958514.8337385.2
Age (years)
 19‐29846716.68169.6765190.4<.0001896613.42422.7872497.3<.0001
 30‐39961918.8181818.9780181.110 20015.27147.0948693.0
 40‐4910 86521.3269924.8816675.213 64420.3168312.311 96187.7
 50‐59985919.3256026.0729974.014 46821.6251317.411 95582.6
 ≥6012 23724.0334127.3889672.719 80429.5525426.514 55073.5
Marital Status
 Living w/ spouse33 38365.4770323.125 68076.9<.000144 09665.7688315.637 21384.4.3433
 Living w/o spouse17 66434.6353120.014 13380.022 98634.3352315.319 46384.7
Region
 City16 62132.6356521.41305678.60.03522 17333.1304713.719 12686.3<.0001
 Rural34 42667.4766922.32675777.744 90966.9735916.437 55083.6
Educational level
 Middle school or less779515.3214727.5564872.5<.000118 88628.2509827.013 78873.0<.0001
 High school15 34430.1383025.01151475.020 18830.1315515.617 03384.4
 College or over27 90854.752572265128 00841.8215325 855
Household Income
 Low874017.1222525.5651574.5<.000115 40123.0376024.411 64175.6<.0001
 Mid‐low857416.8208324.3649175.711 18416.7191817.1926682.9
 Mid‐high15 39530.2340711 98818 05626.9240515 651
 High18 33835.9351919.21481980.822 44133.5232310.420 11889.6
Occupational categories a
 White14 53428.5293220.211 60279.8<.000115 56423.212708.214 29491.8<.0001
 Pink619212.1127020.5492279.512 04418.0177514.710 26985.3
 Blue20 47740.1492924.115 54812 62018.8273021.69890
 Inoccupation984419.3210321.4774178.626 85440.0463117.222 22382.8
Smoking
 Non smoker15 18029.7266617.612 51482.4<.000163 02794.0967315.353 35484.7<.0001
 past smoker17 36234.0421824.313 14475.719983.033116.6166783.4
 smoker18 50536.3435023.514 15576.520573.140219.5165580.5
BMI
 Non‐obesity48 11594.310 14521.137 97078.9<.000164 86596.7972515.055 14085.0<.0001
 Obesity29325.7108937.1184362.922173.368130.7153669.3
Diagnose of diabetes
 Yes31526.279425.2235874.8<.000133235.074922.5257477.5<.0001
 No47 89593.810 44021.837 45578.263 75995.0965715.154 10284.9
Physical activity‐walk
 Yes28 24055.3622622.02 201478.00.81040 05459.7632315.833 73184.20.017
 No22 80744.7500822.017 79978.027 02840.3408315.122 94584.9
Menopausal status
 Yes32 88249.0757623.025 30677.0<.0001
 No34 20051.028308.331 37091.7
Alcohol use disorder
 Mild drinking & Non‐drinking16 56032.4315319.013 40781.044 91867.0751216.737 40683.3
 Moderate drinking15 74630.8317420.212 57279.8<.000112 59518.8149711.911 09888.1<.0001
 Heavy drinking18 74136.7490726.213 83473.8956914.3139714.6817285.4

Three groups(White, Pink, Blue) based on International Standard Classification Occupations codes. Inoccupation group includes housewife

General characteristics of the study population Three groups(White, Pink, Blue) based on International Standard Classification Occupations codes. Inoccupation group includes housewife Table 2 reports the findings of logistic regression analysis for the association between change in facial flushing and hypertension stratified by sex. Men in the NF group had a higher OR of hypertension than other groups (men: OR 1.42, CI 1.14–1.76); among women, there was no statistically significant relationship between change in facial flushing and hypertension. Additionally, participants who drink moderately (men: OR 1.20, CI 1.11–1.30, women: OR 1.16, CI 1.07–1.27) and heavily (men: OR 1.83, CI 1.69–1.98, women: OR 1.93, CI 1.76–2.13) were strongly associated with an increased risk for hypertension.
TABLE 2

Results of factors associated with hypertension

Hypertension
MenWomen
VariablesOR95% CIOR95% CI
Facial flushing change
 Non‐drinking1.001.00
 non‐flushing →non‐flushing1.11(0.99 ‐ 1.25)0.93(0.86 ‐ 1.01)
 flushing →flushing1.09(0.97 ‐ 1.22)1.03(0.94 ‐ 1.13)
 non‐flushing →flushing1.42(1.14 ‐ 1.76)1.11(0.90 ‐ 1.37)
 flushing →non‐flushing1.08(0.93 ‐ 1.24)0.93(0.81 ‐ 1.06)
Age (years)
 19‐291.001.00
 30‐392.48(2.22 ‐ 2.77)2.98(2.50 ‐ 3.56)
 40‐493.79(3.38 ‐ 4.24)5.71(4.82 ‐ 6.77)
 50‐594.35(3.87 ‐ 4.90)6.98(5.68 ‐ 8.57)
 ≥605.21(4.57 ‐ 5.94)9.28(7.47 ‐ 11.54)
Marital Status
 Living wtih spouse1.001.00
 Living without spouse1.32(1.23 ‐ 1.42)1.09(1.01 ‐ 1.16)
Region
 City1.001.00
 Rural0.99(0.94 ‐ 1.05)1.01(0.96 ‐ 1.08)
Occupational categories a
 White1.001.00
 Pink0.95(0.86 ‐ 1.04)1.06(0.95 ‐ 1.17)
 Blue1.04(0.97 ‐ 1.12)1.12(1.00 ‐ 1.25)
 Inoccupation1.05(0.95 ‐ 1.15)1.11(1.01 ‐ 1.22)
Educational level
 Middle shool or less1.33(1.20 ‐ 1.47)1.72(1.54 ‐ 1.92)
 High school1.22(1.14 ‐ 1.30)1.31(1.20 ‐ 1.42)
 College or over1.001.00
Household income
 Low1.12(1.02 ‐ 1.22)1.25(1.14 ‐ 1.37)
 Mid‐low1.17(1.08 ‐ 1.28)1.20(1.10 ‐ 1.32)
 Mid‐high1.11(1.04 ‐ 1.19)1.13(1.05 ‐ 1.23)
 High1.001.00
Smoking
 Non smoker1.001.00
 Past smoker1.06(0.98 ‐ 1.14)1.36(1.16 ‐ 1.61)
 smoker1.04(0.97 ‐ 1.12)1.28(1.10 ‐ 1.48)
BMI
 Non‐obesity1.001.00
 Obesity3.25(2.94 ‐ 3.59)3.57(3.08 ‐ 4.14)
Diagnose of diabetes
 Yes1.001.00
 No1.17(1.05 ‐ 1.31)1.06(0.94 ‐ 1.20)
Physical activity‐walk
 Yes1.001.00
 No0.91(0.87 ‐ 0.97)0.96(0.90 ‐ 1.01)
Menopausal status
 Yes1.17(1.03 ‐ 1.34)
 No1.00
Alcohol use disorder
 mild drinking & non‐drinking1.001.00
 moderate drinking1.20(1.11 ‐ 1.30)1.16(1.07 ‐ 1.27)
 heavy drinking1.83(1.69 ‐ 1.98)1.93(1.76 ‐ 2.13)

(White, Pink, Blue) based on International Standard Classification Occupations codes. Inoccupation group includes housewife

Results of factors associated with hypertension (White, Pink, Blue) based on International Standard Classification Occupations codes. Inoccupation group includes housewife Figure 1 shows the results of stratified analyses of the association of the changes in facial flushing on hypertension according to alcohol consumption. Overall, taking the non‐drinking group as the reference category, the OR of the NF was high in mild and moderate drinking levels among men. (mild drinking: OR 1.95, CI 1.40–2.71; moderate drinking: OR 2.02 CI, 1.41–2.90). Also, the OR of the NF was high in moderate and heavy drinking levels among women. (moderate drinking: OR 1.71, CI 1.16–2.52; heavy drinking: OR 1.90 CI, 1.19–3.04)
FIGURE 1

Stratified analysis of the changes in facial flushing with respect to hypertension by alcohol consumption

Stratified analysis of the changes in facial flushing with respect to hypertension by alcohol consumption Finally, Table 3 reports the subgroup analysis stratified by independent variables. Men diagnosed with diabetes had an increased association with hypertension in the NF group (OR 2.24, CI 1.22–4.11). Additionally, men who did not exercise had an increased risk of hypertension in the NF group (OR 1.68, CI 1.26–2.25).
TABLE 3

The results of subgroup analysis stratified by independent variables

VariablesHypertension
Facial flushing change
No‐drinkingnon‐flushing → non‐flushingflushing → flushingnon‐flushing → flushingflushing → non‐flushing
OROR95% CIOR95% CIOR95% CIOR95% CI
Men
Age
 19‐291.001.17(0.77 ‐ 1.77)1.11(0.72 ‐ 1.72)1.16(0.49 ‐ 2.75)1.11(0.64 ‐ 1.91)
 30‐391.001.16(0.83 ‐ 1.63)0.95(0.67 ‐ 1.34)1.52(0.84 ‐ 2.76)1.05(0.69 ‐ 1.58)
 40‐491.001.29(0.98 ‐ 1.71)1.22(0.93 ‐ 1.62)1.61(1.00 ‐ 2.60)1.17(0.85 ‐ 1.61)
 50‐591.000.96(0.74 ‐ 1.24)1.10(0.85 ‐ 1.42)1.40(0.86 ‐ 2.28)1.00(0.74 ‐ 1.36)
 ≥601.001.04(0.88 ‐ 1.24)1.14(0.97 ‐ 1.35)1.39(1.00 ‐ 1.94)1.13(0.90 ‐ 1.43)
Diagnose of diabetes
 Yes1.000.97(0.67 ‐ 1.40)0.97(0.66 ‐ 1.43)2.24(1.22 ‐ 4.11)0.68(0.42 ‐ 1.13)
 No1.001.13(1.01 ‐ 1.28)1.11(0.98 ‐ 1.25)1.35(1.07 ‐ 1.70)1.12(0.96 ‐ 1.29)
BMI
 non‐obesity1.001.13(1.01 ‐ 1.27)1.10(0.98 ‐ 1.24)1.40(1.11 ‐ 1.76)1.10(0.95 ‐ 1.28)
 Obesity1.000.91(0.62 ‐ 1.35)1.00(0.68 ‐ 1.48)1.58(0.73 ‐ 3.41)0.80(0.48 ‐ 1.34)
Physical activity
 Yes1.001.01(0.86 ‐ 1.20)0.97(0.82 ‐ 1.14)1.18(0.85 ‐ 1.63)0.91(0.73 ‐ 1.13)
 No1.001.21(1.03 ‐ 1.42)1.22(1.04 ‐ 1.42)1.68(1.26 ‐ 2.25)1.25(1.04 ‐ 1.52)
Women
Age
 19‐291.001.25(0.68 ‐ 2.29)1.28(0.66 ‐ 2.46)0.45(0.09 ‐ 2.14)0.69(0.29 ‐ 1.63)
 30‐391.001.03(0.71 ‐ 1.51)0.93(0.61 ‐ 1.41)0.65(0.28 ‐ 1.48)1.23(0.75 ‐ 2.04)
 40‐491.001.39(1.10 ‐ 1.76)1.56(1.21 ‐ 2.01)0.97(0.56 ‐ 1.69)1.28(0.94 ‐ 1.75)
 50‐591.000.96(0.82 ‐ 1.12)1.14(0.96 ‐ 1.35)1.79(1.26 ‐ 2.56)1.00(0.78 ‐ 1.28)
 ≥601.000.82(0.73 ‐ 0.91)0.92(0.80 ‐ 1.07)1.13(0.79 ‐ 1.62)0.89(0.71 ‐ 1.11)
Diagnose of diabetes
 Yes1.001.07(0.82 ‐ 1.39)1.11(0.79 ‐ 1.56)0.69(0.35 ‐ 1.38)0.76(0.44 ‐ 1.33)
 No1.000.93(0.86 ‐ 1.01)1.02(0.93 ‐ 1.12)1.14(0.92 ‐ 1.42)0.93(0.81 ‐ 1.07)
BMI
 Non‐obesity1.000.91(0.84 ‐ 0.99)1.01(0.92 ‐ 1.12)1.12(0.88 ‐ 1.43)0.93(0.81 ‐ 1.07)
 Obesity1.001.47(1.02 ‐ 2.12)1.43(0.96 ‐ 2.13)1.17(0.53 ‐ 2.58)1.08(0.56 ‐ 2.08)
Physical activity
 Yes1.000.92(0.82 ‐ 1.04)1.03(0.90 ‐ 1.19)1.15(0.82 ‐ 1.61)0.87(0.71 ‐ 1.06)
No1.000.94(0.85 ‐ 1.04)1.03(0.91 ‐ 1.16)1.07(0.82 ‐ 1.40)0.99(0.83 ‐ 1.18)

Adjusted for other covariates

The results of subgroup analysis stratified by independent variables Adjusted for other covariates

DISCUSSION

We found that change in facial flushing reaction was associated with a higher risk of hypertension. Especially, individuals with facial flushing reaction in the present but not in the past increased the likelihood of hypertension, and we also examined individuals who consumed similar alcohol levels. The association between flushing changes and hypertension was different for each alcohol consumption level. Among those who drink mild or moderate, men who did not have facial flushing reaction in the past but did in the present were the highest likelihood of hypertension. And women who did not have facial flushing reaction in the past but did in the present were the highest likelihood of hypertension among moderate drinking group. Some studies link hypertension and alcohol‐induced facial flushing. , The likelihood of hypertension was higher in people with facial flushing than in those without facial flushing in previous study. In the result of our study, the difference between the two group was not significant. Since previous studies considered only current facial flushing, different results may have been derived from our study. While polymorphisms partly explained the association in alcohol metabolism genes, these studies did not find any evidence that facial flushing reaction is associated with the risk of hypertension. , Therefore, further studies are necessary. In this study, we assessed the association between the presence of facial flushing and alcohol consumption. The reasons for the change in facial flushing can be explained as follows. Facial flushing is a well‐known symptom of acetaldehyde accumulation and intolerance to alcohol. Some studies showed that the genotype of ADH and ALDH was associated with liver disease. , , , Chronic alcoholics have a higher tolerance to alcohol than others because of the metabolic adaptation of the central nervous system and increased ethanol elimination rate. Increased ethanol elimination increases both blood and tissue acetaldehyde levels in chronic alcoholics. People with liver injury experience decreasing activities of ADH and proportionally low‐K ALDH (ALDH2). It is speculated that the decrease in ADH could be due to centrilobular cell necrosis. , Thus, decrease in liver function may be associated with a decrease in the activity of the enzyme that metabolizes alcohol. This, in turn, leads to the accumulation of alcohol and acetaldehyde in the body and induces symptoms such as facial flushing. Therefore, people who have liver disease with non‐facial flushing in the past may develop a facial flushing reaction later. In our study, people who did not have a facial flushing reaction in the past but did in the present were significantly associated with the risk of hypertension among those who were diagnosed with diabetes or did not exercise. Although the mechanism causing flushing is unknown, it is clear that this is not a good indication or reaction in the body. Research findings have indicated that ALDH2 polymorphism that causes facial flushing is related to cancer risk incidence according to alcohol intake. It is noteworthy that these studies mainly focused on upper oral pharyngeal and laryngeal cancer and esophageal squamous cell carcinoma. , , Thus, if people have never had facial flushing to alcohol before but experience facial flushing now, people need to exercise caution with their alcohol intake. However, as there are no studies in the literature supporting this result, it is difficult to determine an absolute judgment. This study has some limitations. First, this study was based on data from a cross‐sectional survey. Therefore, although the association could be confirmed, the causality could not be evaluated. Second, our data were self‐reported; thus, it is subject to recall bias and underreporting of drinking habits or experience of facial flushing. Therefore, the association of facial flushing with drinking may not be accurate. Moreover, we do not know how long it has been since changes in facial flushing were observed by participants. Third, although the cut‐off points used for facial flushing are in accordance with KCHS, it may be difficult to compare our findings in different settings or populations. Fourth, residual confounding factors may exit because taking some medication like steroid that cause facial flushing have not been identified due to data limitation. These factors should be considered in future studies. Finally, due to lack of similar studies, it is difficult to explain all the findings in this study. Therefore, it is necessary to perform precise measurements of facial flushing in further studies. Despite these limitations, this study has several strengths. We used the most recent nationally representative database to determine the association between facial flushing and hypertension. Therefore, the results obtained are highly representative of adults in South Korea. Furthermore, in our analysis, we adjusted for several social factors that are known potential confounders for facial flushing pattern or hypertension, including sex, socioeconomic status, and health behaviors, to appropriately estimate the associations across different drinking behavior patterns. In conclusion, this study found a significant association between change in facial flushing and hypertension among adults in South Korea. In particular, individuals who changed from non‐flushing to flushing reactions had an increased association with hypertension than those in the other groups. Compared to people at the same drinking level, people with non‐flushing to flushing reactions were highly associated with hypertension at moderate drinking level.

CONFLICT OF INTEREST

None declared.

AUTHOR CONTRIBUTIONS

Soo Hyun Kang conceived of the presented idea. Yu Shin Park and Soo Hyun Kang developed the theory and performed the computations. Yu Shin Park and Soo Hyun Kang verified the analytical methods. Eun Cheol Park and Suk Yong Jang encouraged Yu Shin Park to investigate facial flushing mechanism and supervised the findings of this work. All authors discussed the results and contributed to the final manuscript. SUPPORTING INFORMATION Click here for additional data file.
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Journal:  Alcohol       Date:  1990 Sep-Oct       Impact factor: 2.405

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Authors:  A Yoshida; M Ikawa; L C Hsu; K Tani
Journal:  Alcohol       Date:  1985 Jan-Feb       Impact factor: 2.405

4.  Association between the incidence of hypertension and alcohol consumption pattern and the alcohol flushing response: A 12-year follow-up study.

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Journal:  Alcohol       Date:  2020-07-21       Impact factor: 2.405

5.  Two aldehyde dehydrogenases from human liver. Isolation via affinity chromatography and characterization of the isozymes.

Authors:  N J Greenfield; R Pietruszko
Journal:  Biochim Biophys Acta       Date:  1977-07-08

6.  Role of hepatic acetaldehyde dehydrogenase in alcoholism: demonstration of persistent reduction of cytosolic activity in abstaining patients.

Authors:  M Thomas; S Halsall; T J Peters
Journal:  Lancet       Date:  1982-11-13       Impact factor: 79.321

7.  Alcohol sensitivity in Taiwanese men with different alcohol and aldehyde dehydrogenase genotypes.

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Journal:  J Formos Med Assoc       Date:  2002-11       Impact factor: 3.282

8.  Influence of liver disease on hepatic alcohol and aldehyde dehydrogenases.

Authors:  J Panés; X Soler; A Parés; J Caballería; J Farrés; J Rodés; X Parés
Journal:  Gastroenterology       Date:  1989-09       Impact factor: 22.682

Review 9.  Alcohol intake and blood pressure: a systematic review implementing a Mendelian randomization approach.

Authors:  Lina Chen; George Davey Smith; Roger M Harbord; Sarah J Lewis
Journal:  PLoS Med       Date:  2008-03-04       Impact factor: 11.069

10.  Effect of alcohol and aldehyde dehydrogenase gene polymorphisms on alcohol-associated hypertension: the Guangzhou Biobank Cohort Study.

Authors:  Wei Sen Zhang; Lin Xu; Catherine Mary Schooling; Chao Qiang Jiang; Kar Keung Cheng; Bin Liu; Tai Hing Lam
Journal:  Hypertens Res       Date:  2013-04-25       Impact factor: 3.872

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1.  Association between changes in facial flushing and hypertension across drinking behavior patterns in South Korean adults.

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