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A specific protein-enriched enteral formula decreases cortisolemia and improves plasma albumin and amino acid concentrations in elderly patients
Nutrition & Metabolism volume 7, Article number: 58 (2010)
Old age is associated with an involuntary and progressive but physiological loss of muscle mass. The aim of this study was to evaluate the effects of exclusive consumption for 6 months of a protein-enriched enteral diet with a relatively high content of branched-chain amino acids on albuminemia, cortisolemia, plasma amino acids, insulin resistance, and inflammation biomarkers in elderly patients.
Thirty-two patients from the Clinical Nutrition Outpatient Unit at our hospital exclusively consumed a protein-enriched enteral diet for 6 months. Data were collected at baseline and at 3 and 6 months on anthropometric and biochemical parameters and on plasma concentrations of amino acids, cortisol, adrenocorticotropic hormone, urea, creatinine, insulin resistance, and inflammation biomarkers.
The percentage of patients with albumin concentration below normal cut-off values decreased from 18% to 0% by the end of the study. At 6 months, concentrations of total plasma (p = 0.008) and essential amino acids (p = 0.011), especially branched-chain amino acids (p = 0.031), were higher versus baseline values, whereas 3-methylhistidine (p = 0.001), cortisol (p = 0.001) and adrenocorticotropic hormone (p = 0.004) levels were lower.
Regular intake of specific protein-enriched enteral formula increases plasma essential amino acids, especially branched-chain amino acids, and decreases cortisol and 3-methylhistidine, while plasma urea and creatinine remain unchanged.
The proportion of the elderly is high and steadily rising in Western populations . Aging is associated with an involuntary and progressive but physiological loss of muscle mass, designated sarcopenia , which is currently considered an emerging problem of Public Health . Sarcopenia is accompanied by a reduction in strength and quality that leads to muscle weakness, limiting mobility and increasing vulnerability to injury [1, 3]. Reduced muscle mass in older adults has also been associated with susceptibility to disease and decreased survival rates after critical illness .
Skeletal muscle is the body's main reservoir of amino acids, which contain 50-75% of human body proteins. Skeletal muscle is a vital supplier of amino acids for use as fuel by the brain and immune system and as a substrate for tissue repair during malnutrition, injury, and disease . It is important to maintain the body protein mass in order to live well and remain physically independent.
It has been postulated that age-related muscle mass reduction is due to a multi-factorial process that include genetic and other factors such as cellular apoptosis, changes in protein metabolism, hormonal alterations, loss of neuromuscular function, inappropriate nutrition, lack of regular physical activity, and diseases or their sequelae . The mechanisms underlying the loss of skeletal muscle are not clear but can be linked to a preceding disruption in the regulation of muscle protein turnover, specifically to an imbalance between protein synthesis and breakdown . It has been demonstrated that the combination of prolonged inactivity and hypercortisolemia increases muscle protein catabolism and reduces muscle protein synthesis, even when substrates are available . Likewise, hypercortisolemia has been observed in hypoalbuminemic individuals . Albumin is a good marker of protein malnutrition, and lower concentrations are commonly observed in older subjects and have been associated with poor health outcomes and mortality .
Inflammatory cytokines such as interleukin (IL)-6 and tumor necrosis factor alpha (TNF-α) contribute, together with a reduced concentration of growth factors, to the development of sarcopenia . Insulin resistance (IR) is also implicated in sarcopenia and is frequently observed in elderly subjects, although it is mostly associated with obesity and, recently, with sarcopenic obesity .
Co-ingestion of protein and leucine stimulates muscle protein synthesis rates to the same extent in young and elderly lean men , and the intake of nutrients and proteins affects the albumin synthesis rate in humans . Ingestion of 15 g/d of whey protein, containing 6.5 g of essential amino acids (EAA), has been reported to be strongly anabolic to skeletal muscle in healthy older individuals . Enteral nutrition (EN) formulas are prescribed to elderly patients, when it is necessary, as an exclusive diet or in combination with other foods to achieve recommended dietary intakes. With this background, the aim of this study was to evaluate the effect of a six-month exclusive protein-enriched enteral diet with a relatively high content of branched-chain amino acids (BCAA) and other essential amino acids on albuminemia, cortisolemia, plasma amino acids, IR, and inflammation biomarkers in elderly patients subjected to total enteral nutrition.
An experimental, prospective, intention-to-treat clinical trial was performed in elderly patients recruited from the Clinical Nutrition and Dietetics Outpatient Unit of the Virgen de las Nieves University Hospital (Granada, Spain). The patients were fed exclusively on an essential amino acid-enriched enteral diet for 6 months. The protein blend comprised 50% caseinate, 25% whey protein, and 25% pea protein (T-Diet Plus®, from Vegenat S.A.). A previous study reported the protein efficiency ratio (PER) of this blend to be 4.04 and the apparent digestive coefficient to be 93.91% .
Patients received 1500 mL of this diet to meet their daily energy and nutritional requirements. The actual mean daily intake for the whole study period was 1266 ± 59 kcal. Table 1 shows the nutritional composition of the enriched protein enteral diet and Table 2 the amino acid composition. The diet was administered as a bolus using a nasogastric tube or via a stoma with a large-bore syringe. All patients received 1000-1200 mL of water daily to maintain optimal hydration status.
Thirty-two patients (25 female, 7 male; mean age 70.1 ± 3.7 yrs) from the Clinical Nutrition and Dietetics Outpatient Unit of our hospital participated in the study. Inclusion criteria were: age >65 years, prescription of total enteral nutrition for ≥6 months, and voluntary consent to participate. Exclusion criteria were: unstable clinical condition, fatal illness, inclusion in other clinical trial, or refusal to participate. The patient or next of kin was informed about the purpose and procedures of the study before written consent was obtained. The protocol was performed in accordance with the Declaration of Helsinki and approved by the Ethics Committee of our hospital. At the end of the experimental period, only 17 of the 32 enrolled patients remained in the study; 15 patients were lost to the study due to: refusal to continue in the study (n = 6), death (n = 4), change in diet (n = 3) (two moved to a nursing home in other province, and one was prescribed a specific formula for diabetics due to his clinical condition), and withdrawal of enteral nutrition (n = 2). Table 3 shows the baseline demographic and anthropometric characteristics of the subjects and their concomitant diseases and medication. A large proportion of patients had cognitive deficits and a history of cerebrovascular diseases and cardiovascular events. The majority were receiving gastric protectors and a large proportion psycho-drugs and anticoagulants.
No attempt was made to measure the weight or height of the patients, who were mostly bed-bound. Measurements were taken of the mid-arm circumference (MAC) and tricipital skinfold (TS). The MAC (in cm) was measured midway between the tips of the acromion and olecranon processes, using a flexible tape measure. The TS (in mm) was taken on the dorsal arm midway between the tips of the acromion and olecranon, using a caliper. These measurements were compared with reference tables for the elderly Spanish population classified by age and sex .
Fasting blood samples were obtained from patients between 8:00 and 10:00 am after 8-10 h overnight fasting at baseline (before diet) and again after 3 and 6 months of the study diet. Serum and plasma (EDTA-coated tubes from BD Vacutainer, Plymouth, UK) were separated by centrifugation (15 min at 1750 g) and immediately processed or divided into aliquots and frozen at -80°C until their analysis.
Plasma urea (Coefficient of Variation [CV 2.8%]), creatinine (CV 3.2%), albumin (CV 3%), and glucose (CV 1%) were determined by standardized spectrophotometric techniques using a Roche Hitachi Modular DDP clinical analyzer system (Roche Diagnostics Spain, S.L., Barcelona). Cortisol (CV 1.7%) and adrenocorticotropin hormone (ACTH) (CV 8.9%) were determined by chemiluminescence using a LIAISON Immunoassay Analyzer (Soaring S.T.A, Saluggia, Italy). Fasting insulin (CV 2.6%) was analyzed by standardized electrochemiluminescence using an E-170 Elecsys Modular Analytics system (Roche Diagnostics España, S.L., Barcelona). All biochemical analyses were performed in the Virgen de las Nieves University Hospital. IR was calculated by using the homeostatic assessment model (HOMA-IR), defined by the equation HOMA-IR = fasting glucose (mM) × fasting insulin (μU/mL)/22.5.
LINCOplex™kits (Linco Research, MO) were used on a Luminex® 200™System (Luminex Corporation, TX) to determine IL-6 (CV 7.8%), IL-8 (CV 7.9%), TNF-α (CV 7.8%) (Cat. #HADK2-61K-B), and adiponectin (CV 9.2%) (Cat. #HCVD1-67AK). C-reactive protein (C-RP) (CV 4%) was determined with a particle-enhanced turbidimetric immunoassay (PETIA) (Dade Behring Inc., IL).
Amino acid analysis
Plasma amino acids were determined by high-performance liquid chromatography (HPLC) using a Beckman system gold HPLC (Beckman Coulter Inc. Fullerton, CA), which includes a solvent module 126AA, post column reactor 232, detector 168, autosampler 508, and a 3×250-mm spherogel AA lithium column (sulfonated polystyrene-divinylbenzene copolymers), as previously described by Le Boucher et al . Lithium column eluents Li-292, Li-365, and Li-375 and trione ninhydrin reagent were from Pickering Laboratories (Mountain View, CA), and norleucine was from Sigma (St. Louis, MO).
Plasma cortisol, ACTH, urea, creatinine, IR, inflammation biomarkers, and amino acids are expressed as mean values with standard error of the mean (SEM). The anthropometric and albumin values are expressed as a percentage of reference values for healthy individuals . Variables were checked for normality and homogeneous variance by using the Kolmogorov-Smirnov and the Levene tests, respectively. As most of the data did not follow a normal distribution, the non-parametric Friedman test for three repeated measures was used to assess differences as a function of treatment time. The Wilcoxon test was used for post hoc comparisons to analyze specific differences between times. Percentages were compared using a chi-square test. Correlations between different variables were assessed using the rank Spearman test. A value of p < 0.05 was considered significant. SPSS 15.01 for Windows (SPSS Inc., Chicago, IL) was used for the data analyses.
No significant differences in anthropometric measurements were found between before and after consumption of the enriched-protein enteral formula for 6 months. However, the percentage of subjects with albumin below the normal plasma cut-off value fell from 18% at baseline to 0% at 6 months (Table 4).
As shown in Figure 1A, reductions from baseline values were observed in plasma ACTH (baseline, 15.37 ± 1.08 pmol/L; 3 months, 9.85 ± 0.83 pmol/L; 6 months, 9.56 ± 1.18 pmol/L; p = 0.004) and in plasma cortisol (baseline, 423 ± 23 nmol/L; 3 months, 361 ± 35 nmol/L, 6 months, (257 ± 29 nmol/L; p = 0.001).
Total plasma amino acids progressively increased (Figure 1B) from 1963 ± 195 μmol/L at baseline to 2809 ± 175 μmol/L at six months (p = 0.008); essential amino acids increased from 558 ± 64 μmol/L at baseline to 731 ± 34 μmol/L (p = 0.023) at three months and remained fairly constant later on. No changes were observed over the study period in plasma urea or creatinine (Figure 1C), which remained at normal concentrations, while 3-methylhistidine (Figure 1D) was unchanged at three months but lower (p = 0.003) at six months. Total plasma amino acids were negatively correlated with plasma cortisol (r = -0.406, P < 0.007).
Specific plasma amino acid concentrations are reported in Table 5. Between three and six months, there were increased concentrations of leucine (p = 0.002), valine (p = 0.006), cysteine (p = 0.002), citrulline (p = 0.006), glutamine (p = 0.008), asparagine (p = 0.001), phenylalanine (p = 0.015) and tyrosine (p = 0.017). In comparison to baseline values, threonine was higher at three months (p = 0.017) and arginine at six months (p = 0.004), while proline, histidine, and methionine were higher at three months (p = 0.048, p = 0.009, and p = 0.012, respectively) but the same as baseline concentrations at six months. Taurine increased progressively from baseline to six months (p = 0.001), while alanine, glycine, isoleucine, serine, glutamic and aspartic acids, lysine, ornithine, and hydroxyproline remained largely unchanged.
Amino acid indexes of nutritional and metabolic interest are shown in Table 5. The ratio of nonessential to essential amino acids (NEAA/EAA) was lower at three months (p = 0.041) but similar to baseline at six months. Between three and six months of the diet, BCAA, Cys/Met ratio, and Whitehouse index increased (p = 0.002, p = 0.002, p = 0.001, respectively) and the Ala/Leu and Ala/BCAA ratios decreased (p = 0.006, p = 0.012, respectively). The Ala/Thr was lower at six months than at baseline (p = 0.001). No changes were observed during the trial (at 3 or 6 months) in other indexes (Table 5) or in insulin, HOMA-IR, adiponectin, C-RP, IL-6, or IL-8 values (Table 6). TNF-α slightly increased from three to six months (p = 0.041).
The main findings of this study were that after six months on an exclusive diet of specific protein-enriched enteral formula with a relatively high content of BCAA and other EAA, elderly patients showed a decrease in plasma cortisol concentrations and an increase in total plasma amino acid concentrations, especially of the essential amino acids leucine, valine and the conditionally essential amino acids arginine and glutamine. The plasma concentration of 3-methylhistidine, a biomarker of protein breakdown, was also decreased in these patients, but no changes were observed in creatinine, IR, or inflammation biomarkers, except for a slight increase in TNF-α at 6 months. There was a trend to a decrease in the percentage of patients with albumin levels below normal range over the duration of the diet (P = 0.06, Kendall's tau b), thus, this percentage decreased to zero after six months of the exclusive diet. These results suggest that plasma albumin concentrations can be increased by an adequate amount and quality of amino acid intake.
The Aging and Body Composition  study reported an association between low serum albumin concentration and greater loss of skeletal muscle mass. Comparison of the fractional synthesis rate (FSR) of albumin between young and old individuals indicated that this rate was not affected by increasing age. However, the FSR was reduced in individuals with an inadequate protein intake due to a reduction in the availability of amino acid substrate . Moreover, the ingestion of 15 g/d of a mixture of EAA for 3 months in older women in a between meal fashion resulted in an increased basal FSR and improvement of the lean body mass , although these authors did not attempt to evaluate whether the inclusion of both EAA and NEAA would yielded the same results.
Efforts have been spent to mitigate sarcopenia in the elderly using a variety of hormones without satisfactory results . However, the oral ingestion of EAA stimulates muscle protein synthesis, without affecting muscle proteolysis [10, 11]. Sarcopenia has been associated with an elevated cortisol concentration, and ACTH and cortisol concentrations were reduced in our patients as a result of the protein-enriched enteral diet. Cortisol is known to stimulate the degradation and inhibit the synthesis of muscle proteins . One study of 26 middle-aged and 21 elderly men found a negative relationship between cortisol and muscle strength of the knee extensor , and another study found a negative relationship between cortisol and high physical performance in elderly subjects.
A major increase in leucine was achieved with the present diet, suggesting a possible increase in protein synthesis. In fact, leucine and insulin are the main regulators of body protein synthesis, which is mediated by the mTOR signaling pathway, involving type 1 phosphoinositide-3 kinase (PI3K) and protein kinase B (PKB/Akt) . Studies in old rats showed that protein synthesis was stimulated by supplementation with leucine . The same effect was observed by Rieu et al  in the elderly and by Koopman et al. in both elderly and young individuals . Recent studies indicated that a novel class type 3 PI3K, vacuolar protein sorting 34 (Vps34), which is stimulated by amino acids, primarily by leucine, increases the production of PI3P. PI3P recruits proteins containing FYVE or PX to enhance phosphorylation and activation of mTOR, which finally inhibits 4EBP-1 and activates S6K1 . Compared with the composition of the FAO/WHO reference protein intake , the enteral diet used in the present study supplied about twice the content of BCAA.
Some EAA and NEAA, including arginine, glutamine, and proline, are important regulators of key metabolic pathways that are necessary for maintenance, growth, reproduction, and immunity in organisms, enhancing protein secretion and improving health . Glutamine and proline metabolisms are interconnected via glutamate and pyrroline-5-carboxilate and both amino acids can serve as an important precursor for arginine . Glutamine participates in protein synthesis, gluconeogenesis, inter-organ nitrogen transfer, nucleic acid biosynthesis, immune response, regulation of cellular redox state, and ammonia detoxification  by shuttling ammonia to the gut and kidney for excretion and as a precursor to arginine and urea synthesis . Arginine is synthesized in the liver, but there is no net synthesis via the hepatic urea cycle, because there is high arginase activity to hydrolyze this amino acid. In adults, the endogenous synthesis of arginine involves the intestinal-renal axis . Citrulline is synthesized from glutamine, glutamic acid, and proline in the enterocyte, released from the small intestine, and taken up primarily by kidneys for arginine production. Besides the kidney, citrulline is readily converted into arginine in nearly all types of cells . In our study, citrulline increased from 3 to 6 month of the enteral diet, indicating that it provided sufficient substrates (i.e., glutamate and glutamine) for its synthesis and explaining the increased plasma arginine levels. The protein source used in the present study is not only rich in glutamine but also in proline (high proportion of casein) and arginine (pea protein content).
Other amino acids, such as those containing sulfur, are of importance in health. The major end-products of methionine and cysteine metabolism are glutathione (GSH), homocysteine, and taurine, which have key roles in the antioxidant defense system and in the intestinal immune response. GSH is the major intracellular low-molecular weight thiol and plays an important part in regulating the homeostasis of free radicals and cytoprotective events . The increase in cysteine levels between three to six months on our diet is of interest, because cysteine is the rate-limiting amino acid for GSH synthesis. There was also an increase in taurine, which participates in maintaining the antioxidant system and is the main component of the free amino acid pool of lymphocytes, indicating its potential importance in immune and proinflamatory responses. Taurine is also involved in detoxification, membrane stabilization, and retinal and cardiac function . Hence, dietary supplementation using a protein source with a high biological value and an adequate distribution of both essential and semi-essential amino acids  appears to be a good strategy to maintain plasma amino acid levels and reduce glucocorticoids and muscle breakdown in the elderly. Thus, a decrease in plasma 3-methylhistidine intake was achieved with our enteral diet, indicating a lesser protein breakdown, since this metabolite cannot be reincorporated into proteins after its release by protein degradation. Furthermore, there was no change in creatinine, a biomarker of protein degradation, suggesting maintenance of the muscular mass without reduction of the arginine pool.
An inflammatory state is usually present in sarcopenia, although it is more frequent in cancer patients. In the elderly, however, the degree to which sarcopenia is associated with a reduced insulin response and/or the presence of inflammatory factors is not clear. The increase in IL-6 with age is well documented. Bautman et al. observed an association between lower muscle performance and higher IL-6 levels in hospitalized geriatric patients , and Yende et al reported low quadriceps strength in elderly individuals with high levels of IL-6 and TNF-α . In the present study, the enteral diet produced no changes in IR or increase in inflammation biomarkers, (IL-6, IL-8 and C-RP), except in the case of TNF-α which increased but remaining within normal ranges, indicating that it did not induce an inflammatory state or influence levels of pro-inflammatory cytokines, while maintaining the homeostasis of nitrogen metabolism.
Our study has some limitations, including the large number of subjects who did not complete it, although its duration was sufficient for some specific metabolic changes to be observed. We were not able to measure the FSR or other parameters directly related to protein synthesis and muscle strength because of the clinical condition of our patients, with the majority having cognitive deficits.
Based on our findings, we can conclude that an enteral diet with a specific blend of protein source with a high proportion of BCCA, glutamate/glutamine, and arginine, among other essential and conditionally essential amino acids, increases plasma essential amino acids, especially leucine, and decreases cortisol and 3-methylhistidine, suggesting that protein synthesis is enhanced and protein degradation is reduced.
tumor necrosis factor alpha
essential amino acids
branched-chain amino acids
protein efficiency ratio
coefficient of variation
homeostatic assessment model
particle-enhanced turbidimetric immunoassay
high-performance liquid chromatography
SEM standard error of the mean
nonessential amino acids
fractional synthesis rate
protein kinase B
vacuolar protein sorting 34
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Authors would like to thank the patients and institutions that participated in the study. This study was financed by Vegenat S.A. Vegenat S.A. has designed the new formula for EN.
MP is a member of the Research and Development Department of Vegenat, the company that funded the present study, and she was involved in the development of the product T-Diet Plus. AG has no contractual relationship with Vegenat but participated in the product design as part of a research contract between the University of Granada Foundation and Vegenat (Contract n° 2388).
JO carried out the study, the statistical analyses and participated in the drafting of the manuscript; MDM was involved in the data analyses; RP participated in the amino acid and hormone analyses; CMA took part in the inflammatory biomarker analyses; MP conceived of the study and was responsible for the design of the product; RMT was involved in the study design and coordination of institutions; APC participated in the design of the product and the study; AG participated in the design of the product, was responsible for coordinating the study, and collaborated in the data analysis and drafting of the manuscript. All authors read and approved the final manuscript.
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Olza, J., Mesa, M.D., Poyatos, R.M. et al. A specific protein-enriched enteral formula decreases cortisolemia and improves plasma albumin and amino acid concentrations in elderly patients. Nutr Metab (Lond) 7, 58 (2010). https://doi.org/10.1186/1743-7075-7-58
- Essential Amino Acid
- Plasma Amino Acid
- Fractional Synthesis Rate
- Enteral Diet