Journal of Nutrition Science Research
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
  • Prospective   
  • J Nutr Sci Res 2022, Vol 7(3): 169
  • DOI: 10.4172/snt.1000169

Metabolic Effect of Orthodox Fasting Dietary Pattern in Type 2 Diabetic Patients

Alemayehu Michael*
Hawassa University, College of Natural and Computational Science, Hawassa, Sidama regional State, Ethiopia
*Corresponding Author: Alemayehu Michael, Hawassa University, College of Natural and Computational Science, Hawassa, Sidama regional State, Ethiopia, Email: alemayehumichael1@yahoo.com

Received: 15-May-2022 / Manuscript No. snt-22-64855 / Editor assigned: 17-May-2022 / PreQC No. snt-22-64855(PQ) / Reviewed: 01-Jun-2022 / QC No. snt-22-64855 / Revised: 04-Jun-2022 / Manuscript No. snt-22-64855(R) / Published Date: 11-Jun-2022 DOI: 10.4172/snt.1000169

Abstract

Background: Lenten fasting is commonly practiced by Ethiopian Orthodox Christian with energy restriction and only vegan diets as ritual activities. In addition to religious benefits, protective role of Lenten fasting on some noncommunicable diseases, cardio-metabolic and serum biochemicals have not been well explored.

Methods: A prospective longitudinal study design was conducted from February 27 to April 30, 2019 among n=52(n=27 fasting group and n=25 non-fasting group) T2DM patients. Structured questionnaire was used to collect all relevant data. The study followed at two time points: at baseline (week 0) and at the end (last week of fasting). Body fat composition determined by Bio-electric impedance analyzer (Tanita® BC-418®, Japan), while serum biochemicals analyzed by random access chemistry analyzer (A25™ Biosystem, Spain). Epidata version 3.4 and SPSS 23 were used for data entry and statistical analysis.

Results: Calorie restriction with vegan diets significantly drops systolic blood pressure (SBP), body fat mass and lean mass among fasters compared to controls (p<0.01). Body fat percentage decreased (p=0.025) significantly among fasters compared to non-fasters. Serum levels of total cholesterol, LDL-cholesterol, non-HDL-cholesterol, total cholesterol/HDL-cholesterol, triglycerides, fasting blood sugar and uric acid also significantly decreased in fasting group than non-fasting (p<0.01). While BMI, diastolic blood pressure, HDL-c, hip and waist circumference insignificantly differed among fasting group compared to non-fasting. Moreover, fasting led to a decreased cardiovascular risks among fasters like SBP ≥130mmHg (26.9%), DBP ≥85mmHg (3.8%), TC ≥200 mg/dL (38.5%) and TC/HDL-c (7.7%) when compared to baseline.

Conclusion: Simultaneous energy restriction (ER) and vegan dietary (VD) pattern during Lenten fasting improved lipid profiles, glycemic control and blood pressure among T2DM patients. This may reflect ER+VD become non-pharmacological option to protect/avert risks of established cardiometabolic risks and morbidity.

Keywords

Lenten fasting; Body composition; Serum biochemical; Blood pressure

Introduction

Currently, in developing countries, rapid shift of healthy traditional eating pattern to excessive energy intake, manifested by increasing consumption of calorie-dense foods containing refined carbohydrates, fats, red meats, and low fiber that worthy increased incidence of obesity, chronic diseases including type 2 diabetes mellitus (T2DM) and the metabolic syndrome (MetS) [1, 2].

In past, to overcome ill effect of energy imbalance, different mechanisms were implemented. For example, long-term interdisciplinary therapy such as decreasing the intake of calories, carbohydrates and fats suggested positively change in body composition and reduced anthropometric measurements [3]. In other hand, continuous eight day fasting on non-obese healthy adults by limiting energy and using 2L water showed significant increase in total serum cholesterol and LDL cholesterol. But no change was observed (did not affect) serum concentrations of triacylglycerol and HDL cholesterol in fasting group [4]. In contrary, in randomly controlled explorative study of medically treated patients with oral hypoglycemic agents and/ or insulin of T2DM for 7-day fasting program followed by dietary advice or to usual care and only dietary advice. The results suggested decrease in mean body weight and systolic/diastolic blood pressure while glycated hemoglobin (HbA1c), insulin and homeostatic model assessment (HOMA) index showed no significant improvements. This fasting were well accepted, there were no serious adverse events [5].

Recently, energy restriction and/or intermittent fasting become more popular strategies to alleviate/reduces non-communicable diseases and cardio-vascular problems. For example, in experimental research of calorie restriction by means of intermittent fasting in different form reduces incidence of age-associated chronic diseases such as cardiovascular diseases, cancer, kidney disease and diabetes mellitus as well as prolonged lifespan [6, 7].

Likewise, reduced energy intake were practiced in many religious groups by incorporating periods of fasting into their rituals including Muslims, fast from dawn until dusk during the month of Ramadan [8]. Similarly, most Orthodox Christian communities, fasting achieved by ingesting no or minimal amounts of food and caloric beverages with caloric restriction for periods typically range from 12 hr. to 10 weeks [9, 10]. More recently, Sinaga et al., 2020, studied the metabolic effect of fasting among Ethiopian Orthodox followers in healthy subjects but this study exhibited inherent limitation of retrospective cohort studies [11]. Unfortunately, long-term evaluation of fasting practice is not available in diabetic patients.

Therefore, the present study aimed to evaluate long term effect of Ethiopian orthodox Christian fasting that combine simultaneous energy restriction and vegan diet, abstain animal source foods, intermittent fasting (Wednesday and Friday)/week, and overnight fast during Lenten on level of on body weight, body mass index (BMI), lipid profile, fasting blood sugar (FBS), blood pressure (BP) and uric acids (UA) in free living insulin resistance patients.

Problem description

Simultaneous energy restriction and vegan and/or vegetarian diet type were seen in free living people of Ethiopian Orthodox Christian fasters but little is known about its’ metabolic effects.

Available Knowledge

Recently, beneficial effect of intermittent fasting, dietary habits and caloric restrictions are well established in improving metabolic activities in health of animal model, human model as well as some extreme human fasting cases (Monks).

Rationale

Caloric restriction and/or consumption of vegan diet using different forms of intermittent fasting and some religious fasting explore health benefits. This study try to look at the beneficial effect of Lenten fasting, combine both caloric restriction and consumption of vegan diet together.

Specific aim

This study aimed to evaluate metabolic effect of Lenten fasting dietary pattern among T2DM patients.

Methods

Intervention

This prospective longitudinal study design was conducted among 52 T2DM patients in Hawassa city administration, Sidama Regional State, Southern Ethiopia from February 27/2019 to April 30/2019. Two groups are involved in the study, fasting group (case) and non-fasting (control).

Study of the Intervention and group allocation

The subjects were Orthodox Christian communities with diabetes and hypertension with age range of 30-50 years old. The subjects were permanently living in the study area with no plan of leaving before the completion of the study. In addition, those patients who have only a good adherence towards diabetes self-care practice were eligible for the study. The group allocation was done based on an Ethiopian Orthodox church fasting season and dietary pattern during Lenten fasting. Following this, 29 subjects (16 males, 13 females) with mean (± standard deviation (SD)) age of 42.31 ± 4.81years old those who have been rigorously fasting experiences for mean of 19 ± 15 years, and aiming to continue to fast and adopt to use simultaneously vegan diet and energy restriction during study period were included in the study group (fasters). Whereas 27 subjects (15 males, 12 females) with mean (±SD) age of 41.27 ± 4.34 years old, those who have stopped fasting (fasted for 17 ± 10 years) before one of study period and those not willing to continue fasting during study period were included in the control group (non-fasters). However, pregnant mothers or lactating mothers, participants on lipid lowering therapy or antiretroviral treatments, patients having chronic liver disease and or renal disease were excluded in figure 1.

journal-nutrition-science-figure

Figure 1:

journal-nutrition-science-figure2

Figure 2:

Measures

Two measurements were taken from the study subjects for each parameter, which means before fasting, at baseline (week 0) and end of fasting (last week of fasting). Structured questionnaires were used to collect socio-demographic, anthropometric, clinical and other pertinent information. Following this, measurements of blood pressure [12], height and weight, hip and waist circumference of the study subjects was done by trained clinical nurses. A digital electronic sphygmomanometer (Omron, Healthcare, Japan) was used to measure blood pressure after patients rested and completely stabilized for at least 5 min in the assessment room [12]. Two readings of BP was taken within 2-3 min differences to maintain the accuracy of measurement and lastly the mean value was taken and documented to assess BP status. In addition, the third BP measurement was taken, when the two measurements varied by 10 mmHg within 2-3 min differences in a single study subject, and lastly the mean value of three measurements was taken to determine BP status.

Body weight, height waist and hip circumference were assessed based on world health organization (WHO) stepwise techniques was applied to collect data [13]. Weight and height was measured when patients stood wearing light cloths and wearing no shoes. A digital electronic Adult scale (ASTO) that contain both weight scale and height scale was used to measure body weight to the nearest 0.1kilogram(kg), and height to the nearest 0.1 centimeter (cm). Moreover, body mass index (BMI) was calculated as weight in kilogram divided by squared height in meter.

Hip circumference (HC) was measured at the level of the above trochanter with stretching resistant tape. While waist circumference (WC) was measured at the navel using a non-stretching type of tape (to the nearest 0.1 cm) when participants stood in upright position after the end of a usual exhalation [14].

Body composition of the subjects was measured using bio-electric impedance analyzer (Model Tanita® BC-418®, Tokyo, Japan) with a range of 0-200 kg and with an accuracy of within 100 g. Measurements were taken between meals among well-hydrated subjects, without shoes and clothing (except underwear), that is, proper time gap should be there between measurement/analysis and meal.

Blood specimen collection and laboratory diagnosis

About 4-5 milliliter of venous blood for prospective determination of serum biochemicals was collected at baseline (before start of fasting) and at last of week of fasting (fasting end time) from each study participant after 12 hours overnight fasting in the morning (from 9:00 to 9:30AM) using serum separator tube (SST). Then, the collected blood sample was allowed to form proper clot within 20-25 min at room temperature. Following this, the samples were centrifuged at 2500-3000 rotation per minute (rpm) to separate serum from clot. Moreover, the serum specimen of each participant was analyzed to determine total cholesterol (TC), high density lipoprotein cholesterol (HDL-c), low density lipoprotein cholesterol (LDL-c), triglycerides (TGs), fasting blood sugar (FBS) and uric acid (UA) using A25™ Biosystem random chemistry analyzer (BioSystems™, Barcelona, Spain).

Finally, enzymatic colorimetric assay technique was applied for UA (Uricase-Peroxidase method), FBS by glucose-oxidase method (GOD-PAP), TC (CHODPAP method) and triglyceride (GPO-PAP method). Whereas HDL-c and LDL-c were determined by the direct homogeneous enzymatic colorimetric assay approach. All biochemicals assay reagents were from Linear manufacturers (Linear chemicals, Montgat, Spain).

Operational definitions

Fasting and abstinence in the Ethiopian Orthodox Tewahedo Church

There are 250 fasting days through the year in Ethiopian Orthodox Christian church. Of these, 180 days are considered as obligatory and the others only for the clergy. The Lenten fasting, known as Abiy Tsom/ Hudade in Amharic or great fasting, is the longest continuous fasting period, lasting 55 days. The consumption of meat, milk products, or eggs are not allowed during these days. Ethiopian cuisine contains many dishes that can be considered vegan diet such as split peas and lentils or vegetables such as potatoes, carrots and chard are common in fasting dishes. Sauce, made from ground chickpeas, is also particularly popular as a fasting food [15].

Dyslipidemia: It was defined according to the United States National Cholesterol Education Program, Adult Treatment Panel (NCEP-ATP) III guideline, which describes as TC ≥ 200 mg/dl, HDL-c < 40 mg/dl, LDL-c ≥ 130 mg/dl, TG ≥ 150 mg/dl and TC/HDL-c ratio ≥ 5 [16].

Glycemic control for diabetes patients: Based on the American Diabetic Association (ADA) 2017 guideline recommendation, good glycemic control is defined as those diabetes patient whose fasting blood glucose level is in between 80-130 mg/dL while those patients who have fasting blood glucose of > 130 mg/dL categorized under poor glycemic control [17].

Hypertension: defined as either having a systolic blood pressure (SBP) ≥ 140 mmHg and/or a diastolic blood pressure (DBP) ≥90 mmHg and/or self-report of earlier diagnosis of hypertension by a health professionals and/or if presently receiving anti-hypertensive agents.

Outcome measurement

The study outcome of anthropometric, body composition and cardiovascular parameters like BMI, WC, HC, fat percent and fat mass, fat free mass, SBP and DBP were assessed between week 0 (baseline) and last of week of fasting (end time) of fasting. For each study subject at each specific study time was calculated as value at last week minus value at baseline divided by concentration at baseline multiplied by 100 [18]. In addition, the study outcome of TC, UA, FBS, and HDL-c, LDL-c, non-HDL-c, TC: HDL-c ratio, and TGs between baseline of fasting and last week of fasting (fasting end time) were assessed in similar manner. For each patient, we calculated percent change as concentration at last week of fasting minus concentration at baseline divided by concentration at baseline, multiplied by 100.

Data quality issue

Data collection tool was evaluated by pretesting of 20% questionnaires before collecting actual data and all vital amendment was done following a pretest result feedback. Data collection was done by trained clinical nurses; while blood sample collection and laboratory analysis was managed by laboratory technologists. In addition, at the initial day of contact, patients have got detailed information about the study and its protocol. In the study baseline and end time, blood samples were drawn from those who come only with overnight fasting. Standard operating procedure was strictly followed from patient preparation to result releasing, while the accuracy and precision of laboratory determination, instrument condition and technical performance were maintained by running commercially prepared quality control samples (controls with known target value) before actual samples and along with actual samples.

Data processing and statistical analysis

All data were visually checked for consistency and its completeness, coded and entered into Epidata version 3.4. Statistical Package for Social Sciences (SPSS) version 23.0 software was used statistically for data analysis. Normality of the continuous data distribution was checked using Shapiro-Wilk test. Descriptive statistics like frequency and percentages were also used to describe dependent variable in relation to different categorical data, while mean (percent increase) and SD or standard error was used for continuous data. In addition, estimate of variances in means of study groups was assessed using student’s t-test at 95% confidence interval (CI) level and finally a p-values< 0.05 was considered for statistical significance.

Ethical approval and consent to participate

The protocol and the questionnaires were reviewed and cleared by the institution review board of Natural and Computational Science of Addis Ababa University, Ethiopia (IRB/035/2018). The nature of the study was fully explained to the study participant and written consent was obtained from each participant prior to conducting the study. All studies on humans defined in the current study were conducted with the endorsement of the accountable ethics committee and in agreement with national law and the Helsinki Declaration of 1975 (in its recent, revised form).

Results

General characteristics of study participants

Of the 57 previously diagnosed known diabetes + hypertensive (29 fasting and 28 non-fasting group) patients were enrolled in the study; however, 5 participants (2 from fasting and 3 from non-fasting group) were lost to follow-up. Therefore data of these 5 patients were not considered in this statistical analysis. A total number of 52[28(53.8%) males and 24(46.2%) females] were participated in the study and completed study follow-up. The mean age of the study subjects was 41.8 ± 4.6 with the age range of 32 to 50 years. Regarding marital status, 63.5% (n=33), 11.5% (n=6), 21.2% (n =11) and 3.8% (n=2) of the study participants were married, unmarried, separated and widowed respectively. Majority, 90.4% (n=47) and 78.8% (n=41) study participants were educationally greater than or equal to college levels and government employed respectively. The physical activity status of about 40.4% (n =21), 21.2% (n=11), and 38.5% (n=20) study participants were identified as having sedentary, less physically active and moderate to intensive physical activity performance respectively. The mean monthly income of the study participants was 4966.7 ± 1417.8 with the range of 3200 to 9000 of Ethiopian Birr. Regarding behavioral characteristics, none of study participants drank alcohol, chewing chat and smoke cigarette.

Baseline characteristics of the study participants

From a total of 52 patients with type 2 diabetes and hypertension (27 were fasting group and rest 25 were non-fasting group). The mean age of fasting group was 42.31 ± 4.81, while the mean age of non-fasting group was 41.27 ± 4.34 (p >0.05). Anthropometric parameters such as BMI, WC and HC and body composition such as fat percent, fat mass and fat free mass were done for 52 participants and they did not show a significant difference between the study groups (p>0.05). Diastolic blood pressure also did not show a significant difference between fasting and non-fasting group, while systolic blood pressure and TC/HDL-c ratio were significantly higher in fasting group when compared to non-fasting group (144.1±14.1 vs. 131.8±13, p= 0.001), and (6.1±1.6 vs. 5.1± 1.7, p=0.003) respectively. In addition, lipid profiles (TC, HDL-c, LDL-c, TG, and non-HDL-c) and other serum biochemicals like FBS and UA also were insignificantly differ at baseline between groups (Table 1).

Variables Study groups Mean(±SD) t statistics p-value
WC Non-fasting 83.5(10.93) -0.251 0.803
Fasting 84.1 (5.18)
Non-fasting
BMI Fasting 25.8(2.38) -0.528 0.6
Non-fasting 26.1(1.89)
HC Fasting 96.1(11.45) 0.647 0.52
Non-fasting 94.5(5.55)
Fat percent Fasting 32.3(5.82) 1.104 0.275
Non-fasting 30.6(5.13)
Fat mass Fasting 23.1(4.49) -0.866 0.391
Non-fasting 24.1(3.87)
FFM Fasting 46.2(3.61) 1.367 0.178
Non-fasting 44.1(6.84)
SBP Fasting 131.8(12.97) -3.669 0.001
Non-fasting 144.1(11.15)
DBP Fasting 79.7(10.32) -1.176 0.245
Non-fasting 82.8(8.19)
FBS Fasting 153.1(56.27) -1.471 0.147
Non-fasting 172.6(37.02)
TG Fasting 399.2(97.40) 0.27 0.788
Non-fasting 392.7(73.50)
TC Fasting 179.92(39.347) -1.329 0.19
Non-fasting 192.19(25.94)
LDL Fasting 90.62(15.74) 0.34 0.191
Non-fasting 89.30(11.84)
HDL Fasting 38.12(9.73) 1.843 0.071
Non-fasting 33.46(8.42)
UA Fasting 5.93(1.99) -0.069 0.945
Non-fasting 5.97(1.60)
Non-HDL-c Fasting 141.8(39.5) -1.8 0.08
Non-fasting 158.7(28.1)
TC/HDL-c Fasting 5.1(1.7) -2.2 0.03
6.1(1.6)
BMI, body mass index; WC, circumference; HC, hip circumference; SBP, systolic blood pressure; DBP, diastolic blood pressure; FBS, fasting blood sugar; TG:,  triglyceride; TC, total cholesterol; LDL, low density lipoprotein; HDL, high density lipoprotein; UA, uric acid.

Table-1: Baseline characteristics of anthropometric, cardiovascular and biochemical parameters among the study participants

Changes in Anthropometric parameters, blood pressure and body composition

All changes within the treatment groups on body composition levels were statistically significant at last week of fasting except anthropometric parameters like BMI, WC and HC. There was no statistically a significant change observed in WC in the fasting group (0.0%) when compared to non-fasting group (1.2%), (95% CI: -3.3 to 0.89), p = 0.25). In contrast, the decrease of fat percentage was 3.0% (95% CI: -0.4 to -5.7) and larger in the non-fasting group (6.67%) than in the fasting group (3.6%). This change was statistically significant (p = 0.025). The decrease in fat mass was higher in the fasting group (6.7%) than in the non-fasting group (3.3%), and this difference (3.4%; 95% CI: 5.0 to 1.7) was statistically significant (p < 0.0001) (Table 2).

Variables  Fasting group (n=27) Non fasting (n=25) Difference (95% CI) p-value
Baseline Last Week % increase Baseline Last Week % increase (Fasting-Non fasting) for difference
  Mean ±SD Mean ±SD Mean ±SE Mean ±SD Mean ±SD Mean ±SE    
BMI (Kg/M2) 26.1(1.89) 25.93(1.81) -.86(1.47) 25.8(2.38) 25.72(2.49) -.51(2.21) -0.34(-1.4 to 0.7) 0.513
WC (cm) 84.1 (5.18) 84.15(5.18) .00(.00) 83.5(10.93) 84.52(11.36) 1.21(5.32) -1.2(-3.3 to 0.89) 0.252
HC (cm) 94.5(5.55) 94.50(5.55) .00(.00) 96.1(11.45) 96.09(11.45) -.02(.10) 0.02(-0.02 to 0.06) 0.322
Fat% 30.6(5.13) 31.77(5.37) 3.64(2.01) 32.3(5.82) 34.47(6.29) 6.67(6.37) -3.0(-0.4 to -5.7) 0.025
Fat mass 24.1(3.87) 25.65(4.03) 6.72(2.74) 23.1(4.49) 23.79(4.55) 3.32(3.18) -3.4 (5.0 to 1.7) <0.0001
FFM 44.1(6.84) 41.91(6.68) -5.10(2.35) 46.2(3.61) 45.63(3.81) -1.31(2.29) -3.8(-2.5 to -5.1) <0.0001
BMI, body mass index; cm, centimeter; CI, confidence interval; SD, standard deviation  Kg, kilogram; M, meter; HC, hip circumference; Fat%, fat percent; FFM, fat free mass; WC, waist circumference

Table-2: Anthropometric and body composition parameters at baseline and last week of fasting and their mean percentage change

The change of SBP was 14.5% (95% CI: -11.7 to-17.2) and it was decreased 7.3% in the fasting group and increased 7.18% in the nonfasting group. This difference was statistically significant (p < 0.0001). In contrast, the DBP was decreased 0.63% in the non-fasting group but it increased 2.69% in the fasting group, this difference was not statistically significant (3.3%; 95% CI:-2.0 to 8.6; p= 0.216) (Table 3).

  Fasting group (n=27) Non fasting (n=25) Difference (95% CI) p-value
Variables Baseline Last Week % increase Baseline Last Week % increase (Fasting-Non fasting) for difference
  Mean ±SD Mean ±SD Mean ±SE Mean ±SD Mean ±SD Mean ±SE    
SBP (mmHg) 144.1(11.15) 133.19(6.64) -7.29(5.52) 131.8(12.97) 141.19(13.56) 7.18(4.40) -14.5(-11.7 to -17.2) <0.0001
DBP(mmHg) 82.8(8.19) 84.23(3.67) 2.69(11.04) 79.7(10.32) 79.11(11.26) -.63(7.83) 3.3(-2.0 to 8.6) 0.216
DBP, diastolic blood pressure; CI, confidence interval; mmHg, millimeter of mercury; SBP, systolic blood pressure; SD, standard deviation

Table-3: Blood pressure at Baseline and last week and their mean percentage change

Changes in lipids profiles and other serum biochemicals

Except HDL-c concentration, all changes within the study groups such as lipid profile, fasting blood glucose, uric acid as well as TC: HDL-c ratio were statistically significant at last week of fasting, The change of TC was 15.1% (95%: -19.2 to -11.1) at last week of fasting and decreased 10.16% in the fasting group but increased 4.97% in the nonfasting group, the difference was statistically significant (p<0.0001).

TC: HDL-c ratio was decreased 18.2% in the fasting group but it increased 1.9% in the non-fasting group (p<0.0001). The decrease of TGs was 36.9% (95% CI: -13.6 to -60.2) and lesser in the fasting group (82.59%) than in the non-fasting group (119.5%). This difference was statistically significant (p<0.0001). Moreover a significant decrease in FBS and UA was observed in the fasting group when compared to nonfasting group (p <0.001 for both parameters) (Table 4).

  Fasting group (n=27) Non fasting (n=25) Difference (95% CI) p-value
(Fasting-Non fasting)
Parameter Baseline Last Week % increase Baseline Last Week % increase for difference
  Mean ±SD Mean ±SD Mean ±SE Mean ±SD Mean ±SD Mean ±SE    
FBS (mg/dL) 172.6(37.02) 148.08(21.06) -12.79(8.24) 153.1(56.27) 170.00(49.42) 18.33(31.74) -31.1(-18.2 to -44) <0.0001
TG (mg/dL) 392.7(73.50) 347.45(57.63) -82.58(29.86) 399.2(97.40) 388.76(95.62) 119.48(51.0) -36.9(-13.6 to -60.2) <0.0001
TC (mg/dL) 192.19(25.9) 172.31(27.14) -10.16(9.65) 179.92(39.35) 188.35(39.31) 4.97(3.54) -15.1(-11.1 to -19.2 ) <0.0001
LDL-c (mg/dL) 89.30(11.8) 83.91(14.39) -6.25(7.81) 90.62(15.74) 91.31(17.94) .75(8.28) -7.0(-11.5 to -2.5) 0.003
HDL-c (mg/dL) 33.46(8.42) 35.86(8.50) 7.78(9.55) 38.12(9.73) 39.41(9.99) 3.85(9.28) 3.9(-1.3 to 9.2) 0.138
UA (mg/dL) 5.97(1.60) 4.48(1.04) -22.60(15.61) 5.93(1.99) 5.71(1.89) 6.72(49.03) -29.3(-9.1 to -49.6) 0.005
Non-HDL-c (mg/dL) 158.7(28.1) 136.4(28.3) -13.9(2.3) 141.8(39.4) 148.9(38.2) 5.8(1.1) -19.7(-14.6 to -24.8) <0.0001
TC/HDL-c ratio 6.1(1.6) 5.0(1.3) -16.4(1.8) 5.1(1.7) 5.1(1.6) 1.9(1.9) -18.2(-13 to -23.4) <0.0001
FBS, fasting blood sugar; TG, triglyceride; TC, total cholesterol; LDL-c, low density lipoprotein cholesterol; HDL-c, high density lipoprotein cholesterol; UA, uric acid

Table 4: Serum biochemical tests at baseline and last week and mean percentage change of the study participants

In contrast, the increase in HDL-c was higher in the fasting group (7.78%) when compared to the non-fasting group (3.85%), but the difference was not statistically significant (3.9%; 95% CI: -1.3 to 9.2, p=0.138). Some abnormal parameters showed decreasing pattern at last week of fasting when compared to baseline value like SBP (from 100 to 73.1%), FBS (from 96.1 to 76.9%), TC (from 53.8 to 15.4%) and TC/HDL-c ratio (from 65.4 to 57.7%). Other lipid profile such as TG and LDL-c and HDL-c did not show any change at last week of fasting in comparison with baseline abnormality according to NCEP ATP III

Discussion

The fasters abstain from the consumption of animal source foods but they experienced by energy restriction with only utilization of vegan diets for 10 weeks prolonged time according to Ethiopian Orthodox Church ritual practice. During this period participants consume only plant origin diets such as whole grains, cereals, green leafy vegetables, legumes, peas, beans, fruits [19].

This study compared the changes on anthropometric, blood pressure, body composition and biochemical parameters of diabetic fasters (study group) with diabetic non-fasters (controls) for about 10 weeks. Both groups were similar with age, sex distribution and geographical location. We found out that abstinence of meat, dairy products and eggs for 10 weeks in the Lent period was significantly associated with lower mean of SBP, fat percentage, fat mass, and fat free mass among fasters when compared to non-fasters.

In addition, we observed significantly lower in mean change of FBS, TGs, TC, LDL-c, UA, non-HDL-c and TC/HDL-c ratio) in the fasters when compared to non-fasters. But insignificantly increased HDL-c value was seen among fasters than non-fasters. Moreover, fasting led to highly decreased abnormal values like SBP≥130mmHg, FBS >130mg/dL, and TC≥200 mg/dL at least 19% in each parameters the fasters at last week of fasting, while fasting did not show any change on TG≥150 mg/dL and HDL-c<40mg/dL. Our finding in line with higher compliance and promise strategies of intermittent fasting in the improvement of metabolic risk factors, body composition, and weight loss in obese and diabetic patients [20-22].

We noticed that Ethiopian orthodox Christian Lenten fasting showed insignificant change on anthropometric parameters such as BMI, HC and WC. Studies from Egyptian Christian Lenten fasting was consistent with our results but other two studies in Ramadan fasting have reported insignificant change [23, 24]. On the contrary, several studies reported a significant improvement on anthropometric measurements (body weight, BMI, WC and HC) and a significant decrease in body weight and BMI following Lenten fasting [25-27].

Fasting led to a significant decrease of mean body fat percent among fasters compared to non-fasters. The finding is in line with the studies conducted in a different place [28, 29].

Our study noted that Lenten fasting for 10 weeks is associated with a significantly lower SBP levels when compared to non-fasters. The finding is comparable with the studies conducted in elsewhere [26, 30, 31]. The consumption of vegan diet [32], intake of high-fiber, low-fat, low-protein and vegan diet effect and or consumption of vegetables that augmented with fibers and potassium content might be a plausible reason for the decreasing effect of blood pressure among fasters [32, 33].

A significant low mean change of FBS, TGs, TC, LDL-c, TC/ HDL-c ratio and non-HDL-c were seen in the fasters when compared to non-fasters after 10 weeks of vegan diet consumption. Comparably different international studies reported that vegan diet significantly decreased the described serum biochemical profile [7, 34-38]. Similarly, the consumption of vegetables particularly in Lenten could have a good opportunity to consume increased amount of fiber containing vegetables when compared to non-fasters and this might have a chance to improve lipid profiles among fasters [39]. However, the study conducted in Addis Ababa, Ethiopia indicates insignificant increasing of TGs after 7 weeks of fasting [30]. This is not in line with the finding of present study, which indicates a significant decrease of mean TG after 10 weeks of fasting. The difference in sample size between the studies and individuals’ trend in the consumption of varieties of vegan diet might be a possible reasons for the variation, that is why some studies have pointed out an association between raised TGs level and an intake of a vegetarian diet [40].

Similarly, our results is agreed with study of intermittent fasting in adults on lipid profile for about six weeks ∼12 h during day time, three times per week indicated larger reduction in body weight, BMI and waist circumference in intermittently fasting group than control. Lipid profiles such as total cholesterol, triglycerides, LDL-c were significantly decreased while HDL-c significantly increased [41]. These beneficial effects are due in part of shifting from the utilization of glucose to fatty acids and ketones as the body’s preferred source of fuel during fasting. During this transition/reprogramming in the body, switches from the synthesis and storage of lipids to mobilization of fat in the form of ketone that highlighted as a potential mechanism for many of the beneficial effects of intermittent fasting. [20]. Fasting in free living Ethiopian Orthodox may follow the same mechanisms of metabolism as intermittent fasting.

Even, our finding in line with different studies during Ramadan fasting. It is resulted by significantly decreased in blood lipid profile such as increase of HDL-c while decrease in total cholesterol, LDL-c and blood glucose after fasting among normal healthy individuals and diabetic patients [42-44]. Also, after Ramadan it is noted significant decrease in blood glucose level, triglycerides, cholesterol and creatinine in diabetic patients [44,45]. Controversially, no significant effect on fasting/postprandial glucose levels and blood lipid levels was observed in insulin resistance [46].

We noted that fasting led to highly decreased cardiovascular/ metabolic risks like SBP≥130mmHg, TC≥200 mg/dL and TC/HDL-c among fasters after week 10 when compared to baseline value. Our study is supported by several studies that revealed fasting is the utmost reasonable intervention that limits cardiovascular diseases and other risks of cardiovascular diseases [47, 48]. Besides, one reports from Ramadan fasting indicated a significant improvement in10 year’s coronary heart disease risk (according to Framingham risk score) as well as other cardiovascular risk factors [27]. Further, consuming diets especially plant source during religious fasting as well as in our daily life play an important role to avert risks of cardiovascular diseases [30].

In general, even though it may be difficult to convince patients to give up or severely restrict calories for an entire 24 h period fasting like Ethiopian orthodox Christian was good practice for T2DM patients to reduce risk of chronic diseases. As patients become more comfortable with overnight fasting, energy restriction and vegan diet eating pattern and abstinence of animal source foods, the feeding window can be restricted further to16 h fast followed by an 8 h feed by checking nutrient balance.

Limitations

The principal limitation of this study was small sample size, which focus only on fasting dietary pattern and we did not comprise the nondiabetic population as a comparative group. Furthermore, it is also true that the hydration status of the participants could have modified the results of the body fat% measured with bioelectrical impedance analysis which is not tightly followed. Since, most BIA prediction equations assume that the fat mass and fat-free mass consist of 73% water [49]. Irrespective of the described limits, this study adds supportive information in the limited data condition of Ethiopia.

Conclusion

In conclusion, energy restriction with vegan dietary pattern in the Lenten fasting significantly improved TC, LDL-c, TG, Non-HDL-c, FBS, SBP, UA and some body composition variables in patients with type 2 diabetes mellitus. The findings of this study suggested that Ethiopian Lenten fasting may be beneficial to improve CVD and metabolic syndrome (MetS) risk factors. There is also a need for large and well-designed randomized control trials to identify clinical characteristics and to assess more imperative clinical outcomes in order to prevent and or limit adverse effects in people living with type 2 diabetes mellitus.

Abbreviations

BMI, body mass index; CI, confidence interval; DM, diabetes mellitus; FBS, fasting blood sugar; HDL-c, HDL-cholesterol; LDL-c, LDL-cholesterol; TC, total cholesterol; HP, hip circumference; SD, standard deviation; WC, waist circumference; TG, triglycerides; SPSS, Statistical package for social sciences; UA, uric acid

Acknowledgement

We want to acknowledge Mr. Endale Work who was working in the Hawassa University, Comprehensive Specialized Hospital clinical chemistry laboratory for his support during serum biochemicals analysis. In addition, our gratefulness is also extended to our study participants (diabetic patients) for their keenly participation in the study.

Authors’ contributions

All authors were involved in the study. AM and KB designed the research; AM performed the research; AM and KB analyzed data and prepared the manuscript including critical appraisal. All authors read and approved final version of the manuscript.

Funding

This study was financially supported by Addis Ababa University

Availability of data and materials

The dataset of this article is not openly accessible, but it can be available on reasonable request from the corresponding author.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interest with respect to the research, authorship, and/or publication of this article.

References

  1. Misra A, Singhal N, Khurana L (2010) Obesity, the metabolic syndrome, and type 2 diabetes in developing countries: role of dietary fats and oils. J Am Coll Nutr 29: 289-301
  2. Indexed at, Google Scholar, Crossref

  3. Roche HM (2005) Fatty acids and the metabolic syndrome. Proc Nutr Soc 64: 23-29
  4. Indexed at, Google Scholar, Crossref

  5. Poli, VFS, Sanches RB, Moraes ADS, Fidalgo JPN, Nascimento MA, et al. (2017) The excessive caloric intake and micronutrient deficiencies related to obesity after a long-term interdisciplinary therapy. Nutrition 38: 113-119
  6. Indexed at, Google Scholar, Crossref

  7. Sävendahl L, Underwood LE (1999) Fasting increases serum total cholesterol, LDL cholesterol and apolipoprotein B in healthy, nonobese humans. J Nutr 129: 2005-2008
  8. Indexed at, Google Scholar, Crossref

  9. Li C, Sadraie B, Steckhan N, Kessler C, Stange R, et al. (2017) Effects of a one-week fasting therapy in patients with type-2 diabetes mellitus and metabolic syndrome–A randomized controlled explorative study. Exp Clin Endocrinol Diabetes 125: 618-624
  10. Indexed at, Google Scholar, Crossref

  11. Patterson RE, Laughlin GA, Sears DD, LaCroix AZ, Marinac C, et al. (2015) Intermittent fasting and human metabolic health. J Acad Nutr Diet 115: 1203-1212
  12. Indexed at, Google Scholar, Crossref

  13. Longo VD, Mattson MP (2014) Fasting: molecular mechanisms and clinical applications. Cell Metab 19: 181-192
  14. Indexed at, Google Scholar, Crossref

  15. Aksungar FB, Eren A, Ure S, Teskin O, Ates G, (2005) Effects of intermittent fasting on serum lipid levels, coagulation status and plasma homocysteine levels. Annals of nutrition and metabolism 49: 77-82
  16. Indexed at, Google Scholar, Crossref

  17. Joanides C, Mayhew M, Mamalakis PM (2002) Investigating inter-Christian and intercultural couples associated with the Greek Orthodox Archdiocese of America: A qualitative research project. Am J Fam Ther 30: 373-383
  18. Indexed at, Google Scholar, Crossref

  19. Sarri KO, Linardakis MK, Bervanaki FN, Tzanakis NE, Kafatos AG (2004) Greek Orthodox fasting rituals: a hidden characteristic of the Mediterranean diet of Crete. Br J Nutr 92: 277-284
  20. Indexed at, Google Scholar, Crossref

  21. Sinaga M, Lindstrom D, Teshome MS, Yemane T, Tegene E, et al. (2020) Effect of Behaviour Change Communication on Metabolic Syndrome and Its Markers among Ethiopian Adults: Randomized Controlled Trial. Research Square
  22. Indexed at, Google Scholar, Crossref

  23. Ekhaise F, Omavwoya B (2008) Influence of hospital wastewater discharged from University of Benin Teaching Hospital (UBTH), Benin City on its receiving environment. Am-Eurasian j agric environ sci 4: 484-488
  24. Indexed at, Google Scholar

  25. World Health Organization, Chronic diseases and health promotion: Stepwise approach to surveillance (STEPS). Geneva, Switzerland, 2010
  26. World Health Organization, Waist circumference and waist-hip ratio: report of a WHO expert consultation, Geneva, 8-11 December 2008. 2011
  27. Zellelew TB (2014) Meat abstinence and its positive environmental effect: Examining the fasting etiquettes of the Ethiopian Orthodox Church. Critical Research on Religion 2: 134-146
  28. Indexed at, Google Scholar, Crossref

  29. Detection NCEPEPo, ToHBCi (2002) Adults, Third report of the National Cholesterol Education Program (NCEP) Expert Panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III): The Program
  30. Marathe PH, Gao HX, Close KL (2017) American Diabetes Association Standards of Medical Care in Diabetes 2017. J Diabetes 9: 320-324
  31. Indexed at, Google Scholar, Crossref

  32. Van Leth F, Phanuphak P, Stroes E, Gazzard B, Cahn P, et al. (2004) Nevirapine and efavirenz elicit different changes in lipid profiles in antiretroviral-therapy-naive patients infected with HIV-1. PLoS medicine 1: 19
  33. Indexed at, Google Scholar, Crossref

  34. Arega R (2017) Fasting in the Ethiopian orthodox church. Ethiopian orthodox Tewahedo church Sunday school department–Mahibere Kidusan why fifty-five days
  35. Google Scholar

  36. Anton SD, Moehl K, Donahoo WT, Marosi K, Lee SA, et al. (2018) Flipping the metabolic switch: understanding and applying the health benefits of fasting. Obesity 26: 254-268
  37. Indexed at, Google Scholar, Crossref

  38. Zubrzycki A, Cierpka-Kmiec K, Kmiec Z, Wronska A (2018) The role of low-calorie diets and intermittent fasting in the treatment of obesity and type-2 diabetes. J Physiol Pharmacol 69: 10.26402
  39. Indexed at, Google Scholar, Crossref

  40. Heymsfield SB, Wadden TA (2017) Mechanisms, pathophysiology, and management of obesity. J Medi 376: 254-266
  41. Indexed at, Google Scholar, Crossref

  42. Ahmed DA, El-Toony LF, Herdan OM, Abd El-All AM (2019) The effect of the Lenten fast on diabetes control in patients with type 2 diabetes mellitus. Diabetes Metab Syndr 13: 848-852
  43. Indexed at, Google Scholar, Crossref

  44. Afrasiabi A, Hassanzadeh S, Sattarivand R, Mahboob S (2003) Effects of Ramadan fasting on serum lipid profiles on 2 hyperlipidemic groups with or without diet pattern. Saudi medi J 24: 23-26
  45. Indexed at, Google Scholar

  46. Edae CK (2018) The Effect of Ethiopian Orthodox Christians ‘Abiy Tsom’ (Lent fasting) on Metabolic Syndrome Indices and Serum Electrolytes. J Nutr, Fast Health 6: 60-70
  47. Sarri KO, Tzanakis NE, Linardakis MK, Mamalakis GD, Kafatos AG (2003) Effects of Greek Orthodox Christian Church fasting on serum lipids and obesity. BMC Public Health 3:1-8
  48. Indexed at, Google Scholar, Crossref

  49. Nematy M, Alinezhad-Namaghi M, Rashed MM, Mozhdehifard M, Sajjadi SS (2012) Effects of Ramadan fasting on cardiovascular risk factors: a prospective observational study. Nutri J 11: 1-7
  50. Indexed at, Google Scholar, Crossref

  51. Santos HO, Macedo RC (2018) Impact of intermittent fasting on the lipid profile: Assessment associated with diet and weight loss. Clin nutri ESPEN 24: 14-21
  52. Indexed at, Google Scholar, Crossref

  53. Ashraf S, Ali Z (2018) Effect of Breakfast Skipping on Lipid Profile Parameters, Body Weight, and Metabolic Measures among University Going Adults. J Nutr Food Sci 8: 2
  54. Google Scholar

  55. Sisay T, Tolessa T, Mekonen W (2020) Changes in biochemical parameters by gender and time: Effect of short-term vegan diet adherence. Plos one 15: e0237065
  56. Indexed at, Google Scholar, Crossref

  57. Dourado KF, Campos FACES, Shinohara NKS (2011) Relation between dietary and circulating lipids in lacto-ovo vegetarians. Nutricion hospitalaria 26: 959-964
  58. Indexed at, Google Scholar, Crossref

  59. Abbasnezhad A, et al. (2020) Effect of different dietary approaches compared with a regular diet on systolic and diastolic blood pressure in patients with type 2 diabetes: A systematic review and meta-analysis. Diab res clin pract 163: 108108
  60. Indexed at, Google Scholar, Crossref

  61. Chiu YF, Hsu C, Chiu THT, Lee C, Liu T, et al. (2015) Cross-sectional and longitudinal comparisons of metabolic profiles between vegetarian and non-vegetarian subjects: a matched cohort study. British J Nutri 114: 1313-1320
  62. Indexed at, Google Scholar, Crossref

  63. Morcos NY, Seoudi DM, Kamel I (2013) Effect of Coptic Orthodox Christian church fasting on healthy and diabetic subjects. Intern J Nutri, Pharmacol, Neurol Dis 3: 375
  64. Google Scholar

  65. Sarri KO, Tzanakis NE, Linardakis MK, Mamalakis GD, Kafatos AG (2003) Effects of Greek Orthodox Christian Church fasting on serum lipids and obesity. BMC Public Health 3: 16
  66. Google Scholar, Crossref

  67. Trepanowski JF, RJ Bloomer (2010) The impact of religious fasting on human health. Nutri J 9: 57
  68. Indexed at, Google Scholar, Crossref

  69. Patterson RE, Sears DD (2017) Metabolic effects of intermittent fasting. Annual rev nutri 37
  70. Indexed at, Google Scholar, Crossref

  71. Sinaga M, Teshome MS, Kidane R, Yemane T, Tegene E, et al. (2019) Metabolic Effects of Fasting and Animal Source Food Avoidance in an Ethiopian Adult Cohort. Sci reports 9: 1-9
  72. Google Scholar, Crossref

  73. Sacks FM, Lichtenstein A, Horn LV, Harris W, Kris-Etherton P (2006) Soy protein, isoflavones, and cardiovascular health: a summary of a statement for professionals from the american heart association nutrition committee. Arterioscler Thromb Vasc Biol 26: 1689-1692
  74. Indexed at, Google Scholar, Crossref

  75. De Baise S, Fernandes SFC, Gianini RJ, Duarte JLG (2007) Vegetarian diet and cholesterol and triglyceride levels. Arq Bras Cardiol 88: 35-39
  76. Indexed at, Google Scholar, Crossref

  77. Ahmed N, Farooq J, Siddiqi HS, Meo SA, Kulsoom B, et al. (2021) Impact of intermittent fasting on lipid profile–A quasi-randomized clinical trial. Fron Nutri 7: 371
  78. Indexed at, Google Scholar, Crossref

  79. Shehab A, Abdulle A, Issa AE, Suwaidi JA, Nagelkerke N (2012) Favorable changes in lipid profile: the effects of fasting after Ramadan. PloS one 7: e47615
  80. Indexed at, Google Scholar, Crossref

  81. Meo SA, Hassan A (2015) Physiological changes during fasting in Ramadan. J Pak Med Assoc 65: S6-14
  82. Indexed at, Google Scholar

  83. Bener A, Yousafzai MT (2014) Effect of Ramadan fasting on diabetes mellitus: a population-based study in Qatar. J Egyp Public Health Assoc 89: 47-52
  84. Indexed at, Google Scholar, Crossref

  85. Beltaief K, Bouida W, Trabelsi I, Baccouche H, Sassi M, et al. (2019) Metabolic effects of Ramadan fasting in patients at high risk of cardiovascular diseases. Inter J gen medi 12: 247
  86. Indexed at, Google Scholar, Crossref

  87. Kamble S, Hiremath S (2018) Insulin resistance and blood lipid levels during fasting. Nat J Phys, Pharm Pharmacol 8: 1158-1161
  88. Google Scholar, Crossref

  89. Nestle M (1999) Animal v. plant foods in human diets and health: is the historical record unequivocal? Proceed Nutri Soci 58: 211-218
  90. Indexed at, Google Scholar, Crossref

  91. Le LT, J Sabate (2014) Beyond meatless, the health effects of vegan diets: findings from the Adventist cohorts. Nutri 6: 2131-2147
  92. Indexed at, Google Scholar, Crossref

  93. Jaffrin MY, Morel H (2008) Body fluid volumes measurements by impedance: A review of bioimpedance spectroscopy (BIS) and bioimpedance analysis (BIA) methods. Medi engi phy 30: 1257-1269
  94. Indexed at, Google Scholar, Crossref

Citation: Michael A (2022) Metabolic Effect of Orthodox Fasting Dietary Pattern in Type 2 Diabetic Patients. J Nutr Sci Res 7: 169. DOI: 10.4172/snt.1000169

Copyright: © 2022 Michael A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Top