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Zimmermann, E.* ; Ängquist, L.H.* ; Mirza, S.S.* ; Zhao, J.H.* ; Chasman, D.I.* ; Fischer, K.* ; Qi, Q.* ; Smith, A.V.* ; Thinggaard, M.* ; Jarczok, M.N.* ; Nalls, M.A.* ; Trompet, S.* ; Timpson, N.J.* ; Schmidt, B.* ; Jackson, A.U.* ; Lyytikäinen, L.-P.* ; Verweij, N.* ; Müller-Nurasyid, M. ; Vikström, M.* ; Marques-Vidal, P.* ; Wong, A.* ; Meidtner, K.* ; Middelberg, R.P.* ; Strawbridge, R.J.* ; Christiansen, L.* ; Kyvik, K.O.H.M.* ; Hamsten, A.* ; Jääskeläinen, T.* ; Tjönneland, A.M.* ; Eriksson, J.G.* ; Whitfield, J.B.* ; Boeing, H.* ; Hardy, R.* ; Vollenweider, P.* ; Leander, K.* ; Peters, A. ; van der Harst, P.* ; Kumari, M.* ; Lehtimäki, T.* ; Meirhaeghe, A.* ; Tuomilehto, J.O.I.* ; Jöckel, K.-H.* ; Ben-Shlomo, Y.* ; Sattar, N.A.* ; Baumeister, S.E.* ; Davey Smith, G.* ; Casas, J.P.* ; Houston, D.K.* ; Marz, W.* ; Christensen, K.* ; Gudnason, V.G.* ; Hu, F.B.* ; Metspalu, A.* ; Ridker, P.M.* ; Wareham, N.J.* ; Loos, R.J.F.* ; Tiemeier, H.M.* ; Sonestedt, E.* ; Sørensen, T.I.A.*

Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults.

Obes. Rev. 16, 327-340 (2015)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Summary: Previously, a single nucleotide polymorphism (SNP), rs9939609, in the FTO gene showed a much stronger association with all-cause mortality than expected from its association with body mass index (BMI), body fat mass index (FMI) and waist circumference (WC). This finding implies that the SNP has strong pleiotropic effects on adiposity and adiposity-independent pathological pathways that leads to increased mortality. To investigate this further, we conducted a meta-analysis of similar data from 34 longitudinal studies including 169,551 adult Caucasians among whom 27,100 died during follow-up. Linear regression showed that the minor allele of the FTO SNP was associated with greater BMI (n=169,551; 0.32kgm-2; 95% CI 0.28-0.32, P<1×10-32), WC (n=152,631; 0.76cm; 0.68-0.84, P<1×10-32) and FMI (n=48,192; 0.17kgm-2; 0.13-0.22, P=1.0×10-13). Cox proportional hazard regression analyses for mortality showed that the hazards ratio (HR) for the minor allele of the FTO SNPs was 1.02 (1.00-1.04, P=0.097), but the apparent excess risk was eliminated after adjustment for BMI and WC (HR: 1.00; 0.98-1.03, P=0.662) and for FMI (HR: 1.00; 0.96-1.04, P=0.932). In conclusion, this study does not support that the FTO SNP is associated with all-cause mortality independently of the adiposity phenotypes.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Fto ; Meta-analysis ; Mortality ; Obesity; Genome-wide Association; Major Risk-factors; Middle-aged Men; Body-mass Index; Mendelian Randomization; Waist Circumference; Cohort Profile; Cardiovascular-disease; Myocardial-infarction; Metabolic Syndrome
Sprache englisch
Veröffentlichungsjahr 2015
HGF-Berichtsjahr 2015
ISSN (print) / ISBN 1467-7881
e-ISSN 1467-789X
Zeitschrift Obesity Reviews
Quellenangaben Band: 16, Heft: 4, Seiten: 327-340 Artikelnummer: , Supplement: ,
Verlag Blackwell
Verlagsort Oxford
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)
POF Topic(s) 30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-504100-001
G-504000-002
DOI 10.1111/obr.12263
WOS ID WOS:000351612400006
Scopus ID 84924047195
Scopus ID 84925584409
Erfassungsdatum 2015-03-15
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