4.7 Article

Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures

Journal

NEUROPSYCHOPHARMACOLOGY
Volume 45, Issue 7, Pages 1188-1195

Publisher

SPRINGERNATURE
DOI: 10.1038/s41386-019-0592-4

Keywords

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Funding

  1. European Community [667302, 728018, 643051]
  2. ECNP Network ADHD across the Lifespan
  3. Netherlands Organization for Scientific Research (NWO) Innovation Program (Vici grant) [016-130-669]
  4. Spanish Ministerio de Economia y Competitividad [SAF2015-68341-R]
  5. AGAUR, Generalitat de Catalunya [2017-SGR-738]
  6. Centro de Investigacion Biomedica en Red de Enfermedades Raras (CIBERER, Spain)
  7. DFG [SFB CRC 1193 Z03]
  8. BMBF (BipoLife)
  9. Netherlands Scientific Organization [NWO 480-05-003]
  10. Dutch Brain Foundation
  11. VU University Amsterdam
  12. Medice

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Attention-Deficit/Hyperactivity Disorder (ADHD) and obesity are frequently comorbid, genetically correlated, and share brain substrates. The biological mechanisms driving this association are unclear, but candidate systems, like dopaminergic neurotransmission and circadian rhythm, have been suggested. Our aim was to identify the biological mechanisms underpinning the genetic link between ADHD and obesity measures and investigate associations of overlapping genes with brain volumes. We tested the association of dopaminergic and circadian rhythm gene sets with ADHD, body mass index (BMI), and obesity (using GWAS data of N = 53,293, N = 681,275, and N = 98,697, respectively). We then conducted genome-wide ADHD-BMI and ADHD-obesity gene-based meta-analyses, followed by pathway enrichment analyses. Finally, we tested the association of ADHD-BMI overlapping genes with brain volumes (primary GWAS data N = 10,720-10,928; replication data N = 9428). The dopaminergic gene set was associated with both ADHD (P = 5.81 x 10(-3)) and BMI (P = 1.63 x 10(-5)); the circadian rhythm was associated with BMI (P = 1.28 x 10(-3)). The genome-wide approach also implicated the dopaminergic system, as the Dopamine-DARPP32 Feedback in cAMP Signaling pathway was enriched in both ADHD-BMI and ADHD-obesity results. The ADHD-BMI overlapping genes were associated with putamen volume (P = 7.7 x 10(-3); replication data P = 3.9 x 10(-2))-a brain region with volumetric reductions in ADHD and BMI and linked to inhibitory control. Our findings suggest that dopaminergic neurotransmission, partially through DARPP-32-dependent signaling and involving the putamen, is a key player underlying the genetic overlap between ADHD and obesity measures. Uncovering shared etiological factors underlying the frequently observed ADHD-obesity comorbidity may have important implications in terms of prevention and/or efficient treatment of these conditions.

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