Phosphorus-31 magnetic resonance brain spectroscopy of children at risk for a substance use disorder: Preliminary results

被引:15
|
作者
Moss, HB
Talagala, SL
Kirisci, L
机构
[1] Univ Pittsburgh, Med Ctr, Dept Psychiat, Addict Recovery Serv, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Med Ctr, Dept Radiol, MR Res Ctr, Pittsburgh, PA 15213 USA
关键词
disruptive behavior disorders; antisocial behavior; magnetic resonance spectroscopy;
D O I
10.1016/S0925-4927(97)00067-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of this exploratory investigation was to evaluate the heuristic potential of P-31 magnetic resonance spectroscopy (MRS) in elucidating a neurobiologic component of the liability for a substance use disorder (SUD). We investigated P-31 MRS spectra employing chemical shift imaging (CSI) derived from four distinct anatomic brain locations (i.e. frontal, occipital, right parietal, left parietal) in three groups of peripubertal children who are hypothesized to be at increasing levels of familial SUD risk. Specifically, we studied children with a positive paternal family history of SUD and a disruptive behavior disorder (DBD) diagnosis (SUD+/DBD+; n = 10), in contrast to those with a positive paternal SUD history in the absence of other psychopathology (SUD+/DBD-; n = 13) and matched control children from normal families (SUD-/DBD-; n = 13). In addition, we examined neurocognitive tests of our subjects to determine any associations between cognitive capacities with regional P-31 MRS spectra. The highest-risk sample (SUD+/DBD+) demonstrated a diminished proportion of phosphodiesters confined to the right parietal voxel. This right parietal phosphodiester proportion correlated only with the Information Scale score on a standard intelligence test for children. This suggested a relationship between general learning ability and motivation for academic achievement and right parietal physiology in the highest-risk sample. Variations in synaptic pruning could account for this observation. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:101 / 112
页数:12
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