Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study

SAP90/PSD95‐associated protein (SAPAP) family proteins are post‐synaptic density (PSD) components that interact with other proteins to form a key scaffolding complex at excitatory (glutamatergic) synapses. A recent study found that mice with a deletion of the Sapap3 gene groomed themselves excessive...

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Veröffentlicht in:American journal of medical genetics. Part B, Neuropsychiatric genetics Neuropsychiatric genetics, 2009-07, Vol.150B (5), p.710-720
Hauptverfasser: Bienvenu, O.J., Wang, Y., Shugart, Y.Y., Welch, J.M., Grados, M.A., Fyer, A.J., Rauch, S.L., McCracken, J.T., Rasmussen, S.A., Murphy, D.L., Cullen, B., Valle, D., Hoehn-Saric, R., Greenberg, B.D., Pinto, A., Knowles, J.A., Piacentini, J., Pauls, D.L., Liang, K.Y., Willour, V.L., Riddle, M., Samuels, J.F., Feng, G., Nestadt, G.
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Sprache:eng
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Zusammenfassung:SAP90/PSD95‐associated protein (SAPAP) family proteins are post‐synaptic density (PSD) components that interact with other proteins to form a key scaffolding complex at excitatory (glutamatergic) synapses. A recent study found that mice with a deletion of the Sapap3 gene groomed themselves excessively, exhibited increased anxiety‐like behaviors, and had cortico‐striatal synaptic defects, all of which were preventable with lentiviral‐mediated expression of Sapap3 in the striatum; the behavioral abnormalities were also reversible with fluoxetine. In the current study, we sought to determine whether variation within the human Sapap3 gene was associated with grooming disorders (GDs: pathologic nail biting, pathologic skin picking, and/or trichotillomania) and/or obsessive‐compulsive disorder (OCD) in 383 families thoroughly phenotyped for OCD genetic studies. We conducted family‐based association analyses using the FBAT and GenAssoc statistical packages. Thirty‐two percent of the 1,618 participants met criteria for a GD, and 65% met criteria for OCD. Four of six SNPs were nominally associated (P 
ISSN:1552-4841
1552-485X
DOI:10.1002/ajmg.b.30897