TY - JOUR
T1 - Paradoxical relationship between body mass index and thyroid hormone levels
T2 - A study using mendelian randomization
AU - Taylor, Peter N.
AU - Richmond, Rebecca
AU - Davies, Neil
AU - Sayers, Adrian
AU - Stevenson, Kirsty
AU - Woltersdorf, Wolfram
AU - Taylor, Andrew
AU - Groom, Alix
AU - Northstone, Kate
AU - Ring, Susan
AU - Okosieme, Onyebuchi
AU - Rees, Aled
AU - Nitsch, Dorothea
AU - Williams, Graham R.
AU - Smith, George Davey
AU - Gregory, John W.
AU - Timpson, Nicholas J.
AU - Tobias, Jonathan H.
AU - Dayan, Colin M.
PY - 2016/2
Y1 - 2016/2
N2 - Context: Free T3 (FT3) has been positively associated with body mass index (BMI) in cross-sectional studies in healthy individuals. This is difficult to reconcile with clinical findings in pathological thyroid dysfunction. Objective: We aimed to investigate whether childhood adiposity influences FT3 levels. Design: Mendelian randomization using genetic variants robustly associated with BMI. Setting: Avon Longitudinal Study of Parents and Children, a population-based birth cohort. Participants: A total of 3014 children who had thyroid function measured at age 7, who also underwent dual x-ray absorptiometry scans at ages 9.9 and 15.5 years and have genetic data available. Main Outcome Measures: FT3. Results: Observationally at age 7 years, BMI was positively associated with FT3:-standardized (-[std]) 0.12 (95% confidence interval [CI]: 0.08, 0.16), P 4.02 10α10; whereas FT4 was negatively associated with BMI:-(std) α0.08 (95% CI: α0.12, α0.04), P 3.00 10α5. These differences persisted after adjustment for age, sex, and early life environment. Genetic analysis indicated 1 allele change in BMI allelic score was associated with a 0.04 (95% CI: 0.03, 0.04) SD increase in BMI (P6.4110α17). At age 7, a genetically determined increase in BMI of 1.89 kg/m2 was associated with a 0.22 pmol/L (95% CI: 0.07, 0.36) increase in FT3 (P .004) but no substantial change in FT4 0.01 mmol/L, (95% CI: α0.37, 0.40), P .96. Conclusion: Our analysis shows that children with a genetically higher BMI had higher FT3 but not FT4 levels, indicating that higher BMI/fat mass has a causal role in increasing FT3 levels. This may explain the paradoxical associations observed in observational analyses. Given rising childhood obesity levels, this relationship merits closer scrutiny.
AB - Context: Free T3 (FT3) has been positively associated with body mass index (BMI) in cross-sectional studies in healthy individuals. This is difficult to reconcile with clinical findings in pathological thyroid dysfunction. Objective: We aimed to investigate whether childhood adiposity influences FT3 levels. Design: Mendelian randomization using genetic variants robustly associated with BMI. Setting: Avon Longitudinal Study of Parents and Children, a population-based birth cohort. Participants: A total of 3014 children who had thyroid function measured at age 7, who also underwent dual x-ray absorptiometry scans at ages 9.9 and 15.5 years and have genetic data available. Main Outcome Measures: FT3. Results: Observationally at age 7 years, BMI was positively associated with FT3:-standardized (-[std]) 0.12 (95% confidence interval [CI]: 0.08, 0.16), P 4.02 10α10; whereas FT4 was negatively associated with BMI:-(std) α0.08 (95% CI: α0.12, α0.04), P 3.00 10α5. These differences persisted after adjustment for age, sex, and early life environment. Genetic analysis indicated 1 allele change in BMI allelic score was associated with a 0.04 (95% CI: 0.03, 0.04) SD increase in BMI (P6.4110α17). At age 7, a genetically determined increase in BMI of 1.89 kg/m2 was associated with a 0.22 pmol/L (95% CI: 0.07, 0.36) increase in FT3 (P .004) but no substantial change in FT4 0.01 mmol/L, (95% CI: α0.37, 0.40), P .96. Conclusion: Our analysis shows that children with a genetically higher BMI had higher FT3 but not FT4 levels, indicating that higher BMI/fat mass has a causal role in increasing FT3 levels. This may explain the paradoxical associations observed in observational analyses. Given rising childhood obesity levels, this relationship merits closer scrutiny.
UR - https://www.scopus.com/pages/publications/84959449409
U2 - 10.1210/jc.2015-3505
DO - 10.1210/jc.2015-3505
M3 - Article
C2 - 26595101
AN - SCOPUS:84959449409
SN - 0021-972X
VL - 101
SP - 730
EP - 738
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 2
ER -