Genetic Correlates of Spirituality/Religion and Depression: A Study in Offspring and Grandchildren at High and Low Familial Risk for Depression.
Micheline R Anderson, Lisa Miller, Priya Wickramaratne, Connie Svob, Zagaa Odgerel, Ruixin Zhao, Myrna M Weissman
Spirituality in Clinical Practice March 1, 2017 DOI: 10.1037/scp0000125 (opens in new tab)
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Study at a glance
AI-extracted from the abstract| Characteristics | Longitudinal family study Peer reviewed |
|---|---|
| Population | Offspring and grandchildren of individuals at high and low familial risk for depression |
| Duration | Thirty-year longitudinal study |
| Topics | Depression |
| Key findings | In people at low familial risk for depression, variants in dopamine (DRD2), serotonin (5-HT1B), vesicular transporter (VMAT1), and oxytocin (OXTR) genes were positively associated with high importance of spirituality or religion, and the DRD2 minor allele was linked to both lifetime major depressive disorder and spirituality. No such associations appeared in the high-risk group. OXTR was associated with lifetime MDD across the full sample. |
Abstract
Rationale: Possible genetic correlates of spirituality and depression have been identified in community samples. We investigate some of the previously identified candidates in a sample of families at both high and low-risk for depression.
Method: Offspring and grandchildren of individuals at high and low-risk for depression, participating in a multi-wave thirty-year longitudinal study, were assessed for seven SNPS drawn from four single gene candidates associated with systems implicated in both depression and spirituality: Serotonin (5-HT1B and 5-HT2A), Dopamine (DRD2), Oxytocin (OT) and Monoamine Vesicular Transporter (VMAT1).
Results: Dopamine (DRD2) Serotonin (5-HT1B), their Transporter (VMAT1) and Oxytocin (OXTR) were positively associated with a high level of importance of spirituality or religion (S/R) in the group at low familial risk for depression. DRD2 minor allele was associated with both lifetime major depressive disorder (MDD) and spirituality in the low-risk group for depression. No SNPs were related to S/R in the group at high familial risk for depression. OXTR was associated with lifetime MDD in the full sample.
Conclusion: Genes for dopamine, serotonin, their vesicular transporter, and oxytocin may be associated with S/R in people at low familial risk for depression. Genes for dopamine may be associated both with S/R and increased risk for depression in people at low-risk for depression, suggesting a common pathway or physiology to mild to moderate depression. MDD is associated with oxytocin across risk groups. In the high-risk group, phenotypic expression of S/R may be suppressed.
Implications: The shared association of DRD2 by S/R and depression, generally found to be inversely related, calls for further research on their common physiological pathways, and the phenotypic expression of these pathways based upon use and environment. Prevention for offspring at high familial risk for depression might include support for the development of child spirituality.
Comparable studies
Other observational and cohort studies on depression, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| Metacognitive awareness and prevention of relapse in depression: Empirical evidence. Residually depressed patients and nondepressed controls; recovered depressed patients | 2002 | Observational cohort with intervention components | |
| Psilocybin for treatment-resistant depression: fMRI-measured brain mechanisms. Patients with treatment-resistant depression | 2017 | Observational cohort | n = 19 |
| Antidepressant effects of a single dose of ayahuasca in patients with recurrent depression: a preliminary report Patients with a depressive disorder | 2015 | Observational study | |
| Concomitant BDNF and sleep slow wave changes indicate ketamine-induced plasticity in major depressive disorder Patients with treatment-resistant major depressive disorder | 2012 | Observational cohort | n = 30 |
| Altered peripheral immune profiles in treatment-resistant depression: response to ketamine and prediction of treatment outcome Healthy controls and actively depressed patients with treatment-resistant depression... | 2017 | Observational cohort | n = 59 |
Citations in the library
Cited by 2
Cites 6
- The Serotonin System and Spiritual Experiences American Journal of Psychiatry November 1, 2003
- Effects of oxytocin administration on spirituality and emotional responses to meditation Social Cognitive and Affective Neuroscience June 17, 2016
- Self-transcendence trait and its relationship with in vivo serotonin transporter availability in brainstem raphe nuclei: An ultra-high resolution PET-MRI study. Brain Research December 10, 2015
- Developmental Depression in Adolescents: A Potential Sub-type Based on Neural Correlates and Comorbidity. Journal of Religion and Health June 1, 2015
- 5-HT 1A polymorphism and self-transcendence in mood disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics August 5, 2005
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