TY - JOUR
T1 - Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders
T2 - Evidence through univariate and multivariate mega-analysis including 6420 participants from the ENIGMA MDD working group
AU - ENIGMA-Major Depressive Disorder W
AU - Opel, Nils
AU - Thalamuthu, Anbupalam
AU - Milaneschi, Yuri
AU - Grotegerd, Dominik
AU - Flint, Claas
AU - Leenings, Ramona
AU - Goltermann, Janik
AU - Richter, Maike
AU - Hahn, Tim
AU - Woditsch, Georg
AU - Berger, Klaus
AU - Hermesdorf, Marco
AU - Mcintosh, Andrew
AU - Whalley, Heather C.
AU - Harris, Mathew A.
AU - Macmaster, Frank P.
AU - Walter, Henrik
AU - Veer, Ilya M.
AU - Frodl, Thomas
AU - Carballedo, Angela
AU - Krug, Axel
AU - Nenadic, Igor
AU - Kircher, Tilo
AU - Aleman, Andre
AU - Groenewold, Nynke A.
AU - Stein, Dan J.
AU - Soares, Jair C.
AU - Zunta-soares, Giovana B.
AU - Mwangi, Benson
AU - Wu, Mon-ju
AU - Walter, Martin
AU - Li, Meng
AU - Harrison, Ben J.
AU - Davey, Christopher G.
AU - Cullen, Kathryn R.
AU - Klimes-dougan, Bonnie
AU - Mueller, Bryon A.
AU - Sämann, Philipp G.
AU - Penninx, Brenda
AU - Nawijn, Laura
AU - Veltman, Dick J.
AU - Aftanas, Lyubomir
AU - Brak, Ivan V.
AU - Filimonova, Elena A.
AU - Osipov, Evgeniy A.
AU - Reneman, Liesbeth
AU - Schrantee, Anouk
AU - Grabe, Hans J.
AU - Van Der Auwera, Sandra
AU - Thompson, Paul M.
PY - 2020/5/28
Y1 - 2020/5/28
N2 - Emerging evidence suggests that obesity impacts brain physiology at multiple levels. Here we aimed to clarify the relationship between obesity and brain structure using structural MRI (n = 6420) and genetic data (n = 3907) from the ENIGMA Major Depressive Disorder (MDD) working group. Obesity (BMI > 30) was significantly associated with cortical and subcortical abnormalities in both mass-univariate and multivariate pattern recognition analyses independent of MDD diagnosis. The most pronounced effects were found for associations between obesity and lower temporo-frontal cortical thickness (maximum Cohen´s d (left fusiform gyrus) = −0.33). The observed regional distribution and effect size of cortical thickness reductions in obesity revealed considerable similarities with corresponding patterns of lower cortical thickness in previously published studies of neuropsychiatric disorders. A higher polygenic risk score for obesity significantly correlated with lower occipital surface area. In addition, a significant age-by-obesity interaction on cortical thickness emerged driven by lower thickness in older participants. Our findings suggest a neurobiological interaction between obesity and brain structure under physiological and pathological brain conditions.
AB - Emerging evidence suggests that obesity impacts brain physiology at multiple levels. Here we aimed to clarify the relationship between obesity and brain structure using structural MRI (n = 6420) and genetic data (n = 3907) from the ENIGMA Major Depressive Disorder (MDD) working group. Obesity (BMI > 30) was significantly associated with cortical and subcortical abnormalities in both mass-univariate and multivariate pattern recognition analyses independent of MDD diagnosis. The most pronounced effects were found for associations between obesity and lower temporo-frontal cortical thickness (maximum Cohen´s d (left fusiform gyrus) = −0.33). The observed regional distribution and effect size of cortical thickness reductions in obesity revealed considerable similarities with corresponding patterns of lower cortical thickness in previously published studies of neuropsychiatric disorders. A higher polygenic risk score for obesity significantly correlated with lower occipital surface area. In addition, a significant age-by-obesity interaction on cortical thickness emerged driven by lower thickness in older participants. Our findings suggest a neurobiological interaction between obesity and brain structure under physiological and pathological brain conditions.
U2 - 10.1038/s41380-020-0774-9
DO - 10.1038/s41380-020-0774-9
M3 - Article
SN - 1359-4184
VL - N/A
SP - 1
EP - 14
JO - Molecular Psychiatry
JF - Molecular Psychiatry
ER -