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1.
J Hum Nutr Diet ; 30(5): 596-603, 2017 10.
Article in English | MEDLINE | ID: mdl-28168764

ABSTRACT

BACKGROUND: Evidence exists for an association between accordance with a Mediterranean diet pattern and slower rates of cognitive decline. However, an 'Americanised' version of the Mediterranean diet screener is needed to assess accordance in the USA. Thus, the Mediterranean Eating Pattern for Americans (MEPA) tool was developed to assess accordance with a Mediterranean-like food pattern when time is limited. The present study aimed to determine whether the MEPA screener captured the key elements of the Mediterranean diet compared to the more comprehensive food frequency questionnaire (FFQ). METHODS: The study comprised a cross-sectional study in which 70 women completed both the VioScreen™ FFQ (Viocare, Princeton, NJ, USA) electronically and the 16-item MEPA screener, either electronically or by telephone, aiming to evaluate the inter-method reliability of the proposed screener. The convenience sample included patients (n = 49) and healthcare providers (n = 21) recruited from a tertiary care medical centre. RESULTS: The overall score from the MEPA screener correlated with corresponding overall MEPA FFQ score (ρ = 0.365, P = 0.002). Agreement between screener items and FFQ items was moderate-to-good for berries (κ = 0.47, P < 0.001), nuts (κ = 0.42, P < 0.001), fish (κ = 0.62, P < 0.001) and alcohol (κ = 0.64, P < 0.001), whereas those for olive oil (κ = 0.33, P = 0.001) and green leafy vegetables (κ = 0.36, P = 0.0021) were fair. Usual intakes of potassium, magnesium, vitamin C, saturated fat, selected carotenoids, folate and fibre derived from the FFQ varied with MEPA screener scores in the anticipated directions. CONCLUSIONS: The MEPA screener captures several components of the Mediterranean style pattern, although further testing of the MEPA screener is indicated.


Subject(s)
Diet Surveys , Diet, Mediterranean , Nutrition Assessment , Adult , Aged , Body Mass Index , Cross-Sectional Studies , Diet, Healthy , Diet, Western , Female , Humans , Middle Aged , Reproducibility of Results , United States , Young Adult
2.
J Nutr Health Aging ; 17(5): 441-5, 2013.
Article in English | MEDLINE | ID: mdl-23636545

ABSTRACT

OBJECTIVE: To examine whether adherence to a Mediterranean-based dietary pattern is predictive of depressive symptoms among older adults. DESIGN: Generalized estimating equation models were used to test the association between a Mediterranean-based dietary pattern and depressive symptoms over time. Models were adjusted for age, sex, race, education, income, widowhood, antidepressant use, total calorie intake, body mass index, smoking, alcohol consumption, number of self-reported medical conditions, cognitive function, and physical disability. SETTING: Chicago, Illinois. PARTICIPANTS: Community-dwelling participants (n=3502) of the Chicago Health and Aging Project aged 65+ years (59% African American) who had no evidence of depression at the baseline. MEASUREMENTS: Adherence to a Mediterranean-based dietary pattern was assessed by the MedDietScore. Dietary evaluation was performed with a food frequency questionnaire at baseline and related to incident depression as measured by the presence of four or more depressive symptoms from the 10-item version of the Center for Epidemiologic Studies Depression scale. RESULTS: Over an average follow-up of 7.2 years, greater adherence to a Mediterranean-based diet was associated with a reduced number of newly occurring depressive symptoms (parameter estimate = -0.002, standard error = 0.001; p = 0.04). The annual rate of developing depressive symptoms was 98.6% lower among persons in the highest tertile of a Mediterranean-based dietary pattern compared with persons in the lowest tertile group. CONCLUSION: Our results support the hypothesis that adherence to a diet comprised of vegetables, fruits, whole grains, fish, and legumes may protect against the development of depressive symptoms in older age.


Subject(s)
Depression/prevention & control , Diet, Mediterranean , Feeding Behavior , Aged , Aged, 80 and over , Chicago/epidemiology , Depression/epidemiology , Diet Surveys , Female , Geriatric Assessment , Humans , Incidence , Male , Models, Biological , Surveys and Questionnaires , Time Factors
3.
Neurology ; 77(13): 1276-82, 2011 Sep 27.
Article in English | MEDLINE | ID: mdl-21947532

ABSTRACT

OBJECTIVE: To investigate the interrelations of serum vitamin B12 markers with brain volumes, cerebral infarcts, and performance in different cognitive domains in a biracial population sample cross-sectionally. METHODS: In 121 community-dwelling participants of the Chicago Health and Aging Project, serum markers of vitamin B12 status were related to summary measures of neuropsychological tests of 5 cognitive domains and brain MRI measures obtained on average 4.6 years later among 121 older adults. RESULTS: Concentrations of all vitamin B12-related markers, but not serum vitamin B12 itself, were associated with global cognitive function and with total brain volume. Methylmalonate levels were associated with poorer episodic memory and perceptual speed, and cystathionine and 2-methylcitrate with poorer episodic and semantic memory. Homocysteine concentrations were associated with decreased total brain volume. The homocysteine-global cognition effect was modified and no longer statistically significant with adjustment for white matter volume or cerebral infarcts. The methylmalonate-global cognition effect was modified and no longer significant with adjustment for total brain volume. CONCLUSIONS: Methylmalonate, a specific marker of B12 deficiency, may affect cognition by reducing total brain volume whereas the effect of homocysteine (nonspecific to vitamin B12 deficiency) on cognitive performance may be mediated through increased white matter hyperintensity and cerebral infarcts. Vitamin B12 status may affect the brain through multiple mechanisms.


Subject(s)
Brain/anatomy & histology , Brain/metabolism , Cognition/physiology , Magnetic Resonance Imaging , Vitamin B 12/blood , Aged , Aged, 80 and over , Brain Infarction/metabolism , Brain Infarction/pathology , Chicago , Cohort Studies , Cross-Sectional Studies , Female , Fumarates/metabolism , Humans , Male , Maleates/metabolism , Neuropsychological Tests , Residence Characteristics , Retrospective Studies
4.
Neurology ; 67(8): 1370-6, 2006 Oct 24.
Article in English | MEDLINE | ID: mdl-17060562

ABSTRACT

OBJECTIVE: To examine the association between rates of cognitive change and dietary consumption of fruits and vegetables among older persons. METHODS: The authors conducted a prospective cohort study of 3,718 participants, aged 65 years and older of the Chicago Health and Aging Project. Participants completed a food frequency questionnaire and were administered at least two of three cognitive assessments at baseline, 3-year, and 6-year follow-ups. Cognitive function was measured using the average z-score of four tests: the East Boston Tests of immediate memory and delayed recall, the Mini-Mental State Examination, and the Symbol Digit Modalities Test. RESULTS: The mean cognitive score at baseline for the analyzed cohort was 0.18 (range: -3.5 to 1.6), and the overall mean change in score per year was a decline of 0.04 standardized units. In mixed effects models adjusted for age, sex, race, and education, compared with the rate of cognitive decline among persons in the lowest quintile of vegetable intake (median of 0.9 servings/day), the rate for persons in the fourth quintile (median, 2.8 servings/day) was slower by 0.019 standardized units per year (p = 0.01), a 40% decrease, and by 0.018 standardized units per year (p = 0.02) for the fifth quintile (median, 4.1 servings/day), or a 38% decrease in rates. The association remained significant (p for linear trend = 0.02) with further control of cardiovascular-related conditions and risk factors. Fruit consumption was not associated with cognitive change. CONCLUSION: High vegetable but not fruit consumption may be associated with slower rate of cognitive decline with older age.


Subject(s)
Aging/psychology , Cognition , Diet , Fruit , Vegetables , Aged , Black People/psychology , Cohort Studies , Female , Humans , Male , Neuropsychological Tests , Prospective Studies , White People/psychology
5.
J Neurol Neurosurg Psychiatry ; 75(8): 1093-9, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15258207

ABSTRACT

BACKGROUND: Dementia can be caused by severe niacin insufficiency, but it is unknown whether variation in intake of niacin in the usual diet is linked to neurodegenerative decline. We examined whether dietary intake of niacin was associated with incident Alzheimer's disease (AD) and cognitive decline in a large, prospective study. METHODS: This study was conducted in 1993-2002 in a geographically defined Chicago community of 6158 residents aged 65 years and older. Nutrient intake was determined by food frequency questionnaire. Four cognitive tests were administered to all study participants at 3 year intervals in a 6 year follow up. A total of 3718 participants had dietary data and at least two cognitive assessments for analyses of cognitive change over a median 5.5 years. Clinical evaluations were performed on a stratified random sample of 815 participants initially unaffected by AD, and 131 participants were diagnosed with 4 year incident AD by standardised criteria. RESULTS: Energy adjusted niacin intake had a protective effect on development of AD and cognitive decline. In a logistic regression model, relative risks (95% confidence intervals) for incident AD from lowest to highest quintiles of total niacin intake were: 1.0 (referent) 0.3 (0.1 to 0.6), 0.3 (0.1 to 0.7), 0.6 (0.3 to 1.3), and 0.3 (0.1 to 0.7) adjusted for age, sex, race, education, and ApoE e4 status. Niacin intake from foods was also inversely associated with AD (p for linear trend = 0.002 in the adjusted model). In an adjusted random effects model, higher food intake of niacin was associated with a slower annual rate of cognitive decline, by 0.019 standardised units (SU) per natural log increase in intake (mg) (p = 0.05). Stronger associations were observed in analyses that excluded participants with a history of cardiovascular disease (beta = 0.028 SU/year; p = 0.008), those with low baseline cognitive scores (beta = 0.023 SU/year; p = 0.02), or those with fewer than 12 years' education (beta = 0.035 SU/year; p = 0.002) CONCLUSION: Dietary niacin may protect against AD and age related cognitive decline.


Subject(s)
Alzheimer Disease/etiology , Alzheimer Disease/prevention & control , Cognition Disorders/etiology , Cognition Disorders/prevention & control , Diet , Hypolipidemic Agents/pharmacology , Niacin/pharmacology , Aged , Female , Humans , Male , Nutritional Status , Prospective Studies , Risk Factors
6.
Neurology ; 62(9): 1573-9, 2004 May 11.
Article in English | MEDLINE | ID: mdl-15136684

ABSTRACT

OBJECTIVE: To examine whether consumption of different types of fat is associated with age-related change in cognition. METHODS: The authors related fat consumption to 6-year change in cognitive function among 2,560 participants of the Chicago Health and Aging Project, ages 65 and older, with no history of heart attack, stroke, or diabetes at baseline. Fat intake was measured by food frequency questionnaire. Cognitive function was measured at baseline and 3-year and 6-year follow-ups, using the average z score of four cognitive tests: the East Boston Tests of Immediate and Delayed Recall, the Mini-Mental State Examination, and the Symbol Digit Modalities Test. RESULTS: In separate mixed models adjusted for demographic and cardiovascular risk factors and intakes of antioxidant nutrients and other dietary fats, higher intakes of saturated fat (p for trend = 0.04) and trans-unsaturated fat (p for trend = 0.07) were linearly associated with greater decline in cognitive score over 6 years. These associations became stronger in analyses that eliminated persons whose fat intake changed in recent years or whose baseline cognitive scores were in the lowest 15%. Inverse associations with cognitive decline were observed in these latter restricted analyses for high intake of monounsaturated fat and a high ratio of polyunsaturated to saturated fat intake. Intakes of total fat, vegetable and animal fats, and cholesterol were not associated with cognitive change. CONCLUSION: A diet high in saturated or trans-unsaturated fat or low in nonhydrogenated unsaturated fats may be associated with cognitive decline among older persons.


Subject(s)
Cognition Disorders/etiology , Cognition/physiology , Dietary Fats/adverse effects , Eating/physiology , Age Factors , Aged , Censuses , Cognition Disorders/diagnosis , Cognition Disorders/epidemiology , Cross-Sectional Studies , Feeding Behavior , Female , Follow-Up Studies , Geriatric Assessment , Humans , Male , Neuropsychological Tests , Nutrition Surveys , Prospective Studies , Racial Groups/statistics & numerical data , United States/epidemiology
7.
Breast Cancer Res Treat ; 71(2): 113-23, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11881909

ABSTRACT

Little information is available about the relationship between quality of life of women who have survived breast cancer (specifically, symptoms including those of menopause and depression) and the quality of their diet. In this cross-sectional study, 117 women with known primary breast cancer completed a self-administered food frequency questionnaire (FFQ) reflecting usual diet during the past year, a Survey of Feelings and Attitudes using the Center for Epidemiologic Studies Depression scale (CES-D) and a survey that includes menopausal symptoms among others common to women with a history of breast cancer. When women's responses to the FFQ were scored using the Healthy Eating Index (HEI), most often diets were evaluated as those that 'need improvement' with a mean total HEI score of 67.2. With regard to the CES-D scores, study women averaged 9.5, with 19 women being classified as clinically depressed. HEI and CES-D scores were inversely related (p = -0.22, p = 0.02). A negative correlation was also observed between energy-adjusted calcium intakes and CES-D scores (p = -0.19, p = 0.04). Clinical depressed women had not only lower HEI scores and calcium intakes, but also lower grain and variety scores. Comparisons to national data for disease-free women and that available for those with breast cancer suggest that our study women consumed diets low in energy and dietary variety. Diet quality may be an important factor influencing the manifestation of depressive symptoms in breast cancer survivors or conversely, poorer diet quality may be an outcome of depression.


Subject(s)
Breast Neoplasms/physiopathology , Diet , Feeding Behavior , Health Behavior , Quality of Life , Survivors , Breast Neoplasms/psychology , Cross-Sectional Studies , Diet/standards , Female , Follow-Up Studies , Humans , Middle Aged , Surveys and Questionnaires , Time Factors
8.
Atherosclerosis ; 159(1): 225-30, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11689225

ABSTRACT

The clinical utility of fibrinogen measurement has been limited by large intraindividual variability. Several approaches that have been shown to improve the repeatability of fibrinogen include acquisition of samples at the same time of day, standardized sample procurement techniques, and multiple replicate sampling. This study employed established pre-analytical and analytical techniques known to reduce fibrinogen variability, including the acquisition of three replicate samples, each analyzed in duplicate, to evaluate the impact of intraindividual variability in fibrinogen measurement at baseline and 3 months on cardiovascular risk in 60 healthy subjects. Classification accuracy was evaluated by the ability to categorize subjects into tertiles of fibrinogen. Only 55% (33/60) of the subjects were correctly assigned to the appropriate fibrinogen tertile. Fibrinogen measurements varied by more than 10% in 45% of subjects and by 5% in 80% of subjects. Intraindividual variability in fibrinogen measurement with a functional assay limits cardiovascular risk assessment even when three replicates are averaged.


Subject(s)
Cardiovascular Diseases/blood , Fibrinogen/analysis , Adult , Aged , Cardiovascular Diseases/classification , Female , Humans , Male , Middle Aged , Reproducibility of Results , Risk Factors
11.
Atherosclerosis ; 155(2): 425-30, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11254913

ABSTRACT

Menopause is accompanied by changes in lipoprotein particles that include an increase in density of low density lipoproteins (LDL) and high density lipoproteins (HDL) particles. The effect of 3 months of oral hormone replacement therapy (HRT) on lipoprotein particle size in postmenopausal women who were randomized to (1) estrogen replacement therapy (ERT) alone (either 17beta-estradiol (1 mg) or conjugated equine estrogens (CEE) (0.625 mg); (2) combination therapy (17beta-estradiol plus medroxyprogesterone acetate (MPA) or CEE plus MPA); and (3) placebo were examined. Lipoprotein subclass concentrations and particle size were quantified by nuclear magnetic resonance spectroscopy (NMR). Combination HRT resulted in significant (P=0.002) increases in HDL particle size as compared with those on placebo formulations or ERT alone. Women assigned to combined HRT had lower concentrations of smaller HDL particles after 3 months (P=0.005) and higher concentrations of larger HDL particles (P=0.02), whereas women assigned to ERT or placebo experienced non-significant changes. In summary, combined HRT increases HDL particle size by altering concentrations of the smallest and largest HDL subspecies.


Subject(s)
Estradiol/pharmacology , Estrogens, Conjugated (USP)/therapeutic use , Hormone Replacement Therapy , Lipoproteins, HDL/chemistry , Medroxyprogesterone Acetate/pharmacology , Administration, Oral , Animals , Estradiol/administration & dosage , Estradiol/therapeutic use , Estrogen Replacement Therapy , Estrogens, Conjugated (USP)/administration & dosage , Estrogens, Conjugated (USP)/pharmacology , Female , Horses , Humans , Lipoproteins, HDL/blood , Magnetic Resonance Spectroscopy , Medroxyprogesterone Acetate/administration & dosage , Medroxyprogesterone Acetate/therapeutic use , Middle Aged , Particle Size , Postmenopause/blood
12.
Atherosclerosis ; 155(2): 463-6, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11254918

ABSTRACT

Statins have a variable response on fibrinogen, and these changes may have implications on cardiovascular events. In this randomized placebo-controlled crossover study, we evaluated whether changes in fibrinogen levels were different between atorvastatin and other statin-treated patients. Adult coronary heart disease (CHD) patients aged 39-83 years with LDL cholesterol levels > or = 130 mg/dl were randomized to atorvastatin 80 mg (n = 84) and one of the following statins: fluvastatin 80 mg (n = 23), lovastatin 80 mg (n = 20), pravastatin 40 mg (n = 22) or simvastatin 40 mg (n = 20) each for 12 weeks in either order. Fibrinogen was analyzed by an automated method of Clauss. Three independently acquired samples were obtained within 1 min of tourniquet application, and each specimen was measured in duplicate. Statistical analyses were performed using a mixed model repeated measures analysis of variance procedure with SAS version 6.12. There were no significant changes in fibrinogen between treatment groups. This study evaluated changes in fibrinogen with established pre-analytical and analytical procedures known to minimize variability in fibrinogen measurement, and we did not observe any differences in fibrinogen levels in the treatment groups.


Subject(s)
Coronary Disease/blood , Fibrinogen/analysis , Heptanoic Acids/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Pyrroles/pharmacology , Adult , Aged , Aged, 80 and over , Atorvastatin , Coronary Disease/drug therapy , Cross-Over Studies , Fatty Acids, Monounsaturated/pharmacology , Fatty Acids, Monounsaturated/therapeutic use , Female , Fluvastatin , Heptanoic Acids/therapeutic use , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Indoles/pharmacology , Indoles/therapeutic use , Lovastatin/pharmacology , Lovastatin/therapeutic use , Male , Middle Aged , Pravastatin/pharmacology , Pravastatin/therapeutic use , Pyrroles/therapeutic use , Simvastatin/pharmacology , Simvastatin/therapeutic use
15.
Arterioscler Thromb Vasc Biol ; 18(12): 1902-5, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9848882

ABSTRACT

Hormone replacement therapy may protect against cardiovascular disease through several mechanisms that have variable actions on the major determinants of plasma viscosity. Plasma viscosity is an important predictor of incident and recurrent cardiovascular events and mortality in coronary heart disease patients. The effect of estrogen alone or in combination with progestin on plasma viscosity is not known. Using a randomized, double-blind design, we examined the impact of the following daily hormone regimens on plasma viscosity in 23 women: (1) 1 mg estradiol and 2.5 mg medroxyprogesterone (n=7); (2) 1 mg estradiol alone (n=8); and (3) placebo (n=8). Plasma viscosity, fibrinogen, and standard lipoprotein levels were determined at baseline and after 12 weeks of intervention. Plasma viscosity was measured at 37 degreesC with a coaxial microviscometer. Fibrinogen was measured by the Clauss method. Significant changes in plasma viscosity (mPa.s) levels occurred among treatment groups (P<0.01) after the intervention. Plasma viscosity was significantly reduced with estrogen replacement therapy (P<0.01). These data demonstrate that estrogen replacement therapy lowers plasma viscosity. This study suggests an additional mechanism for the cardiovascular protection conferred to postmenopausal women on estrogen replacement therapy.


Subject(s)
Blood Viscosity/drug effects , Cardiovascular Diseases/prevention & control , Estrogen Replacement Therapy , Postmenopause/blood , Aged , Double-Blind Method , Estradiol/pharmacology , Female , Fibrinogen/analysis , Humans , Medroxyprogesterone/pharmacology , Middle Aged , Triglycerides/blood
16.
J Am Diet Assoc ; 98(9): 985-8, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9739797

ABSTRACT

OBJECTIVES: The objectives of this study were to examine variability of folate intake in order to estimate the number of days needed to accurately estimate intakes in women of childbearing age and to simulate the effect of folic acid fortification of cereals and grains on individual folate intake. DESIGN: Observational study of food intake over a 60-day period. SAMPLING: A convenience sample of 21 women completed food records on randomly assigned days within a 60-day period. OUTCOMES MEASURED: Folate intake and variance ratios of folate intake. STATISTICAL ANALYSIS: Repeated measures analysis of variance. RESULTS: Six days of food records were needed to describe folate intake of these women of childbearing age (18 to 45 years) with 20% attenuation of a correlation coefficient between dietary folate intake and another biological variable. Seven days of records were needed with simulated folic acid fortification (assuming fortification of 140 micrograms folic acid per 100 g flour) and 5 days were needed with supplements containing 200 to 400 micrograms folic acid in addition to folic acid fortification. Food folate intake was 288 +/- 195 micrograms; only 2 of the participants consumed the recommended 400 micrograms. With fortification, folate intake increased to 550 +/- 279 micrograms without supplements and 609 +/- 327 micrograms with supplements. APPLICATIONS: Individual intakes of folate should be assessed with at least 7 days of dietary records (20% attenuation). In this sample, when folic acid fortification was added to dietary intake, routine supplementation was not necessary to achieve folate intakes of 400 micrograms in the majority of participants. The practice of routine folic acid supplementation should be considered carefully to ensure that individual intakes of folate do not exceed the upper limits of safety.


Subject(s)
Diet , Folic Acid/administration & dosage , Food, Fortified , Neural Tube Defects/prevention & control , Adult , Analysis of Variance , Computer Simulation , Diet Records , Dietary Supplements , Female , Folic Acid/adverse effects , Food, Fortified/adverse effects , Humans
17.
Clin Hemorheol Microcirc ; 18(2-3): 191-4, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9699041

ABSTRACT

Reliable plasma viscosity measurements are required for cardiovascular risk factor assessment. This study was designed to examine the influence of tourniquet pressure and duration on plasma viscosity measurement with a coaxial cylinder at 37 degrees C. Plasma viscosity was evaluated at low (40 mm Hg) and high (mean arterial blood pressure plus 10 mm Hg) tourniquet pressure and at two time intervals following (0-1 and 4-5 min) of tourniquet application in 38 healthy adults. Longer duration of tourniquet application was accompanied by a significant increase in plasma viscosity at both low (1.356 +/- 0.067 mPa s versus 1.393 +/- 0.067 mPa s (p = 0.0001)) and high (1.321 +/- 0.071 mPa s versus 1.430 +/- 0.086 mPa s (p = 0.0002)) tourniquet pressures. Plasma viscosity values were not influenced by the magnitude of tourniquet pressure. The accuracy of plasma viscosity measurements can be improved by sample acquisition within 1 min following tourniquet application.


Subject(s)
Blood Viscosity , Tourniquets , Adult , Female , Humans , Male
18.
J Am Diet Assoc ; 98(8): 863-8, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9710655

ABSTRACT

OBJECTIVE: To identify psychological characteristics and eating behaviors associated with weight cycling and binge eating behaviors in overweight women (body mass index > 27.3). DESIGN: Questionnaires measuring self-esteem, self-efficacy, coping strategies, psychological symptoms, depression, binge eating, restrained eating, disinhibition, and hunger were administered to female weight cyclers who were overweight. Psychological characteristics were compared between subjects grouped by binge eating disorder classification and by binge eating severity. SUBJECTS: A convenience sample of 62 female weight cyclers who were overweight was recruited from the Chicago, Ill, area. Questionnaires were administered individually or in small groups in subjects' homes or other private settings. STATISTICAL ANALYSES: Student's t tests or Mann-Whitney U tests were used to assess differences in psychological characteristics. RESULTS: Thirty-six weight cyclers (58%) met the criteria for binge eating disorder and 26 (42%) did not. Weight cyclers with binge eating disorder reported greater severity of binge eating (P < .0005) and disinhibition (P < .0005) and poorer eating self-efficacy (P < .0005) than weight cyclers without binge eating disorder. Weight cyclers with severe binge eating behaviors reported greater psychological distress (P < .0005) and depression (P < .005) and lower self-esteem (P = .0001) and used less healthful coping strategies (P = .0027) than weight cyclers with no binge eating to moderate binge eating problems. Weight cyclers with severe binge eating behavior also reported more hunger (P < .0005) and used less cognitive restraint (P = .0024) than those with no binge eating to moderate binge eating problems. APPLICATIONS: Operational definitions of weight cycling and binge eating are needed to facilitate research on effective weight-loss treatments. Persons seeking to lose weight (especially weight cyclers) should be assessed for binge eating severity, problematic eating behaviors, and psychological symptoms.


Subject(s)
Feeding Behavior/psychology , Obesity/psychology , Adaptation, Psychological , Adult , Depression , Female , Humans , Hyperphagia/prevention & control , Self Concept , Surveys and Questionnaires
19.
JAMA ; 279(20): 1643-50, 1998 May 27.
Article in English | MEDLINE | ID: mdl-9613915

ABSTRACT

Clinical trials of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors or statin therapy have demonstrated that baseline or treated low-density lipoprotein (LDL) cholesterol levels are only weakly associated with net coronary angiographic change or cardiovascular events. The beneficial effects of statins on clinical events may involve nonlipid mechanisms that modify endothelial function, inflammatory responses, plaque stability, and thrombus formation. Experimental animal models suggest that statins may foster stability through a reduction in macrophages and cholesterol ester content and an increase in volume of collagen and smooth muscle cells. The thrombotic sequelae caused by plaque disruption is mitigated by statins through inhibition of platelet aggregation and maintenance of a favorable balance between prothrombotic and fibrinolytic mechanisms. These nonlipid properties of statins may help to explain the early and significant cardiovascular event reduction reported in several clinical trials of statin therapy.


Subject(s)
Antithrombins/pharmacology , Cardiovascular Diseases/blood , Cardiovascular Diseases/prevention & control , Cholesterol, LDL/blood , Endothelium, Vascular/physiology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Hypolipidemic Agents/pharmacology , Platelet Aggregation , Animals , Antithrombins/therapeutic use , Cholesterol, LDL/physiology , Clinical Trials as Topic , Coronary Disease/blood , Coronary Disease/prevention & control , Fibrinogen , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypolipidemic Agents/therapeutic use , Inflammation , Lovastatin/pharmacology , Lovastatin/therapeutic use , Muscle, Smooth, Vascular/physiology , Pravastatin/pharmacology , Pravastatin/therapeutic use , Simvastatin/pharmacology , Simvastatin/therapeutic use , Thromboplastin , Thrombosis/physiopathology
20.
J Am Coll Nutr ; 17(2): 162-70, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9550460

ABSTRACT

OBJECTIVE: This study was designed with two aims: 1) to determine if the coronary artery bypass graft (CABG) procedure alters plasma vitamin E and C concentrations of adult patients through repeated determinations of vitamin levels at time points before, during and following CABG, and 2) to assess whether plasma vitamin E concentrations reflect myocardial tissue content. METHODS: A consecutive sample of 38 patients undergoing CABG surgery at a Midwest tertiary care hospital was enrolled. Patients receiving blood transfusions before or during surgery were excluded. RESULTS: Plasma vitamin E/total lipid ratios rose with reperfusion, remained elevated immediately following bypass, and fell to preoperative concentrations by 24 hours. Plasma vitamin E/total cholesterol levels varied little throughout this time course. Both plasma uric acid and ascorbate concentrations (corrected for hemodilution) also rose by the preischemic interval, and remained elevated until a return to preoperative levels by 24 hours. Corrected malondialdehyde (MDA) concentrations rose by pre-ischemia but returned more quickly to preoperative levels. Atrial appendage tissue vitamin E concentrations bore a significant relationship to those of plasma prior to surgery (r=+0.49, p=0.004). Reported supplement use, plasma concentrations and body mass index contributed to the variability in atrial tissue concentrations of vitamin E. CONCLUSIONS: In short, when not confounded by transfusions or hemodilution, several peripheral indices of antioxidants increase with the reperfusion segment of CABG procedure and return to baseline levels within 24 hours of surgery. Parallel changes in MDA were observed. The observed changes are consistent with the hypothesis that oxidative stress accompanies the ischemia-reperfusion components of the CABG procedure.


Subject(s)
Ascorbic Acid/blood , Cardiopulmonary Bypass , Vitamin E/blood , Aged , Body Mass Index , Cholesterol/blood , Creatine Kinase/blood , Female , Heart Atria/metabolism , Humans , Isoenzymes , Male , Malondialdehyde/blood , Middle Aged , Prospective Studies , Uric Acid/blood , Vitamin E/administration & dosage , Vitamin E/metabolism
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