TY - JOUR
T1 - Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children
AU - Farook, Vidya S.
AU - Reddivari, Lavanya
AU - Mummidi, Srinivas
AU - Puppala, Sobha
AU - Arya, Rector
AU - Lopez-Alvarenga, Juan Carlos
AU - Fowler, Sharon P.
AU - Chittoor, Geetha
AU - Resendez, Roy G.
AU - Kumar, Birunda Mohan
AU - Comuzzie, Anthony G.
AU - Curran, Joanne E.
AU - Lehman, Donna M.
AU - Jenkinson, Christopher P.
AU - Lynch, Jane L.
AU - DeFronzo, Ralph A.
AU - Blangero, John
AU - Hale, Daniel
AU - Duggirala, Ravindranath
AU - Vanamala, Jairam K.P.
N1 - Publisher Copyright:
© 2017 American Society for Nutrition.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Background: Dietary intake of phytonutrients present in fruits and vegetables, such as carotenoids, is associated with a lower risk of obesity and related traits, but the impact of genetic variation on these associations is poorly understood, especially in children. Objective: We estimated common genetic influences on serum carotenoid concentrations and obesity-related traits in Mexican American (MA) children. Design: Obesity-related data were obtained from 670 nondiabetic MA children, aged 6-17 y. Serum α- and β-carotenoid concentrations were measured in ∼570 (α-carotene in 565 and β-carotene in 572) of these children with the use of an ultraperformance liquid chromatography-photodiode array. We determined heritabilities for both carotenoids and examined their genetic relation with 10 obesity-related traits [body mass index (BMI), waist circumference (WC), high-density lipoprotein (HDL) cholesterol, triglycerides, fat mass (FM), systolic and diastolic blood pressure, fasting insulin and glucose, and homeostasis model assessment of insulin resistance] by using family data and a variance components approach. For these analyses, carotenoid values were inverse normalized, and all traits were adjusted for significant covariate effects of age and sex. Results: Carotenoid concentrations were highly heritable and significant [α-carotene: heritability (h2) = 0.81, P = 6.7 3 10211; β-carotene: h2 = 0.90, P = 3.5 3 10215]. After adjusting for multiple comparisons, we found significant (P ≤ 0.05) negative phenotypic correlations between carotenoid concentrations and the following traits: BMI, WC, FM, and triglycerides (range: α-carotene = 20.19 to 20.12; β-carotene = 20.24 to 20.13) and positive correlations with HDL cholesterol (α-carotene = 0.17; β-carotene = 0.24). However, when the phenotypic correlations were partitioned into genetic and environmental correlations, we found marginally significant (P = 0.051) genetic correlations only between β-carotene and BMI (20.27), WC (20.30), and HDL cholesterol (0.31) after accounting for multiple comparisons. None of the environmental correlations were significant. Conclusions: The findings from this study suggest that the serum carotenoid concentrations were under strong additive genetic influences based on variance components analyses, and that the common genetic factors may influence b-carotene and obesity and lipid traits in MA children.
AB - Background: Dietary intake of phytonutrients present in fruits and vegetables, such as carotenoids, is associated with a lower risk of obesity and related traits, but the impact of genetic variation on these associations is poorly understood, especially in children. Objective: We estimated common genetic influences on serum carotenoid concentrations and obesity-related traits in Mexican American (MA) children. Design: Obesity-related data were obtained from 670 nondiabetic MA children, aged 6-17 y. Serum α- and β-carotenoid concentrations were measured in ∼570 (α-carotene in 565 and β-carotene in 572) of these children with the use of an ultraperformance liquid chromatography-photodiode array. We determined heritabilities for both carotenoids and examined their genetic relation with 10 obesity-related traits [body mass index (BMI), waist circumference (WC), high-density lipoprotein (HDL) cholesterol, triglycerides, fat mass (FM), systolic and diastolic blood pressure, fasting insulin and glucose, and homeostasis model assessment of insulin resistance] by using family data and a variance components approach. For these analyses, carotenoid values were inverse normalized, and all traits were adjusted for significant covariate effects of age and sex. Results: Carotenoid concentrations were highly heritable and significant [α-carotene: heritability (h2) = 0.81, P = 6.7 3 10211; β-carotene: h2 = 0.90, P = 3.5 3 10215]. After adjusting for multiple comparisons, we found significant (P ≤ 0.05) negative phenotypic correlations between carotenoid concentrations and the following traits: BMI, WC, FM, and triglycerides (range: α-carotene = 20.19 to 20.12; β-carotene = 20.24 to 20.13) and positive correlations with HDL cholesterol (α-carotene = 0.17; β-carotene = 0.24). However, when the phenotypic correlations were partitioned into genetic and environmental correlations, we found marginally significant (P = 0.051) genetic correlations only between β-carotene and BMI (20.27), WC (20.30), and HDL cholesterol (0.31) after accounting for multiple comparisons. None of the environmental correlations were significant. Conclusions: The findings from this study suggest that the serum carotenoid concentrations were under strong additive genetic influences based on variance components analyses, and that the common genetic factors may influence b-carotene and obesity and lipid traits in MA children.
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U2 - 10.3945/ajcn.116.144006
DO - 10.3945/ajcn.116.144006
M3 - Article
C2 - 28515064
AN - SCOPUS:85021785104
SN - 0002-9165
VL - 106
SP - 52
EP - 58
JO - American Journal of Clinical Nutrition
JF - American Journal of Clinical Nutrition
IS - 1
ER -