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(Journal of Nutrition. 2000;130:280S-283S.)
© 2000 The American Society for Nutritional Sciences


Supplement

Dietary Glycemic Index and Obesity1 ,2

David S. Ludwig

Division of Endocrinology, Children’s Hospital, Boston, MA 02115


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
Obesity is among the most important medical problems in America today. Currently, ~1 in 4 children and 1 in 2 adults are overweight, prevalence rates that have increased by 50% since the 1960s. In an attempt to combat this problem, the Federal government and various official medical agencies have advocated decreasing intake of total fat and sugar, while increasing consumption of "complex carbohydrate." Despite a recent reduction in fat consumption to near the recommended 30% of total energy, rates of obesity have continued to rise, suggesting that other dietary factors may play a critical role in body weight regulation. One such factor may be glycemic index. This review examines the physiologic effects of glycemic index and argues for the need for controlled clinical trials of a low glycemic index diet in the treatment of obesity.


KEY WORDS: • glycemic index • obesity • diet • dietary carbohydrate • blood glucose


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
Obesity, a condition characterized by excessive body fat, is commonly believed to result in part from excessive fat consumption. Partly for this reason, the U.S. government (U.S. Department of Health and Human Services 1988Citation ), the American Heart Association (1996)Citation and the American Diabetes Association (1997)Citation recommend a low fat diet to prevent and treat obesity. However, the effect of dietary fat on body fat has been questioned in recent years (Katan et al. 1997Citation , Larson et al. 1996Citation , Willett 1998Citation ). Epidemiologic studies do not show consistently that high levels of dietary fat promote weight gain (Kant et al. 1995Citation , Larson et al. 1996Citation , Ludwig et al 1999aCitation , Nicklas 1995Citation ), and weight loss with consumption of low fat diets is characteristically modest and transient (Katan et al. 1997Citation , Lissner and Heitmann 1995Citation ). Moreover, mean fat intake in the United States has decreased since the 1960s, from 42% to ~34% of dietary energy (Lenfant and Ernst 1994Citation , Nicklas 1995Citation , Stephen and Wald 1990Citation ), whereas the prevalence of overweight has risen to 1 in 4 children and 1 in 2 adults (Flegal et al. 1998Citation , Troiano and Flegal 1998Citation ). These observations suggest that dietary factors other than fat play an important role in body weight regulation.


    The glycemic index
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
The concept of glycemic index (GI) was proposed by Jenkins and colleagues in 1981 to characterize the rate of carbohydrate absorption after a meal (Jenkins et al. 1981Citation ). GI is defined as the area under the glucose response curve after consumption of 50 g carbohydrate from a test food divided by the area under the curve after consumption of 50 g carbohydrate from a control food, either white bread or glucose (Wolever et al. 1991Citation ). Over the past two decades, the GI of most commonly consumed carbohydrate-containing foods has been measured (Foster-Powell and Miller 1995Citation ).

Many factors together, including carbohydrate type, fiber, protein, fat, food form and method of preparation, determine the GI of a particular food (Bjorck et al. 1994Citation , Estrich et al. 1967Citation , Welch et al. 1987Citation , Wolever et al. 1991Citation ). Contrary to common belief, carbohydrate digestion rate, and therefore glycemic response, is not related to saccharide chain length. For example, Wahlqvist and colleagues demonstrated similar changes in blood glucose, plasma insulin and plasma fatty acid concentrations after consumption of glucose as a monosaccharide, disaccharide, oligosaccharide or polysaccharide (starch) (Wahlqvist et al. 1978Citation ). In fact, sugar may have a lower GI than some "complex carbohydrates" (Foster-Powell and Miller 1995Citation ) as demonstrated by an improvement in glycemic control among subjects with Type 1 diabetes mellitus after isoenergetic substitution of sucrose for starch (Rickard et al. 1998Citation ). In general, refined grain products and potato have a high GI, exceeding that of table sugar by up to 50%, whereas most vegetables, fruits and legumes have a low GI.


    Low fat vs. low GI
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
Because protein intake for most individuals remains within a fairly narrow range, reductions in dietary fat tend to cause a compensatory rise in carbohydrate consumption. An increase in carbohydrate intake has in fact been observed in the U.S. since the 1970s (Nicklas 1995Citation , Popkin et al. 1992Citation , Stephen et al. 1995Citation ). The carbohydrate that replaces fat in low fat diets is typically high in GI. According to data from the Department of Agriculture, >80% of the carbohydrate consumed by children ages 2–18 y would have a GI equal to or greater than that of table sugar (Subar et al. 1998Citation ). Moreover, carbohydrate absorption rate (and therefore GI) is increased after a low fat meal because fat acts to delay gastric emptying (Estrich et al. 1967Citation , Welch et al. 1987Citation ). Thus, the GI of the American diet has probably increased in recent years. Might this increase have contributed to the rising prevalence of obesity?


    Effects of GI on appetite
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
To date, at least 16 studies have examined the effects of GI on appetite in humans (Table 1Citation ). For example, Leathwood and Pollet (1988)Citation found lower blood glucose levels and slower return of hunger after meals with bean puree (a low GI starch) compared with meals with potato (a high GI starch). Holt and colleagues showed that glycemic and insulinemic responses to various breakfast cereals are inversely related to satiety score (Holt et al. 1992Citation ). In fact, all but one of these 16 studies demonstrated increased satiety, delayed return of hunger or decreased ad libitum food intake after low compared with high GI foods.


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Table 1. Studies comparing glycemic response with changes in hunger, satiety or energy intake

 
To explore the physiologic events that might relate GI to appetite, we compared the effects of three isocaloric test meals differing in GI during three separate 24-h admissions (Ludwig et al. 1999bCitation ). The low GI meal was a vegetable omelet with fruit, the medium GI meal was "steel-cut" oatmeal (a preparatory method that slows digestion rate) and the high GI meal was "instant" oatmeal. The medium and high GI meals were composed of similar foods to control for the effects of other potentially confounding dietary factors, whereas the low GI meal was designed to increase the range of GI in the study beyond that that could be achieved by manipulating food structure alone. Subjects included 12 obese teenage boys, at least 120% of ideal body weight, but otherwise in good health.

After the test breakfasts, area under the blood glucose curve differed between the high, medium and low GI meals as expected [284, 141 and 76.6 (mmol·min)/L, respectively]. The rapid absorption of glucose from the high GI meal resulted in relatively high insulin and low glucagon concentrations. These hormonal changes would be expected to promote uptake of glucose in muscle, liver and fat tissue, restrain hepatic release of glucose and inhibit lipolysis. As a consequence, access to the two major metabolic fuels was effectively impaired in the postabsorptive period, as shown by a "reactive hypoglycemia" (difference in glucose nadir of -0.5 mmol/L, P = 0.02) and lower free fatty acid concentrations 3 to 5 h after the high compared with the low GI meals. Subjects also consumed significantly more energy after the high GI (5.8 MJ) compared with the medium GI (3.8 MJ, P < 0.05) or the low GI (3.2 MJ, P = 0.01) test lunches.


    Obesity
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
High GI foods elicit, calorie for calorie, higher insulin levels and c-peptide excretion than low GI foods (Haber et al. 1977Citation , Jenkins et al. 1987Citation , Wolever and Bolognesi 1996Citation ). The functional hyperinsulinemia associated with high GI diets may promote weight gain by preferentially directing nutrients away from oxidation in muscle and toward storage in fat. Cusin and colleagues reported that rats pretreated with insulin showed increased glucose utilization in white adipose tissue, but decreased utilization in muscle, changes that were associated with increased food intake and weight gain (Cusin et al. 1992Citation ). In humans, high acute insulin secretion after intravenous glucose tolerance tests predicts weight gain among glucose-tolerant offspring of parents with diabetes mellitus (Sigal et al. 1997Citation ). Pima Indian children with elevated fasting insulin levels gain prospectively more weight than those children with normal insulin levels (Odeleye et al. 1997Citation ). Indeed, excessive weight gain is recognized to be a complication of insulin treatment in Type 2 diabetes mellitus (UK Prospective Diabetes Study Group 1998Citation ) and intensive insulin treatment in Type I diabetes mellitus (Diabetes Control and Complication Trial Group 1988Citation ). Thus, hormonal responses to a high GI diet appear to lower circulating levels of metabolic fuels, stimulate hunger and favor storage of fat, events that may promote excessive weight gain.


    SUMMARY
 TOP
 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 
The concept that "a calorie is a calorie" underlies most conventional weight loss strategies. According to this principle, obesity results from an imbalance between energy intake and expenditure. The proposed cure is to eat less and exercise more. However, calorie-restricted, low fat diets have poor long-term effectiveness in the outpatient setting. In a sense, these diets may constitute symptomatic treatment that does not address the physiologic drives to overeat. From a hormonal standpoint, all calories are not alike.

The optimal diet for the prevention and treatment of obesity, if one exists, remains to be determined. In particular, the effects of GI on body weight regulation must be explored in long-term clinical trials. Nevertheless, a growing body of theoretical and experimental work suggests that diets designed to lower the insulin response to ingested carbohydrate (e.g., low GI) may improve access to stored metabolic fuels, decrease hunger, and promote weight loss. Such a diet would contain abundant quantities of vegetables, fruits and legumes, moderate amounts of protein and healthful fats, and decreased intake of refined grain products, potato and concentrated sugars (Fig. 1Citation ). Indeed, this diet bears a close resemblance to that consumed by human ancestors over the last several hundred thousand years (Eaton and Konner 1985Citation ). Finally, reductions in dietary GI may also lower the risks for various conditions associated with hyperinsulinemia, such as diabetes mellitus (Salmeron et al. 1997Citation ) and cardiovascular disease (Frost et al. 1999Citation , Jenkins et al. 1985Citation , Lamarche et al. 1998Citation ).



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Figure 1. A low glycemic index "pyramid."

 


    FOOTNOTES
 
1 Presented at the symposium entitled "Dietary Composition and Obesity: Do We Need to Look Beyond Dietary Fat?" as part of the Experimental Biology 99 meeting held April 17–21 in Washington, DC. This symposium was sponsored by the American Society for Nutritional Sciences and was supported in part by an educational grant from the ILSI Research Foundation. The proceedings of this symposium are published as a supplement to The Journal of Nutrition. Guest editors for this supplement were Susan R. Roberts, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA and Melvin B. Heyman, University of California, San Francisco, CA.

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2 Supported by grants from the Charles H. Hood Foundation, the Children’s Hospital League and the National Institutes of Health (1K08 DK02440).

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 ABSTRACT
 INTRODUCTION
 The glycemic index
 Low fat vs. low...
 Effects of GI on...
 Obesity
 SUMMARY
 REFERENCES
 

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