The authors of this paper do not have any commercial associations that might pose a conflict of interest in connection with this manuscript.
Neurochemical deficits in the cerebellar vermis in child offspring of parents with bipolar disorder
Article first published online: 28 MAR 2011
© 2011 John Wiley and Sons A/S
Volume 13, Issue 2, pages 189–197, March 2011
How to Cite
Singh, M. K., Spielman, D., Libby, A., Adams, E., Acquaye, T., Howe, M., Kelley, R., Reiss, A. and Chang, K. D. (2011), Neurochemical deficits in the cerebellar vermis in child offspring of parents with bipolar disorder. Bipolar Disorders, 13: 189–197. doi: 10.1111/j.1399-5618.2011.00902.x
- Issue published online: 28 MAR 2011
- Article first published online: 28 MAR 2011
- Received 28 May 2010, revised and accepted for publication 19 January 2011
- cerebellar vermis;
- familial bipolar disorder;
Singh MK, Spielman D, Libby A, Adams E, Acquaye T, Howe M, Kelley R, Reiss A, Chang KD. Neurochemical deficits in the cerebellar vermis in child offspring of parents with bipolar disorder. Bipolar Disord 2011: 13: 189–197. © 2011 The Authors. Journal compilation © 2011 John Wiley & Sons A/S.
Objectives: We aimed to compare concentrations of N-acetyl aspartate, myo-inositol, and other neurometabolites in the cerebellar vermis of offspring at risk for bipolar disorder (BD) and healthy controls to examine whether changes in these neuronal metabolite concentrations occur in at-risk offspring prior to the onset of mania.
Methods: A total of 22 children and adolescents aged 9–17 years with a familial risk for bipolar I or II disorder [at-risk offspring with non-bipolar I disorder mood symptoms (AR)], and 25 healthy controls (HC) were examined using proton magnetic resonance spectroscopy at 3T to study metabolite concentrations in an 8-cc voxel in the cerebellar vermis.
Results: Decreased myo-inositol and choline concentrations in the vermis were seen in the AR group compared to HC (p < 0.01).
Conclusions: Decreased cellular metabolism and interference with second messenger pathways may be present in the cerebellar vermis in youth at risk for BD as evident by decreased myo-inositol and choline concentrations in this region. These results may be limited by a cross-sectional design, co-occurring diagnoses, and medication exposure. Longitudinal studies are necessary to determine whether early neurochemical changes can predict the development of mania. Improved methods for identifying children with certain neurochemical vulnerabilities may inform preventive and early intervention strategies prior to the onset of mania.