Abstract
Background: Diarrhoeal disease is a major cause of global infant mortality, and compromises the ability of many countries with respect to achieving sustainable development goals. The WHO’s recommendation of Oral Rehydration Solution (ORS) and zinc in the management of this disease, may not be readily available. Consideration and assessment of cultural practices in its management has been an area of increased interest over the last decade. Aim: This study aims to systematically evaluate efficacy of the consumption of traditional fermented foods as functional products for the treatment and management of diarrhoea. Methods: Following PRISMA guidelines, a systematic review was conducted of electronic databases (Cochrane Library, Ovid Medline and Pubmed) databases with no restrictions on language and publication date for RCTs that investigated the effect of consumption of fermented foods on the treatment of diarrhoea in children under five years of age. Results: Seven RCTs were included. Meta-analysis showed that compared to control, consumption of fermented foods significantly reduced mean duration of diarrhoea, −0.61 days; (95% CI, −1.04, −0.18); length of hospitalization, −0.35 days (95% CI, −0.69, −0.02); but not mean daily frequency of stool −2.00 (95% CI,-7.03, 3.04). Conclusion: Limited available evidence suggests that consumption of fermented foods may help reduce duration and severity of symptoms as a treatment of diarrhoea. More high quality research needs to be undertaken to investigate the efficacy of fermented food as an effective alternative to ORS as a potential WHO recommendation for management of diarrhoeal disease.
Keywords: Diarrhoea, gastrointestinal diseases, fermented foods, fermentation organisms, oral rehydration solution, meta-analysis
Introduction
The consensus definition of diarrhoea, published by the World Health Organisation (WHO) in 1988 as stated by Levine et al., (2017) is the passage of three or more loose stools - one that takes the shape of a container, or watery stools in a 24-h period. According to WHO, diarrhoeal disease is the second leading cause of death among children under the age of 5 in the world (World Health Organisation, 2005). The WHO’s recommendation for the treatment of diarrhoea is oral rehydration solution (ORS), consisting of a solution of clean water, sugar and salt along with a 10-14 day supplemental treatment course of dispersible 20 mg zinc tablets (World Health Organisation, 2005). However, currently there is limited available information of the recommended ORS/zinc treatment especially in rural regions of some African countries (Njume and Goduka, 2012; Wilson et al., 2013). In addition to poor access, a number of indigenous and culturally acceptable alternatives treatments based on fermented foods tend to be used in these regions (Njume and Goduka, 2012).
Fermented foods are consumed across the globe as traditional foods, within many societies and communities using fermented foods for the treatment of diarrhoea, especially in children (Lei et al., 2006; Achi and Asamudo, 2018; Anukam and Reid, 2009). This ancient food processing technique continues to be used both domestically and industrially as a food preservation method, prolonging shelf life of foods and beverages (Franz et al., 2014; Mokoena et al., 2016; Ray et al., 2016). Fermentation additionally has the potential to enhance sensory properties of food product, which leads to some consumers to prefer (Franz et al., 2014; Karovicova, 2007). To date, some research data support the potential of fermented foods in providing therapeutic benefits in the management or prevention of some gastrointestinal diseases and disorders (Marsh et al., 2014). Though not clearly understood, there are various hypotheses with respect to the possible ways in which fermented foods and beverages may be able to offer health benefits. Components of the fermented product matrix, including the fermentation organisms, fermentation products, including de novo organic compounds and exopolysaccharides produced during fermentation, which could collectively or individually result in the varied effects of fermented food products are reported in the literature (Hill et al., 2014).
The most commonly found organisms in fermented foods and beverages are lactic acid bacteria (LAB) and yeast strains, which are generally regarded as safe (Ali, 2010; Chelule et al., 2010; Tamang et al., 2016). These organisms are particularly common in dairy and cereal fermentation (Nyanzi and Jooste, 2012; Widyastuti and Febrisiantosa, 2014). Some species of these organisms, particularly those of Lactobacilli and Saccharomyces have the potential to confer health benefits through mechanisms such as enhancement of gut immune response, competition with pathogenic organisms for biological niches in the gastrointestinal tract (GIT) or production of antibacterial substances (Beausoleil et al., 2007; Song et al., 2012). Such organisms may be described as probiotic if they are able to survive the harsh environment of the upper GIT in order to reach the colon in significant numbers, where they may be able to enhance gut epithelial function (Donot et al., 2012; Franz et al., 2014; Liu et al., 2010). However, a fermentation organism does not have to be probiotic in order to confer health benefits, as even dead cells may stimulate the production of helper T cells in the colon (Gosálbez and Ramón, 2015; Park and Jeong, 2015; Vinderola et al., 2005). This was initially proposed by Adams (2010), who reported that dead LAB cells may enhance immune response in the GIT in an in-vivo model using rats. Upon reaching the gut, Lactobacilli along with other LAB, produce lactic acid which is metabolised by other organisms into butyrate (Morrison and Preston, 2016; Rautiola, 2013), a SCFA reported to have anti-inflammatory and anti-carcinogenic properties in the human GIT, whilst also boosting the GIT and systemic immune function (Nicholson et al., 2012).
Diarrhoea occurs as a result alteration of the movement of water and ions in the colon where the absorption of water and electrolyte primarily takes place (Hodges and Gill, 2010; Kiela and Ghishan, 2016). This can be induced by pathogenic infection or as a result of gut dysbiosis, for example, in antibiotic associated diarrhoea (Allen et al., 2010; Pimentel, 2003). Extracellular polysaccharides (EPS) are carbohydrate polymers formed from simple or complex carbon substrates by the bacterial cells including fermentative organisms in foods and beverages (Nwodo et al., 2012), as a protective surface in response to a hostile environment, enhancing colonization by the EPS producing organism (Salazar et al., 2016). EPS production influences the rheological and textural properties of fermented foods as seen in the viscosity of fermented milk. Some EPS produced by Lactobacilli organisms such as α-D-glucans, inulin-type fructans, oligosaccharides, (Sanlibaba and Çakmak, 2016), may act as prebiotics in the human GIT (Das et al., 2014; Hutkins et al., 2016; Roberfroid, 2007; Whelan, 2013), selectively stimulating the growth of beneficial organisms in the colon (Gibson et al., 2004; Gibson and Roberfroid, 1995). Furthermore, enhanced production of SCFAs in the human gut has also been associated with EPS with the explanation that it serves as substrate for organisms, such as LAB and Bifidobacteria, which are involved in the production of SCFAs in the gut (O'Callaghan and van Sinderen, 2016).
In summary, fermented products may be useful in the prevention and management or treatment of diarrhoea by enhancing immune responses, potentially and/or selectively increasing the population of the beneficial organisms in the gut, inhibiting the growth of gut pathogenic organisms and enhancing gut homeostasis.
Although the potential of fermented products as alternative treatment for diarrhoeal disease has emerging supportive evidence in adults, there is a need for research to investigate its efficacy as an alternative treatment to ORS, especially in children. Randomised controlled trials (RCTs) and other clinical studies have examined the effect of fermented foods on diarrhoea amongst other gastrointestinal diseases or symptoms in adults (Beniwal et al., 2003; Gomi et al., 2018; Lei et al., 2006; Merenstein et al., 2009; Ringel-Kulka et al., 2015), but results have been inconsistent. To date, there is limited evidence and systematic analyses have investigated the efficacy of fermented foods in the prevention and treatment of diarrhoea jointly, using dairy products as the intervention (Agostoni et al., 2007; Patro-Golab et al., 2015a; Patro-Gołąb et al., 2015b; Szajewska et al., 2015), although the potential mechanisms for both effects appear to be similar. This systematic review and meta-analysis aim to evaluate the available evidence with respect to the efficacy fermented foods and beverages in comparison with unfermented or heat treated products, including dairy and cereal products, focussing on the treatment of diarrhoea in infants.
Methods
The protocol for the systematic review and meta-analysis was registered with PROSPERO, registration number CRD42020201411. Cochrane Collaboration and Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) (Moher et al., 2009) guidelines for undertaking a systematic review and meta-analysis were followed.
Outcome measures
The primary outcome measure for this review was duration of diarrhoea. The secondary outcome measures were mean number of stools per day and duration of hospitalisation. A lack of data regarding these outcomes was not an exclusion criterion.
Electronic search
Electronic searches of the Cochrane Central Register of Controlled Trials (COCHRANE CENTRAL), OVID MEDLINE and PUBMED databases were undertaken in December 2020. There was no language restriction and publication date was left open till the date of search (December 2020) to avoid limited number of search output. Reference lists of relevant review articles, RCTs, systematic reviews and meta-analyses were hand search to identify any articles that the initial search may have missed. The search strategy included the use of validated filters in combination with topic-specific strategies. Search terms were included fermented food(s), diarrhoea/diarrhea, and gastrointestinal disease(s). The search strategy used both keywords and MeSH terms.
Inclusion and exclusion criteria
Randomised control trials (RCTs), clinical trials, controlled clinical trials or quasi-randomized trials were considered eligible for inclusion in this analysis. Studies must have included human subjects, with age no more than 5 years and with acute/chronic diarrhoea and must have had duration of diarrhoea as an outcome measure. Studies which included participants treated with antibiotics were excluded. Intervention had to be consumption of any fermented food product at any dosage scheme and duration of delivery with control being placebo, consumption of unfermented or ultra-heat treated or pasteurized fermented food product similar to the intervention or no intervention. Studies with no control, unspecified control and non-heat treated fermented controls were excluded.
Selection of studies
The title, abstract, and key words of every article identified during the search were initially screened. Articles that were irrelevant following an initial screening based on title, abstract and keywords were excluded. Full text of potentially relevant studies were then obtained for further screening. Consensus was reached by two reviewers (AO and NP) on the final chosen articles.
Data extraction
Information extracted from each article include: author; year of publication; baseline characteristics of the participants (age, setting, country of origin) sample size; type of intervention and comparator; dosage of intervention; duration of the intervention; definition of diarrhoea; outcome measures and results. Where comparable data were available, meta-analysis was undertaken using Review Manager (RevMan) (Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). Mean difference between the experimental and control groups was selected to be the effect size of the continuous outcome with 95% confidence intervals. Duration of diarrhoea was identified as the only common outcome variable in the selected studies and therefore used in the meta-analysis. Where there were more than 1 intervention group, either similar experimental groups were combined to create a single pair-wise comparison or the more appropriate group was selected (Higgins, 2011). A conversion of result of outcome measure, shown as median and range to mean and standard deviation was achieved as recommended by (Hozo et al., 2005; Luo et al., 2018; Wan et al., 2014), in order to pool data together. It is however important to note that conversions such as this could result in overestimation of mean and standard deviation (Patro-Gołąb et al., 2015b), therefore, interpretation of pooled results of this meta-analysis would need to be made with caution.
Assessment of risk of bias in included trials
Risk of bias was assessed using the Cochrane Collaboration tool which includes the following criteria: adequacy of random sequence generation; allocation concealment; blinding of participants; personnel, and outcome assessors; incomplete outcome data and selective reporting. In all cases, an answer of “ + ”, “-” and “?” indicated low risk, high risk and unclear risk respectively. There was no formal assessment of publication bias using funnel plot due to small number (< 10) of selected articles (Sterne et al., 2011).
Results
Seven RCTs (Agarwal and Bhasin, 2002; Bhatnagar et al., 1998; Boudraa et al., 2001; Isolauri et al., 1991; Pedone et al., 1999), were identified to have met the inclusion criteria. Figure 1 is the flow diagram showing the process of identification for the eligible trials and the characteristics of the excluded trials, with reasons for exclusion. Characteristics of these articles, assessment of risk of bias and Grading of Recommendations, Assessment, Development and Evaluations (GRADE#0 analysis can be found in Tables 1, 2 and 3 respectively. Agarwal and Bhasin (2002) undertook these two studies independently and simultaneously in two different settings, the community and the hospital. Data from these settings were separately, hence eight studies were included for analysis. Only children aged between 3 months and 5 years old were recruited as participants in all selected studies. Two, of the 8 studies were not carried out with in-patients. These were studies by Pedone et al., (1999) with children recuited from day care centres and Agarwal and Bhasin (2002), who recruited children from Nand Nagri for the community based study.
Figure 1.
Shows the PRISMA flow chart for literature search.
Table 1.
Characteristics of included articles.
| Title, Authors, Country | Population | Blinding | Intervention | Comparator | Duration of intervention | Definition of Diarrhoea | Results |
|---|---|---|---|---|---|---|---|
| Effect of feeding yogurt versus milk in children with acute
diarrhoea and carbohydrate malabsorption Boudraa et al., (2001); Oran, Algeria |
112 well-nourished children, aged 3 to 24 months, admitted to Cabral Clinic, Oran with acute watery diarrhoea of less than 5 days | Double | Yogurt made from Infant formula fermented with Lactobacillus bulgaricus (108) and Streptococcus thermophilus (108). N = 56 |
M group Infant formula N = 56 |
180 ml / kg*day was offered to each participant for no less than 5 days. | More than 3 watery stools during the previous 24 h | • Duration of diarrhoea was significantly reduced in group Y 44.1 h; 95% (CI 36–54) compared with group M 61.7 h; 95% CI (52–71), p < 0.05 • Number of stools per day significantly reduced in group Y 12; 95% (CI 9–15) compared with group M 17; 95% CI (14–20), p < 0.05 |
| The effect of supplementation with milk fermented by
Lactobacillus casei (strain DN-114 001) on acute diarrhoea in
children attending day care centres Pedone et al., (1999). Val de Marne, Paris France |
287 (265 analysed; no ITT) children aged between 6 to 36 months, in whom dairy product had been introduced for more than a month before the beginning of the study, attending 1 of 12 selected day care 5 days a week and having both lunch and a 4 pm snack | Double | a) Standard yoghurt containing 107 cfu/ml of
L. bulgaricus and S.
thermophilus N = 92 b) milk fermented with L. bulgaricus and S. thermophilus with the addition of L. casei (3.2*103 cfu/ml) yogurt with L. casei N = 86 |
Jellied milk (JM) free of LAB N = 87 |
125 g / day for children between 6 and 18 months for 6
months 250 g/day for children over 18 months for 6 months |
Diarrhoea defined as 3 or more loose or watery stools per 24 h. | • Yogurt with L.c asei significantly reduced severity (duration) of diarrhoea attacks over the 6 months of intervention 4.3 (2.7) days compared with standard yogurt - 5.3 (2.5) days and JM – 8.0 (5.3) days, p = 0.009 • Both yogurtssignificantly reduced duration of ‘one episode of diarrhoea’ (3.9 [2.4] and 4.8 [2.3] days respectively) when compared with JM (6.9 [3.0] days) p = 0.002 |
| Clinical trial of fermented maize-based oral rehydration
solution in the management of acute diarrhoea in
children Yartey et al., (1995); Accra, Ghana |
108 children aged between 4 and 27 months presenting with acute diarrhoea of no more than 7 days duration, with mild to moderately severe dehydration | Not stated | Fermented maize N = 36 Unfermented maize N = 35 |
WHO/UNICEF ORS N = 37 |
Unlimited quantities aiming to achieve full hydration within 24
h Up to 48 h of intervention |
Three or more loose or watery stools per 24-h period. | • Mean duration of diarrhoea (hours) after admission; 17.8 (16.8–18.8), 20.6 (19.7–21.5) and 21.1 (20.0–21.1) for fermented maize, unfermented maize and WHO/UNICEF ORS groups respectively, were not s.d. • Mean number of stools within 24 h of admission; 4.2 (2.3), 4.3 (2.7) and 4.0 (2.2) for fermented maize, unfermented maize and WHO/UNICEF ORS groups respectively, were not s.d. |
| Efficacy of milk versus yogurt offered as part of a mixed diet
in acute non-cholera diarrhoea among malnourished
children Bhatnagar et al., (1998); New Delhi, India |
Malnourished boys aged 4 to 48 months with diarrhea for 96 h or less and passage of five or more liquid stools in the preceding 24 h were enrolled |
Double | 120 ml/kg/24 h of yoghurt made from a combination
of Streptococcus thermophilus and Lactobacillus Bulgaricus N = 47 |
120 ml/kg/24 h of milk formula N = 49 |
Minimum of 3 days or till recovery, whichever was later. | five or more liquid stools in 24 h |
• The median (range) duration of diarrhoea (hours) was 45 [4, 183] for MF and 52 [7, 173] for YF, (p = 0.94). |
| Feasibility studies to control acute diarrhoea in children by
feeding fermented milk preparations Actimel and Indian
Dahi Agarwal and Bhasin (2002); Delhi and Nand Nagri, India |
75 children (6 months to 5 y) with diarrhoea were admitted for
the study to the University College of Medical Sciences and Guru
Teg Bahadur Hospital. Simultaneously, the study was also carried out on 75 children of the same age with diarrhoea in a slum area named (community study) in one of its dispensaries run by the State Government of Delhi. |
Double | Group 1: Fermented milk containing 108 Lactobacillus casei DN-114001 per gram (Actimel by Danone, France). Community n = 25 Hospital n = 23 Group 2: Dahi containing 108 Lactococcus lactis, Lactococcus lactis cremoris and Leuconostac mesenteroids cremoris per gram Community n = 25 Hospital n = 27 |
Ultra-heat-treated fermented milk (no bacteria) Community n = 25 Hospital n = 25 |
100 ml, 2 times daily for children between 6 and 12 months and 3 times for other children until recovery | three loose stools per day without blood/ mucus |
• Mean duration of diarrhoea (days) were 1.5 (SD = 0.48) and 1.9 (SD = 0.8) for Group 1 (Actimel) at the hospital and the community respectively • Mean duration of diarrhoea (days) were 1.8 (SD = 0.61) and 2.2 (SD = 1.0) for Group 2 (Dahi) at the hospital and the community respectively • Mean duration of diarrhoea (days) were 2.1 (SD = 0.72) and 2.4 (SD = 0.9) for Group 3 (control) at the hospital and the community respectively • P value were < 0.01 and < 0.05 between groups at the hospital and community respectively |
| A human Lactobacillus strain (Lactobacillus casei sp strain GG)
promotes recovery from acute diarrhoea in children Isolauri et al., (1991); Tampere, Finland |
4 and 45 months admitted at Tampere University Hospital or Satakunta Central Hospital for acute diarrhea of less than 7 days’ duration and with more than three watery stools during the previous 24 h. All patients were given ORT of at least two times the fluid deficit n = 71 |
Not stated | Group 1: L.casei sp strain
GG (Lactobacillus GG)-fermented milk product, (1010−11 cfu) N = 24 Group 2: Lactobacillus GG given as a freeze dried powder N = 23 |
Group 3: Fermented and pasteurized yoghurt with insignificant
amount of LAB N = 24 |
Group 1 and placebo: 125 g of milk, 2ce daily for 5
days Group 2, 1 dose of powder containing 1010−11 cfu twice daily for 5 days 1 month follow up |
More than three watery stools during 24 h. |
• Mean (SD) duration of the diarrhoea was 1.4 (0.8) days in group 1 (n = 22), 1.4 (0.9) days in group 2 (n = 17), and 2.4 (1.1) days in group 3 (n = 19); F = 12.46, P < .001 • Mean (SD) number of days of hospital stay was 3.5 (1.6) days in group 1, 3.2 (1.2 in group 2 and 3.6 (1.4) in group 3; P = 0.66 • The percentage of patients who had watery diarrhoea on days 3 and 4 was 12.5% in group 1, 22% in group 2 and 58% in group 3; P = 0.001; 0% in group 1, 4% in group 2 and 21% in group 3; P = 0.02 respectively. |
| Evaluation of yogurt effect on acute diarrhoea in
6-24-month-old hospitalized infants Pashapour and Iou, (2006); Urmia, Iran |
6-24 months with moderate dehydration and acute non-bloody, non-mucoid diarrhoea for fewer than four days admitted in Urmia Imam Hospital n = 80 |
Not blinded | At least 15 ml/kg/day of pasteurized cow milk yogurt (fat 2.5%, sugar 3%, lactic acid 1%, water 74%, Lactobacillus bulgaris 50,000/ml, Streptococcus thermophilus 50,000/ml and pH = 4.7) orally plus routine hospital treatment N = 40 |
Timely routine hospital treatment only: a compound of
intravenous serum therapy, ORS and mother’s milk in breast-feeding infants and complementary food according to their month of age n = 40 |
From admission to discharge | Increase in the frequency, fluidity and volume of faeces |
• Mean (SD) duration of hospitalization was 2.7 (0.91) days vs 3.1 (0.74) days for experimental vs control groups, respectively; p = 0.035 • Mean (SD) reduction in diarrhoea frequency was 4.30 (1.74) vs 3.60 (1.23) times for experimental and control groups, respectively; p = 0.017 |
Table 2.
Risk of bias assessment using the cochrane risk assessment tool.
| Author | Random sequence generation | Allocation Concealment | Blinding of participants and personnel | Blinding of outcome assessment | Incomplete outcome data | Selective reporting |
|---|---|---|---|---|---|---|
| Boudraa et al. (2001) |
|
|
|
|
|
|
| Pedone et al. (1999) |
|
|
|
|
|
|
| Yartey et al. (1995) |
|
|
|
|
|
|
| Bhatnagar et al. (1998) |
|
|
|
|
|
|
| Agarwal & Bhasin (2002) |
|
|
|
|
|
|
| Isolauri et al. (1991) |
|
|
|
|
|
|
| Pashapour & Iou (2006) |
|
|
|
|
|
|
Table shows the summary of risk of bias based on authors’ judgement using the Cochrane Collaboration tool. In all cases, an answer of “ + ”, “-” or “?” indicates low risk, high risk and unclear risk respectively.
Table 3.
GRADE analysis - fermented foods compared to comparator for childhood diarrhoea.
| Certainty assessment | Summary of findings | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Participants (studies) Follow-up |
Risk of bias | Inconsistency | Indirectness | Imprecision | Publication bias | Overall certainty of evidence | Study event rates (%) | Relative effect (95% CI) |
Anticipated absolute effects | ||
| With Comparitor | With Probiotics | Risk with Comparitor | Risk difference with Probiotics | ||||||||
| Duration of diarrhoea | |||||||||||
| 603 (7 RCTs) |
seriousa | seriousb | not serious | not serious | none | ⊕⊕◯◯ Low |
301 | 302 | - | The mean duration of diarrhoea was 3.82 days | mean 0.61 days fewer (0.18 fewer to 1.04 fewer) |
| Mean daily stool frequency | |||||||||||
| 183 (2 RCTs) |
seriousa | seriousb | not serious | not serious | none | ⊕⊕◯◯ Low |
91 | 92 | - | The mean mean daily stool frequency was 12 stools per day | mean 2 stools per day fewer (3.04 more to 7.03 fewer) |
| Duration of hospitalisation | |||||||||||
| 128 (2 RCTs) |
seriousa | seriousb | not serious | not serious | none | ⊕⊕◯◯ Low |
64 | 64 | - | The mean duration of hospitalisation was 3.29 days | mean 0.35 days fewer (0.69 fewer to 0.02 fewer) |
CI: confidence interval.
Explanations.
a. Only 2 of the studies which accounted for <50% of the weighting had a low risk of bias.
b. Heterogeneity seen through varied dosages and length of administration. with a high I2 of 98%.
Pashapour and Iou (2006) and Yartey et al., (1995) used WHO’s recommendations of oral rehydration solution (ORS), as control in their study. Boudraa et al., (2001), Pedone et al., (1999), Bhatnagar et al., (1998) compared the effects of fermented milk against unfermented milk on the outcomes of diarhoea whilst studies by Agarwal and Bhasin (2002) and Isolauri et al., (1991) used heat treated fermented milk as control. Bhatnagar et al., (1998) and Boudraa et al., (2001) administered ORS to all participants in both groups. However, whilst Bhatnagar et al., (1998) continued to administer the solution throughout the study, Boudraa et al., (2001) stopped the administration of ORS before patients were randomised into groups.
Duration of diarrhoea
This outcome was reported by six out for the seven RCT included in the current study using a total population of 603 children. The pooled results from the articles (Figure 2), showed that overall mean duration of diarrhoea was significantly less, in the experimental group in comparison with the control group, −0.61 days; 95% CI (−1.04, −0.18). Subgroup analysis separating studies which utilised a non-fermented control and ORS from those that used heat-treated fermented food as control found mean duration of diarrhoea was significantly lower in the group administered fermented foods in comparison with the heat-treated and ORS control group, −0.58 days; 95% CI (−0.97, −0.20) and −0.61 days; 95% CI (−0.19, −0.09) respectively, but not significantly different when compared with the non-fermented control −0.74 days; 95% CI (−1.52, 0.05).
Figure 2.
Forest plot showing the effect of intake of fermented food on duration of diarrhoea.
Secondary outcomes
Two RCTs each report mean daily number of stools and mean length of hospitalisation (days). Fermented foods did not significantly reduce mean daily stool frequency −2.00 95% CI (−7.03, 3.04), but significantly reduced the length of hospitalisation, −0.35 days 95% CI (−0.69, −0.02) in comparison to the control group (Figure 3).
Figure 3.
Forest plot showing the effect of intake of fermented food on A) mean daily stool frequency B) duration of hospitalisation. Data shows outcome of random effect models for both analysis analyses.
Discussion
This systematic review and meta-analyses of pooled data from six studies suggests that administering fermented foods during an episode of diarrhoea in infants under five years of age, may reduce the duration of the disease in comparison to the control groups. Fermented foods were shown to reduce the duration of diarrhoea compared to heat treated fermented food controls. This beneficial effect was observed when ORS was used as control, suggesting that fermented foods may have a potential role in the management of diarrhoeal disease. There was no clear effect on daily stool frequency, but duration of hospitalisation was reduced following administration of fermented foods.
The significant treatment effect observed in the mean duration of diarrhoea between the experimental group administered with fermented foods using the HT fermented food or ORS as control could an effect associated with a number of potentially active components within the fermented foods including the fermentation organisms and the products of fermentation process. The difference in the therapeutic effect observed in fermented foods versus heat treated fermented food is suggestive that the beneficial effects may be associated with the presence of viable fermentation organisms in the product. However, the plausible complementary effects of other fermentation by-products should not be ignored. Studies have investigated the effect of fermentation organisms in the fermented product, testing for probiotic effects of these organisms and using heated treated matching fermented product or products that do not contain the organism of interest as the comparator (de Vrese et al., 2011; Merenstein et al., 2009; Pitkälä et al., 2007). Species of LAB including Lb kefiri, Lb fermentum, Lb. acidophilus, Lb. rhamnosus, Lb. plantarum, Lb. casei, have been investigated in in vitro and in vivo studies and have been reported to have probiotic properties (Bao et al., 2010; Millette et al., 2008; Pisano et al., 2014; Rivera-Espinoza and Gallardo-Navarro, 2010; Watson and Preedy, 2015; Zheng et al., 2013). Nevertheless, LAB are able to also produce heat-stable bacteriocins as well as heat-labile antimicrobial proteins (Grosu-Tudor et al., 2014), which may be effective in the restoration of gut health during an incident of diarrhoea.
According to the meta-analysis by Ritchie and Romanuk (2012), Lb rhamnosus GG (LGG) and Lb casei are LAB organisms which have most commonly been investigated for the management of gastrointestinal diseases including diarrhoea. The authors further reported in their study that these LAB had the potentials for preventive and therapeutic management of infectious diarrhoea but not for travellers’ diarrhoea in adults. There were variations in factors such as duration of administration, quantity administered varied and age of subject, across the studies included in the meta-analysis which may have caused the variations in the outcomes of both types of diarrhoea. Furthermore, the specificity of the health benefits that may be derived from organisms with probiotic properties may have contributed to inconsistencies that may have been observed between studies, as strains of the same species may not proffer the same health benefit to their host (Campana et al., 2017; Ramos et al., 2013; Ritchie and Romanuk, 2012; Rivera-Espinoza and Gallardo-Navarro, 2010). Ritchie and Romanuk (2012) reported a more significant probiotic effect in combined species of Lactobacilli compared to studies that used only one species but higher doses of probiotic organisms did not significantly enhance the therapeutic effect of probiotics organisms against gastrointestinal diseases. They therefore suggested that dosage size of metabolites formed in fermented foods on the other hand may be crucial to the effectiveness of these foods in enhancing gastrointestinal health.
Majority of the studies found during the search, investigated the efficacy of fermented foods in the prevention rather than treatment of diarrhoea and other related gastrointestinal diseases (Beausoleil et al., 2007; de Vrese et al., 2011; Fox et al., 2015; Wenus et al., 2008) with a combination of heat treated and unfermented controls. However, in vivo studies that have investigated the effect of cell free or heat treated fermented foods versus unfermented foods were unavailable. Such in vivo studies may be able to give insights on the effect of the combined components of the complex matrix of fermented food, excluding the fermentation organisms, on health. Though the results of this current study may indicate that the fermentation organisms may help improve gut health during an episode of diarrhoea, it also supports the possibility that the complex matrix of the fermented food, which includes the organisms, end-products and by-products of fermentation may be of greater significance, than the isolation of each component.
Furthermore, there is limited number of studies that have investigated treatment of diarrhoea using fermented foods other than dairy products in both adults and infants (Fox et al., 2015; Patro-Golab et al., 2015a; Patro-Gołąb et al., 2015b; Rivera-Espinoza and Gallardo-Navarro, 2010). The potential of fermented cereals having similar outcomes as fermented dairy products should not be overlooked. Only one article, Yartey et al., (1995) which was included in the current study. Lei et al., (2006), also investigated that effect of a fermented cereal product in diarrhoea but was excluded from this study as it did not meet the inclusion criteria. Sub-analysis of fermented corn versus ORS in the current study suggests that fermented maize may be more effective in reducing the duration of diarrhoea than ORS, though the analysis was done with one article. This could imply that fermented corn may be a plausible effective alternative when ORS is not easily available especially in locations where corn is a staple meal. Furthermore, Pashapour and Iou, (2006) reported a significant difference, though marginal, in the reduction in the daily stool frequency with the group that was administered fermented milk having a decreased frequency compared to the group that was administered intravenous serum therapy and oral rehydration solution (ORS). This therefore buttresses the need for further research to be undertaken to investigate the efficacy of fermented food in the management of diarrhoea.
Limitation of meta-analysis
Due to limited number of studies that have investigated the effectiveness of fermented foods, in the treatment of diarrhoea, only seven articles were included in the current review due to the limited number of studies of fermented foods in infants. On the other hand, many more studies have investigated the effectiveness of fermentation organisms particularly those that have tested for probiotic potentials (Allen et al., 2010; Marsh et al., 2014; Millette et al., 2008; Mokoena et al., 2016) in the prevention or treatment of diarrhoea, especially in adults. Secondly, the disappearance of a significant outcome in the comparison between fermented foods versus unfermented foods in the sub-group analysis may be related to the variation in the types of controls that were used in the studies. But more importantly, the plausible overestimation of mean and standard deviation resulting from the conversion of the median and range values reported the included study by Bhatnagar et al., (1998) may have also notably contributed to the disappearance of this statistical significance. Thirdly, a significant degree of statistical heterogeneity was observed but not surprising as there were marked diversity in the ages of the participants, population size, location of study, duration and dosage of intervention between studies. Also, only 2 studies included in the review (Agarwal and Bhasin, 2002; Pedone et al., 1999) showed low risk of bias using the Cochrane assessment tool. The quality of trials included in a meta-analysis will have a great impact on the validity of the results (Agarwal and Bhasin, 2002; Greco et al., 2013). Isolauri et al., (1991) declared support from DANONE and Foundation for Nutrition Research respectively for their studies.
Conclusion and future research
Fermented food products are widely available and consumed around the world. Probiotic potential of the organisms involved in the fermentation process have been documented. Health benefits of some of the end-products and by products of fermentation have also been suggested. Fermented foods are traditionally consumed in some African and Asian communities, not only for the nutritional benefits but also for possible therapeutic effects they are perceived to have in the treatment of gastrointestinal diseases such as diarrhoea. There is however limited number of studies to evidence this perception. The current review has attempted to do this using limited amount of data available on the effect of fermented food on infant diarrhoea. Results indicate that fermented foods may be helpful in the treatment of diarrhoea in infants up to the age of five, maybe to the same degree as, or better than as suggested by Yartey et al., (1995) and Pashapour et al., (2006), the ORS recommended by the WHO. Given the small number of trials and methodological limitations of the included studies, the evidence in this review should be viewed with caution. However, the efficacy of fermented foods has shown promise and warrants further investigation to inform health workers of the benefits gained in nutrition, health and well-being particularly amongst very young children. More good quality trials are required to investigate the complex matrix of fermented food products, other than dairy foods, in the management, particularly treatment of gastrointestinal diseases such as diarrhoea.
Abbreviations
- WHO
World Health Organisation
- GIT
gastrointestinal tract
- LAB
lactic acid bacteria
- ORS
oral rehydration solution
- SCFA
Short Chain Fatty Acid
- EPS
Extracellular polysaccharides
- RCTs
Randomised controlled trials
- PRISMA
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
Footnotes
Ethical approval: This analysis was exempt from ethics because there was no direct involvement of animal or human subjects.
Guarantor: Not Applicable
Contributorship: AO: Conceptualised the idea; Article is part of the PhD thesis; Undertook writing, data extraction and meta- analysis
DM: Draft review and organisation
YK: Draft review, organisation and re-write where necessary
NP: PhD supervisor, data extraction, draft review
Availability of data and materials: The data that support the findings of this study are available on request from the corresponding author.
Consent for publication: All authors have approved the version of the manuscript submitted and agreed to publish this in Nutrition and Health. All authors also declare that this study is not published or submitted elsewhere for peer review.
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.
ORCID iDs: Adetokunbo Olayanju https://orcid.org/0000-0002-5021-2832
Duane Mellor https://orcid.org/0000-0002-1369-3868
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