AJCN North Carolina Research Campus
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.
Agricola
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.
American Journal of Clinical Nutrition, Vol. 74, No. 5, 585-591, November 2001
© 2001 American Society for Clinical Nutrition

Original Research Communication

Site-specific differences in the fatty acid composition of abdominal adipose tissue in an obese population from a Mediterranean area: relation with dietary fatty acids, plasma lipid profile, serum insulin, and central obesity1,2,3

Marta Garaulet, Francisca Pérez-Llamas, Millán Pérez-Ayala, Pedro Martínez, Fermín Sánchez de Medina, Francisco J Tebar and Salvador Zamora

1 From the Department of Physiology and Pharmacology, University of Murcia, Murcia, Spain; the Department of Biochemistry, University of Granada, Granada, Spain; and the Departments of Biochemistry and Endocrinology, Arrixaca Hospital, Murcia, Spain.

2 Supported by a grant from the Official College of Pharmacists of Murcia.

3 Address reprint requests to F Pérez-Llamas, Department of Physiology and Pharmacology, University of Murcia, 30100-Murcia, Spain. E-mail: frapella{at}um.es.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Background: Abdominal obesity is associated with coronary risk, although causality is not well established.

Objective: In an obese Mediterranean population, we measured the fatty acid composition of adipose tissue, its relation with dietary fatty acids and central fat deposition, and its influence on plasma lipids and insulin.

Design: Adipose tissue samples were obtained from 84 obese patients (29 men, 55 women) aged 30–70 y (body mass index, in kg/m2: 27–35). We measured concentrations of insulin and lipids in plasma and fatty acids in subcutaneous, omental, and perivisceral fat. Dietary fatty acid intake was assessed with a 7-d diet record.

Results: The population studied was normolipidemic and normoinsulinemic. There were important differences in fatty acid composition between tissue sites: saturated fatty acids were higher and monounsaturated fatty acids were lower in perivisceral than in subcutaneous fat (P < 0.05). Significant correlations were found for oleic, linoleic, {alpha}-linolenic, and total n-6 polyunsaturated fatty acids between the subject's habitual diet and adipose tissue composition. Oleic and n-3 fatty acids from adipose regions were negatively correlated with apolipoprotein B and triacylglycerols; adipose tissue 22:1n-9, 20:2n-6, stearic acid, and eicosapentaenoic acid were positively correlated with HDL and apolipoprotein A; and adipose tissue myristic acid was negatively correlated with apolipoprotein A (P < 0.05). Central obesity was positively associated with n-6 polyunsaturated fatty acids and inversely associated with monounsaturated fatty acids and n-3 polyunsaturated fatty acids in adipose tissue (P < 0.05).

Conclusion: The differences found in the composition and metabolism of perivisceral, omental, and subcutaneous fats may indicate that their atherogenic capacities also differ.

Key Words: Obesity • central obesity • cardiovascular risk • adipose tissue • body fat • dietary fatty acids • Mediterranean diet • heart disease • coronary artery disease • cardiovascular disease • atherosclerosis • dietary fat


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Cardiovascular disease accounts for a large proportion of deaths among adults in the Western world. Abdominal obesity, especially visceral obesity, is associated with coronary risk, although causality is not well established. The relation is not simply a function of overall obesity, because increased waist-to-hip ratio (WHR) is associated with increased coronary risk even in nonobese persons (1). This raises the question of why intraabdominal fat mass is so strongly related to several diseases and their risk factors. Insulin resistance may be a key factor in this link. Many studies have pointed to an association between insulin resistance and intraabdominal fat accumulation (2, 3).

Adipose tissue may play an important role in the development of atherosclerosis because adipose tissue fatty acids are in constant interchange with plasma (4), and plasma triacylglycerols are probably the major source of endogenous and exogenous fatty acids for the synthesis of complex lipids. Varying proportions of fatty acids from adipose tissue may be related to atherosclerosis and other diseases and might exert a direct influence on serum lipids that may differ depending on the adipose tissue region. It was suggested that intraabdominal fat has a higher turnover rate than does subcutaneous fat (5), and therefore the former may have a greater influence on the plasma lipid profile. There is conflicting information about differences between the fatty acid composition of subcutaneous and deep visceral adipose tissue. Some authors suggest that intraabdominal adipose tissue is enriched with saturated fatty acids and that this composition could contribute to the coronary risk associated with abdominal obesity (6).

The fatty acid composition of adipose tissue is partially dependent on dietary intake (7). Changing the nature of the fat consumed has a profound influence on the fatty acids available to the body. Therefore, modifying the sources of dietary fat may alter the composition of adipose tissue. On the other hand, the endogenous synthesis of nonessential fatty acids, predominantly in the form of saturated and monounsaturated fatty acids, may also be a contributing factor to human adipose tissue composition, although the significance of this contribution to the fatty acid pool in humans was questioned (8, 9).

Few studies have related the factors discussed above with consumption of a typical Mediterranean diet, even though it was established that diets high in olive oil, and consequently high in oleic acid, are strongly associated with the low cardiovascular disease mortality found in Spain and most other Mediterranean countries of Europe (10). The aim of the present study was to determine the fatty acid composition of intra- and extraabdominal adipose tissue, its relation with dietary fatty acids and central fat deposition, and its influence on plasma insulin and the lipid profile in an obese population of a Mediterranean area of southeast Spain.


   SUBJECTS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Subjects
A total of 84 subjects (29 men and 55 women, aged 30–70 y) were selected from the outpatient clinics of the University Virgen de la Arrixaca, the General University, and the Morales Meseguer hospitals in Murcia, Spain. All the subjects were obese, with a body mass index (BMI; in kg/m2) of 27–35, and were being admitted to the hospital for abdominal surgery or laparoscopy for gallbladder disease without icterus, ulcer, or umbilical hernia. Potential subjects were excluded from the study if they were following a special diet or taking steroid or thyroid medication, or they had diabetes mellitus, chronic renal failure, hepatic disease, or cancer. All subjects gave their written, informed consent, and the study was approved by the Ethics Committee of the Virgen de la Arrixaca Hospital.

Adipose tissue sample collection, anthropometrics, and body composition
Abdominal adipose tissue samples were obtained during surgery. Subcutaneous samples were taken from the periumbilical region and intraabdominal samples were taken from the perivisceral fat (surrounding the gallblader) and the omental fat. Depending on the type of surgery (laparotomy or laparoscopy) and the pathology (gallbladder, eventration, or ulcer), omental or perivisceral fat was obtained. Samples were stored at -70°C until analyzed. Body weight was measured to the nearest 0.1 kg while subjects were dressed in their underwear, and height was measured to the nearest centimeter. From these data, the BMI was calculated. Total body fat (%) was derived from the biceps, triceps, suprailiac, and subscapular skinfold-thickness measurements (11). All measurements were obtained on the right side, with the subject upright and relaxed. A Harpenden caliper (Holtain Ltd, Crymmych, United Kingdom) with a constant pressure of 10 g/mm2 was used. Body fat distribution was assessed by measuring waist circumference at the level of the umbilicus and hip circumference over the widest part of the greater trocanters. Measurements were made 3 times by a single operator. The WHR and conicity index [waist circumference/(0.109 , where waist circumference and height are in m and weight is in kg] were calculated (12). Visceral and subcutaneous adipose tissue areas were measured with computed tomography on the basis of the recommendations of Sjöstrom (13) with a Toshiba CBTB007A scanner (Toshiba Corp, Shimoshiqui, Otowawara, Japan). A single 10-mm scan at the L4–L5 level (determined to the nearest 1 mm with a skeleton radiogram) was performed with a 512 x 512 matrix, a window size of 300 Hounsfield units, and a center of 40 Hounsfield units. The subcutaneous abdominal (SA) and visceral abdominal (VA) fat areas were determined from a tomodiagram section by image analysis with a MIP-Microm Image Processing System (Microm, Barcelona, Spain) on the basis of the IMCO 10 (Kontron, Eching, Germany). The ratio of VA to SA was then calculated (14). Note that VA includes both perivisceral and omental fat.

Adipose tissue fatty acid composition
To determine the fatty acid composition of adipose tissue, a direct transesterification procedure was carried out in methanol-benzene (4:1) with acetyl chloride (15). Fatty acids were identified as methyl esters on a Perkin-Elmer 84-10 gas chromatograph (Perkin-Elmer, Norwalk, CT) equipped with a 30 m x 0.25 mm fused-silica capillary column (SP-2380; Teknokroma, Barcelona, Spain). Detection was by flame ionization. The injector and detector temperatures were 210 and 280°C, respectively. Nitrogen was used as the carrier gas. Chromatography was performed with a temperature program that increased from 160 to 208°C by increments of 2°C/min and from 208 to 230°C by increments of 3°C/min. The column temperature was held at 230°C for 7 min. The instrument output was quantified with a Perkin-Elmer GP-100 integrator. The peaks were identified by comparison with standards (Supelco, Bellefonte, PA).

Plasma lipids and insulin
Venous blood samples were obtained after subjects fasted overnight. Plasma concentrations of triacylglycerols, total cholesterol, HDL, LDL, and apolipoprotein (apo) A and B were determined with commercial kits (Roche Diagnostics GmbH, Mannheim, Germany). Serum insulin concentrations were determined with a radioimmunoassay (MNIA, Serono, Italy).

Dietary data
Subjects recorded their dietary intakes for 7 d, after they had undergone surgery. The recorded intakes were typical of their usual diets. We calculated their nutrient intakes with a computer program (16) written on the basis of the Spanish food tables (17). The intakes of fatty acids were calculated from Spanish food-composition tables (18). For each subject, each nutrient intake was calculated as the mean daily intake for the 7 d. These calculations allowed us to estimate the intakes of the major saturated fatty acids (SFAs), monounsaturated fatty acids (MUFAs), and polyunsaturated fatty acids (PUFAs), including linoleic acid (18:2n-6), {alpha}-linolenic acid (18:3n-3), and n-3 fatty acids of marine origin.

Statistical analyses
Data are presented as means ± SDs. The Student's t test was performed to analyze differences between the sexes. To determine differences in the composition of the 3 adipose tissue regions studied, a two-way (type of fat and subject) analysis of variance (ANOVA) with a post hoc test of least significant difference with Bonferroni correction was used. Pearson's product-moment correlation coefficients were used to quantify the relations between adipose tissue composition, dietary fatty acids, and plasma lipids.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Subject characteristics including age, body weight, BMI, percentage body fat, and measures of body fat distribution (WHR, conicity index, and VA:SA) are shown by sex in Table 1Go. There were no significant differences in age, BMI, or waist circumference between the sexes. Percentage body fat was greater in women, whereas the WHR and VA:SA were significantly higher in men. Fasting triacylglycerol, total cholesterol, LDL, HDL, apo A and B, insulin, and glucose concentrations are shown separately for men and women in Table 2Go.


View this table:
[in this window]
[in a new window]
  		TABLE 1. Subject characteristics1
 

View this table:
[in this window]
[in a new window]
  		TABLE 2. Fasting serum concentrations of lipids, insulin, and glucose1
 
The fatty acid composition of the adipose tissue regions and the subjects' habitual diets is shown in Table 3Go. Because there were no significant differences between the sexes in the proportions of fatty acids, the data are reported for the total subject population combined. The single fatty acid present in the greatest amount was oleic acid (18:1n-9), followed by palmitic acid (16:0) and 18:2n-6. The mean daily intake of dietary fat was 102 ± 41 g for the total subject population. When the fatty acid composition of the subjects' habitual diets was correlated with the composition of adipose tissue by using Pearson's product-moment correlations, significant correlations were found for n-6 PUFAs, 18:2n-6, 18:3n-3, and 18:1n-9 (Table 4Go).


View this table:
[in this window]
[in a new window]
  		TABLE 3. Fatty acid composition of adipose tissue regions and habitual diets of the total subject population1
 

View this table:
[in this window]
[in a new window]
  		TABLE 4. Pearson's product-moment correlation coefficients (r values) between fatty acid contents of the diet and those of different adipose tissue regions1
 
Differences in fatty acid composition between the 3 adipose tissue regions are shown in Figure 1Go. A two-way (type of fat and subject) ANOVA indicated that the perivisceral fat was the most saturated and contained less MUFA than did the other adipose regions.



View larger version (25K):
[in this window]
[in a new window]
  		FIGURE 1. Mean (±SD) fatty acid content (%) of subcutaneous, perivisceral, and omental adipose tissue in the subject population (men and women combined). Note that perivisceral and omental adipose tissues are both part of the visceral abdominal fat area. Differences between the adipose tissue regions were tested with a two-way (type of fat and subject) ANOVA with a post hoc test of least significant difference and a Bonferroni correction. *Significantly different from the other 2 adipose tissue regions, P < 0.05. SFA, saturated fatty acids; MUFA, monounsaturated fatty acids; PUFA, polyunsaturated fatty acids.

 
Pearson's product-moment correlations between plasma lipid concentrations and the fatty acid contents of subcutaneous (n = 76), perivisceral (n = 57), and omental (n = 24) adipose tissue regions in this obese population were calculated. This indicated that the palmitoleic acid (16:1n-7) content of omental fat was inversely correlated with the total and LDL-cholesterol concentrations (r = -0.39 and -0.55, respectively; P = 0.05 for both). In addition, the n-3 fatty acid content of subcutaneous fat was inversely associated with the triacylglycerol concentration (r = -0.26, P < 0.05). The 18:1n-9 content of perivisceral fat was inversely correlated with the apo B concentration (r = -0.26, P < 0.05), whereas the stearic acid (18:0) and 22:1n-9 contents of omental fat and the eicosapentaenoic acid (20:5n-3) content of subcutaneous fat were positively correlated with the HDL concentration (r = 0.57, P < 0.01; r = 0.74, P < 0.001; and r = 0.25, P < 0.05, respectively). The 22:1n-9 content of omental fat and the 20:2n-6 content of subcutaneous fat were positively associated with the plasma apo A concentration (r = 0.60, P < 0.01, and r = 0.31, P < 0.01, respectively); however, in the latter case, 2 values much above the mean may have determined the correlation. In contrast, the vaccenic acid (18:1n-7) content of perivisceral fat was positively correlated with LDL (r = 0.47, P < 0.01) and the myristic acid (14:0) content of omental fat was inversely correlated with apo A concentrations (r = -0.41, P < 0.05). The 14:0 content of both intraabdominal fats tended to be positively correlated with apo B concentrations, although the correlations were not significant. In addition, the adipose tissue 18:2n-6 concentration tended to be correlated with the plasma LDL concentration (r = 0.22, P = 0.09). Of all the adipose tissue regions, omental fat showed the greatest number of correlations with the plasma lipid profile. There were no significant correlations between serum insulin values and the fatty acid compositions of the 3 adipose tissue regions or the n-3-to-n-6 ratio.

Correlations between degree of obesity (defined by BMI and percentage body fat), central distribution of fat (defined by WHR and VA), and the fatty acid contents of different adipose tissue regions in the total subject population are shown in Table 5Go. The degree of obesity and central distribution of body fat were positively correlated with the total n-6 PUFA content of adipose tissue (especially 18:2n-6 content) and negatively correlated with the MUFA and n-3 PUFA contents of adipose tissue. Serum insulin values were positively correlated with the degree of obesity (r = 0.29, P < 0.01 for BMI, and r = 0.28, P < 0.05 for percentage body fat) and with the amount of subcutaneous fat (r = 0.38, P < 0.001).


View this table:
[in this window]
[in a new window]
  		TABLE 5. Correlations (r) of degree of obesity, indicated by BMI and percentage body fat, and central distribution of fat, indicated by waist-to-hip ratio (WHR) and visceral abdominal fat area (VA), with the fatty acid contents of different adipose tissue regions1
 

   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
Visceral obesity has been defined as the condition in which the VA:SA is >0.4 (14). On the basis of this index, the subject population in this study can be defined as having the visceral type of obesity. In addition, the mean waist circumference of our subjects exceeded values established as being associated with cardiovascular disease risk (19). This suggests that our obese population might have high plasma lipid and insulin values. However, plasma lipids and insulin were within the normal ranges for subject age and sex.

The fatty acid composition of adipose tissue observed in this study is consistent with the results of other studies showing that oleic acid is the major component of adipose tissue; however, our values were higher than those found in other populations (20, 21). The PUFA values in this study were also higher, whereas SFA values were much lower than those observed in other countries (20, 21). Fat intake in the present study was also different from that recorded in other non-Mediterranean countries: MUFA intake was much higher and SFA intake was much lower in our subjects (22–24). These findings suggest that the population studied, despite being obese with a central distribution of fat, had a fatty acid profile (both in the diet and in adipose tissue) that might be considered protective against cardiovascular disease (25). This might also explain the normal plasma lipid and insulin concentrations observed.

The mean 18:1n-9 concentrations in the subcutaneous and perivisceral adipose tissue were positively associated with dietary intake of oleic acid in our subject population. This finding differs from conclusions reached by using the mathematical model of Beynen et al (26) and by other authors (24). The quantity of oleic acid consumed by our population was high (48.3 g/d), and several studies in animals suggested that the storage of different fatty acids varies with the quantity ingested (27, 28). However, our results agree with those found in a Greek population that also consumed a Mediterranean diet (29).

Our data indicate that there was a positive correlation between the fatty acid composition of the subjects' habitual diets and that of their adipose tissue for n-6 PUFAs, especially 18:2n-6, a finding consistent with Beynen's mathematical model (26). On the other hand, no general association between the 18:3n-3 content of adipose tissue and dietary estimates of 18:3n-3 intake was found; such an association was confined to the omental adipose tissue. This fatty acid, unlike 18:2n-6, was ingested in small amounts (1.59%). Furthermore, despite being an essential fatty acid, 18:3n-3 plays no important metabolic role other than acting as a precursor of other fatty acids of the n-3 family. It is rapidly converted into 20:5n-3 and docosahexaenoic acid (22:6n-3), and therefore is not stored in any appreciable quantities in the adipose tissue (30).

The results showed no associations between the concentrations of n-3 fatty acids or 20:5n-3 and 22:6n-3 in adipose tissue and those in the habitual diet, which contrasts with the findings of other authors who manipulated dietary fat (31, 32). There are several possible reasons such a relation was not evident in this study. First, in our study the intake of this type of fatty acid was low (eg, 0.25 g 22:6n-3/d), whereas intakes were up to 25 times greater (eg, 6 g/d) in intervention studies (33). Second, because of their metabolic importance and molecular structure, these fatty acids can easily move from the tissues in which they accumulate (34). Third, 20:5n-3 and 22:6n-3 can be synthesized endogenously from 18:3n-3.

The mean concentrations of some of the fatty acids were similar in body fat and the diet, although 14:0, 16:0, 16:1n-7 and arachidonic acid (20:4n-6) were present in greater amounts in adipose tissue, whereas concentrations of 18:1n-9 and 18:0 were significantly greater in the diet (P < 0.05). These results suggest that 18:1n-9 and 18:0 are preferentially used in the different metabolic pathways, oxidized for energy production, or desaturated or elongated to produce other fatty acids. The higher concentrations of 14:0, 16:0, and 16:1n-7 in the adipose tissue could be a result of their endogenous synthesis from carbohydrate. The low dietary consumption of arachinoic acid and the fact that it is synthesized endogenously from 18:2n-6 (35) might explain the significantly higher concentration found in adipose tissue than in the diet.

When the different adipose tissue sites were compared with each other to ascertain any site-specific differences in fatty acid composition, perivisceral fat was found to be the most saturated, whereas subcutaneous fat was much richer in MUFA. These results differ from those of studies that suggested a homogenous composition of fat throughout the body (36), but they agree with findings that the superficial or subcutaneous fat is softer than the deeper fat (37, 38).

There were no significant differences between the different adipose regions with regard to total PUFA content. These results are consistent with those of many studies (23, 38, 39). The essential fatty acids 18:2n-6 and 18:3n-3 and their metabolic products cannot be synthesized de novo, therefore the diet determines their concentrations in adipose tissue.

The different effects of dietary n-3 fatty acids on cardiovascular diseases have been described comprehensively (40). However, the influence of different adipose tissue concentrations of these fatty acids on plasma lipids is still not clear. The present findings suggest that n-3 fatty acids in subcutaneous adipose tissue are negatively correlated with triacylglycerols and positively correlated with HDL and apo A. These results agree with data obtained in epidemiologic studies from Scotland, Finland, and Italy (41). In our subjects, the degree of obesity (BMI) was negatively correlated with the concentration of n-3 fatty acids in omental fat. The accumulation of central fat (indicted by WHR), especially in the intraabdominal region (VA), was also associated with a lower n-3 fatty acid content in both intraabdominal fats.

Our data also show that the plasma concentrations of apo A decreased significantly as the concentration of 14:0 increased in perivisceral fat, whereas apo B concentrations increased. This suggests that 14:0 in the adipose tissue may play an atherogenic role in obese individuals.

It was suggested that 16:0 is one of the most atherogenic fatty acids in the diet (42). However, our findings showed no relation between the 16:0 contents of adipose tissue and plasma lipids, which is consistent with other studies (41). These results underline the differences between the fatty acids from dietary sources (exogenous) and those of an endogenous origin. When an excess of carbohydrates is consumed, there is a rapid synthesis of 16:0, 18:0, and 18:1n-9, but no corresponding increase in plasma cholesterol concentrations (43).

Despite the fact that 18:0 is an SFA, its concentration in omental adipose tissue was positively correlated with plasma HDL concentrations, as was also found by Berry et al (7) and Hudgins et al (41). Emken (44) suggests that this results in part from the high capacity of the liver to desaturate this fatty acid.

In the present study, perivisceral 18:1n-9 was associated with low apo B concentrations in plasma. Omental 22:1n-9 was correlated with high HDL and apo A concentrations, whereas the 16:1n-7 of this adipose region was associated with low plasma concentrations of LDL and total cholesterol. If we consider that the degree of obesity (BMI and percentage body fat) and central fat distribution (VA) were inversely associated with MUFA concentrations, especially those of 18:1n-9 in every adipose tissue region studied, these data as a whole suggest a protective role of 18:1n-9 against cardiovascular diseases (45). Analyses of all the above data showed that omental fat was the region most strongly correlated with the plasma lipid profile. These findings could be explained by the higher degree of turnover characteristic of this adipose tissue region and could help explain the greater medical risk associated with central obesity.

Insulin values, although within the normal range, were positively correlated with degree of obesity and body fat distribution. Many studies have supported an association between insulin resistance and intraabdominal fat accumulation (2, 3). However, the data indicate that insulin values were positively correlated with subcutaneous fat accumulation. Subcutaneous fat probably plays a major role in determining systemic plasma fatty acid concentrations, which are relevant in determining insulin resistance (5). No correlations were found between insulin values and adipose tissue composition. These results differ from those of in vitro studies that suggested lipids may interact with insulin-stimulated glucose transport (46), but they agree with results of in vivo studies that show no association between the fatty acid profile and insulin sensitivity (47).

In summary, our data show that the studied population, despite being obese, apparently has normal plasma lipid concentrations. These lipid concentrations could be associated with the higher 18:1n-9 and PUFA contents and the lower SFA content found in the diet and adipose tissue compared with non-Mediterranean populations. The differences in composition and metabolism between perivisceral, omental, and subcutaneous abdominal fats indicate that the relations of these different adipose regions with plasma metabolites, and the atherogenic capacity of these adipose regions, also differ.


   ACKNOWLEDGMENTS
 
We are indebted to Per Björntorp from the Departments of Medicine and Heart and Lung Diseases, Wallenger Laboratory, Sahlgren's Hospital, University of Göteborg, Sweden, for advice about the scientific design of this project. We also thank all the staff from the Surgery, Endocrinology, Radiology, and Biochemistry Services at the Arrixaca Hospital, Spain, for their skilled technical assistance.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Folsom AR, Kaye SE, Sellers TA, et al. Body fat distribution and 5-yr risk of death in older women. JAMA 1993;29:483–7.
  2. Clandinin MT, Cheema S, Field CJ, Garg ML, Venkatraman J, Clandinin TR. Dietary fat: exogenous determination of membrane structure and cell function. FASEB J 1991;5:2761–9.[Abstract]
  3. Björntorp P. Hormonal control of regional fat distribution. Hum Reprod 1997;12(suppl):21–5.
  4. Lands WE. Long-term fat intake and biomarkers. Am J Clin Nutr 1995;61(suppl):72S–5S.
  5. Frayn KN. Visceral fat and insulin resistance: causative or correlative? Br J Nutr 2000;83(suppl):721S–5S.
  6. Lapidus L, Bengtsson C, Larsson B, Pennert K, Rybo E, Sjöström L. Distribution of adipose tissue and risk of cardiovascular disease and death: a 12 year follow-up of participants in the population study of women in Gothenberg, Sweden. Br Med J (Clin Res Ed) 1984;289:1257–61.
  7. Berry EM, Hirsch J, Most J, McNamara DJ, Thornton J. The relationship of dietary fat to plasma lipid levels as studied by factor analysis of adipose tissue fatty acid composition in a free-living population of middle-aged American men. Am J Clin Nutr 1986;44: 220–31.[Abstract/Free Full Text]
  8. Kessler L, Baum C, Schoeller D. Direct measure of human de novo fatty acid synthesis using stable isotopes. FASEB J 1992;6:A1648 (abstr).
  9. Hellerstein MK, Christiansen M, Kaempfer S, et al. Measurement of de novo hepatic lipogenesis in humans using stable isotopes. J Clin Invest 1991;87:1841–52.
  10. Uemura K, Pisa Z. Trends in cardiovascular disease mortality in industrialized countries since 1950. World Health Stat Q 1988;41: 155–78.[Medline]
  11. Durnin JVGA, Rahaman MM. The assesment of the amount of fat in the human body from measurements of skinfold thickness. Br J Nutr 1967;21:681–9.[Medline]
  12. Valdez R, Seidell JC, Ahn YI, Weiss KM. A new index of abdominal adiposity as an indicator of risk for cardiovascular disease. A cross-population study. Int J Obes Relat Metab Disord 1993;17:77–82.[Medline]
  13. Sjöström L. A computer tomography based multicompartment body composition technique and anthropometric prediction of lean body mass, total and subcutaneous adipose tissue. Int J Obes 1991;15: 19–30.
  14. Tauri S, Tokunaga K, Fujioka S, Matsuzawa Y. Visceral fat obesity. Anthropological and pathophysiological aspects. Int J Obes 1991; 15(suppl):1S–8S.
  15. Lepage G, Roy CC. Direct transesterification of all classes of lipids in a one-step reaction. J Lipid Res 1986;27:114–20.[Abstract]
  16. Villegas JA, Iniesta JM. Investigación en informática aplicada a la alimentación humana. (Research in informatics applied to human food intake.) Murcia, Spain: Universidad Católica San Antonio, 1998 (in Spanish).
  17. Mataix J, Mañas M, Llopis J, Martínez E. Tabla de composición de alimentos españoles. (Table of composition of Spanish foods.) Granada, Spain: Instituto de Nutrición y Tecnología, Universidad de Granada, 1995 (in Spanish).
  18. Moreiras O, Carvajal A, Cabrera L. Tablas de composición de alimentos. (Tables of composition of foods.) Madrid: Ediciones Pirámide, SA, 1995.
  19. Thang S, van Leer E, Seidell J, Lean M. Waist circumference as a screening tool for cardiovascular risk factors: evaluation of receiver operating chacracteristics (ROC). Obes Res 1996;4:533–47.[Medline]
  20. Hegsted DM, Jack CW, Stare FJ. The composition of human adipose tissue from several parts of the world. Am J Clin Nutr 1962;10:11–8.[Medline]
  21. Scott RF, Lee KT, Kim DN, Morrison ES, Goodale F. Fatty acids of serum and adipose tissue in six groups eating natural diets containing 7 to 40 per cent fat. Am J Clin Nutr 1964;14:280–90.[Abstract/Free Full Text]
  22. Field CJ, Angel A, Clandinin MT. Relationship of diet to the fatty acid composition of human adipose tissue structural and stored lipids. Am J Clin Nutr 1985;42:1206–20.[Abstract/Free Full Text]
  23. Tjonneland A, Overvad K, Thorling E, Ewertz M. Adipose tissue fatty acids as biomarkers of dietary exposure in Danish men and women. Am J Clin Nutr 1993;57:629–33.[Abstract/Free Full Text]
  24. Garland M, Sacks FM, Colditz GA, et al. The relation between dietary intake and adipose tissue composition of selected fatty acids in US women. Am J Clin Nutr 1998;67:25–30.[Abstract]
  25. Keys A, ed. Seven countries: a multivariate analysis of death and coronary heart diseases. Cambridge, MA: Harvard University Press, 1980.
  26. Beynen AC, Hermus RJ, Hautvast JG. A mathematical relationship between the fatty acid composition of the diet and that of the adipose tissue in man. Am J Clin Nutr 1980;33:81–5.[Abstract/Free Full Text]
  27. Tove SB, Smith FH. Kinetics of the depletion of linoleic acid in mice. Arch Biochem Biophys 1959;85:325–65.
  28. Ostwald R, Okey R, Shannon A, Tinoco J. Changes in tissue lipids in response to diet. Fatty acids of subcutaneous, mesenteric and interscapular fat. J Nutr 1962;76:340–52.
  29. Fordyce MK, Christakis G, Kafatos A, Duncan R, Cassadi J. Adipose tissue fatty acid composition of adolescents in a U.S.-Greece cross-cultural study of coronary heart disease risk factors. J Chronic Dis 1983;36:481–6.[Medline]
  30. Crawford MA, Doyle W, Williams G, Drucy PJ. The role of fats and EFAs for energy and cell structure in growth of the fetus and neonate. In: Vergroesen AJ, Crawford MA, eds. The role of fat in human nutrition. London: Academic Press, 1989:82–115.
  31. London SJ, Sacks FM, Caesar J, Stampfer MJ, Siguel E, Willett WC. Fatty acid composition of subcutaneous adipose tissue and diet in postmenopausal US women. Am J Clin Nutr 1991;54:340–5.[Abstract/Free Full Text]
  32. Leaf DA, Connor WE, Barstad L, Sexton G. Incorporation of dietary n-3 fatty acids into the fatty acids of human adipose tissue and plasma lipid classes. Am J Clin Nutr 1995;62:68–73.[Abstract/Free Full Text]
  33. Nelson GJ, Schmidt PC, Bartolini GL, Kelley DS, Kyle D. The effect of dietary docosahexaenoic acid on plasma lipoproteins and tissue fatty acid composition in humans. Lipids 1997;32:1137–46.[Medline]
  34. Raclot T, Miokowski E, Bach AC, Groscolas R. Selectivity of fatty acid mobilization: a general metabolic feature of adipose tissue. Am J Physiol 1995;296:1060–7.
  35. Holman RT. Biological activities and requirements for polyunsaturated acids. In: Progress in the chemistry of fats and other lipids. New York: Pergamon Press, 1970:607–82.
  36. Schoeo RE, Evans KW, Sankey SS, Weissfeld JL, Kuller L. Does visceral adipose tissue differ from subcutaneous adipose tissue in fatty acid content? Int J Obes Relat Metab Disord 1996;20:346–52.[Medline]
  37. Kokatnur MG, Oalmann MC, Johnson WD, Malcom GT, Strong JP. Fatty acid composition of human adipose tissue from two anatomical sites in a biracial community. Am J Clin Nutr 1979;32:2198–205.[Abstract/Free Full Text]
  38. Calder PC, Harvey DJ, Pond CM, Newsholme EA. Site-specific differences in the fatty acid composition of human adipose tissue. Lipids 1992;27:716–20.[Medline]
  39. Phinney SD, Stern JS, Burke KE, Tang AB, Miller G, Holman RT. Human subcutaneous adipose tissue shows site-specific differences in fatty acid composition. Am J Clin Nutr 1994;60:725–9.[Abstract/Free Full Text]
  40. Nestel PJ. Fish oil and cardiovascular disease: lipids and arterial function. Am J Clin Nutr 2000;71(suppl):228S–31S.[Abstract/Free Full Text]
  41. Hudgins LC, Hirsch J, Emken EA. Correlation of isomeric fatty acids in human adipose tissue with clinical risk factors for cardiovascular disease. Am J Clin Nutr 1991;53:474–82.[Abstract/Free Full Text]
  42. Keys A, Anderson JT, Grande F. Serum cholesterol responses to changes in the diet. IV. Particularly saturated fatty acids in the diet. Metabolism 1965;14:776–87.
  43. Nelson GL. Dietary fatty acids and lipid metabolism. In: Chow CK, ed. Fatty acids in foods and their health implications. New York: Marcel Dekker, 1992:437–72.
  44. Emken EA. Metabolism of dietary stearic acid relative to other fatty acids in human subjects. Am J Clin Nutr 1994;60(suppl):1023S–8S.[Abstract/Free Full Text]
  45. Berry E, Eisenberg S, Friedlander Y, et al. Effects of diets rich in monounsaturated fatty acids on plasma lipoproteins. The Jerusalem Nutrition Study: monounsaturated vs saturated fatty acids. Nutr Metab Cardiovasc Dis 1995;5:55–62.
  46. Thomson AL, Lim-Fraser MY, Kraegen EW, Cooney GJ. Effects of individual fatty acids on glucose uptake and glycogen synthesis in soleous muscle in vitro. Am J Physiol Endocrinol Metab 2000;279: 577–84.
  47. Brynes AE, Edwards CM, Jadhav A, Ghatei MA, Bloom SR, Frost GS. Diet-induced change in fatty acid composition of plasma triacylglycerols is not associated with change in glucagon-like peptide 1 or insulin sensitivity in people with type 2 diabetes. Am J Clin Nutr 2000;72:1111–8.[Abstract/Free Full Text]
Received for publication August 1, 2000. Accepted for publication January 26, 2001.




This article has been cited by other articles:


Home page
 J. Am. Coll. Nutr.Home page
J. Mataix, M. Lopez-Frias, E. Martinez-de-Victoria, M. Lopez-Jurado, P. Aranda, and J. Llopis
Factors Associated with Obesity in an Adult Mediterranean Population: Influence on Plasma Lipid Profile
J. Am. Coll. Nutr., December 1, 2005; 24(6): 456 - 465.
[Abstract] [Full Text] [PDF]

Home page
 J. Nutr.Home page
A. Baylin and H. Campos
Arachidonic Acid in Adipose Tissue Is Associated with Nonfatal Acute Myocardial Infarction in the Central Valley of Costa Rica
J. Nutr., November 1, 2004; 134(11): 3095 - 3099.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
H. S Kahn and R. Valdez
Fatty acid composition of abdominal adipose tissue
Am. J. Clinical Nutrition, June 1, 2002; 75(6): 1123 - 1123.
[Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
M. Garaulet, F. Perez-Llamas, S. Zamora, F. S. de Medina, M. Perez-Ayala, P. Martinez, and F. J Tebar
Reply to HS Kahn and R Valdez
Am. J. Clinical Nutrition, June 1, 2002; 75(6): 1124 - 1124.
[Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.
Agricola
Right arrow Articles by Garaulet, M.
Right arrow Articles by Zamora, S.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS