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The role of ADHD genetic risk in mid-to-late life somatic health conditions

The role of ADHD genetic risk in mid-to-late life somatic health conditions
The role of ADHD genetic risk in mid-to-late life somatic health conditions
Growing evidence suggests that ADHD, an early onset neurodevelopmental disorder, is associated with poor somatic health in adulthood. However, the mechanisms underlying these associations are poorly understood. Here, we tested whether ADHD polygenic risk scores (PRS) are associated with mid-to-late life somatic health in a general population sample. Furthermore, we explored whether potential associations were moderated and mediated by life-course risk factors. We derived ADHD-PRS in 10,645 Swedish twins born between 1911 and 1958. Sixteen cardiometabolic, autoimmune/inflammatory, and neurological health conditions were evaluated using self-report (age range at measure 42–88 years) and clinical diagnoses defined by International Classification of Diseases codes in national registers. We estimated associations of ADHD-PRS with somatic outcomes using generalized estimating equations, and tested moderation and mediation of these associations by four life-course risk factors (education level, body mass index [BMI], tobacco use, alcohol misuse). Results showed that higher ADHD-PRS were associated with increased risk of seven somatic outcomes (heart failure, cerebro- and peripheral vascular disease, obesity, type 1 diabetes, rheumatoid arthritis, and migraine) with odds ratios ranging 1.07 to 1.20. We observed significant mediation effects by education, BMI, tobacco use, and alcohol misuse, primarily for associations of ADHD-PRS with cardiometabolic outcomes. No moderation effects survived multiple testing correction. Our findings suggests that higher ADHD genetic liability confers a modest risk increase for several somatic health problems in mid-to-late life, particularly in the cardiometabolic domain. These associations were observable in the general population, even in the absence of medical treatment for ADHD, and appear to be in part mediated by life-course risk factors.
Garcia-Argibay, Miguel
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Rietz, Ebba du
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Lu, Yi
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Martin, Joanna
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Haan, Elis
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Lehto, Kelli
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Bergen, Sarah E.
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Lichtenstein, Paul
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Larsson, Henrik
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Brikell, Isabell
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Garcia-Argibay, Miguel
e5a6941e-4dcc-401a-9de4-09557c8856ef
Rietz, Ebba du
fcfdb832-03aa-4236-8fb4-147bf166f13c
Lu, Yi
42c9df18-0785-449a-a720-14ff7531cc8b
Martin, Joanna
e31bf359-7647-4787-8b70-76e3a69e2425
Haan, Elis
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Lehto, Kelli
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Bergen, Sarah E.
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Lichtenstein, Paul
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Larsson, Henrik
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Brikell, Isabell
8ce0666a-d578-4128-9385-20358b875b7c

Garcia-Argibay, Miguel, Rietz, Ebba du, Lu, Yi, Martin, Joanna, Haan, Elis, Lehto, Kelli, Bergen, Sarah E., Lichtenstein, Paul, Larsson, Henrik and Brikell, Isabell (2022) The role of ADHD genetic risk in mid-to-late life somatic health conditions. Translational Psychiatry, 12. (doi:10.1038/s41398-022-01919-9).

Record type: Article

Abstract

Growing evidence suggests that ADHD, an early onset neurodevelopmental disorder, is associated with poor somatic health in adulthood. However, the mechanisms underlying these associations are poorly understood. Here, we tested whether ADHD polygenic risk scores (PRS) are associated with mid-to-late life somatic health in a general population sample. Furthermore, we explored whether potential associations were moderated and mediated by life-course risk factors. We derived ADHD-PRS in 10,645 Swedish twins born between 1911 and 1958. Sixteen cardiometabolic, autoimmune/inflammatory, and neurological health conditions were evaluated using self-report (age range at measure 42–88 years) and clinical diagnoses defined by International Classification of Diseases codes in national registers. We estimated associations of ADHD-PRS with somatic outcomes using generalized estimating equations, and tested moderation and mediation of these associations by four life-course risk factors (education level, body mass index [BMI], tobacco use, alcohol misuse). Results showed that higher ADHD-PRS were associated with increased risk of seven somatic outcomes (heart failure, cerebro- and peripheral vascular disease, obesity, type 1 diabetes, rheumatoid arthritis, and migraine) with odds ratios ranging 1.07 to 1.20. We observed significant mediation effects by education, BMI, tobacco use, and alcohol misuse, primarily for associations of ADHD-PRS with cardiometabolic outcomes. No moderation effects survived multiple testing correction. Our findings suggests that higher ADHD genetic liability confers a modest risk increase for several somatic health problems in mid-to-late life, particularly in the cardiometabolic domain. These associations were observable in the general population, even in the absence of medical treatment for ADHD, and appear to be in part mediated by life-course risk factors.

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e-pub ahead of print date: 11 April 2022

Identifiers

Local EPrints ID: 488846
URI: http://eprints.soton.ac.uk/id/eprint/488846
PURE UUID: 66ad3ffa-bef9-4cd6-b327-07882b27a8fd
ORCID for Miguel Garcia-Argibay: ORCID iD orcid.org/0000-0002-4811-2330

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Date deposited: 08 Apr 2024 16:42
Last modified: 13 Apr 2024 02:11

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Contributors

Author: Miguel Garcia-Argibay ORCID iD
Author: Ebba du Rietz
Author: Yi Lu
Author: Joanna Martin
Author: Elis Haan
Author: Kelli Lehto
Author: Sarah E. Bergen
Author: Paul Lichtenstein
Author: Henrik Larsson
Author: Isabell Brikell

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