Context Coffee has several metabolic effects that could reduce
the risk of gallstone formation.
Objective To examine the association between coffee consumption
and the risk of symptomatic gallstone disease in men.
Design and Setting The Health Professionals Follow-up Study, a
prospective cohort study, in which the consumption of coffee and other
caffeinated drinks was assessed starting in 1986 as part of the
131-item food frequency questionnaire given to US male health
professionals with follow-up through 1996.
Participants A total of 46,008 men, aged 40 to 75 years in
1986, without history of gallstone disease.
Main Outcome Measures Newly symptomatic gallstone disease
(diagnosed by ultrasonography or x-ray) or a cholecystectomy.
Results During 404,166 person-years of follow-up, 1081
subjects reported symptomatic gallstone disease, of whom 885 required
cholecystectomy. After adjusting for other known or suspected risk
factors, compared with men who did not consume regular coffee in 1986
and 1990, the adjusted relative risk (RR) for those who consistently
drank 2 to 3 cups of regular coffee per day was 0.60 (95% confidence
interval [CI], 0.42-0.86) and for those who drank 4 or more cups per
day the RR was 0.55 (95% CI, 0.33-0.92). All coffee brewing methods
showed a decreased risk. The risk of symptomatic gallstone disease also
declined with increasing caffeine intake (P for
trend=.005). After controlling for known or suspected
risk factors, the RR for men in the highest category of caffeine intake
(>800 mg/d) compared with men in the lowest category (≤25 mg/d) was
0.55 (95% CI, 0.35-0.87). In contrast, decaffeinated coffee was not
associated with a decreased risk.
Conclusions In this cohort of US men, coffee consumption may have
helped to prevent symptomatic gallstone disease.
Gallstone disease affects more than 20 million Americans and causes
800,000 hospitalizations each year,1 with a direct
cost of more than $2 billion.2 Coffee is one of the most
widely consumed beverages in the country,3 and coffee and
individual coffee constituents affect various metabolic processes that
are involved in cholesterol lithogenesis. Coffee stimulates
cholecystokinin release,4 increases gallbladder
motility,5 and possibly enhances large bowel
motility.6 Caffeine inhibits biliary cholesterol
crystallization,7 decreases gallbladder fluid
absorption,8 and increases hepatic bile flow.9
Cafestol, a lipid component contained in coffee beans, may affect bile
cholesterol concentration.10 Thus, metabolic studies
addressing the effects of coffee suggest a possible preventive role of
coffee consumption on risk for gallstone formation.4-9
Given widespread consumption of coffee and the high prevalence of
gallstone disease, any association between these would have
considerable clinical and public health relevance. However,
epidemiological evidence regarding the relationship between coffee
consumption and gallstone disease is sparse, with most studies
compatible with a decreased risk of gallstone disease among persons
with high coffee intakes,11-15 but some suggesting an
increased risk.16-18 The lack of a statistically
significant association observed in all but 1 prospective
study11 may be due to imprecise assessments of coffee
intake, limited control for potential confounders, or small sample
sizes.
Although gallstone occurrence and mild symptoms related to
gallstones are less frequent in men than in women,19 severe
biliary events leading to surgery are equally common among both sexes
after gallstones have developed.20 To address further the
association between coffee and caffeine consumption and symptomatic
gallstone disease, we examined intake of coffee, tea, decaffeinated
coffee, caffeinated soft drinks, and caffeine from all sources as well
as coffee brewing methods in relation to risk of symptomatic gallstone
disease in a large cohort of US men.
The Health Professionals Follow-up Study began in 1986 when
51,529 US male dentists, veterinarians, optometrists,
osteopathic physicians, and podiatrists who were 40 to 75 years of age
returned a mailed questionnaire regarding diet and medical
history.21 Follow-up questionnaires were sent biennially to
update information on exposures and newly diagnosed illnesses. Diet was
assessed in 1986, 1990, and 1994. For this analysis, we excluded men
who reported a cholecystectomy or gallstone diagnosis at baseline, men
with cancer (other than nonmelanoma skin cancer) prior to 1986, men
with an energy intake outside the range of 3347 to 17,572 kJ/d
(800-4200 kcal/d), men with 70 or more blank food items, and men
providing no information on beverage consumption. After exclusions, the
study population consisted of 46,008 eligible men who were
followed up from 1986 to 1996. The overall follow-up response was 94%.
The consumption of regular coffee, decaffeinated coffee, tea, and
caffeinated soft drinks was assessed in 1986 as part of a 131-item
semiquantitative food frequency questionnaire.22 For each
beverage, a commonly used portion size was specified, and the
participants were asked how often, on average over the past year, they
consumed that amount. There were 9 possible response categories ranging
from "never" or "less than once per month" to "6 times or
more per day." Standard portion sizes were specified as 1 cup for
coffee or tea, and 1 glass, bottle, or 354 mL (12 oz) can for
caffeinated soft drinks. Caffeine intake was calculated by multiplying
the frequency of consumption of each beverage by the caffeine content
of the specified portion size. Total caffeine intake for each
participant was computed as the sum of the contributions from regular
coffee (79% of the total for all participants), tea (12%),
caffeinated soft drinks (7%), and decaffeinated coffee, cocoa,
chocolate, cookies, brownies, and candies (2%). To distinguish between
methods of preparing coffee, on the 1990 questionnaire participants
were asked to report whether they consumed mainly filtered, instant, or
espresso type coffee.
To assess the validity of self-reported coffee consumption,
estimated intakes from the food frequency questionnaire were compared
with those from two 7-day dietary records in a sample of 127 Boston,
Mass, area participants who had returned the 1986 baseline
questionnaire and a second questionnaire in 1987.22 The
Spearman correlation coefficient between coffee use as assessed by the
questionnaires compared with the diet records was 0.82.23
(The Spearman correlation coefficient is a nonparametric measure of the
strength and the direction of the relationship ranging from −1.0,
perfect inverse correlation; 0, no correlation; +1.0, perfect positive
correlation).
Assessment of Gallstone Cases
In 1986 and on each follow-up questionnaire, participants were asked
whether they had undergone a cholecystectomy or had been diagnosed as
having gallstones by a physician. Subjects were also asked whether the
gallstone diagnosis had been confirmed by ultrasonography or x-ray and
whether their gallstones were symptomatic. To verify the self-reports
of cholecystectomy and diagnosed but unremoved gallstones, we reviewed
a sample of 441 medical records of subjects who reported a
cholecystectomy or gallstones and of these, all but 5 confirmed the
diagnosis. Furthermore, all self-reported symptoms and all but 1 of the
self-reported diagnostic procedures were confirmed by medical record
review. Although we did not assess the composition of the gallstones,
in a similar cohort of men, nearly 80% were cholesterol or mixed
stones.24
For each participant, follow-up time accrued from the month of return
of the 1986 questionnaire and ended at the month of cholecystectomy,
diagnosis of symptomatic gallstones, death, or the end of the study
period, whichever occurred first. Relative risks (RRs) were calculated
as the incidence rate of symptomatic gallstone disease among men in
different categories of exposure compared with the incidence rate among
men in a specified reference group. Age-adjusted RRs were calculated
using the Mantel-Haenszel rate ratio,25 and tests for trend
were computed using the Breslow and Day χ statistic.26
For multivariate analyses, pooled logistic regression with 2-year time
increments27 was used to estimate the RRs of symptomatic
gallstone disease. This method accounts for varying time to the outcome
event and is asymptotically equivalent to Cox regression if the time
intervals are short and the probability of an event is small for each
interval.28 The basic model included biennially updated
age, body mass index (calculated as weight in kilograms divided by the
square of height in meters), recent weight change, history of diabetes
mellitus, smoking, physical activity, intake of cholesterol-lowering
drugs, thiazide diuretics, and nonsteroidal anti-inflammatory drugs.
Intakes of alcohol, energy-adjusted dietary fiber, energy-adjusted
carbohydrates, and energy-adjusted dietary fat were also included in
the basic model and were updated every 4 years. Tests for linear trend
were calculated by assigning the median coffee intake for categories
treated as a continuous variable.
In a subanalysis, we corrected the RR estimate of coffee consumption
for measurement error by using data from our validation
study.29 This procedure provides an estimate of the
association unattenuated by the effects of measurement
error.30 All RRs are presented with 95% confidence
intervals (CIs), and reported P values are based on 2-sided
tests.
During 404,166 person-years of follow-up, we
documented 1081 cases of self-reported symptomatic gallstone disease,
of which 885 required cholecystectomy. Sixty-nine percent of the
participants reported drinking regular coffee, 52% drank decaffeinated
coffee, 56% drank tea, and 64% drank caffeinated soft
drinks at least once per month. Compared with nondrinkers, men who
drank regular coffee smoked more, consumed more dietary fat and less
dietary fiber, and exercised less; but they drank more alcohol and had
a lower carbohydrate intake (Table
1).
In multivariate analyses, intake of regular coffee had a strong,
inverse association with risk of symptomatic gallstone disease
(P value, test for trend, <.001). Compared with men with no
consumption of regular coffee, the RR for those who drank 4 or more
cups of regular coffee per day was 0.67 (95% CI, 0.53-0.84) (Table 2).
To examine the possibility that latent gallstone symptoms caused a
decrease in coffee consumption, thereby biasing our results, we
conducted an analysis excluding all cases that occurred during the
first 2-year follow-up period. The relationship became slightly
stronger (RR for men consuming ≥4 cups of regular coffee per day
compared with men with no consumption of regular coffee, 0.64; 95% CI,
0.49-0.84).
To evaluate the potential for bias due to an increased medical
surveillance among men with no consumption of regular coffee, we
additionally excluded men without a routine medical check-up between
1986 and 1988. The RR for men consuming 4 or more cups of regular
coffee per day compared with men with no consumption of regular coffee
was 0.59 (95% CI, 0.42-0.82). When we additionally excluded cases that
occurred during the first 4 years of follow-up, the RR was 0.75 (95%
CI, 0.53-1.06).
We further addressed the possibility of detection bias by excluding
cases with unremoved gallstones (who were presumably less symptomatic)
and limiting the analysis to cholecystectomy cases. The RR for men
consuming 4 or more cups of regular coffee per day compared with men
with no consumption of regular coffee was 0.69 (95% CI, 0.53-0.89).
We next cumulatively updated coffee exposure in 1990 and in 1994 to
provide a better estimate of the effect of long-term average coffee
consumption. Specifically, the incidence of symptomatic gallstone
disease from 1986 through 1990 was related to the average intake
reported on the 1986 questionnaire, the incidence from 1990 through
1994 was related to average intake reported on the 1986 and 1990
questionnaires, and the incidence from 1994 through 1996 was related to
average intake reported on the 1986, 1990, and 1994 questionnaires. The
RR among men drinking 4 or more cups of regular coffee per day compared
with men with no consumption of regular coffee was 0.60 (95% CI,
0.46-0.79).
The inverse association was stronger among men with evidence of
consistent coffee intake over time. Considering cases that occurred
after 1990 only, men who consistently reported drinking 2 to 3 cups of
regular coffee
per day in the 1986 and 1990 questionnaires had
an RR of 0.60 (95% CI, 0.42-0.86), and those drinking 4 or more cups
of regular coffee per day had an RR of 0.55 (95% CI, 0.33-0.92)
compared with men who in 1986 and in 1990 consistently reported no
consumption of regular coffee (Table
3).
To examine the impact of measurement error in our assessment of
coffee intake, we used regular coffee as a continuous variable in a
multivariate logistic model. An increase in coffee consumption of 1 cup
per day was associated with an RR of 0.94 (95% CI, 0.91-0.98). After
correction for measurement error, the RR was 0.91 (95% CI, 0.86-0.98).
We also looked for possible differences in the association of coffee
brewing method with symptomatic gallstone disease. For this
subanalysis, we used 469 cases of gallstone disease occurring between
1990 and 1996 with no missing information on brewing methods. After
mutually adjusting for brewing methods and using nondrinkers of regular
coffee as the common reference group, the RR of symptomatic gallstone
disease for men consuming any level of regular filtered coffee was 0.77
(95% CI, 0.62-0.96), for men consuming regular instant coffee, the RR
was 0.74 (95% CI, 0.53-1.04), and for men consuming regular espresso,
the RR was 0.68 (95% CI, 0.43-1.08).
We examined the association between caffeine and risk for symptomatic
gallstone disease. Higher intakes of caffeine were associated with a
decreasing risk of gallstone disease (P value, test for trend,
.005). The RR for men in the highest category of caffeine intake
(>800 mg/d, equivalent to ≥5-6 cups of coffee per day) compared with
men in the lowest category (≤25 mg/d, equivalent to less than one
fifth of a cup of coffee per day) was 0.55 (95% CI, 0.35-0.87) (Table 4).
No significant associations were observed between the consumption of
tea, decaffeinated coffee, or low-calorie types of caffeinated soft
drinks and the risk of gallstone disease. A positive association was
observed for regular types of caffeinated soft drinks and gallstone
disease (based on 22 cases), although the trend was not statistically
significant (Table 2).
In this large prospective cohort study among men, we found a strong
inverse association between consumption of regular
coffee and risk of symptomatic gallstone disease. All brewing methods
showed a decreased risk. No association was observed with intake of
decaffeinated coffee or tea. The lack of association we observed with
decaffeinated coffee and tea may be due to the low amount of caffeine
in these beverages in our study population; men drinking 4 or more cups
of decaffeinated coffee per day consumed only 140 mg/d of caffeine from
all sources (approximately equivalent to 1 cup of regular coffee), and
tea usually contains less than half the caffeine of regular coffee. In
spite of the fact that we found a positive association with caffeinated
soft drinks, only 1 multivariate RR value was statistically
significant, and this finding was based on a small sample of 22 cases.
Furthermore, the data did not appear to follow any significant
dose-dependent trend.
Epidemiological data concerning the relationship between coffee and
gallstone disease are sparse. Our results are consistent with a
previous prospective Italian study using ultrasonography to assess
cholelithiasis, which reported an odds ratio of 0.62 (95% CI,
0.40-0.98) for any vs no coffee drinking.11 One prospective
study,12 1 case-control study,13 and 2
cross-sectional surveys14,15 also found inverse
associations with coffee drinking.
In contrast, 1 cross-sectional survey16 and 1 case-control
study17 observed positive associations with coffee intake,
and 1 prospective study18 reported an inverse relationship
with brewed coffee and a positive relationship with instant coffee.
Thus, most studies that have examined this relationship support a
benefit of coffee consumption in preventing gallstone disease. However,
most studies were not statistically significant,12-18 some
did not address the dose-response relationship,11,12 and
others could not rule out that coffee consumption may have been altered
by the disease.14-16
Because our study restricted the outcome to men with symptomatic
gallstone disease, the results may not be generalizable to all
gallbladder disease. However, our analysis focuses on the clinically
most relevant fraction of the disease.
Because no systematic screening of the study subjects with
ultrasonography or other imaging tests for the presence of gallstones
was performed, it is likely that there was considerable
underascertainment of gallstones in this population, as most gallstones
are asymptomatic.31 Thus, some of the gallstone cases were
present but undiagnosed at baseline and may have preceded the reporting
of coffee consumption. However, because it seems unlikely that the
presence of asymptomatic gallstones at baseline is associated with the
men's reporting of coffee consumption, this bias could not have been
responsible for the decreased risk of symptomatic gallstone disease
that we observed among men who consumed coffee in this study.
We considered the possibility of detection bias because coffee may
cause pain in gallstone patients.32 Although some men who
may have reduced or avoided coffee consumption because they had
gastrointestinal symptoms could have consulted a physician more
frequently, thus increasing the detection rate of gallstone disease,
the magnitude of this bias would have to be substantial to account for
the strong observed inverse association. Moreover, the relationship
persisted after we excluded the first 2 years of follow-up, men without
a routine medical check-up between 1986 and 1988, and men with
unremoved gallstones who were presumably less symptomatic and more
prone to detection bias.
The possibility of misclassification was of concern because information
on
coffee intake was collected by self-report.
However, this cohort provides accurate and reliable information on
coffee consumption.23 Moreover, the correlation coefficient
for consumption in 1986 and 1990 was 0.57, indicating that coffee
intake tracks over time. Because the data concerning coffee consumption
were gathered before the onset of symptoms of gallstone disease,
misclassification would be nondifferential between cases and noncases
and would tend to weaken any true relationship.
Extensive information on multiple risk factors enabled us to adjust for
the effects of known confounding variables. However, we cannot rule out
the possibility that the associations we observed were partly
attributable to unmeasured dietary, behavioral, or genetic factors.
Several physiological mechanisms support a causal relationship between
coffee intake and lower risk of gallstone disease. Coffee stimulates
cholecystokinin release,4 enhances gallbladder
contractility,5 and may increase colonic
motility,6 factors that are related to development of
cholesterol gallstone disease.
The inverse association between coffee intake and gallstone
disease may be due specifically to the effect of caffeine. In animal
models, caffeine prevents cholesterol crystallization,7
possibly by inhibiting gallbladder fluid absorption,8 which
is increased in the early stages of cholesterol
lithogenesis.33 Caffeine and other methylxanthines are
excreted via the bile34 and may decrease bile cholesterol
saturation by increasing bile flow35 or by stimulating
ileal bile acid absorption36 and hepatic bile acid
uptake.37 In addition, caffeine possesses significant
thermogenic properties and could exert a preventive influence on
gallstone development by increasing energy expenditure and reducing
body fat stores.38
In addition to caffeine, 1 or more of the many ingredients in coffee
may contribute to the inverse relationship. For example, an insoluble
hemicellulose fiber contained in coffee39 may decrease the
colonic absorption of deoxycholic acid. Because coffee is rich in
antioxidative compounds such as caffeic acid and other
phenolics,40 the protective effect of coffee on gallstone
formation could be mediated by an inhibition of reactive oxygen
metabolites,41 which appear to precede the formation of
cholesterol monohydrate crystals.42 Coffee may act through
the effect of magnesium, which is a coffee constituent43
and was inversely associated with gallstone disease in our data and in
a recent survey.44 Magnesium correlates inversely with
γ-glutamyltransferase levels and is essential in maintaining membrane
integrity and energy production,45 suggesting that it may
modulate hepatic enzyme activity and gallbladder motility.
A more speculative possibility linking coffee intake with decreased
gallstone risk is that certain lipid components contained in coffee
modulate hepatic cholesterol metabolism. Unfiltered coffee contains
cafestol and kahweol, which raise serum cholesterol
levels,46 possibly by decreasing hepatic low-density
lipoprotein receptor activity.47 The mechanism underlying
the downregulation of low-density lipoprotein receptors may involve
7α-hydroxylase and 3-hydroxy-3-methylglutaryl coenzyme A reductase
activity.10,47 If coffee diterpines decrease bile
cholesterol saturation, one might expect a lower risk of gallstone
disease among consumers of unfiltered coffee, such as espresso. Our
results show similar associations for filtered and unfiltered coffee.
In summary, these prospective data suggest a decreased risk of
symptomatic gallstone disease with higher intake of regular coffee. Our
results are most obviously generalizable to US men aged 40 years and
older. The magnitude of the association, the evidence of a
dose-response effect, the failure to explain this relationship on the
basis of other risk factors for gallstone disease, the existence of
several plausible metabolic pathways, and the consistency with results
from experimental studies all support the causal nature of this
association.
The fact that symptomatic gallstones are associated with
considerable morbidity and are currently the most common
digestive-related cause of hospitalization in the United
States48 underscores the significant implications of these
findings for health-related quality of life and the use of health care
resources. Further studies are needed to evaluate the apparent benefits
of coffee consumption for preventing gallstone disease and to assess
the potential therapeutic effects of coffee and individual coffee
components on gallstone disease. Because the overall effect of coffee
intake on health may vary considerably according to acute or chronic
consumption, level of intake, source and type of coffee, methods of
roasting and preparation of the brew, and the development of
tolerance,49 clinical recommendations on coffee consumption
should be based on the patients' individual health risks and benefits.
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