Abstract
Globally, there has been a shift in the causes of illness and death from infectious diseases to noncommunicable diseases. This changing pattern has been attributed to the effects of an (ongoing) epidemiologic transition. Although researchers have applied epidemiologic transition theory to questions of global health, there have been relatively few studies exploring its relevance especially in the context of emerging allergic disorders in sub-Saharan Africa (SSA). In this article, we address the growing burden of noncommunicable diseases in sub-Saharan Africa through the lens of epidemiologic transition theory. After a brief review of the literature on the evolution of the epidemiologic transition with a particular emphasis on sub-Saharan Africa, we discuss existing frameworks designed to help inform our understanding of changing health trends in the developing world. We subsequently propose a framework that privileges “place” as a key construct informing our understanding. In so doing, we use the example of allergic disease, one of the fastest growing chronic conditions in most parts of the world.
The epidemiologic transition describes a steady decline in mortality, fertility, and changing trends in cause-specific mortality (Omran, 1971). Evidence for a global epidemiologic transition is often associated with the worldwide increase in life expectancy (United Nations, Department of Economic and Social Affairs, Population Division, 2012). Along with increased longevity, we have seen a global shift from infectious diseases to noncommunicable diseases (NCDs) as the primary cause of mortality and morbidity (World Health Organization [WHO], 2009). This is in part a result of improving national incomes, integration into the global market, urbanization, and lifestyle changes (Stuckler, 2008).
The epidemiologic transition literature is useful for exploring and characterizing global health trends, though not without both theoretical and methodological challenges (e.g., Santosa, Wall, Fottrell, Högberg, & Byass, 2014). While usefully employed to explain historical patterns of health changes in European and North American contexts, with few exceptions there is a dearth of literature reflecting how the transition has affected sub-Saharan Africa (SSA; Defo, 2014a) despite evidence of changing burdens of disease. For example, type 2 diabetes now accounts for over 90% of diabetes in SSA (Hall, Thomsen, Henriksen, & Lohse, 2011). In South Africa, cardiovascular diseases have increased by 65% in adults aged 65 years and older while deaths from malignant neoplasms have more than doubled (Tollman et al., 2008). The increasing burden of NCDs in SSA calls for targeted public health interventions. Unpacking place-based influences (e.g., sociocultural and politicoeconomic) on population health can provide insights into the nature of changing health risks and help identify gaps for policy actions that address both the waning current burden of infectious disease and anticipate future health needs from NCDs.
Current studies on the epidemiologic transition in low- and middle-income (LMI) settings are often based on the aggregation of national characteristics to the global scale (Byass, de Savigny, & Lopez, 2014), which masks our understanding of the complex and diverse ways in which space and place matter for population well-being. This invariably put constraints on the ability to explore nuances at the local level, where people live, work, and play (Macintyre, Ellaway, & Cummins, 2002). As progress is sustained in reducing infectious disease cases and economic growth and urbanization in SSA become spatially dispersed and diverse, the experience of health and risk factors for disease will also vary and invariably be place-sensitive (Poland, Lehoux, Holmes, & Andrews, 2005). Consequently, this article argues for a “place-based” exploration of the dimensions of settings to aid understanding of disparities in health and the experience of health in places.
This article addresses the growing burden of NCDs in SSA through the lens of epidemiologic transition theory. In so doing, literature on the evolution of the epidemiologic transition with a particular emphasis on SSA is reviewed and examined to help us understand and analyze changing health trends in LMI countries. We next review “new” emerging health risks related to allergic disorders in SSA within the broader context of chronic disease. Following this, we propose a framework that allows for conceptualizing “place” as a concept to inform our understanding and to address changing health patterns in SSA. This framework is illustrated using the example of allergic disease, one of the fastest growing NCDs in many if not most parts of the world (Du Toit et al., 2015; Pawankar, Canonica, Holgate, & Lockey, 2011).
The Epidemiologic Transition
Past and contemporary reflections on the epidemiologic transition have raised some critical conceptual and methodological issues (e.g., Caldwell, 1992; Frenk, Bobadilla, Sepúlveda, & Cervantes, 1989; Harper & Armelagos, 2010; McKeown, 2009; Zuckerman, 2014; Zuckerman, Harper, Barrett, & Armelagos, 2014) leading to alternative theorizations (e.g., Caldwell, 1992; Defo, 2014a, 2014b; Frenk et al., 1989) that highlight the role of multiple factors and the complexity of changing health and disease patterns across the human life course.
Explicit in existing empirical studies has been the overreliance on quantitative research designs with little or no discussion of the use of qualitative methodologies. While recognizing that in the research process the question determines the method (Elliott, 1999), the scarcity of a critical reflection on qualitative approaches can largely be situated in the implicit theoretical foundations of the epidemio-logic transition. Conceptually, because of its attention to relationships between mortality, morbidity, disability, birth rates, and life expectancy, it evokes a biomedical perspective of health. In this sense, past and current practices have seen the widespread application of multivaried statistical tools that seek to, for example, identify risk factors influencing health and model changing trends of health and disease over time. While such techniques may demonstrate empirical evidence for associations, they nonetheless often obscure explanations and reasons for the impact of place on health—“the local context of health, disease and social process” (Kearns, 1993, p. 139). To gain contextual knowledge as Kearns (1994,) has argued is to relax “conventional (positivist) scientific rigor and the adoption of methods which are no less rigorous and scientific, but ones that grant subjectivity and ultimately involves the researcher and researched [italics added] in the research process” (p. 113).
Attention to the role of “place” enriches our understanding of how, why, and to what extent characteristics of the local social and physical environment shape disease prevalence and incidences (Dunn & Cummins, 2007) as well as the embodied experiences and meanings of health that bridge interest in understanding how compositional and contextual factors influence health and disease. A place-based perspective demands a need to recognize transition trends characterized by variances in population groups, pace, timing, patterns of change, and meanings of health and disease, particularly given the intricate sociocultural, economic, and environmental contexts in which health unfolds in countries. Given discussions of a rapid ongoing epidemiologic transition in developing regions, particularly the diverse paths that the transition can take, a “place-based” perspective provides an entry point that can enrich our understanding of the heterogeneity of the epidemiologic transition particularly in contexts such as SSA.
Changing Health and Disease in Sub-Saharan Africa
While there is a general belief that societies in Western Europe and North America have successfully completed their epidemiologic transition from diseases of infection to NCDs, in SSA, research suggests a distinct trajectory characterized by heterogeneity in the region’s healthscapes (National Research Council, 2012). A detailed review of country-specific shifts in disease and heterogeneity is beyond the scope of the current article, though some illustrations have been provided. The evidence in SSA, however, suggests that despite a context of persistent and high burden of infectious and childhood diseases, chronic NCDs and injuries are increasingly becoming critical health issues (e.g., WHO, 2009). For example, findings from the Global Burden of Disease 2010 study indicate that infectious diseases, childhood illnesses, and maternal-related deaths were responsible for close to 70% of the burden of disease in most countries in the region (WHO, 2012). This notwithstanding, progress has also been made in reducing age-specific mortality trends (e.g., the child mortality rate has declined by 65% since 1970; Defo, 2014a; Institute for Health Metrics and Evaluation [IHME] & Human Development Network, The World Bank [HDN-WB], 2013).
At the same time, populations in SSA along with those in Asia and Latin America are dealing with the rise of chronic NCDs and injuries. Diabetes and depression are estimated to have risen by 88% and 61% respectively between 1990 and 2010 in SSA. NCDs-related disability-adjusted life years were estimated at 25% in 2010, a rise of about 20% from 1990 (IHME & HDN-WB, 2013). Similarly, countries like Ghana have seen a significant rise in NCDs-related disability-adjusted life years—ischemic heart disease, 130%; diabetes, 110%; and stroke, 100% (IHME & HDN-WB, 2013). Furthermore, emerging NCDs disproportionately affect vulnerable groups such as women, and the poor living in urban slums (Miszkurka et al., 2012; van der Vijver, Oti, Agyemang, Gomez, & Kyobutungi, 2013).
Given increased life expectancy, shifting lifestyle practices, poverty, rapid urbanization, and globalization, it is projected that by 2030, chronic disease will become the leading triggers of death in SSA (Marquez & Farrington, 2013). While traditional NCDs (e.g., cancer, cardiovascular disease, diabetes) receive the most attention, allergic disease (e.g., asthma, rhinitis, eczema, food allergy) is largely unacknowledged as a significant health problem especially in SSA. This is due in part to limited health infrastructures to diagnose allergies and the relatively high-priority focus on the burden of infectious disease (Mbugi & Chilongola, 2010; Obeng, Hartgers, Boakye, &Yazdanbakhsh, 2008). A preliminary search in PubMed (1990-2014) suggests a concentration of studies on asthma in countries such as South Africa, Nigeria, and Ethiopia (see Appendix 1). Large-scale multicenter epidemiologic studies such as the International Study of Asthma and Allergies in Childhood (ISAAC) Phase III study in 16 African countries provide some insights into the state of allergies in Africa. ISAAC found a relatively high prevalence of symptoms of asthma, rhinitis, and eczema with centers in countries such as South Africa (Cape Town, 20.3%; Polokwane, 18.0%) and Congo (Brazzaville, 19.9%), showing rates comparable to those in Western societies (Ait-Khaled et al., 2007). In South Africa, a time trend study reported significant increases in wheeze, a marker of asthma (from 16% to 27.7%); allergic rhinitis (from 29.1% to 41.5%); and eczema (from 9.6% to 16.7%) between 1995 and 2002 (Zar, Ehrlich, Workman, & Weinberg, 2007). Similar studies in Ghana demonstrate an increase in prevalence of exercise-induced bronchospasm—a marker of asthma—and of allergic sensitization from 3.1% to 5.2% and 7.6% to 13.6% over a decade, respectively (Addo-Yobo et al., 2007). Falade, Olawuyi, Osinusi, and Onadeko (2004) also show growing atopic conditions among children in Ibadan Nigeria, with the cumulative prevalence of reported symptoms of wheezing, rhinitis, and eczema estimated at 7.2%, 11.3%, and 10.1%, respectively. These studies highlight a socio-economic and rural–urban gradient in the risk of developing allergic disease.
Concerns have also been raised about “new” atopic conditions such as food allergy, which has lagged behind asthma and eczema even in developed countries until recently (Prescott & Allen, 2011). Our preliminary search (Appendix 1) shows a dearth of studies in particular on rhinitis and food allergy in SSA. With respect to food allergy, an emerging body of evidence (Boye, 2012; Kung, Steenhoff, & Gray, 2012; Prescott et al., 2013) using a range of diagnostic techniques points toward a “burgeoning reality” of food allergy. In South Africa, one study estimated the overall prevalence of sensitization to food allergens—egg white (3.3%), milk (2%), peanut (1%), and potato (1%)—as measured by a positive skin prick test at 5% (Levin, Muloiwa, & Motala, 2011). Similarly, Obeng et al. (2011) reported prevalence of adverse reactions to food at 11%, with 5% showing a positive skin prick test reaction mainly to peanut (2%) and pineapples (2%) in Ghanaian schoolchildren. Recently, an audit review of allergic sensitization profiles of patients in Zimbabwe found high levels of sensitization to potato (16%) and peanut (15%; Sibanda, 2013). More recently, Gray et al. (2014) found that, 40% of children had at least one IgE-mediated food allergy to egg, peanut, tree nut, cow milk, and fish in a high-risk population in South Africa. In Western societies, food allergy has become an important heath issue. For example, national studies indicate that approximately 7.5% of the overall population in Canada (Soller et al., 2012) and 8% of children in the United States (Gupta et al., 2011) self-report food allergy.
These extant studies challenge the popular view that SSA may be “protected” from allergic disease, highlighting the need to enhance our understanding of changing biological, environmental, and socioeconomic dynamics shaping allergic disease. In developed countries where the epidemiologic transition appears “complete,” allergic disease is on a substantial upward trajectory (Zuckerman et al., 2014), paralleling NCDs. Given the trajectory of the epidemiologic transition in SSA, will we see the same situation in the near future? We propose a framework for exploring allergic disorders that privileges “place” as a key construct in our understanding.
Toward a “Place-Based” Framework for Understanding Allergic Disease
Space and place represent enduring lenses for understanding health, particularly within health geography. Traditionally, studies explicating the role of “space” and “place” on health have been characterized by spatial and locational analyses (employing mostly statistical techniques) that conceptualize “space” as a container of things and or as attributes of phenomenon (Kearns & Moon, 2002). From this perspective, space is seen as the platform on which health-related activities are manifest and consequently is treated as independent from the social phenomenon it embodies. Similarly, “place” has typically been explored in terms of location (as implied in different scales such as community or neighborhood) by exploring its social and/or physical attributes (Kearns & Moon, 2002). Consequently, studies primarily dealt with, for example, modeling and mapping the spatial determinants of disease, distribution and diffusion of diseases, as well as accessibility and utilization of health services (Andrews, 2002). In the context of allergic disease, studies have generally explored spatio-temporal patterns of allergic disease (e.g., Asher et al., 2006, examined worldwide trends in asthma, rhinitis, and eczema prevalence). Similar studies have also investigated allergy-specific national disparities in prevalence such as asthma (Obaseki, Awoniyi, Awopeju, & Erhabor, 2014), eczema (Hogewoning et al., 2012), and food allergies (Soller et al., 2015). In addition, studies have also examined risk factors for allergies, focusing on socioeconomic index of areas, geographic remoteness, and childhood food allergy and anaphylaxis in space (Mullins, Clark, & Camargo, 2010).
While important, these studies restrict our understanding of space and place as “the canvas on which events happen while the nature of the locality and its role in restructuring health status and health-related behaviors and by extension allergic disease [italics added] is neglected” (Jones & Moon, 1993, p. 515). In this sense, the intricacies of “place” go beyond just emphasizing where a location (e.g., physical settings) is, to encapsulating how sets of situated social dynamics (Poland et al., 2005) involve iterate and interactive relations between “experience of both literal place and people’s perceived “place-in-the-world” mediates health and well-being (Kearns & Moon, 2002, p. 610). For example, Fenton, Elliott, and Clarke (2013) explored space, place, and the health experience of Canadian food allergic children and showed how the school environment mediates interactions through the construction of bodily constraints and emotions of allergic children as they move through “spaces of risk”—for example, class room, cafeteria—searching and discerning known and unknown safe havens. Thus our understanding of changes in health and disease ought to be deeply embedded in the mutually linked notions of composition (type of people in places) and context (constructing places; Cummins, Curtis, Diez-Roux, & Macintyre, 2007; Macintyre et al., 2002).
As processes such as economic growth, globalization, and urbanization trigger changes in patterns of health and disease, it is essential we understand how these shape and are being shaped by social processes and their spatial outcomes (e.g., distribution of allergies). While attention to macro-level changes may set the context for health policy, it is also essential to explore micro-level practices shaping health behaviors. Allergic disorders are only recently gaining attention, and in the context of SSA, very few studies have explored this burden. In addition, the available research focuses on place and health through the lens of spatial and locational analyses, using quantitative methodologies (e.g., Gray et al., 2014; Obeng et al., 2011) that do not inculcate in-depth explorations of sociocultural dimensions and how these shape allergic disorders in SSA.
We propose a framework that seeks to account for both macro-level and local production of health and by extension allergies with the key levels of influences being micro/individual context, area-level influences, sociocultural environment, and macro-structural context (Figure 1). In this framework, “place” is not just the “physical setting” shaping allergic disease but also a “set of ‘situated’ social dynamics” that is “multidimensional, contestable, and embedded [italic added] with different meanings to different social and professional groups” (Poland et al., 2005, p. 172) within which allergies can become embodied. This iterative framework views allergic disease as influencing and being influenced by the micro-level, area level, sociocultural, and macro-level contexts. For example, individuals who may have a genetic disposition (individual level) who also are exposed to environmental triggers (area level) may be more vulnerable to developing allergies.

A “place-based” framework for understanding allergic disease.
Individual/Micro Context
At the individual level, family history (indirect measure of genetic risk) of allergy is an important pathway to allergic disease notwithstanding environmental risks factors (Wang, 2005). Twin studies, for example, show associations of genetic influence on dermatitis, asthma, and allergic rhinitis (Tan, Ellis, Saffery, & Allen, 2012) while heritability has been found to account for variance in peanut allergy (Sicherer et al., 2000).
Allergic disease risks are also associated with some measures of socioeconomic status (SES) in places although there are variations by allergic phenotype. Studies have found that exposure to low-income environments from birth is associated with the risk of developing persistent asthma (Kozyrskyj, Kendall, Jacoby, Sly & Zubrick, 2010). Similarly, Almqvist, Pershagen and Wickman (2005) note that risk of asthma, rhinitis, and sensitization to food allergens in children decreases with increasing SES particularly if both parents have higher level white-collar employments. On the other hand, higher SES factors (e.g., income, formal education) are surrogate risk indicators for self-reported food allergy, allergic sensitization, and anaphylaxis development (Ben-Shoshan et al., 2012; Mullins et al., 2010).
Area-Level Contexts
Where you live is associated with allergic disease especially for populations moving from traditional/rural to modern/urban societies (Obeng et al., 2011). Exposure to urban living environment, for example, pollution, household exposure to allergens, and Westernized lifestyles (e.g., modern housing, better hygiene, sanitation, and dietary changes) have been identified as risk markers for allergic disease (Robinson et al., 2011). There are, however, intra-urban variations in specific allergic disease risks. For example, while prevalence of allergic sensitization and allergic rhino-conjunctivitis increased with increasing urbanization, the same effects have not been observed in relation to asthma (Viinanen et al., 2005). In rural areas in SSA, van Gemert, van der Molen, Jones, and Chavannes (2011) found that, asthma is less predominant in comparison to urban communities. Beyond the rural–urban gradient, household and community characteristics and presence or absence of health services can shape health behavior and by extension allergy disease risk, knowledge, and diagnosis.
Sociocultural Context
Chronic disease conditions are embedded in the norms and beliefs of societies. Using qualitative techniques, Lu, Elliott, and Clarke (2014) illustrate that knowledge about and perceptions of food allergy vary between migrants and their host populations. They also point out the lack of a defined name for food allergy in migrant places of origin. Thus, the concept of allergies differs across geographic areas and population groups. In addition, poor health-related knowledge of allergies may hamper early diagnosis, which may partly be an outcome of a lack of access and quality of health services. In such cases, direct and indirect bodily experience of allergies may be an important mechanism shaping health-seeking action and choice of therapeutic treatments. Given food allergies are newly emerging health risks, understanding how existing norms and disease etiology affect diagnosis and treatment-seeking behavior is essential to our understanding.
The Macro-Structural Context
Though allergic disease occurs at the individual level, a lack of attention to the macro-level interwoven socio-political and economic processes can mask underlying influences that lead to health inequalities (Krieger, 2011). Decisions related to the allocation of resources, type of health care, and disease priority are influenced by multiple stakeholders at various spatial scales. For instance, until recently, global and national health policy emphasized the prevention of infectious diseases in developing countries. Implicit in such prioritization is the perception that chronic disease (e.g., diabetes, asthma, and allergies) exists only in affluent Western societies. Thus, a focus on macro determinants such as issues of power, financial resources, policy, as well as the agency of multiple stakeholders can expand the pathways to understand how decisions about health are made and their implications for allergic disorders in LMI countries (Bousquet, Ndiaye, Ait-Khaled, Annesi-Maesano, & Vignola, 2003).
Discussion and Conclusions
Chronic diseases are projected to be an increasingly significant health burden in LMI countries as progress is sustained in tackling infectious diseases (Stuckler, 2008). In this article, we addressed NCDs through the lens of epidemiologic transition theory. The article emphasizes that notwithstanding its challenges, it is still a useful structural framework for understanding changing health and disease patterns. We have also pointed out that existing frameworks for analyzing changing epidemiologic patterns in SSA and elsewhere must pay attention to how the specificity of “place” becomes pathways through which chronic diseases such as allergic disorders become embodied in populations. Engagement with “place effects” demands thinking about possibilities of multiple epidemiologic transitions at and across various analytic scales—for example, regional, national, and socioeconomic groups—if we are to comprehend differing health trends in SSA.
As we are unable to provide an in-depth country-specific synthesis of the epidemiologic transition over time, this article may not be generalizable across countries vis-à-vis the pace and stages of the epidemiologic transition. However, the broad trends described are generally consistent with the changes occurring in most countries in SSA. Furthermore, given that allergic disorders such as food allergy is “newly” emerging, we only make reference to published studies for countries in the subregion for which data were available.
Questions remain regarding the prevalence of allergic disease in SSA. Furthermore, little is known about its etiology, its social constructions, as well as the mechanisms through which policies might mediate allergic disease risk. As a way to address data gaps, we suggest that validated questions about allergic disorders could be incorporated into existing health and national population-based surveys (e.g., Census, the Demographic and Health Surveys, Multiple-Indicator Cluster Surveys, Living Standards Surveys) to help provide evidence for policy planning. Beyond building the evidence base, “place”- focused research implies multiple perspectives in research design, policy formulation, and policy implementation. Thus, we follow Elliott (2011) to suggest that research and practice need a transdisciplinary approach to understand the epidemiology of allergic diseases in SSA. Much can be gained from best practices in developed countries employing transdisciplinary teams of researchers to understand biological risks factors and immunological pathways as well as social dimensions related to allergies (Ben-Shoshan et al., 2012; Minaker, Elliott, & Clarke, 2014). At the very least, the few extant studies provide signposts for anticipating future added health burdens from allergic diseases in SSA. As a starting point, health policy ought to take a balanced approach reflective of the current burden of infectious disease as well as of future health needs from NCDs, and allergic disorders more specifically. Currently, only South Africa has prepared eczema and rhinitis guidelines (Green et al., 2012; Sinclair, Aboobaker, Jordaan, Modi, & Todd, 2008). It is important that health policy makers begin to adopt more proactive steps to incorporate allergic disorders as part of their broader agenda for NCD prevention. Furthermore, training health professionals to recognize allergic disorders can provide an effective entry point to reach populations at risk. Given that allergic disorders primarily affect children, this can be integrated into maternal and child health programs.
Footnotes
Appendix
Studies of Allergic Disorders in Anglophone-Speaking Countries in Sub-Saharan Africa, 1990 to 2014.
| Country | Asthma | Eczema | Rhinitis | Food allergy |
|---|---|---|---|---|
| Bostwana | X | X | X | X |
| Cameroon | Mugusi et al., 2004; Ait-Khaled et al., 2007 a ; Kengne et al., 2008 | Ait-Khaled et al., 2007; Bissek et al., 2012 | Ait-Khaled et al., 2007 | X |
| Eriteria | X | X | X | X |
| Ethiopia | Zemedkun et al., 2014; Belyhun et al., 2010; Denboba et al., 2008; Ait-Khaled et al., 2007; Venn et al., 2005; Davey et al., 2005; Dagoye et al., 2004; Hailu et al., 2003; Dagoye et al., 2003; Venn et al., 2001; Scrivener et al., 2001; Selassie et al., 2000; Melaku & Berhane, 1999; Yemaneberhan et al., 199; Seyoum & Amaro, 1992; Silverman, 2003 | Morrone, 2014; Gimbel & Legesse, 2012; Amberbir et al., 2011; Bilcha et al., 2010; Belyhun et al., 2010; Bilcha et al., 2009; Accorsi et al., 2009; Ait-Khaled et al., 2007 a ; Haileamlak, Dagoye, et al., 2005; Haileamlak, Lewis, 2005; Hailu et al., 2003; Shibeshi, 2000 | Ait-Khaled et al., 2007 | X |
| Gambia | Walraven et al., 2001; Weber et al., 1999 | X | X | X |
| Ghana | Obeng et al., 2014; Stevens et al., 2011; Addo-Yobo et al., 2007, 2001, 1997, Hesse, 1995 | Hogewoning et al., 2012, 2010 | X | Amoah et al., 2013; Obeng et al., 2011 |
| Kenya | Ait-Khaled et al., 2007 a ; Perzanowski et al., 2002; Ng’ang’a et al., 1998; Odhiambo et al., 1998; Ng’ang’a et al., 1997; Odhiambo et al., 1994; Odhiambo & Chwala, 1992; De Souza, 1992 a ; Gathua & Aluoch, 1990 | Ait-Khaled et al., 2007; Esamai et al., 2002 a ; Esamai & Anabwani, 1996; De Souza, 1992 | Ait-Khaled et al., 2007; Esamai et al., 2002; De Souza, 1992 | De Souza, 1994 |
| Lesotho | X | X | X | X |
| Liberia | X | X | X | X |
| Malawi | X | X | X | X |
| Namibia | X | X | X | X |
| Nigeria | Ayuk et al., 2014; Desalu et al., 2013; Thacher et al., 2013; Adeyeye et al., 2013; Oviawe & Osarogiagbon, 2013; Adetoun Mustapha et al., 2013; Oluwole et al., 2013; Onazi et al., 2012; Desalu et al., 2012; Fawibe et al., 2011; Ige et al., 2011; Desalu et al., 2011; Oni et al., 2011; Desalu, Oluboyo, et al., 2009 a ; Desalu, Salami, et al., 2009; Falade et al., 2009 a ; Adeyeye & Onadeko, 2008; Aguwa et al., 2007; Erhabor et al., 2006; Erhabor & Mosaku, 2004; Erhabor, 2003; Anetor et al., 2003; Oladipo et al., 2003; Erhabor et al., 2002; Ayres et al., 1999; Gbadero et al., 1995; Onadeko et al., 1994; Famodu et al., 1994; Fagbule & Ekanem, 1994, Erhabor et al., 1993 | Falade et al., 2009; Ayanlowo & Olumide; 2007; Nnoruka, 2005, 2004; Ogunbiyi et al., 2003 | Desalu, Oluboyo, et al., 2009; Falade et al., 2009; Aguwa et al., 2007; Takwoingi et al. 2003; Nwawolo & Olusesi, 2001, Ibekwe et al., 1990 | Onyemelukwe, 2011 |
| Rwanda | Musafiri et al., 2011 | Hogewoning et al., 2012 | 0 | 0 |
| Seychelles | X | X | X | X |
| Sierra Leone | X | X | X | X |
| South Africa | Shirinde et al., 2014; Abbott et al., 2013; van der Walt et al., 2013; Singh et al., 2013; Levin et al., 2011; Carroll et al., 2012; Mash et al., 2009; Calvert & Burney, 2010; Greenblatt et al., 2010; Maluleke & Worku, 2009; White et al., 2009; Jeebhay et al., 2009; Green et al., 2008; Wichmann et al., 2009, 2007; Ait-Khaled et al., 2007; van der Merwe et al., 2006; Mashalane et al., 2006; Ehrlich et al., 2005; Poyser et al., 2002; de Klerk et al., 2002; Macintyre et al., 2001; Zar & Weinberg, 2001; Zar et al., 2001; Esterhuizen, Hnizdo, & Rees, 2001; Esterhuizen, Hnizdo, Rees, Lalloo, et al., 2001; Ehrlich, Jordaan, et al., 2001; Green et al., 2001; Hnizdo et al., 2001; Buck et al., 2001; Jones et al., 2000; Nriagu et al., 1999; Ehrilich et al., 1998; Kirkby & Ker, 1998; Bheekie et al., 1998; Green & Luyt, 1997; Moosa & Henley, 1997; Ehrlich et al., 1996; Cowie & Mabena, 1996; Ehrlich et al., 1995; Luyt et al., 1995; Ehrlich & Weinberg, 1994; Ehrlich & Bourne, 1994; Roux et al.,1993; Terblanche & Stewart, 1990 | Levin et al., 2011 a ; Wichmann et al. 2009 a , 2008, 2007; Zar et al., 2007; Ait-Khaled et al., 2007 a ; Mercer et al., 2004 a ; Hartshorne, 2003; Jessop et al., 2002 | Potter et al., 2013; Seedat et al., 2010; Wichmann et al., 2009; Zar et al., 2007 a ; Green et al., 2007; Ait-Khaled et al., 2007; Mercer et al., 2004, 2002 | Levin et al., 2011; Hooper et al., 2008; Nieuwenhuizen et al., 2006; Frank et al., 1999; Zinn et al., 1997 |
| Swaziland | X | X | X | X |
| Uganda | Nantanda, Tumwine, Ndeezi, & Ostergaard, 2013; Nantanda, Ostergaard, Ndeezi, & Tumwine, 2013; Kirenga & Okot-Nwang, 2012; Mpairwe et al., 2008 a | Mpairwe et al., 2008; Mpairwe et al., 2011 | X | X |
| Tanzania | Berntsen, 2011; Goebbels et al., 2010; Berntsen et al., 2009; Justin-Temu et al. 2008 a ; Mugusi et al., 2004; Sunyer et al. 2001; Sunyer et al. 2000 | Komba & Mgonda, 2010; Satimia et al., 1998; Justin-Temu et al., 2008 | X | X |
| Zambia | X | X | X | X |
| Zimbabwe | Sibanda, 2003; Kambarami et al., 1999a | Sibanda, 2013; Kambarami et al., 1999 | Kambarami et al., 1999 | Sibanda, 2013 |
Note. X = No results found.
Studies involve more than one type of allergy.
1. Asthma
Ait-Khaled, N., Odhiambo, J., Pearce, N., Adjoh, K. S., Maesano, I. A., Benhabyles, B., . . . Zar, H. J. (2007). Prevalence of symptoms of asthma, rhinitis and eczema in 13- to 14-year-old children in Africa: The International Study of Asthma and Allergies in Childhood Phase III. Allergy, 62, 247-258.
Bissek, A.-C., Tabah, E. N., Kouotou, E., Sini, V., Yepnjio, F. N., Nditanchou, R., . . . Muna, W. F. T. (2012). The spectrum of skin diseases in a rural setting in Cameroon (sub-Saharan Africa). BMC Dermatology, 12, 7. doi:10.1186/1471-5945-12-7
Kengne, A. P., Sobngwi, E., Fezeu, L. L., Awah, P. K., Dongmo, S., & Mbanya, J. C. (2008). Nurse-led care for asthma at primary level in rural sub-Saharan Africa: The experience of Bafut in Cameroon. Journal of Asthma, 45, 437-443. doi:10.1080/02770900802032933
Mugusi, F., Edwards, R., Hayes, L., Unwin, N., Mbanya, J. C., Whiting, D., . . . Rashid, S. (2004). Prevalence of wheeze and self-reported asthma and asthma care in an urban and rural area of Tanzania and Cameroon. Tropical Doctor, 34, 209-214.
1. Asthma
Ait-Khaled, N., Odhiambo, J., Pearce, N., Adjoh, K. S., Maesano, I. A., Benhabyles, B., . . . Zar, H. J. (2007). Prevalence of symptoms of asthma, rhinitis and eczema in 13- to 14-year-old children in Africa: The International Study of Asthma and Allergies in Childhood Phase III. Allergy, 62, 247-258.
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Dagoye, D., Bekele, Z., Woldemichael, K., Nida, H., Yimam, M., Hall, A., . . . Lewis, S. A. (2003). Wheezing, allergy, and parasite infection in children in urban and rural Ethiopia. American Journal of Respiratory and Critical Care Medicine, 167, 1369-1373.
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2. Eczema
Accorsi, S., Barnabas, G. A., Farese, P., Padovese, V., Terranova, M., Racalbuto, V., & Morrone, A. (2009). Skin disorders and disease profile of poverty: Analysis of medical records in Tigray, northern Ethiopia, 2005-2007. Transactions of the Royal Society of Tropical Medicine and Hygiene, 103, 469-475. doi:10.1016/j.trstmh.2008.11.028
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Bilcha, K. D., Ayele, A., Shibeshi, D., & Lovell, C. (2010). Patch testing and contact allergens in Ethiopia: Results of 514 contact dermatitis patients using the European baseline series. Contact Dermatitis, 63, 140-145. doi:10.1111/j.1600-0536.2010.01740.x
Bilcha, K. D., Shibeshi, D., Grangsjo, A., & Hiletework, M. (2009). Patch test reaction on Ethiopian subjects with eczema. International Journal of Dermatology, 48, 979-983. doi:10.1111/j.1365-4632.2009.04070.x
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1. Asthma
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1. Asthma
Addo-Yobo, E. O., Custovic, A., Taggart, S. C., Asafo-Agyei, A. P., & Woodcock, A. (1997). Exercise induced bronchospasm in Ghana: Differences in prevalence between urban and rural schoolchildren. Thorax, 52, 161-165.
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Obeng, B. B., Amoah, A. S., Larbi, I. A., de Souza, D. K., Uh, H. W., Fernández-Rivas, M., . . . Hartgers, F. C. (2014). Schistosome infection is negatively associated with mite atopy, but not wheeze and asthma in Ghanaian schoolchildren. Clinical & Experimental Allergy, 44, 965-975. doi:10.1111/cea.12307
Stevens, W., Addo-Yobo, E., Roper, J., Woodcock, A., James, H., Platts-Mills, T., & Custovic, A. (2011). Differences in both prevalence and titre of specific immunoglobulin E among children with asthma in affluent and poor communities within a large town in Ghana. Clinical & Experimental Allergy, 41, 1587-1594. doi:10.1111/j.1365-2222.2011.03832.x
2. Eczema
Hogewoning, A. A., Bouwes Bavinck, J. N., Amoah, A. S., Boakye, D. A., Yazdanbakhsh, M., Kremsner, P. G., . . . Lavrijsen, A. P. (2012). Point and period prevalences of eczema in rural and urban schoolchildren in Ghana, Gabon and Rwanda. Journal of the European Academy of Dermatology and Venereology, 26, 488-494. doi:10.1111/j.1468-3083.2011.04106.x
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3. Food Allergy
Amoah, A. S., Obeng, B. B., Larbi, I. A., Versteeg, S. A., Aryeetey, Y., Akkerdaas, J., . . . Yazdanbakhsh, M. (2013). Peanut-specific IgE antibodies in asymptomatic Ghanaian children possibly caused by carbohydrate determinant cross reactivity. Journal of Allergy and Clinical Immunology, 132, 639-647. doi:10.1016/j.jaci.2013.04.023
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1. Asthma
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2. Eczema
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3. Food Allergy
De Souza, M. (1994). Allergies and skin testing: A Nairobi experience. East African Medical Journal, 71, 473-475.
1. Asthma
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2. Eczema
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3. Rhinitis
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4. Food allergy
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1. Asthma
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2. Eczema
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1. Asthma
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Declaration of Conflicting Interests
The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The authors received no financial support for the research, authorship, and/or publication of this article.
Supplement Issue Note
This article is part of a Health Education & Behavior supplement, “Noncommunicable Diseases in Africa and the Global South,” which was supported by SAGE Publishing, with additional support from the National Heart, Lung, and Blood Institute Contract No. HHSN268201500073P. The entire supplemental issue is available open access for one year at
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