SciELO - Scientific Electronic Library Online

 
vol.45 suppl.2Early warning system for high temperatures and heat waves: The need for a public health policy in ColombiaGenomic fragment detection and infectivity evaluation of rotaviruses isolated from wastewater used for irrigation in western Bogotá, D. C. author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Biomédica

Print version ISSN 0120-4157On-line version ISSN 2590-7379

Biomed. vol.45  supl.2 Bogotá Dec. 2025  Epub Nov 27, 2025

https://doi.org/10.7705/biomedica.7897 

Original article

Outbreaks and incidence of vector-borne diseases in Colombia (2007-2024): Impact of climate change and deforestation

Brotes e incidencia de enfermedades transmitidas por vectores en Colombia (20072024): impacto del cambio climático y la deforestación

Mario J. Olivera1  2  * 
http://orcid.org/0000-0002-6885-6353

Julián Felipe Porras-Villamil3 
http://orcid.org/0000-0003-1861-4601

Màrius Vicent Fuentes2 
http://orcid.org/0000-0002-9508-6390

1Grupo de Parasitología, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Bogotá, D. C., Colombia

2Grupo de Investigación Parásitos y Salud, Facultat de Farmàcia i Ciències de l’Alimentació, Universitat de València, València, España

3Facultad de Ciencias de la Salud, Universidad de la Salle, Bogotá, D. C., Colombia


Abstract

Introduction.

Vector-borne diseases pose a public health challenge in Colombia, influenced by climatic and environmental factors. El Niño and deforestation can alter vector habitats, affecting the incidence of dengue, Zika, chikungunya, malaria, cutaneous leishmaniasis, and yellow fever. This study analyzes the relationship between these variables and vector-borne diseases incidence in Colombia (2007-2024).

Materials and methods.

An ecological study was conducted using incidence and outbreak data for six vector-borne diseases, linked to climate information, El Niño, and deforestation. Regression models and random forests were applied to assess associations.

Results.

Between 2007 and 2024, 3,283,259 cases of vector-borne diseases were reported in Colombia. Of these, 49.9% (1,639,120) were dengue and 39.8% (1,307,351) malaria, accounting for 89.7% of total cases. El Niño was associated with increased incidence of dengue (β = 213.24; 95% CI: 86.05-338.43), chikungunya (β = 26.41; 95% CI: 17.54-70.36), and Zika (β = 14.12; 95% CI: 10.06-89.30). Maximum temperature showed a positive relationship with dengue (β = 5.74; 95% CI: 2.15-13.63) and malaria (β = 17.28; 95% CI: 3.81-30.75). Deforestation was associated with malaria (β = 12.35; 95% CI: 4.6220.08) and cutaneous leishmaniasis (β = 8.67; 95% CI: 2.21-15.13). Mean precipitation had negative associations with chikungunya and leishmaniasis.

Conclusions:

Climate change and deforestation impact the epidemiology of vector-borne diseases in Colombia. Integrated public health and environmental conservation strategies are needed to mitigate their effects.

Key words: Vector borne diseases; climate change; conservation of natural resources; epidemiologic studies; Colombia

Resumen

Introducción.

Las enfermedades transmitidas por vectores representan un desafío para la salud pública en Colombia, influenciadas por factores climáticos y ambientales. El Niño y la deforestación pueden alterar los hábitats de los vectores, afectando la incidencia de dengue, fiebre de chikunguña, enfermedad por el virus del Zika, malaria, leishmaniasis cutánea y fiebre amarilla.

Objetivo.

Analizar la relación entre estas variables y la incidencia de las enfermedades transmitidas por vectores en Colombia (2007-2024).

Materiales y métodos.

Se realizó un estudio ecológico utilizando los datos de incidencia y brotes de seis enfermedades transmitidas por vectores, vinculados con información climática, El Niño y deforestación. Se aplicaron modelos de regresión y bosques aleatorios para evaluar asociaciones.

Resultados.

Entre el 2007 y el 2024, se registraron en Colombia 3'283.259 casos de enfermedades transmitidas por vectores. De estos, el 49,9 % (1’639.120) correspondieron a dengue y el 39,8 % (1’307.351) a malaria, representando el 89,7 % del total. El Niño se asoció con un aumento en la incidencia de dengue (β = 213,24; IC 95%: 86.05-338.43), fiebre de chikunguña (β = 26,41; IC 95%: 17,54-70,36) y enfermedad por el virus del Zika (β = 14,12; IC 95%: 10,06-89,30). La temperatura máxima mostró una relación positiva con el dengue (β = 5,74; IC 95%: 2,15-13,63) y la malaria (β = 17,28; IC 95%: 3,81-30,75). La deforestación se asoció con malaria (β = 12,35; IC 95%: 4,62-20,08) y leishmaniasis (β = 8,67; IC 95%: 2,21-15,13). La precipitación media tuvo asociaciones negativas con fiebre de chikunguña y leishmaniasis.

Conclusiones.

El cambio climático y la deforestación impactan la epidemiología de las enfermedades transmitidas por vectores en Colombia. Se requieren estrategias integradas de salud pública y conservación ambiental para mitigar sus efectos.

Palabras clave: enfermedades transmitidas por vectores; cambio climático; conservación de los recursos naturales; estudios epidemiológicos; Colombia

Vector-borne diseases pose a persistent challenge to public health in Colombia and other tropical regions 1. Diseases such as dengue, malaria, yellow fever, leishmaniasis, chikungunya, and Zika have shown variable incidence patterns in response to environmental and climatic factors 2,3. Among these factors, climate change and deforestation have been identified as key determinants influencing vector dynamics and, consequently, the spread of these diseases 2,3.

The El Niño-Southern Oscillation (ENSO) is a recurring climate phenomenon that includes both El Niño and La Niña phases, which affect global temperature and precipitation patterns through complex oceanatmosphere interactions 4. In Colombia, the El Niño phase has been particularly associated with hotter and drier conditions that favor vector survival and increase the transmission potential of diseases such as dengue, Zika, and chikungunya 5. Although La Niña may influence disease dynamics in different ways, this study focused on El Niño given its stronger and more documented association with arboviral outbreaks in the region.

It is also important to note that while these diseases are endemic in Colombia and maintain an expected baseline incidence, certain environmental conditions -such as those induced by El Niño- can amplify transmission, leading to epidemic outbreaks. Similarly, deforestation and other land-use changes create new habitats for vectors, affecting human populations’ exposure to these pathogens and modifying transmission patterns 6.

Vector-borne diseases remain one of the leading causes of morbidity in Colombia. According to the latest epidemiological data, dengue is the most prevalent arboviruses, with recurrent epidemic cycles and a significant burden on the healthcare system 7,8. Malaria, though more geographically concentrated in endemic regions, continues to pose a challenge in rural and marginalized communities 9,10. Meanwhile, emerging diseases such as chikungunya and Zika have caused major outbreaks following their introduction into the country, whereas cutaneous leishmaniasis and yellow fever maintain a stable incidence but present a risk of re-emergence in jungle areas 11,12.

While previous studies have explored the relationship between these diseases and environmental factors, most have focused on specific outbreaks or individual diseases 13. However, a comprehensive approach is needed to assess both outbreaks and incidence rates over time across multiple vector- borne diseases relevant to public health. Combining statistical models with spatial analysis might provide a deeper understanding of epidemiological patterns and their relationship with climate variability and environmental transformation 14.

The objective of this study was to evaluate the impact of ENSO and deforestation on the incidence and outbreaks of six vector-borne diseases (dengue, malaria, yellow fever, leishmaniasis, chikungunya, and Zika) in Colombia from 2007 to 2024. Using robust analytical methodologies, this research aimed to provide evidence on how these factors have shaped the burden of vector-borne diseases in the country, offering key insights for epidemiological surveillance and public health decision-making to design more effective prevention and control strategies.

Materials and methods

Study design

An ecological study was conducted based on incidence and outbreak data of vector-borne diseases in Colombia from 2007 to 2024. The six previously mentioned vector-borne diseases (dengue, yellow fever, malaria, cutaneous leishmaniasis, chikungunya, and Zika) were analyzed assessing the relationship between disease events and environmental factors such as ENSO, temperature, precipitation, and deforestation were evaluated.

Data sources

Vector-borne diseases incidence and outbreak data were obtained from official records of the Sistema Nacional de Vigilancia en Salud Pública, SIVIGILA (https://www.ins.gov.co/Paginas/Inicio.aspx). Climatic variables related to temperature (mean, minimum, and maximum) and precipitation (minimum, mean, and maximum) were collected from national and international meteorological databases, including the Instituto de Hidrología, Meteorología y Estudios Ambientales, IDEAM (https://www.ideam.gov.co/) and the National Oceanic and Atmospheric Administration (NOAA) (https://www.noaa.gov/). These variables were processed with departmental spatial resolution and monthly temporal resolution to align them with epidemiological data.

Deforestation data were sourced from the Global Forest Watch platform and IDEAM, with spatial resolution at the departmental level and annual temporal resolution. All data were georeferenced and integrated into a unified analytical framework, allowing spatial and temporal analyses to assess the relationship between environmental factors and vector-borne diseases incidence.

Data analysis

Data was organized and tabulated in a structured database using Microsoft Excel (Microsoft, Redmond, WA, USA), and statistical analyses were performed using R software. Map visualizations were created using QGIS. Continuous variables included the annual incidence of each vector- borne disease, temperature (mean, minimum, and maximum), precipitation (minimum, mean, and maximum), and deforested area. Categorical variables, such as the presence or absence of the El Niño phenomenon and the occurrence of epidemic outbreaks, were presented as frequencies and proportions. Data distribution was assessed, and annualized incidence rates were calculated by department and disease.

Annualized incidence rates were obtained by dividing the number of new cases of each vector-borne disease each year by the at-risk population during the same period, multiplying the result by 100,000 inhabitants. For spatial analysis, incidence rates were estimated at the departmental level using official population projections.

ENSO was operationalized as a binary variable (presence/absence) for each year based on publicly available climatological classifications. Its influence was examined both descriptively and analytically by comparing incidence rates in years with and without ENSO events.

Poisson regression models with a population offset were used to assess the association between vector-borne diseases incidence and environmental variables. Predictors included ENSO, temperature (mean, minimum, and maximum), precipitation (minimum, mean, and maximum), and deforestation. While ENSO is known to be influenced by broader socioeconomic and ecological dynamics, this study focused on its localized climatic expression and statistical association with disease incidence in Colombia.

To evaluate the influence of climate change and deforestation on outbreak incidence, machine learning models using random forests were implemented to determine the relative importance of each predictor variable. Additionally, incidence rates in years with and without ENSO events were compared using parametric and non-parametric statistical tests, complemented by graphical analyses to identify trends and potential associations.

Mucosal and visceral forms of leishmaniasis were excluded, focusing on those with the greatest epidemiological impact in the region. The significance level of p < 0.05 was considered statistically significant for all analyses.

Results

Burden of vector-borne diseases in Colombia

Between 2007 and 2024, a total of 3,283,259 vector-borne disease cases were reported in the country. Of these, 49.9% (1,639,120) corresponded to dengue and 39.8% (1,307,351) to malaria, collectively accounting for 89.7% of all reported cases. Cutaneous leishmaniasis represented 4.6% of cases, with a total of 151,038 reports during the study period. Since the introduction of chikungunya in 2014, a total of 78,966 cases were recorded by the end of 2024. Similarly, following the emergence of the Zika virus in 2015, 106,738 cases were reported (table 1). While the overall incidence of Zika and chikungunya has declined after initial epidemic waves, their peak years overlapped with El Niño events, which allowed for statistically significant associations in our models.

Table 1 Total cases and outbreak frequency of vector-borne diseases in Colombia (2007-2024) 

Disease Total cases Percentage of total cases Years with outbreaks Percentage of years with outbreaks
Dengue 1,639,120 49.9 8 30.8
Malaria 1,307,351 39.8 5 19.2
Cutaneous leishmaniasis 151,038 4.6 4 15.4
Zika 106,738 3.3 2 7.7
Chikungunya 78,966 2.4 3 11.5
Yellow fever 46 <0.01 4 15.4
Total 3,283,259 100 26 100

Trends in the incidence of vector-borne diseases in Colombia and their relationship with environmental factors

The analysis of the influence of climatic and environmental factors on incidence rates, conducted using regression models and random forests, revealed significant variations in vector-borne diseases incidence. An increase in dengue incidence (β = 213.24; 95% CI: 86.05-338.43), chikungunya (β = 26.41; 95% CI: 17.54-70.36), and Zika (β = 14.12; 95% CI: 10.06-89.30) was observed in years associated with ENSO events. In contrast, malaria (β = 17.28; 95% CI: 3.81-30.75), yellow fever, and cutaneous leishmaniasis (β = 8.67; 95% CI: 2.21-15.13) exhibited more heterogeneous patterns, influenced by variations in temperature, precipitation, and deforestation (figure 1).

Figure 1 Spatial and temporal patterns of vector-borne disease incidence in Colombia (2007-2023). A. Geographic distribution of incidence rates by department. B. National incidence trends over time. 

Association between El Niño and the incidence of diseases

The presence of ENSO was significantly associated with an increase in the incidence of dengue, chikungunya, and Zika (p < 0.05). However, in the case of malaria, yellow fever, and leishmaniasis, the relationship was less evident (table 2 and figure 2).

Table 2 Association between ENSO events and the incidence of vector-borne diseases in Colombia (2007-2024) 

Disease β coefficient 95% CI p value
Dengue 213.24 86.05 - 338.43 < 0.05
Chikungunya 26.41 17.54 - 70.36 < 0.05
Zika 14.12 10.06 - 89.30 < 0.05
Leishmaniasis 74.36 -27.16 - 175.88 NS
Malaria 156.03 -43.38 - 355.44 NS
Yellow fever 0.0030 -0.0070 to - 0.0130 NS

NS: Not significant

Note: Coefficients derived from Poisson regression models adjusted for population size.

Statistically significant associations (p < 0.05) are highlighted in bold.

Figure 2 Comparison of the average incidence of each vector-borne disease in years with and without El Niño 

Impact of environmental factors on the incidence of vector-borne diseases

Deforestation was a significant predictive factor for the incidence of leishmaniasis (β = 8.67; 95% CI: 2.21-15.13) and malaria (β = 12.35; 95% CI: 4.62-20.08), while its association with other diseases was inconclusive. Similarly, maximum temperature was positively associated with the incidence of dengue (β = 5.74; 95% CI: 2.15-13.63) and malaria (β = 17.28; 95% CI: 3.81-30.75). In contrast, mean precipitation had a more variable effect, showing negative associations with chikungunya (β = -3.25; 95% CI: -5.90 to -0.60) and leishmaniasis (β = -1.02; 95% CI: -2.91 to -0.87) (table 3).

Table 3 Multivariable associations between environmental predictors and the incidence of vector-borne diseases (2007-2024) 

Disease Deforestation β (95% CI) Max temperature β (95% CI) Mean precipitation β (95% CI)
Malaria 12.35 (4.62 - 20.08)* 17.28 (3.81 - 30.75)* 4.56 (1.32 - 7.80)*
Leishmaniasis 8.67 (2.21 - 15.13)* -0.025 (-0.048 - 0.002) -1.02 (-2.91 to -0.87)*
Dengue -3.89 (-7.65 - 0.13) 5.74 (2.15 - 13.63)* 2.14 (-1.55 - 5.83)
Chikungunya -5.21 (-9.75 - 0.67) -10.16 (-18.25 - 2.07) -3.25 (-5.90 to -0.60)*
Zika -7.48 (-14.92 - 0.04) -15.51 (-29.38 - 1.64) -2.89 (-6.04 - 0.26)
Yellow fever 0.0003 (-0.0009 - 0.0015) 0.0002 (-0.0012 - 0.0016) 0.0001 (-0.0005 - 0.0007)

* Coefficients derived from Poisson regression models.

Statistically significant values (p < 0.05) are marked with an asterisk.

Frequency of epidemic outbreaks and their relationship with El Niño

During the study period, 26 epidemic outbreaks were recorded, of which 30.8% were associated with dengue, 19.2% with malaria, and 11.5% with chikungunya. These outbreaks were more frequent in years affected by El Niño, indicating a potential link between anomalous climatic conditions and epidemic intensity (figure 3).

Figure 3 Incidence rates in years with and without El Niño 

Key factors in outbreak prediction

The random forest model indicated that ENSO was the most influential variable in predicting outbreaks, followed by mean precipitation and deforestation (table 4 and figure 4).

Table 4 Multivariable regression model of environmental predictors associated with vector-borne diseases outbreak occurrence (2007-2024) 

Variable β estimate 95% CI p value
Intercept -9.322 -9.356 to -9.288 -
El Niño 0.4064 0.4029 - 0.4099 < 0.05
Deforestation 0.0001 0.0001073 - 0.0001097 < 0.05
Max temperature 0.0516 0.0505 - 0.0527 < 0.05
Mean precipitation 0.0194 0.0188 - 0.0199 < 0.05

Note: All predictors shown were statistically significant in the final model. Values were rounded to four decimals for interpretability.

Figure 4 Variable importance in outbreak prediction (random forest) 

Discussion

This study analyzed the incidence and outbreaks of vector-borne diseases in Colombia between 2007 and 2024, exploring their relationship with climatic and environmental factors, with a particular focus on the impact of the ENSO phenomenon and deforestation 15. The findings indicate that increased temperature and reduced precipitation during ENSO years were strongly associated with a rise in the incidence of diseases such as dengue, chikungunya, and Zika. Additionally, deforestation emerged as a key factor, primarily affecting malaria and cutaneous leishmaniasis 15-17.

These results align with previous studies that have identified ENSO as a driver of dengue epidemics in Latin America, due to temperature and humidity conditions favorable for the proliferation of the Aedes aegypti mosquito 18-20. In the case of chikungunya and Zika, although with relatively fewer longitudinal studies, recent research has suggested a pattern similar to dengue in tropical regions 21,22. In this aspect, rising temperatures accelerate viral development within the mosquito and shorten the vector’s reproductive cycle, while reduced precipitation can lead to water accumulation in artificial containers, creating breeding sites for urban mosquitoes 23,24. This would explain why outbreaks and incidence of these arboviral diseases are more frequent during these periods.

It is important to highlight that chikungunya and Zika are relatively new diseases in Colombia, with the first autochthonous cases reported in 2014 and 2015, respectively 25; their introduction was accompanied by significant epidemic outbreaks due to the lack of population immunity and the widespread presence of A. aegypti25,26. While our analyses indicate that these viruses follow a pattern similar to dengue in relation to ENSO, the recent emergence of these diseases suggests that long-term trends should still be interpreted with caution. As population immunity accumulates and climatic conditions continue to change, the transmission dynamics may differ from those observed in this first decade after their introduction.

In contrast, malaria showed a less evident relationship with the ENSO phenomenon. While previous studies have suggested that changes in temperature and precipitation can influence Plasmodium spp. transmission 27, our results indicate that its incidence and outbreaks are more closely related to deforestation and alterations in the hydrography of endemic regions 28,29. This suggests that the expansion of the agricultural frontier and urbanization may be intensifying transmission.

The link between deforestation and malaria has been widely documented in the Amazon and other tropical regions, where the loss of vegetation cover creates more suitable habitats for Anopheles spp. vectors, altering their behavior and facilitating human contact 30-32. Additionally, in deforested areas, the presence of exposed water bodies with higher temperatures may favor vector larval development, suggesting that environmental transformation plays a more determining role than large-scale climate fluctuations 30-32.

Similarly, cutaneous leishmaniasis showed a stronger association with deforestation than with the ENSO phenomenon, supporting the hypothesis that ecosystem disruption increases human exposure to Leishmania spp. vectors (Phlebotomus spp. sandflies) 6,33. In Colombia, cutaneous leishmaniasis is endemic in various rural regions, and its transmission depends on the ecological balance between vectors, reservoirs, and humans.

The link with deforestation can be explained through several mechanisms. First, habitat fragmentation forces sandflies to adapt to more open and human-modified environments, increasing the likelihood of human contact 6. Second, human activities associated with deforestation, such as agricultural expansion, livestock farming, illegal mining, and infrastructure development, can increase local populations’ exposure to these vectors 34. Additionally, biodiversity loss may reduce the availability of natural reservoirs for the parasite, facilitating transmission to humans 35.

These findings suggest that, unlike arboviruses, where interannual climate variability plays a key role, cutaneous leishmaniasis is more closely linked to long-term environmental changes 36. This reinforces the need for public health strategies that not only respond to climatic factors but also integrate environmental conservation policies and vector control measures in deforested areas.

Another key finding is the importance of temperature as a predictor of incidence, particularly for dengue and malaria. Studies have shown that rising temperatures accelerate mosquito development and shorten the extrinsic incubation period of viruses and parasites within their vectors 37. For dengue, chikungunya, and Zika, this effect is amplified during ENSO years due to reduced precipitation and the proliferation of breeding sites in urban environments 1,38. For malaria, although no clear relationship with ENSO was observed, temperature remains a crucial factor, as it influences the development rate of the Plasmodium spp. parasite within Anopheles spp. mosquitoes and transmission dynamics 39. However, other elements may modulate its impact, such as ecosystem alterations due to deforestation, insecticide resistance, and human migration patterns 40. These results suggest the need for a more detailed approach to malaria studies, incorporating data on land-use changes, urbanization, and vector resistance to control interventions.

Unlike other arboviruses, yellow fever showed a less evident relationship with the analyzed climatic variables. This may be due to the complexity of its transmission, which involves both sylvatic cycles (with non-human primates as reservoirs and Haemagogus spp. and Sabethes spp. mosquitoes as vectors) and urban cycles (A. aegypti as the primary vector). Some studies have found that yellow fever outbreaks in South America may be influenced by changes in precipitation and temperature patterns 41,42, but in this analysis, no strong association with ENSO was identified. However, deforestation and habitat fragmentation have been documented to increase human exposure to sylvatic vectors 43, suggesting that additional ecological factors may be modulating the incidence of the disease in Colombia.

Another aspect to consider is the influence of yellow fever vaccination on epidemiological dynamics. Unlike diseases such as dengue and malaria, which lack widely implemented vaccines, yellow fever has an effective vaccine that may be reducing incidence in certain areas 44. However, in regions with insufficient vaccine coverage, outbreaks may be more frequent and more closely related to agricultural frontier expansion and human mobility.

This study presents some limitations that should be considered when interpreting the results. First, incidence data may be subject to underreporting or variability in epidemiological surveillance over time, which could affect the accuracy of the estimates. Second, although key climatic factors were included, other determinants such as human mobility, public health interventions, and socioeconomic dynamics were not analyzed in depth, which could influence the distribution and persistence of these diseases. Finally, the spatial scale of the analysis, focusing on departmental levels, might obscure relevant local patterns that require more detailed studies at the municipal or village level.

Nonetheless, this study has significant strengths. The distinction between outbreaks and incidence rates allowed for a better understanding of the transmission dynamics of vector-borne diseases. While outbreaks reflect a sudden increase in the number of cases over a short period, annual incidence captures the overall disease burden in the population, providing a comprehensive view of epidemiological behavior. This approach enhances the interpretation of associated factors and facilitates the design of differentiated strategies for the prevention and control of these diseases in various epidemiological and environmental contexts.

In conclusion, these findings underscore the need to integrate public health strategies with environmental conservation and climate change mitigation policies. Strengthening epidemiological surveillance during ENSO years is essential to anticipate vector-borne diseases outbreaks, while targeted vector control actions are especially needed in deforested areas where malaria and cutaneous leishmaniasis remain highly prevalent.

Given the context of climate change and accelerated environmental degradation, it is critical to develop localized predictive models that incorporate environmental, social, and health system variables. Moreover, deforestation should not be viewed solely as an ecological phenomenon but as a complex socio-environmental process driven by land use practices, economic activities, population dynamics, and governance factors, which interact with climate variability to amplify disease transmission risks.

From a policy perspective, the study results highlight the need to incorporate climatic and ecological indicators, such as ENSO alerts, temperature anomalies, and forest-cover loss, into national epidemiological surveillance system coordinated by the Instituto Nacional de Salud. Vector control actions should be aligned with the Decennial Public Health Plan (2022-2031), and vector-borne diseases risk mapping should inform the national zero deforestation strategy and territorial climate change plans. Furthermore, land-use planning instruments (e.g., Plan de ordenamiento territorial, and Plan de ordenación y manejo de cuencas hidrográficas) must embed epidemiological risk assessments to curb disease emergence in rapidly transforming territories.

Sustained, coordinated action among the health, environment, and planning sectors is essential to leverage shared data systems, maintain updated risk maps, and jointly monitor vector-borne diseases trends amid ongoing climatic and ecological pressures.

Acknowledgments

The authors would like to express their gratitude to the knowledge management, research, and innovation network in malaria for their support during this study

References

1. Molina-Guzmán LP, Gutiérrez-Builes LA, Ríos-Osorio LA. Models of spatial analysis for vector-borne diseases studies: A systematic review. Vet World. 2022;15:1975-89. https://doi.org/10.14202/vetworld.2022.1975-1989 [ Links ]

2. El-Sayed A, Kamel M. Climatic changes and their role in emergence and re-emergence of diseases. Environ Sci Pollut Res Int. 2020;27:22336-52. https://doi.org/10.1007/s11356-020-08896-w [ Links ]

3. Yadav N, Upadhyay RK. Global effect of climate change on seasonal cycles, vector population and rising challenges of communicable diseases: A review. J Atmospheric Sci Res. 2023;6:21-59. https://doi.org/10.30564/jasr.v6i1.5165 [ Links ]

4. Cai W, Santoso A, Collins M, Dewitte B, Karamperidou C, Kug J-S, et al. Changing El Niño- Southern oscillation in a warming climate. Nat Rev Earth Environ. 2021;2:628-44. https://doi.org/10.1038/s43017-021-00199-z [ Links ]

5. Chretien J-P, Anyamba A, Small J, Britch S, Sánchez JL, Halbach AC, et al. Global climate anomalies and potential infectious disease risks: 2014-2015. PLoS Curr. 2015;26:7. https://doi.org/10.1371/currents.outbreaks.95fbc4a8fb4695e049baabfc2fc8289f [ Links ]

6. Ortiz DI, Piche-Ovares M, Romero-Vega LM, Wagman J, Troyo A. The impact of deforestation, urbanization, and changing land use patterns on the ecology of mosquito and tick-borne diseases in Central America. Insects. 2021;13:20. https://doi.org/10.3390/insects13010020 [ Links ]

7. Segura NA, Muñoz AL, Losada-Barragán M, Torres O, Rodríguez AK, Rangel H, et al. Minireview: Epidemiological impact of arboviral diseases in Latin American countries, arbovirus-vector interactions and control strategies. Pathog Dis. 2021;79:ftab043. https://doi.org/10.1093/femspd/ftab043 [ Links ]

8. Khan A, Yasin M, Aqueel MA, Farooqi MA, Akram MI, Yousuf HMB, et al. Vector-borne disease and climate change. In: Shields VDC, editor. Arthropods-new advances and perspectives. IntechOpen; 2023. https://doi.org/10.5772/intechopen.107120 [ Links ]

9. Padilla-Rodríguez JC, Olivera MJ, Padilla MC, Abril EP. Malaria epidemics in Colombia, 1970-2019. Rev Soc Bras Med Trop. 2022 29:55:e05592021. https://doi.org/10.1590/0037-8682-0559-2021 [ Links ]

10. Cardona-Arias JA, Salas-Zapata W, Carmona-Fonseca J. A systematic review of mixed studies on malaria in Colombia 1980-2022: What the “bifocal vision” discovers. BMC Public Health. 2023;23:1169. https://doi.org/10.1186/s12889-023-16098-5 [ Links ]

11. Freitas LP, Carabali M, Yuan M, Jaramillo-Ramírez GI, Balaguera CG, Restrepo BN, et al. Spatio-temporal clusters and patterns of spread of dengue, chikungunya, and Zika in Colombia. PLoS Negl Trop Dis. 2022;16:e0010334. https://doi.org/10.1371/journal.pntd.0010334 [ Links ]

12. Mantilla-Granados JS, Sarmiento-Senior D, Manzano J, Calderón-Peláez M-A, Velandia-Romero ML, Buitrago LS, et al. Multidisciplinary approach for surveillance and risk identification of yellow fever and other arboviruses in Colombia. One Health. 2022:15:100438. https://doi.org/10.1016/j.onehlt.2022.100438 [ Links ]

13. Thomson MC, Stanberry LR. Climate change and vectorborne diseases. N Engl J Med. 20224;387:1969-78. https://doi.org/10.1056/NEJMra2200092 [ Links ]

14. Colón-González FJ, Sewe MO, Tompkins AM, Sjõdin H, Casallas A, Rocklõv J, et al. Projecting the risk of mosquito-borne diseases in a warmer and more populated world: a multi-model, multi-scenario intercomparison modelling study. Lancet Planet Health. 2021;5:e404-e414e404-14. https://doi.org/10.1016/S2542-5196(21)00132-7 [ Links ]

15. Colonia CB, Vásquez-Rodríguez AB, Alexander N, de la Hoz Restrepo F. Malaria, relationship with climatic variables and deforestation in Colombia, Latin America and the Caribbean from 2000 to 2020: A systematic review. Malaria J. 2024;23:347. https://doi.org/10.1186/s12936-024-05140-5 [ Links ]

16. Marinho RdSS, Duro RLS, Mota MTdO, Hunter J, Diaz RS, Kawakubo FS, et al. Environmental changes and the impact on the human infections by dengue, chikungunya and Zika viruses in northern Brazil, 2010-2019. Int J Environ Res Public Health. 2022;19:12665. https://doi.org/10.3390/ijerph191912665 [ Links ]

17. Romero-Vega LM, Piche-Ovares M, Soto-Garita C, Barantes Murillo DF, Chaverri LG, Alfaro-Alarcón A, et al. Seasonal changes in the diversity, host preferences and infectivity of mosquitoes in two arbovirus-endemic regions of Costa Rica. Parasit Vectors. 2023;16:34. https://doi.org/10.1186/s13071-022-05579-y [ Links ]

18. Gagnon AS, Bush AB, Smoyer-Tomic KE. Dengue epidemics and the El Niño southern oscillation. IntJBiometeorol. 2002;46:81-9. https://doi.org/10.1007/s00484-001-0119-6 [ Links ]

19. Petrova D, Lowe R, Stewart-Ibarra A, Ballester J, Koopman SJ, Rodó X. Sensitivity of large dengue epidemics in Ecuador to long-lead predictions of El Niño. Climate Services. 2019;15:100096. https://doi.org/10.1016/j.cliser.2019.02.003 [ Links ]

20. Ruiz-Polo AA, Santillan-Valdivia RE, Saavedra-Ríos CY, Núñez-Rodriguez CM, Niño- Mendoza LE. Comportamiento alimentario de Aedes aegypti en brotes de dengue de dos zonas rurales del Perú durante el ciclón Yaku y El Niño Global del 2023. Revista Peruana de Medicina Experimental y Salud Pública. 2024;41:266-72. [ Links ]

21. Ruiz-Polo AA, Santillan-Valdivia RE, Saavedra-Ríos CY, Núñez-Rodríguez CM, Niño- Mendoza LE. Aedes aegypti feeding behavior during dengue outbreaks in two rural areas of Perú during the Yaku cyclone and El Niño phenomenon of 2023. Revista Peruana de Medicina Experimental y Salud Pública. 2024;41:266-72. [ Links ]

22. Messina JP, Kraemer MU, Brady OJ, Pigott DM, Shearer FM, Weiss DJ, et al. Mapping global environmental suitability for Zika virus. Elife. 2016:5:e15272. https://doi.org/10.7554/eLife.15272 [ Links ]

23. Ruiz-Polo AA, Barrera-Rivera LV. Efecto de la temperatura en el ciclo biológico del Aedes aegypti en condiciones de laboratorio. Revista Peruana de Medicina Experimental y Salud Pública. 2024;41:327-8. [ Links ]

24. Valdez LD, Sibona GJ, Condat C. Impact of rainfall on Aedes aegypti populations. Ecological Modelling. 2018;385:96-105. https://doi.org/10.1016/j.ecolmodel.2018.07.003 [ Links ]

25. Padilla JC, Lizarazo FE, Murillo OL, Mendigaña FA, Pachón E, Vera MJ. Epidemiología de las principales enfermedades transmitidas por vectores en Colombia, 1990-2016. Biomédica. 2017;37(Supl.2) :27-40. https://doi.org/10.7705/biomedica.v37i0.3769 [ Links ]

26. Guzmán NA, Zakzuk J, Moranth RV, Olaciregui AA, Padilla DP. Dengue, Chikunguña y Zika en Colombia 2015-2016. Revista MVZ (Córdoba). 2017;22:2. [ Links ]

27. Paaijmans KP, Blanford S, Bell AS, Blanford JI, Read AF, Thomas MB. Influence of climate on malaria transmission depends on daily temperature variation. Proc Natl Acad Sci USA. 2010;107:15135-9. https://doi.org/10.1073/pnas.1006422107 [ Links ]

28. Laporta GZ, Ilacqua RC, Bergo ES, Chaves LS, Rodovalho SR, Moresco GG, et al. Malaria transmission in landscapes with varying deforestation levels and timelines in the Amazon: A longitudinal spatiotemporal study. Sci Rep. 2021;11:6477. https://doi.org/10.1038/s41598-021-85890-3 [ Links ]

29. Laporta GZ. Amazonian rainforest loss and declining malaria burden in Brazil. Lancet Planet Health. 2019;3:e4-e5. https://doi.org/10.1016/S2542-5196(18)30243-2 [ Links ]

30. Valle D, Clark J. Improving the modeling of disease data from the government surveillance system: A case study on malaria in the Brazilian Amazon. PLoS Comput Biol. 2013;9:e1003312. https://doi.org/10.1371/journal.pcbi.1003312 [ Links ]

31. Valle D, Clark J. Conservation efforts may increase malaria burden in the Brazilian Amazon. PLoS ONE. 2013;8:e57519. https://doi.org/10.1371/journal.pone.0057519 [ Links ]

32. Hahn MB, Olson SH, Vittor AY, Barcellos C, Patz JA, Pan W. Conservation efforts and malaria in the Brazilian Amazon. Am J Trop Med Hyg. 2014;90:591-4. https://doi.org/10.4269/ajtmh.13-0323 [ Links ]

33. Rodrigues MGdA, Sousa JDdB, Dias ÁLB, Monteiro WM, Sampaio VdS. The role of deforestation on American cutaneous leishmaniasis incidence: Spatial-temporal distribution, environmental and socioeconomic factors associated in the Brazilian Amazon. Trop Med Int Health. 2019;24:348-55. https://doi.org/10.1111/tmi.13196 [ Links ]

34. Burkett-Cadena ND, Vittor AY. Deforestation and vector-borne disease: Forest conversion favors important mosquito vectors of human pathogens. Basic and applied ecology. 2018;26:101-10. Basic Appl Ecol. 2018:26:101-10. https://doi.org/10.1016/j.baae.2017.09.012 [ Links ]

35. Kocher A, Cornuault J, Gantier Jc, Manzi S, Chavy A, Girod R, et al. Biodiversity and vector- borne diseases: Host dilution and vector amplification occur simultaneously for Amazonian leishmaniases. Mol Ecol. 2023;32:1817-31. https://doi.org/10.1111/mec.16341 [ Links ]

36. Caminade C, McIntyre KM, Jones AE. Impact of recent and future climate change on vector- borne diseases. Ann N Y Acad Sci. 2019;1436:157-73. https://doi.org/10.1111/nyas.13950 [ Links ]

37. Mordecai EA, Caldwell JM, Grossman MK, Lippi CA, Johnson LR, Neira M, et al. Thermal biology of mosquito-borne disease. Ecol Lett. 2019;22:1690-708. https://doi.org/10.1111/ele.13335 [ Links ]

38. Molleda P, Serra GV. El Niño Southern Oscillation and the prevalence of infectious diseases. La Granja: revista de Ciencias de la Vida. 2024;40:9-37. https://doi.org/10.17163/lgr.n40.2024.01 [ Links ]

39. Kemarau RA, Eboy OV. Spatial-temporal distribution of malaria risk and its association with El Niño Southern Oscillation (ENSO). Malaysian Journal of Social Sciences and Humanities. 2021;6:276-86. https://doi.org/10.47405/mjssh.v6i4.768 [ Links ]

40. Fletcher IK, Grillet ME, Moreno JE, Drakeley C, Hernández-Villena J, Jones KE, et al. Synergies between environmental degradation and climate variation on malaria reemergence in southern Venezuela: A spatiotemporal modelling study. Lancet Planet Health. 2022;6:e739-e48. https://doi.org/10.1016/S2542-5196(22)00192-9 [ Links ]

41. Hamlet A, Gaythorpe KA, Garske T, Ferguson NM. Seasonal and inter-annual drivers of yellow fever transmission in South America. PLoS Negl Trop Dis. 2021;15:e0008974. https://doi.org/10.1371/journal.pntd.0008974 [ Links ]

42. Hamrick PN, Aldighieri S, Machado G, Leonel DG, Vilca LM, Uriona S, et al. Geographic patterns and environmental factors associated with human yellow fever presence in the Americas. PLoS Negl Trop Dis. 2017;11:e0005897. https://doi.org/10.1371/journal.pntd.0005897 [ Links ]

43. Aliaga-Samanez A, Romero D, Murray K, Cobos-Mayo M, Segura M, Real R, et al. Climate change is aggravating dengue and yellow fever transmission risk. Ecography. 2024;2024:e06942. https://doi.org/10.1111/ecog.06942 [ Links ]

44. Hansen CA, Barrett AD. The present and future of yellow fever vaccines. Pharmaceuticals (Basel). 2021;14:891. https://doi.org/10.3390/ph14090891 [ Links ]

Citation: Olivera MJ, Porras-Villamil JF,Fuentes MV. Outbreaks and incidence of vector-borne diseases in Colombia (2007-2024): Impact of climate change and deforestation. Biomédica. 2025;45(Supl.2):17-29. https://doi.org/10.7705/biomedica.7897

Author's contributions:

Mario Javier Olivera: Study conception and design; information organization; statistical data analysis and manuscript writing.

Julián Felipe Porras-Villamil and Màrius Vicent Fuentes: Information organization; statistical data analysis; manuscript writing and revision.

Funding:

This study was funded by the Instituto Nacional de Salud.

Use of artificial intelligence tools No artificial intelligence tools were used in the preparation, analysis, writing, or editing of this manuscript.

Received: March 03, 2025; Revised: July 07, 2025; Accepted: July 17, 2025; Published: July 18, 2025

*Corresponding author: Mario J. Olivera, Grupo de Parasitología, Dirección de Investigación en Salud Pública, Instituto Nacional de Salud, Calle 26 N°51-20, Bogotá, D. C., Colombia Phone: (57) (601) 220 7700, extensión 1323 molivera@ins.gov.co

Conflicts of interest:

The authors declare no conflicts of interest.

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License