Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents

Qibin Qi; Mary K Downer; Tuomas Oskari Kilpeläinen; H Rob Taal; Sheila J Barton; Ioanna Ntalla; Marie Standl; Vesna Boraska; Ville Huikari; Jessica C Kiefte-de Jong; Antje Körner; Timo A Lakka; Gaifen Liu; Jessica Magnusson; Masayuki Okuda; Olli Raitakari; Rebecca Richmond; Robert A Scott; Mark E S Bailey; Kathrin Scheuermann; John W Holloway; Hazel Inskip; Carmen R Isasi; Yasmin Mossavar-Rahmani; Vincent W V Jaddoe; Jaana Laitinen; Virpi Lindi; Erik Melén; Yannis Pitsiladis; Niina Pitkänen; Harold Snieder; Joachim Heinrich; Nicholas J Timpson; Tao Wang; Hinoda Yuji; Eleftheria Zeggini; George V Dedoussis; Robert C Kaplan; Judith Wylie-Rosett; Ruth J F Loos; Frank B Hu; Lu Qi

doi:10.2337/db14-1629

Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents

Qibin Qi, Mary K Downer, Tuomas Oskari Kilpeläinen, H Rob Taal, Sheila J Barton, Ioanna Ntalla, Marie Standl, Vesna Boraska, Ville Huikari, Jessica C Kiefte-de Jong, Antje Körner, Timo A Lakka, Gaifen Liu, Jessica Magnusson, Masayuki Okuda, Olli Raitakari, Rebecca Richmond, Robert A Scott, Mark E S Bailey, Kathrin ScheuermannJohn W Holloway, Hazel Inskip, Carmen R Isasi, Yasmin Mossavar-Rahmani, Vincent W V Jaddoe, Jaana Laitinen, Virpi Lindi, Erik Melén, Yannis Pitsiladis, Niina Pitkänen, Harold Snieder, Joachim Heinrich, Nicholas J Timpson, Tao Wang, Hinoda Yuji, Eleftheria Zeggini, George V Dedoussis, Robert C Kaplan, Judith Wylie-Rosett, Ruth J F Loos, Frank B Hu, Lu Qi

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Abstract

The FTO gene harbors variation with the strongest effect on adiposity and obesity risk. Previous data support a role for FTO variation in influencing food intake. We conducted a combined analysis of 16,094 boys and girls aged 1-18 years from 14 studies to examine the following: 1) the association between the FTO rs9939609 variant (or a proxy) and total energy and macronutrient intake; and 2) the interaction between the FTO variant and dietary intake, and the effect on BMI. We found that the BMIincreasing allele (minor allele) of the FTO variant was associated with increased total energy intake (effect per allele = 14.3 kcal/day [95%CI 5.9, 22.7 kcal/day], P = 6.5 3 1024), but not with protein, carbohydrate, or fat intake. We also found that protein intake modified the association between the FTO variant and BMI (interactive effect per allele = 0.08 SD [0.03, 0.12 SD], P for interaction = 7.2 3 1024): the association between FTO genotype and BMI was much stronger in individuals with high protein intake (effect per allele = 0.10 SD [0.07, 0.13 SD], P = 8.2 3 10210) than in those with low intake (effect per allele = 0.04 SD [0.01, 0.07 SD], P = 0.02). Our results suggest that the FTO variant that confers a predisposition to higher BMI is associated with higher total energy intake, and that lower dietary protein intake attenuates the association between FTO genotype and adiposity in children and adolescents.

Originalsprog	Engelsk
Tidsskrift	Diabetes
Vol/bind	64
Udgave nummer	7
Sider (fra-til)	2467-76
Antal sider	10
ISSN	0012-1797
DOI	https://doi.org/10.2337/db14-1629
Status	Udgivet - jul. 2015

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10.2337/db14-1629

American Diabetes Association. Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents. Diabetes 64(7):2467-76. American Diabetes Association 2015. Copyright and all rights reserved. Material from this publication has been used with the permission of American Diabetes Association.Forlagets udgivne version, 1,18 MBLicens: Ikke-specificeret
2467.full.pdfForlagets udgivne version, 1,15 MB

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Qi, Q., Downer, M. K., Oskari Kilpeläinen, T., Taal, H. R., Barton, S. J., Ntalla, I., Standl, M., Boraska, V., Huikari, V., Kiefte-de Jong, J. C., Körner, A., Lakka, T. A., Liu, G., Magnusson, J., Okuda, M., Raitakari, O., Richmond, R., Scott, R. A., Bailey, M. E. S., ... Qi, L. (2015). Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents. Diabetes, 64(7), 2467-76. https://doi.org/10.2337/db14-1629

Qi, Q, Downer, MK, Oskari Kilpeläinen, T, Taal, HR, Barton, SJ, Ntalla, I, Standl, M, Boraska, V, Huikari, V, Kiefte-de Jong, JC, Körner, A, Lakka, TA, Liu, G, Magnusson, J, Okuda, M, Raitakari, O, Richmond, R, Scott, RA, Bailey, MES, Scheuermann, K, Holloway, JW, Inskip, H, Isasi, CR, Mossavar-Rahmani, Y, Jaddoe, VWV, Laitinen, J, Lindi, V, Melén, E, Pitsiladis, Y, Pitkänen, N, Snieder, H, Heinrich, J, Timpson, NJ, Wang, T, Yuji, H, Zeggini, E, Dedoussis, GV, Kaplan, RC, Wylie-Rosett, J, Loos, RJF, Hu, FB & Qi, L 2015, 'Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents', Diabetes, bind 64, nr. 7, s. 2467-76. https://doi.org/10.2337/db14-1629

@article{3ddca8d99473497f8e8f41dbf379f7f8,

title = "Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents",

abstract = "The FTO gene harbors variation with the strongest effect on adiposity and obesity risk. Previous data support a role for FTO variation in influencing food intake. We conducted a combined analysis of 16,094 boys and girls aged 1-18 years from 14 studies to examine the following: 1) the association between the FTO rs9939609 variant (or a proxy) and total energy and macronutrient intake; and 2) the interaction between the FTO variant and dietary intake, and the effect on BMI. We found that the BMIincreasing allele (minor allele) of the FTO variant was associated with increased total energy intake (effect per allele = 14.3 kcal/day [95%CI 5.9, 22.7 kcal/day], P = 6.5 3 1024), but not with protein, carbohydrate, or fat intake. We also found that protein intake modified the association between the FTO variant and BMI (interactive effect per allele = 0.08 SD [0.03, 0.12 SD], P for interaction = 7.2 3 1024): the association between FTO genotype and BMI was much stronger in individuals with high protein intake (effect per allele = 0.10 SD [0.07, 0.13 SD], P = 8.2 3 10210) than in those with low intake (effect per allele = 0.04 SD [0.01, 0.07 SD], P = 0.02). Our results suggest that the FTO variant that confers a predisposition to higher BMI is associated with higher total energy intake, and that lower dietary protein intake attenuates the association between FTO genotype and adiposity in children and adolescents.",

author = "Qibin Qi and Downer, {Mary K} and {Oskari Kilpel{\"a}inen}, Tuomas and Taal, {H Rob} and Barton, {Sheila J} and Ioanna Ntalla and Marie Standl and Vesna Boraska and Ville Huikari and {Kiefte-de Jong}, {Jessica C} and Antje K{\"o}rner and Lakka, {Timo A} and Gaifen Liu and Jessica Magnusson and Masayuki Okuda and Olli Raitakari and Rebecca Richmond and Scott, {Robert A} and Bailey, {Mark E S} and Kathrin Scheuermann and Holloway, {John W} and Hazel Inskip and Isasi, {Carmen R} and Yasmin Mossavar-Rahmani and Jaddoe, {Vincent W V} and Jaana Laitinen and Virpi Lindi and Erik Mel{\'e}n and Yannis Pitsiladis and Niina Pitk{\"a}nen and Harold Snieder and Joachim Heinrich and Timpson, {Nicholas J} and Tao Wang and Hinoda Yuji and Eleftheria Zeggini and Dedoussis, {George V} and Kaplan, {Robert C} and Judith Wylie-Rosett and Loos, {Ruth J F} and Hu, {Frank B} and Lu Qi",

note = "{\textcopyright} 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.",

year = "2015",

month = jul,

doi = "10.2337/db14-1629",

language = "English",

volume = "64",

pages = "2467--76",

journal = "Diabetes",

issn = "0012-1797",

publisher = "American Diabetes Association",

number = "7",

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TY - JOUR

T1 - Dietary intake, FTO genetic variants and adiposity

T2 - a combined analysis of over 16,000 children and adolescents

AU - Qi, Qibin

AU - Downer, Mary K

AU - Oskari Kilpeläinen, Tuomas

AU - Taal, H Rob

AU - Barton, Sheila J

AU - Ntalla, Ioanna

AU - Standl, Marie

AU - Boraska, Vesna

AU - Huikari, Ville

AU - Kiefte-de Jong, Jessica C

AU - Körner, Antje

AU - Lakka, Timo A

AU - Liu, Gaifen

AU - Magnusson, Jessica

AU - Okuda, Masayuki

AU - Raitakari, Olli

AU - Richmond, Rebecca

AU - Scott, Robert A

AU - Bailey, Mark E S

AU - Scheuermann, Kathrin

AU - Holloway, John W

AU - Inskip, Hazel

AU - Isasi, Carmen R

AU - Mossavar-Rahmani, Yasmin

AU - Jaddoe, Vincent W V

AU - Laitinen, Jaana

AU - Lindi, Virpi

AU - Melén, Erik

AU - Pitsiladis, Yannis

AU - Pitkänen, Niina

AU - Snieder, Harold

AU - Heinrich, Joachim

AU - Timpson, Nicholas J

AU - Wang, Tao

AU - Yuji, Hinoda

AU - Zeggini, Eleftheria

AU - Dedoussis, George V

AU - Kaplan, Robert C

AU - Wylie-Rosett, Judith

AU - Loos, Ruth J F

AU - Hu, Frank B

AU - Qi, Lu

PY - 2015/7

Y1 - 2015/7

N2 - The FTO gene harbors variation with the strongest effect on adiposity and obesity risk. Previous data support a role for FTO variation in influencing food intake. We conducted a combined analysis of 16,094 boys and girls aged 1-18 years from 14 studies to examine the following: 1) the association between the FTO rs9939609 variant (or a proxy) and total energy and macronutrient intake; and 2) the interaction between the FTO variant and dietary intake, and the effect on BMI. We found that the BMIincreasing allele (minor allele) of the FTO variant was associated with increased total energy intake (effect per allele = 14.3 kcal/day [95%CI 5.9, 22.7 kcal/day], P = 6.5 3 1024), but not with protein, carbohydrate, or fat intake. We also found that protein intake modified the association between the FTO variant and BMI (interactive effect per allele = 0.08 SD [0.03, 0.12 SD], P for interaction = 7.2 3 1024): the association between FTO genotype and BMI was much stronger in individuals with high protein intake (effect per allele = 0.10 SD [0.07, 0.13 SD], P = 8.2 3 10210) than in those with low intake (effect per allele = 0.04 SD [0.01, 0.07 SD], P = 0.02). Our results suggest that the FTO variant that confers a predisposition to higher BMI is associated with higher total energy intake, and that lower dietary protein intake attenuates the association between FTO genotype and adiposity in children and adolescents.

AB - The FTO gene harbors variation with the strongest effect on adiposity and obesity risk. Previous data support a role for FTO variation in influencing food intake. We conducted a combined analysis of 16,094 boys and girls aged 1-18 years from 14 studies to examine the following: 1) the association between the FTO rs9939609 variant (or a proxy) and total energy and macronutrient intake; and 2) the interaction between the FTO variant and dietary intake, and the effect on BMI. We found that the BMIincreasing allele (minor allele) of the FTO variant was associated with increased total energy intake (effect per allele = 14.3 kcal/day [95%CI 5.9, 22.7 kcal/day], P = 6.5 3 1024), but not with protein, carbohydrate, or fat intake. We also found that protein intake modified the association between the FTO variant and BMI (interactive effect per allele = 0.08 SD [0.03, 0.12 SD], P for interaction = 7.2 3 1024): the association between FTO genotype and BMI was much stronger in individuals with high protein intake (effect per allele = 0.10 SD [0.07, 0.13 SD], P = 8.2 3 10210) than in those with low intake (effect per allele = 0.04 SD [0.01, 0.07 SD], P = 0.02). Our results suggest that the FTO variant that confers a predisposition to higher BMI is associated with higher total energy intake, and that lower dietary protein intake attenuates the association between FTO genotype and adiposity in children and adolescents.

U2 - 10.2337/db14-1629

DO - 10.2337/db14-1629

M3 - Journal article

C2 - 25720386

SN - 0012-1797

VL - 64

SP - 2467

EP - 2476

JO - Diabetes

JF - Diabetes

IS - 7

ER -

Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents

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