TY - JOUR
T1 - Fetal growth and subsequent maternal risk of thyroid cancer
AU - Crump, Casey
AU - Sundquist, Jan
AU - Sieh, Weiva
AU - Winkleby, Marilyn A.
AU - Sundquist, Kristina
N1 - Publisher Copyright:
© 2015 UICC.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Thyroid cancer has peak incidence among women of reproductive age, and growth factors, which have procarcinogenic properties, may play an important etiologic role. However, the association between fetal growth rate during a woman's pregnancy and her subsequent risk of thyroid cancer has not been previously examined. We conducted a national cohort study of 1,837,634 mothers who had a total of 3,588,497 live-births in Sweden in 1973-2008, followed up for thyroid cancer incidence through 2009. There were 2,202 mothers subsequently diagnosed with thyroid cancer in 36.8 million person-years of follow-up. After adjusting for maternal age, height, weight, smoking, and sociodemographic factors, high fetal growth (birth weight standardized for gestational age and sex) was associated with a subsequent increased risk of thyroid cancer in the mother (incidence rate ratio [IRR] per additional 1 standard deviation, 1.05; 95% CI, 1.01-1.09; p = 0.02). Each 1,000 g increase in the infant's birth weight was associated with a 13% increase in the mother's subsequent risk of thyroid cancer (IRR, 1.13; 95% CI, 1.05-1.22; p = 0.001). These findings appeared to involve both papillary and follicular subtypes, and did not vary significantly by the mother's height, weight or smoking status. In this large national cohort study, high fetal growth during a woman's pregnancy was independently associated with a subsequent increased risk of her developing thyroid cancer. If confirmed, these findings suggest an important role of maternal growth factors in the development of thyroid cancer, and potentially may help facilitate the identification of high-risk subgroups of women. What's new? Thyroid cancer rates continue to rise among women, with the majority of cases involving relatively unknown etiological pathways. Among women of reproductive age, likely suspects include growth pathways that feature insulin-like growth factor I (IGF-I), which is procarcinogenic and positively associated with fetal growth during pregnancy. In this cohort study, high infant birth weight was directly associated with an increased risk of thyroid cancer in the mother subsequent to childbirth. The findings indicate that fetal growth factors influence thyroid cancer risk and may be useful markers for identifying women at high risk of the disease.
AB - Thyroid cancer has peak incidence among women of reproductive age, and growth factors, which have procarcinogenic properties, may play an important etiologic role. However, the association between fetal growth rate during a woman's pregnancy and her subsequent risk of thyroid cancer has not been previously examined. We conducted a national cohort study of 1,837,634 mothers who had a total of 3,588,497 live-births in Sweden in 1973-2008, followed up for thyroid cancer incidence through 2009. There were 2,202 mothers subsequently diagnosed with thyroid cancer in 36.8 million person-years of follow-up. After adjusting for maternal age, height, weight, smoking, and sociodemographic factors, high fetal growth (birth weight standardized for gestational age and sex) was associated with a subsequent increased risk of thyroid cancer in the mother (incidence rate ratio [IRR] per additional 1 standard deviation, 1.05; 95% CI, 1.01-1.09; p = 0.02). Each 1,000 g increase in the infant's birth weight was associated with a 13% increase in the mother's subsequent risk of thyroid cancer (IRR, 1.13; 95% CI, 1.05-1.22; p = 0.001). These findings appeared to involve both papillary and follicular subtypes, and did not vary significantly by the mother's height, weight or smoking status. In this large national cohort study, high fetal growth during a woman's pregnancy was independently associated with a subsequent increased risk of her developing thyroid cancer. If confirmed, these findings suggest an important role of maternal growth factors in the development of thyroid cancer, and potentially may help facilitate the identification of high-risk subgroups of women. What's new? Thyroid cancer rates continue to rise among women, with the majority of cases involving relatively unknown etiological pathways. Among women of reproductive age, likely suspects include growth pathways that feature insulin-like growth factor I (IGF-I), which is procarcinogenic and positively associated with fetal growth during pregnancy. In this cohort study, high infant birth weight was directly associated with an increased risk of thyroid cancer in the mother subsequent to childbirth. The findings indicate that fetal growth factors influence thyroid cancer risk and may be useful markers for identifying women at high risk of the disease.
KW - fetal development
KW - mothers
KW - pregnancy
KW - risk factors
KW - thyroid neoplasms
UR - https://www.scopus.com/pages/publications/84955511070
U2 - 10.1002/ijc.29857
DO - 10.1002/ijc.29857
M3 - Article
C2 - 26379007
AN - SCOPUS:84955511070
SN - 0020-7136
VL - 138
SP - 1085
EP - 1093
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 5
ER -