- Research article
- Open Access
- Open Peer Review
Secular trends of salted fish consumption and nasopharyngeal carcinoma: a multi-jurisdiction ecological study in 8 regions from 3 continents
© Lau et al.; licensee BioMed Central Ltd. 2013
- Received: 20 July 2012
- Accepted: 1 June 2013
- Published: 19 June 2013
Despite salted fish being a classical risk factor of Nasopharyngeal Carcinoma (NPC), whether secular trends in salted fish consumption worldwide accounted for changes in NPC rates were unknown. The relationship between vegetable and cigarette consumption to NPC risk worldwide were also largely uncertain. We investigated the longitudinal trends in standardised NPC incidence/mortality rates across 8 regions and their associations with secular trends in salted fish, vegetable and tobacco consumptions.
Age standardised mortality rate (ASMR) and age standardised incidence rate (ASIR) of NPC were obtained from the WHO cancer mortality database and Hong Kong Cancer Registry. Per capita consumption of salted fish, tobacco and vegetables in Hong Kong and 7 countries (China, Finland, Japan, Portugal, Singapore, United Kingdom and United States) were obtained from the Food and Agriculture Organization of the United Nation (FAO) and Hong Kong Trade and Census Statistics. Pearson correlation and multivariate analysis were performed to examine both crude and adjusted associations.
There were markedly decreasing trends of NPC ASIR and ASMR in Hong Kong over the past three decades, which were correlated with corresponding secular changes in salted fish consumption per capita (Pearson r for 10 cumulative years : ASIR = 0.729 (male), 0.674 (female); ASMR = 0.943 (male), 0.622 (female), all p < 0.05 except for female ASMR). However such associations no longer correlated with adjustments for decreasing tobacco and increasing vegetable consumption per capita (Pearson r for 10 cumulative years: ASIR = 2.007 (male), 0.339 (female), ASMR = 0.289 (male), 1.992 (female), all p > 0.05). However, there were no clear or consistent patterns in relations between NPC ASIR and ASMR with salted fish consumption across 7 regions in 3 continents.
Our results do not support the notion that changes in salted fish consumption had played an important role in explaining secular trends of NPC rates in Hong Kong and worldwide. Further studies should explore other lifestyle and genetic factors. However, our findings do support the potentially protective effects of vegetable consumption against NPC.
- Nasopharyngeal carcinoma
- Salted fish consumption
- Secular trend
- Ecological study
The distribution of nasopharyngeal carcinoma (NPC) has a distinctive geographic variation. Being a rare malignancy worldwide, it has particularly high rates in Southern China . Residual risk remained high among migrants of Chinese descent  to non-endemic areas, with intergenerational decline , suggesting that the aetiology of NPC is a complex interplay between genetic influences and environmental exposures distinct in these populations.
Among known environmental exposures relevant to the aetiology of NPC; dietary consumption of salted fish is the most well recognised risk factor. First suggested by Ho and colleagues  to have a link with the high incidence of NPC in Southern China Guangdong Province in the early 1970s, subsequent studies quite consistently reported positive associations between salted fish consumption and risk of NPC in Chinese  and other ethnicities  such as Thai and Tunisian , and that early exposures during the weaning period in childhood may play a critical role [1, 8]. What makes salted fish an intriguing item to look at is that nitrosamine in Cantonese style salted fish is carcinogenic to humans and this food item is rated as a group 1 carcinogen by the International Agency for Research on Cancer (IARC), whereas other salted fish are only classified as group 3 carcinogen . This can be explained by the different levels of nitrosamines in various types of salted fish, depending on the method of preservation . However, the low disease rates of NPC even in endemic regions render case-control studies to be the only feasible epidemiological method, of which limitations and deficiencies are well-recognised. The extent to which notorious effects of recall bias , lack of adjustment of caloric intake  and other confounders may affect the validity of the study findings remains unknown. Whether any publication bias may exist due to active reporting of salted fish consumptions as a classical risk factor of NPC is also uncertain. Although Cantonese-style salted fish has been classified by IARC as a group 1 carcinogen , the putative main biological active component N-nitrosodimethylamine, is only classified as a group 2A carcinogen . Such incoherence makes the aetiological role of salted fish especially worthwhile for more thorough re-exploration.
In the past 30 to 40 years, the incidence and mortality rates of NPC have dropped noticeably in several Asia regions particularly among some Chinese subpopulations [14, 15]. Given the wide range of the relative risk of high salted fish consumption ranging from 2.5–17.2 ,which translates into population attributable risk (PAR) of 39%–78%, adopting exposure prevalence of salted fish consumption in the population, it would be of interest to investigate whether the secular trend of NPC disease rates is explained by a corresponding change in salted fish consumption in relevant jurisdictions. To our best knowledge, reports of such studies were not available.
We, therefore, carried out this Hong Kong and multi-site ecological study to investigate the relationship between secular trends of salted fish consumption and standardised NPC incidence and mortality rates over 30 years. We also included an analysis in Hong Kong taking into account other key lifestyle related factors, including tobacco smoking  and vegetable  consumption, which were reported to be a risk and protective factor of NPC respectively.
In this ecological study, we focused on Hong Kong, an endemic area of NPC, and 7 countries in 3 continents including: China, Finland, Japan, Portugal, Singapore, United Kingdom and United States. Hong Kong was chosen due to its high prevalence of NPC, with the advantage of a comprehensive cancer statistics database and the availability of relevant risk/protective factor profiles. China was also selected for investigation, since there is a substantial variation in NPC risk of Chinese who lived in different parts of China. For example those who live in the Northern parts of China have a lower incidence rate than people who live in Southern China . Another area with a relatively high NPC mortality rate is Singapore, which attracted much attention in previous NPC case control studies [19, 20]. For low risk areas, Japan, Finland, Portugal, United Kingdom and United States were selected because of their rather complete cancer statistics.
NPC incidence and mortality statistics
NPC age-standardised mortality rates (ASMR) and age-standardised incidence rates (ASIR) were obtained from various sources. NPC age-standardised incidence and mortality rates in Hong Kong during 1978 to 2008 were derived from Hong Kong Cancer Registry with the world 1966 standard population as reference. NPC mortality statistics of other jurisdictions were collected from the WHO cancer mortality database [22–24], and age-standardised rates were also adjusted to the world standard population 1966. The code of cancer site followed the International Classification of Disease (ICD) coding system, with NPC coded as 147 (ICD-8, WHO 1967; ICD-9, WHO 1977) and C11 (ICD-10, WHO 1992).
Salted fish consumption per capita
Hong Kong SAR trade statistics and census
Salted fish consumption in Hong Kong was estimated from import, export and re-export volumes of dried fish, and whether or not salted but not smoked provided by the Service Centre on Trade Statistics, Census and Statistics Department, Hong Kong SAR Government. The database contains monthly and annual tallies of quantity, value and import by country of origin (of the product), import by country of consignment (origin of shipment), country of export, and country of re-export according to Harmonized Commodity Description and Coding System of the World Customs Organization. Domestic consumption was calculated from the difference between exports, re-exports and imports. All these data were acquired from the archive database of Census and Statistics Department. Salted fish consumption per capita for each year was then estimated according to the formula: (imports − exports − re-exports) ÷ mid-year population in Hong Kong retrieved from Population Census and By-census, Demographic Statistics Section, Census and Statistics Department, 1978–2008 .
Food and Agriculture Organisation (FAO), United Nations
Worldwide salted fish consumptions were compiled by productions, imports, exports and re-exports on fish, dried, salted or smoked from Fishery and Aquaculture Statistics Database, FAO , United Nations. This database contains statistics on the annual production, imports, exports and re-exports of fishery commodities by country and commodities in terms of volume and value from 1976. For every country, per capita consumption was calculated from the difference between exports, re-exports, imports and production, i.e. [(import + production) – export– re-export] ÷ total population of the defined jurisdiction in each year. Total population is estimated from FAOSTAT Population module .
Tobacco consumption per capita
Per capita cigarette consumption in Hong Kong was estimated by Hong Kong Council on Smoking and Health (COSH) via General Household Survey and Thematic Household Survey 2008 in reporting average daily cigarette consumption among smokers(sticks), number of smokers and percentage of smokers in Hong Kong from 1982–2008. Per capita consumption was calculated by: Daily average consumption × No. of daily smokers (aged 15 and over) ÷ Population (all age) × 365 days = Per capita consumption (stick/capita/year). Statistic on tobacco tax was also collected from COSH. Data on percentage increase in tobacco tax was plotted with per capita consumption of tobacco.
Vegetable consumption per capita
Per capita fresh vegetable consumption data in Hong Kong from 1991 to 2009 were obtained from the Department Annual Report by Agriculture, Fisheries and Conservation Department HKSAR . All per capita calculations in Hong Kong were divided by mid-year population obtained from Population Census and By-census 1991–2009, Demographic Statistics Section, Census and Statistics Department .
NPC incidence and mortality rates were estimated from 1978–2008, as cases or deaths per 100,000 persons. The rates were age-standardised to the world 1966 standard population for all localities using 18 age groups (<1, 1–4, 5–9,…, 80–84, 85+). Age-standardised mortality/incidence and male/female ratio in age-standardised incidence and mortality rates were also calculated.
Non-linear regression of least square method was used for fitting any incomplete data point from 1978–2008. Pearson correlation analysis was used to examine the relations between cumulative consumption of salted fish, vegetable and tobacco in relation to ASIR and ASMR from 1991–2008 in Hong Kong. Multivariable linear regression analysis was performed to adjust for potential confounding effects of tobacco and vegetable consumption during the period of 1991–2008. Repeated analysis using various duration of cumulative salted fish intake prior to the NPC disease rate outcomes was performed to test the robustness of estimates based on differential assumptions in the latency period of cancer development subsequent to relevant exposures (range: 0, 5, 10 years). A p value smaller than 0.05 (two-sided) was considered statistically significant. All the data was analysed by SPSS Statistics 17.0.
Age-standardised incidence and mortality rates in Hong Kong from 1978–2008
The age standardised mortality/incidence ratio (Figure 1c) for both genders, albeit with notable fluctuations, followed an overall slowly declining trend over the past 30 years with estimates for males being consistently higher than females. The male/female ratios for ASIR and ASMR, as presented in Figure 1d, maintained a value of around 3 over the past 30 years with a slowly rising trend. The ASMR male/female ratio was higher than that for ASIR throughout the whole period.
Secular trend of salted fish consumption estimates in Hong Kong from 1978–2008
Relation between salted fish consumption and NPC in Hong Kong
Correlation coefficient (r) from Pearson correlation analysis between cumulative salted fish consumption per capita (per kg) and age-standardized incidence and mortality rates in Hong Kong, 1991–2008
(a) FAO commodity statistics
Year of cumulative salted fish consumption per capita
Age-standardized incidence rate
Age-standardized mortality rates
(b) Hong Kong trade statistics
Year of cumulative salted fish consumption per capita
Age-standardized incidence rate
Age-standardized mortality rates
Tobacco consumption and relations with NPC in Hong Kong
Correlation coefficient (r) from Pearson correlation analysis between cumulative cigarette consumption per capita (per stick) and age-standardized incidence and mortality rates in Hong Kong, 1991–2008
Year of cumulative cigarette consumption per capita
Age-standardized incidence rate
Age-standardized mortality rates
Vegetable consumption and relations with NPC in Hong Kong
Correlation coefficient (r) from Pearson correlation analysis between cumulative fresh vegetable consumption per capita (per kg) and age-standardized incidence and mortality rates in Hong Kong,1991–2008
Year of cumulative fresh vegetable consumption per capita
Age-standardized incidence rate
Age-standardized mortality rates
Beta (β) regression coefficient from multivariate regression analysis of NPC age-standardized incidence and mortality rates on cumulative salted fish (per kg), cigarette (per stick) and fresh vegetable consumption (per kg) in Hong Kong, 1991–2008
Cumulative window (Years)
Age-standardized incidence rate
Age-standardized mortality rates
Multi-jurisdiction ecological analysis
This is the first multi-jurisdiction ecological study that examined the associations between secular trends of NPC risk and salted fish consumption per capita. We also adjusted for the potentially confounding effects of two most important lifestyle factors, namely tobacco and vegetable consumption, using per capita estimates. We included 7 regions in 3 continents to include both endemic and low-risk areas, to analyse the pattern with a more global perspective.
We observed a decline in both ASIR and ASMR of NPC in Hong Kong over the past three decades. Higher NPC ASMR was observed in males than females in most of the jurisdictions included, consistent with previous studies [11, 30, 31], which may be due to a combination of differential risk factor exposures such as greater tobacco consumption in males and genetic factors. The rather consistent; more than 3-fold risk in males compared with females needs further investigation. Our results showed markedly decreasing trends in salted fish intake and tobacco consumption, but an increasing trend in vegetable consumption in Hong Kong over the past several decades. All of these environmental risk factors were individually highly correlated with ASMR and ASIR. The decrease in salted fish consumption may represent a change in dietary culture with westernisation of dietary patterns among Hong Kong citizens from a traditional Cantonese diet and from increased awareness of the carcinogenicity of salted fish. Decrease in intake of salted fish should lower the risk of an individual getting NPC if the relationship is causal .
There were no substantial changes in the proportion of Cantonese residing in Hong Kong, thus any changes noted should not be confounded by migration effect. Additional file 1: Tables S1-S3 show the population structure in Hong Kong from 1961–2006. Nevertheless, in the multivariable model, the relations between salted fish consumption and NPC ASIR and ASMR were attenuated and became mostly insignificant. In contrast, the negative association between vegetable consumption and NPC ASIR remained statistically significant after adjustment and was robust across varying estimates of cumulative exposure windows prior to NPC outcomes. Consistent with findings from previous case-control studies [18, 32], dietary intake of fruits and vegetables may have a protective effect against NPC due to its antioxidant contents, potentially interfering with the actions of nitrosamines . World Cancer Research Fund (WCRF) panel suggested fruit and vegetable consumption have limited to suggestive levels of evidence for protection against NPC , which is consistent with the result found in this study. Although positive association was observed for cigarette consumption and NPC ASIR in males, previous literature suggested that for lung cancer, of which smoking is known as one of the major risk factor, the lag year for the disease from exposure to cancer onset was 25–30 years , it is expected that the lag for NPC should not be shorter if not similar to lung cancer. As our study is ecological, further analytical studies, such as case control studies with genetic, viral and other biomarkers are warranted to examine the link between salted fish and NPC in Hong Kong, taking into account smoking, vegetable consumption and other potential confounders.
Despite the parallel secular trends of salted fish consumption and NPC rates in Hong Kong, the same pattern was not observed in all other jurisdictions. For instance, in China, salted fish consumption increased over the years and there was no sign in apparent increase of ASMR in both males and females. Similarly, there are jurisdictions where NPC ASIR/ASMR had markedly decreased, but with no accompanying drop in salted fish consumption. Caution needs to be taken in interpretation, since the salted fish consumed in other countries might not be the Cantonese-styled salted fish, which is categorised as a group I carcinogen by IARC. The effect of salted fish on NPC development might only have a notable impact among Hong Kong Chinese but not in other populations, due to the higher underlying disease rates of NPC in Hong Kong, or could be due to genetic differences e.g. nitrosamine metabolism . Indeed, the vast majority of previous case-control studies on salted fish consumption and NPC were only conducted in Chinese [1, 4, 5, 37]. It remains uncertain whether the same carcinogenesis mechanism could apply to different Chinese sub-group or non-Chinese populations.
Our findings highlight the importance of examining the relations between key risk factor exposures and NPC on multiple jurisdictions rather than focusing on a single locality and a single exposure in an ecological study. Furthermore, since NPC includes a spectrum of squamous, and keratinising versus non-keratinising subtypes which are linked to differential risk factors, this may also be an important reason underlying the varying patterns of ecological associations found across different jurisdictions. Thus an ecological study investigates the links between risk and protective factors and different subtypes would be of interest, especially when the pathogenesis processes for various NPC subtypes appear to be distinct. Therefore it is important to first elucidate the secular trend of salted fish consumption and NPC incidence/mortality rates between multiple areas. The findings from this study have encouraged us to further examine the time trend of different NPC subtypes across regions, and so far our literature review has shown that a more thorough review and deeper understanding is needed of different NPC histological classification between China and the West, but such data are often scarce. Also, the differences between Chinese and WHO classifications need to be further examined and resolved. We believe this would warrant a separate paper for a detailed discussion.
There are several limitations in our study. First of all we could not be certain that the capture of NPC incidence and mortality was 100% complete and accurate in each jurisdiction, but most data were derived from cancer registries where completeness of data; especially that of mortality, is good with high accuracy. Variations of diagnostic criteria could exist but this effect is minimised by using International Classification of Disease (ICD 8–10) since NPC is a rare and uncommon cancer. Secondly, per capita consumption was calculated by taking the difference between export, import, production and re-export of salted fish. Consequently, there was a possibility of over or underestimating the actual amount of salted fish being consumed. Nevertheless, data obtained from Hong Kong Trade and Statistics and from the FAO were largely consistent. Even though we tried to obtain all the salted fish related data as precisely as possible, the data we used might include other dried fish products rather than just Cantonese style salted fish, details of which could not be obtained from other jurisdictions. Moreover, the uncertainty of latency period between the consumption patterns and ASIR/ASMR is well acknowledged, for that we included the sensitivity analysis by using year of cumulative consumption for regression and result were shown to be robust. Furthermore, vegetable consumption in Hong Kong was not available from Agriculture, Fisheries and Conservation Department HKSAR prior to 1991, thus multivariable analysis was done only between 1991–2008 but not from 1978–2008.
Finally, the limitations of ecological studies due to the ecological fallacy are well recognised, and unknown, unmeasured or immeasurable confounding factors may be present. We tried to take account of important and known factors by accounting for tobacco consumption, vegetable consumption and migration effects, which is the first example of its kind in NPC epidemiological studies. In future studies, age-specific rather than age-standardised mortality and incidence rates could be more informative to investigate disease risk across different ages and in different populations. Because NPC is endemic mainly in Southern China, ecological analysis focusing on the endemic regions of China would yield more important information than a national study. Data specifically in Southern China on salted fish, vegetable and cigarette consumptions, together with NPC incidence and mortality rates (with subtypes) would be highly valuable if such data are available in the near future and more in depth analysis is warranted.
In this study, we found markedly decreasing trends of NPC ASIR and ASMR in Hong Kong over the past 3 decades, which was correlated with corresponding secular changes in salted fish consumption per capita. However, this association no longer held after adjustment for tobacco and vegetable consumption per capita. Our result showed vegetable had a protective role in NPC ASIR. There was no clear or consistent pattern in the relations between NPC ASIR and ASMR with salted fish consumption across 7 regions in 3 continents. Whether the pathogenic role of salted fish consumption is specific to NPC among Hong Kong Chinese requires further studies.
This study was supported by Hong Kong RGC Area of Excellence Scheme (Grant Number AoE/M-06/08), and by World Cancer Research Fund UK (WCRF UK) and Wereld Kanker Onderzoek Fonds (WCRF NL), as part of the WCRF International grant programme (grant 2011/460).
- Yu MC, Ho JHC, Lai SH, Henderson BE: Cantonese-style salted fish as a cause of nasopharyngeal carcinoma: report of a case-control study in Hong Kong. Cancer Res. 1986, 46 (2): 956-961.PubMedGoogle Scholar
- Bray F, Haugen M, Moger TA, Tretli S, Aalen OO, Grotmol T: Age-incidence curves of nasopharyngeal carcinoma worldwide: bimodality in low-risk populations and aetiologic implications. Cancer Epidemiol Biomarkers Prev. 2008, 17 (9): 2356-2365. 10.1158/1055-9965.EPI-08-0461.View ArticlePubMedGoogle Scholar
- Yu W, Hussain S: Incidence of nasopharyngeal carcinoma in Chinese immigrants, compared with Chinese in China and South East Asia: review. J Laryngol Otol. 2010, 123 (10): 1067-1074.View ArticleGoogle Scholar
- Ho JHC, Huang DP, Fong YY: Salted fish and nasopharyngeal carcinoma in southern Chinese. Lancet. 1978, 2 (8090): 626-View ArticlePubMedGoogle Scholar
- Ning JP, Yu MC, Wang QS, Henderson BE: Consumption of salted fish and other risk factors for nasopharyngeal carcinoma factor in Tianjin, a low risk region for NPC in the People’s Republic of China. J Natl Cancer Inst. 1990, 82 (4): 291-296. 10.1093/jnci/82.4.291.View ArticlePubMedGoogle Scholar
- Sriamporn S, Vatanasapt V, Pisani P, Yongchaiyudha S, Rungpitarangsri V: Environmental risk factors for nasopharyngeal carcinoma: a case-control study in northeastern Thailand. Cancer Epidemiol Biomarkers Prev. 1992, 1 (5): 345-348.PubMedGoogle Scholar
- Jeannel D, Hubert A, Vathaire FD, Ellouz R, Camoun M, Ben Salem M, Garnier S, De-The G: Diet, living conditions and nasopharyngeal carcinoma in Tunisia-a case control study. Int J Cancer. 1990, 46 (3): 421-425. 10.1002/ijc.2910460316.View ArticlePubMedGoogle Scholar
- Zheng YM, Tuppin P, Hubert A, Jeannel D, Pan YJ, Zeng Y, The Gd: Environmental and dietary risk factors for nasopharyngeal carcinoma: a case-control study in Zangwu County, Guangxi, China. Br J Cancer. 1994, 69 (3): 508-514. 10.1038/bjc.1994.92.View ArticlePubMedPubMed CentralGoogle Scholar
- Some naturally occurring substances: Food items and constituents, heterocyclic aromatic amines and mycotoxins. Summary of data reported and evaluation. IARC monographs on the evaluation of carcinogenic risks to humans. vol. 56. 1997, Lyon, France: WHOGoogle Scholar
- Zou XN, Lu SH, Liu B: Volatile N-nitrosamines and their precursors in chinese salted fish-a possible etological factor for NPC in China. Int J Cancer. 1994, 59 (2): 155-158. 10.1002/ijc.2910590202.View ArticlePubMedGoogle Scholar
- Feng B-J, Jalbout M, Ayoub WB, Khyatti M, Dahmoul S, Ayad M, Maachi F, Bedadra W, Abdoun M, Mesli S, et al: Dietary risk factors for nasopharyngeal carcinoma in Maghrebian countries. Int J Cancer. 2007, 121 (7): 1550-1555. 10.1002/ijc.22813.View ArticlePubMedGoogle Scholar
- Albanes D: Caloric intake, body weight, and cancer: a review. Nutr Cancer. 1987, 9 (4): 199-217. 10.1080/01635588709513929.View ArticlePubMedGoogle Scholar
- Vainio H, Wilbourn J: Identification of carcinogens within the IARC monograph program. Scand J Work Environ Health. 1992, 18 (Suppl 1): 64-73.PubMedGoogle Scholar
- Hsu C, Shen YC, Cheng CC, Hong RL, Chang CJ, Cheng AL: Difference in the incidence trend of nasopharyngeal and oropharyngeal carcinomas in Taiwan: implication from age-period-cohort analysis. Cancer Epidemiol Biomarkers Prev. 2006, 15 (5): 856-861. 10.1158/1055-9965.EPI-05-0821.View ArticlePubMedGoogle Scholar
- Lee AWM, Foo W, Mang O, Sze W, Chappell R, Lau W, Ko W: Changing epidemiology of nasopharyngeal carcinoma in Hong Kong over a 20-year period (1980–99): An encouraging reduction in both incidence and mortality. Int J Cancer. 2003, 103 (5): 680-685. 10.1002/ijc.10894.View ArticlePubMedGoogle Scholar
- Alberg AJ, Boyd K, Tao XG, Matanoski G, Balick L, Caulfield LE, Chen LW, Gallicchio L, Guallar E, Herman JG, et al: The association between food, nutrition and physical activity and the risk of cancer of the nasopharynx and underlying mechanism. 2006, Baltimore, Maryland, USA: John Hopkins University, John Hopkins UniversityGoogle Scholar
- Yuan JM, Wang XL, Xiang YB, Gao YT, Ross RK, Yu MC: Non dietary risk factors for nasopharyngeal carcinoma in Shanghai, China. Int J Cancer. 2000, 85 (3): 364-369. 10.1002/(SICI)1097-0215(20000201)85:3<364::AID-IJC12>3.0.CO;2-C.View ArticlePubMedGoogle Scholar
- Y-t L, Dai J-j X, C-h L, Y-k FY-y, X-l Z, C-x Z, Y-m C: Greater intake of fruit and vegetables is associated with lower risk of nasopharyngeal carcinoma in Chinese adults: a case-control study. Cancer Causes Control. 2012, 23 (4): 588-599.Google Scholar
- Lee HP, Gourley L, Duffy SW, Lee J, Day NE: Preserved foods and nasopharyngeal carcinoma: a case control study among Singapore Chinese. Int J Cancer. 1994, 59 (5): 585-590. 10.1002/ijc.2910590502.View ArticlePubMedGoogle Scholar
- Friborg JT, Yuan JM, Wang R, Koh WP, Lee HP, Yu MC: A prospective study of tobacco and alcohol use as risk factors for pharyngeal carcinomas in Singapore Chinese. Cancer. 2007, 109 (6): 1183-1191. 10.1002/cncr.22501.View ArticlePubMedGoogle Scholar
- Hong Kong Cancer Registry: Incidence and mortality rates from. 1983, [http://www3.ha.org.hk/cancereg/e_a1a.asp], –2009
- Demographic data: United Nations, World Population Prospects, the. 2010, [http://www.un.org/esa/population/unpop.htm], revision
- Number of deaths: World Health Organisation, mortality database. [http://www.who.int/healthinfo/mortality_data/en/index.html]
- WHO cancer mortality database: [http://www-dep.iarc.fr/WHOdb/WHOdb.htm]
- Hong Kong Demographic Statistics 1961–2011: [http://www.censtatd.gov.hk/showtableexcel2.jsp?tableID=002]
- Annual production of fishery commodities and imports, exports and re-exports of fishery commodities from 1976–2009: [http://www.fao.org/fishery/statistics/global-commodities-production/query/en]
- FAOSTAT Population module: [http://faostat.fao.org/site/550/default.aspx#ancor]
- Census and Statictic Department(C&SD): Thematic Household Survey Report No. 36. 2008, Hong Kong SAR, China: Census and Statictic Department(C&SD)Google Scholar
- Hong Kong Agriculture, Fisheries and Conservation Department annual report: Department Annual Report. 2001-2009, Hong Kong SAR, China: Hong Kong Agriculture, Fisheries and Conservation DepartmentGoogle Scholar
- Yu MC, Yuan JM: Epidemiology of nasopharyngeal carcinoma. Semin Cancer Biol. 2002, 12 (6): 421-429. 10.1016/S1044579X02000858.View ArticlePubMedGoogle Scholar
- Ji XM, Zhang WD, Xie CH, Wang BH, Zhang G, Zhou FX: Nasopharyngeal carcinoma risk by histologic type in central China: impact of smoking, alcohol and family history. Int J Cancer. 2011, 129 (3): 724-732. 10.1002/ijc.25696.View ArticlePubMedGoogle Scholar
- Ward MH, Pan W-H, Cheng Y-J, Li F-H, Brinton LA, Chen CJ, Hsu MM, Chen IH, Levine PH, Yang CS, et al: Dietary exposure to nitrite and nitrosamines and risk of nasopharyngeal carcinoma in Taiwan. Int J Cancer. 2000, 86 (5): 603-609. 10.1002/(SICI)1097-0215(20000601)86:5<603::AID-IJC1>3.0.CO;2-H.View ArticlePubMedGoogle Scholar
- Ikken Y, Morales P, Martínez A, Marín ML, Haza AI, Cambero MI: Antimutagenic effect of fruit and vegetable ethanolic extracts against N-nitrosamines evaluated by the Ames test. J Agric Food Chem. 1999, 47 (8): 3257-3264. 10.1021/jf990166n.View ArticlePubMedGoogle Scholar
- Food, nutrition, physical activity, and the prevention of cancer: a global perspective. 2007, Washington DC: World Cancer Research Fund/American Institute of Cancer ResearchGoogle Scholar
- Shibuya K, Inoue M, Lopez AD: Statistical modeling and projections of lung cancer mortality in 4 industrialized countries. Int J Cancer. 2005, 117 (3): 476-485. 10.1002/ijc.21078.View ArticlePubMedGoogle Scholar
- Cho EY, Hildesheim A, Chen CJ, Hsu MM, Chen IH, Mittl BF, Levine PH, Liu MY, Chen JY, Brinton LA: Nasopharyngeal carcinoma and genetic polymorphisms of DNA repair enzymes XRCC1 and hOGG1. Cancer Epidemiol Biomarkers Prev. 2003, 12 (10): 1100-1104.PubMedGoogle Scholar
- Armstrong RW, Imrey PB, Lye MS, Armstrong MJ, Yu MC, Sani S: Nasopharyngeal carcinoma in Malaysian Chinese: salted fish and other dietary exposures. Int J Cancer. 1998, 77 (2): 228-325. 10.1002/(SICI)1097-0215(19980717)77:2<228::AID-IJC11>3.0.CO;2-7.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2407/13/298/prepub
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