Abstract
Background
In Brazil, the incidence of dengue greatly increased in the last two decades and there are several factors impeding the control of the disease. The present study focused on describing the space-time evolution of dengue in Brazil from 2001 to 2012 and analyzing the relationship of the reported cases with socio-demographic and environmental factors.
Methods
The analytic units used in the preparation of thematic maps were municipalities. Statistical tests and multilevel regression models were used to evaluate the association between dengue incidence and the following factors: climate, diagnostic period, demographic density, percentage of people living in rural areas, Gross Domestic Product, Gini index, percentage of garbage collection and the rate of households with a sewage network.
Results
The largest accumulation of dengue cases in Brazil was concentrated on the Atlantic coast and in the interior part of São Paulo State. The risk of dengue in subtropical and tropical climates was 1.20–11 times lower than that observed in semi-arid climates. In 2009–2010 and 2011–2012, the risks were ten and six times higher than in 2003–2004, respectively.
Conclusion
Dengue is a common infection in the Brazilian population, with the largest accumulation of dengue cases concentrated on the Atlantic coast and in the interior area of São Paulo State. The high dengue rates observed in the Brazilian coastal region suggest that the cases imported from neighboring countries contribute to the spread of the disease in the country. Our results suggest that several socio-demographic and environmental factors resulted in the increase of dengue in the country over time. This is likely applicable to the occurrence of other arboviruses like Zika and chikungunya. To reverse the situation, Brazil must implement effective public policies that offer basic services such as garbage collection and sanitation networks as well as reduce vector populations.
Introduction
Dengue is a mosquito-borne viral disease (arbovirus) caused by a flavivirus, which infects about 390 million inhabitants of several countries every year. Currently, there are four known types of dengue virus (DENV): DENV1, DENV2, DENV3 and DENV4 [1].
The role of arboviruses in public health has increased globally [2–5]. Around 40% of the world population is at risk to acquire some arbovirus in Asia, the Americas, Africa and the Eastern Mediterranean [6, 7].
The incidence of dengue increased greatly over the past two decades in Brazil, affecting all regions except the South. The Brazilian Health Ministry reported that the incidence of dengue rose from 273.9/100,000 in 2014 to 756.9/100,000 in 2015 [8]. Attempts to reduce the dengue incidence have not been a simple task for Brazilian’s health managers. Several factors impede the ability to control the disease: different serotypes of the DENV can circulate simultaneously, Brazil has the appropriate environmental conditions for vector reproduction [6, 7], and there is fast and disordered growth of the population in urban centers, impacting other problems such as poor sanitation and inadequate garbage collection [7]. This influences the increase of the incidence of arboviruses, like dengue, Zika and chikungunya, in the Brazilian population. The present study focused on describing the profile of the space-time evolution of dengue in Brazil from 2001 to 2012 and analyzing the relationship of the notified cases with socio-demographic and environmental factors.
Methods
This is an ecological study using public access data collected from government websites: Informatics Department of Brazilian Unified Health System (DATASUS), Brazilian Institute of Geography and Statistics (IBGE) and Information System of Compulsory Notification of Diseases (SINAN) [9–13]. Municipalities were the analytic units used in the preparation of thematic maps. In Brazil, there are 27 states incorporating 5,570 municipalities.
We used the geo-referenced mesh of Brazilian municipalities (shapefile file), available on the IBGE website [14], and collected notification data of dengue cases according to the diagnostic year for each municipality from the SINAN website. We determined the municipal population for each year according to the census data and inter-census projections of IBGE.
To compute the spatial statistics, we formulated a binary spatial weight matrix (ω), in which two counties are neighbors if they share a common physical boundary. The Queen matrix, used in the present study, also considers two neighboring regions that share a common border by analyzing the vertices. We calculated Global Moran Index and the rate of dengue per 100,000 inhabitants for the 2001–2006 and 2007–2012 periods using the Global Empirical Bayesian technique.
We defined the climatic distribution according to Koppen-Geiger classification (Af, Aw, Am, BSh, Cfb, Cfa, Cwa and Cwb) [11, 15, 16] (Table 1), and the municipalities sharing borders with others countries according to the neighbor country (border with Uruguay, Argentina, Paraguay, Bolivia, Guyana, Surinam, French Guiana, Venezuela, Colombia and Peru). We collected information about the percentage of garbage collection by cleaning service, the rate of households with a sewage network per 1,000 dwellings, the percentage of the population living in rural areas, the demographic density (measured by the number of inhabitants per square kilometer), the Gross Domestic Product (GDP) per capita/1,000 dollar, and the Gini Index per capita household income from the DATASUS website [17]. We calculated the incidence of dengue per 100,000 inhabitants using the notified records and its respective population.
Table 1. Division of Brazilian climate characteristics using Koppen-Geiger classification.
Group | Climate | Characteristics | Prevailing area |
---|---|---|---|
Tropical | Am | High total rainfall | North |
Short dry season | |||
Af | Humid climate | North | |
No dry season | |||
Aw | Rainy season in the summer | Midwest | |
Dry winter | Northeast | ||
Arid (hot) | BSh | Dry climate | Northeast |
High temperatures | |||
Strong sunlight | |||
Little and irregular rainfall | |||
Torrential flooding | |||
Subtropical (temperate) | Cfa | Hot summer | South |
No dry season | Southeast | ||
Cfb | Mild summer | South | |
No dry season | Southeast | ||
Cwa | Hot summer | Southeast | |
Dry winter | Midwest | ||
Cwb | Mild summer | Southeast | |
Dry winter |
For each municipality, we assessed the Gini index to evaluate the degree of inequality between individuals according to per capita household income. This index ranges from zero to one, where zero indicates the absence of inequality and one indicates complete inequality.
Information about garbage collection, sewage network and Gini Index was only available for the years 2000 and 2010.
Statistical analysis
We used chi-square tests to evaluate the association between dengue incidence and the following factors: climate, diagnostic period, demographic density and percentage of people living in rural areas.
We used Quasi Poisson regression models to evaluate the association between dengue occurrence and the following factors: GDP, Gini index, garbage collection and sewage networks. We calculated both crude and adjusted relative risks (RR) using a different model for each factor. To get adjusted estimates, we added the covariate “percentage of the population living in rural areas” in the model. Excluding information on the relationship between GDP and dengue, in which information was available for the entire period (2001–2012), we only used data from 2010 of the 5,570 Brazilian municipalities to perform the other analyses.
We fitted three multilevel Poisson regression models to explain the risk of dengue (response variable) from 2001 to 2012. The first model included the diagnostic period in the first level and climate, demographic density, GDP, municipality and state in the second level. The second model included climate in the first level, and diagnostic period, demographic density, GDP, municipality and state in the second level. The third model included demographic density in the first level and diagnostic period, climate, GNP, municipality and state in the second level.
Poisson regression is frequently used to model count data, but it is often inadequate for over-dispersion situations [18]. Therefore, we applied the multilevel Poisson regression [19] and the quasi-Poisson regression to circumvent over-dispersion in the study context and to permit the inclusion of contextual effects in the model specification.
We used tables and maps to present the results. All analyses were performed using ArcGis (version 10.4) and R-Project (version 3.2.4) software.
Results
Since the early 2000s, the largest accumulation of dengue cases in Brazil has been concentrated on the Atlantic coast (Northeast and Southeast regions) and in the interior area of Southeast region (São Paulo State). From the 2001–2006 to the 2007–2012 period, there was a spread of cases toward the interior of the country, especially in the Midwest region (Fig 1).
There was an increase in the dengue epidemic at international borders and in the Midwest of the country. From 2001 to 2011, the global incidence in the municipalities that share borders with French Guiana, Bolivia and Venezuela was higher than 400/100,000.
The Global Moran Index for the 2001–2006 and 2007–2012 periods were 0.35 (p-value < 0.001) and 0.41 (p-value < 0.001), respectively.
Over the 2001–2006 period, most of the municipalities indicating a high rate of dengue were located in the Northeast and Southeast of Brazil. Over the 2007–2012 period, the rates increase in the Midwest of the country and in some municipalities of the North (Fig 2).
The incidence of dengue in Brazil ranged from 47.20/100,000 in 2004 to 467.62/100,000 in 2010. The simple analysis indicated an association between most of the socio-demographic and environmental factors with dengue incidence (Table 2). Comparing the 2001–2002 with the 2011–2012 period, there was not a significant difference. The high incidence in 2001–2002 decreased by 65% in 2003–2004 and then subsequently increased until 2009–2010. In 2011–2012, there was a decrease of about 40%. The incidence rates in every time period were statistically different from the 2003–2004 and 2009–2010 periods, which correspond to the greater declining and peak periods, respectively.
Table 2. Descriptive analysis of incidence of dengue per 100,000 by sociodemographic and environmental factors.
Factors | Category | Rate/100,000 | P-value |
---|---|---|---|
Diagnostic period1 | 2001–2002 | 212.96 | 0.0001 |
2003–2004 | 74.76 | ||
2005–2006 | 206.78 | ||
2007–2008 | 224.71 | ||
2009–2010 | 354.10 | ||
2011–2012 | 211.81 | ||
Climate2 | Af | 112.05 | 0.0001 |
Am | 263.54 | ||
Aw | 254.89 | ||
BSh | 321.88 | ||
Cfa | 116.14 | ||
Cfb | 30.69 | ||
Cwa | 191.39 | ||
Cwb | 213.61 | ||
Demographic Density (inhab/km2) | <100 | 216.67 | 0.20 |
100–499 | 208.38 | ||
500–999 | 234.82 | ||
≥1000 | 241.50 | ||
Rural percentage | < 35 | 244.44 | 0.0001 |
35–49 | 214.74 | ||
≥ 50 | 161.67 |
inhab/km2 = inhabitants per square kilometer; 12-years annual average rate; 2Climate: defined according to Koppen-Geiger classification: Cfb—temperate climate; Cfa—subtropical climate; Cwb—subtropical highland climate; Cwa—subtropical climate; Af—wet or very wet tropical or subtropical climate; Aw—tropical climate mainly; Am—wet or very wet tropical climate; and BSh—hot semi-arid climate.
The areas with a temperate Cfb climate had the lowest dengue rates (p<0.05). The highest rate was observed in the BSh semi-arid climate (about 320/100,000) (p<0.05, except for the comparison with subtropical highland climate—Cwb). We observed high rates (around 250/100,000) in areas with Aw and Am tropical climates. The incidence of dengue in areas with Cfa and Cfb subtropical climates were 63.92% and 90.47% lower than those observed in areas with a semi-arid climate (BSh), respectively; and 12.18%, 20.81% and 65.19%, lower in areas with Am, Aw and Af tropical climates, respectively (Table 2).
The simple analysis indicated an inverse association between the occurrence of dengue and the proportion of people living in rural areas, indicating that the greater the city's urban population, the greater the risk of dengue (Table 2).
In Table 3, adjusted analysis by the percentage of the population living in rural areas indicated: 1) an inverse association between GDP per capita and risk of dengue, i.e., the higher the GDP, the lower the risk of dengue (Relative Risk (RR) = 0.98; p-value <0.0001); 2) a direct association between the levels of the Gini index and risk of dengue, i.e., the higher the Gini index, the greater the risk of dengue (RR = 3.64; p <0.001); and 3) an inverse association between having a sewerage network and the risk of dengue, i.e., the lower the rate of a sewerage network, the greater the risk of dengue (RR = 0.98; p <0:02).
Table 3. Adjusted association between sociodemographic factors and the risk of dengue.
Factors | Crude RR | P-value | Adjusted RR | P-value |
---|---|---|---|---|
GDP per capita /1,000 dollar | 1.01 | 0.0001 | 0.98 | 0.0001 |
Gini index | 1.70 | 0.16 | 3.64 | 0.0001 |
Sewerage network/1,000 dwellings | 1.03 | 0.001 | 0.98 | 0.02 |
Garbage collection percentage | 3.40 | 0.0001 | 0.65 | 0.29 |
GDP = Gross Domestic Product (the conversion real to dollar considered: 1 real = 0,272892 dollars); RR = Relative Risk; Adjusted RR = estimates got from four different models (one for each factor) adjusted by percentage of population living in rural area.
We used Quasipoisson regression models in the analysis.
Excepted for GPD, which the information is available for the entire period (2001–2012), we used only 2010 data to estimate the RR.
The risk of dengue was 4–10 times higher in all periods than that observed in 2003–2004. In 2009–2010 and 2011–2012, the risks were ten and six times higher than in 2003–2004, respectively (p-value <0.05) (Table 4).
Table 4. Adjusted association between dengue occurrence in Brazil and sociodemographic and environmental factors.
Explanatory variables | Category | RR (1/RR) | P-value |
---|---|---|---|
Diagnostic period1 | 2001–2002 | 4.52 | 0.0001 |
Reference category: 2003–2004 | 2005–2006 | 4.52 | 0.0001 |
2007–2008 | 4.59 | 0.0001 | |
2009–2010 | 10.44 | 0.0001 | |
2011–2012 | 5.82 | 0.0001 | |
Climate2 | Af | 0.45 (2.20) | 0.0001 |
Reference category: BSh | Am | 0.68 (1.47) | 0.001 |
Aw | 0.81 (1.23) | 0.01 | |
Cfa | 0.19 (5.19) | 0.0001 | |
Cfb | 0.09 (11.00) | 0.0001 | |
Cwa | 0.53 (1.89) | 0.0001 | |
Cwb | 0.50 (1.99) | 0.01 | |
Demographic Density3 (1,000 inhab/km2) | 1.10 | 0.0005 |
RR = Relative Risk.
We used multilevel Poisson regression models to explain the risk of dengue (response variable).
1The first model included diagnostic period in the first level (fix effect), and climate, demographic density, gross domestic product per capita, municipality and state in the second level (random effects).
2The second model included climate in the first level (fix effect), and diagnostic period, demographic density, gross domestic product per capita, municipality and state in the second level (random effects).
3The third model included demographic density in the first level (fix effect), and diagnostic period, climate, gross domestic product per capita, municipality and state in the second level (random effects).
We used Koppen-Geiger to classify climate.
For all climatic areas with tropical and subtropical climates, the risk of dengue was 1.20–11 times lower than that observed in the semiarid climate (BSh). Compared to BSh, the risk was nearly 11 times lower for the Cfb climate, five times lower for the Cfa climate, two times lower for Af, Cwa and Cwb climates, and less than 50% lower for Am and Aw climates (p-value <0.05) (Table 4).
There was a direct association between the risk of dengue and population density, indicating that the higher the population density, the greater the risk of dengue. Data indicated a 10% increase in dengue risk for each increase of 1,000 inhabitants/km2 in the city (p-value < 0.05) (Table 4).
Discussion
From the 2001–2002 to the 2011–2012 period, dengue incidence rates were not significantly reduced. Brazil had the lowest and the highest incidence of dengue in 2004 and 2010, respectively. There was a high incidence of dengue in the 2001–2002 period. After 2003–2004 (the greater declining period), the rates of dengue increased in Brazil. The specific serotypes, which circulate more intensely in the population in a specific period, combined with the immunity level for each serotype, may explain the space-temporal distribution of dengue’s incidence and the variation of the level of the disease over the time [20].
By the end of 2000, Brazil had already experienced epidemics of DENV1 and DENV2. In January 2001, the introduction of DENV3 was confirmed and isolated in Rio de Janeiro [21]. After the entry of this serotype, the epidemic spread in Brazil in 2002. At this time, the DENV1, DENV2 and DENV3 were all simultaneously circulating [22, 23]. Yet, the dengue pandemic was already affecting much of the American continent (69 countries) with over 1,000,000 registered cases of the disease [24]. DENV2 and DENV3 predominated in most Brazilian states in the 2002–2006 and 2007–2009 periods, respectively. The DENV1 re-emerged in 2009 in the Southeast, being detected in about half of the affected patients. The DENV2 and DENV3 were also circulating at this time, and were detected in about 30% and 20% of the cases, respectively [25, 26]. In 2010, the DENV4 resurfaced in the North, spreading to several regions of the country [27]. The increase in the incidence of dengue in Brazil in 2010 can be attributed to the re-emergence of DENV1 and DENV4, together with the circulation of the other serotypes. [20, 26, 28].
Since dengue vectors usually live near people, they are common in urban centers of Brazil. Previous research has indicated that the major risk areas for dengue are: urban areas, areas with high population density, areas with informal settlements and in places where sanitation conditions are not satisfactory. In those areas, the female mosquito finds conditions in which it can feed and reproduce [29, 30]. Further, the Brazilian coast is densely populated since the major Brazilian urban centers are located on the coast or near it (e.g., São Paulo, Rio de Janeiro and Salvador). Problems like high population density, informal settlements and poor sanitation conditions are common in these areas, especially in slums, which are very frequent in urban centers. According to the 2010 Brazilian Census, 77.1% of the homes located in informal settlements are found in municipalities with more than 2,000,000 inhabitants (e.g. 19% in São Paulo and 15% in Rio de Janeiro). There is a lack of essential public services, like garbage collection and a water/sewage network in these houses [31].
The role of the transmission of the disease across international borders is reported in scientific literature [32]. Our findings detected a high incidence of dengue in the municipalities’ neighbors of French Guiana, Bolivia and Venezuela. The dengue vector is found from Uruguay to the southern United States, and outbreaks of dengue have been recorded in countries such as Venezuela, Cuba and Paraguay. Some research indicates the possibility that dengue was introduced to Brazil in the 1980s from the northern countries of South America [24].
The present study detected high dengue rates in Northeastern and Northern municipalities. Before the 2000s, the vast majority of reported dengue cases were from Northeastern and Southeastern municipalities [33]. In 2002, the rates increased significantly not only in the Southeast and Northeast, but also in the Midwest [34]. By 2006, there was an increase in dengue cases in the Southeast and Midwest [34]. The following year, states from the Southeast and Midwest had the highest number of reported cases [34]. In 2009, the dengue cases decreased in almost all Brazilian regions [35].
According to the Ministry of Health, 80% of cases were concentrated in the Southeast and Northeast in 2012, while the remaining 20% were mainly concentrated in the Midwestern and Northern regions. Compared to 2011, the number of cases in the country in 2012 decreased more than 40% [36].
The space-time fluctuations in the number of cases in the different regions are related not only to the serotypes and susceptible populations, but also to the great mobility between the populations from these states and unplanned urban expansion, which results in problems such as poor sanitation and inadequate garbage collection [34].
Environmental factors are predictors of dengue’s incidence. We observed that in areas with milder temperatures, the incidence of dengue was smaller. It is known that the drop in temperature to levels below 20°C impacts mosquito development and reproduction and consequently causes a reduction in the number of cases of dengue [37, 38]. The areas with lower dengue incidence in Brazil were those with a subtropical climate, located in the Southern region, and those with a tropical climate, located mainly in the west of the Amazon and in the narrow coastal strip stretching from the Southeast to the Northeast of the country [16].
Our findings indicate that there were higher dengue rates in areas with semiarid climates, which is predominant in the Northeast. Regions with a tropical climate that have a dry winter and a humid or sub-humid tropical climate had a high incidence as well (greater than 200/100,000). Tropical climates (Aw and Am) occupy the greatest part of Brazilian territory. The Aw climate is mainly found in the Northeast and the Midwest, while the Am climate is principally located in the north of the country [16]. According to literature, the Aedes aegypti mosquito (the main vector of dengue) grows faster in warmer areas, explaining the high dengue rates in the semiarid region [39]. Moreover, the rise in temperatures over the years due to climate change and the growing urban population may have affected the growth and spread of the mosquito population. This explains why the regions whose climate has the highest average temperatures (BSh, Aw and Am) were the ones that had the highest dengue incidence. Despite the lack of rainfall and the short time frame of the rainy season in regions with a hot semi-arid climate, massive flooding occurs when it rains [16]. Even when there are occasional droughts, characteristic of semi-arid climates, they do not prevent the reproduction of the vector, since their eggs can resist desiccation up to one year without water [37, 38]. As a result, the high temperatures in these regions, combined with the poor sanitary conditions of the population, favors the presence of domestic water reservoirs. In general, these reservoirs do not have a proper seal, thereby providing the ideal environment for vector reproduction [40].
The results of this study indicate that the greater the urbanization and population density of a city, the greater the risk of dengue. It is known that the transmission of arboviruses is more frequent in overpopulated areas [41], which likely explains the low incidence of dengue in the most northern areas. In Brazil, urbanization has taken place in an unplanned and rapid manner, leading to the establishment of informal settlements and socioeconomically segregated urban environments, which has resulted in the precariousness of the provision of basic services and inadequate living conditions [34, 42]. The scale of environmental problems, such as unsanitary conditions and difficulty in managing solid waste, has increased in the Brazilian metropolitan urban areas, especially in areas of informal settlements. These specific areas probably contribute the most to the spread of arboviruses in these metropolises [42].
Further, the highest GDP areas are concentrated in the Southern and Southeastern urban regions. In large urban areas with high population density, there is also great socioeconomic inequality. Since the first survey of mosquito infestation in Rio de Janeiro at the beginning of the last century, the direct relationship between the presence of Aedes aegypti and population density was already described [37].
This study has some limitations. First, information about the Gini Index, garbage collection, and the sewage network were only available for the years 2000 and 2010. Second, not all dengue cases are reported by health professionals, especially during major outbreaks. This occurs because of the high demand and inadequate number of health services and professionals. Third, we could not assess the dengue seasonality throughout the year in this study, since the Brazilian Ministry of Heath does not provide monthly data information about the occurrence of the cases for each municipality.
Since the 1980s, there have been records of Aedes aegypti in coastal cities of Brazil, which have since expanded to the interior of the country over time. The increase in waste production, such as containers and debris that accumulate rainwater and are discharged in streets, backyards and vacant lots, favors the proliferation of mosquitoes. All of this, coupled with the weakness of government’s basic services and protective public health actions, creates a favorable setting for arbovirus epidemics.
The fight against mosquitoes in the early twentieth century was easier, considering both the lower production of waste (mostly organic) and population density. Currently, the urban context is different due to the greater number of inhabitants living in urban cities (about 80% higher than in the early century) and the greater production of non-organic waste [43]. In addition, there are the socioeconomic, political, cultural, environmental and geographic differences linked to the urban environment as well as the complexity of urban life [34].
In large Brazilian cities, there are areas of high and low socioeconomic status. In the latter, the populations live in poor housing with inadequate sanitary conditions and irregular garbage collection, contributing to the increase of the vectors and the incidence of dengue [44]. In recent decades, government policies aimed at the prevention of arboviruses have been fragmented. In 1990, due to the end of the Superintendence of Public Health Campaigns (SUCAM) and the decentralization of monitoring actions of vector outbreaks by surveillance officers, there was a partial break in the continuity of actions [45]. When dengue rates began to increase again, some actions were resumed, though only occasionally, to combat outbreaks or during the peak months of the epidemic. Another important factor was the failure of the implementation of the sanitary network (water and sewage) throughout the country. In 2007, the intended expansion of the sewage system by the Growth Acceleration Program (PAC) in order to meet the Millennium Development Goals did not happen as scheduled [46].
Conclusion
Dengue is a common infection in the Brazilian population, with the largest accumulation of dengue cases concentrated on the Atlantic coast and in the interior area of São Paulo State. The high dengue rates observed in the Brazilian coastal region suggest that the cases imported from neighboring countries contribute to the spread of the disease into the country. Our results suggest that several socio-demographic and environmental factors resulted in the increase of dengue in the country over the time. This is likely applicable to the occurrence of others arbovirosis, such as Zika and chikungunya. To reverse this situation, Brazil must implement effective public policies that offer basic services such as garbage collection and sanitation networks as well as reduce vector populations.
Data Availability
Data are available from the DATASUS website: http://www2.datasus.gov.br/DATASUS/index.php.
Funding Statement
The authors received no specific funding for this work.
References
- 1.Grange L, Simon-Loriere E, Sakuntabhai A, Gresh L, Paul R, Harris E. Epidemiological risk factors associated with high global frequency of inapparent dengue virus infections. Front Immunol. 2014;5:280 10.3389/fimmu.2014.00280 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.PLOS Neglected Tropical Diseases: Spatial Distribution of the Risk of Dengue and the Entomological Indicators in Sumaré, State of São Paulo, Brazil 2015. Available from: http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0002873. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.PLOS Neglected Tropical Diseases: Spatio-Temporal Distribution of Dengue and Lymphatic Filariasis Vectors along an Altitudinal Transect in Central Nepal 2015. Available from: http://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0003035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Abrao EP, Fonseca BA. Infection of Mosquito Cells (C6/36) by Dengue-2 Virus Interferes with Subsequent Infection by Yellow Fever Virus. Vector Borne Zoonotic Dis. 2016. 10.1089/vbz.2015.1804 . [DOI] [PubMed] [Google Scholar]
- 5.Jaenisch T, Junghanss T, Wills B, Brady OJ, Eckerle I, Farlow A, et al. Dengue expansion in Africa-not recognized or not happening? Emerg Infect Dis. 2014;20(10). 10.3201/eid2010.140487 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.WHO WHO. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva, Switzerland: 2009. [PubMed] [Google Scholar]
- 7.WHO WHO. Global strategy for dengue prevention and control 2012–2020. Geneva, Switzerland: 2012. [Google Scholar]
- 8.HM BHM. [Comparison of the probable cases of dengue between 2014 and 2015]. Brasília, Brazil: 2016.
- 9.The_World_Bank. Equity and Development. Washington DC: 2006 32204.
- 10.IPEA. [Economic and Applied Research] 2016 [cited 2016 02162016]. Available from: http://www.ipea.gov.br/portal/.
- 11.Sampaio MdS, Alves MdC, Carvalho LG, Sanches L. [Use of Geographic Information System to compare climate classification Koppen-Geiger and Thornthwaite]. Anais XV Simpósio Brasileiro de Sensoriamento Remoto—SBSR—INPE. 2011:8857.
- 12.IBGE BIoGaS. [Estimates of Resident Population in Brazil and Federal Units with Reference Date in July 1st, 2014] Rio de Janeiro/Brazil: IBGE—Brazilian Institute of Geography and Statistics; 2014. Available from: ftp://ftp.ibge.gov.br/Estimativas_de_Populacao/Estimativas_2014/estimativas_2014_TCU.pdf.
- 13.DATASUS. [Health Information] Brazil2015 [cited 2014 02/16/2014]. Ministério da Saúde do Brasil]. Available from: http://www2.datasus.gov.br/DATASUS/index.php.
- 14.IBGE. IBGE malhas digitais Rio de Janeiro/Brazil2015 [cited 2015 05/28/2015]. Available from: http://mapas.ibge.gov.br/bases-e-referenciais/bases-cartograficas/malhas-digitais.
- 15.Rolim GdS, Camargo MBPd, Lania DG, Moraes JFLd. Classificação climática de Köppen e de Thornthwaite e sua aplicabilidade na determinação de zonas agroclimáticas para o estado de são Paulo. Bragantia. 2007;66:711–20. [Google Scholar]
- 16.EMBRAPA EBdPA. [Climate] Brasília, Brazil: Brazilian Ministry of Agriculture; [cited 2016 03/09/2016]. Available from: http://www.cnpf.embrapa.br/pesquisa/efb/clima.htm.
- 17.RIPSA RIdIpS. Indicadores e Dados Básicos—Brasil—2012 Brasília, Brasil2012 [cited 2015 26/10/2015]. Available from: http://tabnet.datasus.gov.br/cgi/idb2012/matriz.htm.
- 18.Ismail N, Jemain AA. Handling Overdispersion with Negative Binomial and Generalized Poisson Regression Models. Casualty Actuarial Society Forum [Internet]. Winter 2007 201/29/2016:[103–58 pp.]. Available from: http://www.casact.org/pubs/forum/07wforum/07w109.pdf.
- 19.Gelman A, Hill J. Data Analysis Using Regression and Multilevel/Hierarchical Models. New York (United States of America): Cambridge University Press; 2007. [Google Scholar]
- 20.Teixeira MG. Few characteristics of dengue's fever epidemiology in Brazil. Rev Inst Med Trop Sao Paulo. 2012;54 Suppl 18:S1–4. . [DOI] [PubMed] [Google Scholar]
- 21.Nogueira RM, Schatzmayr HG, de Filippis AM, dos Santos FB, da Cunha RV, Coelho JO, et al. Dengue virus type 3, Brazil, 2002. Emerg Infect Dis. 2005;11(9):1376–81. 10.3201/eid1109.041043 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Siqueira JB, Martelli CM, Coelho GE, Simplicio AC, Hatch DL. Dengue and dengue hemorrhagic fever, Brazil, 1981–2002. Emerg Infect Dis. 2005;11(1):48–53. 10.3201/eid1101.031091 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Rocco IM, Kavakama BB, Santos CL. First isolation of dengue 3 in Brazil from an imported case. Rev Inst Med Trop Sao Paulo. 2001;43(1):55–7. . [DOI] [PubMed] [Google Scholar]
- 24.Barreto ML, Teixeira MG. Dengue in Brazil: epidemiological situation and contribution to a research agenda. Estudos Avançados. 2008;22:53–72. [Google Scholar]
- 25.Muhamad M, Kee LY, Rahman NA, Yusof R. Antiviral actions of flavanoid-derived compounds on dengue virus type-2. Int J Biol Sci. 2010;6(3):294–302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Nogueira RM, Eppinghaus AL. Dengue virus type 4 arrives in the state of Rio de Janeiro: a challenge for epidemiological surveillance and control. Mem Inst Oswaldo Cruz. 2011;106(3):255–6. . [DOI] [PubMed] [Google Scholar]
- 27.de Souza RP, Rocco IM, Maeda AY, Spenassatto C, Bisordi I, Suzuki A, et al. Dengue virus type 4 phylogenetics in Brazil 2011: looking beyond the veil. PLoS Negl Trop Dis. 2011;5(12):e1439 10.1371/journal.pntd.0001439 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Bertolacci-Rocha LG, Cunha RV, Lichs GG, Dal Fabbro MM, Motta-Castro AR. Introduction of the dengue virus type 4 in the State of Mato Grosso do Sul, Brazil. Cad Saude Publica. 2014;30(8):1789–92. . [DOI] [PubMed] [Google Scholar]
- 29.Chahad-Ehlers S, Gentile C, Lima JB, Peixoto AA, Bruno RV. Analysis of cycle gene expression in Aedes aegypti brains by in situ hybridization. PloS one. 2013;8(1):e52559 10.1371/journal.pone.0052559 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Gentile C, Rivas GB, Lima JB, Bruno RV, Peixoto AA. Circadian clock of Aedes aegypti: effects of blood-feeding, insemination and RNA interference. Mem Inst Oswaldo Cruz. 2013;108 Suppl 1:80–7. 10.1590/0074-0276130471 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.IBGE. [Subnormal Clusters—Territorial Information]. Brasília, Brazil: 2010.
- 32.Chowell G, Cazelles B, Broutin H, Munayco CV. The influence of geographic and climate factors on the timing of dengue epidemics in Perú, 1994–2008. BMC infectious diseases. 2011;11:164 10.1186/1471-2334-11-164 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Câmara FP, Theophilo RLG, Santos GTd, Pereira SRFG, Câmara DCP, Matos RRCd. [Regional and dynamics characteristics of dengue in Brazil: a retrospective study]. Revista da Sociedade Brasileira de Medicina Tropical. 2007;40:192–6. [DOI] [PubMed] [Google Scholar]
- 34.Mendonça FdA, Souza AVe, Dutra DdA. [Public health, urbanization and dengue's fever in Brazil]. Sociedade & Natureza. 2009;21:257–69. [Google Scholar]
- 35.HM BHM. Dengue no Brasil Informe epidemiológico 17/2009. Brasília, Brazil: 2009.
- 36.HM BHM. [Epidemiological Bulletin—Dengue: epidemiological situation]. Brasília, Brazil: 2012.
- 37.FIOCRUZ FOC. [The Aedes aegypti mosquito is part of history and is spreading around the world from the period of colonization] Rio de Janeiro, Brazil: Fundação Oswaldo Cruz; 2016 [cited 2016 03/21/2016]. Available from: http://www.ioc.fiocruz.br/dengue/textos/longatraje.html.
- 38.Peryassu AG. Os Culicideos do Brasil. São Paulo, Brasil1908.
- 39.Glasser CM, Gomes AdC. [Climate and the superimposed distribution of Aedes aegypti and Aedes albopictus on infestation of São Paulo State, Brazil]. Revista de Saúde Pública. 2002;36:166–72. [DOI] [PubMed] [Google Scholar]
- 40.Barcellos C, Monteiro AMV, Corvalán C, Gurgel HC, Carvalho MS, Artaxo P, et al. [Climatic and environmental changes and their effect on infectious diseases: scenarios and uncertainties for Brazil]. Epidemiologia e Serviços de Saúde. 2009;18:285–304. [Google Scholar]
- 41.Ribeiro AF, Marques GR, Voltolini JC, Condino ML. [Association between dengue incidence and climatic factors]. Rev Saude Publica. 2006;40(4):671–6. . [DOI] [PubMed] [Google Scholar]
- 42.Jacobi P. [Urban environmental impacts risk to seeking sustainability]2004:[169–84 pp.].
- 43.UJVARI SC. [The story and its epidemics: the coexistence of man with microorganisms]. Revista do Instituto de Medicina Tropical de São Paulo. 2003;45:212-. [Google Scholar]
- 44.Vlahov D, Freudenberg N, Proietti F, Ompad D, Quinn A, Nandi V, et al. Urban as a determinant of health. J Urban Health. 2007;84(3 Suppl):i16–26. 10.1007/s11524-007-9169-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.FUNASA BHM. [Historical Public Health Chronology] Brasília, Brazil2011 [cited 04/08/2016]. Available from: http://www.funasa.gov.br/site/museu-da-funasa/cronologia-historica-da-saude-publica/.
- 46.MP BPM. PAC Brasília, DF2016 [cited 2016 04/08/2016]. Available from: http://www.pac.gov.br/.
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data are available from the DATASUS website: http://www2.datasus.gov.br/DATASUS/index.php.