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PLOS ONE logoLink to PLOS ONE
. 2014 Feb 11;9(2):e88547. doi: 10.1371/journal.pone.0088547

Taiwanese Vegetarians and Omnivores: Dietary Composition, Prevalence of Diabetes and IFG

Tina H T Chiu 1,2, Hui-Ya Huang 3, Yen-Feng Chiu 4, Wen-Harn Pan 2,5, Hui-Yi Kao 4, Jason P C Chiu 6, Ming-Nan Lin 3,7,*, Chin-Lon Lin 1,8,9
Editor: Marià Alemany10
PMCID: PMC3921224  PMID: 24523914

Abstract

Introduction

Vegetarian diets have been shown to improve glucose metabolism and reduce risk for diabetes in Westerners but whether Chinese vegetarian diets have the same benefits is unknown.

Methods

We evaluated the association between diet and diabetes/impaired fasting glucose (IFG) among 4384 Taiwanese Buddhist volunteers and identified diabetes/IFG cases from a comprehensive review of medical history and fasting plasma glucose.

Results

Vegetarians had higher intakes of carbohydrates, fiber, calcium, magnesium, total and non-heme iron, folate, vitamin A, and lower intakes of saturated fat, cholesterol, and vitamin B12. Besides avoiding meat and fish, vegetarians had higher intakes of soy products, vegetables, whole grains, but similar intakes of dairy and fruits, compared with omnivores. The crude prevalence of diabetes in vegetarians versus omnivores is 0.6% versus 2.3% in pre-menopausal women, 2.8% versus 10% in menopausal women, and 4.3% versus 8.1% in men. Polytomous logistic regression adjusting for age, body mass index, family history of diabetes, education, leisure time physical activity, smoking and alcohol, showed that this vegetarian diet was negatively associated with diabetes and IFG in men (OR for diabetes: 0.49, 95% CI: 0.28–0.89; OR for IFG: 0.66, 95% CI: 0.46–0.95); in pre-menopausal women (OR for diabetes: 0.26, 95% CI: 0.06–1.21; OR for IFG: 0.60, 95% CI: 0.35–1.04); and in menopausal women (OR for diabetes: 0.25, 95% CI: 0.15–0.42; OR for IFG: 0.73, 95% CI: 0.56–0.95).

Conclusion

We found a strong protective association between Taiwanese vegetarian diet and diabetes/IFG, after controlling for various potential confounders and risk factors.

Background

The diabetes epidemic in Asia and particularly in China emerged simultaneously with increased meat consumption and higher proportion of energy intake from animal protein and fat [1]. Compared with Westerners, Asians tend to incur diabetes at a younger age and at a lower body mass index (BMI), possibly due to genetic susceptibility in combination with environmental exposures [2]. Vegetarian diets have been associated with a lower prevalence [3] and incidence [4] of diabetes among Seventh day Adventists. Previous clinical trials have shown vegetarian diets improve glycemic control [5] and insulin sensitivity [6]. Although several small studies reported lower glucose level and better insulin sensitivity in Taiwanese vegetarians than omnivores [7][9], no study thus far has examined whether a vegetarian diet protects against diabetes in Chinese ethnic Asian population, a high risk population that may incur diabetes despite having a normal BMI value [2]. Moreover, Asian diets tend to be lower in meat and higher in plant foods compared with Western diet. It remains unknown whether a diet completely avoiding meat and fish would further extend the protective effect of a plant-based diet. In addition, most studies on Asian vegetarians tend to compare vegetarians from religious groups with omnivores from the general population [7]. Religious and spiritual practices (a main determinant of vegetarian dietary practice in Asia) may be associated with social and emotional support which may confound health outcomes [10], [11].

This study examines within a Buddhist group, the cross-sectional association between vegetarian diet and two stages of impaired glucose metabolism – impaired fasting glucose (IFG) and diabetes.

Methods

The Tzu Chi Health Study

The Tzu Chi Health Study enrolled 6002 Taiwanese adults, of which 77% were Tzu Chi commissioners – a devoted group of volunteers of the Buddhist Tzu Chi Foundation who receive a free health examination every 2 to 3 years at one of four Tzu Chi hospitals. Tzu Chi Commissioners are required to abstain from alcohol, tobacco, and are encouraged to adopt a vegetarian diet for reasons of compassion and environmental conservation.

The current study was conducted at the Buddhist Dalin Tzu Chi Hospital between 2007 and 2009, where all participants received a health examination during an overnight stay at the hospital. Height was measured on a scale with participants standing erect. Body weight and body fat were measured on a Bioelectrical Impedance Analyzer (Tanita TBF-410). Waist circumference was measured at navel, with the participants standing. All measurements were performed with the participants wearing light clothes and without shoes. BMI was computed by dividing weight in kilograms by the square of height in meters. Venous blood was collected the next morning after an overnight fasting. Serum glucose was measured using the hexokinase glucose-6-phosphate dehydrogenase method (INTEGRA 800 system, Roche, USA).

Trained research dietitians interviewed each participant on demographic, lifestyle, diet, leisure time physical activity (LTPA), and medical history. Participants were identified as having a family history of diabetes if they reported one or more of their parents, grandparents, or siblings as having diabetes. Detailed diet was assessed through a 64-item food frequency questionnaire (FFQ), which had been validated in a subgroup of the present cohort [12], and the detail procedure of administering this FFQ had been reported previously [12]. Nutrients were calculated based on Taiwan's Food Composition Table [13]. Heme iron content was estimated using the following percentages of total iron: 65% for beef and lamb, 39% for pork, 26% for chicken and fish [14]. Only those who completely avoid meat, fish, and all animal flesh for at least one year up until entry into the study were considered vegetarians. Current smoker is defined as the use of any cigarette in the past 6 months. Alcohol drinking habit is defined as drinking of alcohol for at least once per week. The institutional review board at the Buddhist Dalin Tzu Chi Hospital approved the study, and all participants gave written informed consent.

Disease ascertainment

Potential cases of diabetes were initially identified using self-reported history of diabetes ascertained from the baseline medical history questionnaire or having a fasting plasma glucose ≥7.0 mmol/L. Two physicians (HYH and MNL) subsequently confirmed the self-reported diabetes with the electronic medical records in Tzu Chi hospitals. For those who did not have medical records (28%), the physicians made telephone calls to confirm with the participants about their diabetes diagnosis. Participants who did not self-report a history of diabetes but had a fasting plasma glucose ≥7.0 mmol/L were regarded as having diabetes if one of the following criteria was further confirmed in medical record or with the participants in a telephone follow-up: (1) physician diagnosis of diabetes; (2) prescription of diabetes medication; (3) an additional fasting plasma glucose ≥7.0 mmol/L; (4) an additional HbA1C≥6.5%. Participants with one fasting plasma glucose ≥7.0 mmol/L but subsequent check-up showing no diabetes were classified as having IFG. Participants with fasting plasma glucose <5.6 mmol/L and 5.6–6.9 mmol/L were classified as normal and IFG respectively [15]. For participants who self reported diabetes during baseline questionnaire interview, the duration of their diabetes (how many years they have known to have diabetes up until entry to the study) was asked.

Statistical analysis

After excluding 1377 non Tzu Chi commissioners, 35 participants who reported adopting vegetarian diet after diagnosis of diabetes, 10 participants with incomplete data on covariates, 267 participants with extreme average daily energy intakes (male: <3.3 MJ [800 kcal] or >16.7 MJ [4000 kcal], female: <2.1 MJ [500 kcal] or >14.6 MJ [3500 kcal]), and 13 participants whose diabetes status could not be confirmed (due to only one measurement of fasting blood glucose ≥7.0 mmol/L), a total of 4384 participants were included in the present analysis.

Demographic characteristics were compared using analysis of variance (continuous variables), or the Chi square test (categorical variables). Fisher's exact test was applied for categorical variables with a cell number less than 5. Dietary intake was compared using Wilcoxon two-sample test. Polytomous logistic regression was used to compare the outcomes of IFG and diabetes with normal glucose as the reference group, with adjustment for age, family history of diabetes, education, LTPA, BMI, smoking (men only), and alcohol (men only). All analyses were completed using SAS 9.2.

Results

Table 1 shows the characteristics of participants with normal glucose, IFG, and diabetes. Diabetes individuals had the oldest age, highest BMI, waist circumference, body fat, and were the most likely to have family history of diabetes. Nearly all women were never smokers, while less than 5% of the men were current smokers. Among menopausal women, diabetes individuals reported more LTPA than those without diabetes.

Table 1. Characteristics of participants with normal glucose, impaired fasting glucose, and diabetes.

Pre-menopausal women Menopausal women Men
Normal IFG Diabetes P-value Normal IFG Diabetes P-value Normal IFG Diabetes P-value
n 866 75 16 1382 285 122 1253 266 119
Age (years) 45±6 47±5 48±4 0.0001 58±7 60±7 62±8 <0.0001 54±10 58±9 59±8 <0.0001
BMI (kg/m2) 23±3 24±4 27±4 <0.0001 23±3 25±3 25±4 <0.0001 24±3 25±3 25±3 <0.0001
Waist (cm) 72±7 77±8 83±9 <0.0001 74±7 79±9 80±8 <0.0001 82±8 86±9 87±9 <0.0001
Body fat (%) 29±6 32±8 35±7 <0.0001 29±6 31±7 32±7 <0.0001 21±5 22±6 22±5 0.0004
Family history of diabetes 35% 33% 63% 0.068 28% 28% 63% <0.0001 24% 27% 58% <0.0001
Education
Elementary or lower 9% 12% 44% <0.0001* 39% 50% 58% <0.0001 17% 23% 16% 0.0093
Secondary 65% 77% 50% 46% 40% 29% 48% 50% 59%
College or higher 26% 11% 6% 15% 10% 13% 35% 27% 25%
Smoking
Current 0% 0% 0% 0.15* 0% 0% 0% 0.013* 4% 3% 5% 0.56
Past 2% 0% 0% 1% 1% 0% 33% 29% 36%
Never 98% 100% 100% 99% 98% 100% 63% 67% 59%
Alcohol
Current 1% 4% 0% 0.004* 1% 0% 0% 0.0042* 8% 10% 8% 0.69
Past 1% 0% 6% 1% 1% 1% 23% 23% 24%
Never 97% 96% 94% 98% 99% 99% 70% 67% 68%
LTPA per week
0–30 minutes 49% 55% 50% 0.0005* 31% 33% 22% 0.023 29% 29% 29% 0.33
31–180 minutes 33% 31% 31% 34% 32% 28% 33% 28% 28%
>180 minutes 18% 15% 19% 35% 35% 50% 37% 42% 43%
Diet
Vegetarian 37% 27% 13% 0.0006* 48% 39% 18% <0.0001 23% 16% 13% 0.0014
Omnivore 63% 73% 88% 52% 61% 82% 77% 84% 87%

Data are presented as either mean ± standard deviation or percent. IFG  =  impaired fasting glucose BMI  =  body mass index. LTPA  =  leisure time physical activity.

*Fisher's exact test.

Table 2 shows the crude prevalence of diabetes, IFG, and other characteristics of vegetarians and omnivores. Vegetarians had lower prevalence of diabetes and IFG than omnivores. All groups had average BMI≤25 kg/m2, and had lower average waist circumference than recommended for Asians (men: <90 cm, and women <80 cm) [16]. Among men, vegetarians were less likely to ever use alcohol or tobacco.

Table 2. Crude prevalence of impaired glucose metabolism and other characteristics of vegetarians and omnivores.

Pre-menopausal women Menopausal women Men
Vegetarians Omnivores P-value Vegetarians Omnivores P-value Vegetarians Omnivores P-value
n 343 614 792 997 349 1289
Impaired glucose metabolism
Diabetes 0.6% 2.3% 0.0006* 2.8% 10% <0.0001 4.3% 8.1% 0.0014
Impaired fasting glucose 5.8% 9.0% 14% 18% 12% 17%
Age (years) 46±5 45±6 0.0071 59±8 58±7 0.25 55±9 55±10 0.14
BMI (kg/m2) 23±3 23±3 0.023 23±3 24±3 <0.0001 23±3 24±3 <0.0001
Waist (cm) 72±7 73±8 0.0083 75±8 76±8 0.0008 81±8 84±8 <0.0001
Body fat (%) 28±5 30±7 <0.0001 28±6 31±6 <0.0001 19±5 22±5 <0.0001
Education
Elementary or lower 10% 10% 0.90 44% 41% 0.35 19% 17% 0.65
Secondary 67% 65% 42% 45% 50% 49%
College or higher 24% 25% 14% 14% 31% 34%
Family history of diabetes 34% 36% 0.50 27% 33% 0.0097 28% 27% 0.85
Smoking
Current 0% 0.5% 0.043* 0% 0% 0.09* 0% 5% <0.0001*
Past 2% 1.5% 1% 1% 31% 33%
Never 98% 98% 99% 99% 69% 62%
Alcohol
Current 1% 2% 0.012* 1% 1% 0.025* 1% 10% <0.0001*
Past 1% 1% 1% 1% 26% 22%
Never 98% 97% 98% 98% 72% 68%
LTPA per week
0–30 min 51% 49% 0.65 33% 28% 0.057 32% 29% 0.037
31–180 min 31% 33% 32% 35% 35% 31%
>180 min 19% 17% 34% 37% 33% 40%

Data are presented as either mean ± standard deviation or percent. BMI  =  body mass index. LTPA  =  leisure time physical activity.

*Fisher's exact test.

Overall, our study participants consumed a predominantly plant-based diet such that even the omnivores consumed little meat and fish (Table 3). Men consumed significantly more energy and most nutrients (except for calcium, folate, and vitamin C) than women. Vegetarians had a higher percent of energy intake as carbohydrate, and lower percent as fat and protein, while having higher intake of fiber, calcium, magnesium, non-heme iron, folate, vitamin A, and lower intake of saturated fat, cholesterol, and vitamin B12. Vegetarians also consumed more soy products, total and green leafy vegetables, nuts, whole grains; less tea; and a similar amount of dairy products and fruits, compared with omnivores. The majority (72% of men and 82% of women) did not report consumption of any sweetened beverage in the FFQ.

Table 3. Comparison of average daily dietary composition between vegetarians and omnivores as assessed by a food frequency questionnaire.

Pre-menopausal women Menopausal women Men
Vegetarians Omnivores P-value Vegetarians Omnivores P-value Vegetarians Omnivores P-value
Median p25, p75 Median p25, p75 Median p25, p75 Median p25, p75 Median p25, p75 Median p25, p75
Energy (MJ) 7.17 5.41, 9.16 6.57 5.03, 8.50 0.0014 6.67 5.26, 8.20 6.15 4.73, 7.85 <0.0001 9.04 6.86, 11.47 8.89 6.92, 11.09 0.28
Protein (% energy) 12 11, 13 13 12, 15 <0.0001 12 11, 13 13 12, 15 <0.0001 11 10, 13 13 11, 14 <0.0001
Animal protein (g) 4 2, 7 13 8, 21 <0.0001 3 1, 7 12 7, 19 <0.0001 4 2, 8 19 11, 30 <0.0001
Plant protein (g) 46 33, 59 35 25, 46 <0.0001 42 33, 53 34 26, 44 <0.0001 55 41, 71 43 33, 55 <0.0001
Fat (% energy) 26 22, 32 29 24, 34 <0.0001 24 19, 29 26 21, 31 <0.0001 22 17, 27 25 19, 31 <0.0001
SFA (g) 9 6, 13 10 7, 15 0.0019 7 5, 11 8 6, 12 <0.0001 10 6, 14 12 8, 17 <0.0001
MUFA (g) 13 9, 19 14 10, 22 0.011 11 7, 17 12 8, 18 0.051 14 8, 20 17 11, 25 <0.0001
PUFA (g) 12 7, 19 11 7, 18 0.13 10 6, 15 9 5, 15 0.15 13 8, 21 13 8, 21 0.21
Carbohydrate (% energy) 63 57, 67 59 53, 65 <0.0001 65 60, 70 62 56, 67 <0.0001 67 62, 72 63 56, 69 <0.0001
Dietary fiber (g) 23 17, 30 19 14, 26 <0.0001 21 16, 29 19 14, 26 <0.0001 24 18, 33 20 15, 27 <0.0001
Cholesterol (g) 98 39, 155 146 87, 220 <0.0001 69 24, 111 104 58, 165 <0.0001 82 31, 151 159 100, 252 <0.0001
Potassium (g) 2.2 1.6, 3.0 2.1 1.5, 2.8 0.036 2.2 1.7, 2.9 2.1 1.6, 2.8 0.059 2.4 1.8, 3.1 2.3 1.7, 2.9 0.020
Calcium (mg) 602 408, 870 514 353, 751 0.0012 626 425, 931 572 380, 833 0.0005 645 445, 909 541 376, 781 <0.0001
Magnesium (mg) 284 210, 380 244 184, 321 <0.0001 290 211, 383 258 189, 352 <0.0001 325 231, 439 286 217, 380 <0.0001
Iron (mg) 13 9, 20 11 8, 16 <0.0001 12 9, 17 11 8, 15 <0.0001 14 10, 20 12 9, 16 <0.0001
Heme iron (mg) 0 0, 0 0.1 0.0, 0.3 <0.0001 0 0, 0 0.1 0.0, 0.2 <0.0001 0 0, 0 0.2 0.1, 0.4 <0.0001
Non-heme iron (mg) 13 9, 20 11 8, 16 <0.0001 12 9, 17 10 7, 15 <0.0001 14 10, 20 11 9, 16 <0.0001
Zinc (mg) 8.1 6.1, 12 7.7 5.7, 11 0.083 8.8 6.4, 14 8.3 6, 13 0.028 11.0 8.1, 14.3 10.4 7.9, 14 0.90
Thiamin (mg) 1.4 0.8, 2.8 1.0 0.6, 1.8 <0.0001 1.5 0.8, 3.0 1.2 0.7, 2.2 <0.0001 1.8 1.1, 3.3 1.3 0.8, 2.3 <0.0001
Riboflavin (mg) 1.0 0.7, 1.9 1.1 0.7, 1.7 0.88 1.1 0.7, 2.3 1.1 0.7, 2.2 0.75 1.1 0.8, 2.0 1.2 0.8, 1.9 0.43
Niacin (mg) 20 14, 31 20 13, 30 0.64 19 12, 31 20 13, 31 0.88 20 14, 31 22 15, 33 0.043
Vitamin B6 (mg) 1.2 0.9, 2.1 1.2 0.8, 1.8 0.52 1.2 0.9, 2.8 1.2 0.8, 2.4 0.43 1.4 1.0, 2.2 1.5 1.1, 2.3 0.17
Folate (µg) 451 308, 701 403 265, 598 0.0019 488 316, 713 433 288, 656 0.0003 493 321, 709 413 280, 607 <0.0001
Vitamin B12 (µg) 1.1 0.6, 3.5 2.7 1.5, 5.6 <0.0001 1.2 0.6, 7.1 2.9 1.4, 8.9 <0.0001 1.1 0.6, 3.2 4.1 2.2, 9.7 <0.0001
Vitamin C (mg) 169 119, 245 160 109, 224 0.078 165 116, 232 164 117, 238 0.85 176 123, 243 165 116, 222 0.017
Vitamin A (mg RE) 2.37 1.47, 3.48 2.04 1.21, 3.22 0.001 2.45 1.64, 3.73 2.18 1.39, 3.39 0.0001 2.70 1.61, 3.82 2.05 1.33, 3.17 <0.0001
Fish (g) 0 0, 0 5 1, 15 <0.0001 0 0, 0 7 2, 20 <0.0001 0 0, 0 15 4, 35 <0.0001
Fresh meat (g) 0 0, 0 11 2, 34 <0.0001 0 0, 0 7 1, 19 <0.0001 0 0, 0 20 7, 49 <0.0001
Processed meat (g) 0 0, 0 1 0, 5 <0.0001 0 0, 0 1 0, 3 <0.0001 0 0, 0 2 0, 6 <0.0001
Eggs (g) 16 6, 31 24 9, 32 <0.0001 7 2, 15 16 6, 24 <0.0001 15 4, 23 18 8, 31 <0.0001
Dairy products (g) 34 4, 115 41 2, 154 0.31 36 2, 144 50 1, 168 0.12 46 1, 161 46 1, 154 0.71
Soy products (g) 96 53, 176 68 30, 112 <0.0001 88 41, 144 52 23, 104 <0.0001 104 53, 176 63 27, 112 <0.0001
Total vegetables (g) 430 280, 650 380 250, 570 0.0013 440 290, 660 400 240, 590 <0.0001 470 300, 650 370 230, 550 <0.0001
Green leafy vegetables (g) 160 86, 200 110 71, 200 0.0014 200 100, 300 160 80, 200 <0.0001 170 80, 290 100 57, 200 <0.0001
Cruciferous vegetables (g) 86 43, 170 80 43, 150 0.34 86 43, 170 86 43, 160 0.28 100 43, 200 80 43, 150 0.0083
Other vegetables (g) 160 91, 270 150 78, 240 0.0019 140 75, 250 130 67, 220 0.0005 160 97, 260 130 70, 210 <0.0001
Fruits (g) 120 68, 240 120 60, 240 0.18 120 68, 240 120 64, 240 0.86 120 68, 240 120 60, 240 0.37
Nuts (g) 2 0, 9 1 0, 3 <0.0001 2 0, 7 1 0, 5 <0.0001 2 0, 8 2 0, 5 0.0006
Whole grain (% total grain) 28 12, 51 20 6, 42 <0.0001 32 12, 60 27 11, 52 0.02 20 8, 46 15 4, 37 <0.0001
Coffee (ml) 13 0, 129 21 0, 143 0.16 0 0, 25 0 0, 43 0.015 5 0, 36 8 0, 57 0.06
Tea (ml) 33 0, 286 100 8, 350 0.00013 0 0, 71 10 0, 214 <0.0001 86 0, 408 151 0, 504 0.0007
Sweeten beverage (ml) 0 0, 0 0 0, 8 0.02 0 0, 0 0 0, 0 0.28 0 0, 0 0 0, 12 0.0131

SFA  =  saturated fatty acid, MUFA  =  monounsaturated fatty acid, PUFA  =  polyunsaturated fatty acid, p25  =  25th percentile, p75  =  75th percentile.

Vegetarian diet is negatively associated with both IFG and diabetes in men, pre-menopausal, and menopausal women (Table 4). The protective association for diabetes is even stronger without controlling for BMI in men (OR: 0.43, 95% CI: 0.24–0.77), in pre-menopausal women (OR: 0.21, 95% CI: 0.05–0.97), and in menopausal women (OR: 0.23, 95% CI: 0.14–0.37). This association in pre-menopausal women was no longer statistical significant after adjusting for BMI as there were only 16 cases of diabetes in this group. BMI is highly correlated with waist circumference (the correlation coefficients r for male: 0.84, female: 0.74) and body fat (r for male: 0.76, female: 0.84). When either waist circumference or body fat was adjusted instead of BMI, similar results were found (data not shown). Family history of diabetes is significantly associated with diabetes but not with IFG. In men, current smoker (versus never smoker) is associated with diabetes, though not significant due to a low number of current smokers. In women, higher education (versus elementary school) is negatively associated with diabetes.

Table 4. Polytomous logistic regression analysis of the association between diet and impaired glucose metabolism.

Men Pre-menopausal women Menopausal women
IFG Diabetes IFG Diabetes IFG Diabetes
OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI
Age 1.05 1.03, 1.06 1.08 1.05, 1.10 1.10 1.04, 1.16 1.08 0.96, 1.22 1.03 1.01, 1.05 1.08 1.05, 1.11
BMI 1.12 1.07, 1.17 1.14 1.07, 1.22 1.13 1.05, 1.20 1.25 1.11, 1.42 1.14 1.10, 1.19 1.13 1.07, 1.20
Family history of diabetes vs none 1.29 0.94, 1.76 5.15 3.42, 7.75 0.92 0.55, 1.54 3.54 1.20, 10.44 1.01 0.75, 1.36 5.19 3.40, 7.93
Vegetarian vs omnivorous diet 0.66 0.46, 0.95 0.49 0.28, 0.89 0.60 0.35, 1.04 0.26 0.06, 1.21 0.73 0.56, 0.95 0.25 0.15, 0.42
Education
Secondary vs elementary or lower 1.06 0.73, 1.53 1.65 0.93, 2.93 1.42 0.65, 3.11 0.26 0.08, 0.84 0.88 0.66, 1.19 0.56 0.35, 0.89
College or higher vs elementary or lower 0.87 0.58, 1.32 1.15 0.60, 2.19 0.60 0.21, 1.67 0.10 0.01, 0.89 0.68 0.43, 1.07 0.65 0.35, 1.22
LTPA per week
31–180 min versus 30 min or less 0.82 0.57, 1.17 0.82 0.49, 1.39 0.79 0.46, 1.38 0.74 0.22, 2.49 0.91 0.66, 1.26 1.07 0.62, 1.86
> = 180 min vs 30 min or less 0.88 0.63, 1.24 0.87 0.53, 1.43 0.58 0.28, 1.18 0.93 0.22, 3.91 0.82 0.59, 1.13 1.52 0.91, 2.52
Smoking
Current smokers vs never 0.67 0.31, 1.43 1.36 0.52, 3.52 - - - - - - - -
Past smokers vs never 0.71 0.51, 0.99 1.01 0.64, 1.60 - - - - - - - -
Alcohol drinking
Current drinkers vs never 1.38 0.85, 2.26 0.88 0.41, 1.87 - - - - - - - -
Past drinkers vs never 1.23 0.86, 1.76 1.00 0.60, 1.67 - - - - - - - -

IFG  =  impaired fasting glucose. OR  =  odds ratio. BMI  =  body mass index. LTPA  =  leisure time physical activity.

As diabetes patients are often advised to change diet and lifestyle, we conducted a sensitivity analysis excluding those who self reported history of diabetes at baseline (n = 216), and counted only diabetes cases that were newly detected in this present study (n = 41). We found a similar protective association between vegetarian diet and diabetes in menopausal women (OR: 0.34, 95% CI: 0.12–0.95). The results were insignificant in men and pre-menopausal women due to limited number of cases of new diabetes.

Discussion

In this Buddhist population consuming a plant-based diet with little meat and fish, true vegetarians who completely avoid animal flesh, while eating more soy, vegetables, nuts and whole grain, have lower odds for IFG and diabetes, after accounting for various confounders, risk factors, and BMI. The protective association is consistent in men and women although the association in pre-menopausal women was not significant due to a small number of diabetes cases.

Our result is consistent with the Adventist Health Study 2 (AHS-2), which found lower prevalence [3] and incidence [4] of diabetes in vegetarians. Similar to AHS-2 [17], we found vegetarians consumed a higher percentage of energy as carbohydrate, a lower percentage as fat and protein, and higher levels of plant protein, fiber, iron, and magnesium compared with omnivores in respective studies. We did not analyze subtypes of vegetarians (vegan, lacto-ovo-, or pesco-), as the AHS-2 did, since most of our vegetarians were of lacto-ovo type, with a small number of vegans (n = 69), and there were no cases of diabetes found within the vegan group. Consumption of eggs and dairy, however, was low, suggesting that the vegetarian diet in our population may resemble that of a vegan diet more than a typical Western lacto-ovo vegetarian diet when compared with AHS-2 [17] and EPIC-Oxford [18].

Despite similar or higher energy consumption, our vegetarians had lower BMI than omnivores. A similar finding is also observed in AHS-2 [3], [17]. Energy content of foods estimated by Atwater factors (for food composition tables and food labels) may not accurately reflect the actual energy utilized by the body due to the complexity in human digestion, and the variation in bioavailability as influenced by cooking and food processing methods, cell wall structures, and microbiome of the individual intestinal track [19][21].

The association between meat and diabetes has been reported recently in a large prospective study of European adults and a previous meta-analysis of prospective cohorts [22], [23], but not in a Shanghai study [24]. Although the Shanghainese population has a more similar ethnicity, the diabetes ascertainment depended on self-reported data; this could be a limitation for caution because the percent of undiagnosed diabetes (64% in urban China, 2000 to 2001) [25] is much higher than most Western countries (29% for the US, NHANES 1999–2000) [26]. Heme iron in meat had been suggested as a potential mediator leading to diabetes, as iron overload produces oxidative stress and induces insulin resistance [27], [28]. Although vegetarians had higher iron intake in both our study and in AHS-2, the iron is of non-heme form, which is absorbed to a lesser degree than that of heme iron from meat [29].

The higher intake of green leafy vegetables and magnesium may potentially contribute to the protective association between vegetarian diet and diabetes. Studies suggest that consuming more leafy green vegetables and a greater variety of fruits and vegetable are associated lower risk of diabetes in Europeans [30], [31]. A dietary pattern characterized by fruits, vegetables, and soy has also been associated with lower risk of diabetes in non-smoking Chinese [32]. A meta-analysis found magnesium to be protective of diabetes, and suggested that magnesium deficiency may induce insulin resistance [33].

Strength and limitation

While our findings suggest a negative association between a vegetarian diet and diabetes/IFG, the temporal association is unclear due to the cross-sectional nature of the study. Although we have accounted for several confounders in our models, it is likely that other residual confounders still remain. The null association between LTPA and diabetes may have been influenced by reverse causation, as diabetes individuals may have increased physical activities in order to manage their disease. The measurements of body fat by Bioelectrical Impedance Analysis should be interpreted with caution as it has a poor accuracy for estimating absolute body composition [34].

The current study also has several strengths. The questionnaires were interviewed instead of self-administered – this enabled us to clarify questions, engage participants, and minimize potential inaccuracy due to fatigue or missing data. In addition, our study participants were relatively homogenous with similar religion and a very low proportion of smokers and alcohol-drinkers. This may minimize potential unadjusted confounders.

Our finding suggests that a vegetarian diet characterized by complete avoidance of meat and fish, and higher intake of soy products, vegetables, nuts, and whole grain may be more beneficial than an omnivorous diet with a moderate portion of meat and fish. Future follow-up on disease outcomes of this cohort will be needed to ascertain this finding and to delineate the impact of dietary components on the development of diabetes.

Funding Statement

The study was supported by a grant (TCRD-I9605-02) from the Buddhist Tzu Chi General Hospital in Taiwan. Tzu Chi Hospital's website: http://www.tzuchi.com.tw/tzuchi/mainpage/Default.aspx. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1. Zhai F, Wang H, Du S, He Y, Wang Z, et al. (2009) Prospective study on nutrition transition in China. Nutr Rev 67 Suppl 1S56–61. [DOI] [PubMed] [Google Scholar]
  • 2. Chan JC, Malik V, Jia W, Kadowaki T, Yajnik CS, et al. (2009) Diabetes in Asia: epidemiology, risk factors, and pathophysiology. JAMA 301: 2129–40. [DOI] [PubMed] [Google Scholar]
  • 3. Tonstad S, Butler T, Yan R, Fraser GE (2009) Type of vegetarian diet, body weight, and prevalence of type 2 diabetes. Diabetes Care 32: 791–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Tonstad S, Stewart K, Oda K, Batech M, Herring RP, et al. (2013) Vegetarian diets and incidence of diabetes in the Adventist Health Study-2. Nutr Metab Cardiovasc Dis 23: 292–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Barnard ND, Cohen J, Jenkins DJ, Turner-McGrievy G, Gloede L, et al. (2009) A low-fat vegan diet and a conventional diabetes diet in the treatment of type 2 diabetes: a randomized, controlled, 74-wk clinical trial. Am J Clin Nutr 89: 1588S–1596S. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Kahleova H, Matoulek M, Malinska H, Oliyarnik O, Kazdova L, et al. (2011) Vegetarian diet improves insulin resistance and oxidative stress markers more than conventional diet in subjects with Type 2 diabetes. Diabet Med 28: 549–59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Hung CJ, Huang PC, Li YH, Lu SC, Ho LT, et al. (2006) Taiwanese vegetarians have higher insulin sensitivity than omnivores. Br J Nutr 95: 129–35. [DOI] [PubMed] [Google Scholar]
  • 8. Kuo CS, Lai NS, Ho LT, Lin CL (2004) Insulin sensitivity in Chinese ovo-lactovegetarians compared with omnivores. Eur J Clin Nutr 58: 312–6. [DOI] [PubMed] [Google Scholar]
  • 9. Chiang JK, Lin YL, Chen CL, Ouyang CM, Wu YT, et al. (2013) Reduced risk for metabolic syndrome and insulin resistance associated with ovo-lacto-vegetarian behavior in female buddhists: a case-control study. PLoS One 8: e71799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Assari S (2013) Race and Ethnicity, Religion Involvement, Church-based Social Support and Subjective Health in United States: A Case of Moderated Mediation. Int J Prev Med 4: 208–17. [PMC free article] [PubMed] [Google Scholar]
  • 11.Seawell AH, Toussaint LL, Cheadle AC. (2013) Prospective associations between unforgiveness and physical health and positive mediating mechanisms in a nationally representative sample of older adults. Psychol Health: in press. [DOI] [PubMed]
  • 12.Chiu TH, Huang HY, Chen KJ, Wu YR, Chiu JP, et al.. (2013) Relative validity and reproducibility of a quantitative FFQ for assessing nutrient intakes of vegetarians in Taiwan. Public Health Nutr: in press. [DOI] [PMC free article] [PubMed]
  • 13.Nutrient Composition Data Bank for Food in Taiwan Area. Taipei: Department of Health, 1988.
  • 14. Balder HF, Vogel J, Jansen MC, Weijenberg MP, van den Brandt PA, et al. (2006) Heme and chlorophyll intake and risk of colorectal cancer in the Netherlands cohort study. Cancer Epidemiol Biomarkers Prev 15: 717–25. [DOI] [PubMed] [Google Scholar]
  • 15. ADA (2010) Diagnosis and classification of diabetes mellitus. Diabetes Care 33 Suppl 1S62–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, et al. (2005) Diagnosis and management of the metabolic syndrome. An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Executive summary. Cardiol Rev 13: 322–7. [PubMed] [Google Scholar]
  • 17.Rizzo NS, Jaceldo-Siegl K, Sabate J, Fraser GE. (2013) Nutrient Profiles of Vegetarian and Nonvegetarian Dietary Patterns. J Acad Nutr Diet: in press. [DOI] [PMC free article] [PubMed]
  • 18. Davey GK, Spencer EA, Appleby PN, Allen NE, Knox KH, et al. (2003) EPIC-Oxford: lifestyle characteristics and nutrient intakes in a cohort of 33 883 meat-eaters and 31 546 non meat-eaters in the UK. Public Health Nutr 6: 259–69. [DOI] [PubMed] [Google Scholar]
  • 19. Carmody RN, Weintraub GS, Wrangham RW (2011) Energetic consequences of thermal and nonthermal food processing. Proc Natl Acad Sci U S A 108: 19199–203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Novotny JA, Gebauer SK, Baer DJ (2012) Discrepancy between the Atwater factor predicted and empirically measured energy values of almonds in human diets. Am J Clin Nutr 96: 296–301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Wollstonecroft MM, Ellis PR, Hillman GC, Fuller DQ, Butterworth PJ. (2012) A calorie is not necessarily a calorie: technical choice, nutrient bioaccessibility, and interspecies differences of edible plants. Proc Natl Acad Sci U S A 109 : E991; author reply E992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Aune D, Ursin G, Veierod MB (2009) Meat consumption and the risk of type 2 diabetes: a systematic review and meta-analysis of cohort studies. Diabetologia 52: 2277–87. [DOI] [PubMed] [Google Scholar]
  • 23. The-InterAct-Consortium (2013) Association between dietary meat consumption and incident type 2 diabetes: the EPIC-InterAct study. Diabetologia 56: 47–59. [DOI] [PubMed] [Google Scholar]
  • 24. Villegas R, Shu XO, Gao YT, Yang G, Cai H, et al. (2006) The association of meat intake and the risk of type 2 diabetes may be modified by body weight. Int J Med Sci 3: 152–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Gu D, Reynolds K, Duan X, Xin X, Chen J, et al. (2003) Prevalence of diabetes and impaired fasting glucose in the Chinese adult population: International Collaborative Study of Cardiovascular Disease in Asia (InterASIA). Diabetologia 46: 1190–8. [DOI] [PubMed] [Google Scholar]
  • 26. Gregg EW, Cadwell BL, Cheng YJ, Cowie CC, Williams DE, et al. (2004) Trends in the prevalence and ratio of diagnosed to undiagnosed diabetes according to obesity levels in the U.S. Diabetes Care. 27: 2806–12. [DOI] [PubMed] [Google Scholar]
  • 27. Rajpathak SN, Crandall JP, Wylie-Rosett J, Kabat GC, Rohan TE, et al. (2009) The role of iron in type 2 diabetes in humans. Biochim Biophys Acta 1790: 671–81. [DOI] [PubMed] [Google Scholar]
  • 28. Hua NW, Stoohs RA, Facchini FS (2001) Low iron status and enhanced insulin sensitivity in lacto-ovo vegetarians. Br J Nutr 86: 515–9. [DOI] [PubMed] [Google Scholar]
  • 29. Craig WJ, Mangels AR (2009) Position of the American Dietetic Association: vegetarian diets. J Am Diet Assoc 109: 1266–82. [DOI] [PubMed] [Google Scholar]
  • 30. Cooper AJ, Forouhi NG, Ye Z, Buijsse B, Arriola L, et al. (2012) Fruit and vegetable intake and type 2 diabetes: EPIC-InterAct prospective study and meta-analysis. Eur J Clin Nutr 66: 1082–1092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Cooper AJ, Sharp SJ, Lentjes MA, Luben RN, Khaw KT, et al. (2012) A prospective study of the association between quantity and variety of fruit and vegetable intake and incident type 2 diabetes. Diabetes Care 35: 1293–300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Odegaard AO, Koh WP, Butler LM, Duval S, Gross MD, et al. (2011) Dietary patterns and incident type 2 diabetes in chinese men and women: the singapore chinese health study. Diabetes Care 34: 880–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Dong JY, Xun P, He K, Qin LQ (2011) Magnesium intake and risk of type 2 diabetes: meta-analysis of prospective cohort studies. Diabetes Care 34: 2116–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Wells JC, Fewtrell MS (2006) Measuring body composition. Arch Dis Child 91: 612–7. [DOI] [PMC free article] [PubMed] [Google Scholar]

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