The study objective is to determine maintenance dietary protein requirements for adult
males who have previously undergone Roux-en-Y-Bypass (RYGB) surgery, using the minimally
invasive Indicator Amino Acid Oxidation (IAAO) method. The study hypothesis is that
dietary protein requirements will be elevated in this population compared to young adults
with no previous bariatric surgery. The null hypothesis states that there is no
difference in dietary protein requirements between adults with previous RYGB surgery and
adults without previous surgery. Protein requirements will be expressed relative to
fat-free-mass (FFM) to account for obesity-related increases in lean mass.
The primary endpoint of the study is the estimated average protein requirements (g/kg
FFM/d) and the upper limit of the 95% confidence interval.
The study comprises a nutritional experimental study using the IAAO method to determine
protein requirements. Indicator amino acid oxidation is measured at seven incremental
protein intake levels, each on a separate study day after two adaptation days. Protein
intake requirements are calculated as the protein intake level where the indicator amino
acid oxidation ceases to decline further despite a further increase in protein intake.
This is referred to as the breakpoint. The sequences of protein intake levels are
randomized for each study participant. Protein requirements are calculated, not per
individual, but for the whole study population, when sufficient oxidation studies are
included at each protein intake level. This implies that the same individual does not
have to complete all the oxidation studies at the seven time points.
The study will consist of one initial screening and planning visit, and 2 to 7 metabolic
trial visits. Each participant can complete at least two, preferably more, and up to all
7 protein intake levels.
Patients who previously consented to be included in a UZ Leuven Obesity Clinic repository
(ClinicalTrials.gov Identifier NCT04614961; S-62590) will be pre-screened according to
the study criteria. Thereafter patients who remain eligible will be contacted and will
receive information regarding the study using the informed consent form. An invitation to
participate in the study will also be circulated through patient support groups of
obesity and bariatric surgery using their social network platforms (See addendum A).
Patients who are interested in participation will be invited to contact the study
coordinator. Patients who complete the pre-screening assessment and remain eligible will
invited to a screening visit.
Patients who remain eligible to partake will receive further information regarding the
study procedures and will be provided with instructions and food items and utensils
needed for the first 3-day metabolic experiment. Patients will also be provided with a
multivitamin-mineral supplement suitable for patients following bariatric surgery to
consume for the duration of the study. Habitual dietary intake will be self-reported
using a 3-day food diary. For patients who do not meet all inclusion criteria, any newly
identified raised blood glucose, blood pressure, abnormal liver function or decreased
kidney function will be reported to the patient and their general practitioner.
The study day will be repeated 7 times, each at a different intake level. The subjects
will randomly receive one of seven protein intakes levels during each IAAO experiment
(figure 1.). Simple randomization will be conducted using RedCap and allocation tables
created in R to allocate a different protein level during each of the visits. Allocation
will be concealed from participants. One investigator will be unblinded to allocation as
he needs to calculate and physically prepare the study diets based on the specific
protein intake level of the given study day. This will not interject bias as the study
outcomes are metabolic processes measured by objective biochemical analysis.
Adaptation days protocol Patients will be contacted, and experimental visits scheduled.
The study protocol is based on the established IAAO method(26). On two adaptation days
prior to the IAAO testing day, patient will consume a maintenance diet providing ad
libitum energy intake and protein intake of at 1.5 g/kg ideal body weight. This amount of
protein meets current upper-limit of protein requirements for individuals after bariatric
surgery(16), and thereby to avoid a catabolic state during the adaptation period.
The maintenance diet will be the participants habitual food intake with the additional of
additional protein supplements as necessary. Participants will be allowed to consume one
cup of coffee or tea and additional water as needed. Food intake during the 2 days will
be recorded to measure protein and energy intake.
Metabolic study days On the study days, patients will visit the ACRONIM study unit at UZ
Leuven. Patients will be instructed to arrive for the study visit after a 12-hour fast
overnight. On arrival, body weight and body composition will be measured as described
above. Patient will receive eight hourly isocaloric meals, each providing 1/12 of their
daily energy requirement, thus 67% of their total daily intake.
The 7 test protein intake levels will be testes. It is important that there are at least
2 intake levels below and above the measured protein requirements to identify a
breakpoint of amino acid oxidation . Therefore, we selected a range of intake levels
which includes two intakes below requirements in healthy men and women, one which is
aligned to healthy requirements, and four at higher levels, anticipating that the
breakpoint will occur before the final two intake levels.
The remainder of the diet will be provided as 40% fat and 40% carbohydrate to meet daily
energy requirements of REE x 1.5. Protein is provided as a crystalline amino acid mixture
with a similar amino acid profile to egg protein. The remainder of the diet will be made
up of protein-free powder, flavouring, oil, and protein-free cookies.
From the 5th meal the tracer protocol will commence. A primer dosage of 0.176 mg/kg
NaH13CO3 and 1.86 mg/kg 1-13C phenylalanine will be provided with the fifth meal. With
the next three meals, 1.2 mg/kg 1-13C phenylalanine will be added.
The phenylalanine tracer will form part of a total dietary phenylalanine intake if 30.5
mg/kg/day, approximately three times the Recommended Daily Allowance (RDA,) to ensure
sufficient supply for protein synthesis. The RDA for an amino acid is the amount of the
amino acid required for protein synthesis, as previously determined by IAAO studies.
Equally total tyrosine intake will be 40 mg/kg/day, well in excess of requirements, to
minimize the conversion of phenylalanine to tyrosine for protein deposition. Both stable
isotopes will be purchased from Cambridge Isotope Laboratories (Woburn, MA, USA).
Breath and urine samples will be collected to measure phenylalanine oxidation and
phenylalanine flux respectively. 3 x12ml breath samples will be collected at three
time-points and 15ml urine samples at 2 time points prior to commencing the tracer
protocol. From 2.5 hours after the start of the tracer protocol until the end of the
experiment (hour eight). Breath samples will be collected 6 times (12ml x 3 each time)
and urine two times (15ml each time). Breath samples will be stored at room temperature
and urine samples will be frozen and stored at -20 ˚C. 13CO2 enrichment of expired air
and Urine 13C phenylalanine enrichment will be measured with the use of Gas
Chromatography-Mass Spectrometry (GC-MS).
Whole-body phenylalanine flux during isotopic steady state will be calculated according
to the model of Matthews et al. as was previously described for IAAO studies.
Phenylalanine flux is measured as the dilution of ingested labelled phenylalanine,
measured as 13C- phenylalanine in urine. The rate of appearance of 13CO2 in expired air
(F13CO2) represents the oxidation of ingested phenylalanine. F13CO2 is calculated
according to the model of Matthews et al., using a factor of 0.82 to account of carbon
dioxide retained in the bicarbonate pool (32).