Study Report
Reference
| Citation | Haefner S, 2008 PubMed |
| Full Info | Haefner S, Baghai TC, Schule C, Eser D, Spraul M, Zill P et al. Impact of gene-gender effects of adrenergic polymorphisms on hypothalamic-pituitary-adrenal axis activity in depressed patients. Neuropsychobiology 2008; 58(3-4): 154-162.
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Study
| Hypothesis or Background |
There is overwhelming evidence that activation of the hypothalamic-pituitary-adrenal (HPA) system plays a major role in depression and cardiovascular disease in genetically susceptible individuals. We hypothesized that due to the multiple interactions between the sympathetic and the HPA systems via adrenoceptors, polymorphisms in these genes could have an impact on HPA axis activity in major depression
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| Sample Information | 89 patients with major depression during the acute state of the disease and after remission. |
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| Method Detail | Using the dexamethasone/corticotrophin-releasing hormone (DEX/CRH) test, we investigated the association of alpha(2)-adrenoceptor (ADRA2A -1291C-->G) and the beta(2)-adrenoceptor gene (ADRB2 Arg16Gly) in 189 patients with major depression during the acute state of the disease and after remission. |
| Method Keywords | genotyping; blood analysis |
| Result | Male ADRA2A -1291G allele homozygotes showed significant pretreatment HPA axis hyperactivity, with increased adrenocorticotropin (ACTH; F = 4.9, d.f. = 2, p = 0.009) and cortisol responses (F = 6.4, d.f. = 2, p = 0.003). In contrast, female ADRB2 Arg/Arg homozygotes had increased pretreatment ACTH (F = 7.17, d.f. = 2, p = 0.001) and cortisol (F = 8.95, d.f. = 2, p = 0.000) levels. Interestingly, in the respective genotypes, the stress hormones remained elevated in the second DEX/CRH test, despite a reduction in depressive symptoms. |
| Conclusions | This study provides evidence that, depending on gender and polymorphisms, there is continuous HPA axis overdrive in a proportion of patients irrespective of the status of depression. Considering the importance of stress hormones for cardiovascular disorders, our data might suggest that these patients are at high risk of comorbidity between depression and cardiovascular disorders. |
Relationships reported by
Haefner S, 2008
| 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)) |
|
Pro-opiomelanocortin (adrenocorticotropin)
|
protein |
ADRB2 (ADRB2) |
gene |
F = 7.17, d.f. = 2, p = 0.001 |
female ADRB2 Arg/Arg homozygotes had increased pretreatment ACTH (F = 7.17, d.f. = 2, p = 0.001) and cortisol (F = 8.95, d.f. = 2, p = 0.000) levels. |
Positive
|
|
Hydrocortisone (cortisol)
|
molecule |
ADRB2 (ADRB2) |
gene |
F = 8.95, d.f. = 2, p = 0.000 |
female ADRB2 Arg/Arg homozygotes had increased pretreatment ACTH (F = 7.17, d.f. = 2, p = 0.001) and cortisol (F = 8.95, d.f. = 2, p = 0.000) levels. |
Positive
|
|
Pro-opiomelanocortin (adrenocorticotropin)
|
protein |
ADRA2A (ADRA2A) |
gene |
F = 4.9, d.f. = 2, p = 0.009 |
Male ADRA2A -1291G allele homozygotes showed significant pretreatment HPA axis hyperactivity, with increased adrenocorticotropin (ACTH; F = 4.9, d.f. = 2, p = 0.009) and cortisol responses (F = 6.4, d.f. = 2, p = 0.003). |
Positive
|
|
Hydrocortisone (cortisol)
|
molecule |
ADRA2A (ADRA2A) |
gene |
F = 6.4, d.f. = 2, p = 0.003 |
Male ADRA2A -1291G allele homozygotes showed significant pretreatment HPA axis hyperactivity, with increased adrenocorticotropin (ACTH; F = 4.9, d.f. = 2, p = 0.009) and cortisol responses (F = 6.4, d.f. = 2, p = 0.003). |
Positive
|
