2009
DOI: 10.1002/gps.2214
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Investigation of dopamine receptors in susceptibility to behavioural and psychological symptoms in Alzheimer's disease

Abstract: Our data, in combination with a review of the literature, reveal a potential role for the VNTR variant of DRD4 in the development of depression in AD patients. The findings presented here need to be replicated in large, well characterised longitudinal cohorts.

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Cited by 25 publications
(16 citation statements)
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“…DRD2 is one of four genes coding for dopamine receptors, and while DRD3 and DRD4 have been associated with AD, DRD2 so far was not. Our results support the association of this gene with non-cognitive symptoms of AD [19,20]. MAG encodes the myelin-associated glycoprotein; its association with AD has been recently investigated with negative results [21].…”
Section: Inference Of Novel Gene-and Drug-disorder Associationssupporting
confidence: 88%
“…DRD2 is one of four genes coding for dopamine receptors, and while DRD3 and DRD4 have been associated with AD, DRD2 so far was not. Our results support the association of this gene with non-cognitive symptoms of AD [19,20]. MAG encodes the myelin-associated glycoprotein; its association with AD has been recently investigated with negative results [21].…”
Section: Inference Of Novel Gene-and Drug-disorder Associationssupporting
confidence: 88%
“…Polymorphisms of the dopaminergic receptors were examined in Alzheimer patients with aggression. Polymorphisms of polymorphisms of the D3 and D4 receptors could be found in Alzheimer patients with agression [9].…”
Section: Dopaminementioning
confidence: 96%
“…It is well established that AD is a heterogeneous disease characterized by a variety of BPSD beyond the well-known progressive cognitive decline [6,7,36]. Different clinical phenotypes might be influenced by underlying genetic variability and behavioral and psychological symptoms.…”
Section: Discussionmentioning
confidence: 99%
“…ed with considerable morbidity for patients and distress for caregivers [6,7]. A genetic predisposition to BPSD in AD has been proposed in family studies [8].…”
Section: Catechol-o-methyltransferase Genetic Variantmentioning
confidence: 99%