SEARCH

SEARCH BY CITATION

Keywords:

  • gallbladder cancer;
  • gallstones;
  • Mapuche;
  • typhoid;
  • genetics

Abstract

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References

Chile's gallbladder cancer rates are among the highest in the world, being the leading cause of cancer deaths among Chilean women. To provide insights into the etiology of gallbladder cancer, we conducted an ecologic study examining the geographical variation of gallbladder cancer and several putative risk factors. The relative risk of dying from gallbladder cancer between 1985 and 2003 was estimated for each of the 333 Chilean counties, using a hierarchical Poisson regression model, adjusting for age, sex and geographical location. The risk of gallbladder cancer mortality was analyzed in relation to region, poverty, Amerindian (Mapuche) population, typhoid fever and access to cholecystectomy, using logistic regression analysis. There were 27,183 gallbladder cancer deaths, with age and sex-adjusted county mortality rates ranging from 8.2 to 12.4 per 100,000 inhabitants. Rates were highest in inland and southern regions. Compared to the northern-coast, the northern-inland region had a 10-fold risk (95% of confidence interval (95% CI): 2.4–42.2) and the southern-inland region had a 26-fold risk (95% CI: 6.0–114.2). Independent of region, other risk factors for gallbladder cancer included a high Mapuche population (Odds ratio (OR):3.9, 95% CI 1.8–8.7), high typhoid fever incidence (OR:2.9, 95% CI 1.2–6.9), high poverty (OR:5.1, 95% CI 1.6–15.9), low access to cholecystectomy (OR:3.9, 95% CI 1.5–10.1), low access to hospital care (OR:14.2, 95% CI 4.2–48.7) and high urbanization (OR:8.0, 95% CI 3.4–18.7). Our results suggest that gallbladder cancer in Chile may be related to both genetic factors and poor living conditions. Future analytic studies are needed to further clarify the role of these factors in gallbladder cancer etiology. © 2008 Wiley-Liss, Inc.

Chile's gallbladder cancer incidence and mortality rates are among the highest in the world, with a mortality rate of 15.6 per 100,000 person–years in women and 7.0 per 100,000 person–years in men.1 Gallbladder cancer is the first cause of cancer death among Chilean women, above breast, lung and cervical cancers (Fig. 1). On the basis of national data, the highest mortality rates in Chile are seen in Southern regions, especially in areas with high poverty, a large Amerindian (Mapuche) population, and insufficient access to health services, including access to gallbladder surgery (cholecystectomy).1, 3

thumbnail image

Figure 1. Crude mortality rates (per 100,000 women) for top 5 causes of cancer deaths among Chilean women, 1990–2005. Elaborated by the author from Chilean Ministry of Health Mortality database.2 [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]

Download figure to PowerPoint

Apart from age, female gender, and a history of gallstones, the etiology of gallbladder cancer remains unclear. Reasons for the very high rates of gallbladder cancer in Chile are not known but both lifestyle and genetic factors have been suggested.4–7 American Indians in the U.S. also have very high rates of gallstones and gallbladder cancer, like the Amerindians in Chile (Mapuche), suggesting a role of genetic susceptibility for both populations.5, 6, 8 Chronic carriage of typhoid has been suggested as a risk factor for gallbladder cancer in India,7 where the incidence of typhoid fever is high. Typhoid fever was endemic in Chile between 1960 and 1982, thus it is possible that typhoid may be contributing to the high risk of gallbladder cancer in Chile.9

To better understand the reasons for the high incidence and mortality of gallbladder cancer in Chile, we conducted a population-based ecologic study examining the relative risks of gallbladder cancer mortality between 1985 and 2002 for each of the 333 counties in Chile. We also examined the relationships between several putative risk factors and the geographic variation of gallbladder cancer mortality using county-specific data.

Material and methods

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References

Study population and data sources

Several national data sources were used for this analysis. Specifically, gallbladder cancer mortality rates for each of the 333 Chilean counties between 1985 and 2002 were calculated, using data from the Ministry of Health of Chile.2 Chilean population estimates (∼15 million in total) by age, sex, race (self-declared) and county were obtained from the 2002 Census.10 Data on the poverty index (the percent of the population in the county whose income does not cover minimum goods and services) was obtained from the 2003 survey Caracterización Socioeconómica Nacional (CASEN),11 and incidence rates of typhoid fever between 1999 and 2004 were based on data from Epidemiological Surveillance Statistics.12

Geographical variations in gallbladder cancer mortality

Since gallbladder cancer is a rare disease and many counties have small populations, we used a Poisson regression model to calculate spatially smoothed gallbladder cancer mortality risks for each county relative to the national average, adjusting for the population size and age-sex composition. We used a hierarchical Poisson regression model, which combines unstructured variability and spatial dependence (structured variability).13 This spatial variability was estimated by an a priori Intrinsic Conditional Autoregressive Distribution (Bayesian analysis).14 The model can be represented by:

  • equation image
  • equation image

In this model, α0 is the intercept that represents the logarithm of the national gallbladder cancer rate (baseline) throughout Chile; bi is the random area-specific effect in the logarithm of relative risk explained by the neighbors of the ith county and hi is the random area-specific unexplained residual. We conducted Bayesian analysis of these models with parameters obtained using Markov–Monte Carlo techniques employed in the program WinBUGS.15 Convergences were evaluated based on standard criteria using the program BOA.16 Comparison and selection of models were based on the Deviance Information Criterion.17 On the basis of the results of this model, counties were dichotomized into high (RR > 1) and low (RR ≤ 1) gallbladder cancer mortality risk, using a ROC curve. To evaluate the change in gallbladder cancer mortality rates between 1985 and 2002, time trend was also summarized using a Poisson regression model.

Risk factors for gallbladder cancer mortality

Multivariate logistic regression analyses were used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for gallbladder mortality in relation to geographic location, percent living in poverty, urbanization (as stated by the National Institute of Statistics), typhoid incidence rate (1999–2004), percent of Amerindians (Mapuche) in the population, access to hospital care for gallbladder cancer patients (estimated as the ratio of the number of gallbladder diseases hospitalizations over the number of deaths from gallbladder cancer) and cholecystectomy (estimated from major surgery in patients with gallbladder disease). Gallbladder cancer mortality risk was evaluated comparing counties with a gallbladder cancer mortality relative risk (RR) greater than 1 with those with RR less than or equal to 1 (risk is relative to the national rate). Geographic location was assessed using 4 regions (north-coast, north-inland, south-coast and south-inland). A county was considered coastal if it touched the coastline, while an inland county has no coastal borders. ROC curve analysis was used to dichotomize the proportion of the Mapuche population (≥ or <3.7%), and typhoid fever incidence (≥ or <7.2 per 100,000 population). Poverty level was categorized as: low (Poverty Index CASEN< 20%), medium (Poverty Index CASEN between 20 and 40%), and high (Poverty Index CASEN >40%) and urbanization as low (<40%), medium (between 40 and 75%), and high (>75%). The ratio of gallbladder diseases hospitalizations over the number of deaths from gallbladder cancer was categorized as: high (>60) medium (30–60), and low (less than 30). Access to cholecystectomy was categorized as: high (>80%), medium (between 50 and 80%) and low (<50%).

Results

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References

Geographic variation in gallbladder cancer mortality by county between 1985 and 2002, relative to average national mortality rates, adjusting for county-specific population size, and age and sex distributions, is shown in Figure 2. As shown, the highest gallbladder cancer mortality rates occurred in the southern part of the country, in particular the south-inland region.

thumbnail image

Figure 2. Geographic variation of relative risk (RR) of gallbladder cancer in Chile (1985–2002) by county with reference to the national average, adjusted for county population size, age-sex distribution and spatially smoothed. [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]

Download figure to PowerPoint

Selected characteristics of the 333 Chilean counties by geographical location are shown in Table I. The Chilean population tended to cluster in the north-inland region, while the Mapuche population was higher in the south, representing 6.5% of the population. Southern regions, both inland and coastal, also had high levels of poverty, were more rural, had a high incidence of typhoid fever, and lower rates of gallbladder surgery. Access to cholecystectomy was highest in the north-inland region and lowest in the south-inland region (81 and 59% of gallbladder disease hospitalizations received surgery respectively). Gallbladder cancer mortality ranged from 8.22 to 12.44 per 100,000 inhabitants, with the south-inland region having the highest rate. The average relative risk for gallbladder cancer mortality was lowest in the north-coastal region and highest in the south-inland region. The northern regions had slightly decreasing mortality risks over the period, while both southern regions had increasing mortality risks.

Table I. Selected Characteristics of the 333 Counties in Chile by Geographic Region
CharacteristicNumber of counties
North-Coast (28)North-Inland (101)South-Coast (67)South-Inland (137)
  • 1

    Prepared by the authors from Ministry of Health hospital statistics, number of major surgery per 100 gallbladder diseases hospitalizations.–

  • 2

    A proxy for access to hospital care for gallbladder disease.

Percent Chilean population12%49%14%24%
Mean percent of Mapuche in population (range)1.0% (0.3–3.0%)2.6% (0.0–10.6%)6.5% (0.2–64.7%)6.5% (0.0–59.5%)
Mean percent living in poverty (range)16.7% (8.2–41.9%)16.7% (1.4–42.0%)26.5% (4.5–59.9%)27.4% (10.9–59.5%)
Mean percent of urbanization (range)78% (0–99%)71% (0–100%)45% (0–99%)47% (0–97%)
Mean typhoid incidence rate 1999–2004 per 100,000 (range)4.2 (0.0–10.5)5.2 (0.0–54.9)7.5 (0.0–38.3)7.0 (0.0–104.1)
Average gallbladder disease hospital discharges 1992–2003 per 100,000 (range)290.8 (50.5–757.1)316.1 (0.0–628.3)352.5 (0.0–747.2)441.1 (65.2–1,207.7)
Mean percent of cholecystectomies 1992–20031 (range)74% (39–100%)81% (47–100%)56% (22–100%)59% (17–100%)
Ratio of gallbladder diseases hospital discharges over gallbladder cancer death2 (range)42 (19–78)37 (0–78)43 (0–102)37 (13–111)
Age-sex adjusted gallbladder cancer mortality rate per 100,000 (range)8.22 (0.0–11.3)8.53 (0.0–23.7)10.41 (0.0–38.3)12.44 (0.0–26.6)
Relative risk for gallbladder cancer mortality (95% CI)0.83 (0.77–0.88)0.93 (0.89–0.98)0.98 (0.91–1.06)1.18 (1.14–1.23)
β (%) for the trend of RR gallbladder cancer mortality 1985–2002 (95% CI)–0.20% (−0.4–0.0)–0.19% (−0.4–0.0)0.21% (0.0–0.4)0.30% (0.12–0.4)

On the basis of the geographical analysis, counties with RR > 1 for gallbladder cancer mortality were classified as high risk, while those with RR < 1 were classified as low risk. A multivariable logistic regression analysis of the gallbladder cancer risk is presented in Table II. Eleven percent of the counties in the north-coastal areas were classified as high-risk, while 67% of the south-inland counties were high-risk. Compared to the north-coast region, north-inland areas had a 10-fold (95% CI 2.4–42.2) risk of gallbladder cancer, and south-inland regions had a 26-fold risk (95% CI 6.0–114.2) of gallbladder cancer mortality (Table II). A large Mapuche population, high rates of typhoid fever, high poverty levels and high urbanization were risk factors for gallbladder cancer mortality, while high access to hospital care and high access to cholecystectomy were protective factors.

Table II. Odds Ratios (OR) and 95% Confidence Intervals (95% CI) for Gallbladder Cancer Mortality Risk in Relation to Selected Factors in 333 Counties in Chile, 1985–2002. Multivariable Logistic Regression.
CharacteristicsNumber of Counties(%) of counties with RR>11OR2 (95% CI)p
  • 1

    Relative risk of gallbladder cancer >1 from the poisson regression analysis.–

  • 2

    Odds ratios for comparisons between two strata within each characteristics, adjusted for geographical location.–

  • 3

    Number of major surgeries per 100 gallbladder diseases hospital discharges.–

  • 4

    Ratio of gallbladder diseases hospital discharges over gallbladder cancer deaths.

Geographic location
 North-Coast28111.0 
 North-Inland1013710.13 (2.4–42.2)0.001
 South-Coast67435.19 (1.1–24.5)0.04
 South-Inland1376726.10 (6.0–114.2)<0.001
Mapuche population
 Low (<3.7%)227411.0 
 High (≥3.7%)106643.92 (1.8–8.7)0.001
Typhoid incidence rate
 Low (<7.2)281441.0 
 High (≥7.2)52692.92 (1.2–6.9)0.014
Poverty
 Low105251.0 
 Medium192563.20 (1.6–6.4)0.001
 High36785.05 (1.6–15.9)0.006
Urbanization
 Low (<40%)121451.0 
 Medium (40–75%)101675.29 (2.5–11.2)<0.001
 High (>75%)111368.01 (3.4–18.7)<0.001
Cholecystectomy3
 High (>80%)115311.0 
 Medium (50–80%)130502.01 (1.0–4.0)0.048
 Low (<50%)88683.86 (1.5–10.1)0.006
Hospital care for gallbladder diseases4    
 High34211.0 
 Medium188475.16 (1.7–15.8)0.004
 Low1115914.25 (4.2–48.7)<0.001

Discussion

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References

In this population-based ecological study of 333 counties in Chile, we show that there is a large geographic variation in gallbladder cancer mortality risk not explained by chance, or the age-sex distribution of the population. The highest gallbladder cancer mortality risk was in the southern regions, in particular the south-inland region. Our results also show that Mapuche ethnicity, typhoid fever and poverty are important gallbladder cancer risk factors in the southern regions of Chile. It is not surprising that counties with a large Mapuche population had a higher risk for gallbladder cancer, since they have Amerindian origin and American Indians have one of the highest rates of gallstones and gallbladder cancer in the world.5, 6, 18–20 The concomitant high rates of gallbladder cancer in Mapuches and American Indians suggest a possible role of genetic susceptibility. Similar to American Indians, Mapuches have high rates of obesity, diabetes, metabolic syndrome and cholesterol gallstones7, 20–23 all of which are risk factors for gallbladder cancer and are conditions with a genetic basis. Several observations have suggested that gallbladder cancer has a strong genetic component. For example, family history of gallstones has been shown to increase the risk of gallbladder cancer24 and certain genetic variants in estrogen metabolism (particularly among obese and diabetic individuals),25 inflammation and lipid metabolism26–28 have been linked to an increased risk of gallstones and gallbladder cancer. Molecular studies of gallbladder cancer have also reported mutations of proto-oncogenes like K-ras and beta-catenin, alterations in some tumor suppressor genes, such as p53 and APC, and instability of microsatellites.29–31 It is possible that the much higher risk of gallbladder cancer in the inland regions is related to a higher homogeneity of the Mapuche population due to a higher degree of inbreeding.32 Although the percent of Mapuche in the population is similar in inland and coastal southern counties (6.5% each), proximity to the sea has permitted for a higher genetic interchange along the coast.32

It is possible that the higher rates of typhoid contribute to the excess risk of gallbladder cancer in Chile. The observation that typhoid fever is a significant risk factor for gallbladder cancer in Chile is consistent with previous reports suggesting a link between chronic typhoid carriage and gallbladder cancer in typhoid-endemic area, such as India.19, 33, 34 Chile has been a highly endemic area for typhoid fever since 1950, with an annual incidence rate of about 60 per 100,000 person–years until 1976.9 Between 1976 and 1985, an epidemic of typhoid surged in most urban areas of Chile due to the deteriorating living conditions, and the incidence increased to 121 per 100,000 person–years. However, in 1985, the incidence of typhoid started to decrease, and this trend continued until 1991, when typhoid incidence rate reached the current level of 3.3 per 100,000 person–years9 (Fig. 3). The precipitous drop in typhoid incidence between 1985 and 1992 was the result of intensive intervention measures taken to avoid the expansion of the cholera epidemic that had been affecting Peru since 1991.9 Typhoid fever is caused by Salmonella typhi (S. typhi). Two to 5% of all individuals who develop clinical or subclinical infection with S. typhi become chronic carriers.35 The propensity to become a chronic carrier after acute infection increases with age and is greater in women.36 Previous studies in Chile have shown that chronic S. typhi carriers had a higher frequency of the erythrocite ABH nonsecretor phenotype than non-carriers, suggesting that the carrier state may be influenced by genetic predisposition and that the ABH carbohydrates secreted in the bile may interfere with S. typhi colonization in the bile tract, resulting in increased gallstone formation and increased probability of becoming chronic carriers (OR = 15).35, 36 It is noteworthy that Chile has one of the highest rates of gallstones and typhoid fever in the world. In Chile, during the hyperendemic period of typhoid (1976–1985), more than 90,000 people were exposed to S.typhi.36 In 1980 the estimated carrier rate was 694 per 100,000 population, with unusually high rates estimated for middle-age-women (aged 30–39, 5,586 per 100,000 and aged 40–49, 4,575 per 100,000).36 Women in these age groups also have usually high rates of gallstones, ranging from 43 to 60%.36 The combination of high rates of chronic typhoid carriage and gallstones is likely to result in an increase in incidence of gallbladder cancer in the future. Gallbladder cancer mortality in Chile has risen steadily and we could expect to see a future surge of incidence as a result of the typhoid epidemic between 1976 and 1985 typhoid endemic. However, since the latency period between typhoid and gallbladder cancer is long, most chronic carriers are still young, and not enough years have elapsed, it is still unclear when the 1976–1985 typhoid epidemic would impact the incidence of gallbladder cancer in Chile. Nevertheless, if cholecistectomy rates increase, particularly in high risk counties, the effect of the chronic S typhi carriers in gallbladder cancer incidence could be averted.

thumbnail image

Figure 3. Temporal trend of typhoid fever incidence rate and of gallbladder cancer (GBC) mortality rate in Chile between 1960 and 2005. Elaborated by the author from Chilean Ministry of Health Mortality database.2 [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]

Download figure to PowerPoint

Poverty is an important risk factor for gallbladder cancer. Many factors, including typhoid infection, diet and access to medical procedures, are related to poverty. In developing countries, cholecystectomy is associated with decreasing rates of gallbladder cancer incidence and mortality.37 In Chile, although economic conditions have improved over time, we have not yet seen a large decrease in gallbladder cancer risk, due largely to the fact that most gallstone patients from high-risk areas do not have access to cholecystectomy procedures.1, 38, 39 A study on the American Indians in New Mexico (a high risk population for gallbladder cancer) showed that their incidence of gallbladder cancer has declined faster than other ethnic groups, presumably because of their better access to cholecystectomy.40

Reasons for the positive association between urbanization and gallbladder cancer are unknown but may be related to westernized lifestyles, better diagnosis or better reporting of gallbladder cancer. Surveys in Chile showed that people in rural areas had fewer risk factor for gallstones, in particular they had lower levels of serum lipids than people in urban areas.41 In addition, the prevalence of diabetes and obesity is higher in urban areas.21 Together, these findings support the observation that more urbanized populations should have higher gallbladder cancer rates.

Certain nutritional factors may be related to the much higher rates of gallbladder cancer in the southern regions, but we do not have the data to evaluate their role. In an earlier study in Chile, consumption of red chili pepper, beef and pork was linked to an increased risk of gallbladder cancer.42 These types of foods are frequently eaten in the southern regions.42, 43 Inland counties have less access to seafood and vegetables, which have been associated with a reduced risk of gallbladder cancer.42, 44

In summary, our ecologic study showed that there is a large geographic variation in gallbladder cancer mortality in Chile, with a much higher rate in the south-inland region. Future studies in Chile are needed to confirm the role of typhoid fever and genetic susceptibility to gallbladder cancer in Amerindians.

Acknowledgements

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References

The authors thank Mr. Alejandro Jara and Ms. Alessandra Gederlini for their assistance in the statistical analysis and to Ms. Elizabeth Salinas for her assistance in mapping the data.

References

  1. Top of page
  2. Abstract
  3. Material and methods
  4. Results
  5. Discussion
  6. Acknowledgements
  7. References
  • 1
    Andia M,Ferreccio C,Gederlini A. Gallbladder cancer: trend and risk distribution in Chile. Rev Med Chile 2006; 134: 56574.
  • 2
    MINSAL, Ministerio de Salud de Chile, Departamento de Estadísticas (DEIS). [Internet] 2007 [cited 2007 October 2]. Available from: www.minsal.cl.
  • 3
    Ferreccio C,Chianale J,González C,Nervi F. Epidemiología descriptiva del cáncer digestivo en Chile (1982–1991): una aproximación desde la mortalidad. Santiago: Edit Alfa Beta, 1995. 147 p.
  • 4
    Pandey M. Risk factors for gallbladder cancer: a reappraisal. Eur J Cancer Prev 2003; 12: 1524.
  • 5
    Randi G,Franceschi S,La Vecchia C. Gallbladder cancer worldwide: geographical distribution and risk factors. Int J Cancer 2006; 118: 1591602.
  • 6
    Lazcano-Ponce E,Miquel J,Muñoz N,Herrero R,Ferreccio C,Wistuba I,Alonso P,Aristi G,Nervi F. Epidemiology and molecular pathology of gallbladder cancer. CA Cancer J Clin 2001; 51: 34964.
  • 7
    Strom BL,Soloway RD,Rios-Dalenz JL,Rodríguez-Martínez HA,West SL,Kinman JL,Polansky M,Berlin JA. Risk factors for gallbladder cancer. An international collaborative case-control study. Cancer 1995; 76: 174756.
  • 8
    Galman C,Miquel JF,Perez RM,Einarsson C,Stahle L,Marshall G,Nervi F,Rudling M. Bile acid synthesis is increased in Chilean Hispanics with gallstones and in gallstone high-risk Mapuche Indians. Gastroenterology 2004; 126: 7418.
  • 9
    Laval E,Ferreccio C. Fiebre Tifoidea: emergencia, cúspide y desaparición de una enfermedad infecciosa en Chile. Invited review. Rev Chil Infect 2007; 24: 43540.
  • 10
    INE, Instituto Nacional de Estadística de Chile, Estadísticas Demográficas y Vitales. [Internet] 2007 [cited 2007 June 2]. Available from: http://www.ine.cl/ine/canales/chile_estadistico/demografia_y_vitales/demo_y_vita.php).
  • 11
    MIDEPLAN, Ministerio de Planificación y Cooperación, Encuesta CASEN. [Internet] 2007 [cited 2007 June 2]. Available from: www.mideplan.cl/casen.
  • 12
    MINSAL, Ministerio de Salud de Chile, Departamento de Epidemiología. [Internet] 2007 [cited 2007 October 2]. Available from: www.minsal.cl.
  • 13
    Wakefield JC,Best NG,Waller LA. Bayesian approaches to disease mapping. In spatial epidemiology: methods and applications. Oxford: Oxford University Press, 2000. 10427.
  • 14
    Besag J,York J,Mollie A. Bayesian image restoration, with two applications in spatial statistics. Ann Inst Stat Math 1991; 43: 159.
  • 15
    Spiegelhalter D,Best N. Bayesian approaches to multiple sources of evidence and uncertainty in complex cost-effectiveness modeling. Stat Med 2003; 22: 3687709.
  • 16
    Smith BJ. Bayesian Output Analysis Program (BOA), Version 0.5.0 for S-PLUS and R, 2000. Available from: http://www.public-health.uiowa.edu/BOA.
  • 17
    Best N,Cowles MK,Vines K. Coda: convergence diagnosis and output analysis software for Gibbs sampling output, Version 0.30. 1995, Technical Report, MRC Biostatistics Unit.
  • 18
    Carey MC,Paigen B. Epidemiology of the American Indians' burden and its likely genetic origins. Hepatology 2002; 36: 78191.
  • 19
    Hsing AW,Rashid A,Devesa SS,Fraumeni JF,Jr. Biliary tract cancer. In: SchottenfeldD,FraumeniJF,Jr, eds. Cancer epidemiology and prevention,3rd edn. New York: Oxford University Press, 2006: 787800.
  • 20
    Miquel JF,Covarrubias C,Villaroel L,Mingrone G,Greco AV,Puglielli L,Carvallo P,Marshall G,Del Pino G,Nervi F. Genetic epidemiology of cholesterol cholelithiasis among Chilean Hispanics, Amerindians, and Maoris. Gastroenterology 1998; 115: 93746.
  • 21
    Carrasco EP,Perez FP,Angel BB,Albala CB,Santos JL,Larenas G,Montalvo D. Prevalence of type 2 diabetes and obesity in two Chilean aboriginal populations living in urban zones. Rev Med Chil 2004; 132: 118997.
  • 22
    Shaffer E. Epidemiology and risk factors for gallstone disease: has the paradigm changed in the 21st century? Curr Gastroenterol Rep 2005; 7: 13240.
  • 23
    Perez F,Santos JL,Albala C,Calvillan M,Carrasco E. Obesity and leptin association in three Chilean aboriginal populations. Rev Med Chil 2000; 128: 4552.
  • 24
    Hsing AW,Bai Y,Andreotti G,Rashid A,Deng J,Chen J,Han TQ,Wang BS,Zhang BH,Shen MC,Fraumeni JF,Jr,Gao YT. Family history of gallstones and the risk of biliary tract cancer and gallstones: a population-based study. Int J Cancer 2007; 121: 8328.
  • 25
    Hou L,Xu J,Gao YT,Rashid A,Zheng SL,Sakoda LC,Shen MC,Wang BS,Deng J,Han TQ,Zhang BH,Meyers DA, et al. CYP17 MspA1 polymorphism and risk of biliary tract cancers and gallstones: a population-based study in Shanghai, China. Int J Cancer 2006; 118: 284753.
  • 26
    Sakoda LC,Gao YT,Chen BE,Chen J,Rosenberg P,Rashid A,Deng J,Shen MC,Wang BS,Han TQ,Zhang BH,Cohen-Webb H, et al. Prostaglandin-endoperoxide synthase 2 (PTGS2) gene polymorphisms and risk of biliary tract cancer and gallstones: a population-based study in Shanghai, China. Carcinogenesis 2006; 27: 12516.
  • 27
    Hsing AW,Gao YT,McGlynn KA,Niwa S,Zhang M,Han TQ,Wang BS,Chen J,Sakoda LC,Shen MC,Zhang BH,Deng J, et al. Biliary tract cancer and stones in relation to chronic liver conditions: a population-based study in Shanghai, China. Int J Cancer 2007; 120: 19815.
  • 28
    Hsing AW,Sakoda LC,Chen J,Rashid A,Chu L,Deng J,Wang BS,Shen MC,Chen E,Rosenberg P,Zhang M,Andreotti G, et al. Variants of inflammation-related genes and the risk of gallstones and biliary tract cancer: a population-based study in China. Cancer Res, in press.
  • 29
    Saetta AA. K-ras, p53 mutations, and microsatellite instability (MSI) in gallbladder cancer. J Surg Oncol 2006; 93: 6449.
  • 30
    Roa J,Roa I,De Aretxabala X,Melo A,Faría G,Tapia O. Mutación del gen K-ras en el cáncer de la vesícula biliar. Rev Med Chil 2004; 132: 95560.
  • 31
    Rashid A,Ueki T,Gao Y,Houlihan P,Wallace C,Wang B,Shen M,Deng J,Hsing AW. K-ras mutation, p53 overexpression, and microsatellite instability in biliary tract cancers: a population-based study in China. Clin Cancer Res 2002; 8: 315663.
  • 32
    Llop E,Harb Z,Moreno R,Rothhammer F. Genetic marker variation in coastal populations of Chile. Homo 2002; 53: 170.
  • 33
    Dutta U,Garg PK,Kumar R,Tandon RK. Typhoid carriers among patients with gallstones are at increased risk for carcinoma of the gallbladder. Am J Gastroenterol 2000; 95: 7847.
    Direct Link:
  • 34
    Mager D. Bacteria and cancer: cause, coincidence or cure? A review. J Transl Med 2006; 28: 414.
  • 35
    Levine MM,Black RE,Lanata C. Precise estimation of the numbers of chronic carriers of Salmonella typhi in Santiago, Chile, an endemic area. J Infect Dis 1982; 146: 7246.
  • 36
    Hofmann E,Chianale J,Rollan A,Pereira J,Ferreccio C,Sotomayor V. Blood group antigen secretion and gallstone disease in the Salmonella typhi chronic carrier state. J Infect Dis 1993; 167: 9934.
  • 37
    Levi F,Lucchini F,Negri E,La Vecchia C. The recent decline in gallbladder cancer mortality in Europe. Eur J Cancer Prev 2003; 12: 2657.
  • 38
    Perez-Ayuso RM,Hernandez V,Gonzalez R,Carvacho C,Navarrete C,Alvarez M,Gonzalez R,Marshall G,Miquel JF,Nervi F. Natural history of cholelithiasis and incidence of cholecystectomy in an urban and a Mapuche rural area. Rev Med Chil 2002; 130: 72330.
  • 39
    Chianale J,Valdivia G,Del Pino G,Nervi F. Mortalidad por cáncer vesicular en Chile y su relación con las tasas de colecistectomía. Análisis de la última década. Rev Med Chil 1990; 118: 12848.
  • 40
    Bakarat J,Dunkelberg J,Ma T. Changing patterns of gallbladder carcinoma in New Mexico. Cancer 2006; 106: 43440.
  • 41
    Ministerio de Salud de Chile, Encuesta Nacional de Salud 2003. Available from: www.minsal.cl.
  • 42
    Serra I,Yamamoto M,Calvo A,Cavada G,Baez S,Endoh K,Watanabe H,Tajima K. Association of chili pepper consumption, low socioeconomic status and longstanding gallstones with gallbladder cancer in a Chilean population. Int J Cancer 2002; 102: 40711.
  • 43
    Pandey M,Shukla V. Diet and gallbladder cancer: a case-control. Eur J Cancer Prev 2002; 11: 3658.
  • 44
    Matsuba T,Qiu D,Kurosawa M,Lin Y,Inaba Y,Kikuchi S,Yagyu K,Motohashi Y,Tamakoshi A. Overview of epidemiology of bile duct and gallbladder cancer focusing on JACC Study. J Epidemiol 2005; 15 ( Suppl 2): S150S156.