Purpose: The overarching goal of this project is to correlate the effects of plasma ceramide with human in vivo vascular function.
Formulation of Research Questions: Following decades of decline in mortality, death due to heart disease is increasing, and remains the #1 cause of death in the United States. Although acute ischemic events are typically due to obstructive plaque within the coronary conduit arteries, strong evidence suggests that dysfunction within the coronary microvasculature is a more powerful predictor of major adverse cardiac events (MACE) than severity of atherosclerosis1. The coronary microvasculature likely also contributes to other forms of cardiovascular disease including heart failure with preserved ejection fraction (HFpEF)2. While assessment of the coronary microvasculature is highly invasive and expensive, interrogation of the peripheral microvasculature offers a more feasible approach. Recent studies have concluded that peripheral microvascular dysfunction mirrors the functional status of the coronary microvasculature3. Further, impaired peripheral microvascular function is associated with increased risk of MACE in patients with stable coronary artery disease (CAD), suggesting that the microvasculature plays a critical role in the pathogenesis of heart disease4.
Elevated plasma ceramides are also associated with risk of MACE in otherwise healthy individuals5 as well as in heart failure both with and without reduced ejection fraction (HFrEF and HFpEF, respectively)6. Recently it was shown that ceramide levels are increased in patients with early CAD that also exhibit impaired coronary microvascular endothelial dysfunction7. Using an in vitro model, the investigators have previously shown that exposure to exogenous ceramide causes microvascular endothelial dysfunction in arterioles from healthy individuals8. However the effect of ceramide on human in vivo peripheral microvascular function represents a critical knowledge gap that needs to be addressed. Increased plasma ceramide may evoke peripheral in vivo microvascular dysfunction that mirrors that of the coronary microvasculature thus providing a less invasive means to assess future cardiovascular risk.
Hypothesis: Following a single high-fat meal, increases in plasma ceramides will correlate with a reduction in peripheral large and small vascular function in the intact human adult.
At Adult TRU:
1. Patient arrives at the Adult Translational Unit (ATRU) and checks in with the nurse at the front desk.
2. TRU nurse informs study team that the subject has arrived.
3. Dr. Freed or study team member consents the subject.
4. Once the subject completes the consent form, the nurse brings them to the patient room.
1. If the subject is female, they are required to take a pregnancy test.
2. The nurse completes the pregnancy test and gives the results to the study team member.
3. The nurse takes baseline vital signs (height, weight, blood pressure, heart rate).
5. Baseline testing begins: (time 0)
1. Baseline blood draw (10mL) to measure plasma ceramide levels.
2. Baseline flow-mediated dilation (FMD) and reactive hyperemia measurements
3. Baseline cytocam assessment
6. High-fat meal: Subjects will be given one high-fat meal by the ATRU dietitian to be ingested within 20 minutes.
7. 2-hour timepoint testing: (time 2)
1. Blood draw (10mL) at 2hrs post initiation of high-fat meal to measure ceramide levels
2. FMD and reactive hyperemia measurements
8. 4-hour timepoint testing: (time 4)
1. Blood draw (10mL) at 4hrs post initiation of high-fat meal to measure ceramide levels
2. FMD and reactive hyperemia measurements
3. 4-hour cytocam assessment
9. After the study is completed, the patient remains in the exam room for 30 min under nurse observation
1. During this time, vital signs are assessed by the nurse
2. The patient may order food off the Froedtert menu
Flow-Mediated Dilation/Reactive Hyperemia Protocol Flow mediated dilation (FMD) and blood flow velocity will be assessed using a portable ultrasound machine with a 13 mHz probe. All images will be continuously captured onto using the Vascular Imager (Medical Imaging, Iowa City, IA) software. Artery diameter will automatically be measured using the boarder sensing function in the Brachial Analyzer (Medical Imaging) software.
After the subjects have rested in the supine position for 15 minutes their arm will be abducted \~80° with the pneumatic cuff placed on their forearm. Baseline brachial artery diameter and blood flow velocity through the artery will be measured 3 cm proximal to the antecubital fossa. The ultrasound probe will be positioned at 90° to the vessel to visualize anterior and posterior lumen-intimal interfaces. After baseline images have been captured, the pneumatic cuff will be inflated to 225 mmHg for 5 minutes to occlude blood flow to the lower leg or forearm. Immediately after cuff release, the increased blood flow velocity due to the reactive hyperemia response will be measured. To assess vasodilation, images will be captured at a rate of 10 images/second for 3 minutes after cuff release.
Cytocam Assessment for Microvascular Function Approximately 10 images will be taken to establish a baseline. The study team will administer 1% acetylcholine (via Q-tip, liquid dropper or gauze) under the tongue for 1 minute. The CytoCam is reinserted to take approximately 10 more images. The patient will be allowed 30 minutes to rest while the nurse retakes vital signs. After 30 minutes, a new set of approximately 10 baseline images are taken. The study team will administer a nitroglycerin tablet (0.3mg) under the tongue. Once the tablet dissolves the CytoCam will be reinserted to image the vessels (approximately 10 images) after 2-3 minutes following tablet administration.
