Study Report
Reference
| Citation | Philibert, 2011 PubMed |
| Full Info | Philibert, R.A., Beach, S.R., Gunter, T.D., Todorov, A.A., Brody, G.H., Vijayendran, M., Elliott, L., Hollenbeck, N., Russell, D. and Cutrona, C. (2011) The relationship of deiodinase 1 genotype and thyroid function to lifetime history of major depression in three independent populations. Am J Med Genet B Neuropsychiatr Genet, 156, 593-599.
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Study
| Hypothesis or Background |
Major depression (MD) is often associated with disturbances of the hypothalamic/pituitary/thyroid (HPT) axis. Unfortunately, whether this association is secondary to common underlying genetic variation or whether the MD-associated disturbances in HPT function are chronic or state-dependent is unknown.
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| Sample Information | 1,555 subjects from three longitudinal ethnically diverse studies that are well-characterized for lifetime MD and thyroid function. |
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| Method Detail | To examine these questions, we genotyped 12 single nucleotide polymorphisms identified in previous genome wide association analyses of thyroid function in DNA contributed by 1,555 subjects from three longitudinal ethnically diverse studies that are well-characterized for lifetime MD and thyroid function. We then examined associations between genetic variants and key outcomes of thyroid stimulating hormone, free thyroxine (FT4) and depression |
| Method Keywords | genotyping |
| Result | We confirmed prior findings that two variants in deiodinase 1 (DIO1), including a variant in the 3'UTR of DIO1 (rs11206244), were associated with altered FT4 levels in both White and African American subjects. We also found that rs11206244 genotype was associated with lifetime MD in White female subjects, in particular those from high-risk cohorts. However, we found no association of current FT4 levels with lifetime MD in either ethnic group. |
| Conclusions | We conclude that genetic variation influencing thyroid function is a risk factor for MD. Given the evidence from prior studies, further investigations of role of HPT variation in etiology and treatment of MD are indicated. |
Relationships reported by
Philibert, 2011
| Component A Approved Name (Name in Paper) |
Component A Type |
Component B Approved Name (Name in Paper) |
Component B Type |
Statistical Result |
Relationship Description |
Result Category (Positive/Negative)) |
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MDD
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syndrome |
rs11206244 (rs11206244) |
SNP |
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We also found that rs11206244 genotype was associated with lifetime MD in White female subjects, in particular those from high-risk cohorts. |
Positive
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