- Open Access
Serum leptin concentrations are not related to dietary patterns but are related to sex, age, body mass index, serum triacylglycerol, serum insulin, and plasma glucose in the US population
© Ganji et al; licensee BioMed Central Ltd. 2009
- Received: 31 August 2008
- Accepted: 14 January 2009
- Published: 14 January 2009
Leptin is known to play a role in food intake regulation. The aim of this study was to investigate the relation between serum leptin concentrations and dietary patterns and demographic, lifestyle, and health factors in the US population.
Data from the third National Health and Nutrition Examination Survey, 1988–1994 were used to study the association between fasting serum leptin and dietary patterns, sex, race-ethnicity, smoking, age, energy and alcohol intakes, body mass index (BMI), plasma glucose, serum triacylglycerol, and serum insulin in 4009 individuals. Factor analysis was used to derive three principle factors and these were labeled as Vegetable, Fruit, and Lean Meat, Western, and Mixed dietary patterns.
Serum leptin concentrations were significantly higher in Vegetable, Fruit, and Lean Meat (8.5 fg/L) and Mixed patterns (8.0 fg/L) compared to Western pattern (6.29 fg/L) (P < 0.0001). When analysis was adjusted for confounding variables, no significant association was observed between serum leptin and dietary patterns (P = 0.22). Multivariate adjusted serum leptin concentrations were significantly associated with sex (higher in women than in men; β = -1.052; P < 0.0001), age (direct relation, β = 0.006, P < 0.0001), BMI, (direct relation, β = 0.082, P < 0.0001), fasting plasma glucose (inverse relation, β = -0.024, P = 0.0146), serum triacylglycerol (direct relation, β = 0.034, P = 0.0022), and serum insulin (direct relation, β = 0.003, P < 0.0001) but not with race-ethnicity (P = 0.65), smoking (P = 0.20), energy intake (P = 0.42), and alcohol intake (P = 0.73).
In this study, serum leptin was not independently associated with dietary patterns. Sex, age, BMI, serum triacylglycerol, plasma glucose, and serum insulin are independent predictors of serum leptin concentrations.
- Dietary Pattern
- Food Frequency Questionnaire
- Food Group
- Mexican American
- Mobile Examination Center
Leptin (16 kDa protein), a product of the obesity gene (Ob/Ob), has generated interest among researchers to examine its role in obesity. Leptin is synthesized and secreted by adipocytes. Circulating leptin concentrations are related to the body fat mass . Leptin has been known to play a role in regulation of energy expenditure and food intake. When energy intake chronically exceeds energy expenditure, the expanding body fat mass secretes leptin in proportion to energy overload. On the other hand, decrease in circulating leptin activates a response to starvation and indicate inadequate amounts of fat energy stored in the adipose tissue . Thus, diet and dietary factors play a direct or indirect role in modulating circulating leptin concentrations.
Although fat mass is directly related to leptin expression, other factors such as alcohol consumption, cigarette smoking, sex, and race-ethnicity are also associated with serum leptin concentrations [3–7]. A few studies documented the role of diet and nutrients in modulating circulating leptin concentrations [8–12]. Reduced carbohydrate intake rather than reduced fat intake has lowered serum leptin in obese humans . Havel et al  reported decreased leptin concentration after ingestion of high fat, low-carbohydrate diet. Others observed no association between macronutrient and serum leptin [13–15].
Several recently published epidemiological studies have characterized individual's diet using factor analysis [16–20]. In factor analysis, foods are separated into food groups based on correlations between foods (factors). Each person receives a score for each derived factor. These factor scores are used to characterize the person's adherence to that pattern. Using factor analysis, Newby et al  derived three dominant patterns (fiber rich pattern, protein and alcohol pattern, and sweets pattern) in Baltimore Longitudinal Study on Aging. Kerver et al  derived two major dietary patterns, i.e., Western (high intake of foods rich in fat) and American-healthy (high intake of vegetables) using the food intake data from the third National Health and Nutrition Examination, 1988–1994 (NHANES III). Feinman et al  using the data from the Active Low-Carber Forum (n = 86,000) reported a low-carbohydrate dietary pattern characterized by high intakes of green and non-starchy vegetables and meat and low intakes of fruits.
To our knowledge, the association between dietary patterns and serum leptin in a representative sample of the US population has never been investigated. The usual approach has been looking at the effect of a single nutrient or food item on leptin. The published results relating leptin to dietary, demographic, and lifestyle factors yielded conflicting results. Considering the role of leptin in obesity, it is important to identify the modifiable factors of circulating leptin concentrations. Additionally, the association between serum leptin and lifestyle factors such as cigarette smoking and alcohol consumption is not well understood. Therefore, the aim of this study was to investigate the relation between serum leptin concentrations and dietary patterns, demographic characteristics, lifestyle factors, energy intake, body mass index (BMI), serum triacylglycerol and insulin, and plasma glucose concentrations.
Data used in this study were derived from the public use data files released by the National Technical Information Service, Springfield, VA [22–24]. The NHANES III was conducted by the National Center for Health Statistics over a 6-y period in two phases (1988–1991 and 1991–1994) at 99 locations. A sample representative of the US civilian, non-institutionalized population aged ≥ 2 mo was selected using a complex, stratified, multistage, probability cluster sampling design. Of 39695 persons sampled, 33994 were interviewed in their homes and they completed the Household Adult Questionnaire. Additional health, nutrition, and laboratory data were collected from 30818 participants by health professionals during visits to the mobile examination centers (MEC). Mexican Americans (MA), non-Hispanic blacks (NHB), children aged 2–5 y, and individuals aged ≥ 60 y were oversampled to yield more reliable estimates for these specific groups. Detailed description of the survey design and operation is published elsewhere .
The Household Adult File included data on sampled person's sex, age, race-ethnicity, BMI, smoking status, and alcohol consumption. The Hispanic category included MA and persons of Hispanic origin. Whether or not the respondent smoked 100+ cigarettes in their lifetime (yes or no) was also collected. Alcohol intake was determined by summing self-reported consumption of beer, wine, and hard liquor. One serving of alcohol was equivalent to 12 ounces (360 mL) of beer, 4 ounces (120 mL) of wine, or 1 ounce (30 mL) of hard liquor.
Blood was collected by venipuncture from participants at the MEC after overnight fasting for varied lengths of time. Specimens were shipped to the Centers for Disease Control and Prevention laboratories for priority analysis. After priority analysis, surplus sera were frozen at -70°C. The sera went through at least 1 freeze-thaw cycle during an average of 8 y of storage before leptin concentrations were measured. Leptin was previously shown to remain stable through 5 freeze-thaw cycles and even after storage for as long as 29 y . Leptin concentrations were only measured in the surplus sera for persons who had fasted ≥ 9 h and age > 20 y. Serum leptin was analyzed by Linco Research, Inc., St. Louis, Missouri . The minimum detectable concentration of the leptin assay was 0.5 fg/L and the limit of linearity was 100 fg/L. Coefficients of variation for within- and between assays ranged from 3.4% to 8.3% and from 3.6% to 6.2%, respectively. Serum insulin was measured with radioimmunoassay method, plasma glucose was measured spectrophotometrically (glucose hexokinase method), and serum triaclyglycerol was measured with microbial lipase method .
Food groups used in the dietary pattern analysis: the NHANES III 1
Foods from the Food Frequency Questionnaire3
1% milk, 2% milk, skim milk, and yogurt/frozen; Swiss, cheddar, and cottage cheeses
Chocolate milk, whole milk, ice cream, ice milk, milk shakes, and cheese dishes
Pizza, calzone, and lasagna
Stew or soup with vegetables
Bacon, sausage, lunch meats, liver, and organ meats
Beef, hamburger, steaks, pork, and ham
Fish and other sea food
Shrimp, clams, oysters, and lobster; Fish: fillets, sticks, and tuna
Chicken (all types)
Scrambled, fried, and omelettes
Fruits: oranges, grape fruit, cantaloupe, honey dew, water melon, peaches, nectarines, apricots, mango, apples, bananas, pears, berries, grapes, and strawberries; Juices: Orange, grapefruit, tangerine, grape, apple, and cranberry
White potatoes, French fries, potato salad, sweet potatoes, yams, squash, and carrots
Tomatoes including fresh and stewed tomatoes, tomato juice, and salsa
Cruciferous and green vegetables
Broccoli, Brussel sprouts, cauliflower, cabbage, coleslaw, sauerkraut, spinach, greens, kale, and tossed salad
Hot red chili peppers, peppers (green, red, and yellow), green beans, corn, peas, mushrooms, and zucchini
Beans, lentils, kidney, pinto, refried, black, and baked
Peanuts, peanut butter, nuts, and seeds
Cooked, hot cereals, oatmeal, cream of wheat/rice, grits, and cold breakfast cereals
Dark breads, whole wheat, and rye
White bread, rolls, English muffins, crackers, corn bread, corn muffins, corn/flour tortillas, and rice
Snacks and sweets
Salted snacks, potato chips, pretzels, popcorn, cakes, cookies, brownies, pies, doughnuts, chocolate candies, and fudge
Oil and vinegar, mayonnaise, and salad dressings
High energy drinks
Hi-C®, Tang®, Hawaiian Punch®, regular colas, and sodas
Diet colas/sodas and crystal light
Coffee and tea
Beer, wine, and hard liquor
Additionally, one 24-h dietary recalls were collected using an automated, microcomputer-based dietary interview and coding system. Participants reported all foods and beverages consumed except plain water for the previous 24-h time period. Nutrient composition of foods reported in food recalls was based on the USDA Survey Nutrient Databases . A number of quality control measures were employed to ensure the accuracy of food recalls. . In this study, energy intake from the food recalls was used as a potential determinant of serum leptin.
The current study sample initially consisted of 6415 participants derived from persons whose fasting serum leptin concentrations were measured in surplus sera. Pregnant (n = 288) and lactating (n = 95) women and diabetic persons (n = 1498) and individuals identified as other race-ethnicity were excluded from the analysis (n = 187). Persons who responded 'yes' to a question whether they were diabetic or whether they were taking diabetic medication were treated as persons with diabetes. Individuals with missing values for sex, race-ethnicity, age, smoking, alcohol and energy intakes, BMI, serum triacylglycerol, plasma glucose, serum insulin, and FFQ were also excluded (n = 338). After applying the above criteria, the final study sample consisted of 4009 participants (men, 1907; women, 2102; NHW, 1907; NHB, 1076; MA, 1026). The average age of the participants was 43.4 ± 0.89 (mean ± SE)
Statistical analyses were performed with SUDAAN (SUDAAN for Windows, version 8.0.2, Research Triangle Institute, Research Triangle Park, NC) and SAS software (Statistical Analysis Software for Windows, version 9.1, Cary, NC) packages. Use of SUDAAN had allowed us to account for the complex survey design. Sample weights were used to account for unequal probabilities of selection, cluster design, and planned oversampling of selected subgroups. Detailed guidelines on the use of sample weights in data analysis are described in NHANES III Analytical and Reporting Guidelines .
Analysis of variance (ANOVA) for continuous variables and chi-square tests for categorical variables were used to determine if there were differences for any demographic characteristics, lifestyle factors, energy intake, BMI, serum triacylglycerol and insulin, and plasma glucose among the 3 dietary pattern groups. Univariate ANOVA was used to determine if mean serum leptin concentrations differed across dietary patterns for all subjects, men, and women (unadjusted analysis). Analysis of covariance (ANCOVA) was used to determine if serum leptin concentrations differed across the different dietary patterns after adjusting for sex, age, race-ethnicity, smoking, alcohol and energy intakes, BMI, serum triacylglycerol and insulin, and plasma glucose. Multiple comparisons among dietary patterns for serum leptin were made using t-test with a Bonferroni correction (P < 0.0167).
Association between serum leptin concentrations and dietary patterns, demographic variables, lifestyle factors, energy intake, BMI, serum triacylglycerol and insulin, and plasma glucose was determined using multivariate regression analysis. Because serum leptin concentrations were not normally distributed, a logarithmic transformation was used to satisfy the distribution requirements in all analyses. An α of 0.05 was used to designate statistical significance.
Subjects were categorized into one of 3 dietary pattern groups based on their factor scores. Persons who received the highest factor scores for food groups that constitute Vegetable, Fruit, and Lean Meat pattern (cruciferous, starch, and other vegetables, fruit/fruit juices, tomatoes, soups, fish/seafood, poultry, low-fat dairy, and legumes) were placed in that pattern. Persons who received the highest factor scores for red meat, processed meat, high-energy drinks, refined grains, eggs, snacks/sweets, pizza/lasagna, alcohol, and coffee/tea groups were placed in the Western dietary pattern group. Lastly, persons who received the highest factor scores for high-fat dairy, fats, nuts, whole grains, starch vegetables, snacks and sweets, and cereals groups were placed in the Mixed pattern group.
Characteristics of study population by dietary patterns in the NHANES III 1
Vegetable, Fruit, and Lean Meat
(n = 1482)
(n = 1503)
(n = 1024)
P value 2
Sex (n, %)
Race-ethnicity (n, %)
Cigarettes smoked (n, %) 3
Age (y) 4
46.2 ± 1.1 5
38.6 ± 0.7
46.6 ± 0.9 5
Alcohol intake (drinks/mo) 4,6
7.8 ± 0.5
10.8 ± 1.3
8.0 ± 0.7
Energy intake (kcal) 4
2022 ± 40 5,7
2553 ± 57 7
2253 ± 45 5
Body mass index (kg/m2) 4
26.4 ± 0.2
26.5 ± 0.3
26.5 ± 0.2
Serum triacylglycerol (mmol/L) 4
1.49 ± 0.06
1.51 ± 0.04
1.49 ± 0.04
Plasma glucose (mmol/L) 4
5.42 ± 0.04
5.32 ± 0.03
5.37 ± 0.03
Serum insulin (pmol/L) 4
61.7 ± 2.5
63.7 ± 2.5
58.8 ± 1.8
Serum leptin concentrations by dietary patterns in the NHANES III 1
Dietary Pattern 2
Vegetable, Fruit and Lean Meat
(n = 1482)
(n = 1503)
(n = 1024)
P value 3
8.50 ± 1.04 4
6.29 ± 1.04 5
8.00 ± 1.04 4
4.90 ± 1.04
4.26 ± 1.04
4.57 ± 1.04
11.82 ± 1.04
12.94 ± 1.05
13.07 ± 1.05
All subjects 6
7.39 ± 1.02
7.69 ± 1.02
7.69 ± 1.02
4.44 ± 1.04
4.57 ± 1.03
4.48 ± 1.03
12.18 ± 1.03
12.68 ± 1.03
12.81 ± 1.03
Association between serum leptin concentrations and dietary patterns, demographic characteristics, and lifestyle and health factors in the NHANES III 1
P value 3
Vegetable, Fruit, Lean Meat
Mixed (referent category)
Women (referent category)
Mexican American (referent category)
Cigarettes smoked 4
No (referent category)
Energy intake (kcal)
Alcohol intake (drinks/mo) 5
Body mass index (kg/m2)
Serum triacylglycerol (mmol/L)
Plasma glucose (mmol/L)
Serum insulin (pmol/L)
Using a subset of a nationally sampled survey, we derived 3 dietary patterns, Vegetable, Fruit, and Lean Meat, Western, and Mixed. Dietary patterns derived from this study are remarkably similar to the patterns identified in other studies using factor analysis [16, 17, 19, 20, 31]. First, Hu et al  and later, Fung et al , in the Health Professionals Follow-up Study derived 2 major food patterns, Prudent (high intakes of vegetables, fruit, legumes, whole grains, and fish and other seafood) and Western (high intakes of processed and red meat, butter, high-fat dairy products, eggs, and refined grains). Khani et al  identified 3 dietary patterns and labeled them as Healthy (vegetables, fish, poultry, tomatoes, whole-grains, low-fat dairy, etc), Western (processed meats, refined grains, high-fat diary, sweets etc), and Drinker. Using the NHANES III data, Kerver et al  derived 2 major food patterns ("American-Healthy" and Western) and 4 minor dietary patterns. They used 35 food groups and had a larger sample size with differing demographic characteristics. Therefore, different dietary patterns emerged in our study. Although there is a slight variation regarding number of factors (patterns) derived from study to study, the first two major dietary patterns, i.e., Prudent (healthy) and Western (not so healthy) have remained by and large consistent over time and between studies.
To our knowledge, this is the first study to examine the relation between dietary patterns and serum leptin in a nationally representative US cohort. Through multivariate-adjusted analysis, we found, dietary patterns are not independently related to serum leptin. In contrast, Fung et al  observed a significant positive correlation between the Western pattern and serum leptin (r = 0.28; P < 0.0001) but not between the Prudent pattern and serum leptin (n = 466). Jensen et al  reported that persons in the highest quintile for whole-grain intake had 11% lower circulating leptin compared to those in the lowest quintile. Winnicki et al  reported that a diet high in fish was associated with lower plasma leptin, independent of body fat or BMI (n = 622). Chu et al  observed no association between serum leptin and fat intake after adjustment for energy and BMI. This lends support to the notion that the relation between serum leptin and dietary patterns is confounded by the amount of energy consumed and body weight. Inconsistent results between these studies may partly be explained by differences in subject characteristics, dietary intake assessment methods employed, and confounding variables used in the data analysis.
Although the association between dietary patterns and circulating leptin is unclear, association between macronutrients and serum leptin has been reported. Dietary carbohydrate appears to play a role in leptin metabolism [4, 10]. Over a 24-h period, a significant decrease in postprandial leptin concentrations was observed after consuming a high-fat, low-carbohydrate diet . Volek et al  reported a 42% decrease in leptin with carbohydrate restricted diet (percentage of energy from carbohydrate:fat:protein = 12:59:28) and a 18% decrease in leptin with low-fat diet (percentage of energy from carbohydrate:fat:protein = 56:24:20) for 12 weeks in overweight subjects. This significant decrease in leptin persisted after normalization of values to body mass and fat mass suggesting that dietary carbohydrate restriction improves leptin resistance more likely due to reduction in body mass [32, 33]. Also, carbohydrate restriction lowered concentrations of serum insulin and triacylglycerol even in the absence of weight loss . Thus, the dietary factor/component (for example carbohydrate restriction) that lowers serum leptin can also improve several indicators of metabolic syndrome such as circulating triacylglycerol and insulin and fat mass [32, 34]. However, in this current study, the adjusted serum leptin concentrations are not related to dietary patterns.
We found a positive relation between serum leptin and insulin concentrations (P < 0.0001). In an experimental study, leptin concentrations increased after 4–6 h of insulin administration . Changes in circulating leptin concentration in response to fasting, refeeding, and macronutrient intake are likely mediated by insulin-stimulated glucose metabolism in adipose tissue . Expression of leptin from adipocytes is directly related to the glucose uptake by adipocytes. Additionally, inhibition of glucose transport and metabolism in adipocytes markedly decreased ob gene expression leading to the reduced production of leptin .
Not only that multivariate-adjusted serum leptin was significantly associated with sex but also that sex was the strongest predictor of serum leptin after including the BMI in the model which suggests that metabolic or physiologic differences might contribute to the differences in serum leptin between men and women. Our finding of no association between serum leptin and race-ethnicity is in agreement with some studies [3, 37, 38]. In contrast, Ruhl et al  reported a higher serum leptin in blacks than in whites independent of anthropometric measures of body fatness. However, the race-related differences in serum leptin may be due to incomplete adjustment for differences in body fat distribution. Blacks have a higher amount of subcutaneous fat than do whites and secretion of leptin is greater from subcutaneous fat compared to visceral fat. When waist circumference was taken into consideration, the association between race and leptin was no longer present .
In this study, no association was found between smoking and serum leptin in the multivariate-adjusted analysis. Previous studies on the association between circulating leptin and lifestyle factors yielded equivocal results [3, 6, 40, 41]. In support of our findings, De Silva et al  found no relation between circulating leptin and smoking. In contrast, Donahue et al  reported that sex-age-race-ethnicity adjusted leptin concentrations were significantly higher in nonsmokers (14.3 ng/ml) than in smokers (8.4 ng/ml) who smoked more than a pack of cigarettes/d (P < 0.001). It has been postulated that smoking may increase tissue sensitivity to leptin and subsequently lead to lower body weight among smokers  which leads to lower concentrations of leptin. Another possible explanation is that smokers tend to have less body fat mass compared to nonsmokers  which in turn leads to lower circulating leptin concentrations. Because we adjusted the analysis for BMI, the lack of association between serum leptin and smoking is rather expected.
Serum leptin concentration was independently and directly related to BMI. A direct relation between serum leptin and body composition is in agreement with the observations made by several investigators [1, 43]. In a study by Racettet et al , leptin concentrations are highly correlated with adiposity measures including BMI, body fat mass, and percentage of body fat. Also, a strong positive correlation (r = 0.85, P < 0.001) was found between serum leptin and the percentage of body fat . Since leptin production was directly related to fat mass, obese subjects had higher serum leptin concentrations when compared to normal-weight subjects (31.3 ng/mL vs. 7.5 ng/mL; P < 0.0001). On the other hand, leptin decreased in response to diet-induced or exercised-induced weight loss . Thus, body fat is an important predictor of serum leptin concentrations. Given a direct relation between BMI and serum triacylglycerol , a positive association between serum leptin and serum triacylgycerol observed in this study is along the expected lines.
FFQ is an important dietary assessment tool used in dietary epidemiological studies because the food intake data derived from it is sufficiently valid , and it is a practical and economical method  with low respondent and investigator burden . Noethlings et al  reported that data on portion sizes add little to the variance in food intake, and the major part of variance in food intake is explained by the frequency of food consumption alone. However, cross-sectional studies that use the FFQ tool are prone to measurement error due to the participants' inability to recall dietary intakes precisely. In the NHANES III, dietary data collected using FFQ reflect intakes a month prior to the survey date. It is not known whether this data represent habitual intake of participants. However, dietary patterns derived in this study are in congruence with the commonly reported food intake patterns in the US, i.e., Western and Prudent [16, 17, 19, 20] which in itself lends sufficient validity to the food intake data collected through the use of FFQ in the NHANES III.
Derivation of dietary patterns using the factor analysis is a reproducible and a valid method . Hu et al  showed reasonable reproducibility and validity of major dietary patterns defined by factor analysis using food consumption data collected through FFQ. Later, Newby et al  in a confirmatory analysis showed a good reproducibility and generalizability of dietary patterns across populations. Dietary patterns derived from the factor analysis were generally stable over a period of time despite changes in eating behavior, food supply, and perceptions of what is regarded as healthy . A limitation of factor analysis was subjectivity used in grouping of individual foods into food groups, extracting number of factors (patterns), and naming dietary patterns . Due to the cross-sectional design of this study, cause and effect analysis is not appropriate.
In the NHANES III subset population, we found no association between serum leptin concentration and dietary patterns after adjusting for certain covariates suggesting that circulating leptin concentrations are independent of dietary intake patterns. Sex, age, BMI, serum triacyglycerol, and serum insulin are independent predictors of serum leptin concentrations. Further studies are needed to evaluate the effect of diet composition relative to leptin expression to better understand the complicated relationship between diet and leptin.
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