Parenteral nutrition is a life-preserving therapy for patients unable to utilize their intestinal tract for nutritional gain. Parenteral nutrition, wherein all nutrition is supplied via the parenteral route, is used by over 350 000 patients annually in the USA, with ∼40 000 patients receiving home-based parenteral nutrition . Despite its nutritional benefits, parenteral nutrition administration is associated with significant complications, primarily infectious in nature. Although these adverse effects have been well documented, the cause of parenteral nutrition-associated septic complications is an area of ongoing investigation. The following review will discuss the inflammatory and infectious complications of parenteral nutrition administration in the setting of enteral nutrient deprivation and potential approaches to limit the impact of these complications for those who require the life-preserving treatment of parenteral nutrition.
THE CASE FOR EARLY ENTERAL BUT DELAYED PARENTAL NUTRITION
The importance of adequate nutrition is well documented, both for the medical and surgical patient. Perioperative malnourishment is associated with poor healing and decreased immunologic function [2▪▪]. The most advantageous mode of nutrition administration, enteral versus parenteral, has been studied extensively. Practically, both enteral and parenteral nutrition are associated with unique risks and complications. Parenteral nutrition is easier to administer and is well tolerated by most patients. In contrast, enteral nutrition is cheaper but more challenging to deliver and is associated with an increased percentage of patient intolerance. gastrointestinal upset, diarrhea, and distention often lead to discontinuation of enteral feeds which in turn leads to periods of undernourishment. In the setting of these practical considerations, morbidity and mortality data overwhelmingly support enteral nutrition. Many early studies focused on the infectious complications with data revealing decreased infection in those receiving enteral nutrition compared to matched patients placed on parenteral nutrition. Current recommendations advise early initiation of enteral nutrition. Studies of initiation of feeds within hours of their operative interventions have shown positive outcomes; mortality is reduced when enteral feeds are initiated within 48 h of ICU admission . In their recommendations regarding enteral feeds, the American Society of Parenteral and Enteral Nutrition guidelines cite multiple studies in which feeds were started within 24 h postoperatively. These patients displayed improved clinical outcomes compared to similar patients in which diet was introduced more slowly, including decreased infectious complications and decreased mortality. These results support their recommendations for early initiation of enteral nutrition, particularly in the critical care setting in which a significant amount of the study and benefit of early enteral feeds has been displayed.
With the known complications of perioperative malnourishment and benefits of early enteral feeds in the surgical patients, the question remained of when to initiate parenteral nutrition for ill patients who cannot meet caloric goals enterally . A recent systematic review by Bost et al. reviewed studies of early initiation versus late initiation of parenteral nutrition. Those in the early group were started on supplemental parenteral nutrition within 48 h of ICU admission, whereas the latter group was initiated on the 8th day after admission (if their caloric goals were not met in the interim). There was no significant difference in mortality, time on mechanical ventilation, time required for renal replacement therapy, days in the ICU, and a hospital stay. Given the equivocal findings and the higher infectious associations of parenteral nutrition administration, later administration of parenteral nutrition is recommended. Current recommendations continue to emphasize a preference for enteral feeding, with delayed administration of parenteral nutrition in adults until 7 days postoperatively with continued reassessment for parenteral nutrition need once initiated [2▪▪].
Despite the known advantages of enteral nutrition, a clinical population unable to tolerate enteral feeds exists. For these patients, parenteral nutrition is a life-sustaining treatment despite its risks. The complications associated with parenteral nutrition are multiple and include hepatic dysfunction, bacterial translocation, metabolic problems, and electrolyte derangements . The cause of these findings is multifactorial in nature, but several contributing factors have been identified: a shift in the mucosa-associated intestinal microbiome, an increased mucosal proinflammatory state, and a subsequent loss of epithelial barrier function (EBF).
ENTERAL DEPRIVATION AND THE INTESTINAL MICROBIOME
The connection between parenteral nutrition-associated sepsis and the gut microbiome was initially suggested by the finding that cultured organisms from the blood of parenteral nutrition-dependent patients are predominantly intestinal microbiota. This has been supported by animal models, and suggests a loss of intestinal EBF and subsequent translocation of gut microbes and bacteria-derived toxins. Although a gut origin of sepsis has been suggested in diverse scenarios of critical illness, this phenomenon has been increasingly observed in the setting of total parenteral nutrition (TPN), with convincing data based on animal models and emerging data from human studies.
First, the deleterious effects of enteral nutrient deprivation on EBF has been shown to occur independently of systemic nutrient delivery. A mouse model in which parenteral nutrition is administered while prohibiting enteral nutrition has demonstrated decreased EBF, as measured by reduced transepithelial resistance, loss of tight junction protein localization, and translocation of intestinally derived bacteria [6,7]. These changes are in contrast to animals that have undergone identical central venous cannulation with saline administration and oral feeding.
As total nutrient delivery remains unchanged between the fed and parenteral nutrition-dependent states, the means by which the nutrition is delivered must drive the changes seen with parenteral nutrition. Increasing evidence suggests a role for altered intestinal microbiota in mediating the proinflammatory effects of enteral nutrient deprivation. The human intestinal microbial population is diverse and plays a profound role in organism homeostasis. Among other roles, gut microbiota allow for the utilization of complex carbohydrates otherwise indigestible by human enterocytes and are necessary for the production of mucosa-maintaining nutrients such as short chain fatty acids. They also help modulate and bolster the host's immune system via cell interaction – primarily with cells of the lamina propria . Through this interaction bacteria can activate toll-like receptors (TLRs), which in turn modulate mucosal inflammation. Parenteral nutrition dependence has been shown to lead to a marked shift in mucosa-associated microbiota after 6 days of enteral deprivation . At the phylum level, this is notable for a reduction in Firmicutes and increased representation of proteobacteria, bacteroidetes, and verrucomicrobia.
The mechanism by which enteral deprivation leads to these changes in the microbiome are currently under investigation. Clearly, in the unfed state, the availability of luminal nutrients for bacterial metabolism is dramatically decreased. This alone might contribute to the survival of more resilient, and potentially more pathogenic, species. Host factors may also drive this microbial shift. Enteral nutrients stimulate the secretion of Paneth cell-derived antimicrobial peptides, and parenteral nutrition dependence has been shown to reduce Paneth cell function [10▪]. An increase in goblet cells, which secrete microbe-regulating mucin, has been observed with parenteral nutrition dependence, and may reflect a compensatory mechanism of the host in response to the altered microbial community.
Though a causal relationship between shifts in the microbiome and parenteral nutrition-associated inflammatory changes has yet to be demonstrated, animal studies have demonstrated a potential mechanism for luminal bacteria to initiate an inflammatory response. Host–microbiome interactions are mediated in part by myeloid cells of the host lamina propria . This interaction takes place via TLR signaling utilizing the membrane-associated protein, MyD88 . Interaction with luminal microbiota and the MyD88 receptor leads to increased expression of proinflammatory cytokines tumor necrosis factor alpha (TNFα) and interferon gamma (IFNγ). Along with increased inflammatory cytokines, this lamina propria interaction downregulates the T-regulatory cells normally present in the lamina propria, leaving the inflammatory cascade unregulated . The role of this bacterial sensing mechanism in the development of parenteral nutrition-associated inflammatory changes has been demonstrated using MyD88 knockout mice, where changes in mucosal inflammation and epithelial barrier function were prevented, despite similar changes in the gut microbiome.
INFLAMMATION AND LOSS OF EPITHELIAL BARRIER FUNCTION
To further understand this phenomenon, multiple inflammatory cytokines have been studied using the aforementioned parenteral nutrition mouse model. Two cytokines that are increased in the circulation of parenteral nutrition-dependent mice are TNFα and IFNγ. These cytokines are associated with epithelial cell apoptosis and loss of EBF integrity . To further study whether the increase of circulating cytokines leads to the loss of barrier function, experimental knockout models have been established. These knockout mice, which are unable to produce and release specific cytokines, allow for study of the individual inflammatory markers in the setting of parenteral nutrition administration. Based on these findings, the following mechanisms have been proposed.
An intact EBF is dependent on a multitude of factors and signaling cascades. A careful balance of growth factors and cell-cycle regulators are necessary to promote both EBF integrity and prevent cellular overgrowth. As previously mentioned, parenteral nutrition delivery results in an increase in TNFα expression. TNFα is commonly associated with cell death but is also key in the regulation of epithelial cell growth, primarily via its interaction with epidermal growth factor (EGF). EGF acts to promote EBF integrity and cell growth, it requires intact TNFα and Erb-1 signaling pathways. Erb-1 is reduced in parenteral nutrition administration, leading to a shift in the ratio of TNF and Erb-1 so that TNFα's primary role is that of cell destruction as opposed to cell growth . Potentiating the intestinal atrophy, TPN administration leads to decreases in both keratinocyte growth factor and glucagon-like peptide. Like EGF, these cellular mediators are associated with an intact epithelial cell barrier and their diminished presence in parenteral nutrition delivery contributes to decreased epithelial integrity.
TNFα incurs further EBF injury activation of downstream cellular mediators, myosin light chain kinase (MLCK), and nuclear factor-κB (NF-κB) . Briefly, TNF receptors lead to activation of MLCK, which when activated causes actin and myosin contractions on the surface of intestinal epithelial cells. This allows for dissociation of tight junction proteins, proteins necessary for an intact EBF. Further loss of function occurs with TNFα downstream activation of NF-κB. NF-κB initiates an inflammatory amplification cascade with potentiates unregulated inflammation and EBF deterioration.
In addition to upregulation of proinflammatory cytokines, there is a decrease in anti-inflammatory interleukin-10 (IL-10) in the setting of parenteral nutrition dependence. IL-10 is one of the most important regulators of the mucosal immune system and in its absence, the inflammatory cascade is left unchecked. IL-10 knockout mice display increased epithelial permeability and parenteral nutrition-dependent mice supplemented with exogenous IL-10 have increased EBF function . Loss of EGF leads to further EBF injury through its association with phosphatidylinositol 3-kinase/p-Akt signaling. EGF is important for P13k/p-Akt signaling and in parenteral nutrition dependency its decreased expression leads to diminished P13k/p-Akt signaling and resulting epithelial cell apoptosis. This finding has been corroborated through study of TPN-dependent mice inoculated with Akt-activating peptide who do not display the same epithelial cell loss .
The proinflammatory state associated with parenteral nutrition has disparate physiologic consequence. For example, another well-known complication associated with parenteral nutrition is cholestasis and liver injury, known as parenteral nutrition-associated liver disease, or PNALD. The cause of PNALD is incompletely understood, but the overall proinflammatory state displayed by patients receiving parenteral nutrition is one possible source. Pathologic findings in PNALD are notable for Kupffer cell hyperplasia and inflammation . One mechanism for this inflammation is increased lipopolysacharride Toll-like receptor-4 (TLR-4) activation in the context of EBF dysfunction and subsequent activation of Kupffer cells. In a study by El. Kasmi et al., small bowel permeability along with parenteral nutrition administration led to increased activation of Kupffer cells and liver injury. Both administration of parenteral nutrition and small bowel permeability were tested in isolation and neither resulted in PNALD in isolation. More recently, this model revealed an expansion of the gut microbial family Erysipelotrichaceae[15▪▪], with attenuation of PNALD after antibiotic treatment and reduction of this bacterial strain. This demonstrates a parallel role of parenteral nutrition-associated changes in the gut microbiome, intestinal inflammation, and altered gut immunity in the pathogenesis of both septic complications and liver injury.
The previously described findings have all been displayed in mice but human data are less abundant. Utilizing healthy volunteers, Buchman et al. reported loss of EBF in subjects maintained on parenteral nutrition for only 2 weeks, yet these losses were to a lesser degree than previously displayed in a murine model. In this human study group, parenteral nutrition dependency led to decreased mucosal thickness, increased villus cell count, and increased intestinal permeability . Recent work by our lab has revealed promising findings in human gut deprived of enteral nutrition [17▪]. Using small bowel harvested during loop ileostomy reversals, fed and unfed intestinal segments from the same patients were studied. Epithelial barrier function first was assessed by comparing transepithelial resistance (TER) in fed and unfed bowel. In unfed bowel, TER was decreased, indicating higher intestinal permeability. To confirm this phenomenon, tracer molecules were introduced to the gut lumen and found to be more likely to translocate in unfed bowel. Immunofluorescence was also used by staining tight junction proteins. Unfed samples showed decreased adherens proteins along with villus atrophy.
Parenteral nutrition administration is a life-preserving therapy for many patients, but it is not without risk. Infectious complications of parenteral nutrition have been well described but the exact pathophysiology of such complications is not fully elucidated. Increased inflammation and marked microbial changes are likely associated with the adverse effects seen. Areas of future study are vast. Environmental modifications, which allow for persistence of a benign microbial population in the setting of parenteral nutrition administration, would likely decrease the natural inflammatory response. Prevention of inflammation via blockade of different signaling cascades is another potential therapeutic option. Bolstering the EBF via EGF administration or direct enterocyte nutrition is another research pursuit we hope to take on in the near future.
Great gains in the understanding of the complications of parenteral nutrition have been made since its relatively recent introduction to the medical field. With continued utilization of both animal in human models of therapy, new treatment techniques will be founded and create a safer TPN for those who require its life-sustaining nutrition.
Financial support and sponsorship
This work was supported by NIH grant 2R01AI-44076-15.
Conflicts of interest
There are no conflicts of interest.
REFERENCES AND RECOMMENDED READING
Papers of particular interest, published within the annual period of review, have been highlighted as:
- ▪ of special interest
- ▪▪ of outstanding interest
1. Pfunter A, Weir L, Stocks C. Most frequent procedures performed in US hospitals, 2010: Statistical Brief #149. Healthcare Cost and Utilization Project (HCUP) Statistical Briefs. Rockville, MD.
2▪▪. Martindale RG, Warren M. Should enteral nutrition
be started in the first week of critical illness? Curr Opin Clin Nutr Metab Care 2015; 18:202–206.
This review provides an excellent summation of the most recent findings regarding the importance of enteral feeds in the critical care setting. The metabolic and immunologic benefits of enteral, even trophic,feedings are discussed.
3. Doig GS, Chevrou-Séverac H, Simpson F. Early enteral nutrition
in critical illness: a full economic analysis using US costs. Clinicoecon Outcomes Res 2013; 5:429–436.
4. Bost RB, Tjan DH, van Zanten AR. Timing of (supplemental) parenteral nutrition
in critically ill patients: a systematic review. Ann Intensive Care 2014; 4:31.
5. El Kasmi KC, Anderson AL, Devereaux MW, et al. Phytosterols promote liver injury and Kupffer cell activation in parenteral nutrition
-associated liver disease. Sci Transl Med 2013; 5:206ra137.
6. Demehri FR, Barrett M, Ralls MW, et al. Intestinal epithelial cell apoptosis and loss of barrier function in the setting of altered microbiota with enteral nutrient deprivation. Front Cell Infect Microbiol 2013; 3:105.
7. Feng Y, Teitelbaum DH. Tumour necrosis factor--induced loss of intestinal barrier function requires TNFR1 and TNFR2 signalling in a mouse model of total parenteral nutrition
. J Physiol 2013; 591:3709–3723.
8. Gourbeyre P, Berri M, Lippi Y, et al. Pattern recognition receptors in the gut: analysis of their expression along the intestinal tract and the crypt/villus axis. Physiol Rep 2015; 3:e12225–e12229.
9. Miyasaka EA, Feng Y, Poroyko V, et al. Total parenteral nutrition
-associated lamina propria inflammation in mice is mediated by a MyD88-dependent mechanism. J Immunol 2013; 190:6607–6615.
10▪. Heneghan AF, Pierre JF, Tandee K, et al. Parenteral nutrition
decreases paneth cell function and intestinal bactericidal activity while increasing susceptibility to bacterial enteroinvasion. JPEN J Parenter Enteral Nutr 2014; 38:817–824.
Administration of parenteral nutrition in the setting of enteral deprivation results in decreased Paneth cell function. This work expands on previous studies and further shows loss of bactericidal activity associated with the loss of Paneth cells.
11. Davies JM, Abreu MT. Host-microbe interactions in the small bowel. Curr Opin Gastroenterol 2015; 31:118–123.
12. Xiao W, Feng Y, Holst JJ, et al. Glutamate prevents intestinal atrophy via luminal nutrient sensing in a mouse model of total parenteral nutrition
. FASEB J 2014; 28:2073–2087.
13. Freeman JJ, Feng Y, Demehri FR, et al. TPN-associated intestinal epithelial cell atrophy is modulated by TLR4/EGF signaling pathways. FASEB J 2015; [Epub ahead of print].
14. Jung WY, Kang JH, Kim KG, et al. Human adipose-derived stem cells attenuate inflammatory bowel disease in IL-10 knockout mice. Tissue Cell 2015; 47:86–93.
15▪▪. Harris JK, El Kasmi KC, Anderson AL, et al. Specific microbiome
changes in a mouse model of parenteral nutrition
associated liver injury and intestinal inflammation. PLoS One 2014; 9:e110396.
Different lipid formulations were utilized for parenteral formulas. These unique lipid formulas resulted in changes in the enteric bacteria in mice. These alterations were seen to result in increased liver injury suggesting the microbiome as an etiology and potential therapeutic target for treatment of parenteral associated liver injury.
16. Buchman AL, Moukarzel AA, Bhuta S, et al. Parenteral nutrition
is associated with intestinal morphologic and functional changes in humans. JPEN J Parenter Enteral Nutr 1995; 19:453–460.
17▪. Ralls MW, Demehri FR, Feng Y, et al. Enteral nutrient deprivation in patients leads to a loss of intestinal epithelial barrier function. Surgery 2015; 157:732–742.
Single center study of epithelial barrier function in fed and unfed bowel utilizing human bowel resection tissue. This work is of special interest as not only does it show loss of EBF in enterally deprived bowel but enterally deprived human bowel, a tissue sample not frequently described.