- Research article
- Open Access
Efficacy of a curcumin extract (Curcugen™) on gastrointestinal symptoms and intestinal microbiota in adults with self-reported digestive complaints: a randomised, double-blind, placebo-controlled study
BMC Complementary Medicine and Therapies volume 21, Article number: 40 (2021)
There is preliminary evidence to suggest curcumin can alleviate digestive symptoms in adults with self-reported digestive complaints and irritable bowel syndrome. However, in all these trials, curcumin was used as a component of a multi-herbal combination and there were consistent concerns associated with risk of bias in most studies. The goal of this study was to investigate the effects of a curcumin extract (Curcugen™) on gastrointestinal symptoms, mood, and overall quality of life in adults presenting with self-reported digestive complaints. Moreover, to determine the potential therapeutic mechanisms of action associated with curcumin, its effects on intestinal microbiota and small intestinal bowel overgrowth (SIBO) were examined.
In this 8-week, parallel-group, double-blind, randomised controlled trial, 79 adults with self-reported digestive complaints were recruited and randomised to receive either a placebo or 500 mg of the curcumin extract, Curcugen™. Outcome measures included the Gastrointestinal Symptom Rating Scale (GSRS), intestinal microbial profile (16S rRNA), Depression, Anxiety, and Stress Scale – 21 (DASS-21), Short Form-36 (SF-36), and SIBO breath test.
Based on self-report data collected from 77 participants, curcumin was associated with a significantly greater reduction in the GSRS total score compared to the placebo. There was also a greater reduction in the DASS-21 anxiety score. No other significant between-group changes in self-report data were identified. An examination of changes in the intestinal microbial profile and SIBO test revealed curcumin had no significant effect on these parameters. Curcumin was well-tolerated with no significant adverse events.
The curcumin extract, Curcugen™, administered for 8 weeks at a dose of 500 mg once daily was associated with greater improvements in digestive complaints and anxiety levels in adults with self-reported digestive complaints. Compared to the placebo, there were no significant changes in intestinal microbiota or SIBO; however, further research using larger samples and testing methods that allow more detailed microbial analyses will be important. An investigation into other potential mechanisms associated with curcumin’s gastrointestinal-relieving effects will also be important such as examining its influence on the intestinal barrier function, inflammation, neurotransmitter activity, and visceral sensitivity.
Australian New Zealand Clinical Trials Registry, Trial ID. ACTRN12619001236189. Registered 6 September 2019.
Turmeric, the dried or fresh rhizome of the plant Curcuma longa L., has been extensively used in traditional medicine. In Ayurvedic medicine (a system of traditional medicine originating from India), turmeric is believed to have many medicinal properties including strengthening the overall energy of the body, relieving gas, dispelling worms, improving digestion, regulating menstruation, dissolving gallstones, and relieving arthritis. In many South Asian countries, it is also used as an antiseptic for cuts, burns, and bruises; and as an antibacterial agent .
Turmeric contains several phytochemicals such as turmerones and various polysaccharides, however, most of its therapeutic activities are believed to result from a group of yellow pigments known as curcuminoids. Curcuminoids are a mixture of curcumin, demethoxycurcumin, bisdemethoxycurcumin, and cyclocurcumin. Of these, curcumin is the principal curcuminoid and has attracted the greatest interest in the scientific literature . Curcumin has been shown to target multiple signalling molecules with most of its benefits believed to be due to its antioxidant and anti-inflammatory effects . There is evidence to suggest it may be beneficial for the treatment of pain and arthritis [4, 5], metabolic syndrome , depression [7, 8], and cognitive impairment . Interest in the effects of curcumin on digestive health is also accumulating and there is preliminary evidence to suggest that it may be beneficial. In a review by Lopresti , it was postulated that curcumin may be helpful for the treatment of gastrointestinal (GI) conditions because of its multiple effects on the GI system including its influence on intestinal microbiota, intestinal permeability, gut inflammation and oxidative stress; and bacterial, parasitic, and fungal infections. In a meta-analysis of 5 clinical trials on the use of curcumin for reducing symptoms associated with irritable bowel syndrome (IBS), it was concluded that there was overall evidence of efficacy . However, in all these trials, curcumin was used as a component of a multi-herbal combination and there were consistent concerns associated with risk of bias in most studies. Beneficial effects from curcumin have also been identified in inflammatory bowel diseases and functional gastrointestinal diseases (FGID) [12,13,14].
The goal of this 8-week, randomised, double-blind, placebo-controlled trial was to investigate the effects of a curcumin extract (Curcugen™) on GI symptoms, mood, and overall quality of life in adults presenting with self-reported digestive complaints. In addition, to determine the potential therapeutic mechanisms of action associated with curcumin, its effects on intestinal microbiota and small intestinal bowel overgrowth (SIBO) were examined. In several animal trials [15,16,17] and one small human trial , curcumin ingestion was associated with changes in gut microbiota. For example, in an animal trial, curcumin intake for 6 weeks resulted in increases in the Firmicutes/ Bacteroidetes ratio compared to a vehicle control , and in a human 8-week trial, turmeric and curcumin supplementation was associated with a 7 and 69% increase in detected species respectively, over time . In another small trial comprising eight healthy adults, the ingestion of curry with turmeric significantly increased the area under the curve of breath hydrogen and shortened small-bowel transit time compared with a curry mixture without turmeric . Despite this preliminary evidence of the GI effects of curcumin, and its potential to impact on intestinal microbiota, there has been no trial specifically examining the GI effects of the curcumin extract, Curcugen™. However, it was hypothesised that based on previous research into turmeric and other curcumin extracts, Curcugen™ may be associated with improvements in digestive symptoms and such changes could be due to its influence on intestinal microbiota.
This was a two-arm, parallel-group, 8-week, randomised, double-blind, placebo-controlled trial (Fig. 1). The trial protocol was prospectively registered with the Australian New Zealand Clinical Trials Registry (Trial ID. ACTRN12619001236189) and approved by the Human Research Ethics Committee at the National Institute of Integrative Medicine (approval number 0056E_2019). To estimate the required sample size (based on a single outcome variable), an a priori power analysis was undertaken. Based on a previously conducted placebo-controlled study on adults with digestive disturbances using a herbal combination containing turmeric , an effect size of 0.6 was predicted. Assuming a type one error rate (alpha) of 5% and a power of 80%, the number of participants required per group to find an effect for the total score on Gastrointestinal Symptom Rating Scale (GSRS) was estimated as 36. After allowing for a 10% drop out rate, we aimed to recruit at least 40 participants per group.
Recruitment and randomisation
Participants were recruited across Australia through social media advertisements between September and December 2019. Interested participants were directed to a website page that provided information about the study and a request to complete an online screening questionnaire. This questionnaire assessed for current digestive symptoms, history of medical and psychiatric disorders, medication use, alcohol, nicotine and other drug use, herb and vitamin intake, and pregnancy/breastfeeding status. If judged as likely eligible, volunteers participated in a phone interview with an investigator. The phone interview comprised a series of questions to further obtain information relating to the eligibility criteria and to acquire further demographic details. Suitable participants then completed online versions of the Gastrointestinal Symptom Rating Scale (GSRS), Depression, Anxiety, and Stress Scale (DASS-21), Short-Form-36 (SF-36), and an informed consent form. Using a randomisation calculator (http://www.randomization.com), eligible and consenting participants were randomly assigned to one of two groups (curcumin or placebo). The randomisation structure comprised 10 randomly-permuted blocks, containing 8 participants per block. Participant identification numbers were allocated according to the order of participant enrolment in the study. All capsules were packed in identical bottles labelled by two intervention codes (held by the study sponsor until final data analysis). Participants and study investigators were blind to treatment group allocation until all outcome data were collected and analysed. No financial compensation was provided to participants for participating in this study, although after the study, participants allocated to the placebo condition were given a complimentary 8-week supply of curcumin capsules.
Male and female participants aged 18 to 65 years, with self-reported symptoms of gastrointestinal complaints were recruited for this study. Participants had a GSRS average rating of between 2 (mild-severity gastrointestinal discomfort) and 5 (moderately-severe gastrointestinal discomfort). All participants were medication-free for at least 4 weeks except for the use of the contraceptive pill and no more than once a week use of pain-relieving medications. Volunteers had had no plan to change their diet or commence new treatments over the study period and had a body mass index (BMI) between 20 and 35. Participants were also fluent in English and have consented (via an online consent form) to all pertinent aspects of the trial.
Participants were ineligible to participate in the study if they were diagnosed with a medical condition including, but not limited to: diabetes, hyper/hypotension, cardiovascular disease, gallbladder disease/gallstones, biliary disease, endocrine disease, psychiatric disorder, or neurological disease (Parkinson’s, Alzheimer’s disease, intracranial haemorrhage, head or brain injury). Participants diagnosed by a medical practitioner with a GI disease (e.g., inflammatory bowel diseases and FGID) were also unable to participate in this study. Participants who reported consuming greater than 14 standard alcoholic drinks per week, a current or 12-month history of illicit drug abuse, used antibiotics in the 4-weeks before study commencement, were taking curcumin supplements, or were currently taking supplements that may affect digestive function (unless they were on a stable dose for 60 days before the baseline assessment) were also ineligible for the study. Women who were pregnant, breastfeeding, or intending to fall pregnant were also ineligible to participate in the study.
Placebo and curcumin capsules were matched for colour, shape, and size. The active treatment, supplied by DolCas Biotech, LLC., contained 500 mg of a standardised curcuminoids extract (Curcugen™). Curcugen™ is a dispersible, 98.5% turmeric-based ingredient, containing 50% curcuminoids, 1.5% essential oils and other native turmeric molecules. By increasing the surface area of the curcuminoids, polar-resins facilitate the self-dispersion of otherwise lipophilic curcuminoids for greater access to absorptive surfaces and extended plasma retention.
The placebo capsules contained the same excipients as the active tablet (microcrystalline cellulose). All capsules were manufactured and packed in a Good Manufacturing Practice facility. All participants were instructed to take one capsule daily with 250 ml of water immediately before sleep for 8 weeks. Medication adherence was monitored by asking participants to count remaining capsules at weeks 4 and 8. The effectiveness of participant treatment blinding was assessed by asking participants to predict group allocation (placebo, curcumin, or uncertain) at the completion of the study. Curcumin and placebo capsules were mailed to participants with directions for use provided on capsule bottles. An information sheet was also provided to participants with details about how to take the capsules. This information was also verbally communicated to participants during their screening telephone interview.
Primary outcome measure
Gastrointestinal symptom rating scale (GSRS) total score
The GSRS is a self-report, 15-item questionnaire that measures the severity of a wide range of gastrointestinal symptoms. Questions are rated on a 7-point scale ranging from no discomfort at all (1) to very severe discomfort (7). A total score is calculated by averaging the ratings provided on all questions. The GSRS has good psychometric properties and in several clinical trials has shown to be sensitive to treatment effects [21, 22]. The GSRS was completed at baseline, week 4, and week 8.
At baseline and week 8, participants collected a stool sample at home after a morning bowel motion. Participants were instructed to collect approximately 1 g of stool into a collection tube (Zymo DNA/RNA Shield faecal collection tube) and return samples via express post to our office for later analysis. DNA/RNA Shield reagent is a DNA and RNA stabilisation solution for nucleic acids that preserves the genetic integrity and expression profiles of samples at ambient temperatures and completely inactivates infectious agents. The DNA and RNA stabilisation solution also prevents degradation from freeze-thaw cycling and unexpected freezer failures. Samples were stored in a − 20-degree Celsius freezer until later analysis. Intestinal microbiota via 16S rRNA (V3-V4 region) gene sequencing was undertaken by Australian Genome Research Facility. Paired-ends reads were assembled by aligning the forward and reverse reads using PEAR (version 0.9.5). Primers were identified and trimmed. Trimmed sequences were processed using Quantitative Insights into Microbial Ecology (QIIME 1.8.4) USEARCH (version 8.0.1623) and UPARSE software. Using USEARCH tools, sequences were quality filtered, full length duplicate sequences were removed and, were sorted by abundance. Singletons or unique reads in the data set were discarded. Sequences were clustered followed by chimera filtered using “rdp_gold” database as a reference. To obtain the number of reads in each operational taxonomic unit (OU) U, reads were mapped back to OTUs with a minimum identity of 97%. Taxonomy was assigned using QIIME. OTU changes in intestinal bacteria at the phylum and family level and changes in microbial diversity (Shannon and Simpson diversity index) from baseline to week 8 were examined.
Secondary outcome measures
Gastrointestinal symptom rating scale (GSRS) cluster scores
In addition to a GSRS total score, five symptom clusters can also be calculated comprising scores for reflux, abdominal pain, indigestion, diarrhoea, and constipation.
Depression, anxiety, and stress scale – 21 (DASS-21)
The DASS-21 is a validated self-report measure assessing symptoms of stress, anxiety, and depression . Twenty one questions are rated on a 4-point scale (0–3), ranging from never to almost always (lower scores indicate a reduction in symptoms). Sub-scale scores for depression, anxiety, and stress are calculated. The DASS-21 was completed at baseline, week 4, and week 8.
Short Form-36 health survey (SF-36)
The SF-36 is a self-report measure assessing quality of life. Scores are calculated for eight areas including (1) energy/fatigue, (2) physical functioning, (3) bodily pain, (4) general health perceptions, (5) physical role functioning, (6) emotional role functioning, (7) social role functioning, and (8) emotional wellbeing. The SF-36 is a commonly-used outcome measure of quality of life with strong psychometric properties [24, 25]. Scoring for the SF-36 was based on the algorithm developed by RAND Health Care . The SF-36 was completed at baseline, week 4, and week 8.
Small intestinal bacterial overgrowth (SIBO)
A 3-h SIBO home breath test was conducted at baseline and week 8. After a 24-h preparatory diet, a lactulose substrate was ingested, and breath samples were collected every 20 min for 3 h. Tests using the QuinTron BreathTracker were used to measure levels of carbon dioxide (CO2), hydrogen, and methane in a single sample of breath (alveolar air). CO2 levels below 1.5% were considered invalid breath collections. Positive, borderline, and negative SIBO results were calculated based on the following criteria:
Elevated hydrogen results: Increases of hydrogen greater than 20 ppm (ppm) over the lowest preceding value within the first 100 min were classified as positive results, and increases occurring 100–120 min later were classified as borderline.
Elevated methane results: Increases of methane greater than 12 ppm over the lowest preceding value within the first 100 min were classified as positive results, and increases occurring 100–120 min later were classified as borderline.
Elevated combined results: Increases of combined hydrogen and methane gas values greater than 15 ppm over the lowest preceding value within the first 100 min were classified as positive results, and increases occurring 100–120 min later were classified as borderline.
Safety and tolerability of supplement intake by participants were examined at weeks 4 and 8 through an online question querying adverse effects that were believed to be associated with supplement intake. Participants were also requested to contact researchers immediately if any adverse effects were experienced.
An independent samples T-test was used to compare demographic variables across the two treatment groups for continuous variables, and Pearson’s Chi-square was used to compare categorical data. To evaluate self-report outcome measures, a repeated-measures analysis of variance (ANOVA) was used to compare within-group changes over time (weeks 0, 4, and 8) and group (curcumin versus placebo) x time interaction effects. A Cohen’s d was also calculated to examine effect sizes. The Shapiro-Wilk normality test was conducted to examine the normality of group data. This demonstrated that data were not normally distributed, and this was not corrected by data transformations. However, a repeated-measures ANOVA was considered the most appropriate option for statistical analyses as it is relatively robust to violations of normality . Where necessary, degrees of freedom were adjusted using the Greenhouse-Geisser approach to correct for violations of the sphericity assumption. Data from participants were included in analyses of self-report outcomes if questionnaire data were obtained at week 4 [last observation carried forward from week 4 for missing values].
To examine SIBO results, a Mann-Whitney U-Test was conducted to examine categorical differences (elevated, borderline, and negative) for hydrogen, methane, and combined gases between the two groups (curcumin and placebo) at the two time points (baseline and week 8). A Wilcoxon signed ranks test was also conducted to evaluate within-group changes in SIBO results over time (baseline and week 8) for the two groups (curcumin and placebo).
Changes in intestinal bacteria were analysed using a permutational multivariate analysis of variance (PERMANOVA) to evaluate the difference between pre- and post-measures, by group (placebo vs curcumin), at the phylum level. A simple t-test on the Simpson and Shannon diversity index to compare the change in bacterial diversity by group at the phylum to genus levels was also conducted. Moreover, a principal component analysis (PCA) was completed to explore the relationship between samples.
A further exploratory analysis was conducted to examine changes in selected individual bacteria over time. Based on the results of several systematic reviews examining differences in gut microbiota between adults with irritable bowel syndrome and healthy adults, the following gut microbiota was chosen for further exploratory analysis: Bacteroidetes (Phyla), Firmicutes (Phyla), Clostridia (class), Enterobacteriaceae (family), Bacteroides (genus), Clostridiales (genus), Faecalibacterium (genus), and Bifidobacterium (genus) [28,29,30]. Moreover, an exploratory analysis was conducted to examine the relationship between change in diversity index and change in GSRS total score. Based on available data from both groups, a Pearson’s correlation coefficient was calculated at the phylum to genus levels. All data were analysed using SPSS (version 26; IBM, Armonk, NY) and R (version 3.6.2 with analysis of bacterial diversity using the package vegan).
Baseline questionnaire and demographic information
From 175 people who completed the initial online screening questionnaire, 79 volunteers met the eligibility criteria and agreed to participate in the study. Self-report data from 77 participants who completed at least week-4 questionnaires were used for statistical analyses of self-report outcome measures. Two participants, one from each group, failed to consume the minimum number of required tablets (i.e., consumed less than 80% of tablets). However, data from these participants were included in the statistical analyses as removal of their results did not significantly influence statistical outcomes. SIBO results were collected from 78 participants at baseline and 69 participants at week 8. A basal hydrogen value of more than 16 ppm is suggestive of non-adherence to the preparatory diet . This occurred in 1 participant at baseline and 9 participants at week 8. However, all collected data were analysed as removal of scores from these participants did not significantly affect statistical results. Stool samples were collected by 71 participants at baseline and 58 participants at week 8. However, valid pre and post stool samples were only available for 50 participants (25 from each group). This was because only one stool sample (either pre or post) was collected/returned by the participant, or an inadequate sample was collected. Statistical analyses of between-group changes were conducted on stool results where both pre and post collections were conducted.
Baseline data for participants are detailed in Table 1. There were no statistically-significant, between-group differences in baseline outcome measures except for the SF-36 pain score, where participants in the curcumin group reported a lower pain score (indicating a higher pain disability). A total of 9 participants withdrew from the study and there were no significant differences in dropout rates between the groups. Reasons for withdrawal included no reason given (n = 4), the commencement of antibiotics (n = 3), excess work commitments (n = 1), and unrelated health issues (n = 1). No participants withdrew from the study due to reported adverse events associated with capsule intake.
GSRS total score (primary outcome measure)
Changes in GSRS total score across the two treatment groups and repeated measures ANOVA significance levels are detailed in Table 2 and Fig. 2. Reductions in the GSRS total score from baseline to week 8, indicating an improvement in symptoms, were significantly greater in the curcumin group than the placebo group (F2,150 = 3.96, p = .021, ES = .57). Curcumin (F2,74 = 36.74, p < .001) and placebo (F2,76 = 25.06, p < .001) administration was associated with statistically-significant reductions in the GSRS total score over time. Within-group analyses revealed that the majority of the changes in the GSRS total score occurred in the first 4 weeks of treatment as there were statistically-significant reductions in the GSRS total score from baseline to week 4 for both the curcumin (F1,37 = 37.08, p < .001) and placebo (F1,38 = 45.39, p < .001) groups. However, between-group contrasts revealed a significant group x time interaction from week 4 to week 8 for GSRS total score (F1, 75 = 6.433, p = .013). From weeks 4 to 8, there was a non-significant decrease in GSRS total score in the curcumin group (F1,37 = 2.92, p = .096) and a non-significant increase in GSRS total score in the placebo group (F1,38 = 3.56, p = .067).
Microbial profile (primary outcome measure 2)
Based on the results of the PERMANOVA, there was a non-significant between-group interaction in changes in intestinal bacteria at the phylum level between the placebo and curcumin groups (F1,48 = 1.730, p = .169). The visual inspection of the PCA (Fig. 3) also revealed that there was no systematic movement in phyla concentrations in the baseline and week 8 samples.
The results of independent samples t-tests examining changes in microbial diversity (Shannon and Simpson index) over time between the two groups revealed there were no statistically-significant between-group differences in changes in the Shannon and Simpson index at the phylum, class, order, or family level (see supplementary Table 1). However, at the genus level, there was a statistically-significant difference between the curcumin and placebo groups for the Shannon (p = .020) and Simpson index (p = 0.06). This was characterised by a decrease in the Shannon [T(24) = − 2.20, p = .038] diversity index in the curcumin group. However, as there were baseline differences in diversity between the two groups, a univariate analysis of variance was conducted with baseline diversity scores included as a covariate. This revealed that between-group differences in changes in diversity scores were no longer significantly different for the Shannon (F2,47 = 3.69, p = .061) and Simpson diversity (F2,47 = 1.92, p = .171) index.
T-tests were conducted to examine OTU changes in selected individual bacteria from the phylum to species level. As detailed in supplementary Table 1 there were no statistically-significant, between-group differences in changes in the selected intestinal bacteria over time.
An exploratory analysis was conducted to examine the relationship between change in the Shannon and Simpson diversity index and change in GSRS total score (supplementary Table 2). Based on the Pearson’s correlation coefficient, there was no significant relationship between change in diversity index at any microbial level and GI symptomatic improvements as measured by the GSRS total score.
GSRS subscale scores (secondary outcome measure 1)
Changes in GSRS cluster scores for the two treatment groups and repeated measures ANOVA significance levels are detailed in Table 2. Concerning changes in all GSRS cluster scores (abdominal pain, reflux, diarrhoea, indigestion, and constipation) across the 8-week intervention, there were no statistically-significant, between-group differences. However, in the curcumin group there were statistically-significant reductions in all GSRS cluster scores comprising abdominal pain (F2,74 = 7.15, p = .001), reflux (F2,74 = 4.04, p = .021), diarrhoea (F2,74 = 8.90, p < .001), indigestion (F2,74 = 28.88, p < .001), and constipation (F2,74 = 14.69, p < .001). In the placebo group, there were statistically-significant reductions in GSRS cluster scores for abdominal pain (F2,76 = 13.59, p < .001), diarrhoea (F2,76 = 8.42, p < .001), indigestion (F2,76 = 23.08, p < .001), and constipation (F2,76 = 5.06, p = .009), but not reflux (F2,76 = 1.06, p = .350).
DASS-21 (secondary outcome measure 2)
Changes in the DASS-21 scores for the two treatment groups and repeated measures ANOVA significance levels are detailed in Table 3. Reductions in the DASS-21 total (F2,150 = 3.19, p = .044, ES = .46) and anxiety scores (F2,150 = 3.85, p = .023, ES = .53) were significantly greater in the curcumin group than the placebo group. However, there were no between-group differences for changes in the DASS-21 depression (F2,150 = 1.02, p = .363, ES = .26) or stress (F2,150 = 1.87, p = .157, ES = .35) scores. In the curcumin group, there were statistically-significant reductions in all DASS-21 scores; total (F2,74 = 14.25, p < .001), depression (F2,74 = 5.58, p = .006), anxiety (F2,74 = 10.81, p < .001), and stress (F2,74 = 9.93, p < .001) scores compared to baseline levels. In the placebo group, there was a statistically-significant reduction in the DASS-21 stress score (F2,76 = 5.29, p = .007), but not the total (F2,76 = 2.96, p = .058), anxiety (F2,76 = .995, p = .375), or depression (F2,76 = .869, p = .423) scores compared to baseline levels.
SF-36 subscale scores (secondary outcome measure 3)
Changes in SF-36 scores for the two treatment groups and repeated measures ANOVA significance levels are detailed in Table 3. Improvements in the SF-36 pain score (F2,150 = 3.85, p = .023, ES = .43) were greater in the curcumin group than the placebo group. However, as pain scores were significantly different at baseline between the two groups, a univariate analysis of variance with baseline pain scores included as a covariate was conducted. This revealed that between-group differences in changes in pain scores were no longer significantly different (F2,74 = 0.175, p = .677). For all other SF-36 subscale scores, there were no statistically-significant, between-group differences.
SIBO (secondary outcome measure 4)
SIBO tests results are detailed in Table 4. A basal hydrogen value of more than 16 ppm is suggestive of non-adherence to the preparatory diet . This occurred in 1 participant at baseline and 9 participants at week 8. However, all collected data were included in analyses as removal of data from these participants did not significantly affect statistical outcomes. Based on the Mann-Whitney U-Test, there were no statistically-significant, between-group differences in the percentage of participants scoring in the elevated, borderline, or negative categories for either hydrogen, methane, or combined gases at either baseline or week 8. A Wilcoxon signed ranks test was conducted to examine changes in SIBO results from baseline to week 8. There were no statistically-significant changes in SIBO from baseline to week 8 in the placebo group for either hydrogen (z = −.502, p = .616), methane (z = −.427, p = .670) or combined gases (z = −.884, p = .377); or the curcumin group for hydrogen (z = − 1.539, p = .124), methane (z = − 1.734, p = .083) or combined gases (z = −.262, p = .794).
Intake of supplements
At week 8, participants recorded their quantity of remaining capsules. Two participants reported taking less than 80% of their capsules over the 8 weeks, although the consistency of use over the 8 weeks could not be ascertained.
No significant adverse events were reported by participants and no participant withdrew from the study due to concerns associated with supplement intake. The frequency of adverse effects is detailed in supplementary Table 3. These were no significant differences in reported adverse effects between the two groups [placebo (11) and curcumin (6)] and reported adverse effects were of mild severity.
Efficacy of participant blinding
To evaluate the efficacy of condition concealment over the study, participants were asked at the completion of the study to predict condition allocation (i.e. placebo, curcumin, or uncertain). Efficacy of group concealment was high as only 31% in the curcumin group and 29% in the placebo group correctly guessed treatment allocation.
In this 8-week, randomised, double-blind, placebo-controlled trial, the administration of a curcumin extract (Curcugen™) at a dose of 500 mg a day was associated with a greater improvement in overall GI symptoms in adults presenting with self-reported digestive complaints compared to the placebo. After 8 weeks of treatment, there was an average 28% reduction in overall digestive symptoms in the curcumin group compared to 18% in the placebo group. Moreover, from weeks 4 to 8, Curcugen™ was associated with improvements in GI symptoms, while the placebo group experienced a worsening in symptoms. In relation to symptomatic improvements, curcumin was also associated with significant reductions in abdominal pain, reflux, diarrhoea, indigestion, and constipation; however, improvements were not significantly different to those observed in the placebo group. Improvements in quality of life and mood were also observed after curcumin administration; however, except for a greater reduction in anxiety, changes were not significantly different from the placebo group. In adults supplemented with curcumin, there was a 52% reduction in anxiety symptoms compared to a 16% reduction in the placebo group. These results suggest curcumin administration was associated with improvements in overall GI symptoms and reductions in anxiety. Curcumin was well-tolerated with no significant differences in adverse effects between the curcumin and placebo groups.
To examine the potential mechanisms associated with curcumin’s influence on the GI system, changes in intestinal microbiota and SIBO were examined over the 8-week intervention. Compared to the placebo, there were no significant changes in microbial diversity (from the phylum to genus level) or in examined selected microbiota comprising Bacteroidetes (Phyla), Firmicutes (Phyla), Clostridia (class), Enterobacteriaceae (family), Bacteroides (genus), Clostridiales (genus), Faecalibacterium (genus), and Bifidobacterium (genus). These intestinal bacteria were chosen for examination as differences in these bacteria have been regularly observed in adults with IBS [28,29,30]. An examination of the effects of curcumin on SIBO also revealed curcumin did not influence SIBO rates. These results suggest that although curcumin was associated with improvements in GI symptoms (and anxiety levels) in adults with self-reported digestive complaints, changes in intestinal bacteria were not responsible for its therapeutic mechanisms of action. Importantly, despite increasing interest in the relationship between microbial diversity and GI conditions, in this study, increases in microbial diversity (from the phylum to genus level) were not associated with GI symptomatic improvements. This finding provides further confirmation that in this examined population of adults with self-reported digestive complaints, therapeutic actions of curcumin were not via its impact on intestinal bacteria. However, it is important to note that 16S rRNA analysis was utilised in this study which lacks the resolution to identify microbial changes at lower taxonomic classifications (e.g., species and strain levels). Other potential mechanisms associated with curcumin’s GI-supporting effects include its influence on intestinal barrier function, inflammation, neurotransmitter activity, and visceral sensitivity; mechanisms which have been identified as compromised in adults with GI disturbances. In a review by Ghosh et al. , it was demonstrated that curcumin decreases the translocation of gut bacteria-derived lipopolysaccharide (LPS) from the intestinal lumen into circulation by maintaining the integrity of the intestinal barrier. In particular, curcumin may modulate intestinal barrier function at several layers including the lumen (via its effect on intestinal alkaline phosphatase), the mucus layer, the epithelium (through its influence on the expression of tight junction proteins), and antibacterial peptides (via its expression of anti-microbial peptides). In an acute study, curcumin supplementation reduced gastrointestinal damage and associated pro-inflammatory cytokine activity in adults exposed to exercise and heat stress . Moreover, curcumin has anti-inflammatory effects and this presents as another mechanism associated with its therapeutic effects. Increased concentrations of systemic LPS are identified in several intestinal and extra-intestinal diseases [34,35,36,37]. Curcumin has been identified in animal studies to attenuate LPS-induced immune response and tissue damage [38,39,40]. Disturbances in the activity of the hypothalamus-pituitary-adrenal (HPA) axis have also been identified in people with IBS and FGID [41,42,43]. Curcumin has been shown in animal studies to influence HPA activity, and in human trials, is associated with lower concentrations of cortisol [44, 45]. Disturbances in serotonergic activity have also been implicated in GI diseases and altered serotonergic signalling may lead to both intestinal and extraintestinal symptoms in IBS . This presents as another mechanism of action associated with curcumin as it has been shown to influence serotonergic activity [47, 48].
Limitations and directions for future research
Even though there were improvements in GI symptoms in adults with self-reported GI complaints, these results should be cautiously generalised to adults presenting with diagnosed GI disorders until confirmation in future clinical trials. How the severity of digestive complaints in the population recruited in this study compares to healthy individuals without GI complaints, or people with diagnosed GI disorders, could not be evaluated as there are no published norms for the GSRS. However, in a study on 516 adults with gastroesophageal reflux disease, an average GSRS total score of 2.27 was identified . This suggests that the population of recruited participants had a mild-to-moderate severity of GI symptoms, as their baseline GSRS score was 2.78 (a higher scores indicates increasing severity of symptoms). Further examination of changes in GI symptoms utilising other outcome measures will be helpful in future trials to provide further analysis of symptomatic changes. Examples include the Bristol Stool Scale , clinician-administered questionnaires, measures of colonic transit time and stool frequency, and provocation tests for the evaluation of visceral sensitivity [50, 51].
In this study, curcumin was administered as a once-daily dose delivering 500 mg of a patented curcumin extract (Curcugen™). This equates to 250 mg of curcuminoids daily. Research confirms that there are significant differences in the bioavailability and composition of curcumin extracts. Curcugen™ is derived from a turmeric oleoresin base with a 50% curcuminoid concentration. In an unpublished study, it was associated with a 39-fold increase in free curcumin compared to standard curcumin. Given the differences in the profile and bioavailability of curcumin extracts, the GI effects of curcumin should be cautiously extended to other curcumin extracts until further confirmatory research is conducted.
In future trials, the efficacy of curcumin should be examined using different doses, frequency of dosing, and treatment duration. This will help to identify optimal treatment regimens for people with GI disorders. Even though no significant changes in intestinal microbiota were identified in this study, different dosages and treatment periods may lead to microbial changes. Moreover, microbial changes may occur in adults with clearly defined and diagnosed GI disorders including IBS, other FGIDs, and inflammatory bowel disease. In this study, adults with self-reported GI complaints with no previous diagnosis of a GI disorder were recruited. In addition, more detailed analysis of microbial changes at different taxonomic levels (e.g., species or strain level) may have revealed changes over time. However, for this greater resolution to occur accurately, whole-genome testing is preferred . Other factors that may have affected the lack of change in intestinal microbiota over time included the recruitment of people taking the contraceptive pill, the inclusion of volunteers with a BMI in the overweight and obese range, and limitations associated with our ability to monitor or control for dietary changes over time. The recruitment of larger samples sizes may also be required to elucidate microbial changes associated with curcumin use. Despite recruiting 79 volunteers, pre- and post-treatment changes in intestinal microbiota were only undertaken on 50 participants but data on GSRS changes were available for 77 participants. This has the potential to confound the results. As already discussed, despite Curcugen™ supplementation being associated with improvements in GI symptoms and reductions in anxiety, its therapeutic mechanisms of action could not be established. It will be important in future trials to examine other potential mechanisms of action of curcumin including examining its effects on intestinal barrier function, inflammation, HPA-axis activity, and serotonergic activity.
The results of this randomised, double-blind, placebo-controlled study demonstrated that the 8-week administration of a curcumin extract, Curcugen™ (500 mg daily), was associated with significant improvements in GI symptoms in adults presenting with self-reported digestive complaints. Compared to the placebo, there were also greater reductions in anxiety. Curcumin was well-tolerated with no reported significant adverse effects. An examination of the potential mechanisms associated with curcumin supplementation suggests its therapeutic effects may not be due to its influence on intestinal microbiota. However, before definitive conclusions about the effects of curcumin on intestinal bacteria can be made, further research using larger sample sizes and testing methods that allow more detailed analysis of microbial changes at lower taxonomic levels (e.g., whole-genome testing) will be important. Further studies on adults with clearly-defined GI disorders, using objective and subjective outcome measures, varying dosages and treatment durations, and differing curcumin extracts are required to elucidate the effects of curcumin on GI symptoms. Further trials are also required to examine the potential therapeutic actions of curcumin.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Analysis of variance
Body mass index
Depression, Anxiety, and Stress Scale – 21
Functional gastrointestinal diseases
Gastrointestinal Symptom Rating Scale
Irritable bowel syndrome
Pperational taxonomic unit
Permutational multivariate analysis of variance
Principal component analysis
Quantitative Insights into Microbial Ecology
Small intestinal bowel overgrowth
Prasad S, Aggarwal BB: Turmeric, the golden spice: from traditional medicine to modern medicine. In: Herbal medicine: biomolecular and clinical aspects. edn. Edited by nd, Benzie IFF, Wachtel-Galor S. Boca Raton: CRC Press/Taylor & Francis 2011.
Lestari ML, Indrayanto G. Curcumin. Profiles Drug Subst Excip Relat Methodol. 2014;39:113–204.
Hewlings SJ, Kalman DS. Curcumin: a review of its' effects on human health. Foods. 2017;6(10):92.
Daily JW, Yang M, Park S. Efficacy of turmeric extracts and curcumin for alleviating the symptoms of joint arthritis: a systematic review and meta-analysis of randomized clinical trials. J Med Food. 2016;19(8):717–29.
Sahebkar A, Henrotin Y. Analgesic efficacy and safety of curcuminoids in clinical practice: a systematic review and meta-analysis of randomized controlled trials. Pain Med. 2015;17(6):1192–202.
Aggarwal BB. Targeting inflammation-induced obesity and metabolic diseases by curcumin and other nutraceuticals. Annu Rev Nutr. 2010;30:173–99.
Lopresti AL, Maes M, Hood SD, Maker GL, Drummond PD. Curcumin for the treatment of major depression: a randomised, double-blind, placebo controlled study. J Affect Disord. 2014;167:368–75.
Fusar-Poli L, Vozza L, Gabbiadini A, Vanella A, Concas I, Tinacci S, Petralia A, Signorelli MS, Aguglia E. Curcumin for depression: a meta-analysis. Crit Rev Food Sci Nutr. 2020;60(15):2643–53.
Sarker MR, Franks SF. Efficacy of curcumin for age-associated cognitive decline: a narrative review of preclinical and clinical studies. Geroscience. 2018;40(2):73–95.
Lopresti AL. The problem of curcumin and its bioavailability: could its gastrointestinal influence contribute to its overall health-enhancing effects? Adv Nutr. 2018;9(1):41–50.
Ng QX, Soh AYS, Loke W, Venkatanarayanan N, Lim DY, Yeo WS. A meta-analysis of the clinical use of curcumin for irritable bowel syndrome (IBS). J Clin Med. 2018;7(10):298.
Grammatikopoulou MG, Gkiouras K, Theodoridis X, Asteriou E, Forbes A, Bogdanos DP. Oral adjuvant curcumin therapy for attaining clinical remission in ulcerative colitis: a systematic review and meta-analysis of randomized controlled trials. Nutrients. 2018;10(11):1737.
Dulbecco P, Savarino V. Therapeutic potential of curcumin in digestive diseases. World J Gastroenterol. 2013;19(48):9256–70.
Yu J, Xu WH, Sun W, Sun Y, Guo ZL, Yu XL. Curcumin alleviates the functional gastrointestinal disorders of mice in vivo. J Med Food. 2017;20(12):1176–83.
Chen YM, Chiu WC, Chiu YS, Li T, Sung HC, Hsiao CY. Supplementation of nano-bubble curcumin extract improves gut microbiota composition and exercise performance in mice. Food Funct. 2020;11(4):3574–84.
Peterson CT, Rodionov DA, Iablokov SN, Pung MA, Chopra D, Mills PJ, Peterson SN. Prebiotic potential of culinary spices used to support digestion and bioabsorption. Evid Based Complement Alternat Med. 2019;2019:8973704.
Zhang Z, Chen Y, Xiang L, Wang Z, Xiao GG, Hu J. Effect of curcumin on the diversity of gut microbiota in ovariectomized rats. Nutrients. 2017;9(10):1146.
Peterson CT, Vaughn AR, Sharma V, Chopra D, Mills PJ, Peterson SN, Sivamani RK. Effects of turmeric and curcumin dietary supplementation on human gut microbiota: a double-blind, randomized, placebo-controlled pilot study. J Evid Based Integr Med. 2018;23:2515690X18790725.
Shimouchi A, Nose K, Takaoka M, Hayashi H, Kondo T. Effect of dietary turmeric on breath hydrogen. Dig Dis Sci. 2009;54(8):1725–9.
Lopresti AL, Gupta H, Smith SJ. A poly-herbal blend (Herbagut(R)) on adults presenting with gastrointestinal complaints: a randomised, double-blind, placebo-controlled study. BMC Complement Altern Med. 2018;18(1):98.
Kulich KR, Madisch A, Pacini F, Pique JM, Regula J, Van Rensburg CJ, Ujszaszy L, Carlsson J, Halling K, Wiklund IK. Reliability and validity of the gastrointestinal symptom rating scale (GSRS) and quality of life in reflux and dyspepsia (QOLRAD) questionnaire in dyspepsia: a six-country study. Health Qual Life Outcomes. 2008;6:12.
Svedlund J, Sjodin I, Dotevall G. GSRS--a clinical rating scale for gastrointestinal symptoms in patients with irritable bowel syndrome and peptic ulcer disease. Dig Dis Sci. 1988;33(2):129–34.
Brown TA, Chorpita BF, Korotitsch W, Barlow DH. Psychometric properties of the depression anxiety stress scales (DASS) in clinical samples. Behav Res Ther. 1997;35(1):79–89.
Ware JE Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992;30(6):473–83.
McHorney CA, Ware JE Jr, Raczek AE. The MOS 36-Item Short-Form Health Survey (SF-36): II. Psychometric and clinical tests of validity in measuring physical and mental health constructs. Med Care. 1993;31(3):247–63.
Hays RD, Sherbourne CD, Mazel RM. The RAND 36-item health survey 1.0. Health Econ. 1993;2(3):217–27.
Tabachnick BG, Fidell LS. Using multivariate statistics. 5th ed. Boston: Allyn; 2007.
Pittayanon R, Lau JT, Yuan Y, Leontiadis GI, Tse F, Surette M, Moayyedi P. Gut microbiota in patients with irritable bowel syndrome-a systematic review. Gastroenterology. 2019;157(1):97–108.
Duan R, Zhu S, Wang B, Duan L. Alterations of gut microbiota in patients with irritable bowel syndrome based on 16S rRNA-targeted sequencing: a systematic review. Clin Transl Gastroenterol. 2019;10(2):e00012.
Wang L, Alammar N, Singh R, Nanavati J, Song Y, Chaudhary R, Mullin GE. Gut microbial dysbiosis in the irritable bowel syndrome: a systematic review and meta-analysis of case-control studies. J Acad Nutr Diet. 2020;120(4):565–86.
Ghoshal UC. How to interpret hydrogen breath tests. J Neurogastroenterol Motil. 2011;17(3):312–7.
Ghosh SS, He H, Wang J, Gehr TW, Ghosh S. Curcumin-mediated regulation of intestinal barrier function: the mechanism underlying its beneficial effects. Tissue Barriers. 2018;6(1):e1425085.
Szymanski MC, Gillum TL, Gould LM, Morin DS, Kuennen MR. Short-term dietary curcumin supplementation reduces gastrointestinal barrier damage and physiological strain responses during exertional heat stress. J Appl Physiol (1985). 2018;124(2):330–40.
Batista CRA, Gomes GF, Candelario-Jalil E, Fiebich BL, de Oliveira ACP. Lipopolysaccharide-induced neuroinflammation as a bridge to understand neurodegeneration. Int J Mol Sci. 2019;20(9):2293.
Caradonna L, Amati L, Magrone T, Pellegrino NM, Jirillo E, Caccavo D. Enteric bacteria, lipopolysaccharides and related cytokines in inflammatory bowel disease: biological and clinical significance. J Endotoxin Res. 2000;6(3):205–14.
Pasternak BA, D'Mello S, Jurickova II, Han X, Willson T, Flick L, Petiniot L, Uozumi N, Divanovic S, Traurnicht A, et al. Lipopolysaccharide exposure is linked to activation of the acute phase response and growth failure in pediatric Crohn’s disease and murine colitis. Inflamm Bowel Dis. 2010;16(5):856–69.
Fluitman S, Denys D, Vulink N, Schutters S, Heijnen C, Westenberg H. Lipopolysaccharide-induced cytokine production in obsessive-compulsive disorder and generalized social anxiety disorder. Psychiatry Res. 2010;178(2):313–6.
Gao F, Shen J, Zhao L, Hao Q, Yang Y. Curcumin alleviates lipopolysaccharide (LPS)-activated neuroinflammation via modulation of miR-199b-5p/IkappaB kinase beta (IKKbeta)/nuclear factor kappa B (NF-kappaB) pathway in microglia. Med Sci Monit. 2019;25:9801–10.
de Gomes MG, Teixeira FEG, de Carvalho FB, Pacheco CO, da Silva Neto MR, Giacomeli R, Ramalho JB, Dos Santos RB, Domingues WB, Campos VF, et al. Curcumin-loaded lipid-core nanocapsules attenuates the immune challenge LPS-induced in rats: neuroinflammatory and behavioral response in sickness behavior. J Neuroimmunol. 2020;345:577270.
Huang W, Li X, Wang D, Sun Y, Wang Q, Bu Y, Niu F. Curcumin reduces LPS-induced septic acute kidney injury through suppression of lncRNA PVT1 in mice. Life Sci. 2020;254:117340.
Kano M, Muratsubaki T, Van Oudenhove L, Morishita J, Yoshizawa M, Kohno K, Yagihashi M, Tanaka Y, Mugikura S, Dupont P, et al. Altered brain and gut responses to corticotropin-releasing hormone (CRH) in patients with irritable bowel syndrome. Sci Rep. 2017;7(1):12425.
Videlock EJ, Shih W, Adeyemo M, Mahurkar-Joshi S, Presson AP, Polytarchou C, Alberto M, Iliopoulos D, Mayer EA, Chang L. The effect of sex and irritable bowel syndrome on HPA axis response and peripheral glucocorticoid receptor expression. Psychoneuroendocrinology. 2016;69:67–76.
Mukhtar K, Nawaz H, Abid S. Functional gastrointestinal disorders and gut-brain axis: what does the future hold? World J Gastroenterol. 2019;25(5):552–66.
Xu Y, Ku B, Tie L, Yao H, Jiang W, Ma X, Li X. Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB. Brain Res. 2006;1122(1):56–64.
Yu JJ, Pei LB, Zhang Y, Wen ZY, Yang JL. Chronic supplementation of curcumin enhances the efficacy of antidepressants in major depressive disorder: a randomized, double-blind, placebo-controlled pilot study. J Clin Psychopharmacol. 2015;35(4):406–10.
Crowell MD. Role of serotonin in the pathophysiology of the irritable bowel syndrome. Br J Pharmacol. 2004;141(8):1285–93.
Abd-Rabo MM, Georgy GS, Saied NM, Hassan WA. Involvement of the serotonergic system and neuroplasticity in the antidepressant effect of curcumin in ovariectomized rats: comparison with oestradiol and fluoxetine. Phytother Res. 2019;33(2):387–96.
Lee B, Lee H. Systemic administration of curcumin affect anxiety-related behaviors in a rat model of posttraumatic stress disorder via activation of serotonergic systems. Evid Based Complement Alternat Med. 2018;2018:9041309.
Riegler G, Esposito I. Bristol scale stool form. A still valid help in medical practice and clinical research. Tech Coloproctol. 2001;5(3):163–4.
Mujagic Z, Keszthelyi D, Aziz Q, Reinisch W, Quetglas EG, De Leonardis F, Segerdahl M, Masclee AA. Systematic review: instruments to assess abdominal pain in irritable bowel syndrome. Aliment Pharmacol Ther. 2015;42(9):1064–81.
Miller LE. Study design considerations for irritable bowel syndrome clinical trials. Ann Gastroenterol. 2014;27(4):338–45.
Ranjan R, Rani A, Metwally A, McGee HS, Perkins DL. Analysis of the microbiome: advantages of whole genome shotgun versus 16S amplicon sequencing. Biochem Biophys Res Commun. 2016;469(4):967–77.
The authors gratefully acknowledge DolCas Biotech, LLC for funding the project and supplying Curcugen™ and placebo capsules used in this study.
This study adheres to CONSORT guidelines
This study was funded by DolCas Biotech, LLC. DolCas Biotech, LLC was not involved in the collection or analysis of the data.
Ethics approval and consent to participate
All participants gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the the National Institute of Integrative Medicine Human Research Ethics Committee (approval number 0056E_2019).
Consent for publication
ALL has received either presentation honoraria or clinical trial grants from nutraceutical companies to complete previous clinical trials. SM is the director of medical & scientific affairs at Dolcas-Biotech LLC. SJS and AR disclose no conflict of interest.
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Changes in OTU of individual bacteria over time. Supplementary Table 2. Pearson’s correlation coefficient between change in diversity index and change in GSRS total score. Supplementary Table 3. Self-reported frequency of adverse effects.
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Lopresti, A.L., Smith, S.J., Rea, A. et al. Efficacy of a curcumin extract (Curcugen™) on gastrointestinal symptoms and intestinal microbiota in adults with self-reported digestive complaints: a randomised, double-blind, placebo-controlled study. BMC Complement Med Ther 21, 40 (2021). https://doi.org/10.1186/s12906-021-03220-6
- Gastrointestinal symptoms