Abstract
Background
We sought to evaluate the associations between frequency of daily laughter with heart disease and stroke among community-dwelling older Japanese women and men.
Methods
We analyzed cross-sectional data in 20 934 individuals (10 206 men and 10 728 women) aged 65 years or older, who participated in the Japan Gerontological Evaluation Study in 2013. In the mail-in survey, participants provided information on daily frequency of laughter, as well as body mass index, demographic and lifestyle factors, and diagnoses of cardiovascular disease, hyperlipidemia, hypertension, and depression.
Results
Even after adjustment for hyperlipidemia, hypertension, depression, body mass index, and other risk factors, the prevalence of heart diseases among those who never or almost never laughed was 1.21 (95% CI, −1.03–1.41) times higher than those who reported laughing every day. The adjusted prevalence ratio for stroke was 1.60 (95% CI, 1.24–2.06).
Conclusions
Daily frequency of laughter is associated with lower prevalence of cardiovascular diseases. The association could not be explained by confounding factors, such as depressive symptoms.
Key words: laughter, aged, stroke, cardiovascular diseases, Japan
Abstract
背景:
普段の笑いの頻度と心疾患および脳卒中有病の関連について、地域在住の日本の高齢者を対象として調査した。
方法:
日本老年学的評価研究(JAGES)の2013年度の調査の対象者のうち65才以上の20,934人(男性10,206人、女性10,728)のデータを分析した。郵送法の自記式調査により笑いの頻度、BMI、人口統計情報およびライフスタイル関連の要因、循環器疾患、高脂血症、高血圧、抑うつ症状についての情報を収集した。
結果:
高脂血症、高血圧、抑うつ症状、BMI、その他の要因を調整した上でも、ほとんど笑わない群の心疾患の有病割合はほぼ毎日笑う群に比べて1.21倍(95%信頼区間:1.03–1.41) 高かった。 同様に脳卒中の有病割合は1.60倍 (95% 信頼区間:1.24–2.06)高かった。
結論:
普段よく笑う高齢者は循環器疾患(心疾患または脳卒中)が少ないという関連が見られた。この関連は抑うつ症状など要因では説明がつかなかった。
キーワード: 笑い, 高齢化, 脳卒中, 循環器疾患, 日本
INTRODUCTION
Laughter is increasingly recognized for its potential health benefits, including ameliorating symptoms of depression,1 dementia,2 and insomnia.3 Several studies have reported beneficial effects of laughter on biomarkers, such as markers of immune function4,5 and HbA1c.6 Laughter has a role in complementary medicine, such as laughter yoga,7 the Smile-Sun technique,8 and laughter and exercise programs.6
Laughter is also believed to improve vascular function,9,10 but most of these studies have been limited to studying the effect of laughter on intermediate outcomes, such as arterial stiffness and endothelial function. Most of these studies are intervention studies, and the effect of laughter in daily life is unclear. Viachopoulos et al investigated the effects of films-induced laughter on arterial stiffness,9 and Miller M et al compared flow-mediated vasodilatation after watching laughter-inducing films and stress-inducing films.10
Although rarely, some studies have looked at “hard” health outcomes (eg, actual disease incidence): Adam et al reported that laughter may prevent coronary heart disease (CHD).11 They carried out a cross-sectional study using questionnaires to measure responsiveness to situational humor and hostility and found that, even after controlling for CHD risk factors, CHD patients were significantly less likely to experience laughter during daily activities. However, the study sample was only 300 patients, and they did not control for depression, a major confounding factor of laughter. Another study looked at the relationship of laughter with stroke, but it focused on recovery following stroke.12
Relatively few epidemiological investigations of the link between laughter and cardiovascular disease have been conducted. In this study, we sought to conduct an analysis of cross-sectional data from a large-scale cohort of community-dwelling Japanese older adults on the association of laughter with cardiovascular disease.
METHODS
Study sample
The present study is based on the Japan Gerontological Evaluation Study (JAGES). The JAGES cohort was established in 2010 to investigate factors associated with health and well-being among non-institutionalized individuals aged 65 years and older. The cohort covers 30 municipalities in Japan. We used the 2013 wave of JAGES, in which questionnaires were mailed to 195 290 community-dwelling individuals aged 65 years and older. Of those, 138 294 individuals responded to the survey (response rate, 70.8%). Aside from basic questions, there were five modules of the survey covering different topics. Module A covered nursing care, medical care, and life styles; module B assessed oral hygiene, optimism, and subjective health; module C covered social capital and history of abuse; module D evaluated subjective quality of life, sleep, and cognitive function; and module E assessed physical activity. We used module B, which includes questions about daily frequency of laughter. Respondents to module B comprised 12 174 men and 14 194 women. We excluded 5434 subjects with missing information on subjective health status, frequency of laughing, depression, sex, or age, ultimately including 20 934 participants (10 206 men and 10 728 women).
Heart diseases and stroke
Our primary objective variables were self-reported history of being diagnosed with heart diseases or stroke. Glymour et al investigated whether self-reported strokes can be used to study stroke incidence and risk factors using the data of Health and Retirement Survey (HRS), which is a self-reported population-based cohort study13; the authors found that HRS estimates were closely comparable to those reported in the Cardiovascular Health Study. On the other hand, Bruce et al reported that underreporting and over-reporting of CVD were common among older adults, while the proportions of false-negative self-reports were small.14
Laughter
Daily frequency of laughter was assessed via a standard single-item question6: “How often do you laugh out loud?” (almost every day, 1–5 days per week, 1–3 days per month, or never or almost never). We selected “almost every day” as the reference category.
Covariates
The 2013 survey also inquired about self-reported history of having been diagnosed with hyperlipidemia or hypertension, as well as a range of other personal characteristics, including the presence of depressive symptoms, age, gender, marital status, smoking habit, alcohol consumption, physical activity, and social participation. For evaluation of depressive symptoms, the 15-item Geriatric Depression Scale (GDS-15) was used. The GDS-15 is scored from 1 to 15, with higher scores indicating more depressive symptomatology. Following previous studies, we used 5 as the cutoff score for indicating moderate-to-severe psychological distress.15 We inquired about the frequency of participation in different civic associations and social groups. After summing the different forms of social participation for each respondent, we categorized individuals into quartiles, using the bottom quartile as the reference group. For the evaluation of physical activity, we asked about the frequency of any physical activity (eg, running, swimming, cycling, tennis, activities in sports clubs, climbing, walking, dancing, gymnastics, golf, gardening, washing cars, stretching, bowling, and washing clothes) and divided subjects into two groups (less than once per week or once or more per week) and used the latter category as the reference. For the evaluation of smoking habit, we used the standard single-item question: “Do you smoke?” (never or almost never, stopped smoking, or currently smoking). For the evaluation of alcohol consumption, we used the standard single-item question: “Do you drink alcoholic beverages?” (never or almost never, stopped drinking, or currently drinking), and used “never or almost never” as the reference category.
Statistical analysis
Poisson regression models were used to calculate the prevalence ratios (PRs) and 95% confidence intervals (CIs) for cardiovascular disease according to frequency of laughing. In Model 1, we statistically adjusted for depressive symptoms, age, gender, marital status, smoking habit, alcohol consumption, and physical activity. The variable of depressive symptoms was included in the model because this could confound the association between laughter and cardiovascular disease: depressed people laugh less often, and depression is an independent risk factor for cardiovascular disease.1 We also controlled for hypertension and hyperlipidemia in the models when heart disease or stroke was the outcome of interest. In these models, hypertension and hyperlipidemia are not necessarily confounding variables but may be related to cardiovascular disease. For all explanatory variables, we set categories that were expected to confer the least health risk as referent categories, based on existing evidence and our hypotheses.
In Model 2, we added social participation as a potential confounder, because social participation could increase the frequency of opportunities for laughter and is an independent inversely associated factor for cardiovascular disease.16 For instance, if the risk ratio for cardiovascular disease becomes attenuated towards the null, we would conclude that social participation is more strongly related to cardiovascular disease than laughter. All statistical analyses were conducted using R version 3.1.0 (R Foundation for Statistical Computing, Vienna, Austria).
Ethical issues
Our study protocol and informed consent procedure were approved by the Ethics Committee on the Research of Human Subjects at Nihon Fukushi University.
RESULTS
Baseline characteristics are shown in Table 1. The prevalence of self-reported heart disease was higher (2238 cases; 10.7%) than that of stroke (676 cases; 3.2%). The prevalence of hypertension was much higher than that of the other three diseases (8998 cases; 42.9%). People who reported having been diagnosed with stroke or hypertension had lower frequency of laughter; however, this was not true for those who reported being diagnosed with hyperlipidemia. People tend to laugh more often if they participated in social activities more frequently, smoked less, drank more, exercised more frequently, and had higher BMI.
Table 1. Frequency of laughing in 4 weeks by participants’ characteristics.
n | Never or almost never (%) |
1–3 days per month (%) |
1–5 days per week (%) |
Almost everyday (%) |
|
Cardiovascular diseases (%) | |||||
Heart diseases | 2238 | 242 (15.2%) | 320 (12.9%) | 863 (11.0%) | 813 (9.0%) |
Stroke | 676 | 102 (6.4%) | 104 (4.2%) | 244 (3.1%) | 226 (2.5%) |
Risk factor diseases (%) | |||||
Hyperlipidemia | 2534 | 158 (9.9%) | 307 (12.4%) | 964 (12.3%) | 1105 (12.2%) |
Hypertension | 8998 | 700 (44.0%) | 1067 (43.2%) | 3381 (43.1%) | 3850 (42.6%) |
Depression (%) | |||||
GDS score ≥5 | 3232 | 715 (44.9%) | 635 (25.7%) | 1198 (15.3%) | 684 (7.6%) |
GDS score <5 | 17 702 | 877 (55.1%) | 1837 (74.3%) | 6639 (84.7%) | 8349 (92.4%) |
Age, years (%) | |||||
65–69 | 6305 | 397 (24.9%) | 706 (28.6%) | 2376 (30.3%) | 2826 (31.3%) |
70–74 | 6408 | 423 (26.6%) | 693 (28.0%) | 2342 (29.9%) | 2950 (32.7%) |
75–79 | 4498 | 359 (22.6%) | 563 (22.8%) | 1675 (21.4%) | 1901 (21.0%) |
≥80 | 3723 | 413 (25.9%) | 510 (20.6%) | 1444 (18.4%) | 1356 (15.0%) |
Body mass index | |||||
1st quintile | 4010 | 365 | 506 | 1547 | 1592 |
2nd quintile | 4017 | 277 | 470 | 1563 | 1707 |
3rd quintile | 4116 | 303 | 458 | 1582 | 1773 |
4th quintile | 3917 | 255 | 467 | 1399 | 1796 |
5th quintile | 3989 | 293 | 453 | 1433 | 1810 |
Missing data | 885 | 99 | 118 | 313 | 355 |
Alcohol consumption (%) | |||||
Never or almost never | 12 118 | 860 (54.0%) | 1265 (51.2%) | 4498 (57.4%) | 5495 (60.8%) |
Stopped drinking | 1045 | 137 (8.6%) | 175 (7.1%) | 380 (4.8%) | 353 (3.9%) |
Currently Drinking | 7538 | 584 (36.7%) | 983 (39.8%) | 2868 (36.6%) | 3103 (34.4%) |
Missing data | 233 | 11 (0.7%) | 49 (2.0%) | 91 (1.2%) | 82 (0.9%) |
Smoking habit (%) | |||||
Never or almost never | 15 025 | 973 (61.1%) | 1570 (63.5%) | 5609 (71.6%) | 6873 (76.1%) |
Stopped smoking | 3410 | 336 (21.1%) | 513 (20.8%) | 1312 (16.7%) | 1249 (13.8%) |
Currently smoking | 2244 | 267 (16.8%) | 342 (13.8%) | 831 (10.6%) | 804 (8.9%) |
Missing data | 255 | 16 (1.0%) | 47 (1.9%) | 85 (1.1%) | 107 (1.2%) |
Physical activity (%) | |||||
Less than once per week | 3173 | 492 (30.9%) | 526 (21.3%) | 1078 (13.8%) | 1077 (11.9%) |
Once or more per week | 17 761 | 1100 (69.1%) | 1946 (78.7%) | 6759 (86.2%) | 7956 (88.1%) |
Missing data | 2888 | 234 (14.7%) | 301 (12.2%) | 1073 (13.7%) | 1280 (14.2%) |
Frequency of social participation per year | |||||
1st quartile | 4623 | 663 | 629 | 1639 | 1692 |
2nd quartile | 3699 | 294 | 501 | 1405 | 1499 |
3rd quartile | 3764 | 207 | 479 | 1413 | 1665 |
4th quartile | 3882 | 122 | 297 | 1514 | 1949 |
Missing data | 4966 | 306 | 566 | 1866 | 2228 |
GDS, Geriatric Depression Scale.
The prevalence of cardiovascular disease according to daily frequency of laughter is shown in Table 2. For cardiovascular diseases (heart disease and stroke), a clear dose-response gradient was observed among both men and women between the daily frequency of laughter and the prevalence of disease. The results of Poisson regression models linking laughter and cardiovascular disease outcomes are shown in Table 3. In the crude model, we found an association between daily frequency of laughter and both heart disease and stroke. Compared to the PR of those who laughed almost every day, the PR of people who never or almost never laughed was 1.69 (95% CI, 1.46–1.95) for heart diseases and 2.56 (95% CI, 2.03–3.24) for stroke. Although these PRs were attenuated by the successive addition of covariates (in models 1 and 2), even in the fully adjusted model (model 2), we found associations between daily frequency of laughter and the two cardiovascular diseases, with adjusted PRs of 1.21 (95% CI, 1.03–1.41) for heart disease and 1.60 (95% CI, 1.24–2.06) for stroke. We also found that depression was associated with increased risks of both stroke (PR 1.37; 95% CI, 1.23–1.52) and heart disease (PR 1.39; 95% CI, 1.15–1.68). Social participation had an inverse association with these cardiovascular diseases, and smoking was somehow associated with decreased risk of heart disease (PR 0.72; 95% CI, 0.61–0.85).
Table 2. Frequency of laughing in 4 weeks by participants’ status of cardiovascular diseases and risk factor diseases.
n | Never or almost never (%) | 1–3 days per month (%) | 1–5 days per week (%) | Almost everyday (%) | |
Men | |||||
Cardiovascular diseases | |||||
Heart diseases | 1382 | 16.4 | 15.0 | 13.2 | 12.5 |
Stroke | 460 | 7.6 | 5.5 | 4.0 | 3.8 |
Cardiovascular risk factors | |||||
Hyperlipidemia | 974 | 8.5 | 10.5 | 9.6 | 9.4 |
Hypertension | 4361 | 42.9 | 43.0 | 42.6 | 42.7 |
Women | |||||
Cardiovascular diseases | |||||
Heart diseases | 856 | 13.0 | 9.8 | 8.9 | 6.4 |
Stroke | 216 | 4.2 | 2.2 | 2.3 | 1.6 |
Cardiovascular risk factors | |||||
Hyperlipidemia | 1560 | 12.5 | 15.4 | 14.9 | 14.3 |
Hypertension | 4637 | 46.0 | 43.4 | 43.6 | 42.6 |
Table 3. Prevalence ratio and confidence intervals for heart diseases and stroke.
Variable | Crude Models | Model 1 | Model 2 | |||
Heart diseases | Stroke | Heart diseases | Stroke | Heart disease | Stroke | |
PR (95% CI) | PR (95% CI) | PR (95% CI) | PR (95% CI) | PR (95% CI) | PR (95% CI) | |
Risk factor diseases | ||||||
Hypertension | 0.98 (0.87–1.12) | 0.93 (0.74–1.17) | 1.10 (0.97–1.25) | 1.07 (0.85–1.35) | 1.10 (0.97–1.25) | 1.08 (0.86–1.37) |
Hyperlipidemia | 1.50 (1.38–1.64) | 1.95 (1.67–2.28) | 1.38 (1.27–1.51) | 1.84 (1.57–2.15) | 1.38 (1.27–1.51) | 1.83 (1.56–2.14) |
Frequency of laughing per month | ||||||
Never or almost never | 1.69 (1.46–1.95) | 2.56 (2.03–3.24) | 1.21 (1.04–1.41) | 1.67 (1.30–2.15) | 1.21 (1.03–1.41) | 1.60 (1.24–2.06) |
1–3 days per month | 1.44 (1.26–1.64) | 1.68 (1.33–2.12) | 1.18 (1.03–1.35) | 1.28 (1.01–1.63) | 1.18 (1.03–1.35) | 1.27 (1.00–1.61) |
1–5 days per week | 1.22 (1.11–1.35) | 1.24 (1.04–1.49) | 1.13 (1.03–1.25) | 1.12 (0.93–1.34) | 1.13 (1.03–1.25) | 1.12 (0.93–1.34) |
Almost everyday | Ref | Ref | Ref | Ref | Ref | Ref |
Depression | ||||||
GDS score ≥5 | 1.57 (1.42–1.74) | 1.84 (1.55–2.19) | 1.37 (1.23–1.52) | 1.45 (1.20–1.75) | 1.37 (1.23–1.52) | 1.39 (1.15–1.68) |
GDS score <5 | Ref | Ref | Ref | Ref | Ref | Ref |
Age, years | ||||||
65–69 | Ref | Ref | Ref | Ref | Ref | Ref |
70–74 | 1.60 (1.42–1.82) | 1.35 (1.09–1.68) | 1.56 (1.38–1.77) | 1.31 (1.05–1.63) | 1.56 (1.38–1.77) | 1.31 (1.05–1.63) |
75–79 | 2.04 (1.80–2.32) | 1.76 (1.41–2.20) | 1.89 (1.66–2.15) | 1.57 (1.25–1.96) | 1.90 (1.66–2.16) | 1.55 (1.23–1.94) |
≥80 | 2.53 (2.23–2.87) | 2.03 (1.62–2.54) | 2.29 (2.00–2.61) | 1.74 (1.37–2.19) | 2.29 (2.01–2.61) | 1.68 (1.33–2.12) |
Gender | ||||||
Men | 1.70 (1.56–1.85) | 2.24 (1.90–2.63) | 1.87 (1.69–2.07) | 2.06 (1.69–2.51) | 1.87 (1.68–2.07) | 2.08 (1.71–2.54) |
Women | Ref | Ref | Ref | Ref | Ref | Ref |
Body mass index | ||||||
1st quintile | 0.92 (0.80–1.06) | 0.80 (0.63–1.02) | 0.99 (0.86–1.14) | 0.92 (0.72–1.18) | 0.99 (0.86–1.14) | 0.91 (0.71–1.16) |
2nd quintile | 0.93 (0.81–1.07) | 0.84 (0.66–1.07) | 0.97 (0.85–1.12) | 0.93 (0.73–1.18) | 0.98 (0.85–1.12) | 0.93 (0.73–1.18) |
3rd quintile | Ref | Ref | Ref | Ref | Ref | Ref |
4th quintile | 1.08 (0.95–1.24) | 0.89 (0.70–1.13) | 1.08 (0.94–1.23) | 0.87 (0.69–1.11) | 1.08 (0.94–1.23) | 0.87 (0.69–1.11) |
5th quintile | 1.29 (1.13–1.46) | 1.03 (0.82–1.30) | 1.25 (1.10–1.42) | 0.97 (0.77–1.22) | 1.25 (1.10–1.42) | 0.96 (0.76–1.21) |
Missing data | 1.08 (0.87–1.35) | 0.83 (0.55–1.26) | 0.94 (0.75–1.18) | 0.73 (0.48–1.11) | 0.94 (0.76–1.18) | 0.72 (0.47–1.10) |
Alcohol consumption | ||||||
Never or almost never | Ref | Ref | Ref | Ref | Ref | Ref |
Stopped drinking | 1.63 (1.40–1.91) | 2.73 (2.13–3.50) | 1.06 (0.89–1.26) | 1.55 (1.18–2.05) | 1.06 (0.89–1.25) | 1.54 (1.17–2.04) |
Currently drinking | 0.95 (0.86–1.03) | 1.29 (1.10–1.52) | 0.75 (0.67–0.83) | 0.93 (0.77–1.12) | 0.75 (0.67–0.83) | 0.95 (0.79–1.14) |
Missing data | 0.73 (0.46–1.16) | 1.43 (0.74–2.78) | 0.61 (0.32–1.14) | 1.92 (0.76–4.88) | 0.61 (0.32–1.15) | 1.93 (0.76–4.90) |
Smoking habit | ||||||
Never or almost never | Ref | Ref | Ref | Ref | Ref | Ref |
Stopped smoking | 1.43 (1.30–1.59) | 1.89 (1.59–2.25) | 1.10 (0.98–1.24) | 1.17 (0.96–1.44) | 1.10 (0.98–1.24) | 1.17 (0.96–1.43) |
Currently smoking | 0.80 (0.69–0.93) | 1.07 (0.82–1.38) | 0.72 (0.61–0.85) | 0.80 (0.61–1.06) | 0.72 (0.61–0.85) | 0.79 (0.60–1.04) |
Missing data | 0.88 (0.59–1.33) | 0.98 (0.46–2.07) | 1.05 (0.60–1.83) | 0.53 (0.18–1.51) | 1.05 (0.60–1.84) | 0.52 (0.18–1.50) |
Physical activity | ||||||
Less than once per week | 1.44 (1.29–1.59) | 1.76 (1.47–2.12) | 1.15 (1.03–1.28) | 1.32 (1.09–1.60) | 1.14 (1.02–1.27) | 1.25 (1.03–1.52) |
Once or more per week | Ref | Ref | Ref | Ref | Ref | Ref |
Missing data | 1.08 (0.96–1.22) | 1.30 (1.05–1.61) | 0.96 (0.85–1.09) | 1.22 (0.98–1.52) | 0.97 (0.86–1.11) | 1.17 (0.94–1.47) |
Frequency of social participation per year | ||||||
1st quartile | 1.31 (1.15–1.49) | 1.95 (1.52–2.50) | 1.02 (0.89–1.17) | 1.43 (1.11–1.86) | ||
2nd quartile | 1.12 (0.97–1.29) | 1.45 (1.10–1.91) | 0.96 (0.83–1.10) | 1.18 (0.89–1.56) | ||
3rd quartile | 1.10 (0.96–1.27) | 1.08 (0.81–1.44) | 1.01 (0.88–1.17) | 0.95 (0.71–1.27) | ||
4th quartile | Ref | Ref | Ref | Ref | ||
Missing data | 1.07 (0.94–1.23) | 1.44 (1.11–1.86) | 0.95 (0.83–1.09) | 1.28 (0.98–1.66) |
CI, confidence interval; GDS, Geriatric Depression Scale; PR, prevalence ratio.
In model 1, we controlled for risk factors of diseases, laughter, depression, age, gender, body mass index, drinking habit, smoking habit, and physical activity.
In model 2, social participation was added to the variables.
Gender-stratified analyses showed almost the same results (eTable 1, eTable 2, eTable 3, eTable 4, and eTable 5). Men had almost twice the prevalence of cardiovascular disease as women, and women laughed more frequently than men (eTable 1). Men also smoked much more, drank more, and were twice as likely to be sedentary (exercising less than once per week). However, men had about the same level of depressive symptoms as women. Men and women also participated in social activities to roughly the same extent.
DISCUSSION
In this cross-sectional study, we found inverse associations between daily frequency of laughter and a self-reported history of having been diagnosed with heart disease or stroke. Risk estimates were attenuated in models adjusting for potential confounders, such as depressive symptoms and extent of social participation. Nonetheless, even in the fully-adjusted models, individuals who reported almost never laughing had a prevalence of heart disease that was 1.21 (95% CI, 1.03–1.41) times higher than those who laughed almost every day. Similarly, the prevalence of stroke was 1.60 (95% CI, 1.24–2.06) times higher among people who reported rarely laughing.
Various mechanisms may account for the association between laughter and heart disease or stroke. First, laughter is known to buffer the effects of psychological stress,17 which is proposed as a major risk factor for cardiovascular disease.18–22 There is evidence that laughter can reduce stress. Kim et al reported that laughter therapy significantly decreased the severity of depression, anxiety, and perceived stress in an experimental group who received laughter therapy compared to those in the control group.23 Bennett et al reported that laughter reduced stress levels and improved natural killer cell activity compared with those assigned to a control condition.24 Second, laughter improves vascular endothelial function,9,10 improving arterial compliance25 and attenuating neuroendocrine hormones involved in the down-regulation of vasodilatation.10 Although evidence is not sufficient at present, laughter may function as a form of exercise or physical activity, which is an important preventive factor for heart disease26 and stroke.27
Caution is warranted in interpreting our findings. First, our study is cross-sectional, so we cannot rule out “reverse causality”, in which people diagnosed with serious illnesses (such as stroke and heart disease) may experience fewer occasions in daily life to feel cheerful. Reverse causation is also applicable in the case of stroke, which may be associated with complications, such as facial paralysis, which may impair people’s ability to laugh.28,29 A definitive answer to the question of temporal sequence must await prospective follow-up of the JAGES cohort to observe incident cardiovascular events. Second, laughter may itself be a marker or proxy of physically and/or mentally positive lifestyles. People who have a more positive outlook on life may be more motivated to engage in healthy behaviors, such as exercise, healthy diet, and moderation in alcohol consumption. Although we controlled for many of these behaviors, the possibility of residual confounding cannot be ruled out. Third, our objective and explanatory variables were self-reported. Although some studies in the United States reported that self-reported information is valid enough to be used in epidemiologic studies, their findings might not be applicable to the Japanese data we used. Validation studies using Japanese data are warranted. Nonetheless, we have some confidence in our results because most of the established risk factors for cardiovascular disease indicated associations in the expected direction (eg, higher BMI, sedentarism, and depression).28–30 The major exception is smoking, which was associated with decreased prevalence of cardiovascular disease in our analysis.31 We think this is mainly due to some deviation in our data: in the JAGES 2013 cross-sectional data, 8787 of 131 920 participants did not report any specific disease but also did not select “do not have any disease”, which may have affected results. Also we excluded 5434 participants with missing data on laughter or depression out of 26 368 total participants. Another possible reason is that some participants may have chosen “smoking” or “never or almost never” arbitrarily, since they were not sure in which category they belonged. Reverse causation may also explain this unexpected finding, since some participants who were diagnosed with heart disease would have stopped smoking. There are many recently developed devices to measure laughter30,31; although self-reported laughter may not be as reliable as these measurement methods, the directions of the associations with cardiovascular disease are consistent with those of previous studies. Lastly, we did not consider different types of laughter. There are many types of laughing; for example, smiling is an indication of fondness and appeasement, while laughter expresses playfulness.31 Duchenne laughter arises from positive emotions, whereas non-Duchenne laughter is not based on humor or positive emotions.32 Further studies are needed to examine the differential impacts according to types of laughter, although this would be difficult to do in a large-scale epidemiological study (where external observation is not possible).
In conclusion, if laughter has inverse associations with cardiovascular disease onset, it would be useful to develop interventions to promote laughter in people’s lives (eg, laughter therapy). Population-based interventions, such as increasing opportunities for social interactions in the community, are also required. Although our study could not clearly show any preventive effect of laughter on cardiovascular diseases due to its cross-sectional nature, the present findings are consistent with such an effect, since those who reported having been diagnosed with stroke or heart disease were found not to laugh as often as those who did not have a history of stroke or heart disease. The mechanisms linking laughter and cardiovascular diseases warrant further study. For instance, a longitudinal study with devices to measure daily laughter may be able to evaluate the preventive effect of laughter on cardiovascular diseases.
ONLINE ONLY MATERIALS
ACKNOWLEGEMENTS
This study used data from the Japan Gerontological Evaluation Study (JAGES), conducted by the Center for Well-being and Society, Nihon Fukushi University, as one of their research projects, which was supported by Health Labour Sciences Research Grant, Comprehensive Research on Aging and Health (H25-Choju-Ippan-003, H26-Choju-Ippan-006, H25-Kenki-Wakate-015, H24-Junkanki(Syosyu)-Ippan-007) from the Ministry of Health, Labour and Welfare, Japan; a grant of the Department of Health and Human Services; Grant-in-Aid for Scientific Research (20319338, 22390400, 23243070, 23590786, 23790710, 24140701, 24390469, 24530698, 24653150, 24683018, 25253052, 25870881, 15KT0007, 15H01972) from the Japan Society for the Promotion of Science; a grant from National Center for Geriatrics and Gerontology, Japan (24-17, 24-23, J09KF00804); and AXA Life Insurance Co. LTD. (CR Fixed Income Fund).
Conflicts of interest: None declared.
REFERENCES
- 1.Fonzi L, Matteucci G, Bersani G. [Laughter and depression: hypothesis of pathogenic and therapeutic correlation]. Riv Psichiatr. 2010. Feb;45(1):1–6. [PubMed] [Google Scholar]
- 2.Takeda M, Hashimoto R, Kudo T, Okochi M, Tagami S, Morihara T, et al. Laughter and humor as complementary and alternative medicines for dementia patients. BMC Complement Altern Med. 2010;10:28. 10.1186/1472-6882-10-28 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Ko HJ, Youn CH. Effects of laughter therapy on depression, cognition and sleep among the community-dwelling elderly. Geriatr Gerontol Int. 2011. Jul;11(3):267–74. 10.1111/j.1447-0594.2010.00680.x [DOI] [PubMed] [Google Scholar]
- 4.Sakai Y, Takayanagi K, Ohno M, Inose R, Fujiwara H. A trial of improvement of immunity in cancer patients by laughter therapy. Jpn Hosp 2013. Jul;(32):53–9. [PubMed] [Google Scholar]
- 5.Hayashi T, Tsujii S, Iburi T, Tamanaha T, Yamagami K, Ishibashi R, et al. Laughter up-regulates the genes related to NK cell activity in diabetes. Biomed Res. 2007. Dec;28(6):281–5. 10.2220/biomedres.28.281 [DOI] [PubMed] [Google Scholar]
- 6.Hirosaki M, Ohira T, Kajiura M, Kiyama M, Kitamura A, Sato S, et al. Effects of a laughter and exercise program on physiological and psychological health among community-dwelling elderly in Japan: Randomized controlled trial: Effects of laughter and exercise on health. Geriatr Gerontol Int. 2013. Jan;13(1):152–60. 10.1111/j.1447-0594.2012.00877.x [DOI] [PubMed] [Google Scholar]
- 7.Dolgoff-Kaspar R, Baldwin A, Johnson MS, Edling N, Sethi GK. Effect of laughter yoga on mood and heart rate variability in patients awaiting organ transplantation: a pilot study. Altern Ther Health Med. 2012. Oct;18(5):61–6. [PubMed] [Google Scholar]
- 8.Takayanagi K. Laughter education for implementation of the smile-sun method to promote natural healing in public and healthcare facilities. Hospitals. 2011;57:57. [PubMed] [Google Scholar]
- 9.Vlachopoulos C, Xaplanteris P, Alexopoulos N, Aznaouridis K, Vasiliadou C, Baou K, et al. Divergent effects of laughter and mental stress on arterial stiffness and central hemodynamics. Psychosom Med. 2009. May;71(4):446–53. 10.1097/PSY.0b013e318198dcd4 [DOI] [PubMed] [Google Scholar]
- 10.Miller M. Impact of cinematic viewing on endothelial function. Heart. 2006. Feb 1;92(2):261–2. 10.1136/hrt.2005.061424 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Clark A, Seidler A, Miller M. Inverse association between sense of humor and coronary heart disease. Int J Cardiol. 2001. Aug;80(1):87–8. 10.1016/S0167-5273(01)00470-3 [DOI] [PubMed] [Google Scholar]
- 12.Ostir GV, Berges IM, Ottenbacher ME, Clow A, Ottenbacher KJ. Associations between positive emotion and recovery of functional status following stroke. Psychosom Med. 2008. May;70(4):404–9. 10.1097/PSY.0b013e31816fd7d0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Capistrant BD, Moon JR, Berkman LF, Glymour MM. Current and long-term spousal caregiving and onset of cardiovascular disease. J Epidemiol Community Health. 2011. Nov 11. doi:10.1136/jech-2011-200040. 10.1136/jech-2011-200040 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Psaty BM, Kuller LH, Bild D, Burke GL, Kittner SJ, Mittelmark M, et al. Methods of assessing prevalent cardiovascular disease in the Cardiovascular Health Study. Ann Epidemiol. 1995. Jul;5(4):270–7. 10.1016/1047-2797(94)00092-8 [DOI] [PubMed] [Google Scholar]
- 15.Wongpakaran N, Wongpakaran T, Van Reekum R. The Use of GDS-15 in Detecting MDD: A Comparison Between Residents in a Thai Long-Term Care Home and Geriatric Outpatients. J Clin Med Res. 2013. Apr;5(2):101–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Ellaway A, Macintyre S. Is social participation associated with cardiovascular disease risk factors? Soc Sci Med. 2007. Apr;64(7):1384–91. 10.1016/j.socscimed.2006.11.022 [DOI] [PubMed] [Google Scholar]
- 17.Berk LS, Tan SA, Fry WF, Napier BJ, Lee JW, Hubbard RW, et al. Neuroendocrine and stress hormone changes during mirthful laughter. Am J Med Sci. 1989;298(6):390–6. 10.1097/00000441-198912000-00006 [DOI] [PubMed] [Google Scholar]
- 18.Kivimäki M, Virtanen M, Elovainio M, Kouvonen A, Väänänen A, Vahtera J. Work stress in the etiology of coronary heart disease—a meta-analysis. Scand J Work Environ Health. 2006. Dec 1;32(6):431–42. 10.5271/sjweh.1049 [DOI] [PubMed] [Google Scholar]
- 19.Trichopoulos D, Zavitsanos X, Katsouyanni K, Tzonou A, Dalla-Vorgia P. Psychological stress and fatal heart attack: the Athens (1981) earthquake natural experiment. Lancet. 1983. Feb 26;321(8322):441–4. 10.1016/S0140-6736(83)91439-3 [DOI] [PubMed] [Google Scholar]
- 20.Truelsen T, Nielsen N, Boysen G, Grønbæk M. Self-reported stress and risk of stroke: the Copenhagen City Heart Study. Stroke. 2003. Apr 1;34(4):856–62. 10.1161/01.STR.0000062345.80774.40 [DOI] [PubMed] [Google Scholar]
- 21.Everson SA, Lynch JW, Kaplan GA, Lakka TA, Sivenius J, Salonen JT. Stress-induced blood pressure reactivity and incident stroke in middle-aged men. Stroke. 2001. Jun 1;32(6):1263–70. 10.1161/01.STR.32.6.1263 [DOI] [PubMed] [Google Scholar]
- 22.Kondo N, Saito M, Hikichi H, Aida J, Ojima T, Kondo K, et al. Relative deprivation in income and mortality by leading causes among older Japanese men and women: AGES cohort study. J Epidemiol Community Health. 2015. doi:10.1136/jech-2014-205103. 10.1136/jech-2014-205103 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Kim SH, Kim YH, Kim HJ, Lee SH, Yu SO. The effect of laughter therapy on depression, anxiety, and stress in patients with breast cancer undergoing radiotherapy. Altern Ther Health Med. 2003;9(2):38–45. [Google Scholar]
- 24.Bennett MP, Zeller JM, Rosenberg L, McCann J. The effect of mirthful laughter on stress and natural killer cell activity. Nurs Fac Publ. 2003;9. [PubMed] [Google Scholar]
- 25.Sugawara J, Tarumi T, Tanaka H. Effect of mirthful laughter on vascular function. Am J Cardiol. 2010. Sep;106(6):856–9. 10.1016/j.amjcard.2010.05.011 [DOI] [PubMed] [Google Scholar]
- 26.Powell KE, Thompson PD, Caspersen CJ, Kendrick JS. Physical activity and the incidence of coronary heart disease. Annu Rev Public Health. 1987;8(1):253–87. 10.1146/annurev.pu.08.050187.001345 [DOI] [PubMed] [Google Scholar]
- 27.Lee CD, Folsom AR, Blair SN. Physical activity and stroke risk: a meta-analysis. Stroke. 2003. Oct 1;34(10):2475–81. 10.1161/01.STR.0000091843.02517.9D [DOI] [PubMed] [Google Scholar]
- 28.Van der Kooy K, van Hout H, Marwijk H, Marten H, Stehouwer C, Beekman A. Depression and the risk for cardiovascular diseases: systematic review and meta analysis. Int J Geriatr Psychiatry. 2007. Jul 1;22(7):613–26. 10.1002/gps.1723 [DOI] [PubMed] [Google Scholar]
- 29.McBride PE. The health consequences of smoking. Cardiovascular diseases. Med Clin North Am. 1992. Mar;76(2):333–53. [DOI] [PubMed] [Google Scholar]
- 30.Hernandez J, Liu Z, Hulten G, DeBarr D, Krum K, Zhang Z. Measuring the engagement level of TV viewers. In: 2013 10th IEEE International Conference and Workshops on Automatic Face and Gesture Recognition (FG) [Internet]. IEEE; 2013 [cited 2015 Mar 27]. p. 1–7. Available from: http://ieeexplore.ieee.org/xpls/abs_all.jsp?arnumber=6553742.
- 31.Kojitani Y and Matsumura M. Long-term monitoring system of laughing voice for relieving stress and promoting health -Laughometer-. International Symposium on Biological and Physiological Engineering, 1B4-1, pp.80–83, 2008.
- 32.Gervais M, Wilson DS. The evolution and functions of laughter and humor: a synthetic approach. Q Rev Biol. 2005. Dec;80(4):395–430. 10.1086/498281 [DOI] [PubMed] [Google Scholar]
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