Greater sensitivity of the circadian system of women to bright light, but not dim‐to‐moderate light

Author:

Vidafar Parisa123,McGlashan Elise M.14,Burns Angus C.1,Anderson Clare1,Shechter Ari5,Lockley Steven W.1678,Phillips Andrew J. K.1,Cain Sean W.1ORCID

Affiliation:

1. School of Psychological Sciences and Turner Institute for Brain and Mental Health Monash University Clayton Victoria Australia

2. Faculty of Medicine and Health, Central Clinical School The University of Sydney Sydney New South Wales Australia

3. Australian Research Council Centre of Excellence for Children and Families over the Life Course Canberra Australian Capital Territory Australia

4. Melbourne School of Psychological Sciences University of Melbourne Parkville Victoria Australia

5. Department of Medicine Columbia University Irving Medical Center New York New York USA

6. Departments of Medicine and Neurology, Division of Sleep and Circadian Disorders Brigham and Women's Hospital Boston Massachusetts USA

7. Division of Sleep Medicine Harvard Medical School Boston Massachusetts USA

8. Department of Clinical and Experimental Medicine, Faculty of Health and Medical Sciences Surrey Sleep Research Centre, University of Surrey Guildford Surrey UK

Abstract

AbstractWomen typically sleep and wake earlier than men and have been shown to have earlier circadian timing relative to the light/dark cycle that synchronizes the clock. A potential mechanism for earlier timing in women is an altered response of the circadian system to evening light. We characterized individual‐level dose–response curves for light‐induced melatonin suppression using a within‐subjects protocol. Fifty‐six participants (29 women, 27 men; aged 18–30 years) were exposed to a range of light illuminances (10, 30, 50, 100, 200, 400, and 2000 lux) using melatonin suppression relative to a dim control (<1 lux) as a marker of light sensitivity. Women were free from hormonal contraception. To examine the potential influence of sex hormones, estradiol and progesterone was examined in women and testosterone was examined in a subset of men. Menstrual phase was monitored using self‐reports and estradiol and progesterone levels. Women exhibited significantly greater melatonin suppression than men under the 400‐lux and 2000‐lux conditions, but not under lower light conditions (10–200 lux). Light sensitivity did not differ by menstrual phase, nor was it associated with levels of estradiol, progesterone, or testosterone, suggesting the sex differences in light sensitivity were not acutely driven by circulating levels of sex hormones. These results suggest that sex differences in circadian timing are not due to differences in the response to dim/moderate light exposures typically experienced in the evening. The finding of increased bright light sensitivity in women suggests that sex differences in circadian timing could plausibly instead be driven by a greater sensitivity to phase‐advancing effects of bright morning light.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Endocrinology

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