The search for circadian clock components in humans: new perspectives for association studies
Open accessAbstract
Individual circadian clocks entrain differently to environmental cycles (zeitgebers, e.g., light and darkness), earlier or later within the day, leading to different chronotypes. In human populations, the distribution of chronotypes forms a bell-shaped curve, with the extreme early and late types _ larks and owls, respectively _ at its ends. Human chronotype, which can be assessed by the timing of an individual's sleep-wake cycle, is partly influenced by genetic factors - known from animal experimentation. Here, we review population genetic studies which have used a questionnaire probing individual daily timing preference for associations with polymorphisms in clock genes. We discuss their inherent limitations and suggest an alternative approach combining a short questionnaire (Munich ChronoType Questionnaire, MCTQ), which assesses chronotype in a quantitative manner, with a genome-wide analysis (GWA). The advantages of these methods in comparison to assessing time-of-day preferences and single nucleotide polymorphism genotyping are discussed. In the future, global studies of chronotype using the MCTQ and GWA may also contribute to understanding the influence of seasons, latitude (e.g., different photoperiods), and climate on allele frequencies and chronotype distribution in different populations.
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The underlying distribution of chronotypes follows a normal bell shape, with tail ends reflecting extreme morning and evening chronotypes.
“there is evidence to suggest that the underlying distribution of chronotypes follows a normal bell shape, with tail ends reflecting extreme morning and evening chronotypes (6).”
From Chronotype: Implications for Epidemiologic Studies on Chrono-Nutrition and Cardiometabolic Health (2019) · cites this paper as [6]
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References 57 · Cited by 84
Research works printed but not linked: 2
- Costa R, Peixoto AA, Barbujani G, Kyriacou CP. A latitudi- nal cline in a Drosophila clock gene. Proc Biol Sci 1992; 250: 43-49.
- Toh KL, Jones CR, He Y, Eide EJ, Hinz WA, Virshup DM, et al. An hPer2 phosphorylation site mutation in familial ad- vanced sleep phase syndrome. Science 2001; 291: 1040- 1043.
- Authors
- Allebrandt, K. V., & Roenneberg, T.
- Affiliations
- Ludwig-Maximilians-Universität München (DE)
- Venue
- Brazilian Journal of Medical and Biological Research
- Publisher
- FapUNIFESP (SciELO)
- Published
- 2008-08
- Volume
- 41
- Issue
- 8
- Pages
- 716-721
- ISSN
- 0100-879X (ISSN-L)
- OpenAlex
- W2136235957
- Cited by
- 84
- References
- 57
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 5 · 2022: 3 · 2021: 5 · 2020: 10 · 2019: 5 · 2018: 6 · 2017: 3 · 2016: 4 · 2015: 6 · 2014: 7 · 2013: 9 · 2012: 3
- FWCI
- 0.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Brazilian Journal of Medical and Biological Research (publishedVersion, cc-by)
- PubMed (publishedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (publishedVersion, other-oa)
- Americanae (AECID Library) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- circadian clock, chronotype, clock genes, genetic association studies, Munich Chronotype Questionnaire, genome-wide association study, single nucleotide polymorphisms, sleep timing, photoperiod, population genetics
- MeSH terms
- Biological Clocks, Genotype, Geography, Humans, Phenotype, Polymorphism, Genetic, Surveys and Questionnaires
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