Dietary intake and biochemical, hematologic, and immune status of vegans compared with nonvegetarians

Citation
Eh. Haddad et al., Dietary intake and biochemical, hematologic, and immune status of vegans compared with nonvegetarians, AM J CLIN N, 70(3), 1999, pp. 586S-593S
Citations number
40
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF CLINICAL NUTRITION
ISSN journal
00029165 → ACNP
Volume
70
Issue
3
Year of publication
1999
Supplement
S
Pages
586S - 593S
Database
ISI
SICI code
0002-9165(199909)70:3<586S:DIABHA>2.0.ZU;2-P
Abstract
Dietary and nutritional status of individuals habitually consuming a vegan diet was evaluated by biochemical, hematologic, and immunologic measures in comparison with a nonvegetarian group. On the basis of 4-d dietary records , the intake of female and male vegans tended to be lower in fat, saturated fat, monounsaturated fat, and cholesterol and higher in dietary fiber than that of vegetarians. With computed food and supplement intakes, vegan diet s provided significantly higher amounts of ascorbate, folate, magnesium, co pper, and manganese in both female and male participants. The body mass ind ex (BMI; in kg/m(2)) of the vegans was significantly lower than that of the nonvegetarians and 9 of the 25 vegans had a BMI <19. Serum ferritin concen trations were significantly lower in vegan men but iron and zinc status did not differ between the sexes. Mean serum vitamin B-12 and methylmalonic ac id concentrations did not differ; however, 10 of the 25 vegans showed a vit amin B-12 deficit manifested by macrocytosis, circulating vitamin B-12 conc entrations <150 pmol/L, or serum methylmalonic acid >376 nmol/L. Vegans had significantly lower leukocyte, lymphocyte, and platelet counts and lower c oncentrations of complement factor 3 and blood urea nitrogen but higher ser um albumin concentrations. Vegans did not differ from nonvegetarians in fun ctional immunocompetence assessed as mitogen stimulation or natural killer cell cytotoxic activity.