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Efficacy of a Probiotic Formulation in Adults With Lactose Intolerance and Methanogenic Intestinal Overgrowth (LAC L-134/33)
Efficacy of a Probiotic Formulation (Lacticaseibacillus Rhamnosus - Limosilactobacillus Fermentum) on Gastrointestinal Symptoms in Adults With Lactose Intolerance and Methanogenic Intestinal Overgrowth
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Lactose intolerance (LI) is a syndrome associated with specific symptoms, including abdominal bloating and pain, nausea, flatulence, borborygmi, and diarrhea following the consumption of foods containing lactose, a disaccharide that is hydrolyzed in the intestine by the enzyme lactase (β-D-galactosidase). However, when there is enzymatic inefficiency or deficiency, malabsorption of the carbohydrate occurs; once present in the large intestine, it is fermented by microorganisms that mediate the production of hydrogen gas (H₂), carbon dioxide (CO₂), methane (CH₄), and short-chain fatty acids. Epidemiological data indicate a global prevalence of LI ranging from 65% to 70%; consequently, a significant percentage of people have difficulty consuming dairy products and must follow a treatment regimen that involves reducing or avoiding their intake. Consequently, the search for tools to manage LI has sparked interest in effective probiotic species capable of acting as an enzymatic source of β-galactosidase in the gastrointestinal tract. In particular, certain strains with β-galactosidase activity can contribute to lactose hydrolysis and symptom relief, such as: Streptococcus thermophilus, Lactobacillus bulgaricus, Lactobacillus reuteri, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bifidobacterium, and Saccharomyces boulardii. Previous clinical trials have noted its use in treating gastrointestinal symptoms and the amount of exhaled H₂ measured by the Hydrogen Breath Test (HBT) before and after probiotic interventions.
However, given that the gut microbiota comprises bacterial communities, viruses, fungi, archaea, and protozoa, it is important to consider its influence on the pathogenesis of certain conditions; in particular, intestinal methanogenic overgrowth (IMO) may have clinical relevance as it is associated with functional gastrointestinal disorders where symptoms may overlap with those of other conditions. It has been suggested that IL may be related to the presence of Small Intestinal Bacterial Overgrowth (SIBO) and share symptoms, since SIBO reduces lactose absorption due to abnormal villus function and the destruction of enzymes in the intestinal mucosa, leading to positive IL cases being secondary to SIBO. Additionally, it has been reported that approximately 30% of SIBO cases present with concomitant IMO. However, the therapeutic targets for IMO include antibiotic administration, dietary modifications, and, it is speculated, the use of probiotics, for which there is limited evidence. Therefore, while it is possible to consider the role of probiotics in modulating the gastrointestinal symptoms associated with IL and IMO, the clinical results of probiotic supplementation are inconclusive. For this reason, we conducted a preliminary pilot efficacy study using the strains Limosilactobacillus fermentum L-33 and Lacticaseibacillus rhamnosus L-134, both isolated from a gastric biopsy and possessing high lactase-producing capacity.
Therefore, the objective of this pilot study was to analyze the efficacy of a capsule formulation containing both probiotics and its effect on gastrointestinal symptoms in adults with lactose intolerance and intestinal methanogenic overgrowth.
Research hypothesis: daily administration, for 12 weeks, of a probiotic formulation with the strains Lacticaseibacillus rhamnosus L-134 and Limosilactobacillus fermentum L-33 with β-galactosidase activity decreases the quantity of exhaled H2 measured through the intervention of HBT and the presentation of gastrointestinal symptoms in adults.
Material and methods: The group of participants was made up of 22 adults of both genders (13 women and 9 men). The group underwent an HBT at the beginning of the intervention to confirm the diagnosis of LI and perform the initial H2 measurement. 12 participants (6 women and 6 men) received a diagnosis of LI. 2 participants tested positive for LI and IMO (2 men) and 8 participants were diagnosed with IMO (7 women and 1 man).
The HBT is the most used diagnostic method for determining LI, is not invasive, is relatively economical and has an optimal sensitivity (> 73.2%) and a specificity of 85.6%. On the other hand, if the golden standard for the diagnosis of SIBO is the aspiration of yeyunal liquid, followed by cultivation and detection of bacterial communities, this intervention stands out for being invasive and expensive, and if it is well known that BT with lactulose or glucose is postulated for the diagnosis of SIBO, in the present pilot study it was possible to identify some subjects positive for IMO from the initial screen specifically targeted at LI (BT with lactose). HBT was applied before and after the intervention to all participants, initially between 2 and 3 weeks before the start of the intervention, indicating the necessary preparation that included a carbohydrate-free diet 48 hours before the test, avoiding the use of antibiotics, laxatives and prokinetic drugs for four weeks beforehand, suspending the habit tobacco the night before and last at least 12 hours.
The specific gastrointestinal symptomatic presentation associated with LI (diarrhea or need to go to the bathroom, vomiting or nausea, cramp or abdominal pain, abdominal cramping or audible intestinal noises and flatulence or abdominal distention) was evaluated through the use of a Questionnaire on symptoms of Lactose Intolerance (QSLT) type visual analogue scale (VAS) which ranges from 0 to 10 with a total score of 50. The form has a sensitivity of 0.75 and a specificity of 0.67 and allows the identification of lactose malabsorption with a cutoff point of 6.5. This questionnaire was applied during the performance of the respective HBT, before and after the intervention. Randomization and masking: The randomized, double-blind and placebo-controlled pilot study was carried out in the facilities of the University of Concepción, Faculty of Pharmacy and/or Biological Sciences during the year 2024. An independent researcher carried out the randomization using a list with the names of participants generated in one Microsoft Office Excel® spreadsheet, which was safeguarded by it to maintain the anonymity and masking of participants throughout the study.
The group of 22 participants was classified into groups: those with LI and those with IMO (positive results for LI + IMO were considered within the LI group). Accordingly, each group was randomized separately and formed into 2 subgroups for each group, having the intervention groups (which received capsules with two probiotic strains) and the placebo groups, over a period of 12 weeks. Liva Company® (Santiago, Chile) provided bottles containing capsules with the biceps probiotic formulation (Lacticaseibacillus rhamnosus L-134 and Limosilactobacillus fermentum L-33) at a concentration of three thousand million CFU of each strain per capsule and placebo capsules were made up of maltodextrin 10-14 dimerco. Both capsules are coated with vegetable cellulose (hydroxypropylmethylcellulose), which are indistinct in appearance. Individuals must administer one capsule daily, in water and in fast with cold water according to the manufacturer's instructions, for 12 weeks. To evaluate self-administration compliance, participants returned the 3 delivered bottles containing non-self-administered capsules.
Nutritional assessment: Includes the measurement of anthropometric and dietary variables, through which body composition, nutritional status and the association between the intake of dairy products and lactose and expressed symptomatology and the result of the intervention are globally analyzed.
Statistical analysis: The size of the sample was defined based on García et al recommendation for pilot studies. The statistical treatment and data tabulation were carried out using the Microsoft Office Excel® version 16.72 program, while the same process and analysis were carried out using the SPSS-24.0® and R 4.4.3 packages. The numerical variables were presented by its mean and standard deviation (D.E), the categorical variables by the frequency and percentage of each one of its levels. Due to the size of the samples, the student test is applied to paired groups. For the statistical analysis, a significance level of 0.05 was used, so every time the value was less than 0.05, the result was considered statistically significant.
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Concepción, Chili, 4030000
- Universidad de Concepcion
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Be of legal age (18 years or older)
- Have a confirmed diagnosis of lactose intolerance
- Currently consume dairy products or derivatives, with or without lactose (which is why the participants' diets were not modified)
Exclusion Criteria:
- Use of probiotics, antibiotics, laxatives, enemas, or prokinetic agents within 1 to 4 weeks prior to the start of the intervention.
- Regular use and/or consumption of lactase enzymes for digestive support within 2 to 4 weeks prior to the start of the intervention.
- Participation in another intervention for the symptomatic management of lactose intolerance.
- Pregnant or breastfeeding women.
- Adults with significant gastrointestinal disease (inflammatory bowel disease, celiac disease, chronic diarrhea, gastroparesis, and gastroenteritis).
- Those who have undergone gastrointestinal surgery within the 6 months prior to the start of the study.
- Individuals with an allergy to any of the excipients included in the probiotic formulation or placebo.
- Individuals with diabetes, whether insulin-dependent or non-insulin-dependent.
- Individuals with cardiac stimulation devices (pacemakers).
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Probiotic
Participants who received the capsules containing the two probiotic strains
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The individuals had to take one capsule daily containing the bi-strain probiotic formulation (Lacticaseibacillus rhamnosus L-134 and Limosilactobacillus fermentum L-33) for 12 weeks.
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Placebo-vergelijker: Placebo
Participants who received the capsules without the probiotic strains
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The individuals had to take one capsule daily containing maltodextrin for 12 weeks.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Hydrogen breath test (HBT)
Tijdsspanne: From enrollment to the end of treatment at 12 weeks
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The HBT was performed orally using lactose as the fermentable substrate (25 g diluted in 125 ml of water).
To measure the concentration of H₂ in breath samples (in ppm), breath samples were collected through a mouthpiece connected to the instrument at serial time intervals (Basal - 15 minutes - 15 minutes - 30 minutes - 30 minutes - 30 minutes).
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From enrollment to the end of treatment at 12 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Questionnaire on symptoms of Lactose Intolerance (QSLT)
Tijdsspanne: From enrollment to the end of treatment at 12 weeks
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The specific gastrointestinal symptoms associated with IL (diarrhea or the urge to use the bathroom, vomiting or nausea, cramps or abdominal pain, borborygmi or audible bowel sounds, and flatulence or abdominal distension) using a Questionnaire on symptoms of Lactose Intolerance (QSLT) based on a visual analog scale (VAS) ranging from 0 to 10, with a total score of 50.
The questionnaire was administered during the respective HBT sessions, before and after the intervention, at 30 minutes, 60 minutes, and 120 minutes.
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From enrollment to the end of treatment at 12 weeks
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie stoel: Cristian A Parra Sepúlveda, MSc, CONTRIBUTOR
Publicaties en nuttige links
Algemene publicaties
- Hsu CA, Lee SL, Chou CC. Enzymatic production of galactooligosaccharides by beta-galactosidase from Bifidobacterium longum BCRC 15708. J Agric Food Chem. 2007 Mar 21;55(6):2225-30. doi: 10.1021/jf063126+. Epub 2007 Feb 23.
- Vasudha M, Prashantkumar CS, Bellurkar M, Kaveeshwar V, Gayathri D. Probiotic potential of beta-galactosidase-producing lactic acid bacteria from fermented milk and their molecular characterization. Biomed Rep. 2023 Feb 8;18(3):23. doi: 10.3892/br.2023.1605. eCollection 2023 Mar.
- Banaszak M, Gorna I, Wozniak D, Przyslawski J, Drzymala-Czyz S. Association between Gut Dysbiosis and the Occurrence of SIBO, LIBO, SIFO and IMO. Microorganisms. 2023 Feb 24;11(3):573. doi: 10.3390/microorganisms11030573.
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- Polkowska-Pruszynska B, Gerkowicz A, Szczepanik-Kulak P, Krasowska D. Small intestinal bacterial overgrowth in systemic sclerosis: a review of the literature. Arch Dermatol Res. 2019 Jan;311(1):1-8. doi: 10.1007/s00403-018-1874-0. Epub 2018 Oct 31.
- Barbone G, Jochum C. [Functional Exams in the gastroenterology - new developments and tips for the common practice]. Dtsch Med Wochenschr. 2021 Apr;146(7):441-445. doi: 10.1055/a-1156-0780. Epub 2021 Mar 29. German.
- Rezaie A, Pimentel M, Rao SS. How to Test and Treat Small Intestinal Bacterial Overgrowth: an Evidence-Based Approach. Curr Gastroenterol Rep. 2016 Feb;18(2):8. doi: 10.1007/s11894-015-0482-9.
- Zafar H, Jimenez B, Schneider A. Small intestinal bacterial overgrowth: current update. Curr Opin Gastroenterol. 2023 Nov 1;39(6):522-528. doi: 10.1097/MOG.0000000000000971. Epub 2023 Sep 18.
- 10.1080
- Ghoshal U, Shukla R, Srivastava D, Ghoshal UC. Irritable Bowel Syndrome, Particularly the Constipation-Predominant Form, Involves an Increase in Methanobrevibacter smithii, Which Is Associated with Higher Methane Production. Gut Liver. 2016 Nov 15;10(6):932-938. doi: 10.5009/gnl15588.
- Guardiola-Arevalo A, Mascort Roca J, Noguerol Alvarez M, Carrillo Munoz R, Mendive Arbeloa JM, Amador Romero J. [Small intestine bacterial overgrowth: Myths and realities]. Aten Primaria. 2025 Apr;57(4):103201. doi: 10.1016/j.aprim.2024.103201. Epub 2025 Jan 11. Spanish.
- Deysine M, Mader M. Thoracic duct lymph flow changes secondary to alterations in serum calcium levels: a proposed mechanism of action. Lymphology. 1980 Mar;13(1):1-8. No abstract available.
- Pimentel M, Saad RJ, Long MD, Rao SSC. ACG Clinical Guideline: Small Intestinal Bacterial Overgrowth. Am J Gastroenterol. 2020 Feb;115(2):165-178. doi: 10.14309/ajg.0000000000000501.
- Plauzolles A, Uras S, Penaranda G, Bonnet M, Dukan P, Retornaz F, Halfon P. Small Intestinal Bacterial Overgrowths and Intestinal Methanogen Overgrowths Breath Testing in a Real-Life French Cohort. Clin Transl Gastroenterol. 2023 Apr 1;14(4):e00556. doi: 10.14309/ctg.0000000000000556.
- Laserna Mendieta EJ, Martin Dominguez V, Perez Lucendo I, Granero Cremades I, Ferreiros Martinez R, Alvarez Male T, Sanz De Benito MA, Santander C. Detection capacity of small intestine bacterial or methanogen overgrowth by lactose and fructose breath testing in the adult population. Adv Lab Med. 2024 Aug 9;5(3):327-332. doi: 10.1515/almed-2024-0115. eCollection 2024 Sep.
- Gingold-Belfer R, Levy S, Layfer O, Pakanaev L, Niv Y, Dickman R, Perets TT. Use of a Novel Probiotic Formulation to Alleviate Lactose Intolerance Symptoms-a Pilot Study. Probiotics Antimicrob Proteins. 2020 Mar;12(1):112-118. doi: 10.1007/s12602-018-9507-7.
- Oliveira LS, Wendt GW, Crestani APJ, Casaril KBPB. The use of probiotics and prebiotics can enable the ingestion of dairy products by lactose intolerant individuals. Clin Nutr. 2022 Dec;41(12):2644-2650. doi: 10.1016/j.clnu.2022.10.003. Epub 2022 Oct 12.
- Oak SJ, Jha R. The effects of probiotics in lactose intolerance: A systematic review. Crit Rev Food Sci Nutr. 2019;59(11):1675-1683. doi: 10.1080/10408398.2018.1425977. Epub 2018 Feb 9.
- 10.1016
- Ahn SI, Kim MS, Park DG, Han BK, Kim YJ. Effects of probiotics administration on lactose intolerance in adulthood: A meta-analysis. J Dairy Sci. 2023 Jul;106(7):4489-4501. doi: 10.3168/jds.2022-22762. Epub 2023 May 22.
- Toca MDC, Fernandez A, Orsi M, Tabacco O, Vinderola G. Lactose intolerance: myths and facts. An update. Arch Argent Pediatr. 2022 Feb;120(1):59-66. doi: 10.5546/aap.2022.eng.59. Epub 2021 Dec 17. English, Spanish.
- 348813230
- 10.1080/07315724.2021.1891587
- Leis R, de Castro MJ, de Lamas C, Picans R, Couce ML. Effects of Prebiotic and Probiotic Supplementation on Lactase Deficiency and Lactose Intolerance: A Systematic Review of Controlled Trials. Nutrients. 2020 May 20;12(5):1487. doi: 10.3390/nu12051487.
- Goosenberg E, Afzal M. Lactose Intolerance. 2025 Aug 6. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK532285/
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Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Metabolisme, aangeboren fouten
- Genetische ziekten, aangeboren
- Metabole ziekten
- Darmziekten
- Ziekten van het spijsverteringsstelsel
- Gastro-intestinale aandoeningen
- Malabsorptiesyndromen
- Koolhydraatmetabolisme, aangeboren fouten
- Aangeboren, erfelijke en neonatale ziekten en afwijkingen
- Voedings- en stofwisselingsziekten
- Lactose intolerantie
- maltodextrin
Andere studie-ID-nummers
- CEBB Nº 1666-2024
Plan Individuele Deelnemersgegevens (IPD)
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