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Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs.

Johansson, S (author)
Halleland, H (author)
Halmøy, A (author)
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Jacobsen, KK (author)
Landaas, ET (author)
Dramsdahl, M (author)
Fasmer, OB (author)
Bergsholm, P (author)
Lundervold, AJ (author)
Gillberg, Christopher, 1950 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Hugdahl, K (author)
Knappskog, PM (author)
Haavik, J (author)
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 (creator_code:org_t)
Wiley, 2008
2008
English.
In: American journal of medical genetics. Part B, Neuropsychiatric genetics. - : Wiley. - 1552-485X .- 1552-4841. ; 147B:8, s. 1470-1475
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Attention deficit hyperactivity disorder (ADHD) is a common and highly heritable psychiatric disorder in children and adults. Recent meta-analyses have indicated an association between genes involved in dopaminergic signaling and childhood ADHD, but little is known about their possible role in adult ADHD. In this study of adults with ADHD, we evaluated the three most commonly studied ADHD candidate genetic polymorphisms; the dopamine receptor D4 (DRD4) exon 3 VNTR repeat, a microsatellite repeat 18.5 kb upstream of the DRD5 locus and the 3'UTR dopamine transporter SLC6A3 (DAT 1) VNTR. We examined 358 clinically diagnosed adult Norwegian ADHD patients (51% males) and 340 ethnically matched controls. We found a nominally significant overall association with adult ADHD for the DRD5 microsatellite marker (P = 0.04), and a trend toward increased risk associated with the 148-bp allele consistent with recent meta-analyses. The strongest overall association (P = 0.02) and increased risk for the 148-bp allele [odds ratio (OR) = 1.27 (95% CI: 1.00-1.61)] were seen in the inattentive and combined inattentive/hyperactive group as previously reported for childhood ADHD. No association was found for the DRD4 or SLC6A3 polymorphisms in this patient sample. In conclusion, our results among adults with a clinical diagnosis of ADHD support an association between ADHD and the DRD5 locus, but not the DRD4 or SLC6A3 loci. It is possible that the latter polymorphisms are associated with a transient form of ADHD with better long-term clinical outcome. (c) 2007 Wiley-Liss, Inc.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

Keyword

Adult
Alleles
Attention Deficit Disorder with Hyperactivity
Diagnosis
Genetics
Case-Control Studies
Dopamine Plasma Membrane Transport Proteins
Genetics
Female
Gene Frequency
Genetic Markers
Humans
Male
Microsatellite Repeats
Polymorphism
Genetic
Receptors
Dopamine D4
Genetics
Receptors
Dopamine D5
Genetics
Retrospective Studies

Publication and Content Type

ref (subject category)
art (subject category)

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