Skip to main content
Download PDF

The effect of berberine and fenugreek seed co-supplementation on inflammatory factor, lipid and glycemic profile in patients with type 2 diabetes mellitus: a double-blind controlled randomized clinical trial

Diabetology & Metabolic Syndrome volume 14, Article number: 120 (2022) Cite this article

Abstract

Background

Type 2 Diabetes mellitus is one of the most common chronic diseases in the world and has many complications. Due to the importance of using alternative therapies in managing symptoms of this disease, the present study was designed and conducted to investigate the effect of co-supplementation of berberine and fenugreek in patients with type 2 diabetes mellitus.

Methods

A randomized controlled clinical trial was conducted on 50 patients with type 2 diabetes mellitus. Participants were randomized in the intervention group, which received 3 capsules/day of 500 mg (300 mg of berberine + 200 mg of fenugreek seed powder) or placebo for 12 weeks. Biochemical and anthropometric variables were measured at the beginning and end of the study.

Results

We observed that fasting insulin, HbA1C, and hs-CRP significantly decreased in the intervention group compared to the baseline. The mean difference in insulin resistance (-0.32 vs. 0.15), fasting blood sugar (-14.40 vs. 1.68), and fasting insulin (- 2.18 vs. 1.34) were clinically significant in comparison to the control group. Almost all domains of SF-12 scores were significantly higher in the intervention group than in the placebo group.

Conclusions

The combination of berberine and fenugreek seed can improve cardio-metabolic status in patients with diabetes and support the anti-diabetic and anti-inflammatory role of herb in the improvement of quality of life.

Background

Type 2 diabetes mellitus (T2DM), which is on the rise, is one of the most prevalent chronic diseases in both developing and developed nations and is expected to impact more than 693 million individuals by the year 2045 [1, 2]. Patients with T2DM are at risk for developing several acute and chronic complications, including cardiovascular disease (CVD), non-alcoholic fatty liver disease (NAFLD), some types of cancer, and microvascular complications [2]. Insulin resistance (IR) is one of the major T2DM risk factors. [3]. Insulin resistance and hyperglycemia increases the production of free radicals and reactive oxygen species (ROS), which leads to lipid peroxidation and degradation of antioxidant enzymes [4]. Many diabetics have dyslipidemia and are at risk for CVD [5].

Hypertriglyceridemia, hypercholesterolemia, increased levels of low-density lipoprotein (LDL), and decreased levels of high density lipoprotein (HDL) are the characteristics of diabetic dyslipidemia, which appears to be an early event in the development of type 2 diabetes mellitus (T2DM) [6].

Traditional herbal medicines have a long history of use in many countries. Active substances obtained from herbs are now a substantial component of the contemporary pharmaceutical industry  [7,8,9,10,11]. Trigonellafoenum-graecum, commonly known as "Fenugreek seed", is a popular herb in Africa, India, Iran, South and Central Asia [12]. This herb has various active compounds, including steroids, lipids, alkaloids, saponins, flavonoids, hydrocarbons, galactomannan fiber, and amino acids. Diosgenin is considered the most bioactive compound in fenugreek seed and has strong antioxidant properties. It has been reported that these active ingredients can prevent diabetes by several mechanisms, including β-cell renewal, insulin secretion stimulation, and increased glucose uptake in HepG2 cells with overexpression of the glucose transporter 2 (GLUT-2) [13]. Moreover, diosgenin increases the mRNA expression levels of CCAAT/enhancer-binding protein (C/EBP) and peroxisome proliferator-activated receptor-γ (PPAR-γ) [13, 14].

Berberine is an alkaloid compound with a wide range of therapeutic activities and is derived from the Hydrastiscanadensis and Coptischinensis [15, 16].

According to experimental investigations, berberine consumption significantly correlated with changes in the gut microbiome, including an increase in good bacterial strains and the production of short-chain fatty acids (SCFA) [17, 18].

Numerous investigations have been undertaken in recent years on the anti-inflammatory, antioxidant, and lipid-lowering benefits of these two substances. Some of these studies have shown encouraging results, while others have yielded insignificant findings [15, 19].

The recent Meta-analysis revealed that berberine consumption is clinically safe and well tolerated by the human body [20], and no adverse effect was observed on participants’ diet [21].

Literature reports berberine's positive effects on managing symptoms of chronic disorders such as glycemic control and improving lipid profiles; however, certain studies were unable to find the strong evidence in this regard [20, 22].

Based on the findings of our investigation, no study has examined the effects of co-supplementing these two herbs on T2DM patients, even though other studies have analyzed the effects of berberine and fenugreek on aspects of glycemic and lipid profiles.

Thus, the goal of the current study was to determine how co-supplementing with berberine and fenugreek seeds affected T2DM patients' glycemic indices, inflammatory marker, and lipid profiles.

Methods

Study population

This study is a double-blinded randomized controlled trial conducted on the research and education association of Diabetes, at Shiraz University of Medical Science, Iran, between 2020 and 2021, Shiraz, Iran. Shiraz Diabetes Educational Research Association received referrals from patients diagnosed with T2DM, who were then recruited as study participants. This study enrolled individuals aged between 18–70 years diagnosed with T2DM for at least one year ago; hemoglobin A1c (HbA1c) > 7.0% or fasting blood glucose (FBG) > 7.0 mmol/L; 3) body mass index (BMI) more than 25 kg/m2 and less than 35; 4) no medical history of type 1 diabetes, cardiovascular, thyroid, kidney disease, cancer, mental disorders and taking medications related to the mentioned diseases; 5) and for female patients, a negative pregnancy test. We did not include patients with a BMI > 35, who had been on weight loss diets or taken weight loss supplements for less than 6 months, a history of fenugreek or berberine allergies, and breastfeeding women. None of the patients regularly smoked, drank alcohol, or took psychiatric medications or insulin. Additionally, individuals were excluded if their drug regimen changed throughout the course of the trial, if they started receiving insulin therapy, if they became pregnant, or if they no longer wanted to comply. All study procedures were approved by the Ethics Committee of Ahvaz Jundishapur university of medical sciences (Ethical NO.IR.AJUMS.REC.1398.735) and registered with the Iranian Clinical Trials Registry (IRCT registration number: IRCT20191229045937N1).

Participant recruitment and screening

Based on the insulin plasma level with a standard deviation of 17.46 in the previous study [23], 19 patients have been estimated for each studied group considering α = 0.05 and a power of 85%. To increase the accuracy and probability of sample loss, 25 patients were considered for each group. All patients signed written informed consent. Current study was designed based on the CONSORT statement for randomized clinical trials [24].

Sixty-two patients with diabetes were initially evaluated, and fifty were eligible to enter the study. Twelve patients were not included in the study due to living in another city, taking medications for depression and cardiovascular disease, as well as coronavirus. Eventually, fifty patients with T2DM were randomly divided into two groups using a block randomization procedure 25 patients in each intervention and placebo groups with three blocks in equal proportions. Randomization was made using computer-generated random numbers by a third person to reduce the bias. Figure 1 shows the flowchart of the participant's enrollment.

Fig.1
figure 1

Flow of study

Full size image

The diagnosis of T2DM was performed based on American Diabetes Association guidelines. Patients with fasting blood sugar (FBS) ≥ 126 mg/dl, 2-h plasma glucose ≥ 200 mg/dl, or Glycated hemoglobin ≥ 6.5% were diagnosed with diabetes mellitus [25].

Study design and interventions

Following the baseline measurements, participants were randomized to receive either 500 mg 3-per-day combination of berberine and fenugreek seed (300 mg of berberine + 200 mg of fenugreek seed powder, Arjuna Natural Pvt. Ltd company, Kerala India) and patients in the placebo group also received 3 capsules containing wheat flour that look similar to the supplements in term of shape, size, and weight. For 12 weeks, participants in both groups were instructed to take the supplements 30 min before the main meals.

Each 500 mg capsule contains 300 mg of berberisaristata extract and 200 mg of fenugreek extract, all of which were standardized to contain 285 mg of berberine hydrochloride NLT and 100 mg of saponins. In the current study, we studied the effect of co-supplementing these herbs in the lower dose, as there have been no side effects documented for any of these herbs at this dose [26], but earlier studies utilized large doses of each of these supplements, and some side effects were observed [26, 27].

The patients and researchers were unaware of the contents of the groups until the study's conclusion. The supplements of the intervention and control groups were coded by a third party (not a relative of the study researcher) using a combination of numeric and alphabetic numbers generated by a computer. To assure the ingestion of the placebo or intervention capsules, calls or texts were made. Each time they came in, patients were requested to bring back their empty supplement boxes so that the remaining ones could be counted if they weren't used. Patients whose compliance was lower than 90% were not included in the trial. The data monitoring committee oversaw the present study's safety and any potential negative effects of the intervention.

Measurements

Demographic information of the patients was recorded, and their physical activity was assessed by the short version of the international physical activity questionnaire (IPAQ).

Each patient's weight was determined during the first and twelve weeks of the study using Seca scales (Seca Company, Model 769, Germany) with an accuracy of 100 g while wearing light clothing, and their height was determined while wearing no shoes using a wall-mounted meter with an accuracy of 0.5 cm. At the start (week 0) and end of the trial, anthropometric measurements such as height, weight, hip circumference (HC), and waist circumference (WC) were taken for each participant.

BMI was determined by dividing the weight in kilograms by the square of the height in meters2. At the beginning and end of the trial, patients underwent telephone or in-person interviews to complete 3-day dietary recalls covering one holiday and two working days. These questionnaires were analyzed using Nutritionist IV (N4) software designed based on the United States Department of Agriculture Food Composition Table, which was modified for Iranian dietary food items [28].

All patients were asked not to change their routine dietary patterns and physical activity.

The gastrointestinal symptoms such as gastroesophageal reflux, dyspepsia, esophageal motility disorders, gastric motility disorders, and colonic motility disorders were assessed by the questionnaire [29]. The severity of the gastrointestinal symptoms were classified as asymptomatic, sometime, and permanent.

The quality of life (QOL) was assessed and scored by the Persian version of the questionnaire (SF-12) [30]. It includes 12 questions and 8 scales: physical functioning (PF-2 items on limitations doing moderate activities and climbing several flights of stairs), role limitations due to physical problems (RP-2 items on less accomplishment than one would like to achieve, and limitation in kind of work or other activities), bodily pain (BP-1 item on pain interference with one's normal work), general health (GH-1 item on general health perception), vitality (VT-1 item on having energy), social functioning (SF-1 item on the interference of physical health or emotional problems with one's social activities), role limitations due to emotional problems (RE-2 items on less accomplishment than one would like to achieve and not being careful in doing activities as usual) and perceived mental health (MH-2 items on feeling calm or peaceful and feeling sad or blue). Response categories for items vary from 2- to 6-point scales, and raw scores for items ranging from 1 to 6. After recoding raw scores for some items (that are BP, GH, VT, and one item from MH); then the raw scores could be transformed to provide eight scale scores, each ranging from 0 (the worst) to 100 (the best), with higher scores indicating better QOL.

All of the patients had to fast for 12–14 h before baseline and endpoint blood samples were obtained. The serum was immediately stored at −80 °C until analysis after the blood samples were immediately centrifuged for 10 min at a speed of 1500–2000 rpm. An auto-analyzer was used to measure fasting blood sugar (FBS) using the enzymatic method (Pars Azmoon Co., Iran). The Monobind insulin kit was used to perform ELISA measurements on fasting insulin concentrations (Monobind Inc., USA, product code: 5825-300). Ion exchange chromatography was used to assess glycated haemoglobin (Hb) A1C using the colorimetric method in Pars Azmoon Co., Iran. The updated homeostasis model of assessment 2 (HOMA-2) [31].

To calculate insulin resistance (IR), sensitivity (S)%, and beta cell function (BCF)% were available from the University of Oxford at (http://www.dtu.ox.ac.uk/homacalculator/index.php). For measuring lipid profiles, including triglyceride (TG), total cholesterol (TC), and HDL (high-density lipoprotein), we used the enzymatic kits (Pars Azmoon, Iran). LDL was calculated using the Friedewald formula. Enzyme-linked immunosorbent assay kits (Monobind Inc. Iran) were applied to measure high-sensitivity C-reactive protein (hs-CRP).

Statistical analysis

We applied SPSS software (version 18; SPSS Inc., Chicago, IL) for statistical analysis. The Kolmogorov– Smirnov test was used to determine data normality. Quantitative and qualitative variables were reported in mean (standard deviation) and frequency (percent frequency), respectively. Comparison of the results within groups after the intervention were assessed using paired sample t test. Independent sample t test was used to compare the results between the two groups (placebo and intervention). The mean changes of measured variables before and after the intervention were reported.In addition, analysis of covariance (ANCOVA), which corrects for baseline values, was used to find any differences between the two groups at the end of the study. Covariates included age, disease duration, dietary energy and macronutrient intake (percent), FBS at baseline, HbA1C at baseline, physical activity, W/H ratio, and body mass index. The intention to treat (ITT) approach was applied to all data. ITT approach involves the analysis of all trial participants who were randomized, regardless of dropout. We initially did the per protocol (complete case) sensitivity analysis and ITT analysis. There was no difference between these two analyses. A straightforward imputation strategy, including baseline data imputation, was used to manage the fully lost at random missing data. The baseline values of the outcome variables, FBS and HbA1C, were taken into account in the study. In addition, qualitative variables were compared by a chi-squared test before and after the intervention. P- value less than 0.05 was considered significant in all analyses.

Results

Forty-five patients completed the study duration (intervention group = 23, placebo group = 22 patients), and 68% of each studied group were female.

Table 1 represents the fundamental traits of patients with type 2 diabetes mellitus. Age, gender, disease duration, education, and PA did not significantly differ between the two study groups at the outset of the investigation. The physical component score (PCS), score changed significantly from baseline to week 12 and was nearly identical in the intervention and control groups. The intervention group, however, showed a tendency to show greater changes in the mental component score (MCS), score from baseline than the placebo group (full table presented as supplementary 1).

Table 1 Basic characteristics of patients with type 2 diabetes
Full size table

Table 2 represent anthropometric measurements of patients. The mean anthropometric parameters at baseline, such as weight, hip circumference, waist circumference (WC), and BMI, did not substantially differ between the two study groups. The mean of WC was considerably lower in both groups at the conclusion of the trial.

Table 2 Basic anthropometric indices of patients with type 2 diabetes
Full size table

Table 3 demonstrated that the baseline mean energy intake of the two study groups was significantly different from the baseline macronutrient consumption of the examined individuals with T2DM.

Table 3 Energy and macronutrients intake of patients with type 2 diabetes
Full size table

In the intervention group, fasting insulin and HbA1c levels were considerably lower at the end of the trial compared to other observed glycemic indices shown in Table 4. There was no discernible difference between the two groups in terms of fasting insulin at the start and conclusion of the trial, according to the crude and modified models, though.

Table 4 Glycemic indices and lipid profile in patients with type 2 diabetes
Full size table

Table 5 indicates that there is no significant difference between the two groups' baseline recorded gastrointestinal problems. The sole difference between the two study groups at the end of the intervention was esophageal motility problems.

Table 5 Severity of the gastrointestinal symptoms before and after intervention with BBR and fenugreek seed
Full size table

Discussion

There is no evidence to our knowledge on the combined effect of berberine and fenugreek seed on T2DM patients and the majority of the evidence is on the single herb. In the current study, taking three capsules of Berberine and Fenugreek seed per day resulted in a significant reduction in FBS and hs-CRP. Furthermore, only the intervention group's BCF % and IS were higher and clinically significant when compared to the control group. Fasting insulin, IR, and FBS levels were all lower and only clinically significant when compared to the control group.

Besides, most the subscales in SF-12 scores were significantly higher in the intervention group than in the placebo group. These findings support that daily co-supplementation of Berberine and Fenugreek could potentially suppress chronic inflammation, better control disease, and improve health-related quality of life.

The permanent esophageal motility disorders were observed only in one intervention group participant. It should be noted that esophageal motility disorder has not previously been reported as a complication of berberine or fenugreek. Hence, it seems that the combination of the two herbs is more appropriate than their single high-dose consumption. Diabetes is a chronic disease that causes severe complications in other vital organs such as the heart, eyes, and kidneys. It also has a negative impact on the economy by increasing the risk of premature death with disability due to diabetes, as well as absence from work and education [32].

Furthermore, gastrointestinal symptoms are common in patients with diabetes, including constipation, bloating, and gastroesophageal reflux [29].

Our findings showed that fasting insulin and HbA1C were significantly improved after intervention and FBS, BCF%, IS, and IR only clinically improved. In line with our findings, Yine et al. found a significant reduction in the serum concentration of FBS, HbA1C, and postprandial blood glucose after the supplementation with 0.5 g berberine thrice a day for 3 months; however, they reported gastrointestinal discomfort in the intervention group [33].

Another RCT study was conducted in the south-west of Iran showed that 500 mg twice daily berberine supplementation for 4 weeks led to a significant reduction in the FBS, but not fasting insulin, HOMA-β%, and HOMA-I than the control group [34]. A recent meta-analysis of 18 clinical trials showed that berberine supplementation significantly reduced TG, FBS, LDL, increased HDL; reduced insulin resistance to improve type II diabetes, and prevent diabetic encephalopathy [21].

Berberine has been shown in clinical studies to be clinically safe and well tolerated by humans. Few unfavorable side effects have been reported, and no adverse effects on the diet of individuals have been detected. Lee et al. discovered that berberine inhibits fat-forming and lipogenic genes, resulting in less fat formation [35].

Heat generation and oxygen demand are enhanced, and glucose and fat metabolism are accelerated when the expression of uncoupling protein mRNA in skeletal muscles is elevated. This herbal composition also acts as an AMP-activated protein kinase (AMPK) agonist, activating AMPK to boost energy generation and decrease energy storage.Upregulation of AMPK can help to correct lipid, glucose, and energy imbalances, as well as ameliorate metabolic imbalances induced by metabolic diseases [36].

Various mechanisms have also been proposed for the glycemic profile enhancing effects of berberine, such as increased insulin sensitivity, activation of protein kinase (AMPK) 1 by adenosine monophosphate 2 (AMP2), inhibition of gluconogenesis, stimulation of glycogenesis, GLP-13 secretion, and expression of LDL receptor mRNA secretion [37]. By enhancing Acetyl-CoA carboxylase (ACC) phosphorylation, stimulating AMPK can also boost Glucose transporter type 4 (GLUT4) translocation, so indirectly accelerating the uptake of glucose in the blood and free fatty acids to the mitochondria, both of which lead to the decline of glucose and lipids [38]. In our study, we did not find any significant difference between the two groups in terms of lipid profile. Contrary to our study, the results of a meta-analysis study showed that supplementation with berberine caused a significant reduction in the serum levels of TC, LDL, and TG [39]. This impact is hypothesized to be caused by the upregulation of LDL-R on hepatocytes related to the stabilization of LDL-R mRNA and the suppression of PCSK9 transcription due to the accelerated breakdown of hepatocyte nuclear factor 1a (HNF1a) and decreased proprotein convertase subtilisin/kexin type 9 (PCSK9) mRNA expression [40,41,42]. Fenugreek plant that contains active ingredients such as galactomannan, saponins, trigonelle, and diosgenin and is used as a spice, herb, food, and medicine [43]. The seeds of the fenugreek plant are the most important and well-studied part of the plant [14]. Fenugreek seed (FS) may be advantageous for modifying human plasma glucose and HbA1C levels, according to earlier studies [44]. Rashid et al. in RCT examined the effects of galactomannan derived from fenugreek in newly diagnosed type-2 diabetics, which is consistent with our findings. For 12 weeks, patients took 1 g/day of galactomannan, the monosaccharide component of Fenugreek gum in capsule form, 1 h before meals at a set time. FBS, HbA1c, TC, TG, and LDL all significantly decreased, according to the findings [45]. Additionally, a multicenter, randomised, placebo-controlled, double-blind experiment among T2DM patients revealed that fenugreek seeds at 500 mg bid significantly lowered FBS and post-prandial plasma sugar levels [46].

Similar results were found in a recent RCT that examined the effects of consuming 5 g of fenugreek seed powder three times per day for eight weeks. The results revealed that fenugreek seed powder supplementation significantly decreased the levels of FBS [27]. Fenugreek seeds have been shown to contain 30% soluble and 20% insoluble fibre, which has been shown to slow down the rate at which glucose is absorbed, presumably as a secondary mechanism for the hypoglycemic action, and to stimulate the release of insulin from pancreatic beta cells [47, 48]. In our study, LDL and HDL concentrations improved more than other lipid profiles, however in the adjusted model, TC rose in both groups while rising even more in the control group. In contrast to the findings of our investigation, Ghahdarijani et al. found that fenugreek ingestion significantly reduced TC, LDL, and TG levels while also raising HDL levels [49].

Polyphenols are the most abundant components in this herb that could improve hyperlipidemia. The Hypocholesterolemia effect of Fenugreek was due to the saponin component in it, which efficiently prevents cholesterol synthesis and therefore effectively reduces TC levels [50]. Additionally, fenugreek contains a gel-like dissolvable fibre that, when combined with bile acids, creates excessively large micelles that are difficult for the digestive system to absorb and lower levels of TG and LDL [51]. The presence of 4-hydroxy isoleucine in fenugreek seed also appears to improve the lipid profile and boost insulin release from pancreatic beta cells, which is another way by which it appears to lower blood cholesterol levels [49].

The other beneficial effect of fenugreek is to modulate intestinal microbiota, which can in turn impact metabolic physiology. Studies have shown that the composition of the gut microbiota is impaired in patients with T2DM, and fenugreek supplementation can delay the progression of T2DM and its complications by improving the gut microbiome [52, 53].

In the current investigation, it was determined that an appropriate strategy for the supportive treatment of diabetes was the combination of low-dose berberine and fenugreek seeds, which caused fewer gastrointestinal symptoms than either dose alone.

In a study, Yin et al. evaluated the effects of 500 mg/TDS berberine consumption on the patients with T2DM, and the results showed the occurrence of gastrointestinal symptoms including constipation, flatulence, and abdominal pain [33].

Additionally, fenugreek has been linked to side effects such diarrhoea, indigestion, stomach distention, and bloating when taken orally, according to a study [54].

Therefore, a low-dose mixture of berberine and fenugreek seeds can be used for diabetics as herbal medicines because there were no variations in the occurrence of gastrointestinal symptoms between the two groups before and after the intervention, with the exception of esophageal (Additional file 1) motility abnormalities. Furthermore, one person in the therapeutic group occasionally experienced an esophageal motility issue alone. It is important to note that esophageal motility issue has not yet been listed as a typical side effect of berberine or fenugreek.

Additionally, none of the subjects experienced significant gastrointestinal issues. On the other hand, numerous studies have demonstrated that some herbal substances have the potential to have beneficial effects on other acute or chronic diseases, the risk of which is higher in individuals with diabetes [55, 56].

It goes without saying that diabetes may have an impact on a patient's health and quality of life. Similar to individuals with type 1 diabetes, those with type 2 diabetes have a lower quality of life than those in good health. As a result, several areas, such as physical and psychological health, would be used to evaluate health-related quality of life.

In the current study, the SF-12 subscale in intervention group significantly improved scores for general health (GH), vitality (VT), and mental health (MH), physical functioning(PH),Role physical(RP),social functioning(SF), role emotional(RE),physical component summary (PCS) score and also increased the mental component summary (MCS) score. Similarly, in other clinical studies, intervention with herbal medicine and symbiotic augmented the quality of life scores for some of the subscales [57, 58].

Moreover, findings of a recent Meta-analysis with the inclusion of eighteen studies concluded that physiological or clinical outcomes, and westernized diet were associated with the QOL of type 2 diabetes mellitus patients [59].

The current study assessed for the first time the combined effect of berberine and fenugreek seed on glycemic indices, inflammatory factor, and lipid profiles in T2DM patients.

Contrary to the findings of earlier research, one of the main reasons for the discrepancy between the results of this investigation and the lack of a significant effect after supplementation with berberine and fenugreek on a number of parameters was connected to the dose utilized. As mentioned, we used the lower dose of these two plants with the aim of better gastrointestinal tolerance, and it seems that this dose does not have a significant effect on some biochemical factors. Despite the strengths of this study, however, it suffered from some limitations.

To begin, the current study was conducted during the COVID-19 epidemic. Despite our advice to avoid lifestyle changes during the intervention, particularly physical activity and dietary intake, their PA decreased compared to baseline, which can affect the accuracy of the results. Previous research has also found that PA decreased during the COVID-19 [60]. Second, due to budget constraints, we were unable to measure additional inflammatory factors. Third, because we used exclusion criteria to reduce the effect of confounding variables, we were unable to generalize these findings to all diabetics. Finally, one of the major issues with herbal compounds is their bioavailability.

Despite the fact that these supplements were provided by a pharmaceutical company, no information on the bioavailability of the phytoconstituents was available. Various measures can be taken to improve the rate of clinical translation of potential phytomolecules [61].

The supplements used in this study were formulated in such a way as to have the desired amounts of active compounds, especially saponins, although the bioavailability of these compounds is not yet clear.

Conclusions

In conclusion, our findings revealed some beneficial effects of berberine and fenugreek seed on glycemic indices, inflammatory factors, and lipid profiles in T2DM patients. Furthermore, there were no significant gastrointestinal side effects with this combination. As a result, consuming a combination of berberine and fenugreek seed appears to be an appropriate strategy for improving diabetes symptoms and quality of life. Further well-designed studies with a longer intervention period, multiple centers, and a larger sample size are suggested without the limitations of our study.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on request.

Abbreviations

ACC:

Acetyl-CoA carboxylase

AMP:

Adenosine monophosphate

AMPK:

Activation of protein kinase

BBR:

Berberine

CVD:

Cardiovascular disease

ITT:

Intention to treat

FI:

Fasting insulin

FG:

Fenugreek

FBS:

Fasting blood sugar

MD:

Mean difference

HDL:

High-density lipoproteins

HOMA-2:

Homeostasis model of assessment

GLUT4:

Glucose transporter type 4

IPAQ:

International physical activity questionnaire

GLUT-2:

Glucose transporter

LDL:

Low-density lipoprotein cholesterol

TG:

Triglyceride

TC:

Total cholesterol T2DM: Type 2 diabetes

VLDL:

Very low–density lipoprotein

QOL:

Quality of life

CCAAT:

Cytosine-cytosine-adenosine-adenosine-thymidine

References

  1. Oguntibeju OO. Type 2 diabetes mellitus, oxidative stress and inflammation: examining the links. Int J Physiol Pathophysiol Pharmacol. 2019;11(3):45.

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Cole JB, Florez JC. Genetics of diabetes mellitus and diabetes complications. Nat Rev Nephrol. 2020;16(7):377–90.

    Article  PubMed  Google Scholar 

  3. Geberemeskel GA, Debebe YG, Nguse NA. Antidiabetic effect of fenugreek seed powder solution (Trigonella foenum-graecum L.) on hyperlipidemia in diabetic patients. J Diabet Res. 2019. https://doi.org/10.1155/2019/8507453.

    Article  Google Scholar 

  4. Lin H-Y, Weng S-W, Chang Y-H, Su Y-J, Chang C-M, Tsai C-J, et al. The causal role of mitochondrial dynamics in regulating insulin resistance in diabetes: link through mitochondrial reactive oxygen species. Oxid Med Cell Longev. 2018. https://doi.org/10.1155/2018/7514383.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Artha IMJR, Bhargah A, Dharmawan NK, Pande UW, Triyana KA, Mahariski PA, et al. High level of individual lipid profile and lipid ratio as a predictive marker of poor glycemic control in type-2 diabetes mellitus. Vasc Health Risk Manag. 2019;15:149.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Adiels M, Olofsson S-O, Taskinen M-R, Borén J. Overproduction of very low–density lipoproteins is the hallmark of the dyslipidemia in the metabolic syndrome. Arterioscler Thromb Vasc Biol. 2008;28(7):1225–36.

    Article  CAS  PubMed  Google Scholar 

  7. Hou Q, He W-J, Wu Y-S, Hao H-J, Xie X-Y, Fu X-B. Berberine: a traditional natural product with novel biological activities. Altern Ther Health Med. 2020;26(S2):20–7.

    PubMed  Google Scholar 

  8. Begum S, Mannan A. A review on Nigella sativa: a marvel herb. J Drug Delivery Ther. 2020;10(2):213–9.

    Article  CAS  Google Scholar 

  9. D’souza MR. Traditional Indian herbs for the management of diabetes mellitus and their herb-drug interaction potentials: an evidence-based review. In: Chen H, Zhang M, editors. Structure and health effects of natural products on diabetes mellitus. Singapore: Springer; 2021.

    Google Scholar 

  10. Nayebi N, Esteghamati A, Meysamie A, Khalili N, Kamalinejad M, Emtiazy M, et al. The effects of a Melissa officinalis L. based product on metabolic parameters in patients with type 2 diabetes mellitus: a randomized double-blinded controlled clinical trial. J Complement Integr Med. 2019. https://doi.org/10.1515/jcim-2018-0088.

    Article  PubMed  Google Scholar 

  11. Sardarbandeh A, Delnavazi MR, Sharifzadeh M, Sepanlou MG, Tamiji Z, Lamardi SNS. Beneficial hypoglycemic, hypolipidemic effects of aerial branches and roots extract of Eryngium caeruleum M. Bieb on Streptozotocin-induced diabetes model in rats. Tradit Integr Med. 2021.

  12. Smith M. Therapeutic applications of fenugreek. Altern Med Rev. 2003;8(1):20–7.

    PubMed  Google Scholar 

  13. Kumar A, Aswal S, Chauhan A, Semwal RB, Kumar A, Semwal DK. Ethnomedicinal investigation of medicinal plants of Chakrata region (Uttarakhand) used in the traditional medicine for diabetes by Jaunsari tribe. Nat Prod Bioprospect. 2019;9(3):175–200.

    Article  PubMed  PubMed Central  Google Scholar 

  14. NagulapalliVenkata KC, Swaroop A, Bagchi D, Bishayee A. A small plant with big benefits: fenugreek (Trigonella foenum-graecum Linn.) for disease prevention and health promotion. Mol Nutr Food Res. 2017;61(6):1600950.

    Article  CAS  Google Scholar 

  15. Ma X, Chen Z, Wang L, Wang G, Wang Z, Dong X, et al. The pathogenesis of diabetes mellitus by oxidative stress and inflammation: its inhibition by berberine. Front Pharmacol. 2018;9:782.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Khashayar A, Bahari Z, Elliyeh M, Ghasemi M. Therapeutic effects of berberine in metabolic diseases and diabetes mellitus. Rev Bras. 2021;31(3):272–81.

    Google Scholar 

  17. Zhang X, Zhao Y, Zhang M, Pang X, Xu J, Kang C, et al. Structural changes of gut microbiota during berberine-mediated prevention of obesity and insulin resistance in high-fat diet-fed rats. PLoS ONE. 2012. https://doi.org/10.1371/journal.pone.0042529.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Han J, Lin H, Huang W. Modulating gut microbiota as an anti-diabetic mechanism of berberine Medical science monitor: international medical journal of experimental and clinical research. Med Sci Monit. 2011. https://doi.org/10.12659/MSM.881842.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Tavakoly R, Maracy MR, Karimifar M, Entezari MH. Does fenugreek (Trigonella foenum-graecum) seed improve inflammation, and oxidative stress in patients with type 2 diabetes mellitus? A parallel group randomized clinical trial. Eur J Integr Med. 2018;18:13–7.

    Article  Google Scholar 

  20. Zhang Y, Li X, Zou D, Liu W, Yang J, Zhu N, et al. Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. J Clin Endocrinol Metab. 2008;93(7):2559–65.

    Article  CAS  PubMed  Google Scholar 

  21. Ye Y, Liu X, Wu N, Han Y, Wang J, Yu Y, et al. Efficacy and safety of Berberine alone for several metabolic disorders: a systematic review and meta-analysis of randomized clinical trials. Front Pharmacol. 2021;12: 653887.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Zhang Z, Zhang H, Li B, Meng X, Wang J, Zhang Y, et al. Berberine activates thermogenesis in white and brown adipose tissue. Nat Commun. 2014;5(1):1–15.

    Article  Google Scholar 

  23. Mathern JR, Raatz SK, Thomas W, Slavin JL. Effect of fenugreek fiber on satiety, blood glucose and insulin response and energy intake in obese subjects. Phytother Res. 2009;23(11):1543–8.

    Article  CAS  PubMed  Google Scholar 

  24. Boutron I, Moher D, Altman DG, Schulz KF, Ravaud P, Group* C. Extending the CONSORT statement to randomized trials of nonpharmacologic treatment: explanation and elaboration. Ann Int Med. 2008;148(4):295–309.

    Article  PubMed  Google Scholar 

  25. Care D. Medical care in diabetes 2018. Diabet Care. 2018;41(1):S105–18.

    Google Scholar 

  26. Li Y, Ma H, Zhang Y, Kuang H, Ng EHY, Hou L, et al. Effect of berberine on insulin resistance in women with polycystic ovary syndrome: study protocol for a randomized multicenter controlled trial. Trials. 2013;14(1):1–5.

    Article  Google Scholar 

  27. Hadi A, Arab A, Hajianfar H, Talaei B, Miraghajani M, Babajafari S, et al. The effect of fenugreek seed supplementation on serum irisin levels, blood pressure, and liver and kidney function in patients with type 2 diabetes mellitus: a parallel randomized clinical trial. Complement Ther Med. 2020;49: 102315.

    Article  PubMed  Google Scholar 

  28. Ghaffarpour M, Houshiar-Rad A, Kianfar H. The manual for household measures, cooking yields factors and edible portion of foods. Tehran: Nashre Olume Keshavarzy. 1999;7(213):42–58.

    Google Scholar 

  29. Shahbazian HHJ, Arghideh M, Fardad F, Latifi M. Prevalence of gastrointestinal symptoms in type 2 patients with diabetes and its association with glycemic control and duration of diabetes. Iran J Endocrinol Metab. 2012;13(5):459–66.

    Google Scholar 

  30. Montazeri A, Vahdaninia M, Mousavi SJ, Omidvari S. The Iranian version of 12-item Short Form Health Survey (SF-12): factor structure, internal consistency and construct validity. BMC Public Health. 2009;9(1):1–10.

    Article  Google Scholar 

  31. Song YS, Hwang Y-C, Ahn H-Y, Park C-Y. Comparison of the usefulness of the updated homeostasis model assessment (HOMA2) with the original HOMA1 in the prediction of type 2 diabetes mellitus in Koreans. Diabetes Metab J. 2016;40(4):318–25.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Saeedi P, Salpea P, Karuranga S, Petersohn I, Malanda B, Gregg EW, et al. Mortality attributable to diabetes in 20–79 years old adults, 2019 estimates: Results from the International Diabetes Federation Diabetes Atlas. Diabetes Res Clin Pract. 2020;162: 108086.

    Article  PubMed  Google Scholar 

  33. Yin J, Xing H, Ye J. Efficacy of berberine in patients with type 2 diabetes mellitus. Metabolism. 2008;57(5):712–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Rashidi H, Namjoyan F, Mehraban Z, Zakerkish M, Ghaderian SB, Latifi SM. The effects of active ingredients of barberry root (Berberine) on Glycemic control and insulin resistance in type 2 diabetic patients. Jundishapur J Nat Pharm Prod. 2018. https://doi.org/10.5812/jjnpp.64180.

    Article  Google Scholar 

  35. Lee YS, Kim WS, Kim KH, Yoon MJ, Cho HJ, Shen Y, et al. Berberine, a natural plant product, activates AMP-activated protein kinase with beneficial metabolic effects in diabetic and insulin-resistant states. Diabetes. 2006;55(8):2256–64.

    Article  CAS  PubMed  Google Scholar 

  36. Srivastava RAK, Pinkosky SL, Filippov S, Hanselman JC, Cramer CT, Newton RS. AMP-activated protein kinase: an emerging drug target to regulate imbalances in lipid and carbohydrate metabolism to treat cardio-metabolic diseases: thematic review series: new lipid and lipoprotein targets for the treatment of cardiometabolic diseases. J Lipid Res. 2012;53(12):2490–514.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Zhou J-Y, Zhou S-W. Protective effect of berberine on antioxidant enzymes and positive transcription elongation factor b expression in diabetic rat liver. Fitoterapia. 2011;82(2):184–9.

    Article  CAS  PubMed  Google Scholar 

  38. Zhang Y-p, Deng Y-j, Tang K-r, Chen R-s, Liang S, Liang Y-j, et al. Berberine ameliorates high-fat diet-induced non-alcoholic fatty liver disease in rats via activation of SIRT3/AMPK/ACC pathway. Curr Med Sci. 2019;39(1):37–43.

    Article  PubMed  CAS  Google Scholar 

  39. Ju J, Li J, Lin Q, Xu H. Efficacy and safety of berberine for dyslipidaemias: a systematic review and meta-analysis of randomized clinical trials. Phytomedicine. 2018;50:25–34.

    Article  CAS  PubMed  Google Scholar 

  40. Li Z, Jiang J-D, Kong W-J. Berberine upregulates hepatic low-density lipoprotein receptor through ras-independent but AMP-activated protein kinase-dependent Raf-1 activation. Biol Pharm Bull. 2014. https://doi.org/10.1248/bpb.b14-00412.

    Article  PubMed  Google Scholar 

  41. Dong B, Li H, Singh AB, Cao A, Liu J. Inhibition of PCSK9 transcription by berberine involves down-regulation of hepatic HNF1α protein expression through the ubiquitin-proteasome degradation pathway. J Biol Chem. 2015;290(7):4047–58.

    Article  CAS  PubMed  Google Scholar 

  42. Allawadhi P, Khurana A, Sayed N, Kumari P, Godugu C. Isoproterenol-induced cardiac ischemia and fibrosis: plant-based approaches for intervention. Phytother Res. 2018;32(10):1908–32.

    Article  PubMed  Google Scholar 

  43. Singh A, Tamarkar A, Shweta NT, Srivastava AK. Antihyperglycaemic effect of an unusual amino acid (4-hydroxyisoleucine) in C57BL/KsJ-db/db mice. Nat Product Res. 2010;24(3):258–65.

    Article  CAS  Google Scholar 

  44. Gong J, Fang K, Dong H, Wang D, Hu M, Lu F. Effect of fenugreek on hyperglycaemia and hyperlipidemia in diabetes and prediabetes: a meta-analysis. J Ethnopharmacol. 2016;194:260–8.

    Article  PubMed  Google Scholar 

  45. Rashid R, Ahmad H, Ahmed Z, Rashid F, Khalid N. Clinical investigation to modulate the effect of fenugreek polysaccharides on type-2 diabetes. Bioact Carbohydr Diet Fibre. 2019;19: 100194.

    Article  CAS  Google Scholar 

  46. Verma N, Usman K, Patel N, Jain A, Dhakre S, Swaroop A, et al. A multicenter clinical study to determine the efficacy of a novel fenugreek seed (Trigonella foenum-graecum) extract (Fenfuroâ„¢) in patients with type 2 diabetes. Food Nutr Res. 2016;60(1):32382.

    Article  PubMed  CAS  Google Scholar 

  47. Bera TK, Ali KM, Jana K, Ghosh A, Ghosh D. Protective effect of aqueous extract of seed of Psoralea corylifolia (Somraji) and seed of Trigonella foenum-graecum L. (Methi) in streptozotocin-induced diabetic rat: a comparative evaluation. Pharmacogn Res. 2013;5(4):277.

    Article  Google Scholar 

  48. Patel D, Prasad SK, Kumar R, Hemalatha S. An overview on antidiabetic medicinal plants having insulin mimetic property. Asian Pac J Trop Biomed. 2012;2(4):320–30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Heshmat-Ghahdarijani K, Mashayekhiasl N, Amerizadeh A, TeimouriJervekani Z, Sadeghi M. Effect of fenugreek consumption on serum lipid profile: a systematic review and meta-analysis. Phytother Res. 2020;34(9):2230–45.

    Article  CAS  PubMed  Google Scholar 

  50. Chen Z, Lei Y-L, Wang W-P, Lei Y-Y, Liu Y-H, Hei J, et al. Effects of saponin from trigonella foenum-graecum seeds on dyslipidemia. Iran J Med Sci. 2017;42(6):577.

    PubMed  PubMed Central  Google Scholar 

  51. Renuka C, Ramesh N, Saravanan K. Evaluation of the antidiabetic effect of Trigonella foenum-graecum seed powder on alloxaninduced diabetic albino rats. Int J PharmTech Res. 2009;1(4):1580–4.

    Google Scholar 

  52. Zentek J, Gärtner S, Tedin L, Männer K, Mader A, Vahjen W. Fenugreek seed affects intestinal microbiota and immunological variables in piglets after weaning. Br J Nutr. 2013;109(5):859–66.

    Article  CAS  PubMed  Google Scholar 

  53. Bruce-Keller AJ, Salbaum JM, Luo M, Blanchard E IV, Taylor CM, Welsh DA, et al. Obese-type gut microbiota induce neurobehavioral changes in the absence of obesity. Biol Psychiat. 2015;77(7):607–15.

    Article  PubMed  Google Scholar 

  54. Haber SL, Keonavong J. Fenugreek use in patients with diabetes mellitus. Am J Health Syst Pharm. 2013;70(14):1196–203.

    Article  PubMed  Google Scholar 

  55. Khurana A, Anchi P, Allawadhi P, Kumar V, Sayed N, Packirisamy G, et al. Superoxide dismutase mimetic nanoceria restrains cerulein induced acute pancreatitis. Nanomedicine. 2019;14(14):1805–25.

    Article  CAS  PubMed  Google Scholar 

  56. Khurana A, Anchi P, Allawadhi P, Kumar V, Sayed N, Packirisamy G, et al. Yttrium oxide nanoparticles reduce the severity of acute pancreatitis caused by cerulein hyperstimulation. Nanomed: nanotechnol. Biol Med. 2019;18:54–65.

    CAS  Google Scholar 

  57. Horvath A, Leber B, Feldbacher N, Tripolt N, Rainer F, Blesl A, et al. Effects of a multispecies synbiotic on glucose metabolism, lipid marker, gut microbiome composition, gut permeability, and quality of life in diabesity: a randomized, double-blind, placebo-controlled pilot study. Eur J Nutr. 2020;59(7):2969–83.

    Article  CAS  PubMed  Google Scholar 

  58. Uchio R, Muroyama K, Okuda-Hanafusa C, Kawasaki K, Yamamoto Y, Murosaki S. Hot water extract of Curcuma longa L. improves serum inflammatory markers and general health in subjects with overweight or prehypertension/mild hypertension: a randomized, double-blind, placebo-controlled trial. Nutrients. 2019;11(8):1822.

    Article  CAS  PubMed Central  Google Scholar 

  59. Jing X, Chen J, Dong Y, Han D, Zhao H, Wang X, et al. Related factors of quality of life of type 2 diabetes patients: a systematic review and meta-analysis. Health Qual Life Outcomes. 2018;16(1):1–14.

    Article  CAS  Google Scholar 

  60. Amini H, Isanejad A, Chamani N, Movahedi-Fard F, Salimi F, Moezi M, et al. Physical activity during COVID-19 pandemic in the Iranian population: a brief report. Heliyon. 2020;6(11): e05411.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Sayed N, Khurana A, Godugu C. Pharmaceutical perspective on the translational hurdles of phytoconstituents and strategies to overcome. J Drug Deliv Sci Technol. 2019;53: 101201.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The M.Sc. thesis of Shima Nematollahi led to the creation of the current study. All of the volunteers in the current study are much appreciated. Many thanks to Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran, and the Nutrition and Metabolic Diseases Research Center and Clinical Sciences Research Institute for approving this research project (IR.AJUMS.REC.1398.735). The Diabetes Research and Education Association at Shiraz University of Medical Science in Shiraz, Iran, is also greatly appreciated. We also extend our sincere gratitude to Arjuna Natural Pvt. Ltd. Company, Kerala, India, for creating the study's supplemental materials.

Funding

This research was supported by the Research Deputy of Ahvaz Jundishapur University of Medical Sciences and Nutrition and Metabolic Diseases Research Center and clinical sciences research institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran (Ethical NO.IR.AJUMS.REC.1398.735).

Author information

Authors and Affiliations

  1. Nutrition and Metabolic Diseases Research Center and Clinical Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

    Shima Nematollahi

  2. Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

    Gholam Reza Pishdad

  3. Health Research Institute, Diabetes Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

    Mehrnoosh Zakerkish

  4. Research center for Traditional Medicine and History of Medicine, Shiraz University of medical sciences, Shiraz, Iran

    Foroogh Namjoyan

  5. Department of Statistics and Epidemiology, School of Health Sciences, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

    Kambiz Ahmadi Angali

  6. Nutrition and Metabolic Disease Research Center and Clinical Sciences Research Institute, Ahvaz Jundishapur University of Medical Science, Ahvaz, Iran

    Fatemeh Borazjani

Authors
  1. Shima Nematollahi
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Gholam Reza Pishdad
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Mehrnoosh Zakerkish
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Foroogh Namjoyan
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Kambiz Ahmadi Angali
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Fatemeh Borazjani
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

SN, FN, and FB came up with the concept and formulated the research question. SN, MZ, and GRP. Supervised the recruitment of managements and participants. Data input and statistical analysis were under KAA supervision. The manuscript was written by FBand SN. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Fatemeh Borazjani.

Ethics declarations

Ethics approval and consent to participate

The Ethical Committee of Jundishapur University of Medical Sciences examined and approved the study, which adhered to the Declaration of Helsinki (IR.AJUMS.REC.1398.735). After outlining the study's goals, each participant in the study provided their written informed consent.

Consent for publication

Not applicable.

Competing interests

There is no potential conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

Baseline and end of trial scores for the SF-12 domains short-form health survey with berberine and fenugreek seed intervention.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nematollahi, S., Pishdad, G.R., Zakerkish, M. et al. The effect of berberine and fenugreek seed co-supplementation on inflammatory factor, lipid and glycemic profile in patients with type 2 diabetes mellitus: a double-blind controlled randomized clinical trial. Diabetol Metab Syndr 14, 120 (2022). https://doi.org/10.1186/s13098-022-00888-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13098-022-00888-9

Keywords

Diabetology & Metabolic Syndrome

ISSN: 1758-5996

Contact us