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We investigated relations between measured body mass index (BMI) and stature and thyroid cancer (3046 cases) in a large Norwegian cohort of more than two million individuals. The risk of thyroid cancer, especially of the papillary and follicular types, increased moderately with increasing BMI and height in both sexes.
Several types of malignancies have been associated with increased weight, as summarised recently (IARC Working Group on the Evaluation of Cancer-Preventive Strategies, 2002). As thyroid cancer is relatively rare, with only a few studies of its association with obesity, the working group did not include it in its review.
In 1993–1997, thyroid cancer comprised 0.5 and 1.4% of all male and female cancer cases, respectively, in the Nordic countries (Møller et al, 2002). In Norway, the (world) age-adjusted incidence rates in 2004 were 1.5 and 5.1 per 100000 persons per year in men and women, respectively (The Cancer Registry of Norway, 2006), the higher rates among women being typical (Parkin et al, 2005). In the US, the rates of thyroid cancer are significantly higher and increasing. In 2001, the age-adjusted incidence rates were 4.2 and 12 per 100000 persons per year in males and females (National Cancer Institute, 2005).
In the present study, we used measurements from Norwegian health surveys to examine the relations between body mass index (BMI) and stature and the risk of thyroid cancer. We have recently published similar analyses for a range of cancers (Engeland et al, 2003a, 2003b and 2003c, 2004, 2005; Bjørge et al, 2004).
The study population and the methods have been described elsewhere (Bjørge et al, 2004). In a number of Norwegian health surveys during 1963–2001, height and weight were measured in 2001727 persons (963709 men and 1038018 women) aged 20–74 years in a standardised way by a trained staff. A major part of the health surveys in the period 1963–1975 was included in a nationwide tuberculosis screening programme (Waaler, 1984), which was compulsory for all Norwegians aged 15 years and above; attendance was about 85%. In 1963–1964 and in 1972–2001, height and weight were also measured in other health surveys connected with coronary heart disease in different parts of Norway (Bjartveit et al, 1979; Bjartveit, 1997). The attendance in these surveys in the mid-1970s was 85–90% and about 75% in the mid-1990s (Bjartveit, 1997).
Deaths, emigrations and cases of thyroid cancer (International Classification of Diseases, seventh revision (ICD-7): 194) in this cohort were identified by linkage to the Death Registry at Statistics Norway (Statistics Norway, 2006) and to the Cancer Registry of Norway (The Cancer Registry of Norway, 2006). Both these registries are population based and cover the entire Norwegian population. A unique 11-digit identification number assigned to all individuals living in Norway after 1960 facilitated the linkages.
The present study included only histologically verified thyroid cancers. Persons with a diagnosis of thyroid cancer before the height and weight measurements were excluded (n=709). In the analyses, the persons in the cohort were followed from the date of measurement until the date of cancer diagnosis, emigration, age 100 years, death or until 31 December 2003. Altogether, 2001018 persons were eligible for the study. A small number of these (39 men and 32 women) were lost to follow-up.
Cox's proportional hazards regression models (Cox and Oakes, 1984), with time since measurement as the time variable, were fitted to obtain relative risk estimates of cancer. In the analyses, categorised variables for age at measurement, year of birth, BMI ((weight in kilograms)/(height in metres)2) and height were included. Body mass index was categorised using the WHO categorisation (World Health Organization Consultation on Obesity, 1998): BMI <18.5 (underweight), 18.5–24.9 (normal), 25.0–29.9 (preobese/overweight) and ≥30.0 kg/m2 (obese).
Analyses were also performed treating BMI and height, respectively, as continuous variables to test for trend in thyroid cancer risk. Separate analyses were performed for papillary, follicular, medullary, anaplastic, other carcinomas and other malignant tumours. All these analyses were performed with the statistical program package SPSS (SPSS Inc., SPSS for Windows, Release 188.8.131.524). The results were presented as relative risks (RR) of cancer with 95% confidence intervals (CI). The hazard functions of thyroid cancer by BMI and height in the Cox model were estimated using spline functions in S-plus (Insightful Corporation, 2002), with 4d.f.
The 2000947 persons (963523 men and 1037424 women) included in this study were followed for on average 23 years (maximum 41 years), constituting 47 million person-years (Table 1). The mean age at measurement was 44 years, and the proportions of obesity were 6 and 13% in men and women, respectively. During follow-up, 3046 thyroid cancer cases were diagnosed among the study subjects on average 15 years after the measurements. The mean age at diagnosis was 62.2 and 57.7 years in men and women, respectively.
The risk of thyroid cancer increased moderately by increasing BMI in both sexes (Table 2). The RR of thyroid cancer per unit increase in BMI was 1.03 (95% CI: 1.00–1.05) in men and 1.02 (95% CI: 1.01–1.03) in women. Excluding the first 5 years of follow-up did not change these results. Splitting the upper BMI category in women gave RRs of 1.27 (95% CI: 1.11–1.47), 1.33 (95% CI: 1.03–1.73) and 1.38 (95% CI: 0.83–2.30) with BMI of 30.0–34.9, 35.0–39.9 and 40 or above, respectively, compared with normal-weighted women.
Histology-specific analyses revealed that the relative risk of follicular carcinoma increased more than the risk of papillary carcinoma with increasing BMI. Further, the risk of medullary carcinoma tended to decrease with increasing BMI in both sexes, being significant among females only. The RR of medullary carcinoma per unit increase in BMI was 0.94 (95% CI: 0.85–1.04) in men and 0.91 (95% CI: 0.86–0.97) in women. The number of cases was low (52 and 107 medullary carcinomas in men and women, respectively). The anaplastic carcinomas showed a strong positive association with BMI in men.
The risk of thyroid cancer increased with increasing height in both sexes (Table 2). The RR of thyroid cancer associated with 10cm increase in height was 1.18 (95% CI: 1.05–1.32) in men and 1.22 (95% CI: 1.13–1.31) in women.
Among males, the elevated risk associated with increased BMI was confined to those measured at the age of 50–74 years (Table 3).
The associations between BMI and stature and the risk of thyroid cancer in women are illustrated in Figure 1. The risk of thyroid cancer increased with increasing height and BMI above 25kg/m2.
In this large cohort, including more than two million individuals, we explored the associations between BMI and height and the occurrence of thyroid cancer. The risk was found to be moderately elevated with increasing BMI and height in both sexes among the follicle-cell derived (papillary and follicular) carcinomas. In medullary carcinomas, an opposite trend was present for BMI, pointing to a different pathogenetic influence.
The associations between BMI and height with thyroid cancer have been difficult to explore in previous small studies owing to the low incidence of this disease. In addition to the large size of the present cohort, we also had an almost complete follow-up with regard to thyroid cancer incidence and deaths. This was made possible by linkages to population-based registries of high quality. Only 0.04% of the study cohort (71 persons) was lost to follow-up, and 0.6% was censored by emigration from Norway.
After a pooled analysis of 12 case–control studies, including 2473 cases, Dal Maso et al (2000) previously found a moderately increased risk of thyroid cancer related to height and weight at diagnosis. Dal Maso et al (2000) used self-reported values for height and weight during the late teens and at diagnosis. In the present study, we relied on height and weight measurements performed on average 15 years before the diagnosis of thyroid cancer. Hence, our estimates were not diluted by a possible influence of individuals weight on the disease.
Iribarren et al (2001) evaluated several potential predictors of thyroid cancer in a large American cohort with long follow-up, including more than 200000 persons. Despite the large size of the cohort and the long follow-up, only 196 thyroid cancers were observed. In this study, no association between BMI, height or weight gain and thyroid cancer was observed.
Dal Maso et al (2000) hypothesised that an association between BMI and thyroid cancer could be owing to a relationship with steroid hormones or other endocrine factors. However, they observed an association between BMI and thyroid cancer of similar magnitude in older and younger women. Also in the present study, there was no difference in the association between BMI and thyroid cancer in older and younger women.
Like Dal Maso et al (2000), we observed a moderately increasing risk of thyroid cancer with increasing height. This association may be owing to dietary influence during childhood or adolescence and possible interactions with growth factors.
In conclusion, the present study showed that the risk of thyroid cancer increased moderately with increasing BMI and height in both males and females.
We are grateful to those who for almost 40 years collected the data used in the present study. These people were connected to the former National Health Screening Service, The Nord-Trøndelag Health Survey (HUNT), The Hordaland Health Survey (HUSK) and The Tromsø Study.