Department of Psychiatry, University of Münster, Albert-Schweitzer-Str. 11, Münster, 48149, Germany.
South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
Neuropsychopharmacology. 2019 Dec;44(13):2212-2219. doi: 10.1038/s41386-019-0461-1. Epub 2019 Jul 8.
Genetic predisposition and brain structural abnormalities have been shown to be involved in the biological underpinnings of anorexia nervosa (AN). Prefrontal brain regions are suggested to contribute through behavioral inhibition mechanisms to body weight. However, it is unknown if and to which extent biological correlates for AN might be present in individuals without clinical AN symptomatology. We therefore investigated the contribution of polygenic load for AN on body weight and prefrontal brain structure in a sample of n = 380 nonclinical individuals. A polygenic score (PGS) reflecting the individual genetic load for the trait of anorexia nervosa was calculated. Structural MRI data were acquired and preprocessed using the cortical parcellation stream of FreeSurfer. We observed a significant PGS × sex interaction effect on body mass index (BMI), which was driven by a negative correlation between PGS and BMI in female participants. Imaging analyses revealed significant interaction effects of sex × PGS on surface area of the lateral orbitofrontal cortex (OFC), the pars orbitalis (PO), the rostral middle frontal gyrus (RMF) and the pars triangularis (PT) of the left frontal cortex. The interaction effects were driven by positive correlations between PGS and prefrontal surface areas in female participants and negative correlations in male participants. We furthermore found sex-specific associations between BMI and left RMF surface area as well as between BMI and left PO and left RMF thickness. Our findings demonstrate a sex-specific association between polygenic load for AN, BMI, and prefrontal brain structure in nonclinical individuals. Hence, this study identifies structural abnormalities associated with polygenic load for AN and BMI in brain regions deeply involved in behavioral inhibition and impulse regulation as candidate brain regions for future research.
遗传易感性和大脑结构异常已被证明与神经性厌食症 (AN) 的生物学基础有关。前额叶脑区被认为通过行为抑制机制对体重产生影响。然而,目前尚不清楚在没有临床 AN 症状的个体中,是否存在与 AN 相关的生物学相关性,以及这种相关性的程度如何。因此,我们在一个包含 380 名非临床个体的样本中,研究了 AN 的多基因负荷对体重和前额叶脑结构的影响。计算了反映 AN 个体遗传负荷的多基因评分 (PGS)。使用 FreeSurfer 的皮质分割流获取和预处理结构 MRI 数据。我们观察到 PGS 和 BMI 之间存在显著的 PGS×性别交互作用,这种交互作用主要是由于女性参与者中 PGS 和 BMI 呈负相关。成像分析显示,性别×PGS 对左侧前额皮质的外侧眶额皮质(OFC)、眶部(PO)、额中回(RMF)和三角部(PT)的表面积有显著的交互作用。这种交互作用的驱动因素是女性参与者中 PGS 和前额叶表面积之间存在正相关,而男性参与者中则存在负相关。我们还发现 BMI 与左侧 RMF 表面积、BMI 与左侧 PO 和左侧 RMF 厚度之间存在性别特异性关联。我们的研究结果表明,非临床个体中 AN 的多基因负荷、BMI 和前额叶脑结构之间存在性别特异性关联。因此,本研究确定了与 AN 的多基因负荷和 BMI 相关的大脑结构异常,这些结构异常与行为抑制和冲动调节中涉及的大脑区域有关,可能是未来研究的候选脑区。