Combining fMRI and SNP data to investigate connections between brain function and genetics using parallel ICA
- PMID: 18072279
- PMCID: PMC2668960
- DOI: 10.1002/hbm.20508
Combining fMRI and SNP data to investigate connections between brain function and genetics using parallel ICA
Abstract
There is current interest in understanding genetic influences on both healthy and disordered brain function. We assessed brain function with functional magnetic resonance imaging (fMRI) data collected during an auditory oddball task--detecting an infrequent sound within a series of frequent sounds. Then, task-related imaging findings were utilized as potential intermediate phenotypes (endophenotypes) to investigate genomic factors derived from a single nucleotide polymorphism (SNP) array. Our target is the linkage of these genomic factors to normal/abnormal brain functionality. We explored parallel independent component analysis (paraICA) as a new method for analyzing multimodal data. The method was aimed to identify simultaneously independent components of each modality and the relationships between them. When 43 healthy controls and 20 schizophrenia patients, all Caucasian, were studied, we found a correlation of 0.38 between one fMRI component and one SNP component. This fMRI component consisted mainly of parietal lobe activations. The relevant SNP component was contributed to significantly by 10 SNPs located in genes, including those coding for the nicotinic alpha-7 cholinergic receptor, aromatic amino acid decarboxylase, disrupted in schizophrenia 1, among others. Both fMRI and SNP components showed significant differences in loading parameters between the schizophrenia and control groups (P = 0.0006 for the fMRI component; P = 0.001 for the SNP component). In summary, we constructed a framework to identify interactions between brain functional and genetic information; our findings provide a proof-of-concept that genomic SNP factors can be investigated by using endophenotypic imaging findings in a multivariate format.
(c) 2007 Wiley-Liss, Inc.
Figures
References
-
- Addis DR,McIntosh AR,Moscovitch M,Crawley AP,McAndrews MP ( 2004): Characterizing spatial and temporal features of autobiographical memory retrieval networks: A partial least squares approach. Neuroimage 23: 1460–1471. - PubMed
-
- Akaike H ( 1974): A new look at statistical model identification. IEEE Trans Automatic Control 19: 716–726.
-
- Amari S ( 1998): Natural gradient works efficiently in learning. Neural Comput 10: 251–276.
-
- Barta PE,Pearlson GD,Powers RE,Richards SS,Tune LE ( 1990): Auditory hallucinations and smaller superior temporal gyral volume in schizophrenia. Am J Psychiatry 147: 1457–1462. - PubMed
-
- Bath KG,Lee FS ( 2006): Variant BDNF (Val66Met) impact on brain structure and function. Cogn Affect Behav Neurosci 6: 79–85. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 MH052886/MH/NIMH NIH HHS/United States
- 5 RO1 MH52886/MH/NIMH NIH HHS/United States
- 1 R01 EB 000840/EB/NIBIB NIH HHS/United States
- R01 EB005846/EB/NIBIB NIH HHS/United States
- R01 EB006841/EB/NIBIB NIH HHS/United States
- R44 MH075481/MH/NIMH NIH HHS/United States
- R01 EB000840/EB/NIBIB NIH HHS/United States
- 2 RO1 MH43775/MH/NIMH NIH HHS/United States
- 1 R01 EB 005846/EB/NIBIB NIH HHS/United States
- R43 MH075481/MH/NIMH NIH HHS/United States
- R01 MH043775/MH/NIMH NIH HHS/United States
- R01 EB020407/EB/NIBIB NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
