College students may be at increased risk for upper respiratory infections (URI) compared to the general adult population due to a multi-stressor environment, characterised by inadequate sleep and psychological stress(Reference Cohen, Doyle and Alper1–Reference Segerstrom and Miller4). Additionally, many live in residence halls or alternative group housing (e.g. sorority or fraternity houses)(2), which facilitates the transmission of viruses from one student to another(Reference White, Kolble and Carlson5). The negative consequences of URI in the present population are missed school days, missed work days, compromised academic performance, burden on the healthcare system and related costs(2, Reference Nichol, D'Heilly and Ehlinger6–8). There is no evidence that over-the-counter (OTC) drugs have any effect on the duration of the viral infection, and they offer only marginal benefits with regard to alleviation of symptoms(Reference Bolser9–Reference Taverner and Latte12). Further, OTC drugs may have unwanted side effects, such as drowsiness(Reference Sutter, Lemiengre and Campbell11), xerostomia (dry mouth)(Reference Sutter, Lemiengre and Campbell11), nervousness(Reference Sutter, Lemiengre and Campbell11), irritability(Reference Sutter, Lemiengre and Campbell11), difficulty sleeping(Reference Sutter, Lemiengre and Campbell11, Reference Taverner and Latte12) and elevated blood pressure(Reference Taverner and Latte12).
Duration and severity of URI symptoms and functional impairment in response to symptoms contribute to health-related quality of life (HRQL)(Reference Wilson and Cleary13, Reference Barrett, Locken and Maberry14). HRQL is subjectively assessed by the patient(Reference Wilson and Cleary13), and most simply defined as ‘the component of overall quality of life that is determined primarily by the person's health and that can be influenced by clinical interventions’(Reference Juniper15). For example, Linder & Singer(Reference Linder and Singer16) demonstrated that various aspects of HRQL were negatively affected during URI, such as physical functioning, bodily pain, vitality, social functioning and mental health. Thus, there is interest in strategies that can improve HRQL in persons suffering from URI.
One such strategy to improve HRQL during URI may involve probiotics, defined by the WHO as ‘live organisms which when administered in adequate amounts confer a health benefit on the host’(17). Prior research studies have demonstrated the ability of certain probiotic strains to modulate immune function(Reference Rizzardini, Eskesen and Calder18–Reference Gleeson, Bishop and Oliveira25). Upper respiratory symptoms result from the inflammatory response of the host towards the virus, not from the viruses themselves(Reference Kirchberger, Majdic and Stockl26). Therefore, immune system adaptations by probiotics may reduce the severity and duration of symptoms via modulation of the inflammatory response to the virus, thus having a positive impact on HRQL during URI. Bifidobacterium animalis ssp. lactis BB-12® (BB-12®) and Lactobacillus rhamnosus LGG® (LGG®) are two particular probiotic strains that may be helpful, according to prior research which showed benefits on immune function in healthy adults(Reference Link-Amster, Rochat and Saudan19–Reference Christensen, Larsen and Kaestel23) and URI outcomes in children(Reference Hatakka, Savilahti and Ponka27–Reference Rautava, Salminen and Isolauri29). However, there is no published research investigating the effect of LGG® and BB-12®, or other probiotic strains, on HRQL during URI, taking into account symptom severity and functional impairment, both important factors of HRQL.
The primary objective of the study was to assess the effect of probiotics on HRQL during URI in college students living on campus in residence halls at the Framingham State University, Framingham, MA. Measures of HRQL were investigated during URI, including self-reported duration, severity of symptoms and functional task impairment. Secondary objectives included self-reported missed school and work days due to URI. It was hypothesised that the probiotics group would have a higher HRQL during URI episodes, as reflected by shorter duration and lower severity scores, compared to the placebo group.
Experimental methods
Study design
The present research study was a prospective, randomised, double-blind, placebo-controlled trial. Daily, for 12 weeks (February–May 2011), subjects were asked to consume probiotics or placebo and complete the Wisconsin Upper Respiratory Symptom Survey-21 (WURSS-21)(Reference Barrett, Brown and Mundt30) to assess HRQL during URI. The Wilson & Cleary(Reference Wilson and Cleary13) HRQL conceptual model provides a framework for indirectly assessing the impact of probiotics on HRQL during URI episodes. Probiotics may directly have an impact on biological and physiological variables (the first stage of the continuum), which will indirectly affect symptoms, functionality, general health perceptions and ultimately overall quality of life (the final stage of the continuum). The present study focused on the impact of probiotics on symptoms (duration and severity of symptoms) and functionality during URI. Once per week, subjects were also asked to complete the weekly questionnaire to assess missed school and work days. Subjects completed all of the aforementioned surveys via the online application, ‘Survey Monkey’ (http://www.surveymonkey.com). Subjects met with the study staff once every 2–3 weeks (to accommodate the academic calendar) during the spring 2011 semester to obtain their supply of probiotics/placebo. The present study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving human subjects/patients were approved by The University of Medicine and Dentistry of New Jersey (Newark, NJ) and the Framingham State University (Framingham, MA) Institutional Review Boards. Written informed consent was obtained from all subjects. Participants received up to $100 in the form of shopping gift-cards for study participation. The Clinicaltrials.gov identifier is NCT01657643.
Participants
All students living on campus in residence halls at the Framingham State University in January 2011 were invited to participate in the study. Study briefings (22 January 2011 to 10 February 2011) consisted of an oral explanation of all study procedures and risks, after which time the interested students were asked to sign the informed consent form. Participants were excluded from participation if: (1) their driver's license or state identification card indicated that they were under 18 years of age or over 25 years of age; (2) they experienced chronic perennial allergies (such as allergies to dust or mould); (3) they were pregnant; (4) they had been diagnosed with medical conditions affecting immune function (e.g. asthma, chronic fatigue syndrome and HIV); or (5) they had acute pancreatitis, were undergoing treatment for cancer or were taking immunosuppressive drugs for an autoimmune disease or post-transplant. Participants were asked to refrain from consuming non-study-related dietary supplements containing probiotics (e.g. Culturelle®) and yogurts with high probiotic content (e.g. DanActive™ or Activia™) during the study, as well as any other dietary supplements which may have an effect on immune function (e.g. Airborne®, Echinacea and quercitin). Participants were reminded of dietary restrictions weekly via the online questionnaire.
Randomisation
Participants were assigned a unique study identification number in the order in which they were enrolled in the study. Specifically, participant numbers were assigned in numerical order (starting with the number 001), based on the order in which the signed consent form was returned to the principal investigator (PI). The randomisation list was generated by the PI using an internet-based random number generator (GraphPad Random Number Generator, 2005), wherein participants were randomised to sticks labelled either ‘2930’ or ‘3220’ based on their unique study identification number. The PI was blinded as to which four-digit code represented probiotics or placebo. A person who was not part of the study staff (i.e. student health services coordinator at the Framingham State University) maintained the randomisation list and the codes indicating placebo or probiotics assignment.
Intervention
The intervention was administered as a daily dose of a strawberry-flavoured powder (5 g), and was packaged in a small foil ‘stick’. Each probiotic stick contained a minimum of 1 billion (or 109) colony-forming units each of LGG® and BB-12® in powder form (Chr. Hansen A/S), which was confirmed before, and within 2 weeks of, study completion. Subjects were advised to store their probiotics/placebo sticks in a cool, dry location ( < 21°C), and to consume only one stick per d.
Blinding
The packaging and contents of the placebo sticks were identical in taste and appearance to the probiotics stick, but did not contain any probiotics. Chr. Hansen A/S manufactured the probiotics and placebo sticks, and labelled each stick with a four-digit number code (2930 or 3220) to identify placebo or active. The PI, study staff and study participants were blinded. The blinding code was provided to the PI after the data cleaning and statistical analysis were completed.
Baseline demographic characteristics and anthropometrics
Baseline data were collected within approximately 1 week of the subjects' consent, after subjects were enrolled and randomised. The following self-reported demographic data were collected via a self-administered questionnaire: sex, age, year in school, race and ethnicity. Criteria for reporting race and ethnicity were based on guidelines from the National Institutes of Health(31).
Primary outcome: health-related quality of life
The WURSS-21 was used to determine if a study participant was suffering from a URI and, subsequently, his/her HRQL during the course of the URI. The WURSS-21 is composed of one global severity item, one global change item, ten symptom-based items and nine functional status items(Reference Barrett, Brown and Mundt30). All subjects answered question no. 1 of the WURSS-21, ‘How sick do you feel today?’ each day during the data collection period. The participant was prompted to answer the remaining twenty questions if, and only if, they did not answer ‘not sick’ to question no.1. A URI episode was recorded if the participant answered affirmatively to question no. 1, 2 d in a row. If a participant reported a URI episode within 7 d of recovering from a previous URI episode (indicated by answering ‘no’ to question no. 1, 2 d in a row), then this episode was considered part of the previous infection(Reference Barrett, Brown and Mundt30).
If a participant indicated that he or she could not access a survey due to technological issues, study staff communicated with the participant to determine whether or not they were suffering from a URI. If the participant indicated that he or she was ‘not sick’, the PI manually completed the survey for him or her on the day in question. If a participant indicated that he or she ‘had a cold’, and was unable to complete the survey, the PI recorded that the participant had a URI on the day in question and this datum was included the analyses; however, remaining WURSS-21 data regarding symptom severity and functionality were considered missing.
Two HRQL scores were generated from the WURSS-21. The first HRQL score was related to duration of the URI episode. Self-reported duration of a URI episode was determined using responses to question no. 1 on the WURSS-21. Start of illness was indicated by an affirmative response to question no. 1, 2 d in a row, while the end of illness was indicated by a negative response to question no. 1, 2 d in a row(Reference Barrett, Brown and Mundt30). Duration was calculated from the first day of an affirmative response up to (but not including) the first day of a negative response. The second HRQL score, generated from the WURSS-21, assessed both symptom severity and functional status, and was expressed in terms of AUC, which was ascertained by adding daily WURSS scores (the possible response range was 0–133 per d) across all days of the illness(Reference Barrett, Brown and Mundt30).
Secondary outcomes: missed school and work days
Subjects self-reported via the Weekly Questionnaire if they missed any school or work (including an internship or practicum) as a consequence of a URI, and the subsequent number of missed school or work days.
Compliance
Subjects received an email and text message daily (7 d/week including weekends and holidays) containing a link to the day's survey and a reminder to take their probiotics/placebo and complete the survey. Daily, subjects were asked to send a text message or email to a designated mobile phone number or email address, respectively, stating that they had taken their probiotics/placebo and completed the survey(s). Study staff followed-up with all subjects who had not sent a text message or email by approximately 19.00 hours each day. Compliance with the probiotics/placebo and questionnaire(s) was recorded daily. Participants were considered ‘compliant’ if they consumed their probiotics/placebo at least five times the week before and during an URI.
Sample size calculation
Sample size estimates were made using SamplePower (release 2.0; SPSS Inc.) paired t test (mean = 0) procedure. The present study aimed to detect a 30 % improvement in HRQL (i.e. symptom severity/functional status score) during URI episodes in response to probiotics v. placebo, based on published literature(Reference Barrett, Brown and Mundt32). Considering an effect magnitude of 93 points, a standard deviation of 250 points(Reference Barrett, Brown and Mundt30) and α set at 0·025 (one-tailed), ninety URI per group were required to have 80 % power in detecting a significant difference between groups. The present study sought to enrol 175 participants in each group to compensate for an estimated 15 % attrition rate and 60 % URI infection rate.
Reporting of adverse events
At the start of the study, participants were provided with the contact information for the PI and asked to communicate any health/medical issues that occurred during the data collection period, regardless of whether or not medical care was sought. Additionally, participants were queried by the PI every 2 to 3 weeks during the data collection period when they were resupplied with probiotics/placebo.
Statistical analysis
Statistical analysis was completed using IBM SPSS statistical software version 19.0 (IBM Corporation) for analysis. All available data were included in the analyses, regardless of compliance with probiotics/placebo and attrition; for example, if a subject withdrew from the study at week 8, all cases of URI that occurred prior to attrition were included in the analyses. Descriptive statistics were obtained for continuous variables and frequencies were calculated for categorical variables. Normal distribution of continuous variables was assessed using the Shapiro–Wilk statistic and visual inspection of histograms. Differences between the probiotics and placebo groups were determined using the Mann–Whitney U test (non-parametric equivalent of the independent samples t test), as data were not normally distributed. For categorical variables, the differences between the probiotics and placebo groups were analysed using the χ2 test. The Bonferroni adjustment was applied to primary outcomes related to HRQL (i.e. duration of URI and symptom severity/functional status score) and significance was established at P≤ 0·001.
Results
Subject disposition and compliance with the intervention
Fig. 1 depicts the recruitment and retention of subjects throughout the study. Of the 231 subjects who initially enrolled, 86 % (n 198; placebo, n 97, 49 % and probiotics, n 101, 51 %) attended the baseline testing session and consumed at least one dose of placebo or probiotics and were included in the statistical analysis. Of these 198 subjects, the retention rate was 91 % (n 180; placebo, n 85, 47 % and probiotics, n 95, 53 %). Compliance with probiotics/placebo was 94 %, wherein probiotics/placebo were consumed at least five times the week before and during a URI in 157 of URI cases (placebo, n 78 cases and probiotics, n 79 cases).
Flow diagram of study participation. * Of the twenty subjects who did not receive the placebo, one participant indicated that they had decided not to participate and the remaining nineteen participants were lost to follow-up. † Of the thirteen participants who did not receive the probiotics, two participants indicated that they had decided not to participate and the remaining eleven participants were lost to follow-up. ‡ Reasons for discontinuation: withdrawn due to new medication (n 1); withdrawn due to health issues related to prior medical diagnosis (n 1); withdrew due to burden of study activities (n 6); withdrew due to gas/bloating (n 3); withdrew due to hospitalisation related to major reconstructive knee surgery (n 1). § Reasons for discontinuation: withdrawn due to withdrawal from the university (n 1); withdrew due to burden of study activities (n 5).
Baseline characteristics
The median age of all participants was 19 years (range 18–24 years). Baseline characteristics (Table 1) were non-significantly different between the placebo and probiotic groups.
Demographic characteristics in the total sample and by group (Number of subjects and percentages)
* There were no significant differences in demographic characteristics between the placebo and probiotic groups.
Primary outcome: health-related quality of life
Available data for HRQL outcomes are shown in Table 2. Of the 167 URI cases reported during the data collection period (placebo, n 83 cases and probiotics, n 84 cases), duration was calculated for 158 cases and severity was calculated for 143 cases due to missing data.
Available data for primary outcome: components of health-related quality of life (Number of subjects and percentages)
URI, upper respiratory infection.
* Total severity score took into account symptom severity and functional status during URI.
Health-related quality of life outcomes are presented in Table 3. URI duration was 33 % (2 d) longer in the placebo group compared to the probiotics group (P= 0·001, one-tailed) and severity scores were 34 % (30 points) higher for the placebo group compared to the probiotics group (P= 0·0003, one-tailed). Significantly fewer days of illness and significantly lower severity scores indicate a higher HRQL in the probiotics group compared to the placebo group(Reference Wilson and Cleary13).
Primary outcome: components of health-related quality of life* (Mean values and standard deviations; medians, ranges and 95 % confidence intervals)
a,b Median values with unlike superscript letters were significantly different between the probiotics and placebo group (duration, P= 0·001 and severity, P= 0·0003).
* Health-related quality of life, as reflected by duration and total severity score.
† Total severity score took into account symptom severity and functional status during upper respiratory infection.
Secondary outcomes: missed work and school days
In the total sample (n 198), nineteen missed work days (10 %; placebo, n 11, 58 % and probiotics, n 8, 42 %) and forty-nine missed school days (25 %; placebo, n 34, 69 % and probiotics, n 15, 31 %) were reported. A total of 94 % of subjects (n 186; placebo, n 92, 50 % and probiotics, n 94, 51 %) indicated that they did not miss any work due to URI, and the number of missed work days did not differ significantly between the placebo group (median = 0; range = 0–3) and the probiotics group (median = 0; range = 0–2), P= 0·429 (one-tailed). The majority of subjects (n 171, 86 %; placebo, n 79, 46 % and probiotics, n 92, 54 %) indicated that they did not miss any school due to URI. The number of missed school days was significantly higher for the placebo group (median = 0; range = 0–4) compared to the probiotics group (median = 0; range = 0–3), P= 0·002 (one-tailed).
Adverse events
There were no significant differences between groups for adverse events (AE), and no serious AE were reported. A total of forty-three AE were reported during the study period (Table 4). Of the forty-three reported AE, diarrhoea or vomiting was the most commonly reported among 198 subjects who consumed at least one dose of placebo or probiotics (n 22, 11 %; placebo, n 10, 45 % and probiotics, n 12, 55 %). Increased flatulence and bloating were the second most common AE, occurring in approximately 4 % of the 198 subjects who consumed at least one dose of placebo or probiotics (n 7; placebo, n 4, 57 % and probiotics, n 3, 43 %).
Adverse events in the total sample and by group* (Number of subjects and percentages)
* Includes subjects who consumed at least one dose of placebo or probiotics (n 198).
† Percentages in this column are representative of subjects who consumed at least one dose of placebo or probiotics (n 198).
‡ These adverse events were diagnosed by a medical doctor.
Discussion
The present study investigated the effect of a probiotic powder containing both LGG® and BB-12® (109 colony-forming units of each strain) on HRQL during URI in college students living on campus in residence halls. Results related to HRQL (the primary outcome) were positive: duration of URI was significantly shorter and URI severity scores were significantly lower in the probiotics group compared to the placebo group. Low occurrence of AE (including gastrointestinal-related symptoms historically associated with probiotics use) and the fact that these symptoms were evenly distributed between groups indicated that the intervention was well-tolerated.
The present study found that median duration of URI was significantly lower by approximately 2 d in the probiotics group compared to the placebo group. The median duration of URI for the placebo group was 6 d; therefore, this finding has practical implications as a 2 d reduction represents 33 % of the total URI duration. Additionally, 2 d represents one-third of a calendar week where productivity may not be lost due to a URI. Three previously published trials also observed significant differences in URI duration in response to probiotics v. placebo (1–2 d mean reduction or approximately 20 %; P <0·05)(Reference Berggren, Lazou Ahrén and Larsson24, Reference de Vrese, Winkler and Rautenberg33, Reference Pregliasco, Anselmi and Fonte34), and the magnitude of between-group differences appears to be similar between the present study and prior studies. In contrast, other studies reported no differences in URI duration between groups(Reference Gleeson, Bishop and Oliveira25, 35–Reference Tiollier, Chennaoui and Gomez-Merino38). Comparisons between studies should be made with caution, as probiotic strains and study populations varied between trials.
The present study also found that median severity of URI was approximately 34 % lower in the probiotics group compared to the placebo group. These findings have practical implications, as severity scores took into account both symptom severity and the effect of URI symptoms on functional tasks. Three prior studies detected no significant differences in total severity scores between groups(Reference Berggren, Lazou Ahrén and Larsson24, Reference Gleeson, Bishop and Oliveira25, Reference Winkler, de and Laue36), while others(Reference de Vrese, Winkler and Rautenberg33, Reference Pregliasco, Anselmi and Fonte34, Reference Cox, Pyne and Saunders37) reported that total severity scores were lower in response to probiotics compared to placebo. The reduction in severity scores in the present study was similar compared to the aforementioned trials (34 v. 20–40 %, respectively)(Reference de Vrese, Winkler and Rautenberg33, Reference Pregliasco, Anselmi and Fonte34, Reference Cox, Pyne and Saunders37). Study populations, methods of assessing symptom severity and probiotic strains were different between studies, thus limiting comparisons.
Results from the present study suggest that the combination of LGG® and BB-12® may be beneficial for mitigating decrements in HRQL during URI in college students living on campus in residence halls. URI symptoms result from the inflammatory response of the host towards the virus, not from the viruses themselves(Reference Kirchberger, Majdic and Stockl26). Therefore, these findings may be partially explained by modulation of the inflammatory response, which has been observed in response to other probiotic strains(Reference Berggren, Lazou Ahrén and Larsson24, Reference de Vrese, Winkler and Rautenberg33, Reference Cox, Pyne and Saunders37, Reference Lavasani, Dzhambazov and Nouri39). For example, de Vrese et al. demonstrated a lower duration of URI in response to a multi-strain probiotics combination of lactobacilli and bifidobacteria compared to placebo, coupled with significantly higher numbers of cytotoxic plus T-suppressor cells (CD8+) and T-helper cells (CD4+) in the probiotics v. placebo group. Berggren et al. demonstrated that the severity score for pharyngeal symptoms was lower in response to two Lactobacillus strains (L. plantarum HEAL 9, DSM 15 312 and L. paracasei 8700:2, DSM 13 434) compared to placebo, and the authors detected a significantly increased number of B lymphocytes in the control group when compared to the probiotics group. The authors speculated that this finding may be indirectly associated with reduced inflammation and pharyngeal symptom severity. Thus, it is possible that the combination of LGG® and BB-12® modulated the inflammatory response in the present study's subjects, and positively made an impact on HRQL during URI. Future research should combine the HRQL outcomes evaluated in the present investigation with outcomes assessing the probiotics' mechanisms of action on the immune system to further elucidate results from the present study.
In the present study, only 14 % (n 27) of subjects in the total sample reportedly missed school due to a URI, and the total number of missed school days was low compared to the total days of reported URI (49 v. 1003 d, respectively). It is feasible that subjects attended school regardless of URI; however, it is also possible that subjects may not have had classes scheduled on days that they were sick. Although the probiotics group missed significantly fewer school days compared to the placebo group (15 v. 34 d, respectively), the effect magnitude was small (0·2 d). Future studies are needed to confirm or refute these findings.
The present study did not detect any significant differences between groups in terms of missed work days due to a URI. These findings are contrary to Tubelius et al. (Reference Tubelius, Stan and Zachrisson40), who found that fewer subjects missed work in response to a different probiotic strain, L. reuteri ATCC55730 v. placebo (26 v. 11 %, P= 0·01). However, the authors(Reference Tubelius, Stan and Zachrisson40) did not differentiate between sick days due to gastrointestinal illness and respiratory tract infections. In the present study, differences between groups may not have been detected for missed work days either because few students worked (possibility of a type II error) or because students were highly motivated to earn money. However, these possibilities cannot be confirmed, as no data were collected regarding work commitments.
The use of OTC medicine was not monitored in the present study; however, this potential confounder was minimised as participants were asked to consider their symptoms when they were not under the influence of OTC medicine (e.g. upon waking). Missing survey data, and assumptions with regard to missing survey data, further limit the study findings. However, these assumptions were based on clinical observations reported in the literature. Further research is warranted to determine if the strains are effective on their own or only in combination. The external validity of the study is further limited to the population studied, and additional research is needed to determine if LGG® and BB-12® are effective for limiting decrements in HRQL during URI in other populations (e.g. athletes), as immune response to URI may be different(Reference Bruunsgaard, Hartkopp and Mohr41–Reference Nieman43).
Lactobacillus may be contraindicated in persons with serious underlying diseases and/or with immunosuppression, based on documented cases of lactobacillaemia, infectious endocarditis and liver abscess(Reference Husni, Gordon and Washington44–Reference Salminen, Tynkkynen and Rautelin48). Besselink et al. (Reference Besselink, van Santvoort and Buskens49) reported that a multi-strain probiotics preparation increased the risk of bowel ischaemia in persons with acute pancreatitis; however, there has been debate as to whether the probiotics were indeed responsible for this negative outcome(Reference Bengmark50). Although these conditions may be unlikely in college students, they should still be given consideration when educating consumers and health care practitioners, when applying the present study's findings in practice and conducting future research. Although the present study showed positive results, a cost–benefit analysis is warranted before a widespread supplementation of LGG® and BB-12® is implemented in the present population. Factors in this equation would be the cost of supplementation itself, healthcare costs, cost of OTC medication use, lost wages and lost productivity at work and school.
Conclusion
The findings from the present study suggest that the combination of LGG® and BB-12® may be beneficial for mitigating decrements in HRQL during URI in college students living on campus in residence halls. Further studies are needed to determine if the combination of LGG® and BB-12® is beneficial for preserving absences from school during URI.
Acknowledgements
The present study was funded by Chr Hansen A/S (Hoersholm, Denmark). Chr Hansen A/S provided the probiotics and placebo products, and provided input towards the study design and final report. However, the company had no involvement in data collection, analysis or interpretation. The authors declare no conflicts of interest. T. J. S. designed the study, coordinated data acquisition, performed the statistical analysis and drafted the manuscript. D. R.-R., R. T.-D., R. D. and T. H. made substantial contributions to study design and critically revised the manuscript for intellectual content. The authors wish to thank study subjects and research assistants from the Framingham State University, Framingham, MA (USA).
