Effect of Tropical Vegetable Oil Consumption on Lipid Profile and Glycaemic Control in Type 2 Diabetics
Received 16 Apr, 2024 |
Accepted 12 Jul, 2024 |
Published 13 Jul, 2024 |
Background and objective: Divergent relationships with several inconsistencies have been established on the effect of vegetable oils consumption on blood glucose and lipid profiles in type 2 diabetes. The study sought to determine the effect of consuming some tropical vegetable oils on glycaemic and lipid control in type 2 diabetes patients in the middle belt of Ghana and evaluate the relationship between lipid profile and FBG.Materials and Methods: In an open-labelled 4-arm parallel prospective dietary cohort study, 62 type 2 diabetic out-patients on metformin medication, consumed meals supplemented with red palm oil (n = 17), groundnut oil (n = 16) or coconut oil (n = 21) as the only source of fat for 4 weeks except control (n = 8) whose diets were not supplemented with vegetable oil or any other oil. A twelve hour fasting venous blood samples were collected at baseline and week 4 (W4), FBG and lipid profile were then determined. Results: There were no significant metabolic changes in the fasting blood glucose and lipid profile generally in the diabetics after the consumption of the vegetable oils. No statistically significant (p>0.05) changes were observed in blood glucose levels across all groups from baseline to W4. Although, serum triglycerides (TG) was significantly increased (p = 0.020) among groundnut oil-treated group from baseline to W4, there were no significant correlations observed between FBG and lipid profile indices across all groups. Conclusion: The consumption of different tropical oils; red palm oil, coconut oil and groundnut oil did not impair glycaemic control or induce dyslipidaemia in type 2 patients.
Copyright © 2024 Berkoh et al. This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
INTRODUCTION
Type 2 diabetes (T2D) has become a major public health problem affecting 425 million people worldwide and is currently described by the International Diabetes Federation (IDF) as an “emerging medical emergency of the 21st century” due to the alarming rate of increase in the number of diagnosed diabetics over the past decade1,2. Decades ago the incidence of diabetes in sub-Saharan Africa was less than 2%3.
In Ghana the prevalence of diabetes is about 6%4. This percentage is believed to be worsening as the country acquires a middle-income status with corresponding changes to increased sedentary lifestyle and the consumption of energy dense diets high in fat but low in carbohydrates5. These lifestyle dietary changes have resulted in an increase in the incidence of diabetes mellitus and other diet-related diseases, including, obesity, hypertension cardiovascular disease and stroke in developing countries6.
Somes studies have related, high fat intake, particularly, rich in saturated fatty acids to reduced insulin sensitivity and secretion7,8 and the aetiology of type 2 diabetes9. Insulin sensitivity has been proven to be decreased by fats and oils10.
The quality of fat in the diet is relevant to the health status of the diabetics and hence it is argued that substituting foods high in saturated and trans fats for those rich in mono and polyunsaturated fatty acids may reduce the risk of CVD and improve glucose metabolism11,12. The World Health Organisation (WHO) in a bid to enforce the consumption of healthy fats introduced the REPLACE action package policy as a strategy to eliminate the consumption of trans fatty acids by 202313. Furthermore, contrasting views from various research findings have been established between fasting blood sugar (FBG) and lipid profile parameters in type 2 diabetes14,15. Studies have shown in a Chinese population, that the consumption of certain fats and oils were associated with an increased risk of type 2 diabetes16. Many clinicians have therefore discouraged patients of type 2 diabetes from consuming fats and oils or at least limit their consumption.
However certain oils including vegetable oils have been shown to have positive effect on diabetes management. Indeed fish oil supplementation has been proven to improve insulin sensitivity in rat study17. Olive oil is a vegetable oil that has also been scientifically proven to have least dyslipidaemic and atherogenic effect18.
In Ghana, particularly in rural and peri-urban settings, red palm oil, coconut oil and groundnut oil are commonly used for cooking due to their availability and the prohibitive cost of imported or refined oils19. It is believed that prudent consumption of these indigenous oils to supplement a balanced diet may be cost-effective and reduce the risk of CVD for diabetic patients living on low income in sub-Saharan Africa20. Ngala et al.21 have shown in animal studies, that rodent chow, supplemented with 10% by weight red palm oil, coconut oil and groundnut oil significantly reduced fasting blood glucose with no dyslipidaemia. Despite the positive effect of these vegetable oils in the rodent study, little is known about the effect of this vegetable oil consumption on FBG and the lipid profile of Ghanaian type 2 diabetes patients and the healthy population. This study therefore investigates the effects of the consumption of three tropical vegetable oils, amist the belief that fats and oils consumption negatively impact glycaemic and lipid control in type 2 diabetes patients.
MATERIALS AND METHODS
Study design and setting: This was an open-labelled, 4-arm parallel prospective dietary cohort study in which 62 diabetic out-patients of both sexes between the ages of 30-75 attending Sunyani and Duayaw Nkwanta Hospitals-Ghana, who had volunteered and given written and/oral consent were recruited between June to December, 2022. Patients consuminmg alcohol or smoking and those with existing malignancies or autoimmune diseases were excluded. All patients were on metformin prescription. A standardised questionnaire was used to collect demographic and clinical data. Patients were administered daily intake of one of the three vegetable oils which were added to their regular meals for four weeks exclusively on their preference. Red palm oil, extract from African oil palm, Elaeis guineensis, groundnut oil extracted from the nuts of Arachis hypogaea) and coconut oil (extracted from the kennel of Cocos nucifera). The quantity of oil administered was based on each individual’s BMI, was calculated and converted into handy measures equivalent to 20-30 g of oil/day/person.
Ethical approval: Ethical approval was obtained from the Kintampo Health Research Centre (KHRC) Institutional Ethics Committee (KHRCIEC/2018-22) with additional permission from the Regional Health Directorate of the Ghana Health Service, Bono Region. Study participants were adequately informed of the purpose, nature, procedures, risks and hazards of the study and signed informed consent forms according to the recommendations of the local ethics review committees that were approved. All work was conducted in accordance with the declaration of Helsinki22.
Blood sample collection and analyses: As 12 hrs fasting venous blood samples were collected into serum separator tubes at baseline and week 4 for lipid profile assessment. Serum samples were separated by centrifuging at 3000 rpm for 10 min from the respective tubes and stored at -20°C until analysis. Fasting blood glucose was measured with a (OneTouch Select Plus Simple®) glucometer while serum concentrations of total cholesterol (TC), High-Density Lipoprotein Cholesterol (HDL-C) and triglycerides (TG) were assayed with standardized enzymatic methods using commercial kits (Medsource Ozone Biomedicals Pvt. Ltd., India). Low-Density Lipoprotein Cholesterol (LDL-C) was calculated using the Friedewald equation:
The LDL-C is low density lipoproteins, TC is total cholesterol, HDL is high density lipoprotein and TG is triglycerides.
Statistical analysis: The results obtained from the FBG and lipid profile analyses were presented as Mean±SEM. A paired t-test was used to compare the mean FBG and lipid profile parameters with a one-way ANOVA to compare the differences among treatment groups. A p<0.05 was considered statistically significant. A multivariate logistic regression (Pearson-Correlation coefficient) was used to assess the correlation between the FBG and lipid profile indices of treatment groups at week 4. The p-values of <0.05 and <0.01 (two-tailed) were considered statistically significant.
RESULTS
Relationship between FBG and lipid profile parameters at W4: Out of the 62 patients recruited (mean age 61±8.5 years), 19 (30.6%) were male while 43 (69.4%) were female. As 18 (28.7%), 33 (53.5%) and 11(17.9%) attended clinics at the Sunyani Regional Hospital, Municipal Hospital and the St. John of God Hospital, Dua-Yaw Nkwanta, respectively. All other demographic data for the level of education, marital status, presence of- and type of comorbidity, religion and family history of diabetes and presence of family support in addition to health insurance cover were presented in Table 1.
The distributions across treatment groups based on patients’ preference for oil are as follows: 8 (12.9%) patients were allocated to the control group while 17 (27.4%), 16 (25.8%) and 21 (33.9%) were assigned to comsume palm coconut and groundnut oils, respectively (Table 2).
There were no significant changes in the plasma glucose level in all the oil treatment in the diabetes patients (Table 3).
There was no significant difference in the absolute glucose values between the control and all the treatment groups (Table 4).
Lipid profile results of respondents from baseline to week 4: There were no significant changes in lipid profile across all groups, total cholesterol (TC) increased among the control, palm oil-treated and groundnut oil-treated groups from baseline to W4 but slightly decreased among the coconut oil-treated group. The HDL, LDL and TC were not significantly changed in all the treatment groups compared to the control.
Table 1: | Demographics of study participants |
Parameter | Frequency | Percentage |
Total | 62 | 100 |
Age Mean±SD (Years) | 61±8.5 | |
Hospital | ||
Regional Hospital | 18 | 28.7 |
Municipal Hospital | 33 | 53.4 |
Duayaw Nkwanta Hospital | 11 | 17.9 |
Gender | ||
Male | 19 | 30.6 |
Female | 43 | 69.4 |
Marital status | ||
Single | 5 | 7.5 |
Married | 33 | 53.9 |
Separated/widowed | 24 | 38.6 |
Educational level | ||
Non-formal | 16 | 26.5 |
Basic | 19 | 30.3 |
Secondary/vocational | 21 | 34.6 |
Tertiary | 5 | 8.6 |
Employment status | ||
Unemployed | 17 | 26.8 |
Employed | 4 | 7 |
Self-employed | 24 | 39.4 |
Pensioner | 17 | 26.8 |
Religion | ||
Christian | 55 | 89 |
Muslim | 7 | 11 |
Presence of family support | ||
Yes | 42 | 67.7 |
No | 20 | 32.3 |
Family history of diabetes | ||
Yes | 38 | 61.9 |
No | 24 | 38.1 |
Presence of comorbidity | ||
Yes | 45 | 72.6 |
No | 17 | 27.4 |
Comorbidities | ||
Hypertension | 39 | 62.9 |
Ulcer | 6 | 9.6 |
Insurance cover | ||
None | 0 | 0 |
NHIS | 62 | 100 |
Table 2: | Distributions of dietary intervention groups |
Variable | Frequency (%) |
Treatment group | |
Control | 8 (12.9) |
Palm oil | 17 (27.4) |
Coconut oil | 16 (25.8) |
Groundnut oil | 21 (33.9) |
Total | 62 (100) |
Table 3: | Fasting blood glucose among treatment groups from baseline to W4 |
Mean FBG (mmol/L) | |||||
Treatment group | Baseline | Week 4 | t-value | Df | p-value |
Control | 9.9±2.8 | 8.3±2.6 | 1.13 | 5 | 0.31 |
Palm oil | 10.0±3.7 | 10.6±3.1 | -0.4 | 11 | 0.697 |
Groundnut oil | 10.8±4.9 | 10.3±2.6 | 0.24 | 13 | 0.817 |
Coconut oil | 10.8±4.6 | 11.8±3.1 | -0.92 | 18 | 0.371 |
Effect of vegetable oils on plasma glucose of diabetes patients. Mean values are expressed as ±SEM. N: 8, 17, 16 and 21 for the control, palm, groundnut and coconut oil groups, respectively, p<0.05, indicate a significant difference between the group and the control |
Table 4: | ANOVA comparison of the absolute differences between the week 4 and baseline FBG among treatment groups against the control group |
Treatment group |
Mean (W4-B_FBG) |
Standard deviation |
Mean difference (I-J) |
Standard error |
p-value | 95% confidence lower bound |
95% confidence upper bound |
Palm oil | 1.93 | 1.56 | -1.06 | 1.27 | 0.91 | 0.93 | 2.92 |
Groundnut oil | 3.64 | 3.08 | 0.65 | 1.24 | 0.47 | 1.86 | 5.41 |
Coconut oil | 2.51 | 2.57 | -0.48 | 1.19 | 0.82 | 1.27 | 3.74 |
Table 5: | Effect of vegetable oil consumption on plasma lipid profile in type 2 diabetes patients after 4 weeks treatment |
Treatment | Baseline | Week 4 | t-value | df | p-value | |
CHOL | Control | 4.19±0.59 | 5.17±0.32 | -2.006 | 6 | 0.092 |
Palm oil | 4.91±0.27 | 5.18±0.21 | -1.341 | 13 | 0.203 | |
Groundnut oil | 4.89±0.24 | 5.11±0.42 | -0.393 | 13 | 0.701 | |
Coconut oil | 5.40±0.28 | 5.35±0.23 | 0.254 | 18 | 0.802 | |
TRIG | Control | 1.39±0.24 | 1.75±0.15 | -1.439 | 6 | 0.2 |
Palm oil | 1.69±0.23 | 1.67±0.20 | 0.112 | 13 | 0.913 | |
Groundnut oil | 1.56±0.10 | 2.06±0.26 | -2.662 | 13 | 0.020* | |
Coconut oil | 1.87±0.22 | 1.97±0.16 | -0.611 | 18 | 0.549 | |
HDL | Control | 1.43±0.26 | 1.3±0.35 | 0.473 | 6 | 0.653 |
Palm oil | 1.51±0.26 | 1.16±0.16 | 1.482 | 13 | 0.162 | |
Groundnut oil | 1.14±0.16 | 1.37±0.18 | -0.888 | 13 | 0.391 | |
Coconut oil | 1.42±0.14 | 1.44±0.22 | -0.034 | 18 | 0.974 | |
LDL | Control | 2.13±0.43 | 3.08±0.54 | -1.475 | 6 | 0.191 |
Palm oil | 2.65±0.22 | 3.04±0.33 | -1.184 | 14 | 0.256 | |
Groundnut oil | 3.04±0.25 | 2.80±0.49 | 0.377 | 13 | 0.712 | |
Coconut oil | 2.97±0.28 | 2.93±0.24 | 0.139 | 18 | 0.891 | |
LDL/HDL ratio | Control | 1.79±1.08 | 3.53±2.46 | -1.737 | 6 | 0.133 |
Palm oil | 2.39±1.51 | 3.39±2.06 | -1.84 | 14 | 0.087 | |
Groundnut oil | 3.21±1.51 | 2.73±2.35 | 0.617 | 13 | 0.548 | |
Coconut oil | 2.70±1.89 | 3.28±2.52 | -0.851 | 18 | 0.405 | |
Effect of vegetable oils on the plasma lipids of diabetes patients. Mean values are expressed as Mean±SEM in each group. TC: Total cholesterol, LDL: Low density lipoprotein, HDL: High density lipoprotein, TG: Triglycerides and compared to controls, p<0.05, indicates a significant difference |
There were also no significant changes in the cardiovascular risk indiex across all groups for all the oils (LDL/HDL).
Only triglyceride was significantly (p = 0.020) increased in the groundnut oil-treated group but not above the physiological upper reference range (Table 5).
The TC, TG and LDL were positively correlated with FBG while HDL negatively (-0.643) correlated with FBG among the control group though not significant. For the palm oil-treated group, all lipid profile parameters were non significantly negatively correlated with FBG while for the groundnut oil-treated group, there was a positive correlation between FBG and TG but a negative correlation was found between TC, LDL, HDL and FBG. There was a positive correlation between FBG and TC, TG and HDL with a negative correlation between LDL and FBG for the coconut oil-treated groups. Although, some of these findings are consistent with other research findings, none were considered to be statistically significant (Table 6).
DISCUSSION
Insulin is the major hormone controlling plasma glucose homeostasis. However this effect is impaired in type 2 diabetes patients, whose predicaments are a result of insulin resistance, hence medication including insulin secretegoques (sulfonylureas and glinides) and insulin sensitizers (metformin, pioglitazone), are administered to achieve a glycaemic control23.
The Ghana Health Service treatment guideline for type 2 diabetes requires metformin as the first line therapy24, therefore all the subjects were on metformin prescription. The antidiabetic effect of metformin on glycaemic control is due to the inhibition gluconeogenesis, reduction of intestinal glucose absorption and improve peripheral glucose uptake and insulin sensitivity25. The activity of metformin is not known to be negatively affected by plasma lipids. Clinical studies have demonstrated that metformin positively modifies lipids metabolism26,27 by altering fatty acid de novo synthesis and the mitochondrial β-oxidation of fatty acids28. However, lipids have been proven to impair insulin sensitivity29, whilst other studies have shown that sesame oil has a synergistic effect with anti-diabetic medication in patients with type 2 diabetes mellitus30.
Table 6: | Correlation between W4-FBS and lipids |
W4-FBG | |||
Treatment group | Lipids | Pearson correlation value | p-value |
Control | W4-CHO | 0.365 | 0.477 |
W4-TG | 0.26 | 0.618 | |
W4-TG/2.2 | 0.26 | 0.618 | |
W4-HDL | -0.643 | 0.168 | |
W4-LDL | 0.553 | 0.255 | |
Palm oil | W4-CHO | -0.571 | 0.085 |
W4-TG | -0.111 | 0.76 | |
W4-TG/2.2 | -0.111 | 0.76 | |
W4-HDL | -0.035 | 0.923 | |
W4-LDL | -0.347 | 0.326 | |
Groundnut oil | W4-CHO | -0.079 | 0.789 |
W4-TG | 0.131 | 0.656 | |
W4-TG/2.2 | 0.131 | 0.656 | |
W4-HDL | -0.179 | 0.539 | |
W4-LDL | -0.072 | 0.806 | |
Coconut oil | W4-CHO | 0.171 | 0.484 |
W4-TG | 0.19 | 0.435 | |
W4-TG/2.2 | 0.267 | 0.27 | |
W4-HDL | 0.303 | 0.207 | |
W4-LDL | -0.181 | 0.457 |
The consumption of the local vegetable oils; coconut, groundnut and red palm oils for four weeks did not significantly alter the blood glucose levels compared to the base line (Table 3). Metformin administration alone (control) did not reduce the blood glucose of the diabetics to the physiological range. Indeed, base line blood glucose levels in all the subjects were higher than the normal reference range (3.4-6.4 mmol/L). Comparison of the absolute differences in the blood glucose levels (Table 4) in the subjects were also not significantly changed.
There are various multifactorial and complex reasons given for poor glycaemic control in T2D31 that are patient- and disease-related or psychosocial. These include factors such as age, physical activity, educational level, lack of knowledge of diabetes and glycaemic targets, smoking, poor or inadequate Self-Monitoring of Blood Glucose (SMBG), duration of diabetes, presence of comorbidities, missing scheduled hospital appointments, poor adherence of medication and diet, anxiety and depression, false beliefs about treatments and availability of family and/or social support32,33 (Table 1).
According to Afaya et al.34 persons aged below 50 years constitute a larger proportion of patients with poor glycaemic control. While some studies report young age to be associated with poor glycaemic control, other studies report no statistically significant relationship between age and glycaemic control35. Again, it is believed that elderly people are more likely to comply with diabetes management regimens and hence have better glycaemic control than young individuals36. Yet, advancement in age can lead to the development of comorbidities and also cause a decline in beta-cell function in diabetic patients31.
Both of these theories could account for the poor glycaemic control observed among the study participants since the average age recorded in this study was 61 years and all patients had at least one comorbidity (Table 1). Furthermore, it is reported that patients with one or more comorbidities such as hypertension or cardiovascular diseases have increased odds of having poorer glycaemic control due to an increased burden of medication from combined drug therapy and hence increases the probability of non-compliance30 (Table 1). The recorded baseline high glucose level, may also imply either a poor compliance with prescribed medication or not following dietary guidelines. Medication adherence is significantly associated with glycaemic control and targets for good glycq1aemic control can be achieved by adhering to appropriate medications37,38. There is evidence to suggest that the practice of following dietary and lifestyle interventions with medication is not completely adhered to worldwide, which could be due to the giving of pharmacotherapy before diet and lifestyle interventions39. It can therefore be inferred that the consumption of these vegetable oils per se did not worsen the glycaemic control as has been observed in the consumption of some oils in a some studies by Zhuang et al.16 and Okuyama et al.40. However, in a similar animal study, lipids-induced improved glycaemic control was observed21.
Studies have long shown that, saturated fatty acids and cholesterol raise the plasma cholesterol high plasma lipid levels havebeen shown to induce insulin resistance in various body organs, including the liver, the adipose tissue, the hypothalamus, the skeletal muscle, the pancreas and the intestines by different mechanisms41. Although, these mechanisms are not fully understood, at the cellular level, the insulin signaling effect from its receptor to its final action is impaired. However, the phosphorylation of insulin receptors at the serine or threonine positions, may exacerbate the breakdown of the phosphorylated protein and therefore impair insulin signaling41,42 level and are a cardiovascular risk, whereas Polyunsaturated Fatty Acids (PUFA) lowers it and have reduced cardiovascular and diabetic risk because of the LDL lowering effect. In addition, soluble fiber and vegetarian diets favorably affect plasma lipid levels43. The administration of the vegetable oils to diabetic patients did not result in dyslipidemic effect (Table 5). The consumption of vegetable oils in the four week period did not induce cadiovascular risk. Indeed the cardiovascular risks calculated 1.79±1.08, 2.39±1.51, 3.21±1.51 and 2.70±1.89 for the controls, palm, groundnut and coconut oils respectively, were within the physiological range of 0-7 (Table 5).
Although, there was a significant increase in triglycerides after the intake of groundnut oil, the triglyceride concentration of 2.06 mmo/L was within the physiological reference range of up to 2.26 mmol/L set up by the laboratory. All the other lipid parameters were not significantly changed compared to the control and not significantly above the upper reference ranges.
The vegetable oils in this study consisted of a mixture of various fatty acids depending on the oil source. The groundnut oil consists of 46 and 32% of Monounsaturated Fatty Acids (MUFA) and Polyunsaturated Fatty Acids (PUFA), respectively. The palm oil contains an almost equal amounts of saturated and unsaturated fatty acids44 and coconut oil though a saturated fat mainly consists of medium-chain fatty acids45,46.
It is therefore not surprising that the oils when consumed at the appropriate amount did not have any dyslipidaemic effect because all the oils were not fully saturated, the unsaturated portion may have had a counter effect on the metabolic activity of the saturated part.
The metabolism of glucose and lipids are interrelated, Randle et al.47 proposed a “glucose-fatty acid cycle” that describes the selectionof fuel by tissues. The cycle explains the inhibition of glucose oxidation by fatty acids. This principle has been investigated by other researchers and new theories explaining the utilization of glucose and fatty acids, including that the changes in lipids and glucose levels which are interconnected through coordinated metabolic pathways and acetyl-CoA formation in which the changes of one pathway can affect the other48.
Hence, blood lipids must be well-controlled in T2D patients to slow down or limit complications and/or mortality rates49. In the diabetic control group of this study, FBG positively correlated with TC, TG and LDL (0.365, 0.260, 0.530) but negatively with HDL (-0.079) (Table 6) which establishes the already existing evidence of the relationship between blood glucose and lipid profile parameters in diabetes. Although, these findings were statistically non-significant but showed the trend of lipid glucose relation. A similar relationship was established between HbA1c and lipid profile where LDL, TC, TG, LDL/HDL ratio, TG/HDL ratio and TC/HDL ratio were positively associated with HbA1c while HDL was negatively associated50. In another study in India, FBG positively correlated with TG, HDL, LDL, VLDL and TC in a diabetic population when compared with healthy population in which FBG positively correlated with TG, VLDL and TC but negatively correlated with HDL and LDL51. These findings are suggestive of the complex and variable nature of lipid and glucose metabolism in both diabetic and non-diabetic populations. The disparities in observations made from these studies could be due to the heterogeneity of study populations, differences in research designs, differences in variable definitions or inadequate adjustment for medical confounders10.
Nutritional or dietary interventions have a significant impact on FBG and lipid profiles49. In the current study, FBG was negatively associated with lipid profile in the palm oil intervention group; while for the groundnut oil-treated group, there was a positive correlation between FBG and TG (0.313, p = 0.020) but a negative correlation was found between TC, LDL and HDL (-0.079, -0.179, -0.072) and FBG. In the coconut oil intervention group, FBG positively correlated with TC, TG and HDL (0.171, 0.190, 0.303) but negatively correlated (-0.181) with LDL. There was no statistically significant relationship between FBG and the lipid profile of all intervention groups compared to the control. This is similar to findings from a study done in India in which, no significant relationship was established between FBG and lipid profile among sedentary individuals consuming a non-vegetarian diet even though high levels of FBG and HbA1c were recorded52.
Even though the vegetable oil intervention did not significantly ameliorate the glycaemic and lipid control as was observed by Ngala et al.21 in the animal study, the oil intervention did not also induce dyslipidamia or hyperglycaemia. The plasma lipid values observed were not significantly higher than the upper reference ranges of the physiological ranges in our Clinical
Laboratory setting (TC: 3.9-5.2, Trg: 0.5-2.6, HDL 0.9-2.2 and LDL 0.0-3.8 mmol/L). It therefore implies the Ghanaian tropical vegetable oils do not impair glycaemic and lipid control in type 2 diabetics contrary to other findings elsewhere10,53. These oils may therefore not be contraindicated in the management of type 2 diabetes. The study was conducted using Ghanaian subjects and locally extracted oils, further studies may be required to acertain the effect in other populations.
CONCLUSION
The consumption of tropical vegetable oils (palm, coconut and groundnut oils) did not negatively impact on blood glucose levels of type 2 diabetes patients.The consumption of the vegetable oils did not also induce dyslipidaemia or impair glyceamic control effect of metformin in the management of type 2 diabetes. This finding therefore provides guide to clinicians monitoring diatary regulations in diabetes patients.
SIGNIFICANCE STATEMENT
High plasma lipids have been shown in several studies to impair glucose metabolism in diabetic patients. Some clinicians therefore prescribe olive oil (believed to be the least atherogenic inducing oil) or reduced fat intake by diabetic patients to make it easy to maintain a glucose homoeostasis. However, lipids are essential in several metabolic processes including energy production, cell membrane synthesis and the biosynthesis of other biomolecules and therefore their consumption cannot be compromised with. Animal studies have shown that the consumption of some tropical vegetable oils rather improve glucose homeostasis and did not induce dyslipidemia in diabetic mice and these oils are cheaper in cost compared to olive. The study therefore investigates the effect of supplementation of some tropical vegetable oils ln the diets of type 2 diabetic patients: palm, coconut and groundnut oil on glucose homeostasis. It is hoped that these oils may have similar effect as was observed in the animal study and may therefore go a long way in reducing the cost of management of type 2 diabetes.
ACKNOWLEDGEMENT
The researchers are greatful to Benso Oil Plantation Ltd for the gift of the palm oil and other logistics Department of Molecular Medicine and Department of Food and Biotechnology Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana for providing laboratory space and support from Technical staff.
REFERENCES
- Harding, J.L., M.E. Pavkov, D.J. Magliano, J.E. Shaw and E.W. Gregg, 2019. Global trends in diabetes complications: A review of current evidence. Diabetologia, 62: 3-16.
- Klisic, A. and I.S. Tzeng, 2023. Editorial: New trends in type 2 diabetes diagnosis and management in primary care. Front. Med., 10.
- Levitt, N.S., 2008. Diabetes in Africa: Epidemiology, management and healthcare challenges. Heart, 94: 1376-1382.
- Doherty, M.L., E. Owusu-Dabo, O.S. Kantanka, R.O. Brawer and J.D. Plumb, 2014. Type 2 diabetes in a rapidly urbanizing region of Ghana, West Africa: A qualitative study of dietary preferences, knowledge and practices. BMC Public Health, 14.
- Popkin, B.M., 1998. The nutrition transition and its health implications in lower-income countries. Public Health Nutr., 1: 5-21.
- Patel, R., R.E. Sina and D. Keyes, 2024. Lifestyle Modification for Diabetes and Heart Disease Prevention. StatPearls Publishing, Treasure Island.
- Riccardi, G., R. Giacco and A.A. Rivellese, 2004. Dietary fat, insulin sensitivity and the metabolic syndrome. Clin. Nutr., 23: 447-456.
- Katan, M.B., P.L. Zock and R.P. Mensink, 1994. Effects of fats and fatty acids on blood lipids in humans: An overview. Am. J. Clin. Nutr., 60: 1017S-1022S.
- Bradley, B.H.R., 2018. Dietary fat and risk for type 2 diabetes: A review of recent research. Curr. Nutr. Rep., 7: 214-226.
- Manco, M., M. Calvani and G. Mingrone, 2004. Effects of dietary fatty acids on insulin sensitivity and secretion. Diabetes Obesity Metab., 6: 402-413.
- Sears, B. and M. Perry, 2015. The role of fatty acids in insulin resistance. Lipids Health Dis., 14.
- Barrea, L., C. Vetrani, M. Caprio, M.E. Ghoch and E. Frias-Toral et al., 2023. Nutritional management of type 2 diabetes in subjects with obesity: An international guideline for clinical practice. Crit. Rev. Food Sci. Nutr., 63: 2873-2885.
- WHO, 2021. REPLACE Trans Fat: An Action Package to Eliminate Industrially Produced Trans-Fatty Acids. World Health Organization, Geneva, Switzerland, ISBN: 9789240021105, Pages: 7.
- Wang, S., X. Ji, Z. Zhang and F. Xue, 2020. Relationship between lipid profiles and glycemic control among patients with type 2 diabetes in Qingdao, China. Int. J. Environ. Res. Public Health, 17.
- Wang, L., N. Yan, M. Zhang, R. Pan, Y. Dang and Y. Niu, 2022. The association between blood glucose levels and lipids or lipid ratios in type 2 diabetes patients: A cross-sectional study. Front. Endocrinol., 13.
- Pan, Z., M. Lei, W. Fei, W. Jun, J. Jingjing and Z. Yu, 2020. Cooking oil consumption is positively associated with risk of type 2 diabetes in a Chinese nationwide cohort study. J. Nutr., 150: 1799-1807.
- Hirabara, S.M., A. Folador, J. Fiamoncini, R.H. Lambertucci and C.F. Rodrigues Jr. et al., 2013. Fish oil supplementation for two generations increases insulin sensitivity in rats. J. Nutr. Biochem., 24: 1136-1145.
- Nagyova, A., P. Haban, J. Klvanova and J. Kadrabova, 2003. Effects of dietary extra virgin olive oil on serum lipid resistance to oxidation and fatty acid composition in elderly lipidemic patients. Bratisl Lek Listy, 104: 218-221.
- Boateng, L., R. Ansong, W. Owusu and M. Steiner-Asiedu, 2016. Coconut oil and palm oil’s role in nutrition, health and national development: A review. Ghana Med. J., 50: 189-196.
- Ngala, R.A., 2021. Managing diabetes and its complications through traditional African dietary intervention. Trends Med. Res., 16: 14-18.
- Ngala, R.A., I. Ampong, S.A. Sakyi and E.O. Anto, 2016. Effect of dietary vegetable oil consumption on blood glucose levels, lipid profile and weight in diabetic mice: An experimental case-control study. BMC Nutr., 2.
- Tanić, N., T. Dramićanin, N. Ademović, T. Tomić and B. Murganić et al., 2022. The impact of TP53 and PTEN tumor suppressor genes on response to different breast cancer treatment modalities. Biomedicinska Istraživanja, 13: 105-117.
- Rena, G., D.G. Hardie and E.R. Pearson, 2017. The mechanisms of action of metformin. Diabetologia, 60: 1577-1585.
- Baker, C., C. Retzik-Stahr, V. Singh, R. Plomondon, V. Anderson and N. Rasouli, 2021. Should metformin remain the first-line therapy for treatment of type 2 diabetes? Ther. Adv. Endocrinol. Metab., 12.
- Kashi, Z., A. Mahrooz, A. Kianmehr and A. Alizadeh, 2016. The role of metformin response in lipid metabolism in patients with recent-onset type 2 diabetes: HbA1c level as a criterion for designating patients as responders or nonresponders to metformin. PloS One, 11, No. 3.
- Lin, S.H., P.C. Cheng, S.T. Tu, S.R. Hsu, Y.C. Cheng and Y.H. Liu, 2018. Effect of metformin monotherapy on serum lipid profile in statin-naïve individuals with newly diagnosed type 2 diabetes mellitus: A cohort study. PeerJ, 6.
- Zabielski, P., H.R. Hady, M. Chacinska, K. Roszczyc, J. Gorski and A.U. Blachnio-Zabielska, 2018. The effect of high fat diet and metformin treatment on liver lipids accumulation and their impact on insulin action. Sci. Rep., 8.
- Samuel, V.T., K.F. Petersen and G.I. Shulman, 2010. Lipid-induced insulin resistance: Unravelling the mechanism. Lancet, 375: 2267-2277.
- Sankar, D., A. Ali, G. Sambandam and R. Rao, 2011. Sesame oil exhibits synergistic effect with anti-diabetic medication in patients with type 2 diabetes mellitus. Clin. Nutr., 30: 351-358.
- Mamo, Y., F. Bekele, T. Nigussie and A. Zewudie, 2019. Determinants of poor glycemic control among adult patients with type 2 diabetes mellitus in Jimma University Medical Center, Jimma Zone, South West Ethiopia: A case control study. BMC Endocr. Disord., 19.
- Alramadan, M.J., A. Afroz, S.M. Hussain, M.A. Batais and T.H. Almigbal et al., 2018. Patient-related determinants of glycaemic control in people with type 2 diabetes in the gulf cooperation council countries: A systematic review. J. Diabetes Res., 2018.
- Cedrick, L.M., J.P.F. Lubaki, L.B. Francois, O.A. Gboyega and L.N. Philippe, 2021. Prevalence and determinants of poor glycaemic control amongst patients with diabetes followed at Vanga Evangelical Hospital, Democratic Republic of the Congo. Afr. J. Primary Health Care Fam. Med., 13.
- Omar, S.M., I.R. Musa, O.E. Osman and I. Adam, 2018. Assessment of glycemic control in type 2 diabetes in the Eastern Sudan. BMC Res. Notes, 11.
- Afaya, R.A., V. Bam, T.B. Azongo, A. Afaya, A. Kusi-Amponsah, J.M. Ajusiyine and T. Abdul Hamid, 2020. Medication adherence and self-care behaviours among patients with type 2 diabetes mellitus in Ghana. PLoS ONE, 15.
- Chetty, R.R. and S. Pillay, 2022. The relationship between age and glycaemic control in patients living with diabetes mellitus in the context of HIV infection: A scoping review. J. Endocrinol. Metab. Diabetes South Africa, 27: 1-7.
- Ayonote, U.A., A.N. Ogbonna and O.M. Akujuobi, 2022. Glycemic control and its associated factors among elderly diabetic patients in a tertiary hospital in Lagos, Nigeria. Curr. Res. Diabetes Obesity J., 16.
- Shameena, A.U., S. Badiger and K.S. Nanjesh, 2017. Medication adherence and health belief model among hypertensive patients attending rural health centres of a tertiary care hospital in South India. Int. J. Community Med. Public Health, 4: 1159-1165.
- Forouhi, N.G., A. Misra, V. Mohan, R. Taylor and W. Yancy, 2018. Dietary and nutritional approaches for prevention and management of type 2 diabetes. BMJ, 361.
- Zhang, Y., X.F. Pan, J. Chen, L. Xia and A. Cao et al., 2020. Combined lifestyle factors and risk of incident type 2 diabetes and prognosis among individuals with type 2 diabetes: A systematic review and meta-analysis of prospective cohort studies. Diabetologia, 63: 21-33.
- Okuyama, H., P.H. Langsjoen, N. Ohara, Y. Hashimoto and T. Hamazaki et al., 2016. Medicines and vegetable oils as hidden causes of cardiovascular disease and diabetes. Pharmacology, 98: 134-170.
- Lovejoy, J.C., 1999. Dietary fatty acids and insulin resistance. Curr. Atherosclerosis Rep., 1: 215-220.
- Soliman, G.A., 2019. Dietary fiber, atherosclerosis, and cardiovascular disease. Nutrients, 11.
- Lisa, B., R. Bernard, W.W. Willett and F.M. Sacks, 1999. Cholesterol-lowering effects of dietary fiber: A meta-analysis. Am. J. Clin. Nutr., 69: 30-42.
- Man, Y.B.C., T. Haryati, H.M. Ghazali and B.A. Asbi, 1999. Composition and thermal profile of crude palm oil and its products. J. Am. Oil Chem. Soc., 76: 237-242.
- Marina, A.M., Y.B.C. Man, S.A.H. Nazimah and I. Amin, 2009. Chemical properties of virgin coconut oil. J. Am. Oil Chem. Soc., 86: 301-307.
- Amarasiri, W.A.D.L., 2006. Coconut fats. Ceylon Med. J., 51: 47-51.
- Randle, P.J., P.B. Garland, C.N. Hales and E.A. Newsholme, 1963. The glucose fatty-acid cycle its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet, 281: 785-789.
- Randle, P.J., 1998. Regulatory interactions between lipids and carbohydrates: The glucose fatty acid cycle after 35 years. Diabetes/Metab. Rev., 14: 263-283.
- Valensi, P. and S. Picard, 2011. Lipids, lipid-lowering therapy and diabetes complications. Diabetes Metab., 37: 15-24.
- Artha, I.M.J.R., A. Bhargah, N.K. Dharmawan, U.W. Pande and K.A. Triyana et al., 2019. 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 Manage., 15: 149-157.
- Khadke, S., S. Harke, A. Ghadge, O. Kulkarni and S. Bhalerao et al., 2016. Association of fasting plasma glucose and serum lipids in type 2 diabetics. Indian J. Pharm. Sci., 77: 630-634.
- Praharaj, A.B., R.K. Goenka, S. Dixit, M.K. Gupta, S.K. Kar and S. Negi, 2017. Lacto-vegetarian diet and correlation of fasting blood sugar with lipids in population practicing sedentary lifestyle. Ecol. Food Nutr., 56: 351-363.
- Kitzmann, M., L. Lantier, S. Hébrard, J. Mercier, M. Foretz and C. Aguer, 2011. Abnormal metabolism flexibility in response to high palmitate concentrations in myotubes derived from obese type 2 diabetic patients. Biochim. Biophys. Acta Mol. Basis Dis., 1812: 423-430.
How to Cite this paper?
APA-7 Style
Berkoh,
D.A., Donkoh,
E.T., Asamoah,
A., Sakibu,
R.A., Ngala,
R.A. (2024). Effect of Tropical Vegetable Oil Consumption on Lipid Profile and Glycaemic Control in Type 2 Diabetics. Trends in Medical Research, 19(1), 247-284. https://doi.org/10.3923/tmr.2024.274.284
ACS Style
Berkoh,
D.A.; Donkoh,
E.T.; Asamoah,
A.; Sakibu,
R.A.; Ngala,
R.A. Effect of Tropical Vegetable Oil Consumption on Lipid Profile and Glycaemic Control in Type 2 Diabetics. Trends Med. Res 2024, 19, 247-284. https://doi.org/10.3923/tmr.2024.274.284
AMA Style
Berkoh
DA, Donkoh
ET, Asamoah
A, Sakibu
RA, Ngala
RA. Effect of Tropical Vegetable Oil Consumption on Lipid Profile and Glycaemic Control in Type 2 Diabetics. Trends in Medical Research. 2024; 19(1): 247-284. https://doi.org/10.3923/tmr.2024.274.284
Chicago/Turabian Style
Berkoh, Dorice, Akosua, Emmanuel Timmy Donkoh, Akwasi Asamoah, Raji Abdul Sakibu, and Robert Amadu Ngala.
2024. "Effect of Tropical Vegetable Oil Consumption on Lipid Profile and Glycaemic Control in Type 2 Diabetics" Trends in Medical Research 19, no. 1: 247-284. https://doi.org/10.3923/tmr.2024.274.284
This work is licensed under a Creative Commons Attribution 4.0 International License.