Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Epidemiology

Adult height in relation to risk of cancer in a cohort of 22,809,722 Korean adults

Abstract

Background

The present study examined whether adult height was associated with all site-combined or site-specific cancers.

Methods

We used a nationwide claim data of 22,809,722 Korean participants including both men and women (2009–2012). The deciles of height from different age and sex groups were merged into a new quintile. We used Cox proportional hazards model to estimate hazard ratios (HRs) and 95% confidence intervals.

Results

During a 5-year follow-up period, 765,651 patients were diagnosed with cancer. Height was positively associated with risk of all site-combined cancers and with malignancy in the oral cavity, larynx, lung, stomach, colorectum, liver, pancreas, biliary tract and gallbladder, breast, ovary, cervix and corpus uteri, prostate, testes, kidney, bladder, central nervous system, thyroid, skin, and lymphatic and haematopoietic systems. The HRs for all-site cancers per 5 cm increment in height was 1.09 and that of each site was the highest in thyroid, breast, lymphoma, testicular, and renal cancers. This association was more prominent in women and male non-smokers than in other counterparts.

Conclusions

Taller adult height was significantly related to an increased risk of most cancers including neoplasm in the gallbladder or biliary tract and testes, but except for oesophagus.

Introduction

Cancer was the second leading cause of death behind cardiovascular diseases. While the association between obesity (or visceral obesity) and cancer has been exhaustedly evaluated, the effect of height on the risk of having malignancy has received far less attention. Some early studies have reported that height is associated with an increased risk of all cancers and of specific cancers at various anatomic sites including the breast, prostate, and colorectum,1,2,3 the results were inconsistent according to gender, smoking status or body mass index (BMI).4,5,6,7 However, literature that included both sexes and a controlled possible compounder, such as weight or smoking, is limited, and most studies were conducted in Western countries. Based on this background, we aimed to investigate the association between attained adult stature and development of cancer using Korean nationwide databases. Additionally, whether different gender or smoking status could affect the association was evaluated.

Methods

Data source

Approximately 97% of the Korean population is registered with the National Health Insurance Corporation (NHIC), a single public health insurance programme, managed by the Korean government. NHIC subscribers undergo mandatory standardised medical examinations at least biennially from 40 years of age. Korean researchers can use the NHIC database with an approval by the official review committee.

From the total population of the Republic of Korea, we recruited 17,391,531 subjects who were older than 20 years and who underwent an initial baseline health check-up by the NHIS between 2009 and 2012. This cohort was then followed up until 2015. From this initial population, we excluded 1,108,167 subjects whose data was missed and 21,484,529 subjects who underwent more than two health check-ups during this period. Finally, 22,809, 722 subjects were included in the baseline cohort and followed up after excluding 448,040 who were diagnosed with any kind of cancer during the preceding years.

Medical record data and standardised self-reporting questionnaires were evaluated. Questionnaires at baseline included cancer risk factors; age (years), sex, smoking, drinking, physical activity and residency (rural and urban). Anthropic variables including blood pressure, height, weight, waist circumference, and values of serum fasting glucose and total cholesterol (mg/dL) were measured.

All procedures involving human participants were performed in accordance with the ethical standards of the institutional and national research committees and the 1964 Helsinki declaration including its later amendments or comparable ethical standards. This study was approved by the Institutional Review Board of Seoul National University Bundang Hospital (X-1608/360-904). Since the study involved routinely collected data, informed consent was not specifically obtained for this study.

Study outcomes

The primary endpoint was newly diagnosed cancer at one of 23 different sites, which was defined using the International Classification of Diseases, 10th revision (ICD-10) codes: oral cavity and pharynx (ICD-10 C00–C14), larynx (C32), oesophagus (C15), stomach (C16), colorectum (C18–20), pancreas (C25), gallbladder and biliary tract (C23–24), lung (C33–34), breast (C50), corpus uteri (C54), cervix uteri (C53), ovary (C56), kidney (C64), bladder (C67), central nervous system (C70–72), skin (C43), non-Hodgkin lymphoma (NHL) (C82–86), multiple myeloma (C90), and leukaemia (C91–95). Codes for the reimbursement for serious diseases were also reviewed to reduce the error in studies with claim data; that is, both codes were required for the definition of cancer patients. The diagnosis was considered new when the patient had no such diagnosis before 2009. All patients with a previous malignancy were excluded. The same method (based on ICD and codes for the reimbursement for cancer) was applied to exclude persons who had history of any malignancy before index date.

Definition of comorbidity and other variables

Regular exercise was defined as engaging in vigorous exercise on a regular basis (periods of high-intensity activity more than three times per week or periods of moderate intensity activity more than five times per week).8 BMI and systolic and diastolic blood pressure (mmHg) were also measured. Subjects were considered as obese when the BMI was ≥ 25 kg/m2 based on criteria for the Asian-Pacific region.9 Waist circumference ≥ 90 cm was defined as abdominal obesity.10 Diabetes mellitus (DM) was defined based on using insulin or oral hypoglycaemic agents, or a fasting plasma glucose level ≥ 126 mg/dL.11 Participants were diagnosed as being hypertensive if the systolic pressure was ≥ 140 mmHg, if the diastolic pressure was ≥ 90 mmHg, or if current antihypertensive medication was used. After overnight fasting for at least 8 h, blood specimens collected from each subject were processed and transported in cold storage to the Central Testing Institute (Neodin Medical Institute, Seoul, Korea). All the blood samples were analysed within 24 h after transportation.

Because height is dependent on age and sex, we divided the population into deciles of height for each age group (20–29 years, 30–39 years, 40–49 years, 50–59 years, 60–69 years and ≥70 years) and sex (Table S1).12 The deciles from the 12 different age and sex groups were merged into new quintiles of height. We analysed these merged quintile groups for incidence and hazard ratio of cancers.

Statistical analyses

Data are presented as mean ± standard deviation for continuous variables and as proportions for categorical variables. Continuous variables were evaluated using analysis of variance (ANOVA), and categorical variables were evaluated using chi-square tests. A Cox proportional hazards model was used to determine the independent effect of height on all sites-combined and site-specific cancer risk, after controlling for age (continuous), sex, BMI, smoking status, alcohol consumption, physical activity, and diabetes. We compared the HR of the highest quintile of height compared with that of the lowest. Additionally, we evaluated the hazard ratios (HRs) in 5 cm increment in height. In Forrest plots, the HRs was represented by lines.

Statistical analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC, United States) and R version 3.2.3 (The R Foundation for Statistical Computing, Vienna, Austria, http://www.Rproject.org). A two-sided P-value of <0.05 was considered to indicate statistical significance.

Results

Characteristics of the study population

A total of 22,809,722 participants among enrolees from 2009 through 2012 were finally analysed and followed up until 2015. They are grouped into the sex and age-adjusted quintile of height, and baseline characteristics at the enrolment were described in Table 1.

Table 1 Baseline characteristics by quintiles of height in study participants of the Korean National Health Insurance Corporation

Approximately, half of the total enrolees were men. Waist circumference and weight increased when the height increased, while BMI deceased. The frequencies of hypertension and dyslipidaemia tended to decrease when the quintile of height increased (P < 0.001 for trend). Taller participants were likely to live in urban places, consume large amount of alcohol, smoke currently, and be more physically active than shorter persons.

Cancer risk stratified by height

Taller adult height was associated with increased risks for total combined-cancers. Compared to participants in the lowest quintile, those in the highest quintile had a 28% increased risk after controlling age, sex, current smoking, current alcohol consumption, regular physical activity, DM and BMI (HR 1.28, 95% CI: 1.27–1.28, P for trend < 0.001) (Table 2).

Table 2 Incidences and adjusted hazard ratios of all-23 cancers and 10 representative site-specific cancers

The HR of all-sites cancers per 5 cm increase in height was 1.09 (95% CI 1.086–1.090) (Fig. 1). Taller adult stature was positively associated with increased risks of cancers at all 23 anatomic sites in a multivariable model that included BMI (Table 2 and Table S2). Compared to persons in the shortest group, HRs and 95% CIs of persons in the tallest group from the multivariable model were as follows: oral cavity (1.09, 95% CI: 1.03–1.15), larynx (1.19, 95% CI: 1.09–1.30), stomach (1.11, 95% CI: 1.09–1.13), colorectum (1.26, 95% CI: 1.24–1.28), lung (1.31, 95% CI: 1.28–1.34), pancreas (1.22, 95% CI: 1.18–1.25), thyroid (1.57, 95% CI: 1.54–1.59), kidney (1.56, 95% CI: 1.48–1.63), bladder (1.31, 95% CI: 1.26–1.37), multiple myeloma (1.29, 95% CI: 1.18–1.40), lymphoma (1.42, 95% CI: 1.35–1.50), leukaemia (1.34, 95% CI: 1.26–1.44), CNS (1.24, 95% CI: 1.16–1.31), melanoma (1.30, 95% CI: 1.17–1.46), breast (1.45, 95% CI: 1.42–1.49), ovary (1.27, 95% CI: 1.21–1.34), prostate (1.30, 95% CI: 1.26–1.33) and testes (1.62, 95% CI: 1.38–1.91). Particularly, there was a dose-dependent increase in the risk of cancers in oral cavity, liver, colorectum, lung, pancreas, breast, ovary, thyroid, bladder, kidney, melanoma, and haematopoietic system (Table 2 and Table S2). With regard to oesophageal cancer, the tallest group had an increased risk for the disease compared with the shortest group; there was a no dose-dependent relationship. HRs for cancers per 5 cm increase in height were highest in thyroid, breast, lymphoma, testicular, and renal cancers (Fig. 1), while oesophageal cancer did not show a significant association due to a lack of a dose-dependent association.

Fig. 1: Hazard ratios and 95% confidence intervals per 5 cm increase in height for all cancers and 23 site-specific cancers.
figure1

HRs are adjusted for age, sex, body mass index, current smoking, current alcohol consumption, regular physical activity, and presence or absence of diabetes mellitus. HR hazard ratio, CI confidence interval, MM multiple myeloma, CNS central nerve system, GB gallbladder, BT biliary tract

Combined effect of height on the development of cancers according to gender and current smoking status

The baseline characteristics were presented by gender (Table S3). Men were more likely to smoke, drink excessively, exercise regularly, and have obesity, hypertension, and diabetes compared to women, while women were older than males with the same height rank, more women lived in cities, and had hyperlipidaemia.

HR of combined all-sites cancers was more prominent in women than in men (women: HR 1.11 95% CI: 1.107–1.114 versus men: HR 1.05, 95% CI: 1.048–1.054) (Fig. 2) Among men, the magnitude of association was highest in thyroid cancer (HR 1.20, 95% CI: 1.19–1.21), while cancers in the larynx and lymphatic system were most associated with height in women (1.20, 95% CI: 1.08–1.33; 1.18, 95% CI: 1.15–1.20) (Fig. 2).

Fig. 2: Hazard ratios per 5 cm increase in height for all cancers and cancers at 23 different sites, stratified by gender.
figure2

HRs are adjusted for age, body mass index, current smoking, current alcohol consumption, regular physical activity, and presence or absence of diabetes mellitus. HR hazard ratio, CI confidence interval, MM multiple myeloma, CNS central nerve system, GB gallbladder, BT biliary tract

The effect of smoking status on the development of all cancers and site-specific cancers was analysed (Fig. 3). Current smoking reduced the magnitude of the association between taller height and the development of all combined-cancer by ~5% compared to non-smoking (non-smoker: 1.10 vs. current smoker: 1.05). Among non-smokers, there was a significant association between increased risk for oral cavity cancer and taller stature. The magnitudes of the association between stature and risk for cancers in oral cavity, larynx, lung, corpus and cervix uteri, stomach, liver, pancreas, multiple myeloma, and melanoma were decreased among current smokers compared with non-smokers (Fig. 3).

Fig. 3: Hazard ratios and 95% confidence intervals per 5 cm increase in height for all cancers and cancers at 23 different sites, stratified by smoking status at enrolment.
figure3

HRs are adjusted for age, sex, body mass index, current alcohol consumption, regular physical activity, and presence or absence of diabetes mellitus among (a) non-smoker and (b) current-smoker. HR hazard ratio, CI confidence interval, CNS central nerve system, GB gallbladder

When each gender was stratified by smoking status, the magnitudes of the association in female were generally larger than those in male irrespective of smoking status (Table S4).

Among men, non-smoker showed a stronger association between taller height and most cancers compared to smokers, but this trend was weak among women (Table S4).

Discussion

In the present nationwide study, which involved a large cohort of Korean individuals, we found that height was positively associated with risk of all sites-combined cancer and with cancers of the larynx, stomach, colorectum, pancreas, biliary tract and gallbladder, lung, liver, breast, ovary, cervix and corpus uteri, kidney, bladder, prostate, testes, CNS, thyroid, skin (excluding non-melanoma), and lymphatic and haematopoietic systems. The HR for all-site cancers per 5 cm increment in height was 1.09 (95% CI: 1.086–1.090), and the magnitude of the associations for specific sites ranged from HR 1.01 (95% CI: 1.00–1.02) for liver cancer to HR 1.18 (95% CI: 1.18–1.19) for thyroid cancer. This association was more prominent in women and non-smokers than in other counterparts.

Several studies have evaluated the association between attained stature and the risk for development of cancer,2,3,4,5,6,7 showed generalised outcomes, i.e., cancer risk increased with increase in stature. For instance, the Million Women Study,7 which is one of the largest studies, presented the positive associations between height and cancers in the colon, rectum, breast, endometrium, ovary, kidney, CNS, skin, and lymphatic and haematopoietic systems. In accordance with the result, our study showed significant associations for all above-mentioned sites. Furthermore, we newly reported positive relationships between taller stature and increased vulnerability to thyroid, gallbladder and biliary tract, and testicular cancers, which the Million Women Study did not report. A previous Korean study has also reported the association of greater stature with a higher risk of biliary cancers in line with our results.5 A recent Danish study has reported that the risk for testicular germ cell tumour was associated with height by age 7 years, not between ages 7 and 13.13 By contrast, the present study showed that taller adult height was significantly associated with a higher chance of testicular cancers in adults. A meta-analysis on the association between adult height and malignancy in testes showed a positive result.14

One of the possible mechanisms which link height to cancers is that the adult height correlates with organ sizes.15 According to this hypothesis, more active cell proliferation for the organs in taller persons could increase the possibility of mutation. Another explanation is an increased level of insulin-like growth factor (IGF) which correlates with calorie intake in animals,16 height in children,17 and risk of colorectal and prostate cancer in adult humans.18 In support of the IGF-malignancy link, there is a positive relationship of stature with carcinoma of the prostate and colorectum in several studies. Some genetic factors linked with height might share mechanisms underlying tumour vulnerability. Recently, Lophatananon et al.19 has reported that height and several genetic variants related to the human growth pathway, such as IGF or growth hormone secretagogue receptor,20 are associated with high-grade prostate cancer risk.

Although gastric, hepatic and cervical cancers traditionally thought to be related with infection, there have been some reports that obesity or metabolic syndrome are associated with the increased risk of them.21,22,23,24,25 For instance, hepatic cellular carcinoma can develop in noncirrhotic livers with non-alcoholic fatty liver disease, particularly in the presence of multiple metabolic risk factors, such as obesity and diabetes.23 Obese women might receive screening for cervical cancer less frequently than normal-weight women.25 Therefore, it is not possible to exclude the possibility that these tumours are linked to IGF hypothesis.

According to literature, the association of height with all-sites cancers was statistically significant after adjustment for potential confounding factors except for the current smoking and usage of hormone therapy.6,26 Our results confirmed that current smoking history is an important effect modifier; that is, height was more strongly related to cancer risk among non-smokers than among smokers.7,27 With regard to gender, similar associations in both genders have been reported.26 Slightly prominent associations among women than among men were shown in the present study. Given that this trend is maintained regardless of whether or not smoking, gender as well as smoking can be a modifier affecting the association between development of height and cancer. To date, no specific mechanism has been known as to whether the association between tall stature and the development of cancer is greater in women or non-smokers.

Another possible modifier is BMI. Weight is correlated with height and could confound the association between height and cancer.28,29 As for oesophageal cancer, which is negatively associated with BMI, the association with height was not significant.

There is some degree of consistency in the impact size of stature on site-specific cancer risks. For instance, melanoma, leukaemia, kidney cancer, and colorectal cancer have been ranked in the highest positions among both sexes.5,6,7,27 When the gender was restricted to men, the Whitehall cohort4 showed melanoma and kidney cancers were the most height-associated, while Sung et al.5 reported thyroid cancer, lymphoma, and melanoma as such. While only our study and the study by Sung et al.5 showed the highest association with taller stature in thyroid cancer, in the present study, skin cancers did not represent the strong association. Ethnic differences may have affected this result because thyroid cancer has been South Korea’s most common cancer, but skin cancers rarely occur in Korea.30 Additionally, a significant association with cancers in the biliary tract and taller persons has been reported in the above two studies. Even though the two studies were based in Korea, there were some differences in results; in the present study, persons with taller stature were at a higher risk of developing stomach and pancreas cancers, while in the study by Sung et al. there was no such clear association between height and stomach and pancreatic cancer.5 This could be because the two studies included in populations from different time periods; thus, resulting in a younger generation in our study. Heliobacter pylori, one of the most potent factors in the carcinogenesis of stomach cancer, is declining over time, from 66.9% in 1998 to 54.4% in 201117; Because H. pylori prevalence is decreasing in Korea and Japan, height may have a greater association with gastric cancer in younger individuals. On the other hand, malignancy in the pancreas has continuously increased, but the incidence is relatively low.30 A huge sample size of the present study could contribute the positive association unlike the study by Sung et al.5 Additionally, Sung et al. previously have shown a marked reduction in the positive association between height and liver cancer after an additional adjustment for hepatitis B viral antigenicity. Therefore, the significant association with liver cancer in taller persons in the present study should be interpreted cautiously because we did not adjust for hepatitis B or C viral antigenicity. Our results suggest a special caution when assessing the association of height with some cancers that are closely associated with weight or infection.

To determine the casualty between anthropometric traits and cancer, Mendelian randomisation study has been used.31 The basic concept is genetic factors influencing height play roles in carcinogenesis. One British study recently have reported that genetically determined taller height is causally associated with greater overall cancer susceptibility and cancer mortality by age 60.32 Further study is necessary to investigate which factors make the association or casualty greater among women or non-smoker.

One of the strengths of our present study is that we used the nationwide database for both sexes to perform a population-based cohort study. Some analyses involved small numbers of events for certain cancer sub-types; this reduced researchers’ ability to detect existing associations. To our knowledge, this is the first study that reported the positive relationship between adult height and cancers in testes among Asian population. This study evaluated as many as 23 site-specific cancers including and biliary tract and gallbladder.

The limitation of the present study is a short follow-up period and the lack of data about menstruation, parity, breast-feeding or use of exogenous hormones. Nonetheless, the result in this study is in accordance with previous studies with 10 years or more follow-up period7 and the consistent impact of height on the development of female organ cancers has been reported after controlling for reproductive factors.26 Authors did not exclude women who had undergone hysterectomy or bilateral oophorectomy at recruitment for the analyses of uterine and ovarian cancer.

Because the study participants were recruited based on health check-up examinee, it cannot be free from the potential selection bias. Further research on the exact mechanisms and potential lifestyle factors which may have a combined synergistic effect for the development of malignancies among individuals of taller stature could provide a clue for better cancer prevention.

Availability of data and material

Data are available from the Korean National Health Insurance Corporation (https://nhiss.nhis.or.kr/bd/ab/bdaba002cv.do) for researchers who meet the criteria for access to confidential data. These are third party data. We did not have any special access privileges that others would not have. If the proposal is accepted by an evaluation committee of NHIC, the researcher would receive the de-identified NHIC dataset after paying some fee.

References

  1. 1.

    De Waard, F. Breast cancer incidence and nutritional status with particular reference to body weight and height. Cancer Res. 35, 3351–3356 (1975).

    PubMed  Google Scholar 

  2. 2.

    Albanes, D., Jones, D. Y., Schatzkin, A., Micozzi, M. S. & Taylor, P. R. Adult stature and risk of cancer. Cancer Res. 48, 1658–1662 (1988).

    CAS  PubMed  Google Scholar 

  3. 3.

    Hebert, P. R. et al. Adult height and incidence of cancer in male physicians (United States). Cancer Causes Control 8, 591–597 (1997).

    CAS  Article  Google Scholar 

  4. 4.

    Batty, G., Shipley, M., Langenberg, C., Marmot, M. & Davey Smith, G. Adult height in relation to mortality from 14 cancer sites in men in London (UK): evidence from the original Whitehall study. Ann. Oncol. 17, 157–166 (2005).

    Article  Google Scholar 

  5. 5.

    Sung, J., Song, Y. M., Lawlor, D. A., Smith, G. D. & Ebrahim, S. Height and site-specific cancer risk: a cohort study of a Korean adult population. Am. J. Epidemiol. 170, 53–64 (2009).

    Article  Google Scholar 

  6. 6.

    Batty, G. D. et al. Adult height and cancer mortality in Asia: the Asia Pacific cohort studies collaboration. Ann. Oncol. 21, 646–654 (2009).

    Article  Google Scholar 

  7. 7.

    Green, J. et al. Height and cancer incidence in the Million Women Study: prospective cohort, and meta-analysis of prospective studies of height and total cancer risk. Lancet Oncol. 12, 785–794 (2011).

    Article  Google Scholar 

  8. 8.

    Lee, Y. H. et al. The combination of vitamin D deficiency and mild to moderate chronic kidney disease is associated with low bone mineral density and deteriorated femoral microarchitecture: results from the KNHANES 2008–2011. J. Clin. Endocrinol. Metab. 99, 3879–3888 (2014).

    CAS  Article  Google Scholar 

  9. 9.

    Oh, S. W. Obesity and metabolic syndrome in Korea. Diabetes Metab. 35, 561–566 (2011).

    Article  Google Scholar 

  10. 10.

    Lee, S. Y. et al. Appropriate waist circumference cutoff points for central obesity in Korean adults. Diabetes Res. Clin. Pract. 75, 72–80 (2007).

    Article  Google Scholar 

  11. 11.

    Choi, Y. J. et al. Elevated serum gamma-glutamyltransferase is associated with an increased risk of oesophageal carcinoma in a cohort of 8,388,256 Korean subjects. PLoS One 12, e0177053 (2017).

    Article  Google Scholar 

  12. 12.

    Park, C. S. et al. Association between adult height, myocardial infarction, heart failure, stroke and death: a Korean nationwide population-based study. Int. J. Epidemiol. 47, 289–298 (2018).

    Article  Google Scholar 

  13. 13.

    McGlynn, K. A., Petrick, J. L., Gamborg, M., Aarestrup, J. & Baker, J. L. Childhood height and risk of testicular germ cell tumors in adulthood. Int. J. Cancer 143, 767–772 (2018).

    CAS  Article  Google Scholar 

  14. 14.

    Lerro, C. C., McGlynn, K. A. & Cook, M. B. A systematic review and meta-analysis of the relationship between body size and testicular cancer. Br. J. Cancer 103, 1467–1474 (2010).

    CAS  Article  Google Scholar 

  15. 15.

    Albanes, D. & Winick, M. Are cell number and cell proliferation risk factors for cancer? J. Natl. Cancer Inst. 80, 772–775 (1988).

    CAS  Article  Google Scholar 

  16. 16.

    Ruggeri, B. A., Klurfeld, D. M., Kritchevsky, D. & Furlanetto, R. W. Caloric restriction and 7, 12-dimethylbenz (a) anthracene-induced mammary tumor growth in rats: alterations in circulating insulin, insulin-like growth factors I and II, and epidermal growth factor. Cancer Res. 49, 4130–3414 (1989).

    CAS  PubMed  Google Scholar 

  17. 17.

    Juul, A. et al. Serum insulin-like growth factor-I in 1030 healthy children, adolescents, and adults: relation to age, sex, stage of puberty, testicular size, and body mass index. J. Clin. Endocrinol. Metab. 78, 744–752 (1994).

    CAS  PubMed  Google Scholar 

  18. 18.

    Renehan, A. G. et al. Insulin-like growth factor (IGF)-I, IGF binding protein-3, and cancer risk: systematic review and meta-regression analysis. Lancet 363, 1346–1353 (2004).

    CAS  Article  Google Scholar 

  19. 19.

    Lophatananon, A. et al. Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium. Br. J. Cancer 117, 734–743 (2017).

    CAS  Article  Google Scholar 

  20. 20.

    Gunnell, D. Height, insulin-like growth factors and cancer risk. Growth Horm. IGF Res. 10, S39–S40 (2000).

    Article  Google Scholar 

  21. 21.

    Lin, Y., Ness-Jensen, E., Hveem, K., Lagergren, J. & Lu, Y. Metabolic syndrome and esophageal and gastric cancer. Cancer Causes Control 26, 1825–1834 (2015).

    Article  Google Scholar 

  22. 22.

    Kim, H. Y. Metabolic syndrome is associated with gastric dysplasia. Eur. J. Gastroenterol. Hepatol. 23, 871–875 (2011).

    CAS  Article  Google Scholar 

  23. 23.

    Vanni, E. & Bugianesi, E. Obesity and liver cancer. Clin. Liver. Dis. 18, 191–203 (2014).

    Article  Google Scholar 

  24. 24.

    Lacey, J. V. Jr et al. Obesity as a potential risk factor for adenocarcinomas and squamous cell carcinomas of the uterine cervix. Cancer 98, 814–821 (2003).

    Article  Google Scholar 

  25. 25.

    Lee, J. K., So, K. A., Piyathilake, C. J. & Kim, M. K. Mild obesity, physical activity, calorie intake, and the risks of cervical intraepithelial neoplasia and cervical cancer. PLoS One 8, e66555 (2013).

    CAS  Article  Google Scholar 

  26. 26.

    Kabat, G. C., Kim, M. Y., Hollenbeck, A. R. & Rohan, T. E. Attained height, sex, and risk of cancer at different anatomic sites in the NIH-AARP Diet and Health Study. Cancer Causes Control 25, 1697–1706 (2014).

    Article  Google Scholar 

  27. 27.

    Kabat, G. C., Heo, M., Kamensky, V., Miller, A. B. & Rohan, T. E. Adult height in relation to risk of cancer in a cohort of Canadian women. Int. J. Cancer 132, 1125–1132 (2013).

    CAS  Article  Google Scholar 

  28. 28.

    Renehan, A. G. Height and cancer: consistent links, but mechanisms unclear. Lancet Oncol. 12, 716–717 (2011).

    Article  Google Scholar 

  29. 29.

    Kabat, G. C., Heo, M., Miller, A. B. & Rohan, T. E. Scaling of weight for height in relation to risk of cancer at different sites in a cohort of Canadian women. Am. J. Epidemiol. 177, 93–101 (2012).

    Article  Google Scholar 

  30. 30.

    Jung, K. W. et al. Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2014. Cancer Res. Treat. 49, 292–305 (2017).

    Article  Google Scholar 

  31. 31.

    Smith, G. D. & Ebrahim, S. ‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease? Int. J. Epidemiol. 32, 1–22 (2003).

    Article  Google Scholar 

  32. 32.

    Ong, J. S. et al. Height and overall cancer risk and mortality: evidence from a Mendelian randomisation study on 310,000 UK Biobank participants. Br. J. Cancer 118, 1262–1267 (2018).

    Article  Google Scholar 

Download references

Author contributions

Study conception and design: L.D.H, S.C.M. Data analysis: H.K. Interpretation of results: all authors. Original draft preparation: C.Y.J. Review, editing and approval of manuscript: all authors.

Author information

Affiliations

Authors

Corresponding author

Correspondence to Dong Ho Lee.

Ethics declarations

Ethics approval and consent to participate

The study was conducted in accordance with the Good Clinical Practice guidelines and the Declaration of Helsinki. The protocol was approved by the ethics committee or institutional review board at of Seoul National University Bundang Hospital, and written informed consent was waived.

Conflict of interest

The authors declare that they have no conflict of interest.

Funding

This work was supported by a grant from the National Research Foundation (NRF) of Korea to the Global Core Research Center (GCRC) funded by the Korean government (Ministry of Science, ICT and Future Planning) [No. 2011-0030001].

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Choi, Y.J., Lee, D.H., Han, KD. et al. Adult height in relation to risk of cancer in a cohort of 22,809,722 Korean adults. Br J Cancer 120, 668–674 (2019). https://doi.org/10.1038/s41416-018-0371-8

Download citation

Further reading

Search

Quick links