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Published on: April 7, 2020
ARNTL, CLOCK and PER3 polymorphisms - links with chronotype and affective dimensions
Konrad S Jankowski1, Monika Dmitrzak-Weglarz2
1a Faculty of Psychology , University of Warsaw , Warsaw , Poland.
Genetic variations in ARNTL, TIM, and PER3 genes showed some associations with affective temperaments in students. However, these single nucleotide polymorphisms (SNPs) did not fully explain the link between sleep-wake cycles and mood. Further research is needed for confirmation.
Area of Science:
- Genetics
- Psychiatry
- Chronobiology
Background:
- Previous research linked specific gene single nucleotide polymorphisms (SNPs) in ARNTL, TIM, and PER3 to affective temperaments in bipolar disorder patients.
- The relationship between chronotype, affective temperaments, and genetic predispositions requires further investigation in non-clinical populations.
Purpose of the Study:
- To investigate if ARNTL, TIM, and PER3 gene SNPs associated with affective temperaments in bipolar patients are also present in a non-clinical student sample.
- To explore the relationship between these SNPs and other affective dimensions, as well as their role in mediating the connection between chronotype and affective traits.
Main Methods:
- Genotyping of seven single nucleotide polymorphisms (SNPs) in the ARNTL, TIM, and PER3 genes.
- Administration of multiple questionnaires assessing temperament, depression, stress, general health, seasonality, and chronotype to 338 university students.
- Statistical analysis to examine associations between SNPs, affective temperaments, dimensions, and chronotype.
Main Results:
- ARNTL rs7107287 showed nominal association with cyclothymic temperament, depressive symptoms, stress, mental health, and seasonality impact.
- TIM rs10876890 was nominally associated with hyperthymic temperament, and TIM rs2291738 with chronotype.
- The study found that different SNPs related to chronotype and affective temperaments, suggesting they do not underpin the observed relationships between eveningness/morningness and affective dysfunction.
Conclusions:
- The study suggests distinct genetic underpinnings for chronotype and affective temperaments/dimensions in a non-clinical sample.
- Observed associations between chronotype (eveningness/morningness) and affective traits (e.g., dysthymic, hyperthymic temperaments, depressive symptoms) were not explained by the investigated SNPs.
- The identified SNP associations require further replication as they did not meet stringent statistical significance criteria (Bonferroni correction).
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