Muscle Protein Synthesis in Dialysis Patients
- Conditions
- Muscle Loss
- Interventions
- Other: Protein MealOther: Stable Isotope Amino Acid Infusion
- Registration Number
- NCT03478722
- Lead Sponsor
- University of Illinois at Urbana-Champaign
- Brief Summary
The most severe form of chronic renal failure is end-stage-renal-disease with maintenance hemodialysis (MHD) as the most common treatment strategy. MHD patients experience a number of metabolic and phenotypic derangements including skeletal muscle wasting. Previously, it has been demonstrated that dialysis treatment leads to increased rates of forearm phenylalanine uptake (proxy for 'muscle' protein synthesis) with an even greater rates of phenylalanine release (proxy for 'muscle' protein breakdown). Hence, the dialysis procedure itself is catabolic and induces a catabolic carryover for several hours after dialysis. This suggests prolonged post-dialysis disturbances in whole body- and skeletal muscle protein metabolism in MHD patients. Moreover, dialysis treatment in itself results in \~20 % losses of circulating amino acids in the dialysate. Collectively, this creates the need for replacement of amino acids by protein supplementation during and/or after dialysis. The ingestion of protein-dense meals in between dialysis treatments likely represents an important dietary strategy to counterbalance dialysis-induced catabolism and to achieve the current recommended protein intakes (set at 1.2 g/kg bodyweight/d) to limit muscle protein loss in MHD patients. However, the effectiveness of protein-rich meal ingestion to augment postprandial whole body and muscle protein metabolic responses in MHD patients outside of the dialysis period remain largely undefined.
The purpose of this study is to compare basal and postprandial whole body leucine body kinetics, muscle anabolic sensing mechanisms, markers of muscle proteolysis, and myofibillar protein synthesis rates to mixed meal ingestion on a non-dialysis day in eight MHD patients, between 20-80 and to compare these outcomes to age- and BMI-matched controls. The investigators will use specifically produced intrinsically L-\[5,5,5-2H3\]leucine labeled eggs combined with primed constant amino acid tracer infusion methods and concomitant blood and muscle direct sampling to make direct assessments of in vivo protein digestion and absorption kinetics and subsequent postprandial muscle protein synthetic responses in MHD patents and controls. On the test day, subjects will remain sedentary for the determination of muscle protein synthesis in both the fasted state and after consumption of the meal.
- Detailed Description
On the day of the infusion trial, participants will report to the laboratory at 0700 h after an overnight fast. MHD patients will be studied \~24 h after their dialysis treatment. A Teflon catheter will be inserted into an antecubital vein for baseline blood sample collection (t=-180 min) after which participants receive priming doses of NaH13CO2 (2.35 µmol·kg), L-\[1-13C\]leucine (7.6 µmol·kg FFM), and L-\[ring-2H5\]phenylalanine (2.0 µmol·kg FFM). Subsequently, a continuous intravenous infusion of L-\[1-13C\]leucine (0.10 µmol·kg FFM ·min) and L-\[ring-2H5\]phenylalanine (0.05 µmol·kg-1 FFM·min) will be initiated (t=-180 min) and maintained until the end of the trial. A second Teflon catheter will be inserted into a heated dorsal hand vein of the same arm for repeated arterialized blood sampling and will remain patent by a 0.9% saline drip. In the postabsorptive state, muscle biopsies will be collected at t=-120 and -0 min of the infusion. Subsequently, participants will consume a mixed meal containing 20 grams of dietary protein and the completion of the meal will mark the start of the postprandial phase (t=0 min). An additional muscle biopsy will be collected at 300 min to determine postprandial myofibrillar protein synthesis rates. Biopsies will be collected from the middle region of the vastus lateralis (15 cm above the patella) with a Bergström needle modified for suction under local anesthesia (2% Lidocaine). The postabsorptive muscle biopsies will be collected from the same incision with the needle pointed to distal and proximal directions, respectively. The postprandial biopsy will be collected through a separate incision 2-3 cm above the postabsorptive incision. All biopsy samples will be freed from any visible blood, adipose, and connective tissue immediately frozen in liquid nitrogen, and stored at -80˚C until subsequent analysis.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 16
- Aged 20-80 years (both healthy controls and MHD patients)
- Medical clearance from a Nephrologist at their respective dialysis clinic to participate (MHD patients)
- Known allergies to egg consumption (both healthy controls and MHD patients)
- Phenylketonuria (both healthy controls and MHD patients)
- Vegans (both healthy controls and MHD patients)
- Diagnosed GI tract diseases (healthy controls)
- Recent (1 year) participation in amino acid tracer studies (both healthy controls and MHD patients)
- Predisposition to hypertrophic scarring or keloid formation (both healthy controls and MHD patients)
- Diabetes (healthy controls)
- Pregnancy (both healthy controls and MHD patients)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Maintenance Hemodialysis Patients Stable Isotope Amino Acid Infusion Protein meal, stable isotope amino acid infusion Control Subjects Stable Isotope Amino Acid Infusion Protein meal, stable isotope amino acid infusion Control Subjects Protein Meal Protein meal, stable isotope amino acid infusion Maintenance Hemodialysis Patients Protein Meal Protein meal, stable isotope amino acid infusion
- Primary Outcome Measures
Name Time Method Fractional synthetic rate of myofibrillar proteins 8 hours Measurement of muscle protein synthesis
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Freer Hall
🇺🇸Urbana, Illinois, United States