Neurochemical correlates of cognitive functions in euthymic patients with bipolar disorder: 1H-MRS study.

We assessed and correlated neurochemical levels and cognitive functions in left dorsolateral prefrontal cortex (DLPFC) and left hippocampus in euthymic patients with bipolar disorder and compared these with healthy controls Twenty-five right-handed euthymic patients (HAM-D score < 7, and YMRS score < 7) with bipolar disorder and 20 age and gender matched controls were compared for neurometabolites (n-acetylaspartate – tNAA, choline – Cho, creatinine – Cr, myoinositol – Ins, and glutamine/glutamate – Glu/Gln) measured in left DLPFC and left hippocampus using single voxel magnetic resonance spectroscopy (MRS) and cognitive functions assessed using trail making test (TMT – A and B), wisconsin card sorting test (WCST), and wechsler memory scale (WMS-III Indian adaptation). The two groups were comparable on socio-demographic variables. tNAA levels in DLPFC and hippocampus, and glutamate levels in hippocampus were found to be significantly lower and Inositol and glutamine levels in hippocampus were found to be significantly higher in patients as compared to controls. Patients performed significantly poorly as compared to controls on TMT A & B, all subscales of WMS – III, 5 subscales of WCST, including perseverative responses and errors. The tNAA and glutamate levels in left DLPFC in patients correlated with scores on TMT A & B, and several subscales of WCST and WMS-III. tNAA concentration in left hippocampus in patients correlated with scores on subscales of WMS-III. Neurochemical dysfunction in select brain areas directly correlates with impairment in cognitive functions seen in patients with bipolar disorder in euthymic phase. • Brain MRS in left DLPFC and left hippocampus in euthymic patients with bipolar disorder (BD) shows abnormalities in neurochemical levels. • In BD, ↓ tNAA levels in DLPFC and hippocampus, ↓ glutamate levels in hippocampus and ↑ Inositol and glutamine levels in hippocampus. • In BD, tNAA and glutamate levels in DLPFC correlate with TMT A & B and several subscales of WCST and WMS-III. • In BD, tNAA concentration in hippocampus correlates with subscales of WMS-III. • In BD, neurochemical levels correlate significantly with the extent of cognitive dysfunction even in euthymic phase. [ABSTRACT FROM AUTHOR]