Increased peripheral blood expression of electron transport chain genes in bipolar depression

Robert D. Beech, Lori Lowthert, Janine J. Leffert, Portia N. Mason, Mary M. Taylor, Sheila Umlauf, Aiping Lin, Ji Young Lee, Kathleen Maloney, Anjana Muralidharan, Boris Lorberg, Hongyu Zhao, Samuel S. Newton, Shrikant Mane, C. Neill Epperson, Rajita Sinha, Hilary Blumberg, Zubin Bhagwagar

Research output: Contribution to journalArticlepeer-review

48 Scopus citations


Objective: To identify specific genetic pathways showing altered expression in peripheral blood of depressed subjects with bipolar disorder (BPD).Methods: Illumina Sentrix BeadChip (Human-6v2) microarrays containing >48,000 transcript probes were used to measure levels of gene expression in peripheral blood from 20 depressed subjects with BPD and in 15 healthy control subjects. Quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) was used to confirm a subset of these differences.Results: A total of 1,180 genes were differentially expressed between subjects with BPD and healthy controls (fold-change >1.3, false discovery rate-corrected p < 0.05, covaried for age and sex). Of these, 559 genes were up-regulated in BPD subjects and 621 were down-regulated. Surprisingly, there was no difference between medicated (n = 11) and unmedicated (n = 9) subjects with BPD for any of these genes. Pathway analysis using GeneGo MetaCore software showed that the most significantly affected pathway was the mitochondrial electron transport chain (ETC). Of the 85 objects (genes or proteins) in this pathway, 22 were up-regulated and 2 down-regulated in subjects with BPD. qRT-PCR confirmed up-regulation of nuclear encoded ETC genes in complexes I, III, IV, and V and, in addition, demonstrated up-regulation of mitochondrially encoded genes in each of these complexes.Conclusion: These results suggest that increased expression of multiple components of the mitochondrial ETC may be a primary deficit in bipolar depression, rather than an effect of medication.

Original languageEnglish (US)
Pages (from-to)813-824
Number of pages12
JournalBipolar Disorders
Issue number8
StatePublished - Dec 2010
Externally publishedYes


  • Bipolar disorder
  • Gene expression
  • Microarray
  • Mitochondria
  • Oxidative phosphorylation

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Biological Psychiatry


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