Altered orbitofrontal sulcogyral patterns in gambling disorder: a multicenter study
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Altered orbitofrontal sulcogyral patterns in gambling disorder : a multicenter study. / Li, Yansong; Wang, Zixiang; Boileau, Isabelle; Dreher, Jean Claude; Gelskov, Sofie; Genauck, Alexander; Joutsa, Juho; Kaasinen, Valtteri; Perales, José C.; Romanczuk-Seiferth, Nina; Ruiz de Lara, Cristian M.; Siebner, Hartwig R.; van Holst, Ruth J.; van Timmeren, Tim; Sescousse, Guillaume.
In: Translational Psychiatry, Vol. 9, 186, 08.2019.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Altered orbitofrontal sulcogyral patterns in gambling disorder
T2 - a multicenter study
AU - Li, Yansong
AU - Wang, Zixiang
AU - Boileau, Isabelle
AU - Dreher, Jean Claude
AU - Gelskov, Sofie
AU - Genauck, Alexander
AU - Joutsa, Juho
AU - Kaasinen, Valtteri
AU - Perales, José C.
AU - Romanczuk-Seiferth, Nina
AU - Ruiz de Lara, Cristian M.
AU - Siebner, Hartwig R.
AU - van Holst, Ruth J.
AU - van Timmeren, Tim
AU - Sescousse, Guillaume
PY - 2019/8
Y1 - 2019/8
N2 - Gambling disorder is a serious psychiatric condition characterized by decision-making and reward processing impairments that are associated with dysfunctional brain activity in the orbitofrontal cortex (OFC). However, it remains unclear whether OFC functional abnormalities in gambling disorder are accompanied by structural abnormalities. We addressed this question by examining the organization of sulci and gyri in the OFC. This organization is in place very early and stable across life, such that OFC sulcogyral patterns (classified into Types I, II, and III) can be regarded as potential pre-morbid markers of pathological conditions. We gathered structural brain data from nine existing studies, reaching a total of 165 individuals with gambling disorder and 159 healthy controls. Our results, supported by both frequentist and Bayesian statistics, show that the distribution of OFC sulcogyral patterns is skewed in individuals with gambling disorder, with an increased prevalence of Type II pattern compared with healthy controls. Examination of gambling severity did not reveal any significant relationship between OFC sulcogyral patterns and disease severity. Altogether, our results provide evidence for a skewed distribution of OFC sulcogyral patterns in gambling disorder and suggest that pattern Type II might represent a pre-morbid structural brain marker of the disease. It will be important to investigate more closely the functional implications of these structural abnormalities in future work.
AB - Gambling disorder is a serious psychiatric condition characterized by decision-making and reward processing impairments that are associated with dysfunctional brain activity in the orbitofrontal cortex (OFC). However, it remains unclear whether OFC functional abnormalities in gambling disorder are accompanied by structural abnormalities. We addressed this question by examining the organization of sulci and gyri in the OFC. This organization is in place very early and stable across life, such that OFC sulcogyral patterns (classified into Types I, II, and III) can be regarded as potential pre-morbid markers of pathological conditions. We gathered structural brain data from nine existing studies, reaching a total of 165 individuals with gambling disorder and 159 healthy controls. Our results, supported by both frequentist and Bayesian statistics, show that the distribution of OFC sulcogyral patterns is skewed in individuals with gambling disorder, with an increased prevalence of Type II pattern compared with healthy controls. Examination of gambling severity did not reveal any significant relationship between OFC sulcogyral patterns and disease severity. Altogether, our results provide evidence for a skewed distribution of OFC sulcogyral patterns in gambling disorder and suggest that pattern Type II might represent a pre-morbid structural brain marker of the disease. It will be important to investigate more closely the functional implications of these structural abnormalities in future work.
U2 - 10.1038/s41398-019-0520-8
DO - 10.1038/s41398-019-0520-8
M3 - Journal article
C2 - 31383841
AN - SCOPUS:85070223903
VL - 9
JO - Translational Psychiatry
JF - Translational Psychiatry
SN - 2158-3188
M1 - 186
ER -
ID: 240626504