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A polymorphism in the microRNA-30e precursor associated with major depressive disorder risk and P300 waveform
1Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Background:
Growing evidence shows that the etiological causes and pathological processes underlying major depressive disorder (MDD) and schizophrenia (SCZ) overlap. Our previous study revealed a strong association between the polymorphism ss178077483 in the miRNA-30e precursor (pre-miR-30e) and the risk of SCZ. We thus hypothesized that this SCZ risk allele at the pre-miR-30e gene also confers risk of MDD.
Methods:
To explore the relationship between miR-30e ss178077483 and MDD, we conducted an association analyses in 1088 MDD patients and 1102 control subjects from the Han Chinese population. We also determined the effects of miR-30e ss178077483 on the development of P300 event-related potential components induced by an auditory odd-ball task.
Results:
We detected a statistically significant positive association between miR-30e ss178077483 and MDD (allelic P=0.0287; genotypic P=0.0275). Moreover, the P300 latency was associated with miR-30e ss178077483 genotypes and the individuals with the C/T genotype have a longer P300 latency than those carrying the C/C genotype (P=0.009).
Limitations:
Larger numbers of subjects and different ethnic groups would confirm and strengthen these preliminary findings.
Conclusions:
To our knowledge, this is the first evidence to suggest that miRNA polymorphisms may play an important role in MDD susceptibility. These findings also imply that certain miRNAs may be involved in the etiology of MDD.
Insights
This study links a specific microRNA (miRNA) gene variant, previously associated with schizophrenia, to an increased risk of major depressive disorder (MDD). The findings suggest miRNA polymorphisms may contribute to MDD susceptibility.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Major depressive disorder (MDD) and schizophrenia (SCZ) share overlapping etiological factors and pathological processes.
- A prior study identified a significant association between the pre-miR-30e gene polymorphism (ss178077483) and SCZ risk.
- This led to the hypothesis that the SCZ risk allele might also confer risk for MDD.
Purpose of the Study:
- To investigate the association between the pre-miR-30e gene polymorphism (ss178077483) and the risk of developing major depressive disorder (MDD).
- To examine the impact of this specific miRNA polymorphism on electrophysiological measures, specifically P300 event-related potential components, in individuals with MDD.
Main Methods:
- Conducted association analyses comparing 1088 MDD patients and 1102 control subjects from the Han Chinese population.
- Assessed the relationship between the miR-30e ss178077483 polymorphism and P300 event-related potential components using an auditory odd-ball task.
Main Results:
- A statistically significant positive association was found between the miR-30e ss178077483 polymorphism and MDD risk (allelic P=0.0287; genotypic P=0.0275).
- P300 latency was significantly associated with miR-30e ss178077483 genotypes.
- Individuals with the C/T genotype exhibited longer P300 latency compared to those with the C/C genotype (P=0.009).
Conclusions:
- This study provides the first evidence suggesting that microRNA (miRNA) polymorphisms may play a role in major depressive disorder (MDD) susceptibility.
- The findings imply that specific miRNAs could be implicated in the underlying etiology of MDD.
- Further research with larger, diverse populations is recommended to confirm and strengthen these preliminary results.
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