Journal article
Circadian Rhythm Profiles in Women with Night Eating Syndrome
Journal of biological rhythms, Vol.24(1), pp.85-94
02/2009
Handle:
https://hdl.handle.net/2376/104855
PMCID: PMC3564642
PMID: 19150931
Abstract
Night eating syndrome (NES) is characterized by evening hyperphagia and frequent awakenings accompanied by food intake. Patients with NES display a delayed circadian pattern of food intake but retain a normal sleep-wake cycle. These characteristics initiated the current study, in which the phase and amplitude of behavioral and neuroendocrine circadian rhythms in patients with NES were evaluated. Fifteen women with NES (mean age ± SD, 40.8 ± 8.7 y) and 14 control subjects (38.6 ± 9.5 y) were studied in the laboratory for 3 nights, with food intake measured daily. Blood also was collected for 25 h (every 2 h from 0800 to 2000 h, and then hourly from 2100 to 0900 h) and assayed for glucose and 7 hormones (insulin, ghrelin, leptin, melatonin, cortisol, thyroid-stimulating hormone [TSH] and prolactin). Statistical analyses utilized linear mixed-effects cosinor analysis. Control subjects displayed normal phases and amplitudes for all circadian rhythms. In contrast, patients with NES showed a phase delay in the timing of meals, and delayed circadian rhythms for total caloric, fat, and carbohydrate intake. In addition, phase delays of 1.0 to 2.8 h were found in 2 food-regulatory rhythms—leptin and insulin—and in the circadian melatonin rhythm (with a trend for a delay in the circadian cortisol rhythm). In contrast, circulating levels of ghrelin, the primary hormone that stimulates food intake, were phase advanced by 5.2 h. The glucose rhythm showed an inverted circadian pattern. Patients with NES also showed reduced amplitudes in the circadian rhythms of food intake, cortisol, ghrelin, and insulin, but increased TSH amplitude. Thus, patients with NES demonstrated significant changes in the timing and amplitude of various behavioral and physiological circadian markers involved in appetite and neuroendocrine regulation. As such, NES may result from dissociations between central (suprachiasmatic nucleus) timing mechanisms and putative oscillators elsewhere in the central nervous system or periphery, such as the stomach or liver. Considering these results, chronobiologic treatments for NES such as bright light therapy may be useful. Indeed, bright light therapy has shown efficacy in reducing night eating in case studies and should be evaluated in controlled clinical trials.
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Details
- Title
- Circadian Rhythm Profiles in Women with Night Eating Syndrome
- Creators
- Namni Goel - Division of Sleep and Chronobiology (Psychiatry), University of Pennsylvania, School of Medicine, Philadelphia, PA, USAAlbert J Stunkard - Center for Weight and Eating Disorders (Psychiatry), University of Pennsylvania School of Medicine, Philadelphia, PA, USANaomi L Rogers - Division of Sleep and Chronobiology (Psychiatry), University of Pennsylvania, School of Medicine, Philadelphia, PA, USAHans P.A Van Dongen - Division of Sleep and Chronobiology (Psychiatry), University of Pennsylvania, School of Medicine, Philadelphia, PA, USAKelly C Allison - Center for Weight and Eating Disorders (Psychiatry), University of Pennsylvania School of Medicine, Philadelphia, PA, USAJohn P O’Reardon - Center for Weight and Eating Disorders (Psychiatry), University of Pennsylvania School of Medicine, Philadelphia, PA, USARexford S Ahima - Division of Endocrinology, Diabetes and Metabolism (Medicine), University of Pennsylvania School of Medicine, Philadelphia, PA, USADavid E Cummings - Division of Metabolism, Endocrinology and Nutrition (Medicine), University of Washington, Seattle, WA, USAMoonseong Heo - Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY, USADavid F Dinges - Division of Sleep and Chronobiology (Psychiatry), University of Pennsylvania, School of Medicine, Philadelphia, PA, USA
- Publication Details
- Journal of biological rhythms, Vol.24(1), pp.85-94
- Academic Unit
- Medical Education and Clinical Science, Department of
- Grant note
- R01 NR004281-13 || NR / National Institute of Nursing Research : NINR
- Identifiers
- 99900546881501842
- Language
- English
- Resource Type
- Journal article