- Research article
- Open Access
Effects of Greek orthodox christian church fasting on serum lipids and obesity
BMC Public Health volume 3, Article number: 16 (2003)
No study to date has focused on the impact of Greek Orthodox Christian fasting on serum lipoproteins and obesity yet.
120 Greek adults were followed longitudinally for one year. Sixty fasted regularly in all fasting periods (fasters) and 60 did not fast at all (controls). The three major fasting periods under study were: Christmas (40 days), Lent (48 days) and Assumption (August, 15 days). A total of 6 measurements were made during one year including pre- and end-fasting blood collection, serum lipoprotein analyses and anthropometric measurements.
Statistically significant end-fasting total and LDL cholesterol differences were found in fasters. Fasters compared to controls presented 12.5% lower end-total cholesterol (p < 0.001), 15.9% lower end-LDL cholesterol (p < 0.001) and 1.5% lower end-BMI (p < 0.001). The end- LDL/HDL ratio was lower in fasters (6.5%, p < 0.05) while the change in end- HDL cholesterol in fasters (4.6% decline) was not significant. Similar results were found when the pre- and end-fasting values of fasters were compared. No change was found in control subjects.
Adherence to Greek Orthodox fasting periods contributes to a reduction in the blood lipid profile including a non-significant reduction in HDL cholesterol and possible impact on obesity.
Fasting, the voluntary abstention from all restricted foods, is a feature of many religions, and the putative health benefits have attracted both scientific and popular interest. Commonly, religious doctrines proscribe foods from animal sources permanently or for particular periods.
There are several religions, such as Hinduism, Buddhism, Judaism, Islam, Seventh-Day-Adventism that have often been studied regarding their relation to health [1–14]. However, the studies on Orthodox Christianity are very limited.
Orthodox Christian holy books recommend a total of 180–200 days of fasting per year. The faithful are advised to avoid olive oil, meat, fish, milk and dairy products every Wednesday and Friday throughout the year. Additionally, there are three principal fasting periods per year: i) a total of 40 days preceding Christmas (meat, dairy products and eggs are not allowed, while fish and olive oil are allowed except on Wednesdays and Fridays), ii) a period of 48 days preceding Easter (Lent). During Lent fish is allowed only two days whereas meat, dairy products and eggs are not allowed. Olive oil consumption is allowed only at weekends, iii) a total of 15 days in August (the Assumption) when the same dietary rules apply as for Lent with the exception of fish consumption which is allowed only on August 6th. Seafood such as shrimps, squid, cuttlefish, octopus, lobsters, crabs as well as snails are allowed on all fasting days throughout the year. The Greek Orthodox fasting practices can therefore be characterized as requiring a periodic vegetarian diet including fish and seafood.
The variant of vegetarianism followed during fasting periods by Orthodox Christians, with a diet of vegetables, legumes, nuts, fruits, olives, bread, snails and seafood, is a type of the so-called Mediterranean diet [15, 16]. To date little is known as to the effects of this 'hidden' element of the traditional Orthodox Christian diet on health and no data exist on the effect of Orthodox Christianity's dietary rules on blood lipid levels and obesity. The objective of this study was therefore to assess the effects of intermittent short-term religious fasting, according to the dietary rules of the Orthodox Christian Church, on blood lipoprotein profile and the prevalence of obesity.
The subjects of this study were selected from an adult population in the region of Heraklion, Crete. One hundred-twenty Orthodox Christians were asked to participate in this study. Sixty individuals (31 males, 29 females), mean age (x ± SD) 41 ± 12 years, fasted regularly according to the dietary rules and the fasting periods of the Christian Orthodox Church. Fasters had been practicing the fasting rituals for a mean of 20 ± 14 years. Another group of sixty subjects (24 males, 36 females), mean age (x ± SD) 38 ± 9 years, were control subjects that did not fast. Among the fasting group, 20 were lay persons (fasted for 13 ± 10 years) and 40 were under religious order (fasted for 23 ± 15 years): 19 nuns living in a convent and 21 priests living with their families in community parishes. The family history of each subject was recorded with regard to diabetes, CHD, smoking, hormonal disturbances and drug intake.
Three pairs of measurements were made over a 1-year period (2000–2001), coinciding with the beginning and end of each of the three major fasting periods of the Christian Orthodox Church: Christmas, Lent and the Assumption. All measurements were made between 8.00–10.00 am and they included fasting blood collection, anthropometric measurements and the completion of questionnaires.
All subjects signed informed consent forms and completed questionnaires on fasting, health habits (coffee and alcohol consumption, smoking), certain items of personal data (marital status, educational level), physical activity, dietary habits (24 h recall, 3-day dietary record). Fasters were defined as those who fasted regularly during all three principal fasting periods, while current smokers as those who smoked at least one cigarette per day.
Body weight was measured all six times by a digital scale (Seca, Hamburg, Germany, Model 770) with an accuracy of ± 100 g. Subjects were weighed barefoot in very light clothing. Standing height was measured once without shoes to the nearest 0.5 cm with the use of a stadiometer with the shoulders in relaxed position and arms hanging freely. Body Mass Index (BMI) was calculated by dividing weight (kg) by height squared (m2). Waist and hip circumferences were measured twice, at the first and sixth measurement of the study . Blood pressure (BP) was measured all six times in the right arm with a traditional sphygmomanometer. Three seated BP measurements were taken for each subject spaced two minutes apart.
Serum lipoprotein concentrations were always determined after 12 h of fasting. Blood samples were transferred to the University hospital of Crete in tanks containing ice packs that maintained the temperature at 3–4°C. Total cholesterol was determined by Allain's method , HDL-C was measured by the heparin-manganese precipitation method  and triacylglycerols were determined using Fossati's method , while LDL-C was calculated as follows: LDL-C = TC - (HDL -C + TG/5) . During the period October 2000 – September 2001 the coefficient of variation for the biochemical analysis of total cholesterol was 2,85%, for HDL was 5,40% and for triacylglycerols was 3,92%. DNA extraction was performed according to the method of Miller et al . Apo E genotype was determined by PCR amplification and subsequent digestion with the restriction enzyme Hha I (New England Biolabs) as described by Reymer et al  in Harokopio University of Athens.
Differences in gender, tobacco use, educational level and apolipoprotein E distribution were compared using χ2 analysis, while differences in age were compared by ANOVA analysis. Regression analysis was used to compare end-fasting lipid concentrations and BMI with age, sex, smoking, educational level, BMI, WHR, fasting and the pre-fasting values. The influence of fasting on end-fasting values was examined using ANCOVA analysis. Paired samples T-test and Mann-Whitney test were used to compare pre and end-fasting values in fasters.
Pre-fasting values comprise the mean of the three measurements that were made before the beginning of the Christmas, Lent and Assumption fasting periods, while end-fasting values are the mean of the three measurements that were made at the end of each one of the fasting periods.
Demographic data on a hundred and twenty subjects are presented in Table 1. Sixty of the subjects were fasters (26% male, 24% female) with a mean age of 42 ± 12; the other sixty were control subjects (20% male, 30% female) with a mean age of 38 ± 9. There was no statistically significant difference in the age of the two groups (ANOVA). The subjects in the fasters group had been observing the fasting rituals for a mean of 20 ± 14 years. The rate of compliance with the fasting rules was 100%. All subjects in both groups did not suffer from any disease like thyroid, diabetes, cancer, cardiovascular diseases, and did not take any medication.
The levels of serum lipids, blood pressure and body measurements of all three periods for fasters and controls are presented in table 2.
Effect of fasting on end-fasting values
Multiple Linear Stepwise Regression Analysis indicated that fasting is a significant determinant for end-total cholesterol, end-LDL cholesterol, end-LDL/HDL ratio and end-BMI (Table 3), showing that fasters have lower levels of these variables.
Females have higher levels of end-HDL cholesterol while men have higher levels of end-TC/HDL and end-LDL/HDL ratios. Waist-to-hip ratio was positively related to end-total cholesterol and end-LDL cholesterol.
Comparisons of end-fasting values between the two groups
Comparisons of mean end-fasting values between fasters and controls are shown in Table 4. Mean end-TC, end-LDL and end-BMI were statistically lower (p < 0.001) in fasters compared to controls. Fasters presented 12.5% lower end-TC, 15.9% lower end-LDL cholesterol and 1.5% lower end-BMI compared to controls. Moreover, fasters had significantly lower LDL/HDL ratios (p < 0.05). All results were adjusted for age, sex, BMI and smoking.
Comparisons of pre and end-fasting values in the fasters' group
The fasters who had 3 complete pairs of measurements were included in this analysis (Table 5). Paired samples T-test showed that fasters presented 9.1% decline in end- total cholesterol, 12.4% decline in end- LDL, 8.5% decline in end- HDL and 1.4% decline in end- BMI compared to their respective pre-values. All these differences were significant (p < 0.001). As for the ratios end- TC/HDL and end- LDL/HDL although they declined the changes were not significant. The same analysis was done in controls that presented no significant changes over the year. A further step was to categorize fasters in two subgroups: 1) nun-priests and 2) lay people and to compare their pre- and end- fasting values. Mann-Whitney test showed that the changes seen in fasters' group remained when each subgroup was analyzed separately though they were not significant. It was observed that between the major fasting periods studied (between the end of Christmas and the beginning of Lent; and between the end of Lent and the beginning of the Assumption fasting period) when fasters returned to their usual dietary habits (non-fasting periods) total cholesterol and LDL cholesterol were increased by 6% and 9% respectively.
Table 6 shows that at end-fasting periods fasters had 10% reduction in energy intake (EI), 17% reduction in total fat (%EI), 23% increase in carbohydrates (%EI) and 43.5% increase in fiber consumption, whereas the respective percentages for the controls are +7%, +1%, +1.7% and +3.3%. All the differences found between the two groups are significant.
Distribution of Apo E polymorphism
Subjects in this study were screened for the common apolipoprotein E (apoE) polymorphism, as genetic variation at the apoE locus has been shown to influence serum lipid responsiveness to dietary interventions and account for much of the interindividual variability in dietary response [24, 25] Several studies, for example, support the concept that the ε4 allele is associated with an increased cholesterol response to dietary manipulation, and that subjects carrying the ε4 allele are the most responsive to diets restricted in saturated fat and cholesterol [24–27].
Fasters and control subjects were classified in three groups according to their apoE genotype: subjects homozygous for the common ε3 allele (apoE3/3 genotype, (38 fasters and 40 controls); subjects with the apoE2/3 genotype (nine fasters and four controls); carriers of the ε4 allele (apoE3/4 and apoE4/4 genotypes; four fasters and six controls, respectively). Chi-square analysis showed that apoE genotype distribution did not differ between fasters and controls (data not shown).
The most important finding of this study is that most serum lipid variables decreased significantly over the fasting periods. Fasters, as compared to controls, had decreased levels of mean end- total cholesterol, LDL-C, LDL/HDL-C ratio and BMI. Several genetic factors account for the variation in cholesterol levels and obesity indices, however, we believe that the possibilities of genetic differences between the two groups are minimal since the population of Crete is stable with a long history over 4000 years. In addition to this, the ApoE genotype distribution found no differences between the two groups (fasters vs controls). In the fasters' group the mean decrease within all three fasting periods was 9% for total cholesterol and 12% for LDL-C. However, it was observed that during non-fasting periods when fasters returned to their usual dietary habits, total cholesterol and LDL-C increased by 6% and 9% respectively. This shows that the reduced end-total and LDL cholesterol concentrations that were observed within the fasting periods were not sustained when the subjects returned to their usual dietary habits even though the increase did not reach the initial pre- levels. The reduction in HDL that occurred in fasters is a common finding with low-fat and vegetarian diets [28–31]. The findings above are in agreement with the results reported by Barnard et al who conducted a strict vegetarian-diet intervention study for 5 weeks on 35 women . The intervention diet consisted of grains, legumes, vegetables and fruit. After the intervention diet phase total cholesterol, LDL and HDL were decreased by 13.2%, 16.9% and 16.5% respectively . BMI was also significantly reduced (p < 0.001) while, in agreement with our findings, the TC/HDL and LDL/HDL ratios remained unchanged (table 5). Similar were the findings in another 6-week vegetarian-diet intervention study by Masarei et al  and in a 12-week low-fat-vegan-diet intervention study by Nicholson et al . Lee  and Hoffman , who compared omnivores with lacto-ovo-vegetarians, found no difference in LDL/HDL ratio between the two groups. The contrasting results on LDL/HDL ratio could be attributed to differences in the population samples studied.
Nieman et al  and Toohey et al  investigated Seventh-Day Adventists with similar demographic and life-style factors and with comparable diets and dietary habits to our cohort. They found that lacto-ovo-vegetarians and lifetime strict vegetarians had lower concentrations of total and LDL cholesterol when compared with non-vegetarians and lacto-ovo-vegetarians respectively (p < 0.05) . Toohey et al found also found lower levels of BMI, triacylglycerols and TC/HDL ratio . The present study showed that women had lower levels of LDL/HDL ratio and TC/HDL ratio, which is also a better predictor for CHD in women [36–38]. This is explained by the higher concentrations of HDL that women have compared to men .
The positive association of waist-to-hip ratio with total and LDL cholesterol is in agreement with other studies that correlate waist-to-hip ratio with coronary risk factors and CHD prevalence [40–42]. Waist-to-hip ratio measurement is a simple and cost-effective measure that contributes in predicting abnormal lipoprotein levels and increased risk of cardiovascular disease.
Both the fasting and control groups had mean BMI in the overweight category. Fasting had a small but statistically significant impact on fasters' BMI at the end of the fasting periods that was not sustained in non-fasting periods. In accordance to the results in this study, Haddad et al studying a group of vegans and nonvegetarians found significantly lower BMI levels in the vegan group . Moreover, others found that vegetarians have lower BMI than meat eaters [44–46]. At the same time following a Mediterranean-style diet has also been proven to be beneficial to weight loss . As regards religious fasting some studies associate it with weight loss and decline in BMI [2, 3] while others do not [4, 5, 48].
Educational level was not found to influence any of the blood lipid variables in this study (Table 3). This was an unexpected result since higher education is associated with better health care and awareness whereas low educational level has been related to unfavorable lipid profile , all-cause and CAD mortality  and hypertension .
The beneficial changes seen in fasters diet during the fasting periods, especially regarding energy intake, total fat and fiber consumption, can also explain the reductions in the biochemical and obesity indices. A recent study of the University of Crete showed that the Christian Orthodox nuns' diet was very low in cholesterol and in saturated fat intake (6% of total energy intake), and high in fiber and antioxidant vitamins . This could be attributed to nuns' high consumption of fruit, vegetables, cereals and legumes. In another study Haddad et al found that vegans consume more grains, vegetables, fruit, legumes and seeds and as a result their diet consists of more dietary fiber and less dietary cholesterol . It is well known that reduced intakes of dietary SFA and cholesterol lower total and LDL cholesterol concentration and are associated with low risk of cardiovascular diseases [52, 53]. The Orthodox Christians' diet, which is based on vegetables, legumes, fruit, cereals, bread and olive oil, is a Mediterranean-type of diet with periodic abstinence from meat and other animal products during the fasting periods. Numerous investigators [54–56] have recognized the beneficial role of the Mediterranean diet in cardiovascular diseases, and the protective effect in terms of cancer and longevity have also been noted [57, 58]. In addition, supplementary studies have associated religiosity with good health . This has been confirmed in a recent study by Chliaoutakis et al , which is the only published work to date which investigates the association between the Orthodox Christian lifestyle and health. Chliaoutakis et al found that devout Orthodox Christians adopt healthier life-styles and that religion has a substantial impact on mental and physical health-related behaviors . In the present study, contrary to Chliaoutakis' findings, the physical activity of the two groups (fasters vs controls) did not differ in any of the testing periods.
Our study attempts to provide an understanding of the impact of Christian Orthodox fasting on serum blood lipids and obesity indices before and at the end of the three major fasting periods. Compared to controls, fasters presented decreased lipoproteins and BMI levels. These results support our hypothesis by highlighting the beneficial influence of Christian Orthodox fasting on lipoprotein profile and prevalence of obesity.
Shatenstein B, Ghadirian P: Influences on diet, health behaviours and their outcome in select ethnocultural and religious groups. Nutrition. 1998, 14 (2): 223-30. 10.1016/S0899-9007(97)00425-5.
Temizhan A, et al: The effects of Ramadan fasting on blood lipid levels. Am J Med. 2000, 109 (4): 341-2. 10.1016/S0002-9343(00)00498-8.
Adlouni A, et al: Fasting during Ramadan induces a marked increase in high-density lipoprotein cholesterol and decrease in low-density lipoprotein cholesterol. Ann Nutr Metab. 1997, 41 (4): 242-9.
Maislos M, et al: Marked increase in plasma high-density-lipoprotein cholesterol after prolonged fasting during Ramadan. Am J Clin Nutr. 1993, 57 (5): 640-2.
Maislos M, et al: Gorging and plasma HDL-cholesterol – the Ramadan model. Eur J Clin Nutr. 1998, 52 (2): 127-30. 10.1038/sj.ejcn.1600526.
Akhan G, Kutluhan S, Koyuncuoglu HR: Is there any change of stroke incidence during Ramadan?. Acta Neurol Scand. 2000, 101 (4): 259-61. 10.1034/j.1600-0404.2000.101004259.x.
Temizhan A, et al: Is there any effect of Ramadan fasting on acute coronary heart disease events?. Int J Cardiol. 1999, 70 (2): 149-53. 10.1016/S0167-5273(99)00082-0.
Akanji AO, Mojiminiyi OA, Abdella N: Beneficial changes in serum apo A-1 and its ratio to apo B and HDL in stable hyperlipidaemic subjects after Ramadan fasting in Kuwait. Eur J Clin Nutr. 2000, 54 (6): 508-13. 10.1038/sj.ejcn.1601047.
Friedlander Y, et al: Coronary heart disease risk factors among religious groupings in a Jewish population sample in Jerusalem. Am J Clin Nutr. 1985, 42 (3): 511-21.
Friedlander Y, Kark JD, Stein Y: Religious observance and plasma lipids and lipoproteins among 17-year-old Jewish residents of Jerusalem. Prev Med. 1987, 16 (1): 70-9.
Fraser GE: Associations between diet and cancer, ischemic heart disease, and all- cause mortality in non-Hispanic white California Seventh-day Adventists. Am J Clin Nutr. 1999, 70 (3 Suppl): 532S-538S.
Fraser GE: Diet as primordial prevention in Seventh-Day Adventists. Prev Med. 1999, 29 (6 Pt 2): S18-23. 10.1006/pmed.1998.0415.
Famodu AA, et al: Blood pressure and blood lipid levels among vegetarian, semi-vegetarian, and non-vegetarian native Africans. Clin Biochem. 1998, 31 (7): 545-9. 10.1016/S0009-9120(98)00067-8.
Nieman DC, et al: Dietary status of Seventh-Day Adventist vegetarian and non-vegetarian elderly women. J Am Diet Assoc. 1989, 89 (12): 1763-9.
Trichopoulou A, et al: Diet and overall survival in elderly people. Bmj. 1995, 311 (7018): 1457-60.
Kafatos A, et al: Mediterranean diet of Crete: foods and nutrient content. J Am Diet Assoc. 2000, 100 (12): 1487-93. 10.1016/S0002-8223(00)00416-8.
Lohman TG, Roche AF, Mastorell R: Anthropometric standardization reference manual. Champaign, IL: Human Kinetics Publishers. 1991
Allain CC, et al: Enzymatic determination of total serum cholesterol. Clin Chem. 1974, 20 (4): 470-5.
Finley PR, et al: Cholesterol in high-density lipoprotein: use of Mg2+/dextran sulfate in its enzymic measurement. Clin Chem. 1978, 24 (6): 931-3.
Fossati P, Prencipe L: Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxide. Clin Chem. 1982, 28 (10): 2077-80.
Friedewald WT, Levy RI, Fredrickson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972, 18 (6): 499-502.
Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988, 16 (3): 1215-
Reymer PW, et al: Apolipoprotein E genotyping on agarose gels. Clin Chem. 1995, 41 (7): 1046-7.
Ordovas JM: The genetics of serum lipid responsiveness to dietary interventions. Proc Nutr Soc. 1999, 58 (1): 171-87.
Dreon DM, Krauss RM: Diet-gene interactions in human lipoprotein metabolism. J Am Coll Nutr. 1997, 16 (4): 313-24.
Lopez-Miranda J, et al: Effect of apolipoprotein E phenotype on diet-induced lowering of plasma low density lipoprotein cholesterol. J Lipid Res. 1994, 35 (11): 1965-75.
Miettinen TA, Gylling H, Vanhanen H: Serum cholesterol response to dietary cholesterol and apoprotein E phenotype. Lancet. 1988, 2 (8622): 1261-10.1016/S0140-6736(88)90862-8.
Masarei JR, et al: Vegetarian diets, lipids and cardiovascular risk. Aust N Z J Med. 1984, 14 (4): 400-4.
Masarei JR, et al: Effects of a lacto-ovo vegetarian diet on serum concentrations of cholesterol, triglyceride, HDL-C, HDL2-C, HDL3-C, apoprotein-B, and Lp(a). Am J Clin Nutr. 1984, 40 (3): 468-78.
Barnard ND, et al: Effectiveness of a low-fat vegetarian diet in altering serum lipids in healthy premenopausal women. Am J Cardiol. 2000, 85 (8): 969-72. 10.1016/S0002-9149(99)00911-X.
Asztalos B, et al: Differential response to low-fat diet between low and normal HDL-cholesterol subjects. J Lipid Res. 2000, 41 (3): 321-8.
Nicholson AS, et al: Toward improved management of NIDDM: A randomized, controlled, pilot intervention using a lowfat, vegetarian diet. Prev Med. 1999, 29 (2): 87-91. 10.1006/pmed.1999.0529.
Lee HY, et al: Serum fatty acid, lipid profile and dietary intake of Hong Kong Chinese omnivores and vegetarians. Eur J Clin Nutr. 2000, 54 (10): 768-73. 10.1038/sj.ejcn.1601089.
Hoffmann I, et al: Giessen Wholesome Nutrition Study: relation between a health-conscious diet and blood lipids. Eur J Clin Nutr. 2001, 55 (10): 887-95. 10.1038/sj.ejcn.1601243.
Toohey ML, et al: Cardiovascular disease risk factors are lower in African-American vegans compared to lacto-ovo-vegetarians. J Am Coll Nutr. 1998, 17 (5): 425-34.
Wang TD, et al: Efficacy of cholesterol levels and ratios in predicting future coronary heart disease in a Chinese population. Am J Cardiol. 2001, 88 (7): 737-43. 10.1016/S0002-9149(01)01843-4.
Solymoss BC, et al: Relation of coronary artery disease in women < 60 years of age to the combined elevation of serum lipoprotein (a) and total cholesterol to high-density cholesterol ratio. Am J Cardiol. 1993, 72 (17): 1215-9.
Hong MK, et al: Usefulness of the total cholesterol to high-density lipoprotein cholesterol ratio in predicting angiographic coronary artery disease in women. Am J Cardiol. 1991, 68 (17): 1646-50.
Price JF, et al: Influence of high-density lipoprotein cholesterol and rheological factors on the sex difference in cardiovascular disease. J Cardiovasc Risk. 2000, 7 (1): 49-56.
Onat A, Sansoy V, Uysal O: Waist circumference and waist-to-hip ratio in Turkish adults: interrelation with other risk factors and association with cardiovascular disease. Int J Cardiol. 1999, 70 (1): 43-50. 10.1016/S0167-5273(99)00049-2.
Mansfield E, McPherson R, Koski KG: Diet and waist-to-hip ratio: important predictors of lipoprotein levels in sedentary and active young men with no evidence of cardiovascular disease. J Am Diet Assoc. 1999, 99 (11): 1373-9. 10.1016/S0002-8223(99)00335-1.
Perry AC, et al: Clinical predictability of the waist-to-hip ratio in assessment of cardiovascular disease risk factors in overweight, premenopausal women. Am J Clin Nutr. 1998, 68 (5): 1022-7.
Haddad EH, et al: Dietary intake and biochemical, hematologic, and immune status of vegans compared with nonvegetarians. Am J Clin Nutr. 1999, 70 (3 Suppl): 586S-593S.
Burr ML, Butland BK: Heart disease in British vegetarians. Am J Clin Nutr. 1988, 48 (3 Suppl): 830-2.
Key TJ, Davey GK, Appleby PN: Health benefits of a vegetarian diet. Proc Nutr Soc. 1999, 58 (2): 271-5.
Key T, Davey G: Prevalence of obesity is low in people who do not eat meat. Bmj. 1996, 313 (7060): 816-7.
De Lorenzo A, et al: Effects of weight loss on body composition and pulmonary function. Respiration. 1999, 66 (5): 407-12. 10.1159/000029423.
el Ati J, Beji C, Danguir J: Increased fat oxidation during Ramadan fasting in healthy women: an adaptative mechanism for body-weight maintenance. Am J Clin Nutr. 1995, 62 (2): 302-7.
Verschuren WM, Boerma GJ, Kromhout D: Total and HDL-cholesterol in The Netherlands: 1987–1992. Levels and changes over time in relation to age, gender and educational level. Int J Epidemiol. 1994, 23 (5): 948-56.
Hardarson T, et al: The relationship between educational level and mortality. The Reykjavik Study. J Intern Med. 2001, 249 (6): 495-502. 10.1046/j.1365-2796.2001.00834.x.
Tedesco MA, et al: Educational level and hypertension: how socioeconomic differences condition health care. J Hum Hypertens. 2001, 15 (10): 727-31. 10.1038/sj.jhh.1001249.
Law M: Dietary fat and adult diseases and the implications for childhood nutrition: an epidemiologic approach. Am J Clin Nutr. 2000, 72 (5 Suppl): 1291S-1296S.
Shahar DR, et al: Seasonal variations in dietary intake affect the consistency of dietary assessment. Eur J Epidemiol. 2001, 17 (2): 129-33. 10.1023/A:1017542928978.
Kafatos A, et al: Heart disease risk-factor status and dietary changes in the Cretan population over the past 30 y: the Seven Countries Study. Am J Clin Nutr. 1997, 65 (6): 1882-6.
Panagiotakos DB, et al: The association of Mediterranean diet with lower risk of acute coronary syndromes in hypertensive subjects. Int J Cardiol. 2002, 82 (2): 141-7. 10.1016/S0167-5273(01)00611-8.
Kris-Etherton P, et al: AHA Science Advisory: Lyon Diet Heart Study. Benefits of a Mediterranean-style, National Cholesterol Education Program/American Heart Association Step I Dietary Pattern on Cardiovascular Disease. Circulation. 2001, 103 (13): 1823-5.
Trichopoulou A, Vasilopoulou E: Mediterranean diet and longevity. Br J Nutr. 2000, 84 (Suppl 2): S205-9.
Trichopoulou A, et al: Cancer and Mediterranean dietary traditions. Cancer Epidemiol Biomarkers Prev. 2000, 9 (9): 869-73.
Chliaoutakis JE, et al: Greek christian orthodox ecclesiastical lifestyle: could it become a pattern of health-related behavior?. Prev Med. 2002, 34 (4): 428-35. 10.1006/pmed.2001.1001.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/3/16/prepub
We appreciate the assistance of Bishop Nektarios of Crete in supporting the study and the Monasteries of Sabbathiana, Isodia Theotokou and Kremaston for their participation. We are also grateful to Dr N.Yiannakouris, Mrs C.Codrington, Dr C.Hatzis, Ms F.Bervanaki, Mr M.Kiriakakis and Mr G.Tsibinos.
Author K.S mainly organized and performed the study, and drafted the manuscript. Author N.T participated in the design of the study and supervised the manuscript. Author M.L performed the statistical analyses. Author G.M performed part of the statistical analysis. Author A.K conceived of the study, participated in its design, and supervised the study and the manuscript.
About this article
Cite this article
Sarri, K.O., Tzanakis, N.E., Linardakis, M.K. et al. Effects of Greek orthodox christian church fasting on serum lipids and obesity. BMC Public Health 3, 16 (2003). https://doi.org/10.1186/1471-2458-3-16
- Greek Orthodox Christian
- serum lipids