Weight Loss Benefits of Rifaximin in an Intermittent Fasting Diet

The Potential Weight Loss Benefits of Rifaximin in an Intermittent Fasting Diet

The epidemic of overweight and obese patients presents a major challenge in chronic disease prevention and overall health across the world. Since the beginning of this century, it is considered the third most important hazard attributable to burden of disease with approximately 350 million obese people (BMI ≥30.0) and over 1 billion overweight people (BMI ≥ 25) in the world. Mechanistic studies have indicated that the microbiota influences energy utilization from the diet and influences host genes that regulate energy expenditure and storage. Thus, it is proposed that alterations in gut microbiota may play a significant role in weight loss potential.

This study seeks to expand on this idea by evaluating whether the incorporation of Rifaximin in an intermittent fasting (IF) diet plays a significant role in weight loss. Rifaximin is a nonsystemic antibiotic that works primarily in the gut to inhibit bacterial growth. It portrays unique eubiotic properties that induces a positive modulation of gut microbiota, favoring the growth of bacteria beneficial to the host without altering overall composition. Thus we propose an agent such as rifaximin would be essential in developing a positively altered gut microbiome.

Based on studies evaluating Rifaximin's role in positive gut modification, we propose that this can play a critical role in weight loss. Rifaximin may be associated with weight loss as it exerts effects that increases the concentration of bacteria more prominent in lean individuals. The choice of incorporating an intermittent fasting (IF) diet, stems from its success in prior studies. By incorporating periods of voluntary abstinence from food and drink, an IF diet has shown short term weight loss among overweight and obese people. We propose that an IF diet with an antibiotic, like Rifaximin, will create more positive alteration in gut microbiota that creates a greater potential for weight loss overall.

A group of subjects with BMI's ranging from 30-35 will be randomly selected and assigned to an experimental and control group. Each subject will be given clear instructions on how to follow a 14:10 intermittent fasting diet, in which they will fast for 14 hours and be able to eat for 10 hours a day. Patients in the experiment group will additionally receive a short-term low dosage of Rifaximin at the start of their diet. Patients will be evaluated with weekly weigh-ins and basic blood work performed at the start and at the completion of the study. The current hypothesis does not incorporate microbiome evaluation due to cost of the kits and limited funding available for the study.

Study Overview

• Status: Unknown
• Conditions: Weight Loss
• Intervention / Treatment: Drug: Rifaximin

Detailed Description

The epidemic of overweight and obese patients presents a major challenge in chronic disease prevention and overall health across the world. Since the beginning of this century, it is considered the third most important hazard attributable to burden of disease with approximately 350 million obese people (BMI ≥30.0) and over 1 billion overweight people (BMI ≥ 25) in the world (Mehrabani, 2018). Although there is a myriad of reasons for obesity, numerous studies have proposed that the intestinal microbiome plays an intrinsic role in overall health and obesity risk. Mechanistic studies have indicated that the microbiota influences energy utilization from the diet and influences host genes that regulate energy expenditure and storage (Davis, 2016). Thus, it is proposed that alterations in gut microbiota may play a significant role in weight loss potential.

This study seeks to expand on this idea by evaluating whether the incorporation of Rifaximin in an intermittent fasting (IF) diet plays a significant role in weight loss. Rifaximin is a nonsystemic antibiotic that works primarily in the gut to inhibit bacterial growth. It portrays unique eubiotic properties that induces a positive modulation of gut microbiota, favoring the growth of bacteria beneficial to the host without altering overall composition (Ponziani et al.,2017). In addition to its bactericidal and bacteriostatic effects, rifaximin downregulates the inflammatory response triggered by the gut microbes through inhibition of nuclear factor (NF)-kB via the pregnane X receptor (PXR) and reduces the expression of pro-inflammatory cytokines IL-1B and tumor necrosis factor alpha. These characteristics are unique to rifaximin in comparison to other antibiotics, prebiotics and probiotics (such as yogurt). These effects of rifaximin play a crucial role in gut modulation by altering bacterial virulence through inhibition of adhesion, internalization and translocation to modify bacterial metabolism (Ponziani et al.,2017). Probiotic agents such as yogurt function to increase bacterial groups (such as Bacteriodes Lactobacilli and Bifdobacteria) and there is no proven effect on gut modulation specifically. Thus we propose an agent such as rifaximin would be essential in developing a positively altered gut microbiome.

One meta-analysis investigating the associated symptoms of Rifaxamin when treating hepatic encephalopathy found weight loss to be one its side effects. (Eltawil et al.,2012). It is currently unknown whether the potential weight loss is a beneficial result of the drug or secondary to its side effects. However, based on studies evaluating Rifaximin's role in positive gut modification, we propose that this can play a critical role in weight loss. The human body is a host to vast number of microbes intrinsically linked with overall health, including obesity risk. Studies investigating the relationship between obesity and microbiota found that a low fecal bacterial diversity is associated with more marked overall adiposity, dyslipidemia, and impaired glucose homeostasis with higher low-grade inflammation. Additionally, the intestines are dominated by two divisions of bacteria: Bacteriodes and Firmictus. Within the study, obese individuals had more Firmicutes bacteria and nearly 90% less Bacteriodes than the lean individuals (Davis, 2016). This supports the reason in which Rifaximin may be associated with weight loss as it exerts effects that increases the concentration of Bifidobacteria and Bacteriodes species (Ponziani et al.,2017). By altering inflammatory cytokines, Rifaximin also plays a crucial role in improving glucose homeostasis and gut inflammation. Finally, one study investigating weight loss capabilities of rifaximin found that patients had lost a mean of 4.5 lbs in the rifaximin group compared to the control loss of 0.7lbs over a 4 month follow up (Vizuete, 2012).

The choice of incorporating an intermittent fasting (IF) diet, stems from its success in prior studies. By incorporating periods of voluntary abstinence from food and drink, an IF diet has shown short term weight loss among overweight and obese people (Ganesan et al,2018). Currently, there are no specific studies evaluating the effects rifaximin has in an IF diet. However, a meta-analysis investigating fasting diets found an alteration of gut microbiota that induced a white adipose tissue to brown adipose tissue transition - which is a beneficial reaction (Li et al, 2020). Additionally, one study investigating microbiome changes specific to a fasting diet found that there was a significantly increased abundance of Bacteriodes fragilis and Akkermansia muciniphila species (Ozkul et al, 2019). As there are already studies investigating the impact of rifaximin and fasting diet effects individually on weight loss, we propose that an IF diet with an antibiotic, like Rifaximin, will create more positive alteration in gut microbiota that creates a greater potential for weight loss overall. Although rifaximin does have some associated side effects, it is important to note that among numerous studies using Rifaximin, patients who had experienced nausea/anorexia claimed it was mild and did not withdraw from the studies (Ying et al., 2020 and Furnari 2019). Overall, this study aims to objectively determine if the use of Rifaximin with an intermittent fasting diet will improve overall weight loss results.

A group of subjects with BMI's ranging from 30-35 will be randomly selected and assigned to an experimental and control group. Each subject will be given clear instructions on how to follow a 14:10 intermittent fasting diet, in which they will fast for 14 hours and be able to eat for 10 hours a day. Patients in the experiment group will additionally receive a short-term low dosage of Rifaximin at the start of their diet. Patients will be evaluated with weekly weigh-ins and basic blood work performed at the start and at the completion of the study. It is important to note, that although we have proposed a change in gut microflora the study will focus on evaluating weight loss results and will later be followed up with another study that evaluates changes in gut microflora through microbiome testing kits. The current hypothesis does not incorporate microbiome evaluation due to cost of the kits and limited funding available for the study.

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Phase 4

Contacts and Locations

Study Locations

• United States
  • Delaware
    • Dover, Delaware, United States, 19901
      • Bayhealth Medical Center- Dover Family Physicians and GI Consultants Office

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• BMI of 30-35

Exclusion Criteria:

• Underlying conditions such as hypertension, hyperlipidemia, diabetes, etc.
• BMI out of range listed above
• Inability to participate in an intermittent fasting diet
• Pregnant patients, as rifaximin should be used with caution in pregnancy due to limited data. (Subjects of childbearing age will undergo a baseline pregnancy test prior to starting the study)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Single Group Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Rifaxamin (R); Patients in the experimental group will receive additional instructions to take 550 mg of Rifaximin 3 times a day for 12 days at the start of the diet. The experimental group will be provided the required doses of Rifaximin at the initial weigh-in and office visit.	Drug: Rifaximin; 550 mg of Rifaximin 3 times a day for 12 days at the start of the diet.
No Intervention: Control; Participants in the control group will undergo no intervention and will only be asked to follow an Intermittent fasting diet.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Weight loss	Patients will be asked to come in for weekly weigh-ins on the same day of the week and time of day (morning, noon or evening). Weight loss will be evaluated as pounds lost or % pounds lost.	Change from Baseline weight at 6 months
BMI	BMI will be calculated at the beginning and at the end of the diet. Weight and height will be combined to report BMI in kg/m^2	Change from Baseline BMI at 6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
HbA1C	HbA1C will be measured at the start and end of the diet to evaluate percent change.	Change from Baseline HbA1C at 6 months
Lipids	Lipid panels will be evaluated at the start and end of the diet.	Change from Baseline lipid results at 6 months

Collaborators and Investigators

• Sponsor: Bayhealth Medical Center
• Investigators: Principal Investigator: Bhavin Dave, MD, Bayhealth Medical Center

Publications and helpful links

General Publications

• Davis CD. The Gut Microbiome and Its Role in Obesity. Nutr Today. 2016 Jul-Aug;51(4):167-174. doi: 10.1097/NT.0000000000000167.
• Eltawil KM, Laryea M, Peltekian K, Molinari M. Rifaximin vs. conventional oral therapy for hepatic encephalopathy: a meta-analysis. World J Gastroenterol. 2012 Feb 28;18(8):767-77. doi: 10.3748/wjg.v18.i8.767.
• Furnari M, De Alessandri A, Cresta F, Haupt M, Bassi M, Calvi A, Haupt R, Bodini G, Ahmed I, Bagnasco F, Giannini EG, Casciaro R. The role of small intestinal bacterial overgrowth in cystic fibrosis: a randomized case-controlled clinical trial with rifaximin. J Gastroenterol. 2019 Mar;54(3):261-270. doi: 10.1007/s00535-018-1509-4. Epub 2018 Sep 19.
• Ganesan K, Habboush Y, Sultan S. Intermittent Fasting: The Choice for a Healthier Lifestyle. Cureus. 2018 Jul 9;10(7):e2947. doi: 10.7759/cureus.2947.
• Li L, Su Y, Li F, Wang Y, Ma Z, Li Z, Su J. The effects of daily fasting hours on shaping gut microbiota in mice. BMC Microbiol. 2020 Mar 24;20(1):65. doi: 10.1186/s12866-020-01754-2.
• Mehrabani J, Ganjifar ZK (2018). Overweight and obesity: a brief challenge on prevalence, complications and physical activity among men and women.MOJ Womens Health;7(1):19-24. DOI: 10.15406/mojwh.2018.07.0016
• Ozkul C, Yalinay M, Karakan T. Islamic fasting leads to an increased abundance of Akkermansia muciniphila and Bacteroides fragilis group: A preliminary study on intermittent fasting. Turk J Gastroenterol. 2019 Dec;30(12):1030-1035. doi: 10.5152/tjg.2019.19185.
• Ponziani FR, Zocco MA, D'Aversa F, Pompili M, Gasbarrini A. Eubiotic properties of rifaximin: Disruption of the traditional concepts in gut microbiota modulation. World J Gastroenterol. 2017 Jul 7;23(25):4491-4499. doi: 10.3748/wjg.v23.i25.4491.
• Li Y, Hong G, Yang M, Li G, Jin Y, Xiong H, Qian W, Hou X. Fecal bacteria can predict the efficacy of rifaximin in patients with diarrhea-predominant irritable bowel syndrome. Pharmacol Res. 2020 Sep;159:104936. doi: 10.1016/j.phrs.2020.104936. Epub 2020 May 26.
• Vizuete, John MD, MPH2; Randall, Charles MD1; Taboada, Carlo MD, et al (2012). Rifaximin for the Treatment of Weight Loss. American Journal of Gastroenterology, 590, Vol. 107
• Zullo A, Ridola L, Hassan C. Rifaximin therapy and Clostridium difficile infection: a note of caution. J Clin Gastroenterol. 2013 Sep;47(8):737. doi: 10.1097/MCG.0b013e31828bea4b. No abstract available.

Study record dates

Study Major Dates

• Study Start (Anticipated): January 1, 2021
• Primary Completion (Anticipated): January 1, 2022
• Study Completion (Anticipated): January 1, 2022

Study Registration Dates

• First Submitted: October 22, 2020
• First Submitted That Met QC Criteria: December 13, 2020
• First Posted (Actual): December 19, 2020

Study Record Updates

• Last Update Posted (Actual): December 19, 2020
• Last Update Submitted That Met QC Criteria: December 13, 2020
• Last Verified: December 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Body Weight Changes; Weight Loss; Body Weight; Anti-Infective Agents; Gastrointestinal Agents; Anti-Bacterial Agents; Rifaximin
• Other Study ID Numbers: 19901

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No