White Adipose Tissue Clocks and High Calorie Feeding
Pilot Study to Examine the Impact of Overfeeding on Peripheral Clock Gene Expression in Humans
2 other identifiers
interventional
10
1 country
1
Brief Summary
Peripheral tissues (e.g. liver, adipose, muscle) express self-sustained circadian clocks that coordinate daily metabolic rhythms. The timing of clock rhythms in peripheral tissues is highly sensitive to feeding-fasting signals across the sleep-wake transition. Nutritional insults such as high fat overfeeding (HF-OF) have been shown to attenuate clock gene expression in peripheral tissues resulting in a deleterious re-programming of the circadian metabolome. Studies in humans have only superficially investigated how the circadian clock machinery is impacted by nutritional signals. The overall goal of this pilot project is to take the first steps toward developing translational methods to investigate links between changes in energy flux and the circadian system in human tissues. Using an innovative ex vivo cell culture approach the investigators will examine the impact of 3-days of HF-OF compared to eucaloric (EU) feeding on the expression of core clock genes in human subcutaneous adipose tissue (SAT). The Investigators hypothesize that compared to EU, the amplitude of clock gene expression in SAT measured over 24hrs will be attenuated following short-term HF-OF. This pilot project will serve as a launch point for designing future studies into the effects of diet and exercise on the circadian control of metabolism in adipose tissue depots as well as other tissues (e.g. muscle).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable healthy
Started Jul 2016
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 7, 2015
CompletedFirst Posted
Study publicly available on registry
June 22, 2016
CompletedStudy Start
First participant enrolled
July 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2017
CompletedJuly 1, 2019
June 1, 2019
1.2 years
December 7, 2015
June 27, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Expression of clock genes in adipose tissue.
Gene expression measured at two time points from abdominal fat.
Measured through study completion, an average of 4 weeks.
Secondary Outcomes (2)
Gene expression of key cellular fuel sensors thought to be controlled. and/or influenced by peripheral clocks
Measured through study completion, an average of 4 weeks.
Expression of clock genes in blood monocytes.
Measured through study completion, an average of 4 weeks.
Study Arms (2)
Eucaloric Feeding
OTHEROverfeeding
OTHERInterventions
Eligibility Criteria
You may qualify if:
- males and females aged 20-35 yr;
- BMI 25-35 kg/m2 and weight stable (±2kg in past 2mo);
- non-smoker;
- sedentary to moderately active (≤3 days of exercise per week ≤30 min of exercise per session);
- sleeping pattern of \>7 hours to 9.25 hrs of sleep/night.
- subjects will be asked to identify themselves as regular consumers of 3 balanced meals per day by answering the question: "Do you eat breakfast, lunch, and dinner on ≥ 5 days per week?"
You may not qualify if:
- Smoker (current or within the previous 3 months);
- Use any medication that could affect lipid metabolism, insulin signaling, or sleep;
- Pregnant women will not be enrolled in the study;
- Have a job that involves shift work;
- Dwelling below Denver altitude (1,600 m) a year prior to testing;
- Travel across more than one time zone 3 wk before a study;
- chronic health conditions such as diabetes, hyper or hypothyroidism, renal or liver disease, anemia, or cancer;
- Regularly go to sleep after midnight;
- o Subjects will be excluded if they are identified as having night eating syndrome (at least 25% of food intake is consumed after the evening meal and/or at least two episodes of nocturnal eating per week);
- Allergy to lidocaine or similar compound;
- Have one or more of the following out-of-range values measured on a fasting blood sample:
- glucose \> 110 mg/dl,
- thyroid stimulating hormone \<0.5 or \>5.0 µU/ml.
- Subjects who may be:
- anemic (hemoglobin \< 14.5 g/dl men, \<12.3 g/dl women ),
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Unknown Facility
Denver, Colorado, 80045, United States
Related Publications (5)
Yoo SH, Yamazaki S, Lowrey PL, Shimomura K, Ko CH, Buhr ED, Siepka SM, Hong HK, Oh WJ, Yoo OJ, Menaker M, Takahashi JS. PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues. Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5339-46. doi: 10.1073/pnas.0308709101. Epub 2004 Feb 12.
PMID: 14963227BACKGROUNDOosterman JE, Kalsbeek A, la Fleur SE, Belsham DD. Impact of nutrients on circadian rhythmicity. Am J Physiol Regul Integr Comp Physiol. 2015 Mar 1;308(5):R337-50. doi: 10.1152/ajpregu.00322.2014. Epub 2014 Dec 17.
PMID: 25519730BACKGROUNDEckel-Mahan KL, Patel VR, de Mateo S, Orozco-Solis R, Ceglia NJ, Sahar S, Dilag-Penilla SA, Dyar KA, Baldi P, Sassone-Corsi P. Reprogramming of the circadian clock by nutritional challenge. Cell. 2013 Dec 19;155(7):1464-78. doi: 10.1016/j.cell.2013.11.034.
PMID: 24360271BACKGROUNDPivovarova O, Jurchott K, Rudovich N, Hornemann S, Ye L, Mockel S, Murahovschi V, Kessler K, Seltmann AC, Maser-Gluth C, Mazuch J, Kruse M, Busjahn A, Kramer A, Pfeiffer AF. Changes of Dietary Fat and Carbohydrate Content Alter Central and Peripheral Clock in Humans. J Clin Endocrinol Metab. 2015 Jun;100(6):2291-302. doi: 10.1210/jc.2014-3868. Epub 2015 Mar 30.
PMID: 25822100BACKGROUNDRynders CA, Morton SJ, Bessesen DH, Wright KP Jr, Broussard JL. Circadian Rhythm of Substrate Oxidation and Hormonal Regulators of Energy Balance. Obesity (Silver Spring). 2020 Jul;28 Suppl 1(Suppl 1):S104-S113. doi: 10.1002/oby.22816. Epub 2020 May 28.
PMID: 32463976DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Daniel Bessesen, MD
University of Colorado School of Medicine
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 7, 2015
First Posted
June 22, 2016
Study Start
July 1, 2016
Primary Completion
September 1, 2017
Study Completion
September 1, 2017
Last Updated
July 1, 2019
Record last verified: 2019-06
Data Sharing
- IPD Sharing
- Will not share