Evidence for a sex-specific contribution of polygenic load for anorexia nervosa to body weight and prefrontal brain structure in nonclinical individuals

Elisabeth J. Leehr, Nils Opel, Janina Werner, Ronny Redlich, Jonathan Repple, Dominik Grotegerd, Katharina Dohm, Janik Goltermann, Joscha Böhnlein, Azmeraw Amare, Lisa Sindermann, Katharina Förster, Susanne Meinert, Verena Enneking, Maike Richter, Tim Hahn, Bernhard T. Baune, Udo Dannlowski

Research output: Contribution to journalArticle

Abstract

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.

LanguageEnglish
JournalNeuropsychopharmacology
DOIs
Publication statusPublished - 8 Jul 2019

ASJC Scopus subject areas

  • Pharmacology
  • Psychiatry and Mental health

Cite this

Leehr, Elisabeth J. ; Opel, Nils ; Werner, Janina ; Redlich, Ronny ; Repple, Jonathan ; Grotegerd, Dominik ; Dohm, Katharina ; Goltermann, Janik ; Böhnlein, Joscha ; Amare, Azmeraw ; Sindermann, Lisa ; Förster, Katharina ; Meinert, Susanne ; Enneking, Verena ; Richter, Maike ; Hahn, Tim ; Baune, Bernhard T. ; Dannlowski, Udo. / Evidence for a sex-specific contribution of polygenic load for anorexia nervosa to body weight and prefrontal brain structure in nonclinical individuals. In: Neuropsychopharmacology. 2019.
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Leehr, EJ, Opel, N, Werner, J, Redlich, R, Repple, J, Grotegerd, D, Dohm, K, Goltermann, J, Böhnlein, J, Amare, A, Sindermann, L, Förster, K, Meinert, S, Enneking, V, Richter, M, Hahn, T, Baune, BT & Dannlowski, U 2019, 'Evidence for a sex-specific contribution of polygenic load for anorexia nervosa to body weight and prefrontal brain structure in nonclinical individuals', Neuropsychopharmacology. https://doi.org/10.1038/s41386-019-0461-1

Evidence for a sex-specific contribution of polygenic load for anorexia nervosa to body weight and prefrontal brain structure in nonclinical individuals. / Leehr, Elisabeth J.; Opel, Nils; Werner, Janina; Redlich, Ronny; Repple, Jonathan; Grotegerd, Dominik; Dohm, Katharina; Goltermann, Janik; Böhnlein, Joscha; Amare, Azmeraw; Sindermann, Lisa; Förster, Katharina; Meinert, Susanne; Enneking, Verena; Richter, Maike; Hahn, Tim; Baune, Bernhard T.; Dannlowski, Udo.

In: Neuropsychopharmacology, 08.07.2019.

Research output: Contribution to journalArticle

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T1 - Evidence for a sex-specific contribution of polygenic load for anorexia nervosa to body weight and prefrontal brain structure in nonclinical individuals

AU - Leehr, Elisabeth J.

AU - Opel, Nils

AU - Werner, Janina

AU - Redlich, Ronny

AU - Repple, Jonathan

AU - Grotegerd, Dominik

AU - Dohm, Katharina

AU - Goltermann, Janik

AU - Böhnlein, Joscha

AU - Amare, Azmeraw

AU - Sindermann, Lisa

AU - Förster, Katharina

AU - Meinert, Susanne

AU - Enneking, Verena

AU - Richter, Maike

AU - Hahn, Tim

AU - Baune, Bernhard T.

AU - Dannlowski, Udo

PY - 2019/7/8

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N2 - 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.

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