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Departments of Community, Occupational and Family Medicine [A. S. H-P. L.], Pathology [M. T.], and Medicine [W-C. T.], National University of Singapore, Singapore 117597; Departments of Pathology [W-T. P.] and Respiratory and Critical Care Medicine [P. E.], Singapore General Hospital, Singapore 169608; Department of Respiratory Medicine, Tan Tock Seng Hospital, Singapore 308433 [Y-T. W.]; and University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, California 90033 [M. C. Y.]
| Abstract |
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| Introduction |
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Heterocyclic amines are a group of compounds formed by pyrolysis of protein-containing foods, through a reaction between creatinine and amino acids and/or sugars (11) . The occurrence of this group of compounds in cooked meat products has been well documented (12, 13, 14, 15) , and they are known to be potent mutagens on the Ames test and carcinogenic in animal studies (16, 17, 18, 19, 20) . The role of these compounds in human carcinogenesis has yet to be confirmed, but recent epidemiological studies suggest that dietary intake of fried, well-done meat may be related to lung cancer (21) and breast cancer (22) . In animal studies, heterocyclic amines have been shown to induce tumors in lung tissue, among other sites (17 , 18) .
Apart from being present on the meat surface, heterocyclic amines have been identified in smoke condensates from frying of beef, pork, and fish (23, 24, 25) , and their formation is similarly temperature and time dependent (26) . Higher levels are produced during frying and grilling than other cooking methods (11) . These observations are consistent with findings that the volatile fraction produced by frying meat contributed a significant proportion of the total mutagenic activity in laboratory systems (23 , 27) . In addition, some but not all studies of occupational groups report an increased risk of respiratory tract cancers among cooks (5 , 28) . In contrast to dietary heterocyclic amines, the role of inhaled heterocyclic amines in cancer risk has not been examined.
Gender differences in smoking-related risk of lung cancer are increasingly being recognized. Women smokers appear to have a higher risk of lung cancer than male smokers in some but not all studies (2 , 29, 30, 31) . For example, the risk among smokers was 12.7 (95% CI 11.513.9) for females compared with 9.1 (8.310.0) for men from population-based data in Missouri (30) . These differences persist after adjusting for lifetime dose (32) and years since quitting (29) .
Compared with women of other ethnicities, Chinese women worldwide are known to have a high risk of lung cancer, despite a low smoking prevalence (9 , 33, 34, 35) . Domestic exposures, such as to fumes from cooking oils, have been implicated as a possible risk factor in studies among Chinese women in Asia (36, 37, 38) , but the exact carcinogens have not been identified. Stir-frying, which involves heating of oil in a wok to high temperatures before ingredients are added, is frequently used in Chinese home cooking and some mutagens identified in heated oils, particularly Chinese rapeseed oil, include formaldehye, acrolein, 1,3-butadiene, and benzene (39 , 40) .
Lung cancer is the third most common cancer among women in Singapore
(41)
, a small island republic with a population of 3.1
million, of which 78% are ethnic Chinese (42)
. Although
the pattern of disease in this country is rapidly evolving toward that
of the West (43)
, reflecting the changing lifestyle of the
population, the smoking prevalence in females is relatively low,
3%
(44)
. Lung cancer comprises 17.8% of cancers diagnosed
annually (41)
, and the incidence has been fairly stable
over the last 25 years (45)
. It was in this context that
we were interested to investigate the risks of lung cancer associated
with cooking exposures among women with a hospital-based case-control
study over a 30-month period from April 1, 1996 to September 30, 1998.
| Materials and Methods |
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During the study period, a total of 418 lung cancer patients were identified in the three hospitals. We excluded 38 cases (9.1%) who were too ill or who otherwise did not satisfy the eligibility criteria, leaving 380 women. Of these, 361 (95.0%) consented to the interview. Forty-four (12.2%) of these patients were diagnosed on clinical or radiological grounds and were excluded from the final analysis. We also excluded 2 (0.6%) patients with carcinoid tumors of the lung and 12 (3.3%) patients where pathological material was not available for review. Thus, in all a total of 303 microscopically confirmed lung cancer cases were included in this analysis. Both cases and controls gave written, informed consent for the interview and the tracing of their medical records.
Selection of Controls.
Controls were selected from hospital patients, frequency matched by
10-year age group, the hospital to which they were admitted, and date
of admission (within 2 months). For each stratum, two to three controls
were recruited per case. Patients who had a history of malignant or
chronic respiratory disease were excluded. We also excluded women with
long-standing illnesses that would preclude carrying out usual
activities, such as severe ischemic heart disease or renal failure.
A total of 789 eligible controls were approached, and of these, 765 (96.9%) consented to be interviewed. Control patients represented a wide range of conditions, of which 32.3% were diseases of the bones, joints, and connective tissue, 20.5% were admissions for acute traumatic injuries, and 12.4% were related to the gastrointestinal tract. An additional 8 and 6% of controls had illnesses of the cardiovascular and neurological systems, respectively.
Study Instrument.
All subjects were interviewed in-person using a standardized
questionnaire. Over the study period, a total of six research nurses
were responsible for data collection, and each interviewed both cases
and controls. Training and supervision were carried out by the same
investigator throughout. Interviewers were not blinded to case or
control status, but possible observer bias was monitored by recording
and reviewing at random a sample of interviews conducted by each nurse.
None of the interviews were carried out solely with next-of-kin, but
where necessary, relatives present with the subject at the time of
interview were allowed to give information that was corroborated by the
subject.
The study instrument elicited information on demographic variables, occupational history, personal and passive tobacco smoking history, past domestic cooking exposure, dietary intake of fruits and vegetables, family history of cancer, and preexisting lung disease among others. Because the only form of tobacco use reported among the subjects in this study was cigarette smoking, a smoker was defined as someone who had ever smoked at least one cigarette a day (either manufactured, hand-rolled cigarettes, or both) for a year or more. This group includes ex-smokers, defined as smokers who had stopped smoking for 1 year at the time of interview. Passive smoke exposure was defined as a positive answer to the question "Did any of your household members smoke (including spouse, parents, children, or any other relative/friend living with you) in your presence more often than once a week?" Intake of fruit and vegetables was measured as the average number of standardized servings per week, over the last 3 years, of 12 fruit items and 19 vegetables widely available and commonly eaten locally. For cooking exposure, patients were asked about the frequency of using various cooking methods, particularly stir-frying (e.g., "How often did you stir-fry food? How often did you stir-fry meat?") and types of oils (e.g., "How often did you use peanut oil for frying?") as their usual practice 2030 years before diagnosis. Subjects were also asked "How often did the air in your kitchen become filled with oily smoke during frying?" For each of these cooking exposures, there were six possible responses ranging from "never/less than yearly," "less than monthly," to "daily" and "more than once a day."
Statistical Analysis.
ORs4
and 95% CIs were calculated for risk of lung cancer for smokers and
nonsmokers separately. Analysis of the association between cooking
exposure and lung cancer risk was carried out using unconditional
logistic regression (46)
adjusting for age, fruit and
vegetable intake (as continuous variables), formal education
(dichotomous; none/one year or more), and place of birth (dichotomous;
local-born/China-born). Among ever smokers, duration of smoking (in
years) and intensity of smoking (number of cigarettes per day in two
groups: 15 sticks and 6+ sticks) were found on stepwise logistic
regression analysis to adequately explain the variation in risk
attributable to smoking. These were therefore entered as covariates
into the logistic regression model for computation of adjusted OR among
smokers. We examined risks associated with higher frequency of
stir-frying, stir-frying of meat, having a fume-filled kitchen during
cooking, and type of oil used. Reported frequency of cooking-related
exposure was grouped as "daily" (including more than once a day)
and "less than daily." The types of oil used for frying were
grouped into unsaturated (peanut and corn oil) and saturated (palm,
blended vegetable which contains mainly palm oil, and lard oil) for the
purposes of analysis. Subjects who indicated daily usage of an
unsaturated oil and less than daily usage of saturated oils were
classified as using "primarily unsaturated oil" and vice
versa. Where there was no clear distinction in frequency of use,
the subject was classified as using "both types equally." The
statistical software SAS 6.12 (SAS Institute, Inc., Cary, NC) was used
for data analysis. All Ps quoted are two-sided.
| Results |
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2 in the oldest age group and 3 in the
4059-year age group. Compared with controls, cases were less likely
to have received formal education (40% versus 53%), be
born in Singapore or Malaysia (67% versus 79%), and to
have ever been used outside the home (66% versus 73%).
There were altogether 227 smokers (current or ex-smokers), of which
63.9% smoked manufactured cigarettes, 25.6% hand-rolled cigarettes,
and 10.6% both types. Cases were markedly more likely to be smokers.
As expected, the median weekly number of servings of fruits and
vegetables was lower among cases than controls (21.7 and 28.0 standard
servings per week, respectively). Among nonsmokers, 391 (47%) reported
ever being exposed to passive smoke from household members more often
than once a week (data not shown).
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We observed significantly elevated risks of lung cancer among ex- and
current smokers compared with lifetime nonsmokers for all histological
types combined, after adjustment for age (Table 2)
. When examined separately by histology, the risk of squamous or small
cell carcinoma among current smokers (OR, 19.8; 95% CI, 11.538.4)
was an order of magnitude higher than for adenocarcinoma (OR, 2.2; CI,
1.33.7). Adjusting for passive smoking did not materially affect
these risk estimates (OR, 18.8 and 2.1, respectively) and the others
given in Table 2
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Table 4
also suggests that among smokers, those using primarily
unsaturated oil for frying experienced a higher risk (OR, 4.3) than
those using saturated oil or both types equally (combined OR, 2.2). The
risk estimates for those using saturated oil (OR, 2.3) or both types
equally (OR, 1.6) were similar, and thus they are grouped together in
Table 4
for stability. Among nonsmokers, there was no significant
association with either cooking oil category.
| Discussion |
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The major strengths of our investigation are the inclusion of incident cases that were microscopically confirmed and reviewed by two pathologists. The study population was homogeneous in terms of gender and ethnicity. All interviews were conducted in-person, and verification of information on smoking status against the medical records indicated a high degree of reproducibility. The potential weaknesses include the use of hospital controls, who may have been admitted for conditions linked to the exposures under study. Such an association, if positive, would bias the results toward the null, or if negative may artificially inflate a negative association between the exposure of interest and lung cancer. To our knowledge, there is no evidence suggesting a link between cooking and other common medical conditions, but nevertheless, we attempted to address this potential bias by drawing controls from as wide a range of medical conditions as possible and excluded those with preexisting malignancies and chronic lung disease. The potential for interviewer bias exists in all case-control studies. Although the research nurses were not blinded to case or control status, they were not apprised of the hypothesis under study. The consistent differential risks observed between smokers and nonsmokers also argue against interviewer bias; in addition, it is relevant to note that questions on cooking preceded those on smoking during the interview. Recall and reporting bias by subjects is an inherent concern in retrospective studies. Our questionnaire elicited information on cooking practices during the period 2030 years before cancer diagnosis, a time frame that was felt to be relevant in the etiology of the disease. Nondifferential misclassification, attributable to memory failure, would have tended again to bias results toward the null. A spurious association could have arisen if cases tended to be more likely to recall, or to overreport, their frequency of meat stir-frying in the past. We feel a situation in which only smokers were subject to this bias, and not nonsmokers, is unlikely. The purported link between cooking method and lung cancer is not common knowledge. Furthermore, in introducing the study, the general term "womens health" was used and not "lung cancer."
The magnitude of the risk associated with smoking by histological type is consistent with the range reported by studies among women in various populations worldwide (29, 30, 31 , 47, 48, 49) . The proportion of adenocarcinomas among our cases is higher than the 3040% overall for female lung cancer patients in the West (8 , 30 , 35 , 50) , where the proportion of smokers ranges from 3080% and is consistent with that reported for predominantly nonsmoking female populations as being between 50 and 80% (33 , 51) .
The most significant finding in this study is the interaction between cigarette smoking and cooking practices, specifically stir-frying of meat. Another model in which the effect of one carcinogen is observed primarily in the presence of another potent carcinogen is that of aflatoxin exposure, which interacts with hepatitis B virus carrier status in its effect on liver cancer risk (52) . The presence of cocarcinogens in cooking fumes is another possible mechanism for the interaction with smoking observed in this study. The possibility that our findings reflect a relationship between meat intake, and hence meat cooking, and smoking should also be considered. There is some evidence from the literature that smokers consume meat more frequently (53 , 54) , and consumption increases with number of cigarettes smoked (53) . In the present study, duration and intensity of smoking were both controlled for in the multivariate model, but the presence of residual confounding by smoking cannot be totally discounted.
In the light of increasing evidence as to the carcinogenicity of heterocyclic aromatic amines, the possibility that the presence of these compounds in cooking fumes increases the risk of lung cancer deserves consideration. We demonstrate specifically that stir-frying of meat enhances risk. It is known that heterocyclic amines are present on pan residues and on the charred surface of broiled or fried meat (12) . Rappaport et al. (27) reported that heating of ground beef to high temperatures resulted in the volatilization of a significant proportion of the basic mutagens formed. Analyses of airborne particulates from domestic environments for mutagenicity levels reported high values for fumes generated during cooking of meat (55) . Other studies, which analyzed the cooking aerosols from fried beef patties (23) and Chinese stir-fried fish (25) , identified these volatile compounds as heterocyclic amines and showed that the mutagenic activity increased with temperature (26) . Our findings suggest that frequent exposure to heterocyclic amines through cooking of meat may pose an additional hazard to health among women who smoke.
If true, the interaction between cooking and smoking lends itself to another interesting hypothesis. As mentioned previously, women smokers exhibit a higher risk of lung cancer than men smokers, after adjusting for dose. Ryberg et al. (56) showed that, among smokers after adjusting for smoking dose, the levels of aromatic DNA adducts in female lung cancer patients was higher than in males. It is possible, and not inconceivable, that exposure to carcinogens in cooking fumes accounts in part for the difference in risks between women smokers, who are more likely to cook, and men, who generally do not cook. The effect of other cooking methods, such as those commonly used in the West, deserves further investigation.
Among subjects who stir-fried meat daily, we also found a higher risk among women who more frequently used unsaturated oil for cooking. Although the numbers supporting this observation are small, we note that this is consistent with previous reports of a higher mutagenicity observed with heated polyunsaturated oils, especially with linolenic acid, relative to saturated oils (39 , 57 , 58) . At high temperatures in the presence of oxygen, fatty acids undergo peroxidation, during which free radicals are produced; the rate of their formation is dependent, among other things, on the initial degree of unsaturation of the fat (59) . Thus far, there is no consistent evidence of any effect of degree of unsaturation of cooking oil on heterocyclic amine formation in particular (60 , 61) , and further research, including experimental approaches, may be helpful in this regard.
In contrast to the strong positive associations in smokers, we did not find any association between frequency of cooking and lung cancer risk among nonsmokers. This is in contrast to a recent study in Taiwan among nonsmoking women (38) , in which the OR for women cooking three meals/day (versus 1 meal) was 3.4 (95% CI, 1.67.0). In Shanghai, Gao et al. (36) reported a relative risk of 2.6 with stir-frying of 30 or more dishes a week among smokers and nonsmokers combined. We note that there are some differences between cooking practices in Singapore and those in China; for example, Chinese rapeseed oil, which has been implicated in a few studies (36 , 39) , is not available here. In addition, the method of rapid stir-frying over very high temperatures ("bao"), which in the case of meat would generate greater amounts of heterocyclic amines, is likely to be less often practiced here. The Singapore Chinese population, however, offers some advantages in terms of heterogeneity of exposure, which may not have been present in more traditional Chinese societies, where >95% of women cooked daily or more (38) or used the same cooking oil (36 , 62) . Our observed lack of association with daily meat frying among nonsmokers should not be viewed as suggesting that such exposure has no effect on lung cancer risk in this subgroup of individuals. Even a moderate interaction effect (such as an interaction relative risk of 2) implies that the relative risk associated with meat frying would be around 1.31.4 in nonsmokers. The statistical power of this study to detect a relative risk of this magnitude is only 33% given a two-sided significance level of 5%. The current study was also not designed to examine the effect of other sources of heterocyclic amines, chiefly dietary (63) , on lung cancer risk.
In conclusion, among Chinese women, we found evidence that exposure to heterocyclic amines in fumes emitted during meat cooking may increase the risk of lung cancer among smokers. Although this is intriguing and deserves further study because of its potential public health implications, we also recognize that because meat cooking and eating are closely related to smoking, traditional epidemiological methods would find it difficult to separate their effects. Further studies, particularly those that incorporate molecular markers relevant to metabolic pathways or genetic changes specific to heterocyclic amines, are needed to confirm or refute these findings.
| Acknowledgments |
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| Footnotes |
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1 This study was funded by Grant NMRC 1996/0155
from the National Medical Research Council. M. C. Y. is supported by
the United States National Cancer Institute Grant R35 CA53890. ![]()
2 To whom requests for reprints should be
addressed, at Department of Community, Occupational and Family
Medicine, Faculty of Medicine (MD3), 16 Medical Drive, Singapore
117597. Phone: 65-8744974; Fax: 65-7791489; E-mail: cofseowa{at}nus.edu.sg ![]()
3 Singapore Cancer Registry, unpublished data. ![]()
4 The abbreviations used are: OR, odds ratio; CI,
confidence interval. ![]()
Received 4/26/00; revised 8/ 9/00; accepted 8/21/00.
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