Effect of whole grains on insulin sensitivity in overweight hyperinsulinemic adults

被引:369
作者
Pereira, MA
Jacobs, DR
Pins, JJ
Raatz, SK
Gross, MD
Slavin, JL
Seaquist, ER
机构
[1] Harvard Univ, Med Sch, Dept Pediat, Cambridge, MA 02138 USA
[2] Childrens Hosp, Dept Med, Boston, MA USA
[3] Univ Minnesota, Gen Clin Res Ctr, Dept Food Sci & Nutr, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Gen Clin Res Ctr, Dept Med, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Gen Clin Res Ctr, Dept Family Practice, Minneapolis, MN 55455 USA
[6] Univ Oslo, Inst Nutr Res, N-0316 Oslo, Norway
关键词
carbohydrate; diet; whole grains; nutrition; insulin; hyperinsulinemia; type; 2; diabetes; insulin response;
D O I
10.1093/ajcn/75.5.848
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Epidemiologic studies have found whole-grain intake to be inversely associated with the risk of type 2 diabetes and heart disease. Objective: We tested the hypothesis that whole-grain consumption improves insulin sensitivity in overweight and obese adults. Design: This controlled experiment compared insulin sensitivity between diets (55% carbohydrate, 30% fat) including 6-10 servings/d of breakfast cereal, bread, rice, pasta, muffins, cookies, and snacks of either whole or refined grains. Total energy needs were estimated to maintain body weight. Eleven over-weight or obese [body mass index (in kg/m(2)): 27-36] hyperinsulinemic adults aged 25-56 y participated in a randomized crossover design. At the end of each 6-wk diet period, the subjects consumed 355 mL (12 oz) of a Liquid mixed meal, and blood samples were taken over 2 h. The next day a euglycemic hyperinsulinemic clamp test was administered. Results: Fasting insulin was 10% lower during consumption of the whole-grain than during consumption of the refined-grain diet (mean difference: -15 +/- 5.5 pmol/L; P = 0.03). After the whole-grain diet, the area under the 2-h insulin curve tended to be lower (-8832 pmol(.)min/L; 95% CI: -18720, 1062) than after the refined-grain diet. The rate of glucose infusion during the final 30 min of the clamp test was higher after the whole-grain diet (0.07 X 10(-4) mmol(.)kg(-1.)min(-1) per pmol/L; 95% Cl: 0.003 X 10(-4), 0.144 X 10(-4)). Conclusion: Insulin sensitivity may be an important mechanism whereby whole-grain foods reduce the risk of type 2 diabetes and heart disease.
引用
收藏
页码:848 / 855
页数:8
相关论文
共 65 条
[1]  
[Anonymous], SAS STAT US GUID VER
[2]   A DATA-BASED APPROACH TO DIET QUESTIONNAIRE DESIGN AND TESTING [J].
BLOCK, G ;
HARTMAN, AM ;
DRESSER, CM ;
CARROLL, MD ;
GANNON, J ;
GARDNER, L .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1986, 124 (03) :453-469
[3]   RELATIONSHIP BETWEEN DEGREE OF OBESITY AND INVIVO INSULIN ACTION IN MAN [J].
BOGARDUS, C ;
LILLIOJA, S ;
MOTT, DM ;
HOLLENBECK, C ;
REAVEN, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (03) :E286-E291
[4]   Beneficial effects of high dietary fiber intake in patients with type 2 diabetes mellitus [J].
Chandalia, M ;
Garg, A ;
Lutjohann, D ;
von Bergmann, K ;
Grundy, SM ;
Brinkley, LJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (19) :1392-1398
[5]   RISK-FACTORS FOR NIDDM IN WHITE-POPULATION - PARIS PROSPECTIVE-STUDY [J].
CHARLES, MA ;
FONTBONNE, A ;
THIBULT, N ;
WARNET, JM ;
ROSSELIN, GE ;
ESCHWEGE, E .
DIABETES, 1991, 40 (07) :796-799
[6]  
DEFRONZO RA, 1979, AM J PHYSIOL, V237, pE214
[7]   INTERNATIONAL TABLES OF GLYCEMIC INDEX [J].
FOSTERPOWELL, K ;
MILLER, JB .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1995, 62 (04) :871S-890S
[8]   A POSSIBLE PROTECTIVE EFFECT OF NUT CONSUMPTION ON RISK OF CORONARY HEART-DISEASE - THE ADVENTIST HEALTH STUDY [J].
FRASER, GE ;
SABATE, J ;
BEESON, WL ;
STRAHAN, TM .
ARCHIVES OF INTERNAL MEDICINE, 1992, 152 (07) :1416-1424
[9]   Are increased plasma nonesterified fatty acid concentrations a risk marker for coronary heart disease and other chronic diseases? [J].
Frayn, KN ;
Williams, CM ;
Arner, P .
CLINICAL SCIENCE, 1996, 90 (04) :243-253
[10]   The effect of low-glycemic carbohydrate on insulin and glucose response in vivo and in vitro in patients with coronary heart disease [J].
Frost, G ;
Keogh, B ;
Smith, D ;
Akinsanya, K ;
Leeds, A .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (06) :669-672