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| ID | Type | Description | Link |
|---|---|---|---|
| R01HL168081 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| University of Colorado, Denver | OTHER |
| National Heart, Lung, and Blood Institute (NHLBI) | NIH |
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People who experience repeated bouts of circadian misalignment, such as shift workers, are at higher risk of cardiovascular disease (CVD) and Type 2 diabetes (T2D) compared to daytime workers. However, the mechanism(s) by which shift work and associated circadian misalignment increase CVD and T2D risk are unknown. This project will examine whether elevated plasma lipids are a mechanism by which circadian misalignment impairs vascular function, insulin sensitivity, glucose homeostasis and muscle lipid accumulation, which could be targeted to prevent and treat cardiometabolic disease in people who chronically experience circadian misalignment, which includes more than 20% of the US workforce.
There is growing recognition that timing of behaviors, such as eating, sleeping, and activity, have a significant impact on human health and disease risk. For example, when people are awake at the "wrong" time of the day (i.e. during the biological night), a mismatch occurs between behavior and biology, termed circadian misalignment. Shift workers experience repeated bouts of circadian misalignment and are at higher risk of cardiovascular disease (CVD) and Type 2 diabetes (T2D) compared to people who work days. However, the mechanism(s) by which shift work and associated circadian misalignment increase CVD and T2D risk are unknown.
Data from the investigators and others demonstrate impaired vascular endothelial function and insulin sensitivity during circadian misalignment, two important risk factors for future development of CVD and T2D. Furthermore, the investigators published and unpublished data support that circadian misalignment increases circulating bioactive lipids known to associate with impaired endothelial function and insulin resistance. Indeed, shift workers also have elevated circulating lipids, though it is not known which specific lipids are elevated, and whether they are associated with impaired vascular function and/or insulin sensitivity. Using a circadian-based eating intervention (time-restricted eating; TRE), we can consistently reduce lipids in circulation, as well as reduce heart rate and blood pressure and improve glucose homeostasis.
Therefore, the overall objective for this project is to examine whether increased plasma lipids are a potential mechanism by which chronic circadian misalignment impairs cardiovascular and metabolic health with the long-term goal of identifying novel therapeutic targets to combat the risks for disease when circadian misalignment is unavoidable. The central hypothesis is that reducing plasma lipids in night shift workers via TRE will improve vascular function, insulin sensitivity and glucose homeostasis, and reduce muscle tissue lipid accumulation. To test the hypothesis, we will conduct a 12-week randomized crossover study in 50 non-rotating night shift workers (25Females/25Males; 18-65years) with existing cardiometabolic risk factors. At the end of each 4-week outpatient condition (TRE vs Control with an intervening 4-week washout period), we will conduct rigorous 3-day inpatient assessment to determine the impact of plasma lipid reduction via TRE in chronic night shift workers on 1) vascular function and blood pressure; and 2) whole body and muscle-specific insulin sensitivity, glucose homeostasis and muscle lipid accumulation.
Achievement of these aims will identify a potential mechanism by which circadian misalignment impairs vascular function and insulin sensitivity (elevated plasma lipids), as well as a non-pharmacological tool (TRE) that could be implemented to reduce cardiometabolic disease risk in populations at elevated risk, in 20% of the US workforce who work nonstandard hours including military personnel, police, paramedics, firefighters, pilots, medical doctors and nurses, as well as people with sleep and circadian disorders.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control eating during overnight work shift | Experimental | For 4 weeks, participants will eat during the biological night as is typically done in night shift workers. |
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| Time-restricted eating during overnight work shift | Experimental | For 4 weeks, participants will refrain from eating during the biological night while maintaining the same sleep opportunity and daily energy intake and macronutrient distribution without changing 24h energy intake. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Time-restricted eating | Behavioral | Night shift workers will participate in 4 weeks of fasting during the biological nighttime while remaining awake during overnight work shifts. |
| Measure | Description | Time Frame |
|---|---|---|
| Blood pressure via 24-hour assessments | Four weeks of TRE during shift work will reduce 24-hour blood pressure versus Control. | Collected during inpatient laboratory visit after 4 weeks of Control and TRE |
| Insulin sensitivity via clamp | Four weeks of TRE during shift work will improve insulin sensitivity versus Control. | Collected during inpatient laboratory visit after 4 weeks of Control and TRE |
| Measure | Description | Time Frame |
|---|---|---|
| Cerebrovascular reactivity via transcranial doppler | Four weeks of TRE during shift work will improve cerebrovascular reactvity versus Control. | Collected during inpatient laboratory visit after 4 weeks of Control and TRE |
| Muscle lipid accumulation via lipidomics |
| Measure | Description | Time Frame |
|---|---|---|
| 24-hour blood sampling for lipids, glucose, insulin, and vascular markers | Four weeks of TRE during shift work will improve 24-hour markers of vascular function versus Control. | Collected during inpatient laboratory visit after 4 weeks of Control and TRE |
Inclusion Criteria:
Exclusion Criteria:
existing diagnosed sleep or eating disorder (e.g. obstructive sleep apnea [OSA], periodic limb movements of sleep [PLMS], narcolepsy, travel more than 1 time zone in 3 weeks before the study; anorexia nervosa, more than one food allergy to maintain flexibility in diet planning);
following any TRE (time-restricted eating) or intermittent fasting plan in the last year;
following any special diet plan, like paleo, keto, gluten-free or vegan, that can affect the primary lipid outcome measures in the last 6 months; any clinically significant surgical condition within the last year;
diagnosed diabetes or cardiovascular disease
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Josiane L Broussard, PhD | Contact | 9704913103 | josiane.broussard@colostate.edu | |
| Ellen Lyon, MS | Contact | 9704913103 | ellen.lyon@colostate.edu |
| Name | Affiliation | Role |
|---|---|---|
| Josiane L Broussard, PhD | Colorado State University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Colorado State University | Recruiting | Fort Collins | Colorado | 80523 | United States |
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| Label | URL |
|---|---|
| Josiane Broussard's Bibliography | View source |
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| Control eating | Behavioral | Night shift workers will participate in 4 weeks of Control eating across the daytime and nighttime hours while remaining awake during overnight work shifts. |
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Four weeks of TRE during shift work will reduce muscle lipid accumulation versus Control. |
| Collected during inpatient laboratory visit after 4 weeks of Control and TRE |
| ID | Term |
|---|---|
| D008659 | Metabolic Diseases |
| D007333 | Insulin Resistance |
| ID | Term |
|---|---|
| D009750 | Nutritional and Metabolic Diseases |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
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