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  1. Article: Sleep duration and metabolic syndrome. A gene-environment association. Schlafdauer und metabolisches Syndrom. Eine Gen-Umwelt-Beziehung

    Allebrandt, K. V.

    Somnologie

    2013  Volume 17, Issue 1, Page(s) 15

    Language German
    Document type Article
    ZDB-ID 1364175-x
    ISSN 1432-9123 ; 1433-7908
    Database Current Contents Medicine

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  2. Article ; Online: The search for circadian clock components in humans: new perspectives for association studies.

    Allebrandt, K V / Roenneberg, T

    Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas

    2008  Volume 41, Issue 8, Page(s) 716–721

    Abstract: 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 ... ...

    Abstract 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.
    MeSH term(s) Biological Clocks/genetics ; Biological Clocks/physiology ; Genotype ; Geography ; Humans ; Phenotype ; Polymorphism, Genetic ; Surveys and Questionnaires
    Language English
    Publishing date 2008-08-28
    Publishing country Brazil
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 786234-9
    ISSN 1414-431X ; 0100-879X
    ISSN (online) 1414-431X
    ISSN 0100-879X
    DOI 10.1590/s0100-879x2008000800013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The search for circadian clock components in humans

    Allebrandt, K. V. / Roenneberg, T.

    Brazilian Journal of Medical and Biological Research

    New perspectives for association studies

    2008  Volume 41 8, Page(s) 716–721

    Abstract: Reviewed population genetic studies to investigate new research avenues for human chronotype study. Differences in clock genes related to individual circadian rhythms can lead to advances in treatment of disease and in the rescheduling of work and school ...

    Title translation Die Suche nach Komponenten der zirkadianen Uhr beim Menschen: Neue Perspektiven für Assoziationsstudien
    Abstract Reviewed population genetic studies to investigate new research avenues for human chronotype study. Differences in clock genes related to individual circadian rhythms can lead to advances in treatment of disease and in the rescheduling of work and school activities allowing for a more flexible approach to normal circadian clocks. A review of genome-wide studies will allow identification of genes related to circadian regulation in humans. Identification of extreme chronotypes will lead to better treatment of patients in an attempt to adjust their clocks to a more suitable social schedule. It will also address disease process treatment that does not involve circadian clock disturbances but does involve an adjustment to the clock. Alterations to school and work schedules may be a topic to be addressed once insight is gained regarding chronotypes.
    Keywords Biologische Rhythmen beim Menschen ; Genom ; Genome ; Human Biological Rhythms ; Schlaf-Wach-Zyklus ; Sleep Wake Cycle
    Language English
    Document type Article
    ZDB-ID 786234-9
    ISSN 0100-879X
    ISSN 0100-879X
    Database PSYNDEX

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  4. Article ; Online: The search for circadian clock components in humans

    K.V. Allebrandt / T. Roenneberg

    Brazilian Journal of Medical and Biological Research, Vol 41, Iss 8, Pp 716-

    new perspectives for association studies

    2008  Volume 721

    Abstract: 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 ... ...

    Abstract 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.
    Keywords Human clock genes ; Chronotype ; Morningness ; Association studies ; Latitudinal hypothesis ; Medicine (General) ; R5-920 ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2008-08-01T00:00:00Z
    Publisher Associação Brasileira de Divulgação Científica
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: Social jetlag and obesity

    Roenneberg, Till / Allebrandt, Karla V. / Merrow, Martha / Vetter, Celine

    Current Biology

    2012  Volume 22, Issue 10, Page(s) 939–943

    Abstract: Obesity has reached crisis proportions in industrialized societies [1]. Many factors converge to yield increased body mass index (BMI). Among these is sleep duration [2-10]. The circadian clock controls sleep timing through the process of entrainment. ... ...

    Abstract Obesity has reached crisis proportions in industrialized societies [1]. Many factors converge to yield increased body mass index (BMI). Among these is sleep duration [2-10]. The circadian clock controls sleep timing through the process of entrainment. Chronotype describes individual differences in sleep timing, and it is determined by genetic background, age, sex, and environment (e.g., light exposure) [11-14]. Social jetlag quantifies the discrepancy that often arises between circadian and social clocks, which results in chronic sleep loss [11, 15]. The circadian clock also regulates energy homeostasis [16], and its disruption-as with social jetlag-may contribute to weight-related pathologies [17-19]. Here, we report the results from a large-scale epidemiological study, showing that, beyond sleep duration, social jetlag is associated with increased BMI. Our results demonstrate that living "against the clock" may be a factor contributing to the epidemic of obesity. This is of key importance in pending discussions on the implementation of Daylight Saving Time and on work or school times, which all contribute to the amount of social jetlag accrued by an individual. Our data suggest that improving the correspondence between biological and social clocks will contribute to the management of obesity.
    Keywords Adipositas ; Biologische Rhythmen beim Menschen ; Body Mass Index ; Human Biological Rhythms ; Obesity ; Schlaf ; Schlaf-Wach-Zyklus ; Sleep ; Sleep Wake Cycle
    Language English
    Document type Article
    ZDB-ID 1071731-6
    ISSN 1879-0445 ; 0960-9822
    ISSN (online) 1879-0445
    ISSN 0960-9822
    DOI 10.1016/j.cub.2012.03.038
    Database PSYNDEX

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  6. Article ; Online: Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.

    Jones, Samuel E / Lane, Jacqueline M / Wood, Andrew R / van Hees, Vincent T / Tyrrell, Jessica / Beaumont, Robin N / Jeffries, Aaron R / Dashti, Hassan S / Hillsdon, Melvyn / Ruth, Katherine S / Tuke, Marcus A / Yaghootkar, Hanieh / Sharp, Seth A / Jie, Yingjie / Thompson, William D / Harrison, Jamie W / Dawes, Amy / Byrne, Enda M / Tiemeier, Henning /
    Allebrandt, Karla V / Bowden, Jack / Ray, David W / Freathy, Rachel M / Murray, Anna / Mazzotti, Diego R / Gehrman, Philip R / Lawlor, Debbie A / Frayling, Timothy M / Rutter, Martin K / Hinds, David A / Saxena, Richa / Weedon, Michael N

    Nature communications

    2019  Volume 10, Issue 1, Page(s) 343

    Abstract: Being a morning person is a behavioural indicator of a person's underlying circadian rhythm. Using genome-wide data from 697,828 UK Biobank and 23andMe participants we increase the number of genetic loci associated with being a morning person from 24 to ... ...

    Abstract Being a morning person is a behavioural indicator of a person's underlying circadian rhythm. Using genome-wide data from 697,828 UK Biobank and 23andMe participants we increase the number of genetic loci associated with being a morning person from 24 to 351. Using data from 85,760 individuals with activity-monitor derived measures of sleep timing we find that the chronotype loci associate with sleep timing: the mean sleep timing of the 5% of individuals carrying the most morningness alleles is 25 min earlier than the 5% carrying the fewest. The loci are enriched for genes involved in circadian regulation, cAMP, glutamate and insulin signalling pathways, and those expressed in the retina, hindbrain, hypothalamus, and pituitary. Using Mendelian Randomisation, we show that being a morning person is causally associated with better mental health but does not affect BMI or risk of Type 2 diabetes. This study offers insights into circadian biology and its links to disease in humans.
    MeSH term(s) Adult ; Aged ; Circadian Rhythm ; Cyclic AMP/metabolism ; Female ; Genetic Loci ; Genome-Wide Association Study ; Glutamic Acid/metabolism ; Humans ; Male ; Middle Aged ; Sleep ; United Kingdom ; Whites/genetics
    Chemical Substances Glutamic Acid (3KX376GY7L) ; Cyclic AMP (E0399OZS9N)
    Language English
    Publishing date 2019-01-29
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-018-08259-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Integrative network analysis highlights biological processes underlying GLP-1 stimulated insulin secretion: A DIRECT study.

    Gudmundsdottir, Valborg / Pedersen, Helle Krogh / Allebrandt, Karla Viviani / Brorsson, Caroline / van Leeuwen, Nienke / Banasik, Karina / Mahajan, Anubha / Groves, Christopher J / van de Bunt, Martijn / Dawed, Adem Y / Fritsche, Andreas / Staiger, Harald / Simonis-Bik, Annemarie M C / Deelen, Joris / Kramer, Mark H H / Dietrich, Axel / Hübschle, Thomas / Willemsen, Gonneke / Häring, Hans-Ulrich /
    de Geus, Eco J C / Boomsma, Dorret I / Eekhoff, Elisabeth M W / Ferrer, Jorge / McCarthy, Mark I / Pearson, Ewan R / Gupta, Ramneek / Brunak, Søren / 't Hart, Leen M

    PloS one

    2018  Volume 13, Issue 1, Page(s) e0189886

    Abstract: Glucagon-like peptide 1 (GLP-1) stimulated insulin secretion has a considerable heritable component as estimated from twin studies, yet few genetic variants influencing this phenotype have been identified. We performed the first genome-wide association ... ...

    Abstract Glucagon-like peptide 1 (GLP-1) stimulated insulin secretion has a considerable heritable component as estimated from twin studies, yet few genetic variants influencing this phenotype have been identified. We performed the first genome-wide association study (GWAS) of GLP-1 stimulated insulin secretion in non-diabetic individuals from the Netherlands Twin register (n = 126). This GWAS was enhanced using a tissue-specific protein-protein interaction network approach. We identified a beta-cell protein-protein interaction module that was significantly enriched for low gene scores based on the GWAS P-values and found support at the network level in an independent cohort from Tübingen, Germany (n = 100). Additionally, a polygenic risk score based on SNPs prioritized from the network was associated (P < 0.05) with glucose-stimulated insulin secretion phenotypes in up to 5,318 individuals in MAGIC cohorts. The network contains both known and novel genes in the context of insulin secretion and is enriched for members of the focal adhesion, extracellular-matrix receptor interaction, actin cytoskeleton regulation, Rap1 and PI3K-Akt signaling pathways. Adipose tissue is, like the beta-cell, one of the target tissues of GLP-1 and we thus hypothesized that similar networks might be functional in both tissues. In order to verify peripheral effects of GLP-1 stimulation, we compared the transcriptome profiling of ob/ob mice treated with liraglutide, a clinically used GLP-1 receptor agonist, versus baseline controls. Some of the upstream regulators of differentially expressed genes in the white adipose tissue of ob/ob mice were also detected in the human beta-cell network of genes associated with GLP-1 stimulated insulin secretion. The findings provide biological insight into the mechanisms through which the effects of GLP-1 may be modulated and highlight a potential role of the beta-cell expressed genes RYR2, GDI2, KIAA0232, COL4A1 and COL4A2 in GLP-1 stimulated insulin secretion.
    MeSH term(s) Animals ; Glucagon-Like Peptide 1/metabolism ; Humans ; Insulin/metabolism ; Insulin Secretion ; Mice
    Chemical Substances Insulin ; Glucagon-Like Peptide 1 (89750-14-1)
    Language English
    Publishing date 2018-01-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0189886
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Depression scores associate with chronotype and social jetlag in a rural population

    Levandovski, Rosa / Dantas, Giovana / Fernandes, Luciana Carvalho / Caumo, Wolnei / Torres, Iraci / Roenneberg, Till / Loayza Hidalgo, Maria Paz / Allebrandt, Karla Viviani

    Chronobiology International

    2011  Volume 28, Issue 9, Page(s) 771–778

    Abstract: Screened an essentially rural population using the Beck Depression Inventory (BDI) and investigated its relation to circadian phenotype (chronotype and social jetlag) assessed via the Munich Chronotype Questionnaire (MCTQ). 4,051 participants of European ...

    Title translation Depressionswerte hängen in einer ländlichen Bevölkerungsgruppe mit Chronotyp und sozialem Jetlag zusammen
    Abstract Screened an essentially rural population using the Beck Depression Inventory (BDI) and investigated its relation to circadian phenotype (chronotype and social jetlag) assessed via the Munich Chronotype Questionnaire (MCTQ). 4,051 participants of European descent (aged 18-65 years) were included. In this study design the authors normalized both chronotype and BDI scores for age and sex (midsleep phase on free days-sleep/age/sex, or MSF(sas) and BDI(as), respectively), calculated individual social jetlag (misalignment of the biological and social time), and investigated the relationship between circadian phenotypes and BDI scores in a population homogeneous in respect to culture, socioeconomic factors, and daily light exposure. 634 (15.65%) of the participants showed mild to severe depressive BDI scores. Late chronotypes had a higher BDI(as) than intermediate and early types, which was independent of whether or not the participants were smokers. Both chronotype and BDI(as) correlated positively with social jetlag. BDI(as) was significantly higher in subjects with more than 2 hours of social jetlag than in the rest of the population. This finding was, again, independent of smoking status. Chronotype was compared with social jetlag distributions between BDI categories (no symptoms, minimal symptoms, and mild to severe symptoms of depression) separately for men and women and for 4 age groups. Specifically in the age group 31 to 40 years, subjects with mild to severe BDI scores were significantly later chronotypes and suffered from higher social jetlag. The authors conclude that misalignment of circadian and social time may be a risk factor for developing depression, especially in 31- to 40-year-olds. The authors suggest that these relationships be further investigated in longitudinal studies to reveal if reduction of social jetlag should be part of prevention strategies.
    Keywords Biologische Rhythmen beim Menschen ; Depression (Emotion) ; Depressive Stimmung ; Human Biological Rhythms ; Individual Differences ; Individuelle Unterschiede ; Schlaf-Wach-Zyklus ; Schlafentzug ; Sleep Deprivation ; Sleep Wake Cycle ; Social Adjustment ; Social Interaction ; Soziale Anpassung ; Soziale Interaktion
    Language English
    Document type Article
    ZDB-ID 998996-1
    ISSN 1525-6073 ; 0742-0528
    ISSN (online) 1525-6073
    ISSN 0742-0528
    DOI 10.3109/07420528.2011.602445
    Database PSYNDEX

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  9. Article: Chronotype and sleep duration

    Allebrandt, Karla V. / Teder-Laving, Maris / Kantermann, Thomas / Peters, Annette / Campbell, Harry / Rudan, Igor / Wilson, James F. / Metspalu, Andres / Roenneberg, Till

    Chronobiology International

    The influence of season of assessment

    2014  Volume 31, Issue 5, Page(s) 731–740

    Abstract: Little is known about human entrainment under natural conditions, partly due to the complexity of human behavior, torn between biological and social time and influenced by zeitgebers (light-dark cycles) that are progressively "polluted'' (and thereby ... ...

    Abstract Little is known about human entrainment under natural conditions, partly due to the complexity of human behavior, torn between biological and social time and influenced by zeitgebers (light-dark cycles) that are progressively "polluted'' (and thereby weakened) by artificial light. In addition, data about seasonal variations in sleep parameters are scarce. We, therefore, investigated seasonal variation in cross-sectional assessments of sleep/wake times of 9765 subjects from four European populations (EGCUT = Estonian Genome Centre, University of Tartu in Estonia; KORA = Cooperative Health Research in the Region of Augsburg in Germany; KORCULA = The Korcula study in Croatia; and ORCADES = The Orkney Complex Disease Study in Scotland). We identified time-of-year dependencies for the distribution of chronotype (phase of entrainment assessed as the mid-sleep time point on free days adjusted for sleep deficit of workdays) in cohorts from Estonia (EGCUT) and Germany (KORA). Our results indicate that season (defined as daylight saving time - DST and standard zonetime periods - SZT) specifications of photoperiod influence the distribution of chronotype (adjusted for age and sex). Second, in the largest investigated sample, from Estonia (EGCUT; N = 5878), we could detect that seasonal variation in weekly average sleep duration was dependent on individual chronotype. Later chronotypes in this cohort showed significant variation in their average sleep duration across the year, especially during DST (1 h advance in social time from the end of March to end of October), while earlier chronotypes did not. Later chronotypes not only slept less during the DST period but the average chronotype of the population assessed during this period was earlier than during the SZT (local time for a respective time zone) period. More in detail, hierarchical multiple regression analyses showed that, beyond season of assessment (DST or SZT), social jetlag (SJl; the discrepancy between the mid sleep on free and work days - which varied with age and sex) contributed to a greater extent to the variation in sleep duration than chronotype (after taking into account factors that are known to influence sleep duration, i.e. age, sex and body mass index). Variation in chronotype was also dependent on age, sex, season of assessment and SJl (which is highly correlated with chronotype - SJl was larger among later chronotypes). In summary, subjective assessments of sleep/wake times are very reliable to assess internal time and sleep duration (e. g. reproducing sleep duration and timing tendencies related to age and sex across the investigated populations), but season of assessment should be regarded as a potential confounder. We identified in this study photoperiod (seasonal adaptation) and SJl as two main factors influencing seasonal variation in chronotype and sleep duration. In conclusion, season of assessment, sex and age have an effect on epidemiological variation in sleep duration, chronotype and SJl, and should be included in studies investigating associations between these phenotypes and health parameters, and on the development of optimal prevention strategies.
    Keywords Biologische Rhythmen beim Menschen ; Human Biological Rhythms ; Jahreszeitliche Schwankungen ; Schlaf ; Schlaf-Wach-Zyklus ; Seasonal Variations ; Sleep ; Sleep Wake Cycle
    Language English
    Document type Article
    ZDB-ID 998996-1
    ISSN 1525-6073 ; 0742-0528
    ISSN (online) 1525-6073
    ISSN 0742-0528
    DOI 10.3109/07420528.2014.901347
    Database PSYNDEX

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  10. Article ; Online: Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

    Samuel E. Jones / Jacqueline M. Lane / Andrew R. Wood / Vincent T. van Hees / Jessica Tyrrell / Robin N. Beaumont / Aaron R. Jeffries / Hassan S. Dashti / Melvyn Hillsdon / Katherine S. Ruth / Marcus A. Tuke / Hanieh Yaghootkar / Seth A. Sharp / Yingjie Jie / William D. Thompson / Jamie W. Harrison / Amy Dawes / Enda M. Byrne / Henning Tiemeier /
    Karla V. Allebrandt / Jack Bowden / David W. Ray / Rachel M. Freathy / Anna Murray / Diego R. Mazzotti / Philip R. Gehrman / Debbie A. Lawlor / Timothy M. Frayling / Martin K. Rutter / David A. Hinds / Richa Saxena / Michael N. Weedon

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 11

    Abstract: GWAS have previously found 24 genomic loci associated with chronotype, an individual’s preference for early or late sleep timing. Here, the authors identify 327 additional loci in a sample of 697,828 individuals and further explore the relationships of ... ...

    Abstract GWAS have previously found 24 genomic loci associated with chronotype, an individual’s preference for early or late sleep timing. Here, the authors identify 327 additional loci in a sample of 697,828 individuals and further explore the relationships of chronotype with metabolic and psychiatric diseases.
    Keywords Science ; Q
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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