Prof. Dr. Christian Cajochen
Head Centre for Chronobiology, Biologist
Prof. Christian Cajochen is heading the Centre for Chronobiology at the University of Basel. He received his PhD in natural sciences from the ETH in Zürich, Switzerland, followed by a 3-y postdoctoral stay at the Harvard Medical School in Boston, USA. His major research interests include investigative work on the influence of light on human cognition, circadian rhythms and sleep, circadian related disturbances in psychiatric disorders, and age-related changes in the circadian regulation of sleep and neurobehavioral performance. He has held a number of honours and has authored more than 200 original papers and reviews in his career.
Publications
2022 |
Benedetti, M; Maierová, L; Cajochen, C; Scartezzini, J -L; Münch, M Optimized office lighting advances melatonin phase and peripheral heat loss prior bedtime Journal Article Scientific Reports, 12 , pp. 4267, 2022. @article{Benedetti2022, title = {Optimized office lighting advances melatonin phase and peripheral heat loss prior bedtime}, author = {M. Benedetti and L. Maierová and C. Cajochen and J.-L. Scartezzini and M. Münch}, url = {https://www.nature.com/articles/s41598-022-07522-8}, doi = {https://doi.org/10.1038/s41598-022-07522-8}, year = {2022}, date = {2022-03-11}, journal = {Scientific Reports}, volume = {12}, pages = {4267}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Gimenez, M; Stefani, O; Cajochen, C; Lang, D; Deuring, G; Schlangen, L J M Journal of Pineal Research, 2022. @article{Gimenez2022, title = {Predicting melatonin suppression by light in humans: unifying photoreceptor-based equivalent daylight illuminances, spectral composition, timing and duration of light exposure}, author = {M. Gimenez and O. Stefani and C. Cajochen and D. Lang and G. Deuring and L.J.M. Schlangen}, doi = { https://doi.org/10.1111/jpi.12786}, year = {2022}, date = {2022-01-03}, journal = {Journal of Pineal Research}, abstract = {Light-induced melatonin suppression data from 29 peer-reviewed publications was analysed by means of a machine learning approach to establish which light exposure characteristics (i.e. photopic illuminance, five α-opic equivalent daylight illuminances (EDIs), duration and timing of the light exposure, and the dichotomous variables pharmacological pupil dilation and narrowband light source) are the main determinants of melatonin suppression. Melatonin suppression in the dataset was dominated by four light exposure characteristics: 1. melanopic EDI, 2. light exposure duration, 3. pupil dilation and 4. S-cone-opic EDI. A logistic model was used to evaluate the influence of each of these parameters on the melatonin suppression response. The final logistic model was only based on the first three parameters, since melanopic EDI was the best single (photoreceptor) predictor that was only outperformed by S-cone-opic EDI for (photopic) illuminances below 21 lux. This confirms and extends findings on the importance of the metric melanopic EDI for predicting biological effects of light in integrative (human centric) lighting applications. The model provides initial and general guidance to lighting practitioners on how to combine spectrum, duration and amount of light exposure when controlling non-visual responses to light, especially melatonin suppression. The model is a starting tool for developing hypotheses on photoreceptors’ contributions to light’s non-visual responses and helps identifying areas where more data is needed, like on the S-cone contribution at low illuminances.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Light-induced melatonin suppression data from 29 peer-reviewed publications was analysed by means of a machine learning approach to establish which light exposure characteristics (i.e. photopic illuminance, five α-opic equivalent daylight illuminances (EDIs), duration and timing of the light exposure, and the dichotomous variables pharmacological pupil dilation and narrowband light source) are the main determinants of melatonin suppression. Melatonin suppression in the dataset was dominated by four light exposure characteristics: 1. melanopic EDI, 2. light exposure duration, 3. pupil dilation and 4. S-cone-opic EDI. A logistic model was used to evaluate the influence of each of these parameters on the melatonin suppression response. The final logistic model was only based on the first three parameters, since melanopic EDI was the best single (photoreceptor) predictor that was only outperformed by S-cone-opic EDI for (photopic) illuminances below 21 lux. This confirms and extends findings on the importance of the metric melanopic EDI for predicting biological effects of light in integrative (human centric) lighting applications. The model provides initial and general guidance to lighting practitioners on how to combine spectrum, duration and amount of light exposure when controlling non-visual responses to light, especially melatonin suppression. The model is a starting tool for developing hypotheses on photoreceptors’ contributions to light’s non-visual responses and helps identifying areas where more data is needed, like on the S-cone contribution at low illuminances. |
2021 |
Spitschan, M; Garbazza, C; Kohl, S; Cajochen, C Sleep and circadian phenotype in people without cone-mediated vision: a case series of five CNGB3 and two CNGA3 patients Journal Article Brain Communications, 2021. @article{Spitschan2021, title = {Sleep and circadian phenotype in people without cone-mediated vision: a case series of five CNGB3 and two CNGA3 patients}, author = {M. Spitschan and C. Garbazza and S. Kohl and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2021/09/fcab159.pdf}, doi = {10.1093/braincomms/fcab159}, year = {2021}, date = {2021-07-18}, journal = {Brain Communications}, abstract = {Light exposure entrains the circadian clock through the intrinsically photosensitive retinal ganglion cells, which sense light in addition to the cone and rod photoreceptors. In congenital achromatopsia (prevalence 1:30–50 000), the cone system is non-functional, resulting in severe light avoidance and photophobia at daytime light levels. How this condition affects circadian and neuroendocrine responses to light is not known. In this case series of genetically confirmed congenital achromatopsia patients (n = 7; age 30–72 years; 6 women, 1 male), we examined survey-assessed sleep/circadian phenotype, self-reported visual function, sensitivity to light and use of spectral filters that modify chronic light exposure. In all but one patient, we measured rest-activity cycles using actigraphy over 3 weeks and measured the melatonin phase angle of entrainment using the dim-light melatonin onset. Owing to their light sensitivity, congenital achromatopsia patients used filters to reduce retinal illumination. Thus, congenital achromatopsia patients experienced severely attenuated light exposure. In aggregate, we found a tendency to a late chronotype. We found regular rest-activity patterns in all patients and normal phase angles of entrainment in participants with a measurable dim-light melatonin onset. Our results reveal that a functional cone system and exposure to daytime light intensities are not necessary for regular behavioural and hormonal entrainment, even when survey-assessed sleep and circadian phenotype indicated a tendency for a late chronotype and sleep problems in our congenital achromatopsia cohort.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Light exposure entrains the circadian clock through the intrinsically photosensitive retinal ganglion cells, which sense light in addition to the cone and rod photoreceptors. In congenital achromatopsia (prevalence 1:30–50 000), the cone system is non-functional, resulting in severe light avoidance and photophobia at daytime light levels. How this condition affects circadian and neuroendocrine responses to light is not known. In this case series of genetically confirmed congenital achromatopsia patients (n = 7; age 30–72 years; 6 women, 1 male), we examined survey-assessed sleep/circadian phenotype, self-reported visual function, sensitivity to light and use of spectral filters that modify chronic light exposure. In all but one patient, we measured rest-activity cycles using actigraphy over 3 weeks and measured the melatonin phase angle of entrainment using the dim-light melatonin onset. Owing to their light sensitivity, congenital achromatopsia patients used filters to reduce retinal illumination. Thus, congenital achromatopsia patients experienced severely attenuated light exposure. In aggregate, we found a tendency to a late chronotype. We found regular rest-activity patterns in all patients and normal phase angles of entrainment in participants with a measurable dim-light melatonin onset. Our results reveal that a functional cone system and exposure to daytime light intensities are not necessary for regular behavioural and hormonal entrainment, even when survey-assessed sleep and circadian phenotype indicated a tendency for a late chronotype and sleep problems in our congenital achromatopsia cohort. |
Weibel, J; Lin, Y -S; Landolt, H -P; Berthomier, C; Brandenwinder, M; Kistler, J; Rehm, S; Rentsch, K; Meyer, M; Borgwardt, S; Cajochen, C; Reichert, C F Regular caffeine intake delays REM sleep promotion and attenuates sleep quality in healthy men Journal Article Journal of Biological Rhythms, 2021. @article{Weibel2021b, title = {Regular caffeine intake delays REM sleep promotion and attenuates sleep quality in healthy men}, author = {J. Weibel and Y.-S. Lin and H.-P. Landolt and C. Berthomier and M. Brandenwinder and J. Kistler and S. Rehm and K. Rentsch and M. Meyer and S. Borgwardt and C. Cajochen and C. F. Reichert }, url = {https://journals.sagepub.com/doi/pdf/10.1177/07487304211013995}, doi = {10.1177/07487304211013995}, year = {2021}, date = {2021-05-23}, journal = {Journal of Biological Rhythms}, abstract = {Acute caffeine intake can attenuate homeostatic sleep pressure and worsen sleep quality. Caffeine intake—particularly in high doses and close to bedtime—may also affect circadian-regulated rapid eye movement (REM) sleep promotion, an important determinant of subjective sleep quality. However, it is not known whether such changes persist under chronic caffeine consumption during daytime. Twenty male caffeine consumers (26.4 ± 4 years old, habitual caffeine intake 478.1 ± 102.8 mg/day) participated in a double-blind crossover study. Each volunteer completed a caffeine (3 × 150 mg caffeine daily for 10 days), a withdrawal (3 × 150 mg caffeine for 8 days then placebo), and a placebo condition. After 10 days of controlled intake and a fixed sleep-wake cycle, we recorded electroencephalography for 8 h starting 5 h after habitual bedtime (i.e., start on average at 04:22 h which is around the peak of circadian REM sleep promotion). A 60-min evening nap preceded each sleep episode and reduced high sleep pres-sure levels. While total sleep time and sleep architecture did not significantly differ between the three conditions, REM sleep latency was longer after daily caffeine intake compared with both placebo and withdrawal. Moreover, the accumulation of REM sleep proportion was delayed, and volunteers reported more difficulties with awakening after sleep and feeling more tired upon wake-up in the caffeine condition compared with placebo. Our data indicate that besides acute intake, also regular daytime caffeine intake affects REM sleep regulation in men, such that it delays circadian REM sleep promotion when compared with placebo. Moreover, the observed caffeine-induced deterioration in the quality of awakening may suggest a potential motive to reinstate caffeine intake after sleep.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Acute caffeine intake can attenuate homeostatic sleep pressure and worsen sleep quality. Caffeine intake—particularly in high doses and close to bedtime—may also affect circadian-regulated rapid eye movement (REM) sleep promotion, an important determinant of subjective sleep quality. However, it is not known whether such changes persist under chronic caffeine consumption during daytime. Twenty male caffeine consumers (26.4 ± 4 years old, habitual caffeine intake 478.1 ± 102.8 mg/day) participated in a double-blind crossover study. Each volunteer completed a caffeine (3 × 150 mg caffeine daily for 10 days), a withdrawal (3 × 150 mg caffeine for 8 days then placebo), and a placebo condition. After 10 days of controlled intake and a fixed sleep-wake cycle, we recorded electroencephalography for 8 h starting 5 h after habitual bedtime (i.e., start on average at 04:22 h which is around the peak of circadian REM sleep promotion). A 60-min evening nap preceded each sleep episode and reduced high sleep pres-sure levels. While total sleep time and sleep architecture did not significantly differ between the three conditions, REM sleep latency was longer after daily caffeine intake compared with both placebo and withdrawal. Moreover, the accumulation of REM sleep proportion was delayed, and volunteers reported more difficulties with awakening after sleep and feeling more tired upon wake-up in the caffeine condition compared with placebo. Our data indicate that besides acute intake, also regular daytime caffeine intake affects REM sleep regulation in men, such that it delays circadian REM sleep promotion when compared with placebo. Moreover, the observed caffeine-induced deterioration in the quality of awakening may suggest a potential motive to reinstate caffeine intake after sleep. |
Stefani, O; Cajochen, C Should We Re-think Regulations and Standards for Lighting at Workplaces? A Practice Review on Existing Lighting Recommendations Journal Article Frontiers in psychiatry, 12 , 2021. @article{Stefani2021, title = {Should We Re-think Regulations and Standards for Lighting at Workplaces? A Practice Review on Existing Lighting Recommendations}, author = {O. Stefani and C. Cajochen }, editor = {S. Rahman }, url = {http://www.chronobiology.ch/wp-content/uploads/2021/09/fpsyt-12-652161.pdf}, doi = {10.3389/fpsyt.2021.652161}, year = {2021}, date = {2021-05-13}, journal = {Frontiers in psychiatry}, volume = {12}, abstract = {Nowadays lighting projects often include temporal variations of the light, both spectrally and in terms of intensity to consider non-visual effects of light on people. However, as of today there are no specific regulations. Compliance with common lighting standards that address visual aspects of light, often means that only little non-visually effective light reaches the eye. In this practice review we confront existing regulations and standards on visual lighting aspects with new recommendations on non-visual aspects and highlight conflicts among them. We conclude with lighting recommendations that address both aspects}, keywords = {}, pubstate = {published}, tppubtype = {article} } Nowadays lighting projects often include temporal variations of the light, both spectrally and in terms of intensity to consider non-visual effects of light on people. However, as of today there are no specific regulations. Compliance with common lighting standards that address visual aspects of light, often means that only little non-visually effective light reaches the eye. In this practice review we confront existing regulations and standards on visual lighting aspects with new recommendations on non-visual aspects and highlight conflicts among them. We conclude with lighting recommendations that address both aspects |
Blume, C; Cajochen, C ‘SleepCycles’ package for R - A free software tool for the detection of sleep cycles from sleep staging Journal Article MethodsX, 2021. @article{Blume2021, title = {‘SleepCycles’ package for R - A free software tool for the detection of sleep cycles from sleep staging}, author = {C. Blume and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2021/09/main.pdf}, doi = {https://doi.org/10.1016/j.mex.2021.101318}, year = {2021}, date = {2021-04-06}, journal = {MethodsX}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Lin, Y -S; Weibel, J; Landolt, H; Santini, F; Meyer, M; Brunmair, J; Meyer-Menches, S; gerner, C; Borgwardt, S; Cajochen, C; Reichert, C F Cerebral Cortex, 2021. @article{Lin2021, title = {Daily Caffeine Intake Induces Concentration-Dependent Medial Temporal Plasticity in Humans: A Multimodal Double-Blind Randomized Controlled Trial }, author = { Y.-S. Lin and J. Weibel and H. Landolt and F. Santini and M. Meyer and J. Brunmair and S. Meyer-Menches and C. gerner and S. Borgwardt and C. Cajochen and C. F. Reichert}, url = {http://www.chronobiology.ch/wp-content/uploads/2021/02/Lin_2021_CC_acc_uncorrect.pdf}, doi = {doi.org/10.1093/cercor/bhab005}, year = {2021}, date = {2021-02-15}, journal = {Cerebral Cortex}, abstract = {Caffeine is commonly used to combat high sleep pressure on a daily basis. However, interference with sleep–wake regulation could disturb neural homeostasis and insufficient sleep could lead to alterations in human gray matter. Hence, in this double-blind, randomized, cross-over study, we examined the impact of 10-day caffeine (3 × 150 mg/day) on human gray matter volumes (GMVs) and cerebral blood flow (CBF) by fMRI MP-RAGE and arterial spin-labeling sequences in 20 habitual caffeine consumers, compared with 10-day placebo (3 × 150 mg/day). Sleep pressure was quantified by electroencephalographic slow-wave activity (SWA) in the previous nighttime sleep. Nonparametric voxel-based analyses revealed a significant reduction in GMV in the medial temporal lobe (mTL) after 10 days of caffeine intake compared with 10 days of placebo, voxel-wisely adjusted for CBF considering the decreased perfusion after caffeine intake compared with placebo. Larger GMV reductions were associated with higher individual concentrations of caffeine and paraxanthine. Sleep SWA was, however, neither different between conditions nor associated with caffeine-induced GMV reductions. Therefore, the data do not suggest a link between sleep depth during daily caffeine intake and changes in brain morphology. In conclusion, daily caffeine intake might induce neural plasticity in the mTL depending on individual metabolic processes.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Caffeine is commonly used to combat high sleep pressure on a daily basis. However, interference with sleep–wake regulation could disturb neural homeostasis and insufficient sleep could lead to alterations in human gray matter. Hence, in this double-blind, randomized, cross-over study, we examined the impact of 10-day caffeine (3 × 150 mg/day) on human gray matter volumes (GMVs) and cerebral blood flow (CBF) by fMRI MP-RAGE and arterial spin-labeling sequences in 20 habitual caffeine consumers, compared with 10-day placebo (3 × 150 mg/day). Sleep pressure was quantified by electroencephalographic slow-wave activity (SWA) in the previous nighttime sleep. Nonparametric voxel-based analyses revealed a significant reduction in GMV in the medial temporal lobe (mTL) after 10 days of caffeine intake compared with 10 days of placebo, voxel-wisely adjusted for CBF considering the decreased perfusion after caffeine intake compared with placebo. Larger GMV reductions were associated with higher individual concentrations of caffeine and paraxanthine. Sleep SWA was, however, neither different between conditions nor associated with caffeine-induced GMV reductions. Therefore, the data do not suggest a link between sleep depth during daily caffeine intake and changes in brain morphology. In conclusion, daily caffeine intake might induce neural plasticity in the mTL depending on individual metabolic processes. |
2020 |
Stefani, O; Freyburger, M; Veitz, S; Basishvili, T; Meyer, M; Weibel, J; Kobayashi, K; Shirakawa, Y; Cajochen, C Changing color and intensity of LED lighting across the day impacts on circadian melatonin rhythms and sleep in healthy men Journal Article Journal of Pineal Research, 70 , 2020. @article{Stefani2020, title = {Changing color and intensity of LED lighting across the day impacts on circadian melatonin rhythms and sleep in healthy men}, author = {O. Stefani and M. Freyburger and S. Veitz and T. Basishvili and M. Meyer and J. Weibel and K. Kobayashi and Y. Shirakawa and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2021/09/Changing-color-and-intensity-of-LED-lighting-across-the-day-impacts-on-circadian-melatonin-rhythms-and-sleep-in-healthy-men.pdf}, doi = {10.1111/jpi.12714}, year = {2020}, date = {2020-12-30}, journal = {Journal of Pineal Research}, volume = {70}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Blume, C; Schmidt, Marlene H; Cajochen, C Effects of the COVID-19 lockdown on human sleep and rest-activity rhythms Journal Article Current Biology, 2020. @article{Blume2020b, title = {Effects of the COVID-19 lockdown on human sleep and rest-activity rhythms}, author = {C. Blume and Marlene H. Schmidt and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2021/09/1-s2.0-S096098222030837X-main.pdf}, doi = {https://doi.org/10.1016/j.cub.2020.06.021}, year = {2020}, date = {2020-06-10}, journal = {Current Biology}, abstract = {In modern societies, human rest-activity rhythms and sleep result from the tensions and dynamics between the conflicting poles of external social time (e.g., work hours and leisure activities) and an individual’s internal biological time. A mismatch between the two has been suggested to induce ‘social jetlag’ [SJL; 1] and ‘social sleep restriction’ (SSR), that is, shifts in sleep timing and differences in sleep duration between work days and free days. Social jetlag [2, 3] and sleep restrictions [4] have repeatedly been associated with negative consequences on health, mental wellbeing, and performance. In a large-scale quasi-experimental design, we investigated the effects of the phase with the strictest COVID-19 restrictions on the relationship between social and biological rhythms as well as sleep during a six-week period (mid-March until end of April 2020) in three European societies (Austria, Germany, Switzerland). We found that, on one hand, the restrictions reduced the mismatch between external (social) and internal (biological) sleep-wake timing, as indexed by significant reductions in SJL and SSR, with a concomitant increase in sleep duration. Sleep quality on the other hand was slightly reduced. The improved individual sleep-wake timing can presumably be attributed to an increased flexibility of social schedules, for instance due to more work being accomplished from home. However, this unprecedented situation also led to a significant increase in self-perceived burden, which was attendant to the decrease in sleep quality. These adverse effects may be alleviated by exposure to natural daylight as well as physical exercising.}, keywords = {}, pubstate = {published}, tppubtype = {article} } In modern societies, human rest-activity rhythms and sleep result from the tensions and dynamics between the conflicting poles of external social time (e.g., work hours and leisure activities) and an individual’s internal biological time. A mismatch between the two has been suggested to induce ‘social jetlag’ [SJL; 1] and ‘social sleep restriction’ (SSR), that is, shifts in sleep timing and differences in sleep duration between work days and free days. Social jetlag [2, 3] and sleep restrictions [4] have repeatedly been associated with negative consequences on health, mental wellbeing, and performance. In a large-scale quasi-experimental design, we investigated the effects of the phase with the strictest COVID-19 restrictions on the relationship between social and biological rhythms as well as sleep during a six-week period (mid-March until end of April 2020) in three European societies (Austria, Germany, Switzerland). We found that, on one hand, the restrictions reduced the mismatch between external (social) and internal (biological) sleep-wake timing, as indexed by significant reductions in SJL and SSR, with a concomitant increase in sleep duration. Sleep quality on the other hand was slightly reduced. The improved individual sleep-wake timing can presumably be attributed to an increased flexibility of social schedules, for instance due to more work being accomplished from home. However, this unprecedented situation also led to a significant increase in self-perceived burden, which was attendant to the decrease in sleep quality. These adverse effects may be alleviated by exposure to natural daylight as well as physical exercising. |
Eze, I C; Jeong, A; Schaffner, E; Rezwan, F I; Ghantous, A; Foraster, M; Vienneau, D; F, Kronenberg F; Herceg, Z; Vineis, P; Brink, M; Wunderli, J M; Schindler, C; Cajochen, C; M, Röösli M; Holloway, J W; Imboden, M; Probst-Hensch, N Environ Health Perspect, 128 (6), pp. 67003, 2020. @article{Eze2020, title = {Genome-Wide DNA Methylation in Peripheral Blood and Long-Term Exposure to Source-Specific Transportation Noise and Air Pollution: The SAPALDIA Study}, author = {I. C. Eze and A. Jeong and E. Schaffner and F. I. Rezwan and A. Ghantous and M. Foraster and D. Vienneau and F. Kronenberg F and Z. Herceg and P. Vineis and M. Brink and J. M. Wunderli and C. Schindler and C. Cajochen and M. Röösli M and J. W. Holloway and M. Imboden and N. Probst-Hensch}, url = {http://www.chronobiology.ch/wp-content/uploads/2020/06/EHP6174.pdf}, year = {2020}, date = {2020-06-01}, journal = {Environ Health Perspect}, volume = {128}, number = {6}, pages = {67003}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Hollinger, A; von Felten, S; Sutter, R; Huber, J; Tran, F; Reinhold, S; Abdelhamid, S; Todorov, A; Gebhard, C E; Cajochen, C; Steiner, L A; Siegemund, M BMJ Open, 2020. @article{Hollinger2020, title = {Study Protocol for a Prospective Randomised Double-Blind Placebo-Controlled Clinical Trial Investigating a Better Outcome With Melatonin Compared to Placebo Administered to Normalize Sleep-Wake Cycle and Treat Hypoactive ICU Delirium: The Basel BOMP-AID Study}, author = {A. Hollinger and S. von Felten and R. Sutter and J. Huber and F. Tran and S. Reinhold and S. Abdelhamid and A. Todorov and C. E. Gebhard and C. Cajochen and L. A Steiner and M. Siegemund}, url = {http://www.chronobiology.ch/wp-content/uploads/2020/05/e034873.full_.pdf}, doi = {10.1136/bmjopen-2019-034873}, year = {2020}, date = {2020-04-30}, journal = {BMJ Open}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Weibel, J; Lin, Y -S; Landolt, H -P; Garbazza, C; Kolodyazhniy, V; Kistler, J; Rehm, S; Rentsch, K; Borgwardt, S; Cajochen, C; Reichert, C F Caffeine-dependent changes of sleep-wake regulation: Evidence foradaptation after repeated intake Journal Article Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2020. @article{Weibel2020, title = {Caffeine-dependent changes of sleep-wake regulation: Evidence foradaptation after repeated intake}, author = {J. Weibel and Y.-S. Lin and H.-P. Landolt and C. Garbazza and V. Kolodyazhniy and J. Kistler and S. Rehm and K. Rentsch and S. Borgwardt and C. Cajochen and C. F. Reichert }, url = {http://www.chronobiology.ch/1-s2-0-s0278584619304798-main-2/}, doi = {10.1016/j.pnpbp.2019.109851 }, year = {2020}, date = {2020-04-20}, journal = {Progress in Neuro-Psychopharmacology and Biological Psychiatry}, abstract = {Background: Circadian and sleep-homeostatic mechanisms regulate timing and quality of wakefulness. To enhance wakefulness, daily consumption of caffeine in the morning and afternoon is highly common. However, the effects of such a regular intake pattern on circadian sleep-wake regulation are unknown. Thus, we investigated if daily daytime caffeine intake and caffeine withdrawal affect circadian rhythms and wake-promotion in habitual consumers. Methods: Twenty male young volunteers participated in a randomised, double-blind, within-subject study with three conditions: i) caffeine (150 mg 3 x daily for 10 days), ii) placebo (3 x daily for 10 days) and iii) withdrawal (150 mg caffeine 3 x daily for eight days, followed by a switch to placebo for two days). Starting on day nine of treatment, salivary melatonin and cortisol, evening nap sleep as well as sleepiness and vigilance performance throughout day and night were quantified during 43 h in an in-laboratory, light and posture-controlled protocol. Results: Neither the time course of melatonin (i.e. onset, amplitude or area under the curve) nor the time course of cortisol was significantly affected by caffeine or withdrawal. During withdrawal, however, volunteers reported increased sleepiness, showed more attentional lapses as well as polysomnography-derived markers of elevated sleep propensity in the late evening compared to both the placebo and caffeine condition. Conclusions: The typical pattern of caffeine intake with consumption in both the morning and afternoon hours may not necessarily result in a circadian phase shift in the evening nor lead to clear-cut benefits in alertness. The time-of-day independent effects of caffeine withdrawal on evening nap sleep, sleepiness and performance suggest an adaptation to the substance, presumably in the homeostatic aspect of sleep-wake regulation.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Background: Circadian and sleep-homeostatic mechanisms regulate timing and quality of wakefulness. To enhance wakefulness, daily consumption of caffeine in the morning and afternoon is highly common. However, the effects of such a regular intake pattern on circadian sleep-wake regulation are unknown. Thus, we investigated if daily daytime caffeine intake and caffeine withdrawal affect circadian rhythms and wake-promotion in habitual consumers. Methods: Twenty male young volunteers participated in a randomised, double-blind, within-subject study with three conditions: i) caffeine (150 mg 3 x daily for 10 days), ii) placebo (3 x daily for 10 days) and iii) withdrawal (150 mg caffeine 3 x daily for eight days, followed by a switch to placebo for two days). Starting on day nine of treatment, salivary melatonin and cortisol, evening nap sleep as well as sleepiness and vigilance performance throughout day and night were quantified during 43 h in an in-laboratory, light and posture-controlled protocol. Results: Neither the time course of melatonin (i.e. onset, amplitude or area under the curve) nor the time course of cortisol was significantly affected by caffeine or withdrawal. During withdrawal, however, volunteers reported increased sleepiness, showed more attentional lapses as well as polysomnography-derived markers of elevated sleep propensity in the late evening compared to both the placebo and caffeine condition. Conclusions: The typical pattern of caffeine intake with consumption in both the morning and afternoon hours may not necessarily result in a circadian phase shift in the evening nor lead to clear-cut benefits in alertness. The time-of-day independent effects of caffeine withdrawal on evening nap sleep, sleepiness and performance suggest an adaptation to the substance, presumably in the homeostatic aspect of sleep-wake regulation. |
Chellappa, S L; Bromundt, V; Frey, S; Schlote, T; Goldblum, D; Cajochen, C; Reichert, C F Intraocular cataract lens replacement and light exposure potentially impact procedural learning in older adults Journal Article 2020. @article{Chellappa2020, title = {Intraocular cataract lens replacement and light exposure potentially impact procedural learning in older adults}, author = {S. L. Chellappa and V. Bromundt and S. Frey and T. Schlote and D. Goldblum and C. Cajochen and C. F. Reichert}, url = {http://www.chronobiology.ch/wp-content/uploads/2020/04/Chellappa-et-al.-JSR_2020.pdf}, doi = {10.1111/jsr.13043}, year = {2020}, date = {2020-04-14}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Rudzik, F; Thiesse, L; Pieren, R; Héritier, H; Eze, I C; Foraster, M; Vienneau, D; Brink, M; Wunderli, J M; Probst-Hensch, N; Röösli, M; Fulda, S; Cajochen, C Ultradian Modulation of Cortical Arousals During Sleep: Effects of Age and Exposure to Nighttime Transportation Noise Journal Article Sleep, 2020. @article{Rudzik2020, title = {Ultradian Modulation of Cortical Arousals During Sleep: Effects of Age and Exposure to Nighttime Transportation Noise}, author = {F. Rudzik and L. Thiesse and R. Pieren and H. Héritier and I. C Eze and M. Foraster and D. Vienneau and M. Brink and J. M. Wunderli and N. Probst-Hensch and M. Röösli and S. Fulda and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2020/05/zsz324.pdf}, doi = {10.1093/sleep/zsz324}, year = {2020}, date = {2020-02-26}, journal = {Sleep}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2019 |
Spitschan, M; Lazar, R; Yetik, E; Cajochen, C No evidence for an S cone contribution to acute neuroendocrine and alerting responses to light Journal Article Current Biology, 2019. @article{Spitschan2019d, title = {No evidence for an S cone contribution to acute neuroendocrine and alerting responses to light}, author = {M. Spitschan and R. Lazar and E. Yetik and C. Cajochen }, url = {https://www.cell.com/current-biology/fulltext/S0960-9822(19)31501-5?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0960982219315015%3Fshowall%3Dtrue}, doi = {10.1016/j.cub.2019.11.031}, year = {2019}, date = {2019-12-16}, journal = {Current Biology}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Spitschan, M; Lazar, R; Cajochen, C Visual and non-visual properties of filters manipulating short-wavelength light Journal Article Ophthalmic Physiol Opt, 2019. @article{Spitschan2019f, title = {Visual and non-visual properties of filters manipulating short-wavelength light}, author = {M. Spitschan and R. Lazar and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2020/01/Spitschan_et_al-2019-Ophthalmic_and_Physiological_Optics-1.pdf}, doi = {10.1111/opo.12648}, year = {2019}, date = {2019-11-01}, journal = {Ophthalmic Physiol Opt}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2017 |
Gabel, V; Reichert, C F; Maire, M; Schmidt, C; Schlangen, L J M; Kolodyazhniy, V; Garbazza, C; Cajochen, C; Viola, A U Scientific Reports, 7 (7620), pp. doi:doi:10.1038/s41598-017-07060-8, 2017. @article{, title = {Differential impact in young and older individuals of blue-enriched white light on circadian physiology and alertness during sustained wakefulness}, author = {V. Gabel and C. F. Reichert and M. Maire and C. Schmidt and L. J. M. Schlangen and V. Kolodyazhniy and C. Garbazza and C. Cajochen and A. U. Viola}, url = {https://www.nature.com/articles/s41598-017-07060-8.pdf}, year = {2017}, date = {2017-08-08}, journal = {Scientific Reports}, volume = {7}, number = {7620}, pages = {doi:doi:10.1038/s41598-017-07060-8}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Reichert, C F; Maire, M; Gabel, V; Viola, A U; Götz, T; Scheffler, K; Klarhöfer, M; Berthomier, C; Strobel, W; Phillips, C; Salmon, E; Cajochen, C; Schmidt, C Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations Journal Article Scientific Reports, 7 , pp. doi:10.1038/s41598-017-05695-1, 2017. @article{644, title = {Cognitive brain responses during circadian wake-promotion: evidence for sleep-pressure-dependent hypothalamic activations}, author = {C. F. Reichert and M. Maire and V. Gabel and A. U. Viola and T. Götz and K. Scheffler and M. Klarhöfer and C. Berthomier and W. Strobel and C. Phillips and E. Salmon and C. Cajochen and C. Schmidt}, url = {http://www.chronobiology.ch/wp-content/uploads/2019/03/Reichert_et_al-2017-Scientific_Reports_Cognitive-brain-responses.pdf}, year = {2017}, date = {2017-07-17}, journal = {Scientific Reports}, volume = {7}, pages = {doi:10.1038/s41598-017-05695-1}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2016 |
Reichert, C F; Maire, M; Schmidt, C; Cajochen, C Sleep-wake regulation and its impact on working memory performance: the role of adenosine Journal Article Biology, 5 (1), pp. E11. doi:10.3390/biology5010011., 2016. @article{, title = {Sleep-wake regulation and its impact on working memory performance: the role of adenosine}, author = {C. F. Reichert and M. Maire and C. Schmidt and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2016/06/Reichert_2016.pdf}, year = {2016}, date = {2016-06-27}, journal = {Biology}, volume = {5}, number = {1}, pages = {E11. doi:10.3390/biology5010011.}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Garbazza, C; Bromundt, V; Eckert, A; Brunner, D P; Meier, F; Hackethal, S; Cajochen, C Non-24-Hour Sleep-Wake Disorder Revisited - A Case Study Journal Article Front Neurol. 2016 Feb 29;7:17 doi: 10.3389/fneur.2016.00017, 2016. @article{, title = {Non-24-Hour Sleep-Wake Disorder Revisited - A Case Study}, author = {C. Garbazza and V. Bromundt and A. Eckert and D.P. Brunner and F. Meier and S. Hackethal and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2016/06/fneur-07-00017-3.pdf}, year = {2016}, date = {2016-02-29}, journal = {Front Neurol. 2016 Feb 29;7:17 doi: 10.3389/fneur.2016.00017}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2015 |
Schmidt, C; Collette, F; Reichert, C F; Maire, M; Vandewalle, G; Peigneux, P; Cajochen, C Pushing the limits: chronotype and time of day modulate working memory-dependent cerebral activity Journal Article Frontiers in Neurology, 25 (6:199), pp. 1-9, 2015. @article{, title = {Pushing the limits: chronotype and time of day modulate working memory-dependent cerebral activity}, author = {C. Schmidt and F. Collette and C. F. Reichert and M. Maire and G. Vandewalle and P. Peigneux and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2015/10/Schmidt_etal_fneur-06-00199_15.pdf}, year = {2015}, date = {2015-10-07}, journal = {Frontiers in Neurology}, volume = {25}, number = {6:199}, pages = {1-9}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Gabel, V; Maire, M; Reichert, C F; Chellappa, S L; Schmidt, C; Hommes, V; Cajochen, C; Viola, A U Dawn simulation light impacts on different cognitive domains under sleep restriction Journal Article Behav Brain Res., doi: 10.1016/j.bbr.2014.12.043, 15 , pp. 281: 258-266, 2015. @article{, title = {Dawn simulation light impacts on different cognitive domains under sleep restriction}, author = {V. Gabel and M. Maire and C. F. Reichert and S. L. Chellappa and C. Schmidt and V. Hommes and C. Cajochen and A. U. Viola}, url = {http://www.chronobiology.ch/wp-content/uploads/2015/08/7.pdf}, year = {2015}, date = {2015-08-20}, journal = {Behav Brain Res., doi: 10.1016/j.bbr.2014.12.043}, volume = {15}, pages = {281: 258-266}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Maire, M; Reichert, C F; Gabel, V; Viola, A U; Phillips, C; Krebs, J; Scheffler, K; Klarhöfer, M; Strobel, W; Cajochen, C; Schmidt, C Fighting Sleep at Night: Brain Correlates and Vulnerability to Sleep Loss Journal Article Ann Neurol., doi: 10.1002/ana.24434., 78(2) , pp. 235-247, 2015. @article{, title = {Fighting Sleep at Night: Brain Correlates and Vulnerability to Sleep Loss}, author = {M. Maire and C. F. Reichert and V. Gabel and A. U. Viola and C. Phillips and J. Krebs and K. Scheffler and M. Klarhöfer and W. Strobel and C. Cajochen and C. Schmidt }, url = {http://www.chronobiology.ch/wp-content/uploads/2015/08/4.pdf}, year = {2015}, date = {2015-08-20}, journal = {Ann Neurol., doi: 10.1002/ana.24434.}, volume = {78(2)}, pages = {235-247}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
vanderLely, S; Frey, S; Garbazza, C; Wirz-Justice, A; Jenni, O G; Steiner, R; Wolf, S; Cajochen, C; Bromundt, V; Schmidt, C Blue blocker glasses as a countermeasure for alerting effects of evening light-emitting diode screen exposure in male teenagers Journal Article J Adolesc Health, doi: 10.1016/j.jadohealth.2014.08.002, 56(1) , pp. 113-119, 2015. @article{, title = {Blue blocker glasses as a countermeasure for alerting effects of evening light-emitting diode screen exposure in male teenagers}, author = {S. vanderLely and S. Frey and C. Garbazza and A. Wirz-Justice and O. G. Jenni and R. Steiner and S. Wolf and C. Cajochen and V. Bromundt and C. Schmidt}, url = {http://www.chronobiology.ch/wp-content/uploads/2015/08/11.pdf}, year = {2015}, date = {2015-08-20}, journal = {J Adolesc Health, doi: 10.1016/j.jadohealth.2014.08.002}, volume = {56(1)}, pages = {113-119}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2014 |
Reichert, C F; Maire, M; Gabel, V; Hofstetter, M; Viola, A U; Kolodyazhniy, V; Strobel, W; Goetz, T; V. Bachmann, ; Landolt, H -P; Cajochen, C; Schmidt, C The Circadian Regulation of Sleep: Impact of a Functional ADA-Polymorphism and Ist Association to Working Memory Journal Article PLoS ONE, 9 (12), pp. 1-23, 2014. @article{, title = {The Circadian Regulation of Sleep: Impact of a Functional ADA-Polymorphism and Ist Association to Working Memory}, author = {C. F. Reichert and M. Maire and V. Gabel and M. Hofstetter and A.U. Viola and V. Kolodyazhniy and W. Strobel and T. Goetz and V. Bachmann and H.-P. Landolt and C. Cajochen and C. Schmidt }, url = {http://www.chronobiology.ch/wp-content/uploads/2014/12/Reichert-2014-napsleep-nback.pdf}, year = {2014}, date = {2014-12-01}, journal = {PLoS ONE}, volume = {9}, number = {12}, pages = {1-23}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Chellappa, S L; Viola, A U; Schmidt, C; Bachmann, V; Gabel, V; Maire, M; Reichert, C F; Valomon, A; Landolt, H P; Cajochen, C Light modulation of human sleep depends on a polymorphism in the clock gene Period3 Journal Article Behavioural Brain Research, 271 , pp. 23-29, 2014. @article{, title = {Light modulation of human sleep depends on a polymorphism in the clock gene Period3}, author = {S.L. Chellappa and A.U. Viola and C. Schmidt and V. Bachmann and V. Gabel and M. Maire and C. F. Reichert and A. Valomon and H.P. Landolt and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/2014/06/BBR_Chellappa_141.pdf}, year = {2014}, date = {2014-06-06}, journal = {Behavioural Brain Research}, volume = {271}, pages = {23-29}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
Reichert, C F; Maire, M; Gabel, V; Viola, A U; Kolodyazhniy, V; Strobel, W; Götz, T; Bachmann, V; Landolt, H P; Cajochen, C; Schmidt, C Insights into Behavioral Vulnerability to Differential Sleep Pressure and Circadian Phase from a Functional ADA Polymorphism Journal Article Journal of Biological Rhythms, 29 (2), pp. 119-130, 2014. @article{, title = {Insights into Behavioral Vulnerability to Differential Sleep Pressure and Circadian Phase from a Functional ADA Polymorphism}, author = {C. F. Reichert and M. Maire and V. Gabel and A.U. Viola and V. Kolodyazhniy and W. Strobel and T. Götz and V. Bachmann and H.P. Landolt and C. Cajochen and C. Schmidt}, url = {http://www.chronobiology.ch/wp-content/uploads/2014/04/Reichert-2014-behavioral-vulnerability1.pdf}, year = {2014}, date = {2014-04-02}, journal = {Journal of Biological Rhythms}, volume = {29}, number = {2}, pages = {119-130}, abstract = {Sleep loss affects human behavior in a nonuniform manner, depending on the cognitive domain and also the circadian phase. Besides, evidence exists about stable interindividual variations in sleep loss–related performance impairments. Despite this evidence, only a few studies have considered both circadian phase and neurobehavioral domain when investigating trait-like vulnerability to sleep manipulation. By applying a randomized, crossover design with 2 sleep pressure conditions (40 h sleep deprivation vs. 40 h multiple naps), we investigated the influence of a human adenosine deaminase (ADA) polymorphism (rs73598374) on several behavioral measures throughout nearly 2 circadian cycles. Confirming earlier studies, we observed that under sleep deprivation the previously reported vulnerable G/A-allele carriers felt overall sleepier than G/G-allele carriers. As expected, this difference was no longer present when sleep pressure was reduced by the application of multiple naps. Concomitantly, well-being was worse in the G/A genotype under sleep loss when compared to the nap protocol, and n-back working memory performance appeared to be specifically susceptible to sleep-wake manipulation in this genotype. When considering psychomotor vigilance performance, however, a higher sensitivity to sleep-wake manipulation was detected in homozygous participants, but specifically at the end of the night and only for optimal task performance. Although these data are based on a small sample size and hence require replication (12 G/A- and 12 G/G-allele carriers), they confirm the assumption that interindividual differences regarding the effect of sleep manipulation highly depend on the cognitive task and circadian phase, and thus emphasize the necessity of a multimethodological approach. Moreover, they indicate that napping might be suitable to counteract endogenously heightened sleep pressure depending on the neurobehavioral domain.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Sleep loss affects human behavior in a nonuniform manner, depending on the cognitive domain and also the circadian phase. Besides, evidence exists about stable interindividual variations in sleep loss–related performance impairments. Despite this evidence, only a few studies have considered both circadian phase and neurobehavioral domain when investigating trait-like vulnerability to sleep manipulation. By applying a randomized, crossover design with 2 sleep pressure conditions (40 h sleep deprivation vs. 40 h multiple naps), we investigated the influence of a human adenosine deaminase (ADA) polymorphism (rs73598374) on several behavioral measures throughout nearly 2 circadian cycles. Confirming earlier studies, we observed that under sleep deprivation the previously reported vulnerable G/A-allele carriers felt overall sleepier than G/G-allele carriers. As expected, this difference was no longer present when sleep pressure was reduced by the application of multiple naps. Concomitantly, well-being was worse in the G/A genotype under sleep loss when compared to the nap protocol, and n-back working memory performance appeared to be specifically susceptible to sleep-wake manipulation in this genotype. When considering psychomotor vigilance performance, however, a higher sensitivity to sleep-wake manipulation was detected in homozygous participants, but specifically at the end of the night and only for optimal task performance. Although these data are based on a small sample size and hence require replication (12 G/A- and 12 G/G-allele carriers), they confirm the assumption that interindividual differences regarding the effect of sleep manipulation highly depend on the cognitive task and circadian phase, and thus emphasize the necessity of a multimethodological approach. Moreover, they indicate that napping might be suitable to counteract endogenously heightened sleep pressure depending on the neurobehavioral domain. |
Maire, M; Reichert, C F; Gabel, V; Viola, A U; Krebs, J; Strobel, W; Landolt, H P; Bachmann, V; Cajochen, C; Schmidt, C Time-on-task decrement in vigilance is modulated by inter-individual vulnerability to homeostatic sleep pressure manipulation Journal Article Frontiers in Behavioral Neuroscience, 8 (59), 2014, ISSN: 1662-5153. @article{, title = {Time-on-task decrement in vigilance is modulated by inter-individual vulnerability to homeostatic sleep pressure manipulation}, author = {M. Maire and C. F. Reichert and V. Gabel and A.U. Viola and J. Krebs and W. Strobel and H.P. Landolt and V. Bachmann and C. Cajochen and C. Schmidt}, url = {http://www.chronobiology.ch/wp-content/uploads/2014/03/Timeontask_MAIREetal2014.pdf}, issn = {1662-5153}, year = {2014}, date = {2014-03-06}, journal = {Frontiers in Behavioral Neuroscience}, volume = {8}, number = {59}, abstract = {Under sleep loss, vigilance is reduced and attentional failures emerge progressively. It becomes difficult to maintain stable performance over time, leading to growing performance variability (i.e., state instability) in an individual and among subjects. Task duration plays a major role in the maintenance of stable vigilance levels, such that the longer the task, the more likely state instability will be observed. Vulnerability to sleep-loss-dependent performance decrements is highly individual and is also modulated by a polymorphism in the human clock gene PERIOD3 (PER3). By combining two different protocols, we manipulated sleep-wake history by once extending wakefulness for 40 h (high sleep pressure condition) and once by imposing a short sleep-wake cycle by alternating 160 min of wakefulness and 80 min naps (low sleep pressure condition) in a within-subject design. We observed that homozygous carriers of the long repeat allele of PER3 (PER35/5) experienced a greater time-on-task dependent performance decrement (i.e., a steeper increase in the number of lapses) in the Psychomotor Vigilance Task compared to the carriers of the short repeat allele (PER34/4). These genotype-dependent effects disappeared under low sleep pressure conditions, and neither motivation, nor perceived effort accounted for these differences. Our data thus suggest that greater sleep-loss related attentional vulnerability based on the PER3 polymorphism is mirrored by a greater state instability under extended wakefulness in the short compared to the long allele carriers. Our results undermine the importance of time-on-task related aspects when investigating inter-individual differences in sleep loss-induced behavioral vulnerability.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Under sleep loss, vigilance is reduced and attentional failures emerge progressively. It becomes difficult to maintain stable performance over time, leading to growing performance variability (i.e., state instability) in an individual and among subjects. Task duration plays a major role in the maintenance of stable vigilance levels, such that the longer the task, the more likely state instability will be observed. Vulnerability to sleep-loss-dependent performance decrements is highly individual and is also modulated by a polymorphism in the human clock gene PERIOD3 (PER3). By combining two different protocols, we manipulated sleep-wake history by once extending wakefulness for 40 h (high sleep pressure condition) and once by imposing a short sleep-wake cycle by alternating 160 min of wakefulness and 80 min naps (low sleep pressure condition) in a within-subject design. We observed that homozygous carriers of the long repeat allele of PER3 (PER35/5) experienced a greater time-on-task dependent performance decrement (i.e., a steeper increase in the number of lapses) in the Psychomotor Vigilance Task compared to the carriers of the short repeat allele (PER34/4). These genotype-dependent effects disappeared under low sleep pressure conditions, and neither motivation, nor perceived effort accounted for these differences. Our data thus suggest that greater sleep-loss related attentional vulnerability based on the PER3 polymorphism is mirrored by a greater state instability under extended wakefulness in the short compared to the long allele carriers. Our results undermine the importance of time-on-task related aspects when investigating inter-individual differences in sleep loss-induced behavioral vulnerability. |
Maire, M; Reichert, C F; Gabel, V; Viola, A U; Strobel, W; Krebs, J; Landolt, H P; Bachmann, V; Cajochen, C; Schmidt, C Sleep ability mediates individual differences in the vulnerability to sleep loss: Evidence from a PER3 polymorphism Journal Article Cortex, http://dx.doi.org/10.1016/j.cortex.2013. , 2014. @article{, title = {Sleep ability mediates individual differences in the vulnerability to sleep loss: Evidence from a PER3 polymorphism}, author = {M. Maire and C. F. Reichert and V. Gabel and A.U. Viola and W. Strobel and J. Krebs and H.P. Landolt and V. Bachmann and C. Cajochen and C. Schmidt}, url = {http://www.chronobiology.ch/wp-content/uploads/2014/01/Maire_Cortex_2013.pdf}, year = {2014}, date = {2014-01-21}, journal = {Cortex}, volume = {http://dx.doi.org/10.1016/j.cortex.2013.}, keywords = {}, pubstate = {published}, tppubtype = {article} } |
2013 |
Gabel, V; Maire, M; Reichert, C F; Chellappa, S L; Schmidt, C; Hommes, V; Viola, A U; Cajochen, C Effects of Artificial Dawn and Morning Blue Light on Daytime Cognitive Performance, Well-being, Cortisol and Melatonin Levels Journal Article Chronobiology International, 30 , pp. 988-97, 2013. @article{180, title = {Effects of Artificial Dawn and Morning Blue Light on Daytime Cognitive Performance, Well-being, Cortisol and Melatonin Levels}, author = {V. Gabel and M. Maire and C. F. Reichert and S.L. Chellappa and C. Schmidt and V. Hommes and A.U. Viola and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/publications/Gabel_2013.pdf}, year = {2013}, date = {2013-07-10}, journal = {Chronobiology International}, volume = {30}, pages = {988-97}, abstract = {Light exposure elicits numerous effects on human physiology and behavior, such as better cognitive performance and mood. Here we investigated the role of morning light exposure as a countermeasure for impaired cognitive performance and mood under sleep restriction (SR). Seventeen participants took part of a 48h laboratory protocol, during which three different light settings (separated by 2 wks) were administered each morning after two 6-h sleep restriction nights: a blue monochromatic LED (light-emitting diode) light condition (BL; 100 lux at 470 nm for 20 min) starting 2 h after scheduled wake-up time, a dawn-simulating light (DsL) starting 30 min before and ending 20 min after scheduled wake-up time (polychromatic light gradually increasing from 0 to 250 lux), and a dim light (DL) condition for 2 h beginning upon scheduled wake time (58 lux). Cognitive tasks were performed every 2 h during scheduled wakefulness, and questionnaires were administered hourly to assess subjective sleepiness, mood, and wellbeing. Salivary melatonin and cortisol were collected throughout scheduled wakefulness in regular intervals, and the effects on melatonin were measured after only one light pulse. Following the first SR, analysis of the time course of cognitive performance during scheduled wakefulness indicated a decrease following DL, whereas it remained stable following BL and significantly improved after DsL. Cognitive performance levels during the second day after SR were not significantly affected by the different light conditions. However, after both SR nights, mood and well-being were significantly enhanced after exposure to morning DsL compared with DL and BL. Melatonin onset occurred earlier after morning BL exposure, than after morning DsL and DL, whereas salivary cortisol levels were higher at wake-up time after DsL compared with BL and DL. Our data indicate that exposure to an artificial morning dawn simulation light improves subjective well-being, mood, and cognitive performance, as compared with DL and BL, with minimal impact on circadian phase. Thus, DsL may provide an effective strategy for enhancing cognitive performance, wellbeing, and mood under mild sleep restriction.}, keywords = {}, pubstate = {published}, tppubtype = {article} } Light exposure elicits numerous effects on human physiology and behavior, such as better cognitive performance and mood. Here we investigated the role of morning light exposure as a countermeasure for impaired cognitive performance and mood under sleep restriction (SR). Seventeen participants took part of a 48h laboratory protocol, during which three different light settings (separated by 2 wks) were administered each morning after two 6-h sleep restriction nights: a blue monochromatic LED (light-emitting diode) light condition (BL; 100 lux at 470 nm for 20 min) starting 2 h after scheduled wake-up time, a dawn-simulating light (DsL) starting 30 min before and ending 20 min after scheduled wake-up time (polychromatic light gradually increasing from 0 to 250 lux), and a dim light (DL) condition for 2 h beginning upon scheduled wake time (58 lux). Cognitive tasks were performed every 2 h during scheduled wakefulness, and questionnaires were administered hourly to assess subjective sleepiness, mood, and wellbeing. Salivary melatonin and cortisol were collected throughout scheduled wakefulness in regular intervals, and the effects on melatonin were measured after only one light pulse. Following the first SR, analysis of the time course of cognitive performance during scheduled wakefulness indicated a decrease following DL, whereas it remained stable following BL and significantly improved after DsL. Cognitive performance levels during the second day after SR were not significantly affected by the different light conditions. However, after both SR nights, mood and well-being were significantly enhanced after exposure to morning DsL compared with DL and BL. Melatonin onset occurred earlier after morning BL exposure, than after morning DsL and DL, whereas salivary cortisol levels were higher at wake-up time after DsL compared with BL and DL. Our data indicate that exposure to an artificial morning dawn simulation light improves subjective well-being, mood, and cognitive performance, as compared with DL and BL, with minimal impact on circadian phase. Thus, DsL may provide an effective strategy for enhancing cognitive performance, wellbeing, and mood under mild sleep restriction. |
2011 |
Chellappa, S L; Viola, A U; Schmidt, C; Bachmann, V; Gabel, V; Maire, M; Reichert, C F; Valomon, A; Götz, T; Landolt, H P; Cajochen, C Human melatonin and alerting response to blue-enriched light depend on a polymorphism in the clock gene PER3 Journal Article J Clin Endocrinol Metab 97(3), 2011. @article{161, title = {Human melatonin and alerting response to blue-enriched light depend on a polymorphism in the clock gene PER3}, author = { S.L. Chellappa and A.U. Viola and C. Schmidt and V. Bachmann and V. Gabel and M. Maire and C. F. Reichert and A. Valomon and T. Götz and H.P. Landolt and C. Cajochen}, url = {http://www.chronobiology.ch/wp-content/uploads/publications/Chellappa_et_al_2011_4.pdf}, year = {2011}, date = {2011-01-01}, journal = {J Clin Endocrinol Metab 97(3)}, keywords = {}, pubstate = {published}, tppubtype = {article} } |