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. 2014 Mar;165B(2):157-66.
doi: 10.1002/ajmg.b.32217. Epub 2014 Jan 30.

A recessive genetic model and runs of homozygosity in major depressive disorder

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A recessive genetic model and runs of homozygosity in major depressive disorder

Robert A Power et al. Am J Med Genet B Neuropsychiatr Genet. 2014 Mar.

Abstract

Genome-wide association studies (GWASs) of major depressive disorder (MDD) have yet to identify variants that surpass the threshold for genome-wide significance. A recent study reported that runs of homozygosity (ROH) are associated with schizophrenia, reflecting a novel genetic risk factor resulting from increased parental relatedness and recessive genetic effects. Here, we explore the possibility of such a recessive model in MDD. In a sample of 9,238 cases and 9,521 controls reported in a recent mega-analysis of 9 GWAS we perform an analysis of ROH and common variants under a recessive model. Since evidence for association with ROH could reflect a recessive mode of action at loci, we also conducted a genome-wide association analyses under a recessive model. The genome-wide association analysis using a recessive model found no significant associations. Our analysis of ROH suggested that there was significant heterogeneity of effect across studies in effect (P = 0.001), and it was associated with genotyping platform and country of origin. The results of the ROH analysis show that differences across studies can lead to conflicting systematic genome-wide differences between cases and controls that are unaccounted for by traditional covariates. They highlight the sensitivity of the ROH method to spurious associations, and the need to carefully control for potential confounds in such analyses. We found no strong evidence for a recessive model underlying MDD.

Keywords: inbreeding; major depression; recessive risk model; runs of homozygosity.

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Conflict of interest statement

Financial Disclosure:

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Beta coefficient from logistic regression of FROH predicting MDD per study (with 95% CI, accounting for covariates). Positive effects suggest that ROHs are a risk factor for MDD. Note that though no combined effect in the mixed model of the full sample, in Illumina studies increased FROH was a risk factor (p=0.02) and in non-Illumina studies it was protective (p=0.007). Note also the consistency in studies from the same country: *Australian studies; ~American studies; # German studies.

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