Cancer Therapy Vol 2, 415-422, 2004
Salted meat consumption and risk of squamous cell carcinoma
of the oesophagus: a case-control study in Uruguay
Eduardo De Stefani1*,
Paolo Boffetta2, Pelayo Correa3, Hugo Deneo-Pellegrini1,
Mar£a Mendilaharsu1 and Alvaro L. Ronco4
1Departamento de Patolog£a,
Instituto Nacional de Oncolog£a, Montevideo, Uruguay.
2International Agency for Research on Cancer, Lyon,
France.
3Department of Pathology, Louisiana State University
Health Sciences, New Orleans, Louisiana, USA.
4Divisi½n de
Epidemiolog£a, Instituto de Radiolog£a y Centro de Lucha contra el C΅ncer,
Hospital Pereira Rossell, Montevideo, Uruguay
__________________________________________________________________________________
*Correspondence: Dr. Eduardo
De Stefani, Avenida Brasil 3080 dep. 402, Montevideo, Uruguay; Tel.: (598) 2
708 23 14; Fax: (598) 2 402 08 10; E-Mail: estefani@adinet.com.uy
Key words: oesophageal
cancer, salted meat, white meat, boiled meat, nitrosamines, salt
Supported by grant from
International Agency for Research on Cancer, Lyon, France
Summary
A
case-control study was conducted in Montevideo, Uruguay in the time period
1996-2003, in order to elucidate the role of meat consumption in oesophageal
carcinogenesis. The study included 200 cases with squamous cell oesophageal
carcinoma and 400 age- and sex-matched controls. Salted meat consumption was
significantly associated with an increased risk for this malignancy (OR 2.34,
95 % CI 1.21-4.53). On the other hand, high intake of white meat was inversely
associated with risk of oesophageal cancer (OR 0.55, 95 % CI 0.36-0.84). Also
boiled meat, frequent component of stews, increased the risk of oesophageal
cancer. The remaining types of meat were not related with the risk of squamous
cell carcinoma of oesophagus.
The role of meat consumption has
been considered controversial in its relationship with squamous cell carcinoma of
the oesophagus. Whereas several studies reported an inverse association with
this malignancy (Pottern et al, 1981; Tuyns et al, 1987; Gao et al, 1994;
Launoy et al, 1998), other reports suggested a positive association with
oesophageal cancer (Victora et al, 1987; De Stefani et al, 1990; Cheng et al,
1992; Rol½n et al, 1995). Since meat industry is the main industry in
Uruguay, this country is particularly well suited for studying the role of
meat, more precisely red meat, in the aetiology of squamous cell oesophageal
cancer. In fact, Uruguay is the leading country in the World regarding beef
consumption (Matos and Brandani, 2002).
A previous Uruguayan study reported
that salted meat and meat from lamb were positively associated with the risk of
oesophageal cancer (De Stefani et al, 1999). This study suffered of a low
statistical power since it included only 82 cases (67 men and 15 women). Since
then our database has been considerably enlarged. Also, our previous study
compared the risks of different types of meat categorized in tertiles. This
comparison was not entirely adequate, since different amounts of intake were
used for it. In fact, for a reliable comparison it is necessary to calculate
all OR using the same fixed amount of intake.
We decided to conduct a new case-control study on the relationship between meat consumption and risk of squamous cell carcinoma of the oesophagus. In this study we will calculate the risk of several sets of meat categorized in quartiles. Furthermore, ORÕs for the same subsets of meat will be calculated as continuous variables after adding a fixed amount of consumption (10 grams per day).
A. Selection of cases
In the period 1996-2003, 208
patients with newly diagnosed and microspically confirmed squamous cell
oesophageal carcinoma were identified in the four major public hospitals
located in Montevideo, Uruguay.
Since hospitals located outside the capital city of Montevideo lacked
facilities for diagnosis and treatment of cancer, almost all patients are
admitted in hospitals of Montevideo. Three patients were diagnosed as
adenocarcinoma of the oesophagus and five patients refused the interview. These
eight patients were excluded from the study, leaving a final total of 200 cases
with squamous cell carcinoma of the oesophagus (response rate 96.1 %). The case
series included 162 males (81 %) and 38 females (19 %).
B. Selection of controls
In the same time period and
in the same hospitals, 723 patients with diseases not related with tobacco
smoking or alcohol drinking and without recent changes in their diets were
considered eligible for the study. Twenty patients refused the interview leaving a final total of 703 potential
controls (response rate 97.2 %). From this pool, 400 controls were frequency matched
to the cases on age (in ten-years intervals) and sex. The patients presented
the following diseases: abdominal hernia (103 patients, 25.7 %), eye disorders
(88, 22.0 %), diseases of the skin (12.0 %), acute appendicitis (37, 9.2 %),
urinary stones (29, 7.3 %), varicose veins (29, 7.3 %), injuries (26, 6.5 %),
hydatid cyst (20, 5.0 %) and blood disorders (20, 5.0 %).
C. Questionnaire
All participants were submitted to a questionnaire shortly
after admittance. The interviews were
conducted by two trained social
workers in the hospitals. No proxy interviews were accepted. The questionnaire
included the following sections: sociodemographics, an occupational history
based in the job titles and its duration, a family history of cancer among
first-degree relatives, a complete tobacco smoking history (including age at
start, age at quit, average number of cigarettes smoked per day, type of
tobacco, type of cigarette), a history of alcohol drinking (including number of
drinks per day or week for beer, wine and hard liquor), a complete history of
matŽ drinking (matŽ is the folk name of a local herbal tea which is drunk hot
or very hot), menstrual and reproductive events and a food frequency
questionnaire (FFQ) on 64 food items. This FFQ allowed the calculation of total
energy intake and was tested for reproducibility with good results.
D. Definition of food groups
All queries concerned the consumption of foods five years before the date of questionnaire. The
following types of meat were included in the FFQ: fried beef, broiled beef,
boiled beef, fried lamb, broiled lamb, boiled lamb, poultry, fish, bacon,
sausage, blood pudding, liver, mortadella, salami, saucisson, hot dog, ham,
salted meat (consumption in the adolescence and current intake). These items were
selected on the basis of the consumption of the Uruguayan population. From
these individual items, the following food groups were created: red meat (beef,
lamb), white meat (poultry, fish), processed meat (bacon, sausage, blood
pudding, mortadella, salami, saucisson, hot dog, ham, salted meat), fried meat
(fried beef, fried lamb), broiled meat (broiled beef, broiled lamb), boiled
meat (boiled beef, boiled lamb) and total meat (red meat, processed meat, white
meat). In order to compare the odds ratios for these nested food groups, each
variable was treated as continuous and the fixed amount of 10 grams per day was
added to each one. Each food item was calculated in grams per day by
multiplying the frequency of consumption per the portion size for a middle age
participant.
E. Statistical analysis
Relative risks of squamous
cell oesophageal cancer for foods, approximated by the odds ratios, were
estimated by multiple unconditional logistic regression (Breslow and Day,
1980). The following variables were included in all models: age (categorical, 5
strata), sex, county of residence (dichotomized as Montevideo and other),
birthplace (categorical, 3 strata), education (categorical, 3 strata), average
number of cigarettes smoked per day (categorical, 5 strata), years since quit
(categorical, 5 strata), smoking status (categorical, 3 strata), alcohol
drinking (categorical, 5 strata), matŽ temperature (categorical, 4 strata),
total energy intake (continuous) and total vegetables and fruits (categorical,
4 strata). Tests for trend were performed after entering categorical variables
as ordinal in the same model. Departure
from the multiplicative model was determined by assessing the likelihood ratio
test statistic. An alpha of 0.05 was used as the indicator of statistical
significance and, accordingly, 95 % CI s were reported. All p-values were
derived from two-sided statistical tests.
All the calculations were done with the STATA programme (1999).
As expected for the frequency
matched design, age and sex were identical (Table 1). There was a higher proportion of dwellers living outside
Montevideo, of rural residents and of subjects born in the Northern part of the
country among cases than among controls.
Cases were significantly less educated than controls (OR 0.6, 95 % CI
0.4-0.9). Income (in US dollars) was rather similar in both series of
participants. Cases were significantly leaner than controls (OR 0.5, 95 % CI
0.3-0.8). The consumption of total energy was slightly higher in cases than in
controls. Heavy smoking was associated with an increased risk of 4.8 (95 % CI
2.6-9.1). There was no difference between smoking of black tobacco and of blond
tobacco cigarettes (OR 1.2, 95 % CI 0.7-1.8). On the other hand, smoking of
hand-rolled cigarettes displayed an OR of 1.7 (95 % CI 1.1-2.7) compared with
commercial cigarettes. Heavy drinking of alcohol was associated with a
four-fold increase in risk and drinking of very hot matŽ displayed an OR of 4.0
(95 % CI 1.5-10.3) compared with drinking of warm matŽ.
Odds ratios
of squamous cell esophageal carcinoma for different types of meat are shown in Table 2. Total meat, red meat and
preserved meat were not associated with risk of esophageal carcinoma.
Similarly, different types of red meat (beef and lamb) were not associated with
this malignancy. On the other hand, white meat consumption (poultry plus fish)
was associated with a significant reduction in risk (OR 0.46, 95 % CI
0.25-0.85, p-value for trend=0.005). When red meat was analyzed by the cooking
method, neither fried nor barbecued meat were associated with risk. In fact,
barbecued meat showed reductions in risk which were close to the significance
level of 0.05. On the other hand, boiled meat was associated with positive
gradient (OR for high consumption of boiled meat 1.90, 95 % CI 1.05-3.46,
p-value for trend=0.01).
Table 1.
Distribution of controls and cases for sociodemographics and selected risk
factors
|
Cases
Controls |
||||
|
Variable |
Category |
N¡ % |
N¡ % |
OR 95 % CI |
|
Age (years) |
40-49 |
15 7.5 |
30 7.5 |
|
|
|
50-59 |
40 20.0 |
80 20.0 |
|
|
|
60-69 |
69 34.5 |
138 34.5 |
|
|
|
70-79 |
61 30.5 |
122 30.5 |
|
|
|
80-89 |
15 7.5 |
30 7.5 |
Not applicable |
Sex
|
Males |
162 81.0 |
324 81.0 |
|
|
|
Females |
38 19.0 |
76 19.0 |
Not applicable |
Residence
|
Montevideo |
76 38.0 |
167 41.8 |
1.0 |
|
|
Other counties |
124 62.0 |
233 58.2 |
1.2 0.8-1.6 |
|
Urban/rural status |
Urban |
149 74.5 |
321 80.3 |
1.0 |
|
|
Rural |
51 25.5 |
79 19.7 |
1.4 0.9-2.1 |
Birthplace
|
Montevideo |
47 23.5 |
135 33.8 |
1.0 |
|
|
South |
69 34.5 |
171 42.7 |
1.1 0.7-1.8 |
|
|
North |
84 42.0 |
94 23.5 |
2.6 1.6-4.0 |
|
Education (yrs) |
0-2 |
69 34.5 |
124 31.0 |
1.0 |
|
|
3-5 |
84 42.0 |
131 32.8 |
1.1 0.8-1.7 |
|
|
6+ |
47 23.5 |
145 36.2 |
0.6 0.4-0.9 |
|
Income (dollars) |
<=146 |
67 33.5 |
173 43.3 |
1.0 |
|
|
147+ |
79 39.5 |
158 39.5 |
1.3 0.9-1.9 |
|
|
Unknown |
54 27.0 |
69 17.2 |
- - |
Family history
|
No |
194 97.0 |
391 97.8 |
1.0 |
|
|
Yes |
6 3.0 |
9 2.2 |
1.3 0.5-3.8 |
|
Body mass index |
<=23.1 |
75 37.5 |
101 25.2 |
1.0 |
|
|
23.2-25.3 |
52 26.0 |
101 25.2 |
0.7 0.4-1.1 |
|
|
25.4-27.3 |
34 17.0 |
98 24.6 |
0.5 0.3-0.8 |
|
|
27.4+ |
39 19.5 |
100 25.0 |
0.5 0.3-0.8 |
Total calories
|
<=1851 |
39 19.5 |
100 25.0 |
1.0 |
|
|
1852-2260 |
56 28.0 |
100 25.0 |
1.4 0.9-2.3 |
|
|
2261-2644 |
47 23.5 |
100 25.0 |
1.2 0.7-2.0 |
|
|
2645+ |
58 29.0 |
100 25.0 |
1.5 0.9-2.4 |
|
Tobacco smoking |
Never smokers |
40 20.0 |
140 35.0 |
1.0 |
|
Ex-smokers (years) |
20+ |
15 7.5 |
33 8.3 |
1.6 0.8-3.2 |
|
|
10-19 |
13 6.5 |
32 8.0 |
1.4 0.7-2.9 |
|
|
1-9 |
29 14.5 |
38 9.5 |
2.7 1.4-4.9 |
|
Current smokers
(cigarettes/day) |
1-9 |
6
3.0 |
20 5.0 |
1.1 0.4-2.8 |
|
|
10-19 |
21 10.5 |
61 15.2 |
1.2 0.6-2.2 |
|
|
20-29 |
36 18.0 |
47 11.8 |
2.7 1.5-4.7 |
|
|
30+ |
40 20.0 |
29 7.2 |
4.8 2.6-9.1 |
Type of tobacco
|
Blond |
77 48.1 |
119 45.8 |
1.0 |
|
|
Mixed |
26 16.3 |
65 25.0 |
0.6 0.4-1.1 |
|
|
Black |
57 35.6 |
76 29.2 |
1.2 0.7-1.8 |
|
Type of cigarette |
Manufactured |
41 25.6 |
94 36.2 |
1.0 |
|
|
Mixed |
21 13.1 |
37 14.2 |
1.3 0.7-2.5 |
|
|
Hand-rolled |
98 61.3 |
129 49.6 |
1.7 1.1-2.7 |
|
Alcohol drinking (1) |
Never drinkers |
62 31.0 |
195 48.8 |
1.0 |
|
|
1-60 |
37 18.5 |
85 21.2 |
1.4 0.8-2.2 |
|
|
61-120 |
41 20.5 |
61 15.2 |
2.1 1.3-3.5 |
|
|
121-240 |
34 17.0 |
39 9.8 |
2.7 1.6-4.8 |
|
|
241+ |
26 13.0 |
20 5.0 |
4.1 2.1-8.0 |
|
MatŽ temperature |
Warm |
11 5.8 |
25 7.4 |
1.0 |
|
|
Hot |
144 75.8 |
295 86.8 |
1.1 0.5-2.5 |
|
|
Very hot |
35 18.4 |
20 5.8 |
4.0 1.5-10.3 |
N¡ patients
|
|
200 100.0 |
400 100.0 |
|
1-In militers of ethanol per day
Table 2. Odds ratios of squamous cell
esophageal carcinoma for different types of meat, categorized in quartiles (1)
|
Type of meat |
Intake
(grams/day) |
Cases/Controls |
OR 95 % CI |
|
Total meat |
<=160.5 |
49/100 |
1.0 |
|
|
160.6-203.0 |
40/100 |
0.48 0.26-0.89 |
|
|
203.1-251.9 |
44/100 |
0.56 0.31-1.01 |
|
|
252.0+ |
67/100 |
0.96 0.54-1.70 |
|
|
p-value for trend |
|
0.80 |
|
Red meat |
<=114.3 |
42/100 |
1.0 |
|
|
114.4-160.2 |
42/100 |
0.65 0.35-1.20 |
|
|
160.3-192.7 |
41/100 |
0.65 0.35-1.19 |
|
|
192.8+ |
75/100 |
1.14 0.64-2.05 |
|
|
p-value for trend |
|
0.49 |
|
Processed meat |
<=7.9 |
46/100 |
1.0 |
|
|
8.0-19.1 |
50/100 |
1.12 0.64-1.99 |
|
|
19.2-39.7 |
57/100 |
1.11 0.63-1.96 |
|
|
39.8+ |
47/100 |
1.15 0.63-2.07 |
|
|
p-value for trend |
|
0.68 |
|
White meat |
<=6.6 |
86/100 |
1.0 |
|
|
6.7-17.1 |
50/100 |
0.64 0.38-1.08 |
|
|
17.2-30.0 |
33/100 |
0.48 0.26-0.86 |
|
|
30.1+ |
31/100 |
0.46 0.25-0.85 |
|
|
p-value for trend |
|
0.005 |
|
Beef |
<=85.4 |
60/100 |
1.0 |
|
|
85.5-146.3 |
43/100 |
0.69 0.39-1.21 |
|
|
146.4-171.3 |
37/100 |
0.46 0.25-0.84 |
|
|
171.4+ |
60/100 |
0.77 0.45-1.34 |
|
|
p-value for trend |
|
0.25 |
|
Lamb |
0 |
85/195 |
1.0 |
|
|
0.1-21.3 |
48/101 |
0.93 0.56-1.54 |
|
|
21.4+ |
67/104 |
1.08 0.65-1.81 |
|
|
p-value for trend |
|
0.80 |
|
Fried meat |
<=21.3 |
62/100 |
1.0 |
|
|
21.4-42.7 |
47/100 |
0.69 0.39-1.21 |
|
|
42.8-64.1 |
48/100 |
0.78 0.45-1.37 |
|
|
64.2+ |
43/100 |
0.73 0.41-1.28 |
|
|
p-value for trend |
|
0.35 |
|
Barbecued meat |
<=10.8 |
65/100 |
1.0 |
|
|
10.9-26.3 |
42/100 |
0.56 0.31-0.99 |
|
|
26.4-53.4 |
44/100 |
0.62 0.35-1.09 |
|
|
53.5+ |
49/100 |
0.58 0.33-1.03 |
|
|
p-value for trend |
|
0.09 |
|
Boiled meat |
<=32.0 |
33/100 |
1.0 |
|
|
32.1-74.7 |
37/100 |
1.02 0.54-1.94 |
|
|
74.8-96.1 |
49/100 |
1.38 0.75-2.55 |
|
|
96.2+ |
81/100 |
1.90 1.05-3.46 |
|
|
p-value for trend |
|
0.01 |
1-Adjusted for age, sex, residence, urban/rural status, birthplace,
education, body mass index, smoking status, number of cigarettes smoked per
day, years since quit, alcohol drinking, matŽ temperature and total energy
intake.
The analysis of types of meat as continuous variables
after the addition of 10 g/day is shown in Table
3. Total meat consumption was not associated with risk of oesophageal
cancer. When total meat was dissected in red meat, preserved meat and white
meat, the last group was significantly and inversely associated with risk of
squamous cell oesophageal cancer (OR 0.57, 95 % CI 0.38-0.86, p-value for
trend=0.008). In model 3, red meat was partitioned in beef and lamb; preserved
meat and white meat were retained in this model. Neither beef nor lamb meat
were associated with risk of oesophageal cancer. In model 4, red meat was
dissected in fried, barbecued and boiled meat, according with the cooking
method. Again preserved meat and white meat were retained in the model. Whereas
fried and barbecued meat were not associated with risk, boiled meat displayed a
modest increased risk which was non-significant (OR 1.29, 95 % CI 0.92-1.81,
p-value for trend=0.14). In model 5, white meat was examined according to its
nested components poultry and fish. Poultry intake was inversely associated
with risk of oesophageal cancer (OR 0.65, 95 % CI 0.39-1.07, p-value for
trend=0.09), whereas fish
Table 3. Odds ratios of squamous cell esophageal carcinoma
for types of meat included in the models as continuous variables after the
addition of 10 g/day (1).
|
Model |
OR 95 % CI |
p-value for linear trend |
|
1 Total
meat |
1.26 0.66-2.40 |
0.40 |
|
2 Red
meat |
1.10 0.68-1.79 |
0.70 |
|
Processed meat |
1.10 0.81-1.49 |
0.55 |
|
White
meat |
0.57 0.38-0.86 |
0.008 |
|
3 Beef |
0.88 0.63-1.24 |
0.48 |
|
Lamb |
1.01 0.77-1.32 |
0.94 |
|
Processed meat |
1.08 0.79-1.47 |
0.63 |
|
White
meat |
0.57 0.38-0.86 |
0.007 |
|
4 Fried
meat |
0.91 0.68-1.21 |
0.51 |
|
Barbecued meat |
0.78 0.58-1.05 |
0.11 |
|
Boiled
meat |
1.29 0.92-1.81 |
0.14 |
|
Processed meat |
1.12 0.82-1.53 |
0.47 |
|
White
meat |
0.57 0.38-0.86 |
0.008 |
|
5 Red
meat |
1.12 0.69-1.81 |
0.66 |
|
Processed meat |
1.11 0.81-1.50 |
0.51 |
|
Poultry |
0.65 0.39-1.07 |
0.09 |
|
Fish |
0.74 0.44-1.24 |
0.26 |
|
6 Red
meat |
1.16 0.70-1.91 |
0.57 |
|
Bacon |
1.38 0.44-4.34 |
0.58 |
|
Sausage |
0.68 0.37-1.26 |
0.32 |
|
Blood
pudding |
0.81
0.41-1.61 |
0.55 |
|
Liver |
0.68 0.38-1.23 |
0.21 |
|
Mortadella |
0.95 0.61-1.47 |
0.81 |
|
Salami |
0.94
0.56-1.59 |
0.83 |
|
Saucisson |
0.99 0.43-2.28 |
0.99 |
|
Hot dog
|
1.34 0.80-2.21 |
0.26 |
|
Ham |
1.26 0.69-2.28 |
0.45 |
|
Salted
meat |
2.34 1.21-4.53 |
0.01 |
|
White
meat |
0.55 0.36-0.84 |
0.006 |
1-Adjusted
for age, sex, residence, urban/rural status, birthplace, education, body mass
index, smoking status, number of cigarettes smoked per day, years since quit,
alcohol drinking, matŽ temperature, total energy intake and total vegetables
and fruits.
According to the results of our
study boiled meat, salted meat and white meat were significantly associated
with risk of oesophageal carcinoma. The remaining varieties of meat were not
related with oesophageal carcinogenesis.
Previous epidemiological studies reported similar
results (Tavani et al, 1994; Bosetti et al, 2000; De Stefani et al, 2003). In
particular, the role of salted meat in the development of oesophageal carcinoma
has been considered a consisting finding (Cheng et al, 1992; De Stefani et al,
1999, 2003). According to Cheng et al, (1992), salted fish is an important
factor in oesophageal carcinogenesis. Also, previous studies conducted in
Uruguay reported similar findings (De Stefani et al, 1999, 2003) for salted red
meat. In fact before the advent of the refrigeration, red meat was preserved in
rural areas of Uruguay by salting and air-drying (ÒcharqueÓ). These areas
displayed very high incidence rates of oesophageal cancer, close to 60 cases
per 100,000 inhabitants. The consumption of ÒcharqueÓ has declined in the last
30-40 years, paralelling the decline in the incidence and mortality of
oesophageal carcinoma (Zheng et al, 1993; De Stefani et al, 1994). Salted meat
is probably more active in the adolescence (Cheng et al, 1992) and is suspected
as a rich source of nitrosamines and salt. Both agents (nitrosamines and salt)
have been considered as important determinants in the process of oesophageal
carcinogenesis (Craddock, 1992; CastellsaguŽ et al, 2000).
Other studies suggested that heterocyclic amines could
be important aetiologic factors for oesophageal cancer (Ward et al, 1997).
Barbecued and fried meat are precisely a rich source of HCA and in previous
studies high consumption of barbecued meat was associated with a high risk of
oesophageal carcinoma (De Stefani et al, 1990; Castelletto et al, 1994). In the
present study, neither fried nor barbecued meat were risk factors for this
malignancy.
Boiled meat, a main component of stew, was
significantly associated with an increased risk of squamous cell oesophageal
cancer in our study. The role of boiled meat was specially evident when this
meat was analyzed as a categorical variable. When boiled meat was entered into
the model as a continuous term, this type of meat was no longer significant. In
is possible that boiled meat acted in the process of oesophageal carcinogenesis
through thermal injury of oesophageal mucosa, since stews are ingested very hot
by the Uruguayan population. This
could induce chronic oesophagitis, considered as the first step in the
development of oesophageal carcinoma (Mu¥oz et al, 1987).
White meat, that is poultry plus fish meat, was the
only protective type of meat in our study. This type of meat is characterized
by a lower amount of saturated fat when compared with red meat. Unfortunately,
our questionnaire did not discriminate cooking methods for poultry and fish. It
has been reported that, whereas low-fat types of white meat (skinless chicken
and unfried fish) are protective, high-fat types of this meat are associated
with risk of other malignancies (Ronco et al, 2003). Thus, it is possible that
our participants consumed mainly low-fat types of white meat. It is not
possible to discard the fact that white meat consumption could be a marker of a
healthy diet. Previous studies reporting ORÕs of oesophageal carcinoma for
white meat consumption, consistently showed inverse associations (De Stefani et
al, 2003). Further studies on mechanisms of white meat consumption in
oesophageal carcinogenesis are needed.
Residual confounding of our results from tobacco
smoking, alcohol drinking, matŽ consumption and diet could result in severe
distortions of the estimates. For these reasons we included terms for tobacco
smoking (8 strata), alcohol drinking (5 strata), matŽ temperature (4 strata)
and total vegetables and fruits (4 strata).
As other hospital-based case-control studies, the
present study has limitations. In first place, selection bias is almost
impossible to exclude. We tried to minimize this bias by frequency matching
cases and controls on age and sex. Also, residence and urban/rural status were
rather similar. Recall bias, which is almost non-existent in prospective
studies, is also a major drawback. We tried to minimize recall bias asking
about the consumption five years before the date of the interview.
Nevertheless, since the process of oesophageal carcinogenesis is of long
duration, is possible that cases experimented difficulties in eating foods like
meat, more difficult to swallow. This could led to differential
misclassification. Since the role of diet in oesophageal carcinoma is mostly
unknown in Uruguay, it is unlikely that both interviewers and participants of
the study could be affected in its attitudes during the interviews. Probably,
the major limitation of our study was the lack of validation of our FFQ. Aside
from this drawback the FFQ was comprehensive and incred queries on 64 food items,
representative of the usual diet of the Uruguayan population. On the other
hand, our study has strengths. Perhaps the major strength is related with the
high response rate observed in both series of patients. Also, the exclusion of
proxy interviews is another strength of the study. Finally, the restriction of
the study to patients afflicted by squamous cell carcinoma of the oesophagus is
a strength.
In summary, our study replicates previous findings
showing that salted meat is a major risk factor for squamous cell carcinoma of
the oesophagus. On the other hand white meat intake was a protective factor,
even after allowing for the effect of plant foods and other major confounders.
Public health measures resulting in a lower intake of salt and in a substitution
of red meat by white meat could prevent the risk of development of squamous
cell oesophageal carcinoma.
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