Association of blood lipids, creatinine, albumin, and CRP with socioeconomic status in Malawi
© Kohler et al.; licensee BioMed Central Ltd. 2013
Received: 10 February 2012
Accepted: 9 January 2013
Published: 28 February 2013
The objective of these analyses is to document the relationship between biomarker-based indicators of health and socioeconomic status (SES) in a low-income African population where the cumulative effects of exposure to multiple stressors on physiological functions and health in general are expected to be highly detrimental for the well-being of individuals.
Biomarkers were collected subsequent to the 2008 round of the Malawi Longitudinal Study of Families and Health (MLSFH), a population-based study in rural Malawi, including blood lipids (total cholesterol, LDL, HDL, ratio of total cholesterol to HDL), biomarkers of renal and liver organ function (albumin and creatinine) and wide-range C-reactive protein (CRP) as a non-specific biomarker for inflammation. These biomarkers represent widely used indicators of health that are individually or cumulatively recognized as risk factors for age-related diseases among prime-aged and elderly individuals. Quantile regressions are used to estimate the age-gradient and the within-day variation of each biomarker distribution. Differences in biomarker levels by socioeconomic status are investigated using descriptive and multivariate statistics.
Overall, the number of significant associations between the biomarkers and socioeconomic measures is very modest. None of the biomarkers significantly varies with schooling. Except for CRP where being married is weakly associated with lower risk of having an elevated CRP level, marriage is not associated with the biomarkers measured in the MLSFH. Similarly, being Muslim is associated with a lower risk of having elevated CRP but otherwise religion does not predict being in the high-risk quartiles of any of the MLSFH biomarkers. Wealth does not predict being in the high-risk quartile of any of the MLSFH biomarkers, with the exception of a weak effect on creatinine. Being overweight or obese is associated with increased likelihood of being in the high-risk quartile for cholesterol, Chol/HDL ratio, and LDL.
The results provide only weak evidence for variation of the biomarkers by socioeconomic indicators in a poor Malawian context. Our findings underscore the need for further research to understand the determinants of health outcomes in a poor low-income context such as rural Malawi.
KeywordsBiomarkers Blood lipids Creatinine Albumin Wide-range CRP Socioeconomic status Variation Malawi
Biomarker-based health indicators of physiological functioning represent a critical link for understanding the relationship between socioeconomic status (SES) and disease presentation because they can reveal common biological pathways between health and its socioeconomic and environmental determinants [1, 2]. For instance, some studies have argued that individuals of low socioeconomic status have a higher prevalence of sub-clinical markers of disease risk , and longitudinal studies of cardiovascular disease (CVD) reveal that the individual’s relative rank on the biomarkers for CVD such as lipids or blood pressure tends to remain stable throughout the life course [4–6]. This suggests that even if currently measured biomarkers do not reveal a present clinical case, they may nevertheless represent a useful tool to identify individuals who are high risk for developing a disease . Currently, however, the evidence about the relationship between SES and biomarkers of physiological health is mixed and derived primarily from studies in developed contexts. For instance, Rosero-Bixby et al.  found that metabolic conditions such as diabetes and cholesterol are not associated with SES, while hypertension and obesity worsen with higher SES. In a comparative multi-country study, Goldman et al.  observed generally negative and significant associations between education and different biomarkers in the United States (U.S.), but non-systematic and only weak associations in Taiwan and Costa Rica. Alley et al.  showed variation of C-reactive protein (CRP) by SES only at very high levels above 10 mg/l, but no difference at moderate or high levels of CRP, suggesting a non-linear relationship between inflammation and SES, at least in the U.S. context. Among the few studies in African contexts, Rossi et al.  found that serum concentration of high-sensitivity CRP was significantly associated with sex, several cardiovascular risk factors, and selected renal function markers in a Seychelles population. Studies have also suggested that the association between SES and biomarkers of health is stronger in developed than in the less-developed contexts, possibly due to the higher levels of social stratification in the industrialized world . In addition, differences in nutritional patterns, ethnic origin, or exposure to environmental pathogens can potentially alter hematological and immunologic indicators and thus contribute to the variation of biomarkers between African and Western populations .
The present study contributes to the emerging literature on biomarker-based health indicators in sub-Saharan Africa (SSA) by analyzing SES differentials in several biomarkers collected as part of the Malawi Longitudinal Study of Families and Health (MLSFH) in the southern region of Malawi (Balaka). The objective of this analysis is to document the relationship between these biomarker-based indicators of health and socioeconomic status (SES) in a low-income African population where the cumulative effects of exposure to multiple stressors on physiological functions and health in general are expected to be highly detrimental for the well-being of individuals.
The MLSFH is a longitudinal study of the rural population in Malawi that provides an exceptional record of the social, economic, and health conditions in one of the world’s poorest nations. The MLSFH is based in three districts in rural Malawi that have been the study sites since 1998: Rumphi in the north, Mchinji in the center, and Balaka in the south. Respondents ( N 2008≈4,000) are evenly split among the three study locations and clustered in 121 villages. The study population is broadly representative of the overall rural population in Malawi , and is similar in many socioeconomic and health conditions to other low-income countries in SSA . MLSFH rounds were collected in 1998, 2001, 2004, 2006, 2008, and 2010. All three MLSFH sites are rural, and subsistence agriculture is the predominant economic activity among study participants. Balaka, which is the site for which biomarkers were collected in 2009, follows a matrilineal system of kinship and lineage system, and it is primarily inhabited by Lomwes and Yaos and has thus the highest proportion of Muslims among MLSFH regions. The Balaka region also exhibits a lower age of sexual debut and larger numbers of lifetime sexual partners than the other MLSFH study regions, and residents tend to be less educated and poorer than those living in the north, leading to higher levels of migration. HIV/AIDS prevalence in the southern region is significantly higher than in the northern and central region .
MLSFH biomarkers and SES indicators
Our analyses focus on three groups of biomarkers: blood lipids (total cholesterol, high-density lipoprotein [HDL], low-density lipoprotein [LDL], and the ratio of total cholesterol to HDL), biomarkers of renal and liver organ function (albumin and creatinine), and wide-range C-reactive protein (CRP) as commonly used and reliable indicator of non-specific inflammation. The three groups represent a fairly broad set of biomarkers that embody multiple physiological processes and have individually as well as cumulatively been linked to important age-related health outcomes, including cardiovascular diseases, cognitive decline, physical performance, and death [15–17]. The selected biomarkers also represent commonly used biological indicators with demonstrated analytical power in population-based studies from both developed and less-developed countries [11, 18–27]. For example, lipids are widely considered a risk factor for cardiovascular disease in the developed and developing countries [26–31], and the ratio of total cholesterol to HDL is a predictor of ischemic heart disease risk in asymptomatic individuals [23, 32, 33]. Low concentrations of albumin have been positively related to coronary artery disease and are also correlated with inflammation and malnutrition, while high levels are positively correlated with dehydration. In HIV-positive or malnourished individuals—both conditions are frequently occurring and co-existing in the Malawian rural population and SSA in general—creatinine levels may be elevated. In addition, renal diseases, and specifically chronic kidney disease, are among the leading causes of morbidity and mortality worldwide, and are understudied in SSA contexts [34–37].
SES indicators available in the MLSFH include: (i) respondent’s level of formal education (measured as no schooling, primary, and secondary schooling); and (ii) wealth indicators such as having a house covered with a metal roof and the wealth tertile based on an index constructed from dwelling characteristics and ownership of household durable assets using principal component analyses . In addition, our analyses include other relevant aspects of the respondent’s demographic and socioeconomic context such as the respondent’s marital status (coded as married versus non-married) and religious affiliation (Christian, Muslim, and others). We also include body mass index (BMI) in the analysis since it is considered as a reliable indicator of current health problems (e.g., malnutrition, presence of HIV infection, and others).
The MLSFH collected blood-serum biomarker data along with a short survey for about 980 randomly selected respondents in the southern region of Balaka in January–February 2009. The details of the MLSFH biomarker collection are described in a companion paper , and IRB approval was obtained from the University of Pennsylvania and the Malawi National Health Sciences Research Council (NHSRC). As stipulated in these IRB protocols and the general regulations for conducting human subjects research, informed consent was obtained from all study participants prior to the participation in this study. The consent form clearly stated that the data are collected as part of a research project. The Balaka region was chosen for the MLSFH biomarker collection because of its relatively high HIV prevalence. All participants for the MLSFH biomarker sample were selected from MLSFH respondents who were successfully interviewed during the 2008 MLSFH wave, and the 2009 MLSFH biomarker sample is linked to all prior and subsequent MLSFH data collected for this study population. The target sample for the MLSFH biomarker collection was selected in two stages from the MLSFH respondent database. First, all respondents who were found HIV positive in a previous MLSFH round were included in the sample. Second, a random sample of approximately 1,500 respondents (aged ≥ 18 years) was drawn from the 2,500 MLSFH respondents residing in Balaka. The biomarker and survey data collection was conducted at respondents’ homes. Because of weather obstacles (rainy season), high levels of work-related migration in this region, and other temporary absences that resulted in failures to re-contact MLSFH respondents, we were able to successfully contact 1,031 individuals in the target sample. These individuals were offered to participate in the MLSFH biomarker study. Forty-nine respondents (4.7%) refused to participate, and the MLSFH successfully collected biomarker specimens for 982 respondents (95.2% of contacted individuals). Sixty-two study participants had previously tested positive for HIV (7.3% among those with known HIV status).
The MLSFH biomarker data collection used LabAnywhere kits (LabAnywhere, Harlem, the Netherlands; formerly known as Demecal) that require only a few drops of blood harvested from a lancet puncture of a sanitized fingertip. The reliability, sensitivity, and specificity of the test kits have been demonstrated by LabAnywhere in the Netherlands, and the applications of test-specific recovery factors yielded a good correlation with results of venous blood samples . The LabAnywhere technology used in our study offers several advantages over the other common means of collecting blood samples in population-based studies such as dried blood spots (DBS) or venipuncture , including the extraction of blood plasma in fieldwork contexts with minimal discomfort for participants and the ability to conduct up to 16 assays with each sample. To collect the specimen for the LabAnywhere kits at respondents’ homes, the MLSFH recruited a team of 25 individuals who had previously been trained by the Malawian Government in finger prick blood collection as part of HIV voluntary counseling and testing. These biomarker collectors underwent an additional one-week of training in the use of the LabAnywhere kits, and each collector then completed about two to four home-based data biomarker and survey collections per day during fieldwork. While in the field during the day, the collected specimen were stored in a cooler. Upon returning from the field each day, the biomarker coordinator checked all samples to verify that they were collected and labeled properly; all plasma samples were stored in a -20°C freezer until they were shipped to the LabAnywhere laboratory on a weekly schedule. Prior to the shipment, all biomarker samples were cross-checked with field records. Shipment was via DHL from Malawi to the LabAnywhere laboratory in the Netherlands. The samples were packed in a special cooler with ice packs provided by LabAnywhere, which were designed specifically for transporting the frozen blood samples, including minimum/maximum thermometers to monitor the cooling conditions. LabAnywhere was able to analyze 910 (92.7%) of the 982 samples they received. None were discarded because of inadequate temperature control. The duration between the collection of each specimen and the analysis by LabAnywhere was almost always less than two weeks.
Descriptive statistics are used to present the distribution of each biomarker by gender. Quantile regressions of the 25th, 50th (median), and 75th percentile of each biomarker distribution on age are used to estimate the age-gradient of each biomarker distribution. Analogous quantile regressions on the time (hour) of the data collection were used to investigate intra-day variation in all biomarker distribution. To investigate differences in biomarker levels by socioeconomic characteristics, we follow the analytical approach of Dowd and Goldman  and apply logistic regressions using as dependent variable whether the biomarker value falls into the highest quartile of the observed distribution. This approach is advantageous compared to a linear specification if a risk for disease is associated with very low or very high values of the biomarkers; this approach is also relatively robust with respect to outliers in the biomarker distributions. Depending on the biomarker of interest, the highest-risk quartile can correspond to either low or high values. For instance, for total cholesterol, HDL, creatinine, CRP, and the ratio of total cholesterol to HDL the highest quartile corresponds to the 75th percentile of the distribution, while for albumin it corresponds to the 25th percentile. The logistic regression analyses are pooled for men and women to increase the statistical power of our analysis. All models control for sex of the respondents, age group (separate for males/females), and currently pregnant (females only). The results obtained from these logistic regression analyses with respect to biomarker differences by socioeconomic characteristics are identical with those obtained from multivariate linear regression using the log biomarker values as outcome (Additional file 1).
Results and discussion
Summary statistics for the study population
# of observations
Age (in 2008)
Married (in 2008)
2008 level of education
Body mass index (BMI) (2008)
Underweight ( BMI<f.5)
Overweight ( 25≤BMI<f)
Obese ( BMI≥30)
Relative health to others in village
Number of recent econ shocks
Summary statistics for the biomarker-based health indicators
Total cholesterol (Chol) (mg/dL)
High-density cholesterol (HDL) (mg/dL)
Low-density cholesterol (LDL) (mg/dL)
C-reactive protein (CRP)
Odds ratios for the probability of being in the highest risk quartiles of the biomarker distributions: BMI, subjective health and other self-reported health measures (logistic regression models, both sexes combined)
Model 1: Schooling
Model 2: Marital status
Married (in 2008)
Model 3: Religion (major groups)
Model 4: Wealth (based on asset-based wealth tertiles)
Model 5: Body mass index (BMI) (reference category: normal)
The lack of significant associations between the MLSFH biomarkers and SES is not due to a lack of statistical power. Our analyses document significant age patterns for several biomarkers, significant associations between BMI and several biomarkers (cholesterol, Chol/HDL ratio, LDL levels), significant differences in the expected direction in four out of the seven biomarkers between HIV+ and HIV– respondents, and associations between CRP and marital status and religion that are in the expected directions. These statistically significant findings suggest that our analyses are in principle adequately powered to detect differences in the MLSFH biomarkers by SES and other indicators (which is consistent with the power calculations used in designing this study). The failure to document important socioeconomic variation in many of our analyses therefore seems not due to an inadequate sample size, but rather due to a lack of strong associations between the MLSFH biomarkers and our socioeconomic indicators.
Biomarker-based health indicators of physiological functioning represent a critical link for understanding the relationship between socioeconomic status (SES) and disease presentation. And yet, current evidence about SES differentials in biomarker-based health measures among prime-aged and elderly individuals remains inconclusive. Our analyses focus on commonly used biomarkers of cardiovascular risk, non-specific inflammation, and renal/liver function that are individually or cumulatively recognized as risk factors for age-related diseases among prime-aged and elderly individuals: total cholesterol, LDL, HDL, ratio of total cholesterol to HDL, albumin, creatinine, and wide-range CRP. And while a large body of research has documented differences in these biomarkers by socioeconomic indicators in other contexts [7–11, 42, 55–60], the variation of these biomarkers in the Malawian—or similar poor high-morbidity contexts in SSA—is still not well established. However, analyses of the SES variation in these biomarker-based health indicators are an important addition to the existing literature on socioeconomic health differentials in adult populations because most existing studies in SSA are often based on self-reported measures of health and disability, and only for HIV and some other infectious diseases, on biomarkers. At this point, little is known from biomarker-based studies about the levels, variations, and determinants of cardiovascular risk, non-specific inflammation, and renal/liver function in poor high-morbidity SSA populations. And as the epidemiological transition in SSA progresses and chronic diseases constitute a growing proportion of the SSA disease burden , these questions will become increasingly important. And quite possibly, the story emerging from biomarker-based indicators of physiological functions and health could point to a more complex interpretation of the determinants of adults health in contexts such as Malawi than conclusions that are often based on self-reported health measures and/or are frequently focused on infectious diseases.
Our analyses are also important from a methodological standpoint. For instance, to which extent are biomarkers such as those collected as part of the MLSFH suitable for identifying health differentials in poor high-morbidity SSA contexts such as Malawi? And to what extent do they provide comparable data on physiological functioning? And do these biomarkers exhibit the same socioeconomic gradients in Malawi that have been documented for these biomarkers in other contexts, or do they exhibit the same gradients as other (mostly self-reported) health indicators?
The key findings of our study point to an important “puzzle”: Despite strong hypothesis for the existence of SES differentials in health (and the MLSFH biomarkers in particular), our results provide only weak evidence for variation in the MLSFH biomarkers for cardiovascular risk, non-specific inflammation, and renal or liver functioning by socioeconomic status. Moreover, only for a small proportions of respondents do any of the MLSFH biomarkers fall outside the limits of the normal clinical ranges as defined by Western standards . Combined these findings are important because it has been suggested that biomarker-based indicators of health can provide a useful tool to model and understand the pathways of how socioeconomic characteristics relate and influence physiological functioning [62–64]. However, the lack of important SES variation and the shifted distribution of the MLSFH biomarker (Table 2) as compared to those observed in more developed contexts raises the possibility that specific contexts of individuals in poor high-morbidity SSA environments importantly affect the distribution of these biomarkers and their association with SES and other behavioral/contextual covariates. Our findings thus underscore the need for further research to understand the determinants of the levels and variations in biomarker-based health indicators that measure cardiovascular risk, inflammation and renal or liver function. In poor high-morbidity SSA contexts, the variation in these indicators is currently understudied. However, a better understanding of the determinants and variation of these biomarker-based health indicators can importantly contribute to an improved understanding of adult health that is construed more broadly than is currently the case in many studies that focus on either self-reported health measures or infectious diseases. Only if the usefulness and validity of such biomarkers can be established does it make sense to further expand biomarker-based health measures in population-based surveys in poor high-morbidity SSA contexts to obtain information about otherwise unobserved dimensions of health. And while the technological challenges for expanding biomarker-based health measures as part of population-based studies in SSA are increasingly surmountable, our findings highlight the potential ongoing challenges in interpreting and comparing these measures within SSA populations and across diverse cross-country contexts.
The strengths of this study include the population-based design; the availability of multiple biomarkers providing indicators of cardiovascular risk, non-specific inflammation, and renal/liver function; a home-based data collection; a high participation rate; and the integration in a longitudinal cohort study with extensive socioeconomic, demographic, and health information. Among the potential limitations of the present analyses is the fact that these results pertain to a small limited population from a discrete region in rural Malawi. Specifically, the analyses are based on data from the southern region of Balaka, an area that is predominantly Muslim. The sample size comprises about 900 individuals and is at most representative for this part of the country, but not of the entire Malawian population. It is possible that while the link between socioeconomic status and blood lipids, creatinine, albumin and wide-range CRP in this setting is similar to the observations in other developed countries, the pathways are different in this cultural setting and are not captured by these analyses. Moreover, while we measure biomarkers that are seen as a standard for health assessment in primarily Western elderly populations, they may not be the best measure for assessing health status in the SSA context. It is also possible that the associations between the biomarkers and the socioeconomic indicators may be confounded by other risk factors such as nutritional deficits and episodic malnutrition, high prevalence of smoking, and presence of co-infections such as HIV, tuberculosis, or endemic parasites. In the present study, we are however not able to control for these potentially confounding factors.
The authors acknowledge support provided by the National Institutes of Heath through grants NICHD R01HD053781, NIA P30 AG12836 and NICHD R24 HD-044964 and the support by the Boettner Center for Pensions and Retirement Security at the University of Pennsylvania.
- Gruenewald TL, Karlamangla AS, Hu P, Stein-Merkin S, Crandall C, Koretz B, Seeman TE: History of socioeconomic disadvantage and allostatic load in later life. Social Sci Med 2012, 74: 75-83. 10.1016/j.socscimed.2011.09.037View ArticleGoogle Scholar
- Crimmins EM, Vasunilashorn S: Links Between Biomarkers and Mortality. In International Handbook of Adult Mortality, Volume 2 of International Handbooks of Population. Edited by: Rogers RG, Crimmins EM. Amsterdam: Springer; 2011:381-398.View ArticleGoogle Scholar
- Seeman T, Crimmins E, Huang M, Singer B, Bucur A, Gruenewald T, Berkman L, Reuben D: Cumulative biological risk and socio-economic differences in mortality: MacArthur studies of successful aging. Social Sci Med 2004,58(10):1985-1997. 10.1016/S0277-9536(03)00402-7View ArticleGoogle Scholar
- McDade T, Williams S, Snodgrass JJ: What a drop can do: dried blood spots as a minimally invasive method for integrating biomarkers into population-based research. Demography 2007,44(4):899-925. 10.1353/dem.2007.0038View ArticlePubMedGoogle Scholar
- Li S, Chen W, Srinivasan S, Berenson G: Childhood blood pressure as a predictor of arterial stiffness in young adults: the Bogalusa Heart Study. Hypertension 2004,43(3):541-546. 10.1161/01.HYP.0000115922.98155.23View ArticlePubMedGoogle Scholar
- Berenson G, Wattigney W, Bao W, Srinivasan S, Radhakrishnamurthy B: Rationale to study the early natural history of heart disease: The Bogalusa Heart Study. Am J Med Sci 1995,310(6):S29.Google Scholar
- Rosero-Bixby L, Dow WH: Surprising SES gradients in mortality, health, and Biomarkers in a Latin American population of adults. J Gerontol: Soc Sci 2009, 64B: 105-117. 10.1093/geronb/gbn004View ArticleGoogle Scholar
- Goldman N, Turra CM, Rosero-Bixby L, Weir D, Crimmins E: Do biological measures mediate the relationship between education and health: A comparative study. Social Sci Med 2011,72(2):307-315. 10.1016/j.socscimed.2010.11.004View ArticleGoogle Scholar
- Alley D, Seeman T, Ki Kim J, Karlamangla A, Hu P, Crimmins E: Socioeconomic status and C-reactive protein levels in the US population: NHANES IV. Brain Behav Immun 2006,20(5):498-504. 10.1016/j.bbi.2005.10.003View ArticlePubMedGoogle Scholar
- Rossi IA, Bochud M, Viswanathan B, Riesen W, Bovet P: Relation between high-sensitivity C-reactive protein and cardiovascular and renal markers in a middle-income country in the African region. Int J Cardiol 2012,156(2):203-208. 10.1016/j.ijcard.2011.09.084View ArticlePubMedGoogle Scholar
- Zeh C, Amornkul P, Inzaule S, Ondoa P, Oyaro B, Mwaengo D, Vandenhoudt H, Gichangi A, Williamson J, Thomas T, et al.: Population-based biochemistry, immunologic and hematological reference values for adolescents and young adults in a rural population in Western Kenya. PloS One 2011,6(6):e21040. 10.1371/journal.pone.0021040View ArticlePubMedPubMed CentralGoogle Scholar
- Anglewicz P, Adams J, Obare F, Kohler HP, Watkins S: The Malawi diffusion and ideational change project 2004–06: data collection, data quality and analyses of attrition. Demographic Res 2009,20(21):503-540.View ArticleGoogle Scholar
- World Bank: Malawi at a Glance. 2011.http://devdata.worldbank.org/AAG/mwi_aag.pdf . [World Bank Country Profile]Google Scholar
- Poulin M, Muula AS: An inquiry into the uneven distribution of women’s HIV infection in rural Malawi. Demographic Res 2011,25(28):869-902.View ArticleGoogle Scholar
- Crimmins E, Kim J, Alley D, Karlamangla A, Seeman T: Hispanic paradox in biological risk profiles. Am J Public Health 2007,97(7):1305-1310. 10.2105/AJPH.2006.091892View ArticlePubMedPubMed CentralGoogle Scholar
- Seeman T, Crimmins E: Social environment effects on health and aging: Integrating epidemiologic and demographic approaches and perspectives. Ann NY Acad Sci 2001, 954: 88-117.View ArticlePubMedGoogle Scholar
- Reynes J, Lasater T, Feldman H, Assaf A, Carleton R: Education and risk factors for coronary heart disease: results from a New England community. Am J Prev Med 1993,9(6):365.PubMedGoogle Scholar
- Adeyinka AO, Ohaeri JU, Osuntokun BO: The correlates of cortical sulci atrophy and central atrophy in a cohort of schizophrenia and manic subjects in Nigeria. Can J Psychiatry 1995,40(2):200-204.PubMedGoogle Scholar
- Gurven M, Kaplan H, Winking J, Finch C, Crimmins EM: Aging and inflammation in two epidemiological worlds. J Gerontol Ser A: Biol Sci Med Sci 2008,63(2):196-199. 10.1093/gerona/63.2.196View ArticleGoogle Scholar
- Khera A, McGuire DK, Murphy SA, Stanek HG, Das SR, Vongpatanasin W, Wians Jr FH, Grundy SM, de Lemos JA: Race and gender differences in C-reactive protein levels. J Am Coll Cardiol 2005,46(3):464-469. 10.1016/j.jacc.2005.04.051View ArticlePubMedGoogle Scholar
- Kuo HK, Bean JF, Yen CJ, Leveille SG: Linking C-reactive protein to late-life disability in the National Health and Nutrition Examination Survey (NHANES) 1999–2002. J Gerontol Ser A: Biol Sci Med Sci 2006,61(4):380. 10.1093/gerona/61.4.380View ArticleGoogle Scholar
- McDade TW, Rutherford JN, Adair L, Kuzawa C: Adiposity and pathogen exposure predict C-reactive protein in Filipino women. J Nutr 2008,138(12):2442. 10.3945/jn.108.092700View ArticlePubMedPubMed CentralGoogle Scholar
- Ridker PM, Stampfer M, Rifai N: Novel risk factors for systemic atherosclerosis. JAMA: J Am Med Assoc 2001,285(19):2481. 10.1001/jama.285.19.2481View ArticleGoogle Scholar
- Ridker PM, Rifai N, Rose L, Buring JE, Cook NR: Comparison of C-reactive protein and low-density lipoprotein cholesterol levels in the prediction of first cardiovascular events. New England J Med 2002,347(20):1557-1565. 10.1056/NEJMoa021993View ArticleGoogle Scholar
- Walker ARP, Walker BF, Segal I: Some puzzling situations in the onset, occurrence and future of coronary heart disease in developed and developing populations, particularly such in sub-Saharan Africa. J R Soc Promotion Health 2004, 124: 40. 10.1177/146642400312400112View ArticleGoogle Scholar
- Farzadfar F, Finucane MM, Danaei G, Pelizzari PM, Cowan MJ, Paciorek CJ, Singh GM, Lin JK, Stevens GA, Riley LM, Ezzati M: National, regional, and global trends in serum total cholesterol since 1980: systematic analysis of health examination surveys and epidemiological studies with 321 country-years and 3.0 million participants. Lancet 2011,377(9765):578-586. 10.1016/S0140-6736(10)62038-7View ArticlePubMedGoogle Scholar
- Bovet P, Romain S, Shamlaye C, Mendis S, Darioli R, Riesen W, Tappy L, Paccaud F: Divergent fifteen-year trends in traditional and cardiometabolic risk factors of cardiovascular diseases in the Seychelles. Cardiovasc Diabetol 2009, 8: 34. 10.1186/1475-2840-8-34View ArticlePubMedPubMed CentralGoogle Scholar
- Gordon T, Castelli W, Hjortland M, Kannel W, Dawber T: High density lipoprotein as a protective factor against coronary heart disease: The Framingham study. Am J Med 1977,62(5):707-714. 10.1016/0002-9343(77)90874-9View ArticlePubMedGoogle Scholar
- Sharrett A, Ballantyne C, Coady S, Heiss G, Sorlie P, Catellier D, Patsch W: Coronary heart disease prediction from lipoprotein cholesterol levels, triglycerides, lipoprotein(a), apolipoproteins AI and B , and HDL density subfractions: The Atherosclerosis Risk in Communities (ARIC) Study. Circulation 2001,104(10):1108-1113. 10.1161/hc3501.095214View ArticlePubMedGoogle Scholar
- Ezzati M, Lopez AD, Rodgers A, Hoorn SV, Murray CJ: Selected major risk factors and global and regional burden of disease. Lancet 2002,360(9343):1347-1360. 10.1016/S0140-6736(02)11403-6View ArticlePubMedGoogle Scholar
- Rosengren A, Hawken S, Ounpuu S, Sliwa K, Zubaid M, Almahmeed WA, Blackett KN, Sitthi-amorn C, Sato H, Yusuf S: Association of psychosocial risk factors with risk of acute myocardial infarction in 11,119 cases and 13,648 controls from 52 countries (the INTERHEART study): case-control study. Lancet 2004,364(9438):953-962. 10.1016/S0140-6736(04)17019-0View ArticlePubMedGoogle Scholar
- Lemieux I, Lamarche B, Couillard C, Pascot A, Cantin B, Bergeron J, Dagenais G, Despres J: Total cholesterol/HDL cholesterol ratio vs LDL cholesterol/HDL cholesterol ratio as indices of ischemic heart disease risk in men: the Quebec Cardiovascular Study. Archives Intern Med 2001,161(22):2685. 10.1001/archinte.161.22.2685View ArticleGoogle Scholar
- Goldman N, Glei D, Chang M: The role of clinical risk factors in understanding self-rated health. Ann Epidemiol 2004, 14: 49-57. 10.1016/S1047-2797(03)00077-2View ArticlePubMedGoogle Scholar
- Sumaili EK, Krzesinski JM, Zinga CV, Cohen EP, Delanaye P, Munyanga SM, Nseka NM: Prevalence of chronic kidney disease in Kinshasa: results of a pilot study from the Democratic Republic of Congo. Nephrol Dial Transplant 2009, 24: 117-122.View ArticlePubMedGoogle Scholar
- Atkins R: The epidemiology of chronic kidney disease. Kidney Int 2005, 67: S14-S18. 10.1111/j.1523-1755.2005.09403.xView ArticleGoogle Scholar
- El Nahas A, Bello A: Chronic kidney disease: the global challenge. Lancet 2005,365(9456):331-340.View ArticleGoogle Scholar
- Naicker S: End-stage renal disease in sub-Saharan and South Africa. Kidney Int 2003, 63: S119—S122.View ArticleGoogle Scholar
- Chin B: Income, health, and well-being in rural Malawi. Demogr Res 2010,23(35):997-1030.View ArticlePubMedPubMed CentralGoogle Scholar
- Kohler IV, Anglewicz P, Kohler HP, Soldo BJ: Evaluating health and disease in sub-Saharan Africa: minimally invasive collection of plasma in the Malawi longitudinal study of families and health. Genus 2012,68(2):1-27.PubMedPubMed CentralGoogle Scholar
- Gootjes J, Tel RM, Bergkamp FJM, Gorgels JPMC: Laboratory evaluation of a novel capillary blood sampling device for measuring eight clinical chemistry parameters and HbA1c. Clinica Chimica Acta 2009,401(1–2):152-157.View ArticleGoogle Scholar
- McDade T: The state and future of blood-based Biomarkers in the health and retirement study. Forum Health Econ Policy 2011.,14(3): 10.2202/1558-9544.1263Google Scholar
- Dowd JB, Goldman N: Do biomarkers of stress mediate the relation between socioeconomic status and health? J Epidemiol Commun Health 2006,60(7):633-639. 10.1136/jech.2005.040816View ArticleGoogle Scholar
- Schifferli JA: Case 40-2006: anemia and low HDL cholesterol. New England J Med 2007, 356: 1893-1895.View ArticleGoogle Scholar
- van der Westhuyzen D, de Beer F, Webb N: HDL cholesterol transport during inflammation. Curr Opin Lipidol 2007,18(2):147-151. 10.1097/MOL.0b013e328051b4feView ArticlePubMedGoogle Scholar
- Gurven M, Kaplan H, Winking J, Rodriguez D, Vasunilashorn S, Kim J, Finch C, Crimmins E: Inflammation and infection do not promote arterial aging and cardiovascular disease risk factors among lean horticulturalists. PLoS One 2009,4(8):e6590. 10.1371/journal.pone.0006590View ArticlePubMedPubMed CentralGoogle Scholar
- Gurven M, Kaplan H, Supa A: Mortality experience of Tsimane Amerindians of Bolivia: regional variation and temporal trends. Am J Human Biol 2007,19(3):376-398. 10.1002/ajhb.20600View ArticleGoogle Scholar
- Gurven M, Kaplan H, Winking J, Finch C, Crimmins E: Aging and inflammation in two epidemiological worlds. J Gerontol Ser A: Biol Sci Med Sci 2008,63(2):196. 10.1093/gerona/63.2.196View ArticleGoogle Scholar
- Snodgrass J, Leonard W, Tarskaia L, McDade T, Sorensen M, Alekseev V, Krivoshapkin V: Anthropometric correlates of C-reactive protein among indigenous Siberians. J Physiol Anthropol 2007,26(2):241-246. 10.2114/jpa2.26.241View ArticlePubMedGoogle Scholar
- Sorensen M, Leonard W, Tarskaya L, Ivanov K, Snodgrass J, Alekseev V, Krivoshapkin V, Rifai N: High-sensitivity C-reactive protein, adiposity, and blood pressure in the Yakut of Siberia. Am J Human Biol 2006,18(6):766-775. 10.1002/ajhb.20547View ArticleGoogle Scholar
- Schultz TP: Health and schooling investments in Africa. J Econ Perspect 1999,13(3):67-88. 10.1257/jep.13.3.67View ArticlePubMedGoogle Scholar
- Waite LJ, Gallagher M: The Case for Marriage: Why Married People are Happier, Healthier, and Better off Financially. New York: Doubleday; 2000.Google Scholar
- Smith JP: Healthy bodies and thick wallets: The dual relation between health and economic status. J Econ Perspect 1999,13(2):145-166. 10.1257/jep.13.2.145View ArticleGoogle Scholar
- Monteiro CA, Moura EC, Conde WL, Popkin BM: Socioeconomic status and obesity in adult populations of developing countries: Areview. Bull World Health Organ 2004, 82: 940-946.PubMedGoogle Scholar
- Prentice AM: The emerging epidemic of obesity in developing countries. Int J Epidemiol 2006, 35: 93-99.View ArticlePubMedGoogle Scholar
- Hemingway H, Shipley M, Brunner E, Britton A, Malik M, Marmot M: Does autonomic function link social position to coronary risk? The Whitehall II study. Circulation 2005,111(23):3071-3077. 10.1161/CIRCULATIONAHA.104.497347View ArticlePubMedGoogle Scholar
- Cohen S, Doyle W, Baum A: Socioeconomic status is associated with stress hormones. Psychosom Med 2006,68(3):414-420. 10.1097/01.psy.0000221236.37158.b9View ArticlePubMedGoogle Scholar
- Loucks E, Magnusson K, Cook S, Rehkopf D, Ford E, Berkman L: Socioeconomic position and the metabolic syndrome in early, middle, and late Life: evidence from NHANES 1999-2002. Ann Epidemiol 2007,17(10):782-790. 10.1016/j.annepidem.2007.05.003View ArticlePubMedGoogle Scholar
- Danese A, Moffitt T, Harrington H, Milne B, Polanczyk G, Pariante C, Poulton R, Caspi A: Adverse childhood experiences and adult risk factors for age-related disease: Depression, inflammation, and clustering of metabolic risk markers. Arch Pediatr Adolesc Med 2009,163(12):1135-1143. 10.1001/archpediatrics.2009.214View ArticlePubMedPubMed CentralGoogle Scholar
- Gruenewald T, Cohen S, Matthews K, Tracy R, Seeman T: 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.2009.05.018View ArticlePubMedPubMed CentralGoogle Scholar
- Alley DE, Seeman TE, Ki Kim J, Karlamangla A, Hu P, Crimmins EM: Socioeconomic status and C-reactive protein levels in the US population: NHANES IV. Brain Behav Immun 2006,20(5):498-504. 10.1016/j.bbi.2005.10.003View ArticlePubMedGoogle Scholar
- National Research Council: The Continuing Epidemiological Transition in sub-Saharan Africa: A Workshop Summary. Washington: National Academies Press; 2012. . [Thomas J. Plewes and Kevin Kinsella, Rapporteurs. Committee on National Population, Division of Behavioral and Social Sciences and Education] [http://www.nap.edu/catalog.php?record_id=13533] . [Thomas J. Plewes and Kevin Kinsella, Rapporteurs. Committee on National Population, Division of Behavioral and Social Sciences and Education]Google Scholar
- Weir D: Elastic powers: The integration of biomarkers into the Health and Retirement Study. In Biosocial Surveys. Edited by: Council NR. Washington: National Academies Press; 2007:78-95.Google Scholar
- Diez Roux A: Integrating social and biologic factors in health research: a systems view. Ann Epidemiol 2007,17(7):569-574. 10.1016/j.annepidem.2007.03.001View ArticlePubMedGoogle Scholar
- McDade T, Williams S, Snodgrass JJ: What a drop can do: dried blood spots as a minimally invasive method for integrating biomarkers into population-based research. Demography 2007,44(4):899-925. 10.1353/dem.2007.0038View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License(http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.