Associations of neighborhood area level deprivation with the metabolic syndrome and inflammation among middle- and older- age adults
BMC Public Health volume 14, Article number: 1319 (2014)
The study examines the association of neighborhood socioeconomic deprivation and metabolic syndrome with inflammation.
The analysis included 19, 079 black and white participants from the REasons for Geographic And Racial Differences in Stroke Study who were age > 45 years at baseline. Logistic regression examined whether neighborhood deprivation was associated with increased odds of METS and CRP-MetS.
Among black adults, residing in the most deprived neighborhoods was associated with increased odds of obesity (p < .01), lower HDL (p < .001), high blood pressure (p < .01), elevated fasting glucose (p < .001), inflammation (p < .01), and CRP-MetS (p < .001). Among white adults, neighborhood deprivation was associated with higher waist circumference (p < .001), lower HDL (p < .001), higher triglycerides (p < .01), higher glucose (p < .001), higher BMI (p < .0001), higher blood pressure (p = .01), METS (p < .001), inflammation (p < .01) and CRP-MetS (p < .001).
These findings highlight the role of neighborhood socioeconomic deprivation on METS and CRP-MetS for black and white adults. Interventions tailored to address the contextual effects of deprived neighborhoods may reduce the observed neighborhood disparities.
In the United States, cardiovascular disease (CVD) remains the leading cause of death and accounts for 16 percent of national health expenditures . Medical costs of CVD have increased at an annual rate of 6 percent and it is projected that by 2030, 40 percent of the population will have some form of CVD . Taken together, these statistics provide evidence of the social and economic consequences of CVD and suggest that CVD will significantly impact the quality of life for a large proportion of the American population. Due to these increased burdens, the identification of CVD predictors and reduction of risk factors are critical to reverse these expected trends. While researchers have devoted significant attention to the biological factors and health-related behaviors that contribute to CVD [3–5], there is a need for increased research focus on the relationship between social determinants, such as neighborhood socioeconomic deprivation, and CVD risk factors, particularly using clinically relevant biological markers of CVD risk.
While there are several plausible mechanisms through which neighborhood socioeconomic deprivation may increase CVD risk such as reduced access to health promoting behaviors, built environmental conditions that impede physical activity and exposure to environmental pollutants [6–8], contextual level socioeconomic status may also be an important pathway through which neighborhoods affect CVD. Individuals in lower socioeconomic status contexts report greater exposure to chronic social stressors, greater severity of stressors, and more daily hassles [9–13]. These SES-related stressors may contribute to biological wear and tear on the body leading to earlier health deterioration, or ‘weathering’, of individuals who reside in socioeconomically deprived neighborhoods . Further, these differential stressor exposures may result in allostatic load which is the chronic overactivity or underactivity of allostatic systems (i.e. hypothalamic pituitary adrenal axis, the autonomic nervous system, insulin, immune and the metabolic systems-thyroid axis) . During times of perceived stress, these systems are activated to protect the body . Repeated activation of these systems may alter blood lipids, blood pressure and result in prolonged circulation of stress hormones and inflammatory cytokines that increase CVD risk [11, 15–17].
Previous studies report associations between neighborhood socioeconomic deprivation and CVD risk factors such as less participation in health promoting behaviors, increased exposure to psychosocial stressors and greater prevalence of obesity, type 2 diabetes and hypertension [6, 18–22]. Cumulatively, these relationships confer increased risks for CVD. The effects of place are further evidenced by the association of neighborhood socioeconomic deprivation with increased CVD among adults in international studies, in the United States and across racial/ethnic groups suggesting that neighborhood context has significant consequences for health [8, 18, 23–25]. While the aforementioned research is informative, the preponderance of evidence addresses health behaviors or single markers of CVD risk. Examining the clustering of factors that relate to CVD, such as the metabolic syndrome and its components may warrant attention. As the metabolic syndrome is an underlying factor for CVD, analyses of the relationships between neighborhood deprivation and metabolic syndrome factors including insulin resistance, impaired fasting glucose, hypertension, high triglycerides, low high-density lipoprotein (HDL), high waist circumference , and metabolic syndrome with an inflammation , may provide further insight into the mechanisms through which CVD differs by level of neighborhood deprivation. Research findings suggest that neighborhood deprivation is significantly associated with the metabolic syndrome, yet this remains a relatively understudied area particularly using population based data that includes a biracial cohort of black and white adults. Therefore, the objective of this research is to assess the associations of socioeconomic status on the metabolic syndrome components beyond individual level socioeconomic status and examine whether neighborhood socioeconomic deprivation is associated with biological markers of the metabolic syndrome among a population based cohort of middle- and older age black and white adults.
The REasons for Geographic and Racial Differences in Stroke (REGARDS) study is a cohort of 30,239 black and white participants who, at the time of enrollment (January 2003-October 2007), were over age 45 and residing in the lower 48 states of the United States. The study was designed specifically to examine racial and regional differences in stroke mortality and therefore oversampled African Americans and those residing in the Southeast, a region commonly referred to as the stroke belt due to the high rates of stroke mortality in this region . In REGARDS, the stroke belt is defined as Tennessee, Arkansas, Louisiana, Mississippi, Alabama, Georgia, South Carolina, and North Carolina. The study has been described elsewhere .
Study related protocol received approval from the Institutional Review Boards at all participating universities. University of Alabama at Birmingham, University of Vermont and State Agricultural College (Burlington), Wake Forest University School of Medicine (Winston-Salem, NC), Alabama Neurological Institute (Brookwood Medical Center), and University of Arkansas for Medical Sciences approved the study methods. REGARDS protocol included both a telephone based interview and an in-home visit. Individuals were identified from commercially available lists of residents, and recruited using an initial mailing followed by telephone contact. Using a computer-assisted telephone interview, trained interviewers obtained demographic information, medical history and indices of quality of life. Consent was obtained verbally and later in writing. Approximately three to four weeks after the telephone interview, trained personnel conducted a brief physical exam that included obtaining blood pressure measurements, blood samples, and an electrocardiogram. Phlebotomy was performed by centrally trained personnel using standardized procedures after a 10–12 hour fast. Within 2 hours of collection, samples were centrifuged and serum or plasma separated and shipped overnight in transfer vials on gel ice packs to the central laboratory at the University of Vermont. Overnight shipping was successful for 94% of participants with available samples. Samples were then re-centrifuged at 30,000 xG and 4 degrees Celsius, and either analyzed (general chemistries) or stored at -80 degrees Celsius.
For the current study, excluded participants included those whose addresses could not be matched at the block group level (n = 6413), who were not fasted (n = 2863), missing any component of the metabolic syndrome (n = 1870), and missing education (n = 14). The final analytic sample included 19,079 participants.
Obesity, metabolic syndrome components and C-reactive protein. Obesity. Height was measured using a portable stadiometer without shoes and to the nearest 0.1 centimeter. Weight was measured using a digital scale. Body mass index (BMI) was calculated using the formula kg/m2. Waist circumference was measured mid-way between the lowest rib and the iliac crest in the standing position. Triglycerides and HDL-cholesterol were measured in serum using the Ortho Vitros Clinical Chemistry System 950IRC instrument (Johnson & Johnson Clinical Diagnostics, Rochester, NY), which uses colorimetric reflectance spectrophotometry on thin film technology. The C.V.’s for HDL and triglyceride were 7% and <2%, respectively. During the in-home visit, systolic (SBP) and diastolic blood pressure (DBP) were measured twice with participants in the seated position. The average of the two measurements was calculated and used for analysis. Fasting glucose was measured in serum using a colorimetric reflectance spectrophotometry on the Ortho Vitros 950 IRC Clinical Analyzer (Johnson & Johnson Clinical Diagnostics, Rochester, NY) with a C.V. of 1%. C-reactive protein (CRP) was measured in SCAT-1 plasma using the BNII nephelometer from Dade Behring (Deerfield, IL) utilizing a validated high-sensitivity particle enhanced immunonepholometric assay. The assay range is 0.175 – 1100 mg/L. Intra-assay C.V.’s range from 2.3 – 4.4% and inter-assay C.V.’s range from 2.1 – 5.7% . Participants self-reported being on lipid lowering, antihypertensive and antidiabetic medications.
Metabolic syndrome was defined using the modified ATP III definition  and included the following criteria:
Triglycerides ≥150 mg/dL
HDL Cholesterol for men <40 mg/dL and for women <50 mg/dL or any lipid lowering medication
Blood Pressure ≥130/85 mm Hg or antihypertensive medication use
Fasting glucose ≥100 mg/dL or antidiabetic medication use
Waist Circumference for men >102 cm (>40 in) and for women >88 cm (>35 in) (high waist circumference)
Prevalence of metabolic syndrome was defined as having three or more of these criteria. Also considered was an alternative definition of metabolic syndrome that has demonstrated associations in prior studies to include CRP as a marker of inflammation (CRP greater than 3 mg/dL) . Even with the six components, we considered having three or more as the definition of metabolic syndrome plus inflammation.
Neighborhood deprivation. As we had address information available, we were able to geocode the home addresses of participants down to the US Census block group level. We used the summary index developed by Diez-Roux  as a measure of neighborhood deprivation. This measure is a compilation of U.S. Census derived indicators of neighborhood SES (median household income, percentage of households with interest, dividend or rental income, median value of housing units, percentage of persons 25 or over with complete high school, percentage persons 25 or over with complete college, and percentage persons in executive, managerial, or professional specialty occupations). First, we created individual Z-scores for each individual indicator and then summed the values across all variables to provide an index of neighborhood level deprivation. We then created quintiles of the Z-score for use in analysis.
Demographic, behavioral and history of cardiovascular disease events. Participants self-reported age, sex, race (African American and white), highest level of education completed, total annual household income, current cigarette smoking and history of cardiovascular disease. We categorized history of cardiovascular disease as any self-reported myocardial infarction or “heart attack”, stroke, coronary artery bypass surgery, coronary angioplasty or stenting, or evidence of myocardial infarction from electrocardiogram.
Due to the hypothesis that neighborhood effects may vary by race-ethnicity , we conducted race-stratified analyses of neighborhood deprivation associations with the metabolic syndrome. We examined the association of neighborhood deprivation and metabolic syndrome using both linear and logistic regression. For the linear regression we examined the distribution of all components of metabolic syndrome and metabolic syndrome plus inflammation and transformed where necessary (results located online as Additional file 1: Table S1). We then standardized each variable by dividing by the standard deviation so we could compare across category. Since we were performing 16 different tests, we used a stricter p value for significance of 0.01. For logistic regression we dichotomized each variable of interest using the cut-point shown above and examined quintiles of neighborhood deprivation as the exposure. We also examined linear tests for trend across quintile. We conducted race-stratified analyses for neighborhood deprivation associations with metabolic syndrome as that was our primary analysis of interest. We also conducted Wald type 3 post hoc analyses to examine whether neighborhood associations with the metabolic syndrome components were significantly different between black and white adults.
Figure 1 presents the individual metabolic syndrome components, the prevalence of metabolic syndrome and metabolic syndrome with inflammation by race. Black adults had higher blood pressure, had higher waist circumference and were more obese. Similar percentages of black and white adults presented with the metabolic syndrome (26.7% and 25.5% respectively). A larger percentage of black adults had elevated C-reactive protein levels. When C-reactive protein was included in the metabolic syndrome criteria, a larger percentage of black adults presented with the metabolic syndrome (42.2% and 34.3% respectively).
Table 1 presents participant characteristics by quintile of neighborhood deprivation. There were statistically significant differences in age by neighborhood deprivation (p = 0.004) however, this translated into less than a one year age difference across neighborhood deprivation quintiles. A significantly greater percentage of black adults, females and individuals residing in the southeast lived in more deprived neighborhood conditions (p < .01). Neighborhood deprivation was significantly and positively associated with obesity, high waist circumference, high blood pressure, high fasting blood glucose, high triglycerides, low-HDL, the metabolic syndrome, and C-reactive protein (all significance levels p < .01). Neighborhood deprivation was also significantly associated with the metabolic syndrome with inflammation (p < .0001), and self-reported history of cardiovascular disease.
Table 2 presents race specific odds ratios and 95% CIs of the metabolic syndrome and individual metabolic syndrome components. The results are presented by quintile of neighborhood deprivation with individuals in the least deprived neighborhoods (quintile 5), as the referent group.
Relative to black adults living in the lowest level of deprivation, black adults residing in the highest level of deprivation had 21% increased odds of obesity (BMI ≥ 30 kg/m2) (OR = 1.27, 95% CI 1.02 to 1.58). Relative to the lowest level of neighborhood deprivation, black adults residing in the highest level of deprivation had 38% higher odds of low HDL (OR = 1.38, 95% CI = 1.09 to 1.61). Black adults in the highest level of deprivation had a 34% increased odds of high blood pressure (OR = 1.34, 95% CI 1.07 to 1.68). Living in the most deprived neighborhood was associated with a 41% increased odds of elevated fasting glucose (OR = 1.41, 95% CI = 1.10 to 1.79). Relative to the least deprived, black adults residing in the highest level of deprivation had 36% increased odds of inflammation (OR = 1.36, 95% CI = 1.09 to 1.70). When inflammation was added to the metabolic syndrome criteria, black adults residing in the highest level of deprivation had 52% higher odds of the metabolic syndrome (OR = 1.52, 95% CI 1.20 to 1.92).
White adults in quintile 1 had a 69% increased odds of obesity relative to white adults living in the least deprived neighborhoods (quintile 1OR = 1.69, 95% CI = 1.36 to 1.84). Residing in the most deprived neighborhood was associated with 58% increased odds of high waist circumference (quintile 1 OR = 1.58, 95% CI = 1.36 to 1.84). White adults residing in the lowest level of deprivation had a 20% increased odds of elevated triglycerides (OR = 1.20, 95% CI = 1.03 to 1.41). Compared to white adults living in the lowest level of deprivation, white adults in the most deprived neighborhoods had 44% increased odds of low HDL (OR = 1.44, 95% CI = 1.23 to 1.67). For white adults residing in the highest level of deprivation, there was a 58% increased odds of elevated fasting glucose (OR = 1.58, 95% CI = 1.32 to 1.89). Relative to individuals in the least deprived neighborhoods, white adults residing in the highest level of neighborhood deprivation had 25% increased odds of inflammation (OR = 1.25, 95% CI = 1.07 to 1.45). Among white adults, residing in the most deprived neighborhood was associated with 78% increased odds of the metabolic syndrome (OR = 1.78, 95% CI = 1.50 to 2.12). When inflammation was added to the metabolic syndrome, residing in the most deprived neighborhood was associated with 65% increased odds of metabolic syndrome (OR = 1.65, 95% CI = 1.41 to 1.93). Post hoc analyses did not indicate any statistically significant differences in the relative odds of metabolic syndrome components across neighborhood quintiles between black and white adults (data not shown).
The current study examines the relationship of area level deprivation and its associations with the metabolic syndrome and inflammation among a national sample of black and white middle- and older age adults. Given the stringent criteria to establish significance and the availability of objective measures of the metabolic syndrome, the study findings provide strong evidence that neighborhood deprivation is associated with the metabolic syndrome. These findings may be lend support to a stressor and allostatic load framework as potential mechanisms through which neighborhood deprivation is associated with the metabolic syndrome. In the race-stratified analyses, independent neighborhood associations persisted after accounting for individual-level socioeconomic status, age, sex, health behaviors and geographic region.
The study findings indicate that living in more deprived neighborhoods is associated with increased odds of the individual metabolic syndrome components for both white and black middle- and older age adults. The findings are also consistent with the research findings among participants in the Canadian Cohort Study in that neighborhood deprivation is associated with increased odds of hypertension . Although the neighborhood economic indicators differ somewhat across studies, the current study findings are also similar to those of Bird et al.,  in that neighborhood deprivation is associated with higher blood pressure and low-HDL cholesterol. The significant relationship of neighborhood deprivation on inflammation is also similar to findings from both MESA and Jackson Heart Study participants which indicate that neighborhood deprivation operates to affect health through inflammatory pathways [8, 33]. Neighborhood deprivation also confers statistically significant increases in the risk of impaired fasting glucose. This contrasts with the research of Andersen et al.,  that suggests non-significant relationships between neighborhood deprivation and fasting glucose. However, that study did not include a national sample of adults and was limited to women. The significant associations evidenced among the REGARDS population align with the general literature suggesting neighborhood associations with insulin and glucose outcomes among MESA participants  and insulin resistance .
While neighborhood deprivation is associated with many of the metabolic syndrome components, the relationships differ for the anthropometric measures BMI and waist circumference. Among white adults, there are clear and significant relationships for high BMI and large waist circumference for each quintile of neighborhood deprivation compared to the least deprived neighborhoods. In contrast, the relationship of waist circumference is insignificant for black adults and the relationship of BMI is only significant for the two highest quintiles of deprivation relative to the least deprived neighborhoods. Research suggests that relationships between neighborhood context and obesity tend to be stronger for women than men and it is possible that if we conducted race-gender specific analyses, then it is possible that neighborhood associations with obesity would be observed among the black participants in REGARDS [22, 33, 36, 37]. However, nationally representative data from the ARIC study suggest that socioeconomic status is not significantly associated with large waist circumference among black participants and white men participants . Among participants in the Baltimore Memory Study, there are weak or non-significant associations between neighborhood deprivation and the odds of obesity for both black and white older adults . This suggests that the relationship between neighborhood deprivation and total body mass are complex and the nature of the relationships may differ across race, gender, and age categories.
Although differences in the odds of the metabolic syndrome are statistically significant for the white participants only, the differences in the odds of the metabolic syndrome with inflammation between the most and least deprived neighborhoods are large for both white and black participants. These findings differ from those of Merkin et al.,  who identified that differences in metabolic and cardiovascular allostatic load scores between the most deprived relative to the least deprived neighborhoods are largest for black participants and non-significant for their white and Mexican American counterparts. However, the current study results are similar to those of Bird et al.,  that there is no evidence of race/ethnic specific patterns in the association of neighborhood deprivation on the risk for high cardiovascular and metabolic allostatic load scores. While there are differences in measurement between the current study and the comparison studies, both suggest the significance of neighborhood deprivation on risk factors for CVD among nationally representative samples of black and white adults. Further, the current study suggests that the inclusion of inflammation in the metabolic syndrome has significant consequences for the black participants and may warrant inclusion in the traditional risk factor panel for metabolic syndrome criteria for this population. Aside from race-specific measures that may be needed to better define metabolic syndrome, conclusions about the relationship between neighborhood deprivation and CVD risk may also be affected by other physiologic mediators of metabolic syndrome that differ by race. For example, Onat et al. have suggested that Lp(a) mediates the incidence of metabolic syndrome via a U-shaped relationship, and non-blacks may be more likely to be in lower tertiles of Lp(a) with more atherogenic lipid profiles [40, 41]. While this is speculative, additional work to explore these hypotheses is necessary to determine if different pathways are at play in the expression of CVD risk that results from being exposed to deprived environments in various race/ethnic groups.
The current study has a number of strengths, including a large national sample of black and white middle to older age adults and the use of objective measurements of the metabolic syndrome. However, there are some limitations, the large proportion of those with missing data, particularly those who could not be geo-coded at the block group level may limit the current findings and the use of cross-sectional data limits the ability to infer causality. We are unable to establish whether individuals with poorer health are concentrated in less economically advantaged neighborhoods as a result of early childhood health problems that limit social mobility (health selection hypothesis) . Longitudinal studies that control for the independent effects of childhood health and lifetime socioeconomic status are warranted to establish the temporal relationship and strength of the effects of neighborhood deprivation on the metabolic syndrome. Further, the Department of Housing and Urban Development sponsored research conducted by Ludwig and colleagues  provides strong evidence that neighborhood factors exert direct and causal effects in the development of metabolic syndrome risk factors. Additionally, the US Census boundaries to denote neighborhood deprivation at the block-group level, while the smallest unit of analysis available, may not correspond with individual participant definitions of neighborhood contexts. However, the Census derived measurements provide standardized neighborhood boundaries that allow for meaningful comparisons across research studies.
The current findings contribute to the growing body of literature suggesting that there are independent neighborhood associations with the clustering of metabolic syndrome components. Future studies should simultaneously examine the multiple pathways (e.g. built, access to resources, environmental exposures, and social stressors) through which neighborhood context affects CVD risk to identify the relative importance of each and to develop meaningful interventions that might reduce the effects of neighborhood context on increased CVD risk.
Metabolic syndrome and inflammation
Body mass index
Systolic blood pressure
Diastolic blood pressure
Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Makuc DM, Marcus GM, Marelli A, Matchar DB, Moy CS, Mozaffarian D, Mussolino ME, Nichol G, Paynter NP, Soliman EZ, et al: Executive summary: heart disease and stroke statistics–2012 update: a report from the American Heart Association. Circulation. 2012, 125 (1): 188-197.
Heidenreich PA, Trogdon JG, Khavjou OA, Butler J, Dracup K, Ezekowitz MD, Finkelstein EA, Hong Y, Johnston SC, Khera A, Lloyd-James DM, Nelson SA, Nichol G, Orenstein D, Wilson PWF, Woo YJ: Forecasting the future of cardiovascular disease in the United States: a policy statement from the American Heart Association. Circulation. 2011, 123 (8): 933-944. 10.1161/CIR.0b013e31820a55f5.
de Oliveira Otto MC, Mozaffarian D, Kromhout D, Bertoni AG, Sibley CT, Jacobs DR, Nettleton JA: Dietary intake of saturated fat by food source and incident cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis. Am J Clin Nutr. 2012, 96 (2): 397-404. 10.3945/ajcn.112.037770.
Li J, Siegrist J: Physical activity and risk of cardiovascular disease–a meta-analysis of prospective cohort studies. Int J Environ Res Public Health. 2012, 9 (2): 391-407.
Liu J, Hickson DA, Musani SK, Talegawkar SA, Carithers TC, Tucker KL, Fox CS, Taylor HA: Dietary Patterns, Abdominal Visceral Adipose Tissue and Cardiometabolic Risk Factors in African Americans: the Jackson Heart Study. Obesity (Silver Spring). 2013, 21 (3): 644-651. 10.1002/oby.20265.
Diez Roux AV: Residential environments and cardiovascular risk. J Urban Health. 2003, 80 (4): 569-589. 10.1093/jurban/jtg065.
Keita AD, Casazza K, Thomas O, Fernandez JR: Neighborhood perceptions affect dietary behaviors and diet quality. J Nutr Educ Behav. 2011, 43 (4): 244-250. 10.1016/j.jneb.2009.07.004.
Nazmi A, Diez Roux A, Ranjit N, Seeman TE, Jenny NS: Cross-sectional and longitudinal associations of neighborhood characteristics with inflammatory markers: findings from the multi-ethnic study of atherosclerosis. Health Place. 2010, 16 (6): 1104-1112. 10.1016/j.healthplace.2010.07.001.
Bak CK, Tanggaard Andersen P, Bacher I, Draghiciu Bancila D: The association between socio-demographic characteristics and perceived stress among residents in a deprived neighbourhood in Denmark. Eur J Pub Health. 2012, 22 (6): 787-792. 10.1093/eurpub/cks004.
Gruenewald TL, Cohen S, Matthews KA, Tracy R, Seeman TE: Association of socioeconomic status with inflammation markers in black and white men and women in the Coronary Artery Risk Development in Young Adults (CARDIA) study. Soc Sci Med. 2009, 69 (3): 451-459. 10.1016/j.socscimed.2009.05.018.
McEwen BS: Protective and damaging effects of stress mediators. N Engl J Med. 1998, 338 (3): 171-179. 10.1056/NEJM199801153380307.
Muennig P, Sohler N, Mahato B: Socioeconomic status as an independent predictor of physiological biomarkers of cardiovascular disease: evidence from NHANES. Prev Med. 2007, 45 (1): 35-40. 10.1016/j.ypmed.2007.04.005.
Myers HF: Ethnicity- and socio-economic status-related stresses in context: an integrative review and conceptual model. J Behav Med. 2009, 32 (1): 9-19. 10.1007/s10865-008-9181-4.
Geronimus AT: The weathering hypothesis and the health of African-American women and infants: evidence and speculations. Ethn Dis. 1992, 2 (3): 207-221.
Maes M, Song C, Lin A, De Jongh R, Van Gastel A, Kenis G, Bosmans E, De Meester I, Benoy I, Neels H, Demedts P, Janca A, Scharpe S, Smith RS: The effects of psychological stress on humans: increased production of pro-inflammatory cytokines and a Th1-like response in stress-induced anxiety. Cytokine. 1998, 10 (4): 313-318. 10.1006/cyto.1997.0290.
McDade TW, Hawkley LC, Cacioppo JT: Psychosocial and behavioral predictors of inflammation in middle-aged and older adults: the Chicago health, aging, and social relations study. Psychosom Med. 2006, 68 (3): 376-381. 10.1097/01.psy.0000221371.43607.64.
Rod NH, Gronbaek M, Schnohr P, Prescott E, Kristensen TS: Perceived stress as a risk factor for changes in health behaviour and cardiac risk profile: a longitudinal study. J Intern Med. 2009, 266 (5): 467-475. 10.1111/j.1365-2796.2009.02124.x.
Bird CE, Seeman T, Escarce JJ, Basurto-Davila R, Finch BK, Dubowitz T, Heron M, Hale L, Merkin SS, Weden M, Lurie N, Alcoa PO: Neighbourhood socioeconomic status and biological 'wear and tear' in a nationally representative sample of US adults. J Epidemiol Community Health. 2010, 64 (10): 860-865. 10.1136/jech.2008.084814.
Diez-Roux AV, Kiefe CI, Jacobs DR, Haan M, Jackson SA, Nieto FJ, Paton CC, Schulz R: Area characteristics and individual-level socioeconomic position indicators in three population-based epidemiologic studies. Ann Epidemiol. 2001, 11 (6): 395-405. 10.1016/S1047-2797(01)00221-6.
Nordstrom CK, Diez Roux AV, Jackson SA, Gardin JM: The association of personal and neighborhood socioeconomic indicators with subclinical cardiovascular disease in an elderly cohort. The cardiovascular health study. Soc Sci Med. 2004, 59 (10): 2139-2147. 10.1016/j.socscimed.2004.03.017.
Smith GD, Hart C, Watt G, Hole D, Hawthorne V: Individual social class, area-based deprivation, cardiovascular disease risk factors, and mortality: the Renfrew and Paisley Study. J Epidemiol Community Health. 1998, 52 (6): 399-405. 10.1136/jech.52.6.399.
van Lenthe FJ, Mackenbach JP: Neighbourhood deprivation and overweight: the GLOBE study. Int J Obes Relat Metab Disord. 2002, 26 (2): 234-240. 10.1038/sj.ijo.0801841.
Chaix B, Bean K, Leal C, Thomas F, Havard S, Evans D, Jego B, Pannier B: Individual/neighborhood social factors and blood pressure in the RECORD Cohort Study: which risk factors explain the associations?. Hypertension. 2010, 55 (3): 769-775. 10.1161/HYPERTENSIONAHA.109.143206.
Cubbin C, Sundquist K, Ahlen H, Johansson SE, Winkleby MA, Sundquist J: Neighborhood deprivation and cardiovascular disease risk factors: protective and harmful effects. Scand J Public Health. 2006, 34 (3): 228-237. 10.1080/14034940500327935.
Winkleby M, Sundquist K, Cubbin C: Inequities in CHD incidence and case fatality by neighborhood deprivation. Am J Prev Med. 2007, 32 (2): 97-106. 10.1016/j.amepre.2006.10.002.
Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, Gordon DJ, Krauss RM, Savage PJ, Smith SC, Spertus JA, Costa F: Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005, 112 (17): 2735-2752. 10.1161/CIRCULATIONAHA.105.169404.
Suzuki T, Katz R, Jenny NS, Zakai NA, LeWinter MM, Barzilay JI, Cushman M: Metabolic syndrome, inflammation, and incident heart failure in the elderly: the cardiovascular health study. Circ Heart Fail. 2008, 1 (4): 242-248. 10.1161/CIRCHEARTFAILURE.108.785485.
Lanska DJ, Kuller LH: The geography of stroke mortality in the United States and the concept of a stroke belt. Stroke. 1995, 26 (7): 1145-1149. 10.1161/01.STR.26.7.1145.
Howard VJ, Cushman M, Pulley L, Gomez CR, Go RC, Prineas RJ, Graham A, Moy CS, Howard G: The reasons for geographic and racial differences in stroke study: objectives and design. Neuroepidemiology. 2005, 25 (3): 135-143. 10.1159/000086678.
Rifai N, Tracy RP, Ridker PM: Clinical efficacy of an automated high-sensitivity C-reactive protein assay. Clin Chem. 1999, 45 (12): 2136-2141.
King KE, Morenoff JD, House JS: Neighborhood context and social disparities in cumulative biological risk factors. Psychosom Med. 2011, 73 (7): 572-579. 10.1097/PSY.0b013e318227b062.
Matheson FI, White HL, Moineddin R, Dunn JR, Glazier RH: Neighbourhood chronic stress and gender inequalities in hypertension among Canadian adults: a multilevel analysis. J Epidemiol Community Health. 2010, 64 (8): 705-713. 10.1136/jech.2008.083303.
Clark CR, Ommerborn MJ, Hickson DA, Grooms KN, Sims M, Taylor HA, Albert MA: Neighborhood disadvantage, neighborhood safety and cardiometabolic risk factors in african americans: biosocial associations in the jackson heart study. PLoS One. 2013, 8 (5): e63254-10.1371/journal.pone.0063254.
Andersen AF, Carson C, Watt HC, Lawlor DA, Avlund K, Ebrahim S: Life-course socio-economic position, area deprivation and Type 2 diabetes: findings from the British Women's Heart and Health Study. Diabet Med. 2008, 25 (12): 1462-1468. 10.1111/j.1464-5491.2008.02594.x.
Auchincloss AH, Diez Roux AV, Brown DG, O'Meara ES, Raghunathan TE: Association of insulin resistance with distance to wealthy areas: the multi-ethnic study of atherosclerosis. Am J Epidemiol. 2007, 165 (4): 389-397.
Chichlowska KL, Rose KM, Diez-Roux AV, Golden SH, McNeill AM, Heiss G: Individual and neighborhood socioeconomic status characteristics and prevalence of metabolic syndrome: the Atherosclerosis Risk in Communities (ARIC) Study. Psychosom Med. 2008, 70 (9): 986-992. 10.1097/PSY.0b013e318183a491.
Coogan PF, Cozier YC, Krishnan S, Wise LA, Adams-Campbell LL, Rosenberg L, Palmer JR: Neighborhood socioeconomic status in relation to 10-year weight gain in the Black Women's Health Study. Obesity (Silver Spring). 2010, 18 (10): 2064-2065. 10.1038/oby.2010.69.
Glass TA, Rasmussen MD, Schwartz BS: Neighborhoods and obesity in older adults: the Baltimore Memory Study. Am J Prev Med. 2006, 31 (6): 455-463. 10.1016/j.amepre.2006.07.028.
Merkin SS, Basurto-Davila R, Karlamangla A, Bird CE, Lurie N, Escarce J, Seeman T: Neighborhoods and cumulative biological risk profiles by race/ethnicity in a national sample of U.S. adults: NHANES III. Ann Epidemiol. 2009, 19 (3): 194-201. 10.1016/j.annepidem.2008.12.006.
Onat A, Can G: Enhanced proinflammatory state and autoimmune activation: a breakthrough to understanding chronic diseases. Curr Pharm Des. 2014, 20 (4): 575-584. 10.2174/138161282004140213145551.
Onat A, Dönmez I, Karadeniz Y, Çakir H, Kaya A: Type-2 diabetes and coronary heart disease: common physiopathology, viewed from autoimmunity. Expert Rev Cardiovasc Ther. 2014, 12 (6): 667-679. 10.1586/14779072.2014.910114.
Elovainio M, Ferrie JE, Singh-Manoux A, Shipley M, Batty GD, Head J, Hamer M, Jokela M, Virtanen M, Brunner E, Marmot MG, Kivimaki M: Socioeconomic differences in cardiometabolic factors: social causation or health-related selection? Evidence from the Whitehall II Cohort Study, 1991–2004. Am J Epidemiol. 2011, 174 (7): 779-789. 10.1093/aje/kwr149.
Ludwig J, Sanbonmatsu L, Gennetian L, Adam E, Duncan GJ, Katz LF, Kessler RC, Kling JR, Lindau ST, Witaker RC, McDade TW: Neighborhoods, obesity, and diabetes–a randomized social experiment. N Engl J Med. 2011, 365 (16): 1509-1519. 10.1056/NEJMsa1103216.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/14/1319/prepub
The authors thank the other investigators, the staff, and the participants of the REGARDS study for their valuable contributions. A full list of participating REGARDS investigators and institutions can be found at http://www.regardsstudy.org.
This work was supported by a cooperative agreement U01 NS041588 from the National Institute of Neurological Disorders and Stroke, National Institutes of Health, Department of Health and Human Service. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Neurological Disorders and Stroke or the National Institutes of Health. Representatives of the funding agency have been involved in the review of the manuscript but not directly involved in the collection, management, analysis or interpretation of the data. Also, the project described was supported by Award Number P30DK056336 from the National Institute Of Diabetes And Digestive And Kidney Diseases and T32DK062710, R00-DK83333. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute Of Diabetes And Digestive And Kidney Diseases or the National Institutes of Health.
National Institutes of Health.
The authors declare that they have no competing interests.
ADK contributed to the conception and design, interpretation of the data, drafting of the manuscript and approval of the final version. SEJ contributed to the conception and design, analysis and interpretation of the data, drafting and revising the manuscript and approval of the final version. VJH, APC and JDA contributed to the drafting and revision of the manuscript and approval of the final version. JRF contributed to the conception and design, drafting and revision and approval of the final version.
Electronic supplementary material
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Keita, A.D., Judd, S.E., Howard, V.J. et al. Associations of neighborhood area level deprivation with the metabolic syndrome and inflammation among middle- and older- age adults. BMC Public Health 14, 1319 (2014). https://doi.org/10.1186/1471-2458-14-1319