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This is a fact canvas intended for wellness professionals. For a reader-friendly overview of Probiotics, come across our consumer fact sheet on Probiotics.

Introduction

The International Scientific Association for Probiotics and Prebiotics defines "probiotics" as "alive microorganisms that, when administered in acceptable amounts, confer a wellness do good on the host" [1]. These microorganisms, which consist mainly of leaner but as well include yeasts, are naturally present in fermented foods, may exist added to other food products, and are bachelor equally dietary supplements. However, non all foods and dietary supplements labeled as "probiotics" on the market accept proven wellness benefits.

Probiotics should not be confused with prebiotics, which are typically complex carbohydrates (such equally inulin and other fructo-oligosaccharides) that microorganisms in the gastrointestinal tract employ as metabolic fuel [two]. Commercial products containing both prebiotic sugars and probiotic organisms are often called "synbiotics." In addition, products containing dead microorganisms and those made past microorganisms (such every bit proteins, polysaccharides, nucleotides, and peptides) are, past definition, not probiotics.

Identification
Probiotics are identified past their specific strain, which includes the genus, the species, the subspecies (if applicable), and an alphanumeric strain designation [iii]. The seven core genera of microbial organisms most often used in probiotic products are Lactobacillus, Bifidobacterium, Saccharomyces, Streptococcus, Enterococcus, Escherichia, and Bacillus. Table 1 shows examples of the classification used for several commercial strains of probiotic organisms.

Table one: Classification for sample commercial strains of probiotics [three]
Genus Species Subspecies Strain Designation Strain Nickname
Lactobacillus rhamnosus none GG LGG
Bifidobacterium animalis lactis DN-173 010 Bifidus regularis
Bifidobacterium longum longum 35624 Bifantis

Mechanisms of action
The human gastrointestinal tract is colonized by many microorganisms, including leaner, archaea, viruses, fungi, and protozoa. The activity and composition of these microorganisms (collectively known equally the gut microbiota, microbiome, or abdominal microflora) can affect human health and illness.

Probiotics exert their effects usually in the alimentary canal, where they may influence the intestinal microbiota. Probiotics tin can transiently colonize the human being gut mucosa in highly individualized patterns, depending on the baseline microbiota, probiotic strain, and alimentary canal region [four].

Probiotics also exert health effects by nonspecific, species-specific, and strain-specific mechanisms [1]. The nonspecific mechanisms vary widely amidst strains, species, or even genera of ordinarily used probiotic supplements. These mechanisms include inhibition of the growth of pathogenic microorganisms in the gastrointestinal tract (by fostering colonization resistance, improving intestinal transit, or helping normalize a perturbed microbiota), production of bioactive metabolites (e.yard., short-chain fatty acids), and reduction of luminal pH in the colon. Species-specific mechanisms tin can include vitamin synthesis, gut bulwark reinforcement, bile salt metabolism, enzymatic activity, and toxin neutralization. Strain-specific mechanisms, which are rare and are used by only a few strains of a given species, include cytokine production, immunomodulation, and effects on the endocrine and nervous systems. Through all of these mechanisms, probiotics might have wide-ranging impacts on human wellness and disease.

Because effects of probiotics can be specific to certain probiotic species and strains, recommendations for their utilize in the dispensary or in enquiry studies need to exist species and strain specific [3,5,vi]. Furthermore, pooling data from studies of different types of probiotics can result in misleading conclusions about their efficacy and rubber.

Sources of Probiotics

Food
Fermented foods are fabricated through the growth and metabolic activeness of a variety of alive microbial cultures. Many of these foods are rich sources of live and potentially beneficial microbes. Some fermented foods, such equally sourdough bread and most commercial pickles, are processed after they are fermented and do not contain alive cultures in the class in which they are consumed. Many commercial yogurts, another type of fermented nutrient, contain probiotic microorganisms, such as Lactobacillus bulgaricus and Streptococcus thermophilus.

The alive microorganisms used to make many fermented foods, including yogurt, typically survive well in the production throughout its shelf life. Still, they usually practise non survive transit through the stomach and might not resist degradation in the small intestine past hydrolytic enzymes and bile salts and, therefore, might not attain the distal gut [7,8]. Notwithstanding, legitimate probiotic strains contained in yogurt or other foods exercise survive intestinal transit.

Fermented foods that incorporate live cultures but do not typically contain proven probiotic microorganisms include many cheeses, kimchi (a Korean fermented cabbage dish), kombucha (a fermented tea), sauerkraut (fermented cabbage), miso (a fermented soybean-based paste), pickles, and raw unfiltered apple cider vinegar made from fermented apple sugars [8].

Certain unfermented foods, such every bit milks, juices, smoothies, cereals, nutrition confined, and baby and toddler formulas, have added microorganisms. Whether these foods are truly probiotics depends on the microorganism levels they comprise when they are eaten, whether they survive abdominal transit, and whether their specific species and strains have health effects.

Dietary supplements
Probiotics are likewise bachelor equally dietary supplements (in capsules, powders, liquids, and other forms) containing a wide variety of strains and doses [9]. These products often contain mixed cultures of live microorganisms rather than single strains. The effects of many commercial products containing "probiotics" take non been examined in research studies, and it is difficult for people not familiar with probiotic inquiry to determine which products are backed by prove. All the same, some organizations accept systematically reviewed the bachelor evidence and developed recommendations on specific probiotics—including appropriate product, dose, and formulation—to employ for preventing or treating various health atmospheric condition [iii,10].

Probiotics are measured in colony forming units (CFU), which point the number of feasible cells. Amounts may exist written on product labels as, for example, i x tennine for one billion CFU or 1 10 1010 for 10 billion CFU. Many probiotic supplements contain 1 to ten billion CFU per dose, but some products contain up to 50 billion CFU or more. However, higher CFU counts practise not necessarily improve the product'due south health furnishings.

Electric current labeling regulations simply require manufacturers to list the total weight of the microorganisms on probiotic products' Supplement Facts labels; this cellular mass tin can consist of both live and dead microorganisms and, therefore, has no relationship with the number of feasible microorganisms in the product [11]. Manufacturers may at present voluntarily list the CFUs in a product in addition to full microorganism weight on the Supplement Facts label. Because probiotics must be consumed alive to have health benefits and they tin can die during their shelf life, users should look for products labeled with the number of CFU at the end of the product's shelf life, not at the time of industry.

Probiotics and Health

The potential health benefits of probiotics are the focus of a great bargain of scientific research. This department focuses on research on the employ of probiotics to forbid or treat vii health conditions: atopic dermatitis, pediatric astute infectious diarrhea, antibiotic-associated diarrhea, inflammatory bowel disease, irritable bowel syndrome, hypercholesterolemia, and obesity.

Atopic dermatitis
Atopic dermatitis, the most common course of eczema, is also i of the well-nigh mutual chronic inflammatory pare disorders, affecting approximately 15% to xx% of children and 1% to 3% of adults worldwide [12].

Numerous probiotic studies accept evaluated the effects of diverse species and strains of leaner on the prevention of atopic dermatitis, and several meta-analyses have synthesized the findings of these studies. These studies and meta-analyses show that exposure to probiotics during pregnancy and in early infancy might reduce the hazard of developing atopic dermatitis in children. For case, a 2018 meta-analysis included 27 randomized controlled trials (RCTs) and 1 controlled cohort written report in a total of 6,907 infants and children exposed to probiotics in utero for 2 weeks to 7 months (via maternal oral supplementation) and/or by oral administration to the infants later birth for ii to 13 months [13]. Between ages 6 months and 9 years, probiotic treatment with unmarried strains or mixtures that included Lactobacillus, Bifidobacterium, and Propionibacterium strains significantly reduced the hazard of atopic dermatitis from 34.7% in the control group to 28.5% in the probiotic grouping.

Subgroup analyses showed that the use of probiotics during both the prenatal and postnatal periods significantly reduced the incidence of dermatitis; even so, probiotics taken either prenatally only or postnatally merely did non. In addition, the effects of probiotic treatment varied by probiotic strain. For instance, supplementation with either Lactobacillus rhamnosus or Lactobacillus paracasei significantly reduced the incidence of atopic dermatitis, whereas supplementation with Lactobacillus reuteri or Lactobacillus acidophilus did not.

In contrast, another meta-analysis of 5 randomized clinical trials with a total of 889 participants found that Lactobacillus rhamnosus GG (LGG) supplementation did not reduce the risk of eczema in children upwards to age iv years, regardless of the timing of administration (to the mothers during pregnancy and/or during breastfeeding or to the infants directly) [14].

Most published meta-analyses have shown that probiotics slightly reduce atopic dermatitis symptoms in infants and children. For example, a meta-assay of 13 RCTs with a total of i,070 participants aged 18 years or younger found that probiotic treatment for 4 to viii weeks of those with atopic eczema significantly reduced SCORing Atopic Dermatitis (SCORAD) values, indicating reduced symptom severity [15]. Subgroup analyses found probiotics had protective effects in children aged one to xviii years (nine trials) but not in infants younger than 1 year (five trials). In add-on, handling with Lactobacillus, Lactobacillus fermentum, or a mixture of probiotic strains, significantly reduced SCORAD values in the children, whereas Lactobacillus rhamnosus GG and Lactobacillus plantarum had no issue.

Another meta-assay included 8 randomized clinical trials with a total of 741 participants from nativity to 36 months of age who were treated with Lactobacillus or Bifidobacterium for 4 to 24 weeks. The results also suggested that probiotics containing Lactobacillus might reduce atopic dermatitis symptoms in infants and toddlers, merely those containing Bifidobacterium did non [16]. The handling significantly improved symptoms in participants with moderate-to-severe forms of the affliction but non in those with balmy forms. A Cochrane review of 39 RCTs of single probiotics and probiotic mixtures for the treatment of eczema in 2,599 participants aged 1 to 55 years (nigh were children) establish that probiotic treatment might slightly reduce SCORAD scores. However, the researchers concluded that the differences were not clinically significant and that the electric current evidence does not support the utilise of probiotics for eczema treatment [17].

Overall, the available show suggests that the employ of probiotics might reduce the risk of developing atopic dermatitis and lead to meaning reductions in atopic dermatitis SCORAD scores, but these products might provide only express relief from the condition. Furthermore, the effects of probiotics vary by the strain used, the timing of assistants, and the patient's age, then it is hard to make recommendations.

Pediatric acute infectious diarrhea
Acute diarrhea is usually defined as loose or liquid stools and/or an increment in the frequency of bowel movements (typically at least three in 24 hours) [xviii]. Acute diarrhea can be accompanied by fever or airsickness, and information technology usually lasts no more than than vii days.

A Cochrane review of 63 RCTs in a full of 8,014 participants (primarily infants and children) found that single- and multi-strain probiotics significantly shortened the elapsing of acute infectious diarrhea by almost 25 hours. These supplements also decreased the risk that the diarrhea would last iv or more than days by 59% and led to approximately ane less bowel motion on the second twenty-four hours in patients who received probiotics compared with patients who did non [19].

An assessment of eleven randomized clinical trials with a total of 2,444 participants showed that Lactobacillus rhamnosus GG is near effective in treating infectious diarrhea at a daily dose of at least tenten CFU [20,21]. A review of 22 randomized clinical trials with a total of 2,440 participants aged 1 month to 15 years found that Saccharomyces boulardii (most commonly 10ix to 10ten CFU/twenty-four hour period for five–x days) reduced both duration of diarrhea and stool frequency [22]. In both of these analyses, Lactobacillus rhamnosus GG and Saccharomyces boulardii reduced the duration of acute infectious diarrhea by approximately one day. However, two subsequent clinical trials found that a five-day course of LGG (1x1010 CFU twice per day taken alone in i trial and a total of 4x109 CFU twice per twenty-four hours of LGG and 50. helveticus R0052 in the other) was no amend than placebo at treating or improving the outcomes of acute gastroenteritis in 1,729 infants and small children presenting to pediatric emergency departments [23,24].

Based on a requirement of at least two adequate and well-controlled studies, each convincing on its own, to constitute an intervention's effectiveness, the European Society for Pediatric Gastroenterology, Hepatology, and Diet identified ii probiotic supplements, Lactobacillus rhamnosus GG (typically at ≥ten10 CFU/day for 5–7 days) and Saccharomyces boulardii (typically at 250–750 mg/day [x9–10ten CFU] for 5–7 days), for which evidence supported utilise as adjuncts to rehydration for managing astute infectious diarrhea in pediatric patients [x]. Yet, contempo studies suggest that probiotics might not be efficacious in developed country emergency departments because most episodes of acute infectious diarrhea are cocky-limiting and crave no handling other than rehydration therapy [23,24]. Therefore, the cost-effectiveness of the use of probiotic supplements to manage astute viral diarrhea lacks consensus [x,19].

Antibiotic-associated diarrhea
Antibiotics are some other mutual crusade of acute-onset diarrhea. Antibiotic treatment frequently disturbs the intestinal microbiome and, by decreasing microbial diversity, can lead to a loss of microbial metabolism (resulting in osmotic diarrhea due to excessive fluid in the intestine), loss of colonization resistance (resulting in increased numbers of infections by other pathogens), and increased intestinal move [25]. Up to 30% of patients who use antibiotics experience antibody-associated diarrhea (AAD) [26].

Individuals receiving inpatient care are at significantly greater risk of developing AAD than individuals receiving outpatient intendance. Similarly, children younger than two years and seniors older than 65 years are at greater take chances of developing AAD than other children and adults. Some antibiotics (eastward.m., erythromycin and penicillin) are associated with AAD more than often than others [25,26].

Meta-analyses indicate that the utilize of any of a few species and strains (described below) of probiotics might reduce the risk of AAD by 51% [27]. Still, the benefits of probiotic apply to preclude AAD depend on the type of antibiotic that caused the AAD, the strain(s) of probiotic used, the life stage of the user (kid, younger developed, or older adult), and whether the user is receiving inpatient or outpatient care. Positive associations between intakes of probiotics and reduced risk of AAD take been plant in children and adults aged xviii to 64 years but not in adults aged 65 years and older [28].

Both Lactobacillus rhamnosus GG and Saccharomyces boulardii accept been shown to reduce the risk of AAD. In a systematic review and meta-assay of 12 RCTs with a total of 1,499 children and adults, treatment with Lactobacillus rhamnosus GG (4 x 108 to 12 ten x10 CFU) compared with placebo or no additional handling for 10 days to 3 months reduced the take a chance of AAD in patients treated with antibiotics from 22.4% to 12.3% [29]. However, when the 445 children and 1,052 adults were evaluated separately, the difference was statistically significant in children only. Although the optimal dose of Lactobacillus rhamnosus GG is unclear, 1 to 2 ten 1010 CFU/twenty-four hour period reduced AAD take chances in children by 71% [29]. Taking probiotics within two days of the first antibody dose is more than effective than starting to take them after.

In a systematic review and meta-assay of 21 RCTs in a full of 4,780 participants, handling with Saccharomyces boulardii compared with placebo or no treatment reduced the risk of AAD in iii,114 adults treated with antibiotics from 17.4% to 8.2% [29]. In the ane,653 children in this study, Saccharomyces boulardii reduced the risk from twenty.9% to 8.eight%. Various doses of Saccharomyces boulardii were tested, and no clear dose-dependent furnishings were observed.

Overall, the bachelor evidence suggests that starting probiotic handling with Lactobacillus rhamnosus GG or Saccharomyces boulardii within two days of the first antibiotic dose helps reduce the adventure of AAD in children and adults aged 18 to 64, merely non in elderly adults. There is no testify to suggest that the benefits are greater when more than one probiotic strain is used.

Inflammatory bowel disease
Inflammatory bowel illness (IBD) is a chronic inflammatory illness that includes ulcerative colitis and Crohn'due south disease [thirty]. The exact cause of IBD is unknown but is probably a combination of inherited and ecology factors, including genetic alterations and allowed system dysfunction [31]. Various treatments for IBD, including oral steroids and other medications, are available, but no cure exists.

Researchers are exploring whether individuals with IBD have alterations in the gut microbiome and whether probiotics might help manage IBD [32]. Several reviews have assessed the effects of probiotics on IBD [31-36]. The authors of all of these reviews reached similar conclusions—that certain probiotics might take modestly beneficial effects on ulcerative colitis, but not Crohn's affliction.

A 2020 systematic review from the American Gastroenterological Association (AGA) examined the role of probiotics in managing gastrointestinal disorders [31]. The review included 12 trials that used probiotics to induce or maintain remission in 689 children and adults with Crohn'south affliction, as well as 17 trials that examined diverse probiotic formulations for inducing or maintaining remission in 1,673 children and adults with ulcerative colitis. The trials used various probiotic strains and combinations—including Saccharomyces boulardii, Lactobacillus GG, Lactobacillus johnsonii NCC 533, Escherichia coli Nissle 1917, and VSL#iii, an 8-strain combination that included Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus, and Streptococcus thermophilus—for several months. The results provided no show that probiotics help induce or maintain remission in children or adults with Crohn'southward illness. The authors could not draw conclusions about whether probiotics benefit patients with severe ulcerative colitis or are effective alternatives to existing therapies. Nevertheless, according to limited evidence, these supplements might modestly reduce illness activity in individuals with mild-to-moderate ulcerative colitis when combined with conventional therapies. Limitations of the evidence included that the bachelor studies used different patient populations, probiotic formulations, treatment durations, and concomitant therapies.

A 2020 Cochrane review of fourteen studies in 865 participants with ulcerative colitis as well indicated that probiotics may assist induce remission and that probiotics combined with 5-ASA (an anti-inflammatory medication commonly used to care for IBD) may exist superior to 5-ASA alone [37]. However, the testify was express and of low certainty. A similar 2020 Cochrane review of 12 studies in 1,473 participants with ulcerative colitis examined the effects of probiotics for maintaining remission [38]. The authors concluded that whether probiotics are helpful is uncertain because of the small-scale number of participants in studies and unreliable methodologies used.

An AGA clinical decision support tool makes no recommendation on the use of probiotics in adults and children with IBD due to knowledge gaps [39]. Similarly, in a clinical practice guideline on the role of probiotics in managing gastrointestinal disorders, AGA recommends the employ of probiotics in adults and children with ulcerative colitis or Crohn's disease merely in the context of a clinical trial [32]. Consensus guidelines published by the British Social club of Gastroenterology in 2019 addressed the management of IBD, including the employ of probiotics [36]. The authors concluded that although probiotics may be modestly beneficial for ulcerative colitis, they should not be routinely used. For Crohn's disease, the authors establish no evidence of any do good.

Additional inquiry, including well-powered RCTs, is needed to place which patients with IBD might benefit from probiotics and which probiotic strains are nigh effective [32,34].

Irritable bowel syndrome
Irritable bowel syndrome (IBS) is a common functional disorder of the gastrointestinal tract characterized by recurrent abdominal discomfort or hurting, bloating, and changes in stool form or frequency. Although the causes of IBS are not completely understood, growing bear witness suggests potential roles for abdominal microbiota in its pathophysiology and symptoms; IBS has besides been linked to stress [40]. According to this enquiry, proinflammatory bacterial species, including Enterobacteriaceae, are abundant in patients with IBS, who typically also have a respective reduction in amounts of Lactobacillus and Bifidobacterium [41]. Probiotic products commonly contain Lactobacillus and Bifidobacterium and, therefore, have the potential to restore some missing microbial functionality and, consequently, help manage IBS symptoms.

Several meta-analyses accept assessed the role of probiotics in patients with IBS [42-46]. Most take constitute that probiotics accept a positive, although small, benign effect. For example, a meta-analysis of 23 RCTs in a total of 2,575 patients found that, overall, probiotics reduced the adventure that IBS symptoms would persist or not amend past 21% [42]. Various species and strains of probiotics had beneficial effects on global IBS symptoms, abdominal hurting, bloating, and flatulence scores, but the quality of the studies was depression. Some combinations of probiotics were superior to individual strains in this assay, but no specific combination was superior to another. A second meta-analysis of 15 randomized- controlled trials in a total of 1,793 patients with IBS found that probiotics reduced overall symptoms and intestinal pain more than placebo after viii to 10 weeks of therapy; in children, these supplements also improved mucosal barrier function [43].

A more contempo systematic review included 35 RCTs of sixteen single-strain and xix multi-strain products in three,406 adults with IBS [47]. Of the studies that found a statistically significant reduction in global symptoms (xiv of 29 trials) or a clinically meaningful reduction in intestinal pain (8 of 34 trials), near used multi-strain probiotic products. Furthermore, but trials of multi-strain products found a clinically meaningful comeback in quality of life [44,45].

Whether dissimilar strains of probiotic leaner take beneficial furnishings on IBS probably depends on the IBS symptom being evaluated [48]. In a meta-analysis of 10 RCTs with a total of 877 adults treated with probiotics or placebo for 4 weeks to half dozen months, hurting scores improved significantly with administration of probiotics containing Bifidobacterium breve, Bifidobacterium longum, or Lactobacillus acidophilus species compared with placebo treatment [49]. In dissimilarity, Streptococcus salivarius ssp. thermophilus, Bifidobacterium animalis, Bifidobacterium infantis, Lactobacillus casei, Lactobacillus plantarum, Lactobacillus bulgaricus, and Saccharomyces boulardii had no meaning consequence. The abdominal distension scores improved with employ of probiotics containing Bifidobacterium breve, Bifidobacterium infantis, Lactobacillus casei, or Lactobacillus plantarum species. Flatulence declined with use of all tested probiotics, but the studies showed no positive effect of probiotics on quality of life.

Overall, the available show indicates that probiotics might reduce some symptoms of IBS. Nevertheless boosted high-quality clinical trials are needed to confirm the specific strain, dose, and elapsing of treatment required as well every bit the type of IBS (such equally with predominant diarrhea or constipation) that can be treated effectively with probiotics.

Hypercholesterolemia
Loftier levels of cholesterol in the claret or cholesterol trapped in arterial walls are a risk factor for cardiovascular affliction (CVD). Depression-density lipoprotein (LDL) carries cholesterol to tissues and arteries. The higher the LDL level, the greater the risk is for CVD. High-density lipoprotein (HDL) carries cholesterol from the tissues to the liver and leads to its excretion. A low level of HDL increases a person'southward chance of CVD.

Researchers have studied the utilize of probiotics to amend lipid profiles. The mechanisms of their effects on cholesterol concentrations include catabolism of cholesterol past increasing:

  • Bile table salt hydrolase activity, which increases the need for new bile acids and thus reduces serum cholesterol levels [50-52];
  • Binding of cholesterol in the pocket-size intestine, which reduces the amount that the body absorbs;
  • Assimilation and incorporation of cholesterol into bacteria [52], thus lowering cholesterol levels in blood;
  • Production by lactobacilli and bifidobacteria of curt-chain fatty acids, which lower hepatic cholesterol synthesis and regulate cholesterol metabolism [50-53].

A meta-analysis of xxx RCTs with 1,624 participants (more often than not adults aged eighteen years or older) demonstrated that those treated with probiotics for 3 to 12 weeks had 7.8 mg/dL lower total cholesterol and 7.three mg/dL lower LDL cholesterol concentrations than those treated with placebo [54]. In subgroup analyses, the benefits of probiotics were slightly greater in studies that lasted eight weeks or longer and in participants who had baseline cholesterol levels higher than 240 mg/dL. Among the strains included in more than three studies, Lactobacillus acidophilus, a mixture of Lactobacillus acidophilus and Bifidobacterium lactis, and Lactobacillus plantarum were associated with significant reductions in total and LDL cholesterol concentrations, simply Lactobacillus helveticus and Enterococcus faecium were not. In a smaller meta-assay of 11 RCTs in 602 adults with normal or high cholesterol levels, those treated with probiotics for 2 to ten weeks had 6.half-dozen mg/dL lower total cholesterol and viii.5 mg/dL lower LDL cholesterol levels than those treated with placebo, but the probiotic handling had no significant effects on HDL cholesterol levels [55]. The effects were most pronounced with consumption of probiotics for more than four weeks by participants with hypercholesterolemia and those aged 45 or older. In both meta-analyses, participants included both good for you adults and adults with hypercholesterolemia, CVD, diabetes, or obesity.

However, the authors of a more than recent review of the influence of probiotics on blood lipid profiles of healthy adults (in 14 studies with a total of 942 adults treated from fifteen–150 days) plant bereft evidence to conclude that probiotics improve claret lipid levels [56]. Another review constitute that use of probiotics containing multiple strains produced statistically significant reductions in full and LDL cholesterol levels (by 12.0 and 20.1 mg/dL, respectively), whereas trials that used a unmarried strain did not [57].

Overall, research suggests that the apply of multiple probiotic strains in combination too as of probiotics containing Lactobacillus acidophilus, a mixture of Lactobacillus acidophilus and Bifidobacterium lactis, or Lactobacillus plantarum might reduce full and LDL cholesterol levels. Nonetheless, more enquiry is needed to ostend these findings.

Obesity
The gut microbiota play an important function in food and energy extraction from food. Inquiry in mice suggests that the gut microbiota touch not only use of energy from the diet, merely also energy expenditure and storage within the host [58]. Whether these effects translate to humans is unknown.

Results of clinical trials that assessed the bear upon of probiotics on obesity-related endpoints have been inconsistent. Ane 12-week clinical trial, for case, randomized 210 healthy adults aged 35 to 60 years who had large amounts of visceral fat to consume 200 g/24-hour interval fermented milk containing 10vii, 106, or 0 (control) CFU of Lactobacillus gasseri SBT2055 (LG2055) per gram of milk [59]. Participants who received 10seven or tensix CFU/g milk of Lactobacillus gasseri experienced significant reductions in visceral fat area (mean reductions of 8.5% and viii.2%, respectively), body mass index, waist and hip circumference, and body fat mass compared with the control group. In another randomized clinical trial, daily supplementation with 3.24 x x8 CFU Lactobacillus rhamnosus CGMCC1.3724 for 24 weeks combined with an energy-restricted nutrition for the showtime 12 weeks (500 kcal/twenty-four hours less than estimated calorie needs) did non significantly impact weight loss compared with placebo in 125 obese adults anile 18 to 55 years [60]. All the same, the Lactobacillus supplementation did significantly reduce body weight after 12 weeks (loss of 1.8 kg) and 24 weeks (loss of 2.6 kg) compared with placebo in the 77 female participants.

A 2017 systematic review of 14 clinical trials, including the two described higher up, in 1,067 overweight or obese individuals showed that probiotics (mostly Lactobacillus administered at various doses for 3 weeks to half-dozen months) significantly decreased torso weight and/or trunk fat in nine trials, had no effect in iii trials, and increased torso weight in two trials [61]. Some other recent systematic review and meta-analysis of 15 RCTs in 957 overweight or obese individuals constitute that supplementation with diverse doses and strains of probiotics for 3 to 12 weeks resulted in larger reductions in body weight (by 0.6 kg), body mass index (by 0.27 kg/m2), and fat percentage (by 0.6%) than placebo [62]. However, these effects were small and of questionable clinical significance.

In contrast, the most contempo systematic review and meta-analysis, which included 19 randomized trials in one,412 participants, found that supplementation with probiotics or synbiotics reduced waist circumference slightly (by 0.82 cm) but had no effect on body weight or body mass alphabetize, although the quality of evidence was depression to moderate [63]. The findings from another meta-analysis of fourteen trials in 881 adults, 5 trials in 726 children, and 12 trials in i,154 infants suggested that probiotics promote loss of a mean of 0.54 kg in adults, gain of a mean of 0.20 kg in children, and no significant weight loss or gain in infants [64].

Taken together, these results indicate that the effects of probiotics on body weight and obesity might depend on several factors, including the probiotic strain, dose, and duration, as well equally certain characteristics of the user, including age, sex activity, and baseline torso weight. Boosted research is needed to understand the potential effects of probiotics on body fat, body weight, and obesity in humans.

Safety Considerations

Many probiotic strains derive from species with a long history of safe use in foods or from microorganisms that colonize good for you gastrointestinal tracts. For these reasons, the common probiotic species—such as Lactobacillus species (acidophilus, casei, fermentum, gasseri, johnsonii, paracasei, plantarum, rhamnosus, and salivarius) and Bifidobacterium species (adolescentis, animalis, bifidum, breve, and longum)—are unlikely to cause impairment [3].

Given the large quantities of probiotics consumed effectually the world, the numbers of opportunistic infections that result from currently marketed probiotics are negligible. For example, probiotics have been administered to thousands of newborn infants, including some who were premature, without a single example of sepsis [65]. Nonetheless, some clinical trials of probiotics are not designed to fairly address questions about prophylactic, leaving gaps in available safety evidence [66-68].

Side furnishings of probiotics are ordinarily minor and consist of self-limited gastrointestinal symptoms, such every bit gas. In a few cases, mainly involving individuals who were severely ill or immunocompromised, the utilise of probiotics has been linked to bacteremia, fungemia (fungi in the blood), or infections that result in astringent illness [69,70]. Nevertheless, some case reports did non confirm that the specific strain of probiotics used was the cause of the infection. In other cases, the probiotic strain used was confirmed to be the opportunistic pathogen. Because species used as probiotics can exist normal residents of a patient's microbiota, such confirmation is important.

At to the lowest degree 60 reports have been published since 1966 of fungemia associated with the utilise of probiotics containing the yeast Saccharomyces cervisiae. In many of these cases, the patients were in an intensive intendance unit of measurement (ICU), were receiving enteral or parenteral diet, had a cardinal venous catheter, or had received broad-spectrum antimicrobial treatment [71]. When LGG was introduced into dairy products in Finland in 1990, monitoring of this country's population through 2000 revealed no increase in rates of bacteremia (bacteria in the claret) acquired by Lactobacillus species [72]. However, an assay of 22,174 ICU patients in a Boston hospital found that those who received LGG (typically through a feeding tube) had a markedly higher risk of developing Lactobacillus bacteremia compared to patients who did not receive the probiotic [73]. Of the 522 patients receiving LGG, a genome-level analysis identified six cases where the ingested LGG was plant in the blood, compared to only ii cases among the 21,652 patients who did not receive the LGG.

For individuals with compromised immune function or other serious underlying diseases, the World Gastroenterology Organisation (WGO) advises restricting probiotic employ to the strains and indications that accept proven efficacy [3].

Probiotic Selection and Use

Proficient bodies of health professionals brand no recommendations for or against probiotic utilize by salubrious people. For people with various health conditions, yet, published studies and reviews provide some guidance (every bit described above) on probiotic species, strains, and doses that might alleviate their symptoms.

The WGO notes that the optimal dose of probiotics depends on the strain and product. The organization therefore recommends that clinicians who advise their patients to apply probiotics specify the probiotic strains, doses, and duration of employ that studies in humans have shown to exist beneficial [iii]. The WGO guidelines include a summary of show on specific probiotic strains used in studies for specific gastrointestinal endpoints [3]. Finally, the WGO recommends that probiotic supplement users check the labels of probiotic supplements for recommended storage weather; for instance, some require refrigeration, whereas others can exist stored at room temperature.

The International Scientific Clan for Probiotics and Prebiotics advises manufacturers to list the total number of CFUs—ideally for each strain—on the "expiration" or "use past" date on the product label [74]. The association likewise suggests that consumers of these supplements avoid products that list the number of CFUs "at time of manufacture" considering this data does not account for declines in CFUs over a product'due south lifespan.

References

  1. Hill C, Guarner F, Reid G, Gibson GR, Merenstein DJ, Pot B, et al. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate utilise of the term probiotic. Nat Rev Gastroenterol Hepatol 2014;11:506-14. [PubMed abstract]
  2. Gibson GR, Hutkins R, Sanders ME, Prescott SL, Reimer RA, Salminen SJ, et al. Practiced consensus certificate: The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus argument on the definition and scope of prebiotics. Nat Rev Gastroenterol Hepatol 2017;14:491-502. [PubMed abstruse]
  3. Globe Gastroenterology System. Probiotics and prebioticsexternal link disclaimer. 2017.
  4. Zmora Due north, Zilberman-Schapira G, Suez J, Mor U, Dori-Bachash M, Bashiardes Southward, et al. Personalized Gut Mucosal Colonization Resistance to Empiric Probiotics Is Associated with Unique Host and Microbiome Features. Cell 2018;174:1388-405.e21. [PubMed abstract]
  5. Sanders ME. Probiotics in 2015: their scope and apply. J Clin Gastroenterol 2015;49 Suppl ane:S2-half dozen. [PubMed abstract]
  6. Sanders ME. Clinical employ of probiotics: what physicians demand to know. Am Fam Physician 2008;78:1026. [PubMed abstruse]
  7. Kailasapathy K, Chin J. Survival and therapeutic potential of probiotic organisms with reference to Lactobacillus acidophilus and Bifidobacterium spp. Immunol Cell Biol 2000;78:80-eight. [PubMed abstruse]
  8. Hogan DE, Ivanina EA, Robbins DH. Probiotics: a review for clinical apply. Gastroenterology & Endoscopy News 2018:i-7.
  9. National Institutes of Health. Dietary Supplement Characterization Database. 2018.
  10. Szajewska H, Guarino A, Hojsak I, Indrio F, Kolacek S, Shamir R, et al. Use of probiotics for management of astute gastroenteritis: a position paper by the ESPGHAN Working Group for Probiotics and Prebiotics. J Pediatr Gastroenterol Nutr 2014;58:531-9. [PubMed abstract]
  11. Food and Drug Administration. Policy regarding quantitative labeling of dietary supplements containing live microbials: Guidance for industryexternal link disclaimer. 2018.
  12. Avena-Woods C. Overview of atopic dermatitis. Am J Manag Intendance 2017;23:S115-S23. [PubMed abstruse]
  13. Li L, Han Z, Niu Ten, Zhang G, Jia Y, Zhang S, et al. Probiotic supplementation for prevention of atopic dermatitis in infants and children: a systematic review and meta-analysis. Am J Clin Dermatol 2018. [PubMed abstruse]
  14. Szajewska H, Horvath A. Lactobacillus rhamnosus GG in the primary prevention of eczema in children: a systematic review and meta-analysis. Nutrients 2018;10. [PubMed abstract]
  15. Huang R, Ning H, Shen M, Li J, Zhang J, Chen X. Probiotics for the treatment of atopic dermatitis in children: a systematic review and meta-analysis of randomized controlled trials. Front Cell Infect Microbiol 2017;7:392. [PubMed abstruse]
  16. Zhao M, Shen C, Ma L. Treatment efficacy of probiotics on atopic dermatitis, zooming in on infants: a systematic review and meta-analysis. Int J Dermatol 2018;57:635-41. [PubMed abstract]
  17. Makrgeorgou A, Leonardi-Bee J, Bath-Hextall FJ, Murrell DF, Tang ML, Roberts A, et al. Probiotics for treating eczema. Cochrane Database Syst Rev 2018;11:CD006135. [PubMed abstract]
  18. Guarino A, Ashkenazi S, Gendrel D, Lo Vecchio A, Shamir R, Szajewska H, et al. European Gild for Pediatric Gastroenterology, Hepatology, and Nutrition/European Society for Pediatric Infectious Diseases prove-based guidelines for the management of acute gastroenteritis in children in Europe: update 2014. J Pediatr Gastroenterol Nutr 2014;59:132-52. [PubMed abstract]
  19. Allen SJ, Martinez EG, Gregorio GV, Dans LF. Probiotics for treating astute infectious diarrhoea. Cochrane Database Syst Rev 2010:CD003048. [PubMed abstruse]
  20. Caffarelli C, Cardinale F, Povesi-Dascola C, Dodi I, Mastrorilli 5, Ricci Thou. Utilize of probiotics in pediatric infectious diseases. Expert Rev Anti Infect Ther 2015;thirteen:1517-35. [PubMed abstract]
  21. Szajewska H, Skorka A, Ruszczynski M, Gieruszczak-Bialek D. Meta-analysis: Lactobacillus GG for treating acute gastroenteritis in children--updated assay of randomised controlled trials. Aliment Pharmacol Ther 2013;38:467-76. [PubMed abstract]
  22. Feizizadeh S, Salehi-Abargouei A, Akbari V. Efficacy and safety of Saccharomyces boulardii for acute diarrhea. Pediatrics 2014;134:e176-91.
  23. Freedman SB, Williamson-Urquhart S, Farion KJ, Gouin South, Willan AR, Poonai Northward, et al. Multicenter Trial of a Combination Probiotic for Children with Gastroenteritis. Northward Engl J Med 2018;379:2015-26. [PubMed abstract]
  24. Schnadower D, Tarr PI, Casper TC, Gorelick MH, Dean JM, O'Connell KJ, et al. Lactobacillus rhamnosus GG versus Placebo for Astute Gastroenteritis in Children. Due north Engl J Med 2018;379:2002-14. [PubMed abstruse]
  25. Ki Cha B, Mun Jung S, Hwan Choi C, Song ID, Woong Lee H, Joon Kim H, et al. The effect of a multispecies probiotic mixture on the symptoms and fecal microbiota in diarrhea-ascendant irritable bowel syndrome: a randomized, double-blind, placebo-controlled trial. J Clin Gastroenterol 2012;46:220-7. [PubMed abstruse]
  26. Silverman MA, Konnikova L, Gerber JS. Impact of antibiotics on necrotizing enterocolitis and antibiotic-associated diarrhea. Gastroenterol Clin North Am 2017;46:61-76. [PubMed abstract]
  27. Blaabjerg S, Artzi DM, Aabenhus R. Probiotics for the prevention of antibiotic-associated diarrhea in outpatients-a systematic review and meta-assay. Antibiotics (Basel) 2017;6. [PubMed abstract]
  28. Jafarnejad S, Shab-Bidar Due south, Speakman JR, Parastui 1000, Daneshi-Maskooni M, Djafarian G. Probiotics reduce the risk of antibody-associated diarrhea in adults (18-64 years) merely non the elderly (>65 years): a meta-assay. Nutr Clin Pract 2016;31:502-13. [PubMed abstract]
  29. Szajewska H, Kolodziej M. Systematic review with meta-analysis: Saccharomyces boulardii in the prevention of antibiotic-associated diarrhoea. Aliment Pharmacol Ther 2015;42:793-801. [PubMed abstract]
  30. Sairenji T, Collins KL Evans DV. An update on inflammatory bowel illness. Prim Care 2017; 44: 673-92. [PubMed abstruse]
  31. Preidis GA, Weizman AV, Kashyap PC Morgan RL. AGA technical review on the role of probiotics in the management of gastrointestinal disorders. Gastroenterology 2020; 159: 708-38. [PubMed abstract]
  32. Su GL, Ko CW, Bercik P, Falck-Ytter Y, Sultan S, et al.. AGA clinical practise guidelines on the role of probiotics in the management of gastrointestinal disorders. Gastroenterology 2020; 159: 697-705. [PubMed abstruse]
  33. Ghouri YA, Richards DM, Rahimi EF, Krill JT, Jelinek KA DuPont AW. Systematic review of randomized controlled trials of probiotics, prebiotics, and synbiotics in inflammatory bowel disease. Clin Exp Gastroenterol 2014; 7: 473-87. [PubMed abstruse]
  34. Derikx LA, Dieleman LA Hoentjen F. Probiotics and prebiotics in ulcerative colitis. Best Pract Res Clin Gastroenterol 2016; 30: 55-71. [PubMed abstract]
  35. Wilkins T Sequoia J. Probiotics for gastrointestinal conditions: a summary of the evidence. Am Fam Physician 2017; 96: 170-viii. [PubMed abstruse]
  36. Lamb CA, Kennedy NA, Raine T, Hendy PA, Smith PJ, et al. British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults. Gut 2019; 68(Suppl 3): s1-s106. [PubMed abstruse]
  37. Kaur L, Gordon M, Baines PA, Iheozor-Ejiofor Z, Sinopoulou Five Akobeng AK. Probiotics for consecration of remission in ulcerative colitis. Cochrane Database Syst Rev 2020; three: Cd005573. [PubMed abstruse]
  38. Iheozor-Ejiofor Z, Kaur L, Gordon 1000, Baines PA, Sinopoulou V Akobeng AK. Probiotics for maintenance of remission in ulcerative colitis. Cochrane Database Syst Rev 2020; 3: Cd007443. [PubMed abstract]
  39. American Gastroenterological Association. Consideration for utilize of probiotics in gastrointestinal diseases: clinical conclusion back up tool. Gastroenterology 2020; 159: 706. [PubMed abstract]
  40. Staudacher HM, Whelan M. Contradistinct gastrointestinal microbiota in irritable bowel syndrome and its modification past diet: probiotics, prebiotics and the depression FODMAP nutrition. Proc Nutr Soc 2016;75:306-eighteen. [PubMed abstract]
  41. Zhuang 10, Xiong L, Li L, Li M, Chen Thou. Alterations of gut microbiota in patients with irritable bowel syndrome: A systematic review and meta-analysis. J Gastroenterol Hepatol 2017;32:28-38. [PubMed abstract]
  42. Ford Air-conditioning, Quigley EM, Lacy Be, Lembo AJ, Saito YA, Schiller LR, et al. Efficacy of prebiotics, probiotics, and synbiotics in irritable bowel syndrome and chronic idiopathic constipation: systematic review and meta-analysis. Am J Gastroenterol 2014;109:1547-61; quiz half-dozen, 62. [PubMed abstract]
  43. Didari T, Mozaffari S, Nikfar S, Abdollahi One thousand. Effectiveness of probiotics in irritable bowel syndrome: Updated systematic review with meta-analysis. World J Gastroenterol 2015;21:3072-84. [PubMed abstruse]
  44. Lorenzo-Zuniga V, Llop E, Suarez C, Alvarez B, Abreu L, Espadaler J, et al. I.31, a new combination of probiotics, improves irritable bowel syndrome-related quality of life. World J Gastroenterol 2014;20:8709-16. [PubMed abstruse]
  45. Williams EA, Stimpson J, Wang D, Plummer S, Garaiova I, Barker ME, et al. Clinical trial: a multistrain probiotic preparation significantly reduces symptoms of irritable bowel syndrome in a double-blind placebo-controlled study. Aliment Pharmacol Ther 2009;29:97-103. [PubMed abstract]
  46. McKenzie YA, Bowyer RK, Leach H, Gulia P, Horobin J, O'Sullivan NA, et al. British Dietetic Association systematic review and show-based do guidelines for the dietary direction of irritable bowel syndrome in adults (2016 update). J Hum Nutr Diet 2016;29:549-75. [PubMed abstract]
  47. McKenzie YA, Thompson J, Gulia P, Lomer MC. British Dietetic Clan systematic review of systematic reviews and show-based practice guidelines for the use of probiotics in the management of irritable bowel syndrome in adults (2016 update). J Hum Nutr Diet 2016;29:576-92. [PubMed abstract]
  48. Principi Northward, Cozzali R, Farinelli E, Brusaferro A, Esposito S. Gut dysbiosis and irritable bowel syndrome: The potential role of probiotics. J Infect 2018;76:111-xx. [PubMed abstruse]
  49. Ortiz-Lucas M, Tobias A, Saz P, Sebastian JJ. Consequence of probiotic species on irritable bowel syndrome symptoms: A bring up to engagement meta-analysis. Rev Esp Enferm Dig 2013;105:19-36. [PubMed abstruse]
  50. Tsai CC, Lin PP, Hsieh YM, Zhang ZY, Wu HC, Huang CC. Cholesterol-lowering potentials of lactic acrid bacteria based on bile-salt hydrolase activity and result of stiff strains on cholesterol metabolism in vitro and in vivo. ScientificWorldJournal 2014;2014:690752. [PubMed abstract]
  51. Kumar R, Grover S, Batish VK. Bile salt hydrolase (Bsh) action screening of lactobacilli: in vitro option of ethnic Lactobacillus strains with potential bile common salt hydrolysing and cholesterol-lowering power. Probiotics Antimicrob Proteins 2012;4:162-72. [PubMed abstract]
  52. Bosch M, Fuentes MC, Audivert S, Bonachera MA, Peiro S, Cune J. Lactobacillus plantarum CECT 7527, 7528 and 7529: probiotic candidates to reduce cholesterol levels. J Sci Food Agric 2014;94:803-9. [PubMed abstract]
  53. Ishimwe N, Daliri EB, Lee BH, Fang F, Du G. The perspective on cholesterol-lowering mechanisms of probiotics. Mol Nutr Food Res 2015;59:94-105. [PubMed abstruse]
  54. Cho YA, Kim J. Effect of probiotics on blood lipid concentrations: a meta-analysis of randomized controlled trials. Medicine (Baltimore) 2015;94:e1714. [PubMed abstract]
  55. Shimizu M, Hashiguchi M, Shiga T, Tamura HO, Mochizuki M. Meta-analysis: effects of probiotic supplementation on lipid profiles in normal to mildly hypercholesterolemic individuals. PLoS One 2015;x:e0139795. [PubMed abstract]
  56. Khalesi S, Bellissimo N, Vandelanotte C, Williams Due south, Stanley D, Irwin C. A review of probiotic supplementation in salubrious adults: helpful or hype? Eur J Clin Nutr 2019;73:24-37. [PubMed abstract]
  57. Sun J, Buys N. Effects of probiotics consumption on lowering lipids and CVD take chances factors: a systematic review and meta-assay of randomized controlled trials. Ann Med 2015;47:430-40. [PubMed abstract]
  58. Davis CD. The gut microbiome and its office in obesity. Nutr Today 2016;51:167-74. [PubMed abstract]
  59. Kadooka Y, Sato M, Ogawa A, Miyoshi One thousand, Uenishi H, Ogawa H, et al. Upshot of Lactobacillus gasseri SBT2055 in fermented milk on intestinal adiposity in adults in a randomised controlled trial. Br J Nutr 2013;110:1696-703. [PubMed abstract]
  60. Sanchez Grand, Darimont C, Drapeau V, Emady-Azar South, Lepage Grand, Rezzonico Due east, et al. Result of Lactobacillus rhamnosus CGMCC1.3724 supplementation on weight loss and maintenance in obese men and women. Br J Nutr 2014;111:1507-19. [PubMed abstract]
  61. Crovesy Fifty, Ostrowski 1000, Ferreira D, Rosado EL, Soares-Mota M. Consequence of Lactobacillus on torso weight and body fatty in overweight subjects: a systematic review of randomized controlled clinical trials. Int J Obes (Lond) 2017;41:1607-14. [PubMed abstruse]
  62. Borgeraas H, Johnson LK, Skattebu J, Hertel JK, Hjelmesaeth J. Effects of probiotics on torso weight, torso mass alphabetize, fat mass and fat per centum in subjects with overweight or obesity: a systematic review and meta-analysis of randomized controlled trials. Obes Rev 2018;19:219-32. [PubMed abstract]
  63. Suzumura EA, Bersch-Ferreira AC, Torreglosa CR, da Silva JT, Coqueiro AY, Kuntz MGF, et al. Effects of oral supplementation with probiotics or synbiotics in overweight and obese adults: a systematic review and meta-analyses of randomized trials. Nutr Rev 2019. [PubMed abstruse]
  64. Dror T, Dickstein Y, Dubourg One thousand, Paul M. Microbiota manipulation for weight alter. Microb Pathog 2017;106:146-61. [PubMed abstract]
  65. AlFaleh M, Anabrees J. Probiotics for prevention of necrotizing enterocolitis in preterm infants. Cochrane Database Syst Rev 2014:Cd005496. [PubMed abstract]
  66. Hempel S, Newberry S, Ruelaz A, Wang Z, Miles JN, Suttorp MJ, et al. Safety of probiotics used to reduce gamble and forestall or treat disease. Bear witness Report/Technology Assessment number 200. Rockville, MD: Bureau for Healthcare Research and Quality; 2011. [PubMed abstract]
  67. Bafeta A, Koh M, Riveros C, Ravaud P. Harms reporting in randomized controlled trials of interventions aimed at modifying microbiota: a systematic review. Ann Intern Med 2018;169:240-seven. [PubMed abstract]
  68. Cohen PA. Probiotic prophylactic--no guarantees. JAMA Intern Med 2018;178:1577-viii. [PubMed abstruse]
  69. Didari T, Solki S, Mozaffari Due south, Nikfar Southward, Abdollahi G. A systematic review of the safety of probiotics. Expert Opin Drug Saf 2014;thirteen:227-39. [PubMed abstract]
  70. Borriello SP, Hammes WP, Holzapfel W, Marteau P, Schrezenmeir J, Vaara M, et al. Safety of probiotics that incorporate lactobacilli or bifidobacteria. Clin Infect Dis 2003;36:775-eighty. [PubMed abstract]
  71. Munoz P, Bouza East, Cuenca-Estrella Yard, Eiros JM, Perez MJ, Sanchez-Somolinos M, et al. Saccharomyces cerevisiae fungemia: an emerging infectious disease. Clin Infect Dis 2005;xl:1625-34. [PubMed abstract]
  72. Salminen MK, Tynkkynen S, Rautelin H, Saxelin M, Vaara M, Ruutu P, et al. Lactobacillus bacteremia during a rapid increment in probiotic use of Lactobacillus rhamnosus GG in Republic of finland. Clin Infect Dis 2002;35:1155-60. [PubMed abstruse]
  73. Yellin I, Flett KB, Merakou C, Mehrotra P, Stam J, Snesrud E, et al. Genomic and epidemiological evidence of bacterial transmission from probiotic sheathing to blood in ICU patients. Nat Med 2019;25:1728-32. [PubMed abstract]
  74. International Scientific Clan for Probiotics and Prebiotics. Deciphering a probiotic labelexternal link disclaimer. 2017.

Disclaimer

This fact sheet by the National Institutes of Health (NIH) Office of Dietary Supplements (ODS) provides data that should not take the identify of medical communication. We encourage you to talk to your healthcare providers (doc, registered dietitian, pharmacist, etc.) about your interest in, questions about, or use of dietary supplements and what may be best for your overall wellness. Any mention in this publication of a specific product or service, or recommendation from an system or professional gild, does not correspond an endorsement by ODS of that production, service, or good advice.

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Source: https://ods.od.nih.gov/factsheets/Probiotics-HealthProfessional/

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