Genetics of ADHD: What Should the Clinician Know?
Open accessAbstract
Purpose of Review: Attention deficit hyperactivity disorder (ADHD) shows high heritability in formal genetic studies. In our review article, we provide an overview on common and rare genetic risk variants for ADHD and their link to clinical practice. Recent findings: The formal heritability of ADHD is about 80% and therefore higher than most other psychiatric diseases. However, recent studies estimate the proportion of heritability based on singlenucleotide variants (SNPs) at 22%. It is a matter of debate which genetic mechanisms explain this huge difference. While frequent variants in first mega-analyses of genome-wideassociation study data containing several thousand patients give the first genome-wide results, explaining only little variance, the methodologically more difficult analyses of rare variants are still in their infancy. Some rare genetic syndromes show higher prevalence for ADHD indicating a potential role for a small number of patients. In contrast, polygenic risk scores (PRS) could potentially be applied to every patient. We give an overview how PRS explain different behavioral phenotypes in ADHD and how they could be used for diagnosis and therapy prediction. Summary: Knowledge about a patient’s genetic makeup is not yet mandatory for ADHD therapy or diagnosis. PRS however have been introduced successfully in other areas of clinical medicine, and their application in psychiatry will begin within the next years. In order to ensure competent advice for patients, knowledge of the current state of research is useful forpsychiatrists.
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Several risk genes have been found in the human genome, but only a limited number of small impact size ADHD genes have been identified.
“Several risk genes have been found in the human genome [59], but only a limited number of small impact size ADHD genes have been identified [60].”
From Molecular Characterisation of the Mechanism of Action of Stimulant Drugs Lisdexamfetamine and Methylphenidate on ADHD Neurobiology: A Review (2022) · cites this paper as [59]
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Shared genetic background between children and adults with attention deficit/hyperactivity disorder
Rovira, P., Demontis, D., Sánchez-Mora, C., Zayats, T., Klein, M., Mota, N. R., Weber, H., Garcia-Martínez, I., Pagerols, M., Vilar-Ribó, L., et al. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0664-5 · Cited by 111 · see citing works
Self-citationAlcohol use disorders and ADHD.
Luderer, M., Ramos Quiroga, J. A., Faraone, S. V., Zhang-James, Y., & Reif, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.07.010 · Cited by 102 · see citing works
Self-citationQuintero, J., Gutiérrez-Casares, J. R., & Álamo, C. (2022) · Neurology and Therapy · doi:10.1007/s40120-022-00392-2 · Cited by 70 · see citing works
“Several risk genes have been found in the human genome [59], but only a limited number of small impact size ADHD genes have been identified [60].”
BackgroundWells, A. C., & Lotfipour, S. (2023) · Advances in Drug and Alcohol Research · doi:10.3389/adar.2023.11628 · Cited by 50 · see citing works
“Globally, 5% of children and adolescents are estimated to have ADHD with a recent meta-analysis of twin studies estimating the heritability of ADHD to be 77% – 88% [64, 65].”
Background
- Authors
- Grimm, O., Kranz, T. M., & Reif, A.
- Affiliations
- Goethe University Frankfurt (DE)
- Corresponding author
- Reif, Andreas
- Venue
- Current Psychiatry Reports
- Published
- 2020-02-27
- Volume
- 22
- Issue
- 4
- Pages
- 18-18
- ISSN
- 1523-3812 (ISSN-L)
- 1535-1645
- PMC
- PMC7046577
- OpenAlex
- W3008672910
- Cited by
- 97
- References
- 13
- Citations by year
- 2026: 16 · 2025: 17 · 2024: 22 · 2023: 16 · 2022: 13 · 2021: 8 · 2020: 5
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Current Psychiatry Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Informationszentrum Lebenswissenschaften (ZB MED) (submittedVersion, cc-by)
- Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) (submittedVersion, cc-by)
- Funders
- Johann Wolfgang Goethe-Universität, Frankfurt am Main
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- attention deficit hyperactivity disorder, ADHD genetics, heritability, single nucleotide polymorphisms, rare variants, polygenic risk score, genetic syndromes, behavioral phenotypes, diagnosis, treatment prediction
- MeSH terms
- Attention Deficit Disorder with Hyperactivity, Humans, Genetic Predisposition to Disease, Multifactorial Inheritance, Polymorphism, Single Nucleotide, Genome-Wide Association Study
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