Probiotics for Diarrhea in Children

when administered in adequate amounts, confer a health benefit to the host” [6]. Following this, the Article ABSTRACT Diarrhea remains the second leading cause of death in children below 5 years of age; in addition it is also the reason for a considerable morbidity in children of all ages throughout the globe. Apart from oral rehydration solution, continued feeding, oral zinc and antibiotics for diarrhea of bacterial etiology, there have been no other proven measures for diarrheal illnesses in children. Probiotics are non-pathogenic live microorganisms. When ingested, probiotics can survive passage through the stomach and small bowel. Probiotics are supposed to have preventive as well as curative effects on several types of diarrhea of different etiologies.


Introduction
Diarrheal disease is responsible for a huge burden on human society. Even with improvements in the case management, diarrhea is responsible for 1.5 million deaths annually, or 1% of deaths in children under 5 years. Although the majority of these deaths occur in the developing world, it is a common reason for medical consultation and hospital admission in Western societies and exacts an enormous social toll in terms of loss of productivity among affected individuals and their caregivers [1].
Probiotics, commonly known as "good bacteria" can offer health benefits in a number of ways when consumed. The use of probiotic microorganisms for the prevention or therapy of gastrointestinal disorders is an obvious measure and perhaps the most usual application of probiotics because most health effects attributed to them are related directly or indirectly to the gastrointestinal tract [2]. In this review, we summarize the available evidence on the use of probiotics for diarrheal diseases in children.

The indigenous intestinal flora
There are an estimated 1014 cells in human body, and out of this only 10% are not bacteria. The gastrointestinal tract of mammals is a complex, dynamic and diverse ecosystem comprising of interactions between aerobic and anaerobic, nonpathogenic bacteria. There are 400 separate species in this complex yet stable colony. The majority of the gut organisms, which represent 40% of the fecal weight, are accounted for by luminal flora; nevertheless, the organisms present in the fecal matter do not necessarily signify the important host-microbial symbiosis of the mucosal bound flora [10]. Within first few days after birth, the newborn's gut is colonized with bacteria. A diverse range of bacteria inoculates the gut initially; this includes Bifidobacteria, Enterobacteria, Bacteroids, Clostridia, and Gram-positive cocci. Later on, there are swift changes in the flora depending on the mode of delivery, gestational age, and diet (breastfeeding/ formula feeding). Vaginally delivered breastfed infants have similar colonization to vaginally born formula-fed infants at 48 hours of life, indicating a similar "inoculums". However, by 7 days, only 22% of breastfed infants are colonized with B. fragilis, as compared to 61% of those fed on formula [11]. Interestingly, there is a minimal role of diet in the composition of fecal flora in the older child and adult [12].
Fungi are present in the stools of up to 65% of individuals, Candida being the predominant genus. It appears that pathogenic colonization by yeast, under normal circumstances, is inhibited by the normal bacterial flora. However, alteration or destruction of the fecal flora by antibiotics would lead to yeast multiplying in great numbers [13].

Mechanism of action of probiotics in diarrhea
Although animal and molecular studies have generated a great deal of data, most theories remain speculative and confirmation of findings in vivo and in human clinical trials have been lacking. Almost certainly multiple mechanisms operate together and it is clear that single strains may act using different mechanisms in different disease processes [14].
Luminal: Many probiotic organisms elaborate 'bacteriocins', restricting the growth or pathogenicity of non-homologous strains. Other probiotic activities including the production of lactic acid, short chain fatty acids and hydrogen peroxide lower intraluminal pH and contribute to a hostile environment for other potentially pathogenic species. Some probiotic products, Journal of Medical Research and Innovation. 2017 May-Aug, Volume 1(2): AV5-AV12 P a g e | AV7 such as proteases produced by Saccharomyces boulardii have been shown to degrade toxins produced by pathogens such as Clostridium deficile, Vibrio cholera or pathogenic Escherichia coli [15]. Additionally, probiotics metabolic activity may have useful nutritional or clinical activity. It has long been appreciated that the enzyme ß-galactosidase produced by lactobacilli may be useful in preventing diarrhea in individuals with acquired deficiency of this enzyme [16].
Mucosal: Some probiotic agents are able to bind directly to invasive species or to otherwise disrupt their ability to interact with or bind to endothelial receptors. Probiotics including several species of Lactobacillus have been shown to upregulate goblet cell production of mucins and protective 'trefoil factors'. They also stimulate crypt located Paneth cells in the production of 'defensins', cationic proteins which are able to insert themselves into microbial membranes to form destructive pores. In addition, probiotics may also influence proteins controlling tight junctions between enterocytes, reducing the potential for the absorption of harmful macromolecules and the ability of luminal pathogens to translocate into the submucosal space [17].
Submucosal: Critical to the development of innate immunity is the system for recognizing microbe-associated molecular patterns (MAMPs)-conserved regions comprising motifs or repeating units from a wide range of molecules including lipopolysaccharides, peptidoglycans, and nucleic acids found more frequently on the surface of microbial species than on host cells. These pattern recognition receptors (PRRs) including the toll-like receptors (TLR) on the surface of host cells (including dendritic cells in the gut) are key determinants of detection and host interaction directing subsequent effector response [18]. Adaptive immune responses have also been shown to be influenced by the presence of probiotic organisms, some of which are able to stimulate immunoglobulin (particularly secretory IgA) production and to modulate the development and activity of regulatory T-lymphocytes. Similarly, probiotics are known to influence the pattern of cytokine release as well.
It is likely that host-microbe signaling takes place continuously rather than awaiting recruitment at the time of disease. The potential for probiotics to influence this series of interactions through the activation of NF-ĸß, thereby controlling DNA transcription, the inflammatory response and the balance of TH1/TH2 activation, hold exciting promise for the ability of these agents to influence chronic inflammatory processes [19]. Such effects are also likely to be important in modulating the immune response to acute infection within the gastrointestinal tract.
The molecular interactions between host and microbiota have been shown to have an influence on the enteric nervous and endocrine systems. Experimental work has identified the activity of certain probiotic species in inducing opioid and cannabinoid receptors in the gastrointestinal tract as well [20].

Probiotics for bacterial diarrhea
Two studies of Lactobacillus rhamnosus GG found no evidence of protection for the 15-20% of children with 'invasive' pathogens, principally Salmonella or Shigella [33]. In the only study specifically addressing bacterial disease, there was an earlier resolution of diarrhea for LGG (co-treated with trimethoprim-sulfamethoxazole) during an outbreak of Shigella dysentery in Estonia [34]. Hwe et al [35] described an AV8 | P a g e Journal of Medical Research and Innovation. 2017 May-Aug, Volume 1(2): AV5-AV12 improvement in stool consistency for 20 children with pathogenic E. coli cultured from the stool. However, a threespecies probiotic mixture including Escherichia faecium was not found to significantly reduce the duration of diarrhea due to Salmonella or Campylobacter in Taiwan [25]. Several studies using combination probiotic products (S. boulardii or E. coli Nissle 1917) in middle-income countries report overall efficacy for groups with significant (10-20%) contributions from pathogenic species but sufficient data is not provided to assess efficacy by diarrheal pathogen [36,37,38,39].
A large community prevention study from India [27] documented a reduction of diarrheal disease with Aeromonas and Cryptosporidium species in Lactobacillus casei Shirota recipients; though other bacteria (including pathogenic E. coli), viral and protozoal species were recovered at equivalent rates.
Another study from urban India reported protection against dysentery (defined by a parental history of bloody diarrhea), although no impact was seen on the overall incidence of diarrhea [40].

Probiotics for parasitic diarrhea
A Cuban study in children with persistent diarrhea (35 out of 40 having giardial cysts in stool) improved with administration of S. boulardii [41]. In cases of amoebic dysentery, reduced duration of bloody diarrhea and a lower rate of cyst excretion on day 5 are reported in 25 Turkish children receiving Saccharomyces [41]. A randomized trial in 48 symptomatic children with Blastocystis hominis demonstrated higher rates of clinical cure and disappearance of cysts from the stool with probiotics [43].

Probiotics for Clostridium defficile associated diarrhea (CDAD)
Although a meta-analysis performed by McFarland for the treatment of CDAD found evidence in favor of treatment with S. boulardii [44], the Cochrane group and other reviewers [45,46,47] have conclude that despite holding promise, currently data are not sufficient to make a recommendation for the use of Saccharomyces or other Probiotics for the treatment of primary or relapsing CDAD.
Five published studies of the use of Saccharomyces in the prevention of antibiotic-associated diarrhea (AAD) have provided secondary outcome measures for CDAD. Reviewers [45, 48,49] have concluded that inadequate evidence currently exists in order to make a recommendation concerning the role of S. boulardii or other Probiotics in the primary prevention of CDAD.

Probiotics for antibiotic associated diarrhea (AAD)
There have been no published RCT investigating the effect of Probiotics for the treatment of non-Clostridium defficile AAD in children; thus, their use cannot be recommended at this time.
A Cochrane meta-analysis of probiotic use of children to prevent or ameliorate (i.e. shorten duration and/ or severity) AAD [50] documents that probiotics produced a statistically significant reduction in the incidence of AAD (RR 0.52; 95% CI 0.38-0.72) with the number needed to prevent one case of AAD being 7. Analysis of secondary outcomes revealed that probiotics decreased the mean duration of diarrhea by threequarters of a day. The difference in mean stool frequency was not statistically significant. Analysis by probiotic strain revealed a significant effect for LG and Lactobacillus sporogenes but not for boulardii.

Probiotics for traveler's diarrhea
Several studies using lactobacilli have suggested benefit in protecting travelers from diarrhea, but in only one study using a mixture of strains (containing Lactobacillus acidophilus, Lactobacillus bulgaricus, Bifidobacterum bifidum and Streptococcus thermophilus) was the reduction in the overall incidence of diarrhea statistically significant [51]. Travelers to a variety of destinations including North Africa, South America, India and Turkey derived some measure of protection from S. boulardii [52]. Several attempts have been made to conduct meta-analysis from these data, estimating risk ratios marginally in favor of probiotics (RR estimates between 0.85 and 0.93) but with confidence intervals close to or encompassing the point of equivalence [53,54,55].

Probiotics for diarrhea in children attending day care centers
One RCT documented that a daily administration of L. reuteri for 3 months in 336 otherwise healthy, Mexican children attending day care centers a significant reduction in the number of episodes of diarrhoea, episodes of diarrhoea per child, mean duration of diarrhoea episodes and days with diarrhea per child both during the intervention and for the next 3-month follow-up period compared to the placebo group [56]. Another RCT carried out in malnourished Indonesian children found that the consumption of regular calcium milk with L. reuteri compared with regular calcium milk alone reduced the risk of diarrhoeal disease [57]. A double-blind RCT from Croatia in 210 children attending daycare centers found that that B. animalis subsp. lactis BB-12 given for months had no effect on the prevention of gastrointestinal [58].

Probiotics for persistent diarrhea
A Cochrane review of probiotics for persistent diarrhea [59] yielded a pooled estimate for reduction in the mean duration of diarrhea from 9 to 4 days, with significantly fewer stools on day 5 (a reduction from a mean of 5 to fewer than 2 stools per day).

Probiotics for acute diarrhea of undetermined etiology
A 2010 Cochrane database of systematic review provides a meta-analysis of 63 studies of probiotic agents involving more than 8000 participants, mostly children, conducted in a variety of geographical and social settings [21]. Overall conclusions suggest that probiotics shorten the duration of diarrhea by 24 hours {95% confidence interval (CI) 16-33 hours} and for a mean difference in stool frequency on day 2 of 0.8 (95% CI 0.4-1.1), with a relative risk of continuing diarrhea on day 4 of 0.4 (95% CI 0.3-0.5). No adverse effects were attributed in these studies to the administration of the probiotic.
There is still clearly much to learn about how best to use probiotics in acute diarrheal disease. Only a few studies have directly compared probiotic products [60][61][62][63] or ranged doses [64,65]. The Cochrane review [21] [78] have concluded that preparations containing probiotics (of the specific strains studied in these trials) both shorten the duration and reduce the severity of acute diarrhea in children.

Safety of probiotics
Probiotics are considered 'generally recognized as safe' (GRAS) and well tolerated in humans but case reports have described bacteremia and fungemia secondary to probiotics. For example, there is a report of a 1-year-old immunocompetent child developing fungemia after receiving S. boulardii for gastroenteritis [79]. The Mayo Clinic reported eight immunocompromised patients post-liver transplant having positive blood culture for Lactobacillus [80]. Furthermore, two infants with short bowel syndrome were found to be bacteremic withprobiotic strains of Lactobacillus GG [81]. Longterm use of probiotics under antibiotic selection pressure could cause antibiotic resistance, and the resistance gene could be transferred to other bacteria [82]. The committee on Nutrition of the European Society of Pediatric Gastroenterology, Hepatology and Nutrition concluded that more studies are required to establish the safety and efficacy of probiotics in children. Till date safety of probiotics is established in healthy infants and children. Caution should be exercised when using these in immunocompromised patients or those with indwelling central venous catheters. It is out of the purview of The American Food and Drug Administration to establish a formal regulatory category for functional foods that includes probiotics. Variations in products do exist and some studies have even found that certain preparations contain no viable bacteria.

Conclusion
A low-cost probiotic intervention capable of reducing the risks of diarrhea in the early years of life, even with modest efficacy, would have an enormous impact on the developing world. Assuming that efficacy is confirmed for prevention and treatment of childhood diarrhea in these settings, a great deal of work will be needed for its broad implementation.