Articles |
From the Lipid Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, and the Division of Endocrinology, Metabolism, and Molecular Medicine, New England Medical Center (E.J.S.), Boston, Mass.
Correspondence to Dr Ernst J. Schaefer, Lipid Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, 711 Washington St, Boston, MA 02111.
| Abstract |
|---|
|
|
|---|
Key Words: LDL cholesterol HDL cholesterol NCEP diet
| Introduction |
|---|
|
|
|---|
The response to dietary restriction of fat, saturated fat, and cholesterol in both normolipidemic and hypercholesterolemic individuals has great clinical and public health relevance. Approximately half of the men and women in the Framingham Offspring Study have plasma LDL cholesterol concentrations above the level defined by the NCEP panel as desirable (3.36 mmol/L, or 130 mg/dL), and 24% of men and 22% of women have plasma LDL cholesterol levels above 4.14 mmol/L (160 mg/dL), the level defined as high risk.9 It is estimated that approximately 52 million Americans are candidates for dietary treatment of hypercholesterolemia.10 Moreover, if in subjects eligible for diet treatment there could be a 15% reduction in LDL cholesterol instead of a 5% reduction, the number of subjects eligible for drug therapy could be reduced by 50%.10 Therefore, dietary restriction of saturated fat and cholesterol may be critical in the general population. However, few studies have evaluated the efficacy of diets similar to the NCEP Step 2 diet in reducing plasma lipid levels in a controlled fashion.11 12 13 There is a need for more information on the effects of NCEP Step 2 diets on plasma lipid levels.
The purpose of the present study was to determine the effects of a diet meeting NCEP Step 2 criteria on plasma lipid levels in middle-aged and elderly normolipidemic and hypercholesterolemic men and women under controlled isocaloric metabolic conditions. Our data indicate that, by complying with an NCEP Step 2 diet, both normolipidemic and hypercholesterolemic subjects may achieve significant reductions in plasma LDL cholesterol levels without significant changes in the total cholesterol/HDL cholesterol ratio. However, our data also indicate a significant biological variability in response to this diet in terms of LDL and HDL cholesterol lowering.
| Methods |
|---|
|
|
|---|
Diets
Meals for the baseline diet and the NCEP Step 2 diet were
prepared by the Metabolic Research Unit of the USDA Human
Nutrition Research Center on Aging at Tufts University and were
provided to the participants. Meals consisted of breakfast, lunch,
dinner, and one or two snacks, on a 3-day cycle menu. Subjects were
requested to consume at least one meal per day at the
Metabolic Research Unit on weekdays. Weekend meals were
packaged and provided to the participants before the weekend. Blood
pressure and body weight were measured at least three times per week.
To keep each subject's body weight constant (±1 kg) throughout the
study, caloric intake was adjusted by means of proportional increments
or decrements of all foods.
The composition of the baseline diet approximated that of the diet
currently consumed in the United States15 ; it consisted of
35.4% of calories as fat and 14.1% of calories as saturated fat, and
contained 147 mg cholesterol per 1000 kcal (Table 1
). The NCEP Step 2 diet consisted of 25.5% of calories
as fat and 4.0% of calories as saturated fat, and contained 45 mg
cholesterol per 1000 kcal. The difference in calories
derived from total fat between the baseline diet and the Step 2 diet
was compensated for by an increase in calories derived from
carbohydrates. Triplicate preparations of each complete 3-day meal
cycle for each of the two diets were analyzed for nutrient
composition by Hazleton Laboratories America Inc. The protein,
carbohydrate, fat, fatty acid, and cholesterol contents of
these diets, as derived from chemical analysis, are provided in
Table 1
. The total fiber content was calculated by use of food
composition tables (GRAND database, release 867,
USDAGrand Forks Human Nutrition Research Center) and was 12.1 g/1000
kcal in the baseline diet and 16.6 g/1000 kcal in the NCEP Step 2 diet.
Typical menus for the baseline and the NCEP Step 2 diets are shown in
Table 2
.
|
|
Laboratory Measurements
In normocholesterolemic subjects, blood samples
for plasma lipid measurements were collected at weeks 4, 5, and 6 of
the baseline diet period and at weeks 4, 8, 12, 16, 20, and 24 of the
NCEP Step 2 diet period. In hypercholesterolemic
subjects, blood was collected at weeks 4, 5, and 6 of both the baseline
diet and the NCEP Step 2 diet. Blood was collected, after a 12-hour
overnight fast, in tubes containing 0.15% EDTA and centrifuged
at 2500 rpm for 20 minutes at 4°C to separate plasma. HDL
cholesterol levels were measured in plasma after
precipitation of apo Bcontaining lipoproteins by the dextran
sulfateMgCl2 method.16 HDL3
cholesterol levels were measured directly from total plasma
by use of a modification of the method of Warnick et al.17
Instead of performing sequential precipitations, in which
HDL3 particles are isolated from the total HDL
supernatants, we performed parallel precipitations directly from
plasma. For the HDL3 precipitation, the concentrations of
dextran sulfate and MgCl2 were adjusted to provide the same
final concentrations as in the original method by addition of a 10%
volume of precipitating reagent containing 19.1 g/L dextran sulfate and
1.95 mol/L MgCl2 to coprecipitate apo Bcontaining and
HDL2 lipoproteins. After incubation at room
temperature for 10 minutes, samples were centrifuged at 3500
rpm for 30 minutes at 4°C and the clear supernatants were used for
cholesterol analysis. HDL2
cholesterol levels were calculated as the difference
between HDL cholesterol and HDL3
cholesterol levels. Plasma was centrifuged at 4°C
in a Beckman 50.3 Ti rotor at 39 000 rpm for 18 hours at a density of
1.006 g/mL to isolate VLDL, according to the Lipid Research Clinics
methodology.18 Plasma total cholesterol and
triglyceride levels, 1.006 g/mL infranatant
cholesterol, and HDL cholesterol and
HDL3 cholesterol levels were measured by
automated enzymatic techniques with an Abbott Diagnostics
Spectrum CCX bichromatic analyzer and Abbott enzymatic
reagents.19 VLDL and LDL cholesterol
concentrations were calculated as follows: VLDL
cholesterol=total cholesterol-1.006 g/mL
infranatant cholesterol, and LDL
cholesterol=1.006 g/mL infranatant
cholesterol-HDL cholesterol.
Our lipid methods are standardized through the Centers for Disease Control and Prevention (CDC) National Heart, Lung, and Blood Institute Lipid Standardization Program, and our laboratory serves as a member of the CDC Cholesterol Reference Method Laboratory Network.
In normolipidemic subjects, plasma apo A-I and apo B concentrations were measured in total plasma by noncompetitive enzyme-linked immunosorbent assays (ELISAs) with immunopurified polyclonal antibodies as previously described,20 21 and plasma Lp(a) was measured with a commercially available ELISA (Strategic Diagnostics Inc) as previously described.22 In hypercholesterolemic subjects, plasma apo A-I, apo B, and Lp(a) concentrations were measured by immunoturbidimetric assays (IncStar). Coefficients of variation for all lipid assays were less than 5%, and for apolipoprotein assays they were less than 8%.
LDL particle size was determined by gradient gel electrophoresis on 2% to 16% nondenaturing polyacrylamide gels.23 The LDL particle score of each subject was calculated taking into account the relative area under the peak of the major and all minor LDL bands, as previously indicated.24 A higher LDL particle score represents a smaller LDL particle size.
Apo A-IV and apo E isoform phenotyping was performed on plasma obtained from all subjects by immunoblotting and isoelectric focusing methods, respectively, as previously described.25 26
Statistical Analyses
The SAS statistical program (SAS Institute) was
used to perform all statistical analyses. PROC
GLM was used to test by ANOVA for differences in mean values at
weeks 4, 5, and 6 of the 6-week diet period and at weeks 4, 8, 12, 16,
20, and 24 of the 24-week diet period. Because no difference among time
points within each dietary phase was observed, mean values for each of
the dietary phases were calculated. A paired Student's t
test was carried out to test for differences between mean values during
the NCEP Step 2 diet and the corresponding baseline value. Correlation
analyses were performed by use of the PROC CORR
procedure.
| Results |
|---|
|
|
|---|
|
The effects of the NCEP Step 2 diet, compared with the baseline diet,
on plasma lipid and apolipoprotein levels in normolipidemic and
hypercholesterolemic subjects are shown in Table 4
. Stabilization of plasma lipid levels during the NCEP
Step 2 diet, under isocaloric conditions, occurred by week 4 in both
groups of subjects (data not shown). During consumption of the NCEP
Step 2 diet, plasma total cholesterol, LDL
cholesterol, and HDL cholesterol levels changed
significantly in both normolipidemic subjects (20%, 21%, and
16%, respectively) and hypercholesterolemic subjects
(16%, 18%, and 15%, respectively). The decrease in plasma HDL
cholesterol levels observed during the NCEP Step 2 diet was
due to decreases in both HDL2 and HDL3
cholesterol levels in both groups of subjects. As a result
of similar decreases in total cholesterol and HDL
cholesterol levels, a small and nonsignificant decrease in
the total cholesterol/HDL cholesterol ratio was
observed in both groups. The decreases in plasma apo B and apo A-I
levels paralleled those in LDL and HDL cholesterol
levels, respectively (Table 4
). Levels of plasma
triglyceride, VLDL cholesterol, and Lp(a) were
not significantly affected by the diet in these subjects (Table 4
).
|
LDL particle size was also measured at the ends of the baseline and the
NCEP Step 2 diet periods (Table 4
). Consumption of the NCEP Step 2 diet
was associated with an increase in LDL particle score, reflecting a
decrease in LDL particle size in both groups of subjects. However, the
diet-associated decrease in LDL size reached statistical significance
only in the hypercholesterolemic group.
The individual LDL cholesterol and HDL
cholesterol responses to diet in normolipidemic and
hypercholesterolemic subjects participating in our
study are shown in Fig 1
. The percent LDL
cholesterol and HDL cholesterol change in
response to the NCEP Step 2 diet in these subjects is shown in Fig 2
. A greater LDL cholesterol response to the
diet in men than in women (-20.7% and -13.4%, respectively;
P<.05) was observed. The percent HDL
cholesterol response to the diet was similar in men and
women (-14.5% and -15.3%, respectively). During the NCEP Step 2
diet, subjects with the apo E3/E4 phenotype (n=8) experienced a
mean 18.6% decrease in LDL cholesterol levels compared
with the baseline diet, whereas subjects with the E3/E3
phenotype (n=18) experienced a mean decrease of 15.2%. The
difference in LDL cholesterol response to the diet in these
apo E phenotype groups did not reach statistical significance.
However, when analyses were performed separately for men and
women, the LDL cholesterol response to the diet was
significantly greater in men with the E3/E4 phenotype (n=5)
than in those with the E3/E3 phenotype (n=10) (-28.7% and
-14.9%, respectively; P<.03). LDL cholesterol
response to the diet in women with the apo E3/E4 phenotype
(n=3, -1.9%) was lower (P<.05) from that in women with
the apo E3/E3 phenotype (n=8, -15.9%). However, this was a
small sample size. Only three of the 32 subjects participating in our
study had the apo A-IV-2 phenotype. This number was
insufficient for statistical analysis. In
univariate analyses, the diet-related percent
change in LDL cholesterol levels was significantly
associated with the percent change in HDL cholesterol
levels (r=.41, P<.02). Body mass index was not
associated with diet responsiveness in these subjects. In this study
there was by design no effect on body weight.
|
|
| Discussion |
|---|
|
|
|---|
As indicated in Table 2
, in our study the reduction in total and
saturated fat in the NCEP Step 2 diet, compared with the average diet
currently consumed in the United States, was achieved by excluding red
meat, substituting low-fat dairy products for full-fat dairy
products, and increasing the intake of fresh fruits, vegetables,
and cereal-based products. These dietary changes are feasible and
can be achieved by motivated individuals in the general population.
Within each population, plasma HDL levels have been inversely associated with the risk of coronary heart disease.34 35 Some concern has been raised about the decrease in HDL cholesterol levels observed with low-fat diets. However, cross-cultural studies indicate that populations with very low intakes of fat in their diet have low rates of coronary heart disease despite low plasma HDL cholesterol levels.36 In addition, there are indications that, when these diets are consumed in a free-living state or when a regular program of physical exercise is associated with diet in overweight subjects, the reduction in HDL cholesterol may be minimized.37
In our subjects, there was a very slight and nonsignificant decrease in the total cholesterol/HDL cholesterol ratio. The decrease in plasma LDL cholesterol levels was paralleled by a similar decrease in apo B levels, suggesting a decrease in the number of circulating LDL particles. However, a change in the structural composition of LDL particles occurred as well, as suggested by a reduction in LDL particle size in both normal and hypercholesterolemic subjects during the consumption of the NCEP Step 2 diet. It has been shown that changes in plasma triglyceride levels are the strongest predictors of changes in LDL particle size.38 Because the consumption of the NCEP Step 2 diet was associated with decreases in both total cholesterol and LDL cholesterol levels without a change in triglyceride levels, it is likely that this relative increase in triglyceride levels was responsible for the LDL size change. Because there is a general concern about the atherogenic potential of small LDL, the change in LDL size that we observed in our subjects after consumption of the NCEP Step 2 diet deserves further attention.
The LDL cholesterol response to the NCEP Step 2 diet was greater in men with the E3/E4 phenotype than in men with the E3/E3 phenotype, in keeping with previous reports showing a greater response to dietary restriction in male subjects with apo E4.26
In this study, greater decreases in the HDL2 subfraction than in the HDL3 subfraction after dietary fat restriction were observed, in agreement with other studies.12 29 39 It has been shown in kinetic studies that a reduction in dietary fat consumption is associated with decreases in apo A-I transport rates.40 Although the mechanism responsible for this phenomenon is not known at present, it is likely that the reduction in circulating apo A-I, without alteration in apo A-II concentrations, may lead to a preferential decrease in HDL particles containing apo A-I only, which are predominantly present in the HDL2 subfraction.41
Overall, our results indicate that an 18% decrease in LDL cholesterol may be achieved with only diet modification in hypercholesterolemic subjects. Recently the efficacy of the NCEP Step 2 diet in the reduction of LDL cholesterol levels in hypercholesterolemic patients has been questioned by a study reporting only a 5% decrease in LDL cholesterol.42 One problem with that study was that hypercholesterolemic subjects were selected who had previously been designated by their physicians to be candidates for drug therapy. Therefore, subjects less responsive to diet may have been selected. In addition, in outpatient diet studies, a major problem encountered by many investigators is the lack of patient compliance. Unlike the case in drug studies, a blinded design is not possible in diet studies, and investigators have relied on dietary questionnaires as instruments of compliance. However, it has been shown that the results of dietary questionnaires may have a high intraindividual variability.43 In addition, when diet records are used, patients may be more compliant with their diet during the recording days. In our study, all meals were provided to the participants, who were required to consume at least one meal every weekday at the Metabolic Research Unit, thus decreasing problems arising from lack of compliance. However, it is possible that the low content of saturated fat in our NCEP Step 2 diet (4%, when levels up to 7% are within the NCEP Step 2 guidelines) played a role in the marked LDL cholesterollowering response that we observed during that diet. It has been projected that if a 15% reduction in LDL cholesterol levels is achieved through dietary means in the US population, compared with only a 5% reduction, the number of subjects requiring drug treatment may be reduced by 50%.10
A final issue is the striking variability in individual response to the diet. In this study, under controlled conditions, we clearly documented a very high degree of variability of response to NCEP Step 2 diets with regard to both LDL and HDL cholesterol lowering. Katan and coworkers44 45 observed similar variability in LDL cholesterol response to high-cholesterol diets. This large individual variability in the LDL cholesterol response to the diet indicates that genetic and environmental factors other than diet play a role in diet responsiveness.
Our data are consistent with a significant and beneficial effect on plasma LDL cholesterol levels of a diet low in total and saturated fat in both normocholesterolemic and hypercholesterolemic middle-aged and elderly men and women. Despite decreases in HDL cholesterol levels, no significant changes in the total cholesterol/HDL cholesterol ratio were observed.
| Acknowledgments |
|---|
| Footnotes |
|---|
Received January 31, 1995; accepted May 8, 1995.
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
D. J. Jenkins, C. W. Kendall, D. A Faulkner, T. Nguyen, T. Kemp, A. Marchie, J. M. Wong, R. de Souza, A. Emam, E. Vidgen, et al. Assessment of the longer-term effects of a dietary portfolio of cholesterol-lowering foods in hypercholesterolemia Am. J. Clinical Nutrition, March 1, 2006; 83(3): 582 - 591. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Fletcher, K. Berra, P. Ades, L. T. Braun, L. E. Burke, J. L. Durstine, J. M. Fair, G. F. Fletcher, D. Goff, L. L. Hayman, et al. Managing Abnormal Blood Lipids: A Collaborative Approach Circulation, November 15, 2005; 112(20): 3184 - 3209. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Desroches, P Y. Chouinard, I. Galibois, L. Corneau, J. Delisle, B. Lamarche, P. Couture, and N. Bergeron Lack of effect of dietary conjugated linoleic acids naturally incorporated into butter on the lipid profile and body composition of overweight and obese men Am. J. Clinical Nutrition, August 1, 2005; 82(2): 309 - 319. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. W. Aude, A. S. Agatston, F. Lopez-Jimenez, E. H. Lieberman, Marie Almon, M. Hansen, G. Rojas, G. A. Lamas, and C. H. Hennekens The National Cholesterol Education Program Diet vs a Diet Lower in Carbohydrates and Higher in Protein and Monounsaturated Fat: A Randomized Trial Arch Intern Med, October 25, 2004; 164(19): 2141 - 2146. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Li, S. Lamon-Fava, J. Otvos, A. H. Lichtenstein, W. Velez-Carrasco, J. R. McNamara, J. M. Ordovas, and E. J. Schaefer Fish Consumption Shifts Lipoprotein Subfractions to a Less Atherogenic Pattern in Humans J. Nutr., July 1, 2004; 134(7): 1724 - 1728. [Abstract] [Full Text] |
||||
![]() |
Y. Henkin and I. Shai Dietary Treatment of Hypercholestrolemia: Can We Predict Long-Term Success? J. Am. Coll. Nutr., December 1, 2003; 22(6): 555 - 561. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. N. Han, L. S. Leka, A. H. Lichtenstein, L. M. Ausman, and S. N. Meydani Effect of a therapeutic lifestyle change diet on immune functions of moderately hypercholesterolemic humans J. Lipid Res., December 1, 2003; 44(12): 2304 - 2310. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Li, J. D. Otvos, S. Lamon-Fava, W. V. Carrasco, A. H. Lichtenstein, J. R. McNamara, J. M. Ordovas, and E. J. Schaefer Men and Women Differ in Lipoprotein Response to Dietary Saturated Fat and Cholesterol Restriction J. Nutr., November 1, 2003; 133(11): 3428 - 3433. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. F Masson, G. McNeill, and A. Avenell Genetic variation and the lipid response to dietary intervention: a systematic review Am. J. Clinical Nutrition, May 1, 2003; 77(5): 1098 - 1111. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J.A. Jenkins, C. W.C. Kendall, A. Marchie, T. L. Parker, P. W. Connelly, W. Qian, J. S. Haight, D. Faulkner, E. Vidgen, K. G. Lapsley, et al. Dose Response of Almonds on Coronary Heart Disease Risk Factors: Blood Lipids, Oxidized Low-Density Lipoproteins, Lipoprotein(a), Homocysteine, and Pulmonary Nitric Oxide: A Randomized, Controlled, Crossover Trial Circulation, September 10, 2002; 106(11): 1327 - 1332. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J Baer, J. T Judd, B. A Clevidence, R. A Muesing, W. S Campbell, E. D Brown, and P. R Taylor Moderate alcohol consumption lowers risk factors for cardiovascular disease in postmenopausal women fed a controlled diet Am. J. Clinical Nutrition, March 1, 2002; 75(3): 593 - 599. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. J Schaefer Lipoproteins, nutrition, and heart disease Am. J. Clinical Nutrition, February 1, 2002; 75(2): 191 - 212. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Sun, F. K Welty, G. G Dolnikowski, A. H Lichtenstein, and E. J Schaefer Effects of a National Cholesterol Education Program Step II Diet on apolipoprotein A-IV metabolism within triacylglycerol-rich lipoproteins and plasma Am. J. Clinical Nutrition, September 1, 2001; 74(3): 308 - 314. [Abstract] [Full Text] |
||||
![]() |
J. A. Metz, J. S. Stern, P. Kris-Etherton, M. E. Reusser, C. D. Morris, D. C. Hatton, S. Oparil, R. B. Haynes, L. M. Resnick, F. X. Pi-Sunyer, et al. A Randomized Trial of Improved Weight Loss With a Prepared Meal Plan in Overweight and Obese Patients: Impact on Cardiovascular Risk Reduction Arch Intern Med, July 24, 2000; 160(14): 2150 - 2158. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. E. Walden, B. M. Retzlaff, B. L. Buck, S. Wallick, B. S. McCann, and R. H. Knopp Differential Effect of National Cholesterol Education Program (NCEP) Step II Diet on HDL Cholesterol, Its Subfractions, and Apoprotein A-I Levels in Hypercholesterolemic Women and Men After 1 Year : The beFIT Study Arterioscler. Thromb. Vasc. Biol., June 1, 2000; 20(6): 1580 - 1587. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Asztalos, M. Lefevre, L. Wong, T. A. Foster, R. Tulley, M. Windhauser, W. Zhang, and P. S. Roheim Differential response to low-fat diet between low and normal HDL-cholesterol subjects J. Lipid Res., March 1, 2000; 41(3): 321 - 328. [Abstract] [Full Text] |
||||
![]() |
E. J Schaefer, J. L Augustin, M. M Schaefer, H. Rasmussen, J. M Ordovas, G. E Dallal, and J. T Dwyer Lack of efficacy of a food-frequency questionnaire in assessing dietary macronutrient intakes in subjects consuming diets of known composition Am. J. Clinical Nutrition, March 1, 2000; 71(3): 746 - 751. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Berglund, E. H Oliver, N. Fontanez, S. Holleran, K. Matthews, P. S Roheim, H. N Ginsberg, R. Ramakrishnan, and M. Lefevre HDL-subpopulation patterns in response to reductions in dietary total and saturated fat intakes in healthy subjects Am. J. Clinical Nutrition, December 1, 1999; 70(6): 992 - 1000. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Velez-Carrasco, A. H. Lichtenstein, F. K. Welty, Z. Li, S. Lamon-Fava, G. G. Dolnikowski, and E. J. Schaefer Dietary Restriction of Saturated Fat and Cholesterol Decreases HDL ApoA-I Secretion Arterioscler. Thromb. Vasc. Biol., April 1, 1999; 19(4): 918 - 924. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. L. Stefanick, S. Mackey, M. Sheehan, N. Ellsworth, W. L. Haskell, and P. D. Wood Effects of Diet and Exercise in Men and Postmenopausal Women with Low Levels of HDL Cholesterol and High Levels of LDL Cholesterol N. Engl. J. Med., July 2, 1998; 339(1): 12 - 20. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Tilly-Kiesi, A. H. Lichtenstein, J. Joven, E. Vilella, M. C. Cheung, W. V. Carrasco, J. M. Ordovas, G. Dolnikowski, and E. J. Schaefer Impact of Gender on the Metabolism of Apolipoprotein A-I in HDL Subclasses LpAI and LpAI:AII in Older Subjects Arterioscler. Thromb. Vasc. Biol., December 1, 1997; 17(12): 3513 - 3518. [Abstract] [Full Text] |