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GWAS Study

A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.

Arias-Vásquez A, Groffen AJ, Spijker S et al.

30659475 PubMed ID
GWAS Study Type
29465 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AA
Arias-Vásquez A
GA
Groffen AJ
SS
Spijker S
OK
Ouwens KG
KM
Klein M
VD
Vojinovic D
GT
Galesloot TE
BJ
Bralten J
HJ
Hottenga JJ
VD
van der Most PJ
KV
Kattenberg VM
PR
Pool R
NI
Nolte IM
PB
Penninx BWJH
FI
Fedko IO
DC
Dolan CV
NM
Nivard MG
DB
den Braber A
VD
van Duijn CM
HP
Hoekstra PJ
BJ
Buitelaar JK
KL
Kiemeney LA
HM
Hoogman M
MC
Middeldorp CM
DH
Draisma HHM
VS
Vermeulen SH
SC
Sánchez-Mora C
RJ
Ramos-Quiroga JA
RM
Ribasés M
HC
Hartman CA
KJ
Kooij JJS
AN
Amin N
SA
Smit AB
FB
Franke B
BD
Boomsma DI
Chapter II

Abstract

Summary of the research findings

We aimed to detect Attention-deficit/hyperactivity (ADHD) risk-conferring genes in adults. In children, ADHD is characterized by age-inappropriate levels of inattention and/or hyperactivity-impulsivity and may persists into adulthood. Childhood and adulthood ADHD are heritable, and are thought to represent the clinical extreme of a continuous distribution of ADHD symptoms in the general population. We aimed to leverage the power of studies of quantitative ADHD symptoms in adults who were genotyped. Within the SAGA (Study of ADHD trait genetics in adults) consortium, we estimated the single nucleotide polymorphism (SNP)-based heritability of quantitative self-reported ADHD symptoms and carried out a genome-wide association meta-analysis in nine adult population-based and case-only cohorts of adults. A total of n = 14,689 individuals were included. In two of the SAGA cohorts we found a significant SNP-based heritability for self-rated ADHD symptom scores of respectively 15% (n = 3656) and 30% (n = 1841). The top hit of the genome-wide meta-analysis (SNP rs12661753; p-value = 3.02 × 10-7) was present in the long non-coding RNA gene STXBP5-AS1. This association was also observed in a meta-analysis of childhood ADHD symptom scores in eight population-based pediatric cohorts from the Early Genetics and Lifecourse Epidemiology (EAGLE) ADHD consortium (n = 14,776). Genome-wide meta-analysis of the SAGA and EAGLE data (n = 29,465) increased the strength of the association with the SNP rs12661753. In human HEK293 cells, expression of STXBP5-AS1 enhanced the expression of a reporter construct of STXBP5, a gene known to be involved in "SNAP" (Soluble NSF attachment protein) Receptor" (SNARE) complex formation. In mouse strains featuring different levels of impulsivity, transcript levels in the prefrontal cortex of the mouse ortholog Gm28905 strongly correlated negatively with motor impulsivity as measured in the five choice serial reaction time task (r2 = - 0.61; p = 0.004). Our results are consistent with an effect of the STXBP5-AS1 gene on ADHD symptom scores distribution and point to a possible biological mechanism, other than antisense RNA inhibition, involved in ADHD-related impulsivity levels.

14,689 European ancestry adults, 14,776 children

Chapter III

Study Statistics

Key metrics and study information

29465
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Netherlands, Spain
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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