Abstract
A large prospective cohort study in the United States examined the association between coffee intake and overall and cause-specific mortality and showed a inverse association between pneumonia and influenza deaths and coffee intake. In Japan, the mortality rate of pneumonia in elderly people is high, and its prevention is an important issue. The present study investigated the association between coffee and green tea intake and pneumonia among the elderly. The design was a hospital-based case control study. The cases were patients over 65 years old newly diagnosed as pneumonia. As a control, patients with the same sex and age (range of 5 years) who visited the same medical institution around the same time (within 2 months after examination of the case) for a disease other than pneumonia were selected. There were two controls per case. Odds ratio (OR) and 95% confidence interval (CI) for pneumonia of coffee and green tea intake during the past month were calculated using a conditional logistic regression model. A total of 199 cases and 374 controls were enrolled. When compared to those who do not drink coffee, the OR for pneumonia of those who drink less than one cup of coffee per day was 0.69 (95% CI 0.39–1.21), OR of those who drink one cup was 0.67 (0.38–1.18), and OR of those who drink two or more cups was 0.50 (0.28–0.88) (Trend p = 0.024). No association was found between pneumonia and green tea consumption. This study suggested a preventive association between coffee intake over 2 cups per day and pneumonia in the elderly.
Subject terms: Medical research, Risk factors
Introduction
Coffee has been consumed all over the world, and many studies are considering its impact on health1,2. A large prospective cohort study in the United States has shown an inverse association between coffee intake and all-cause mortality, and in cause-specific deaths, coffee intake has inversely associated with heart disease, chronic respiratory disease, diabetes, pneumonia and influenza, and suicide3. A cohort study in Japan also showed an inverse association with coffee intake and overall mortality, cause-specific death by heart disease, cerebrovascular disease and respiratory disease4. Green tea intake was inversely associated with overall mortality and cause-specific death by heart disease, and it was inversely associated with cause-specific death by cerebrovascular disease and respiratory disease in men5.
In Japan, elderly people have high age-specific mortality rates of pneumonia, especially high age at 80 years and over6. Because Japan is aging at a pace unparalleled in other countries, the prevention of elderly person pneumonia is an important problem. Epidemiological studies on pneumonia in the elderly have been studied on the effectiveness of vaccination (streptococcus pneumoniae, influenza), but few studies have examined the relationship with lifestyle related factors.
This study investigated the association between coffee and green tea intake, which are often drunk in Japan, and pneumonia in the elderly.
Methods
Study design
This hospital-based, matched case–control study was conducted at 24 hospitals in Tokyo, Chiba, Shizuoka, Aichi, Gifu, Kyoto, and Fukuoka Prefectures between October 1, 2009 and September 30, 2014. Details of this study have been described elsewhere7–9.
Study subjects
As cases, the study included 65 years or older patients who were newly diagnosed with pneumonia by a physician. Pneumonia was diagnosed based on the increased white blood cell count (or elevated levels of C-reactive protein (CRP)), presence of an infiltrative shadow on chest X-rays, and clinical features (cough, sputum, and fever).
As a control, patients with the same sex and age (range of 5 years) who visited the same medical institution at the same time (within 2 months after examination of the case) for a disease other than pneumonia were selected. Two controls (respiratory department, other departments) for each case were selected whenever possible. Exclusion criteria were as follows: nursing home residents, patients with aspiration pneumonia (i.e., pneumonia caused by inhalation during eating or vomiting), patients with malignant tumors, patients currently undergoing treatment with oral steroids or immunosuppressant, and patients with a history of splenectomy.
Information collection
The following information were collected from patient’s self-administered questionnaire and physician’s questionnaire: sex, age, height, body weight, vaccination status (pneumococcal, influenza), underlying diseases (respiratory disease, hypertension, diabetes mellitus, dyslipidemia, heart disease, cerebrovascular disease, kidney disease), activities of daily living (ADL), children ≤ 6 years old living in the same household, current smoking habit, current alcohol drinking habit, and coffee and green tea intake (how often and how much have you drunk for the past month?: Didn't you drink, how many cups did you drink a month, how many cups did you drink per week, how many cups did you drink a day?) (supplementary file).
Statistical analysis
Explanatory variables were categorized into four groups for comparison as follows. Coffee (per day): did not drink, less than one cup, one cup, two or more cups, Green tea (per day): less than one cup, 1–2 cups, 3–4 cups, 5 or more cups.
Adjustment variables were classified as follows. Pneumococcal vaccination status was defined as "vaccinated" if a patient had undergone the vaccination within the previous 5 years, and "not vaccinated" if otherwise. Influenza vaccination (monovalent influenza A (H1N1) pdm09 vaccine, trivalent seasonal influenza vaccine) status was defined as "vaccinated" if the patient had undergone the vaccination within the previous 6 months, and "not vaccinated" if otherwise. During the 2009–2010 season, an influenza A (H1N1) pandemic occurred, but not a seasonal influenza epidemic10. The monovalent influenza A (H1N1) pdm09 vaccine was therefore used as the influenza vaccine. BMI was calculated as weight in kilograms (kg) divided by the square of height in meters (m2), and BMI was categorized as three groups according to WHO classification11; underweight (< 18.5 kg/m2); normal range (18.5–24.9 kg/m2); overweight (pre-obese (25.0–29.9 kg/m2) or obese (≥ 30.0 kg/m2)), and normal range was the reference category. All underlying diseases were categorized as yes, or no. ADL was categorized as "independent" or "not independent (bedridden, semi-bedridden, semi-independent)". Characteristics of cases and controls were compared using a Wilcoxon rank-sum test and chi-square, as appropriate.
We calculated the odds ratios (ORs) and 95% confidence intervals (CIs) for pneumonia using conditional logistic regression model to elucidate the association between coffee and green tea intake and pneumonia. The variables included in the multivariate model were factors that were p < 0.1 in the characteristic comparison of the cases and controls or were medically and biologically meaningful regardless of statistical significance. The following explanatory variables were included in the multivariate models: coffee and green tea intake, vaccination status (pneumococcal, influenza), BMI, underlying disease (respiratory disease, hypertension, diabetes mellitus, heart disease), ADL, children ≤ 6 years old living in the same household, current smoking habit, and current alcohol drinking habit. Trends for association were assessed by assigning ordinal scores to a single intake variable.
Next, following sub-analyses were performed. In our previous study examining control selection, different departments of control (respiratory department, other departments) showed different Vaccine inoculation rates, suggesting different background factors8. So when the characteristics were compared by control departments (respiratory department, other departments), there were patients who did not currently have respiratory disease but visited the respiratory department (52/192), and patients who currently have respiratory disease but visited other departments (18/182) (Table 1(a)). Therefore, as shown in Fig. 1, we investigated the association between coffee intake and pneumonia in following two subjects; Sub analysis (1): all cases (n = 199) and controls without respiratory disease (n = 216), Sub analysis (2): all cases (n = 199) and controls with respiratory diseases (n = 158). In two sub analyses, characteristics of cases (n = 199) and controls (n = 216 or n = 158) were compared using the same methods as the main analysis (Table 1(b)), the ORs of coffee intake for pneumonia were calculated using a logistic model.
Table 1.
Comparison of characteristics.
Characteristic | Cases (N = 199) | Controls (N = 374) | (a) Controls by department | (b) Controls by underlying disease | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Non- respiratory medicine (n = 182) | Respiratory medicine (n = 192) | Without respiratory disease (n = 216) | With respiratory disease (n = 158) | ||||||||||||
n | (%) | n | (%) | P* | n | (%) | n | (%) | n | (%) | P*, † | n | (%) | P*, ‡ | |
Age (years) | |||||||||||||||
Median | 75 | 75 | 0.570 | 74 | 75 | 74 | 0.205 | 76 | 0.622 | ||||||
Range | (65–92) | (65–98) | (65–93) | (65–98) | (65–93) | (65–98) | |||||||||
Male sex | 136 | (68) | 257 | (69) | 0.927 | 124 | (68) | 133 | (69) | 142 | (66) | 0.574 | 115 | (73) | 0.361 |
Vaccinated | |||||||||||||||
Pneumococcal vaccine | 51 | (26) | 102 | (27) | 0.672 | 33 | (18) | 69 | (36) | 49 | (23) | 0.484 | 53 | (34) | 0.102 |
Influenza vaccine | 86 | (43) | 181 | (48) | 0.237 | 82 | (45) | 99 | (52) | 98 | (45) | 0.659 | 83 | (53) | 0.080 |
BMI (kg/m2) | |||||||||||||||
< 18.5 | 49 | (25) | 47 | (13) | < 0.001 | 15 | (8) | 32 | (17) | 22 | (10) | < 0.001 | 25 | (16) | 0.017 |
18.5–24.9 | 121 | (61) | 246 | (66) | 121 | (67) | 125 | (65) | 147 | (68) | 99 | (63) | |||
25–40 | 29 | (15) | 81 | (22) | 46 | (25) | 35 | (18) | 47 | (22) | 34 | (22) | |||
Underlying disease | |||||||||||||||
Respiratory disease | |||||||||||||||
No | 110 | (55) | 216 | (58) | 0.569 | 164 | (90) | 52 | (27) | 216 | (100) | 0 | (0) | ||
Yes | 89 | (45) | 158 | (42) | 18 | (10) | 140 | (73) | 0 | (0) | 158 | (100) | |||
Hypertension | 85 | (43) | 197 | (53) | 0.023 | 107 | (59) | 90 | (47) | 119 | (55) | 0.012 | 78 | (49) | 0.210 |
Diabetes mellitus | 28 | (14) | 95 | (25) | 0.002 | 66 | (36) | 29 | (15) | 67 | (31) | < 0.001 | 28 | (18) | 0.346 |
Dyslipidemia | 31 | (16) | 70 | (19) | 0.348 | 43 | (24) | 27 | (14) | 50 | (23) | 0.052 | 20 | (13) | 0.434 |
Heart disease | 29 | (15) | 77 | (21) | 0.078 | 51 | (28) | 26 | (14) | 51 | (24) | 0.020 | 26 | (16) | 0.625 |
Cerebrovascular disease | 17 | (9) | 27 | (7) | 0.571 | 19 | (10) | 8 | (4) | 21 | (10) | 0.677 | 6 | (4) | 0.070 |
Kidney disease | 4 | (2) | 15 | (4) | 0.203 | 6 | (3) | 9 | (5) | 8 | (4) | 0.304 | 7 | (4) | 0.226 |
Activities of daily living (ADL) | |||||||||||||||
Independent | 176 | (88) | 347 | (93) | 0.080 | 172 | (95) | 175 | (91) | 204 | (94) | 0.028 | 143 | (91) | 0.530 |
Not independent | 23 | (12) | 27 | (7) | 10 | (5) | 17 | (9) | 12 | (6) | 15 | (9) | |||
Live in a household with children ≤ 6 years old | 19 | (10) | 20 | (5) | 0.057 | 10 | (5) | 10 | (5) | 12 | (6) | 0.122 | 8 | (5) | 0.112 |
Current smoker | 22 | (11) | 38 | (10) | 0.739 | 24 | (13) | 14 | (7) | 21 | (10) | 0.656 | 17 | (11) | 0.929 |
Current alcohol drinker | 70 | (35) | 148 | (40) | 0.302 | 79 | (43) | 69 | (36) | 93 | (43) | 0.101 | 55 | (35) | 0.943 |
*Wilcoxon rank-sum test or Chi-square test or Fisher exact test.
†P between all cases (N = 199) and controls without respiratory disease (N = 216).
‡P between all cases (N = 199) and controls with respiratory disease (N = 158).
Figure 1.
Subjects for analysis.
A difference was found in the comorbidities of diabetes mellitus in the characteristic comparison between the cases and the controls. Since coffee intake was often reported to have a protective association with diabetes mellitus12,13, the ORs of coffee intake for pneumonia in participants without diabetes mellitus were calculated using a logistic model (N = 450, sensitivity analysis).
In the sub-analyses and sensitivity analysis, matching could not be maintained, so an unconditional logistic model was used, and same variables as main analysis and matching variables (sex, age) were included in the multivariate models.
The level of statistical significance was taken as p < 0.05. Analysis was performed using SAS version 9.4 software (SAS Institute, Cary, NC).
Ethics approval and consent to participate
The attending physician verbally explained the study using the written to the participants. Participants were informed that they could refuse to participate in this study and were instructed to complete a self-administered questionnaire if they could participant with this study, including providing medical information. All participants were considered to consent the study if they filled out the questionnaire. Informed consent was obtained from all participants. It is based on the research ethics guidelines for people in Japan at that time. This study protocol was approved by the Ethics Committees at the Osaka City University Graduate School of Medicine and was performed in accordance with the Declaration of Helsinki.
Results
199 cases and 374 controls were enrolled. Table 1 shows characteristics of cases and controls. The subjects with BMI less than 18.5 kg/m2 were more frequent in cases than controls. The prevalence of hypertension and diabetes mellitus was significantly higher in the control than in the case. Other variables did not differ significantly between case and control.
Table 2 shows the association between coffee and green tea intake and pneumonia. ORs of coffee intake for pneumonia were 0.69 (95% CI 0.39–1.21) in those who drank less than one cup a day compared to those who did not drink coffee, 0.67 (0.38–1.18) in those who drank one cup, and 0.50 (0.28–0.88) in those who drank two or more cups, and the dose response relationship was significant (tend p = 0.024).
Table 2.
Odds ratio of coffee and green tea intake for pneumonia.
Cases | Controls | Crude OR | 95% CI | P | Adjusted OR * | 95% CI | P | |||
---|---|---|---|---|---|---|---|---|---|---|
(N = 199) | (N = 374) | |||||||||
n | (%) | n | (%) | |||||||
Coffee intake (daily) | ||||||||||
None | 52 | (26) | 66 | (18) | 1.00 | 1.00 | ||||
< 1 cup | 49 | (25) | 89 | (24) | 0.68 | 0.40–1.14 | 0.139 | 0.69 | 0.39–1.21 | 0.192 |
1 cup | 51 | (26) | 103 | (28) | 0.61 | 0.36–1.03 | 0.065 | 0.67 | 0.38–1.18 | 0.169 |
≥ 2 cups | 47 | (24) | 116 | (31) | 0.49 | 0.29–0.83 | 0.008 | 0.50 | 0.28–0.88 | 0.017 |
(Trend p = 0.010) | (Trend p = 0.024) | |||||||||
Green tea intake (daily) | ||||||||||
< 1 cup | 41 | (21) | 83 | (22) | 1.00 | 1.00 | ||||
1–2 cups | 45 | (23) | 76 | (20) | 1.25 | 0.73–2.14 | 0.424 | 1.22 | 0.68–2.19 | 0.502 |
3–4 cups | 65 | (33) | 130 | (35) | 0.998 | 0.59–1.69 | 0.995 | 1.18 | 0.67–2.05 | 0.571 |
≥ 5 cups | 48 | (24) | 85 | (23) | 1.15 | 0.67–1.96 | 0.615 | 1.08 | 0.61–1.93 | 0.788 |
(Trend p = 0.805) | (Trend p = 0.807) |
*Variables included in model: vaccination status (pneumococcal, influenza), BMI, underlying disease (respiratory disease, hypertension, diabetes mellitus, heart disease), ADL, children ≤ 6 years old living in same household, current smoking habit, current alcohol drinking habit, coffee intake, and green tea intake.
ORs of green tea intake for pneumonia were 1.22 (95%CI 0.68–2.19) in those who drank one or two cups a day compared to those who drank less than one cup, 1.18 (0.67–2.05) in those who drank three or four cups, and 1.08 (0.61–1.93) in those who drank five or more cups.
In Sub analysis (1), characteristics of BMI, prevalence of hypertension, diabetes mellitus and heart disease and ADL differed between the cases and the controls (Table 1(b)). As shown in Table 3, the OR of coffee intake for pneumonia was 0.49 (95% CI 0.26–0.93, p = 0.029) in those who drank two or more cups a day compared to those who did not drink coffee. In Sub analysis (2), only the BMI characteristics differed between the cases and the controls (Table 1(b)). The OR of those who drank two or more cups of coffee a day was 0.56 (0.30–1.07, 0.078) (Table 4).
Table 3.
Odds ratio of coffee intake for pneumonia in Sub analysis (1).
Cases | Controls without respiratory disease | Adjusted OR * | 95% CI | P | |||
---|---|---|---|---|---|---|---|
(N = 199) | (N = 216) | ||||||
n | (%) | n | (%) | ||||
Coffee intake (daily) | |||||||
None | 52 | (26) | 34 | (16) | 1.00 | ||
< 1 cup | 49 | (25) | 57 | (26) | 0.60 | 0.32–1.11 | 0.105 |
1 cup | 51 | (26) | 58 | (27) | 0.65 | 0.34–1.21 | 0.174 |
≥ 2 cups | 47 | (24) | 67 | (31) | 0.49 | 0.26–0.93 | 0.029 |
(Trend p = 0.054) |
*Variables included in model: sex, age, vaccination status (pneumococcal, influenza), BMI, underlying disease (hypertension, diabetes mellitus, heart disease), ADL, children ≤ 6 years old living in same household, current smoking habit, current alcohol drinking habit, coffee intake, and green tea intake.
Table 4.
Odds ratio of coffee intake for pneumonia in Sub analysis (2).
Cases | Controls with respiratory disease | Adjusted OR * | 95% CI | P | |||
---|---|---|---|---|---|---|---|
(N = 199) | (N = 158) | ||||||
n | (%) | n | (%) | ||||
Coffee intake (daily) | |||||||
None | 52 | (26) | 32 | (20) | 1.00 | ||
< 1 cup | 49 | (25) | 32 | (20) | 0.98 | 0.51–1.87 | 0.943 |
1 cup | 51 | (26) | 45 | (28) | 0.76 | 0.40–1.42 | 0.386 |
≥ 2 cups | 47 | (24) | 49 | (31) | 0.56 | 0.30–1.07 | 0.078 |
(Trend p = 0.055) |
*Variables included in model: same as Table 3.
In a sensitivity analysis of subjects without diabetes mellitus as an underlying disorder, the OR of those who drank two or more cups of coffee a day was 0.46 (95% CI 0.26–0.83, p = 0.010) compared to those who did not drink coffee (Table 5).
Table 5.
Odds ratio of coffee intake for pneumonia excluding subjects with diabetes mellitus (sensitivity analysis) (N = 450).
Coffee intake (daily) | Cases | Controls | Sex and age adjusted OR | 95% CI | P | Adjusted OR * | 95% CI | P | ||
---|---|---|---|---|---|---|---|---|---|---|
(N = 171) | (N = 279) | |||||||||
n | (%) | n | (%) | |||||||
None | 48 | (28) | 55 | (20) | 1.00 | 1.00 | ||||
< 1 cup | 42 | (25) | 66 | (24) | 0.71 | 0.41–1.24 | 0.231 | 0.74 | 0.42–1.33 | 0.315 |
1 cup | 42 | (25) | 73 | (26) | 0.64 | 0.37–1.11 | 0.115 | 0.66 | 0.37–1.17 | 0.156 |
≥ 2 cups | 39 | (23) | 85 | (30) | 0.50 | 0.28–0.87 | 0.014 | 0.46 | 0.26–0.83 | 0.010 |
(Trend p = 0.014) | (Trend p = 0.010) |
*Variables included in model: sex, age, vaccination status (pneumococcal, influenza), BMI, underlying disease (respiratory disease, hypertension, heart disease), ADL, children ≤ 6 years old living in same household, current smoking habit, current alcohol drinking habit, coffee intake, and green tea intake.
Discussion
We investigated the association between coffee and green tea intake and pneumonia among the elderly using hospital-based case–control study. Our study found a significant reduction in the OR for pneumonia in elderly individuals who drank ≥ 2cups/day of coffee compared to non-coffee drinkers. Our subjects without diabetes mellitus were also shown similar association.
Because in hospital-based case–control studies, it is desirable to select controls for different diseases to reduce bias, we recruited controls from the respiratory department and other departments. However, as a result of visiting a clinical department that has been examined in the past, there were patients who did not currently have respiratory disease but visited the respiratory department, and patients who currently have respiratory disease but visited other departments. So, when we performed the Sub analysis (1) in which the controls were limited to patients without respiratory disease and the Sub analysis (2) in which the controls were limited to patients with respiratory disease, the association between coffee intake and pneumonia were similar.
A large prospective cohort study in the United States showed an inverse association between coffee intake and total death, and there were inverse association between coffee intake and chronic respiratory diseases and pneumonia and influenza in deaths by cause3. Other cohort studies have also reported an inverse association between coffee intake and death from respiratory diseases (pneumonia, influenza, chronic obstructive pulmonary disease, and related symptoms)4,14. These findings suggest that coffee may have a preventive influence for chronic and acute respiratory diseases.
It has been reported that the constituents contained in coffee have various health benefits. There are several reports on the preventive association between coffee consumption and chronic respiratory disease and asthma15. Caffeine contained in coffee has arousal effect, inotropic effect, diuretic effect, and respiratory function improving effect, and theophylline of its metabolites, has bronchodilation, stimulation of respiratory center, and anti-inflammatory effect16. In addition, coffee components such as caffeine, chlorogenic acid, and trigonelline have been reported to have antibacterial activity17–22.
There are also some research reports on the association between coffee and intestinal flora. Mills CE and colleagues have tested in vitro that chlorogenic acid, a type of polyphenol abundant in coffee beans23, improves the balance of the gut flora24. In addition, arabinogalactan contained in coffee beans has an effect of growing specific bifidobacteria25, and bifidobacteria grown in the large intestine have a function of activating immune cells26. Because the intestinal flora changes with aging, for example the number of bifidobacteria that work well for the body reduce significantly after the age of sixty27, these coffee components may have a beneficial effect on the gut flora. The role of these components in coffee may have played a role in reducing the risk of pneumonia in the elderly seen in this study.
Green tea consumption was associated with a lower risk of death from pneumonia in Japanese women28. A Japanese cohort study reported that men who drank green tea had a reduced hazard ratio (HR) for respiratory disease-related mortality.5 We could not elucidate the association between green tea consumption and pneumonia. If caffeine was involved in the development of pneumonia, the amount of caffeine contained in 2 cups of coffee in this study is equivalent to 6 cups of green tea, so it is necessary to consider it in those who drink a lot of green tea (100 ml of beverage contains about 20 mg of caffeine for sencha and about 60 mg for regular and instant coffee29).
In the present study, the following limitations may have influenced the research results. First, information on intake of coffee and green tea was self-reported, and measurement of actual intake amount could not be made. Secondly, we didn't examine the detailed types of coffee and green tea that they ingested, so we could not investigate the association between the constituents of these drinks and pneumonia. The constituents of coffee differ depending on bean type, roasting method, instant, drip, or non-caffeine, and many kinds of tea are drunk in Japan, and the constituents are different depending on the type of green tea. Third, these drinking habits were information within the past month from the time of participation in this study, so the effects of long-term habits may not be considered. Because this study is hospital-based, controls may have changed their lifestyle within the past month due to their medical condition, and the possibility of reverse causality cannot be ruled out. Fourth, the possibility of confounding by associated factors that we did not examine is undeniable. For example, when examining the association between lifestyle and disease, socioeconomic status may affect lifestyle30, but we could not include it in our model as a potential confounder. Finally, because the study was conducted at 24 medical institutions in seven regions of Japan of different sizes, the severity of cases may vary between hospitals and clinics. Therefore, when a stratified analysis was performed at the hospital (with beds) and clinic (without beds), there was no difference in the association between coffee intake and pneumonia (Supplementary Table). However, since our study is a hospital-based case-contol study, in order to apply our result to the general elderly and the elderly with some diseases, further studies with more subjects and regions are needed.
Conclusions
We examined the association between coffee and green tea intake and elderly pneumonia. A decrease in OR for pneumonia was suggested in those who drank more than two cups of coffee per day compared to those who did not. The intake of green tea was not related to pneumonia. Further studies are needed to clarify the association between coffee intake and pneumonia.
Supplementary information
Abbreviations
- ADL
Activities of daily living
- OR
Odds ratio
- CI
Confidence interval
- HR
Hazard ratio
Author contributions
K.K. contributed to the conceptualization, data curation, formal analysis, methodology, software, validation, visualization, writing—original draft and writing—review & editing. K.S. contributed to the conceptualization, methodology, project administration and writing—review & editing. M.W. contributed to the conceptualization, investigation, methodology, resources and writing—review & editing. S.O. and W.F. contributed to the conceptualization, data curation, formal analysis, methodology, software, validation and writing—review & editing. A.M. contributed to the conceptualization, methodology and writing—review & editing. Y.H. contributed to the conceptualization, funding acquisition, methodology, supervision and writing—review & editing. S.A., S.K., S.I., K.Y., N.M., N.F. and the other members of the Pneumonia in Elderly People Study Group contributed to the investigation, resources and writing—review & editing. All authors read and approved the final draft of the article.
Funding
This study was supported by Health and Labour Science Research Grants from the Ministry of Health, Labour and Welfare of Japan (Grant H20-SHINKO-IPPAN-003, H26-SHINKO-GYOSEI-SHITEI-003). The funders of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.
Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Competing interests
The authors declare no competing interests.
Footnotes
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Contributor Information
Kyoko Kondo, Email: kyou@med.osaka-cu.ac.jp.
The Pneumonia in Elderly People Study Group:
Kanzo Suzuki, Masakazu Washio, Kyoko Kondo, Satoko Ohfuji, Akiko Maeda, Wakaba Fukushima, Yoshio Hirota, Satoru Adachi, Sakae Kan, Seiichiro Imai, Kunihiko Yoshimura, Naoyuki Miyashita, Nobumitsu Fujisawa, Noriko Kojimahara, Chiharu Ota, Ikuji Usami, Munehiro Kato, Toshinobu Yamamoto, Kazuhide Yamamoto, Yoichi Nakanishi, Takanari Kitazono, Takafumi Matsumoto, Hideki Tashiro, Masahiko Taketomi, Tomoaki Iwanaga, Hiroko Nogami, Koichi Takano, Ken Tonegawa, Yoshimitsu Hayashi, Ikuo Ikeda, Shigeki Sugiyama, Masahiro Aoshima, Kei Nakashima, Yoshitaka Nakamori, Yasushi Seida, Yoshiko Kichikawa, Atsushi Nakamura, Yasuhito Iwashima, Yasuhiro Kojima, Yasuo Yamada, Hidekazu Kawamura, Toshiaki Niwa, Atsuro Kawai, Yuuji Ito, Emi Aoyama, Noriko Kusada, and Chizuko Sumida
Supplementary Information
The online version contains supplementary material available at 10.1038/s41598-021-84348-w.
References
- 1.Poole R, Kennedy OJ, Roderick P, Fallowfield JA, Hayes PC, Parkes J. Coffee consumption and health: umbrella review of meta-analyses of multiple health outcomes. BMJ. 2017;359:j5024. doi: 10.1136/bmj.j5024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Kim Y, Je Y, Giovannucci E. Coffee consumption and all-cause and cause-specific mortality: a meta-analysis by potential modifiers. Eur. J. Epidemiol. 2019;34(8):731–752. doi: 10.1007/s10654-019-00524-3. [DOI] [PubMed] [Google Scholar]
- 3.Loftfield E, Freedman ND, Graubard BI, Guertin KA, Black A, Huang W-Y, et al. Association of coffee consumption with overall and cause-specific mortality in a large US prospective cohort study. Am. J. Epidemiol. 2015;182(12):1010–1022. doi: 10.1093/aje/kwv146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Saito E, Inoue M, Sawada N, Shimazu T, Yamaji T, Iwasaki M, et al. Association of coffee intake with total and cause-specific mortality in a Japanese population: the Japan Public Health Center-based Prospective Study. Am. J. Clin. Nutr. 2015;101(5):1029–1037. doi: 10.3945/ajcn.114.104273. [DOI] [PubMed] [Google Scholar]
- 5.Saito E, Inoue M, Sawada N, Shimazu T, Yamaji T, Iwasaki M, et al. Association of green tea consumption with mortality due to all causes and major causes of death in a Japanese population: the Japan Public Health Center-based Prospective Study (JPHC Study) Ann. Epidemiol. 2015;25(7):512–518.e3. doi: 10.1016/j.annepidem.2015.03.007. [DOI] [PubMed] [Google Scholar]
- 6.Annual Statistical Report of National Health Conditions Health Welfare Stat. Assoc. 2014;61:49–82. [Google Scholar]
- 7.Kondo K, Suzuki K, Washio M, Ohfuji S, Fukushima W, Maeda A, et al. Association between monovalent influenza A (H1N1) pdm09 vaccine and pneumonia among the elderly in the 2009–2010 season in Japan: a case-control study. Hum. Vaccin. Immunother. 2015;11(5):1088–1093. doi: 10.1080/21645515.2015.1016668. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Kondo K, Suzuki K, Washio M, Ohfuji S, Fukushima W, Maeda A, et al. Effectiveness of 23-valent pneumococcal polysaccharide vaccine and seasonal influenza vaccine for pneumonia among the elderly—selection of controls in a case-control study. Vaccine. 2017;35:4806–4810. doi: 10.1016/j.vaccine.2017.07.005. [DOI] [PubMed] [Google Scholar]
- 9.Suzuki K, Kondo K, Washio M, Nakashima K, Kan S, Imai S, et al. Preventive effects of pneumococcal and influenza vaccines on community-acquired pneumonia in older individuals in Japan: a case-control study. Hum. Vaccin. Immunother. 2019;15(9):2171–2177. doi: 10.1080/21645515.2019.1584023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.National Institute of Infectious Diseases Infectious Disease Surveillance Center Infectious agents surveillance report 2010, 31: 248–250 (in Japanese).
- 11.WHO: Obesity: Preventing and managing the global epidemic: report of a WHO Consultation on Obesity, Geneva, 3–5 June 1997 (WHO, Geneva, 1998).
- 12.Ding M, Bhupathiraju SN, Chen M, van Dam RM, Hu FB. Caffeinated and decaffeinated coffee consumption and risk of type 2 diabetes: a systematic review and a dose-response meta-analysis. Diabetes Care. 2014;37(2):569–586. doi: 10.2337/dc13-1203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Oba S, Nagata C, Nakamura K, Fujii K, Kawachi T, Takatsuka N, Shimizu H. Consumption of coffee, green tea, oolong tea, black tea, chocolate snacks and the caffeine content in relation to risk of diabetes in Japanese men and women. Br. J. Nutr. 2010;103(3):453–459. doi: 10.1017/S0007114509991966. [DOI] [PubMed] [Google Scholar]
- 14.Freedman ND, Park Y, Abnet CC, Hollenbeck AR, Sinha R. Association of coffee drinking with total and cause-specific mortality. N Engl J Med. 2012;366(20):1891–1904. doi: 10.1056/NEJMoa1112010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Welsh EJ, Bara A, Barley E, Cates CJ. Caffeine for asthma. Cochrane Database Syst Rev. 2010;1:CD001112. doi: 10.1002/14651858.CD001112.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Aubier M. Effect of theophylline on diaphragmatic and other skeletal muscle function. J. Allergy Clin. Immunol. 1986;78:787–792. doi: 10.1016/0091-6749(86)90062-X. [DOI] [PubMed] [Google Scholar]
- 17.Pawar P, Bikkad S, Kurhade S, Kadbane S. Evaluation of antibacterial activity of caffeine. International Journal of Research in Ayurveda and Pharmacy. 2011;2(4):1354–1357. [Google Scholar]
- 18.Nonthakaew A, Matan N, Aewsiri T, Matan N. Caffeine in foods and its antimicrobial activity. Int. Food Res. J. 2015;22(1):9–14. [Google Scholar]
- 19.Lou Z, Wang H, Zhu S, Ma C, Wang Z. Antibacterial activity and mechanism of action of chlorogenic acid. J. Food Sci. 2011;76(6):M398–403. doi: 10.1111/j.1750-3841.2011.02213.x. [DOI] [PubMed] [Google Scholar]
- 20.Wang L, Bi C, Cai H, Liu B, Zhong X, Deng X, et al. The therapeutic effect of chlorogenic acid against Staphylococcus aureus infection through sortase A inhibition. Front Microbiol. 2015;6:1031. doi: 10.3389/fmicb.2015.01031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Peddie BA, Wood JE, Lever M, Happer DA, de Zwart F, Chambers ST. Assessment of antimicrobial activity of hydrophilic betaines in osmotically stressed bacteria. Antonie Van Leeuwenhoek. 2003;83(2):175–181. doi: 10.1023/A:1023305326164. [DOI] [PubMed] [Google Scholar]
- 22.Yi TL, Shah M, Raulji D, Dave D. Comparative evaluation of antimicrobial efficacy of coffee extract and 0.2% chlorhexidine mouthwash on the periodontal pathogens Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans: an in vitro study. Adv. Human Biol. 2016;6(2):99–103. doi: 10.4103/2321-8568.190316. [DOI] [Google Scholar]
- 23.Mills CE, Oruna-Concha MJ, Mottram DS, Gibson GR, Spencer JP. The effect of processing on chlorogenic acid content of commercially available coffee. Food Chem. 2013;141(4):3335–3340. doi: 10.1016/j.foodchem.2013.06.014. [DOI] [PubMed] [Google Scholar]
- 24.Mills CE, Tzounis X, Oruna-Concha MJ, Mottram DS, Gibson GR, Spencer JP. In vitro colonic metabolism of coffee and chlorogenic acid results in selective changes in human faecal microbiota growth. Br. J. Nutr. 2015;113(8):1220–1227. doi: 10.1017/S0007114514003948. [DOI] [PubMed] [Google Scholar]
- 25.Hori M, Iwai K, Kimura R, Nakagiri O, Takagi M. Utilization by intestinal bacteria and digestibility of Arabinogalactan from coffee bean in vitro. Jpn. J. Food Microbiol. 2007;24(4):163–170. doi: 10.5803/jsfm.24.163. [DOI] [Google Scholar]
- 26.Namba K, Hatano M, Yaeshima T, Takase M, Suzuki K. Effects of Bifidobacterium longum BB536 administration on influenza infection, influenza vaccine antibody titer, and cell-mediated immunity in the elderly. Biosci. Biotechnol. Biochem. 2010;74(5):939–945. doi: 10.1271/bbb.90749. [DOI] [PubMed] [Google Scholar]
- 27.Odamaki T, Kato K, Sugahara H, Hashikura N, Takahashi S, Xiao J, et al. Age-related changes in gut microbiota composition from newborn to centenarian: a cross-sectional study. BMC Microbiol. 2016;16:90. doi: 10.1186/s12866-016-0708-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Watanabe I, Kuriyama S, Kakizaki M, Sone T, Ohmori-Matsuda K, Nakaya N, et al. Green tea and death from pneumonia in Japan: the Ohsaki cohort study. Am. J. Clin. Nutr. 2009;90(3):672–679. doi: 10.3945/ajcn.2009.27599. [DOI] [PubMed] [Google Scholar]
- 29.Science and Technology Agency. Standard Tables of Food Composition in Japan, The fifth revised edition (in Japanese). Tokyo: Printing Bureau, Ministry of Finance; 2000.
- 30.Wang J, Geng L. Effects of socioeconomic status on physical and psychological health: lifestyle as a mediator. Int. J. Environ. Res. Public Health. 2019;16(2):281. doi: 10.3390/ijerph16020281. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.