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1.
J Racial Ethn Health Disparities ; 3(4): 706-712, 2016 12.
Article in English | MEDLINE | ID: mdl-27294760

ABSTRACT

INTRODUCTION: Evidence from epidemiological studies shows a link between food insecurity and diet intake or quality. However, the moderating effect of race in this relation has not yet been studied. METHODS: Food insecurity (USDA Food Security Module) and diet quality (Healthy Eating Index-2010; HEI) were measured in 1741 participants from the Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study. Data were collected from 2004 to 2009 and analyzed in 2014. Multivariable regression assessed the interaction of race and food insecurity on HEI scores, adjusting for age, sex, poverty status, single parent status, drug, alcohol and cigarette use, and comorbid diseases. RESULTS: The interaction of food insecurity and race was significantly associated with diet quality (p = 0.001). In the absence of food insecurity, HEI scores were similar across race. However, with each food insecurity item endorsed, HEI scores were substantially lower for Whites compared to Blacks. An ad hoc analysis revealed that Blacks were more likely than Whites to participate in SNAP (p < 0.05). Further, race stratified analyses revealed that Blacks participating in SNAP showed diminished associations of food insecurity with diet quality. CONCLUSIONS: Study findings provide the first evidence that the influence of food insecurity on diet quality may be potentiated for Whites, but not Blacks. Additionally, results show that Blacks are more likely to participate in SNAP and show attendant buffering of the effects of food insecurity on diet quality. These findings may have important implications for understanding how food insecurity affects diet quality differentially by race.


Subject(s)
Black People , Diet , Food Supply , Adult , Cross-Sectional Studies , Female , Humans , Male , Poverty , Racial Groups , Urban Population , White People
2.
J Neurol Sci ; 365: 9-14, 2016 Jun 15.
Article in English | MEDLINE | ID: mdl-27206865

ABSTRACT

Hypertension confers increased risk for cognitive decline, dementia, and cerebrovascular disease. These associations have been attributed, in part, to cerebral hypoperfusion. Here we posit that relations of higher blood pressure to lower levels of cerebral perfusion may be potentiated by a prior head injury. Participants were 87 community-dwelling older adults - 69% men, 90% white, mean age=66.9years, 27.6% with a history of mild traumatic brain injury (mTBI) defined as a loss of consciousness ≤30min resulting from an injury to the head, and free of major medical (other than hypertension), neurological or psychiatric comorbidities. All engaged in clinical assessment of systolic and diastolic blood pressure (SBP, DBP) and single photon emission computed tomography (SPECT). Computerized coding of the SPECT images yielded relative ratios of blood flow in left and right cortical and select subcortical regions. Cerebellum served as the denominator. Sex-stratified multiple regression analyses, adjusted for age, education, race, alcohol consumption, smoking status, and depressive symptomatology, revealed significant interactions of blood pressure and head injury to cerebral blood flow in men only. Specifically, among men with a history of head injury, higher systolic blood pressure was associated with lower levels of perfusion in the left orbital (ß=-3.21, p=0.024) and left dorsolateral (ß=-2.61, p=0.042) prefrontal cortex, and left temporal cortex (ß=-3.36, p=0.014); higher diastolic blood pressure was marginally associated with lower levels of perfusion in the left dorsolateral prefrontal cortex (ß=-2.79, p=0.051). Results indicate that men with a history of head injury may be particularly vulnerable to the impact of higher blood pressure on cerebral perfusion in left anterior cortical regions, thus potentially enhancing risk for adverse brain and neurocognitive outcomes.


Subject(s)
Blood Pressure/physiology , Brain Injuries, Traumatic/physiopathology , Brain/physiopathology , Cerebrovascular Circulation/physiology , Aged , Aged, 80 and over , Blood Pressure Determination , Brain/blood supply , Brain/diagnostic imaging , Brain Injuries, Traumatic/diagnostic imaging , Brain Mapping , Female , Humans , Male , Middle Aged , Sex Characteristics , Tomography, Emission-Computed, Single-Photon
3.
BMC Public Health ; 16: 258, 2016 Mar 14.
Article in English | MEDLINE | ID: mdl-26975845

ABSTRACT

BACKGROUND: Examine interactive relations of race and poverty status with cardiovascular disease (CVD) risk factors in a socioeconomically diverse sample of urban-dwelling African American (AA) and White adults. METHODS: Participants were 2,270 AAs and Whites (57% AA; 57% female; ages 30-64 years) who completed the first wave of the Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study. CVD risk factors assessed included body mass index (BMI), waist circumference (WC), total cholesterol (TC), high- and low-density lipoprotein cholesterol (HDL-C, LDL-C), triglycerides (TG), glycated hemoglobin (HbA1c), high-sensitivity C-reactive protein (CRP), and systolic, diastolic, and pulse pressure (SBP, DBP, PP). Interactive and independent relations of race, poverty status, and sex were examined for each outcome via ordinary least squares regression adjusted for age, education, literacy, substance use, depressive symptoms, perceived health care barriers, medical co-morbidities, and medications. RESULTS: Significant interactions of race and poverty status (p's < .05) indicated that AAs living in poverty had lower BMI and WC and higher HDL-C than non-poverty AAs, whereas Whites living in poverty had higher BMI and WC and lower HDL-C than non-poverty Whites. Main effects of race revealed that AAs had higher levels of HbA1c, SBP, and PP, and Whites had higher levels of TC, LDL-C and TG (p's < .05). CONCLUSION: Poverty status moderated race differences for BMI, WC, and HDL-C, conveying increased risk among Whites living in poverty, but reduced risk in their AA counterparts. Race differences for six additional risk factors withstood extensive statistical adjustments including SES indicators.


Subject(s)
Aging , Black or African American/statistics & numerical data , Cardiovascular Diseases/epidemiology , Poverty/statistics & numerical data , White People/statistics & numerical data , Adult , Blood Pressure , Body Mass Index , C-Reactive Protein/metabolism , Cardiovascular Diseases/ethnology , Cross-Sectional Studies , Depression/epidemiology , Female , Glycated Hemoglobin , Health Services Accessibility , Humans , Lipids/blood , Male , Middle Aged , Risk Factors , Socioeconomic Factors , Substance-Related Disorders/epidemiology , Waist Circumference
4.
Ethn Dis ; 24(2): 150-4, 2014.
Article in English | MEDLINE | ID: mdl-24804359

ABSTRACT

BACKGROUND: Higher rates of cardiovascular disease (CVD) and its risk factors are well documented among those with objective indicators of lower socioeconomic status (SES), such as income, education, and occupation. However, relatively little is known about the relationship of subjective SES to CVD risk, particularly within different racial groups. METHODS: Subjective SES and Framingham 10-year CVD risk profile were examined in 1,722 socioeconomically diverse Black and White adults enrolled in the Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study. The sample had a mean age of 47.7 years, was 57% female, 56% African American, and 39% living in poverty. RESULTS: Subjective SES was associated with greater CVD risk after adjustment for poverty status, substance use, BMI, depression, antihypertensives, and co-morbidities (B = -.059, t[1,1711] = -2.44, P = .015). However, when the analysis was race-stratified, subjective SES was associated with CVD risk in Whites (B = -.074, F[1,787] = -2.01, P = .045), but not Blacks. CONCLUSIONS: These results suggest that subjective SES may aid in predicting CVD risk in Whites, but not Blacks. It is important to note that these analyses were adjusted for poverty status, a potent indicator of objective SES. Thus, these findings further suggest that for Whites, subjective SES may influence CVD risk beyond that associated with objective SES. These findings highlight the potential importance of patients' subjective SES in CVD risk detection.


Subject(s)
Black or African American/statistics & numerical data , Cardiovascular Diseases/ethnology , Health Status Disparities , White People/statistics & numerical data , Adult , Black or African American/psychology , Cardiovascular Diseases/economics , Female , Humans , Male , Middle Aged , Risk Factors , Socioeconomic Factors , United States/epidemiology , White People/psychology
5.
J Behav Med ; 37(1): 94-101, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23135529

ABSTRACT

Estrogen may influence coronary heart disease risk in women through the effects of endogenous opioids on autonomic control of blood pressure. In a randomized, placebo-controlled trial, we examined the combined effects of estrogen and the opioid antagonist, naltrexone, on blood pressure responses to psychological stress in 42 postmenopausal women. After 3 months of estrogen or estrogen plus progestin (hormone replacement therapy; n = 27) or placebo replacement, participants completed a mental arithmetic task after administration of .7 mg/kg oral naltrexone or placebo. Systolic blood pressure (SBP), diastolic blood pressure, mean arterial pressure and heart rate (HR) were measured at rest and during the arithmetic stressor. Stress produced significant increases in circulatory measures regardless of estrogen condition or opioid blockade (p's < .001). Interestingly, there was an estrogen by naltrexone interaction on SBP reactivity scores [F(1,38) = 4.36, p < .05], where women on estrogen with intact opioid receptors showed the largest SBP responses to stress, compared with all other conditions. This is consistent with some studies of premenopausal women, suggesting that estrogens may alter opioid function during stress. The interaction between estrogen and endogenous opioids may explain sex differences in opioid effects on stress reactivity in younger premenopausal women.


Subject(s)
Blood Pressure/drug effects , Estrogens/pharmacology , Naltrexone/pharmacology , Postmenopause , Stress, Psychological/physiopathology , Adult , Aged , Blood Pressure/physiology , Female , Heart Rate/drug effects , Heart Rate/physiology , Hormone Replacement Therapy , Humans , Middle Aged , Problem Solving/drug effects , Problem Solving/physiology , Progesterone/pharmacology , Stress, Psychological/psychology
6.
Schizophr Res ; 109(1-3): 24-37, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19223268

ABSTRACT

BACKGROUND: Given the wealth of data in the literature on schizophrenia endophenotypes, it is useful to have one source to reference their frequency data. We reviewed the literature on disease-liability associated variants in structural and functional magnetic resonance images (MRI), sensory processing measures, neuromotor abilities, neuropsychological measures, and physical characteristics in schizophrenia patients (SCZ), their first-degree relatives (REL), and healthy controls (HC). The purpose of this review was to provide a summary of the existing data on the most extensively published endophenotypes for schizophrenia. METHODS: We searched PubMed and MedLine for all studies on schizophrenia endophenotypes comparing SCZ to HC and/or REL to HC groups. Percent abnormal values, generally defined as >2 SD from the mean (in the direction of abnormality) and/or associated effect sizes (Cohen's d) were calculated for each study. RESULTS: Combined, the articles reported an average 39.4% (SD=20.7%; range=2.2-100%) of abnormal values in SCZ, 28.1% (SD=16.6%; range=1.6-67.0%) abnormal values in REL, and 10.2% (SD=6.7%; range=0.0-34.6%) in HC groups. CONCLUSIONS: These findings are reviewed in the context of emerging hypotheses on schizophrenia endophenotypes, as well as a discussion of clustering trends among the various intermediate phenotypes. In addition, programs for future research are discussed, as instantiated in a few recent large-scale studies on multiple endophenotypes across patients, relatives, and healthy controls.


Subject(s)
Phenotype , Schizophrenia/genetics , Biomarkers , Cluster Analysis , Cognition Disorders/diagnosis , Cognition Disorders/genetics , Cognition Disorders/psychology , Family , Humans , Schizophrenia/diagnosis , Schizophrenic Psychology , Statistics as Topic
7.
Alcohol Clin Exp Res ; 33(4): 617-25, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19183133

ABSTRACT

BACKGROUND: Prior studies report that accidents involving intoxicated drivers are more likely to occur during performance of secondary tasks. We studied this phenomenon, using a dual-task paradigm, involving performance of a visual oddball (VO) task while driving in an alcohol challenge paradigm. Previous functional MRI (fMRI) studies of the VO task have shown activation in the anterior cingulate, hippocampus, and prefrontal cortex. Thus, we predicted dose-dependent decreases in activation of these areas during VO performance. METHODS: Forty healthy social drinkers were administered 3 different doses of alcohol, individually tailored to their gender and weight. Participants performed a VO task while operating a virtual reality driving simulator in a 3T fMRI scanner. RESULTS: Analysis showed a dose-dependent linear decrease in Blood Oxygen Level Dependent activation during task performance, primarily in hippocampus, anterior cingulate, and dorsolateral prefrontal areas, with the least activation occurring during the high dose. Behavioral analysis showed a dose-dependent linear increase in reaction time, with no effects associated with either correct hits or false alarms. In all dose conditions, driving speed decreased significantly after a VO stimulus. However, at the high dose this decrease was significantly less. Passenger-side line crossings significantly increased at the high dose. CONCLUSIONS: These results suggest that driving impairment during secondary task performance may be associated with alcohol-related effects on the above brain regions, which are involved with attentional processing/decision-making. Drivers with high blood alcohol concentrations may be less able to orient or detect novel or sudden stimuli during driving.


Subject(s)
Automobile Driving , Central Nervous System Depressants/pharmacology , Computer Simulation , Ethanol/pharmacology , Psychomotor Performance/drug effects , Task Performance and Analysis , Adult , Dose-Response Relationship, Drug , Female , Hippocampus/physiopathology , Humans , Magnetic Resonance Imaging , Male , Poisoning/physiopathology , Prefrontal Cortex/physiopathology , Psychomotor Performance/physiology
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