Prevalence of Malaria Among Individuals Living With Lymphedema in Kamwenge District, Western Uganda
Vicent Mwesigye, Joanita Berytah Tebulwa, Benson Musinguzi, Twinomujuni Muzafaru, Henry Zamarano, Charles Nkubi Bagenda, Edgar Mulogo, Frederick Byarugaba, Itabangi Herbert

TL;DR
This study found a small percentage of people with lymphedema in Uganda also had malaria, suggesting the need for integrated healthcare in regions where both diseases are common.
Contribution
The study provides new insights into the co-occurrence of malaria and lymphedema in a specific Ugandan district.
Findings
Malaria was detected in 3.3% of individuals with lymphedema in Kamwenge District.
Most participants had bilateral lower limb lymphedema and lived in rural areas.
The study highlights the importance of integrated healthcare for co-endemic diseases.
Abstract
Lymphedema, also known as elephantiasis, is a long-term and often debilitating condition characterized by the progressive swelling of limbs due to poor lymphatic drainage. While lymphatic filariasis, a mosquito-borne disease, is a common infectious cause globally, non-infectious forms such as podoconiosis resulting from prolonged exposure to mineral-rich soils are also prevalent in many low-resource, endemic regions. In areas where both malaria and lymphedema occur, malaria may further affect individuals already suffering from chronic swelling. In Kamwenge District, Western Uganda, lymphedema is a recognized public health concern, yet the contributing factors remain poorly understood. This lack of clarity complicates effective diagnosis, treatment, and disease control. This study aimed to assess the presence of malaria among individuals living with lymphedema in this setting. A…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
| Variable | Total* N=154 | |
| Gender | ||
| Male | 44 (28.6%) | |
| Female | 110 (71.4%) | |
| Age (years): Mean ± SD | 54.70 ± 15.6 | |
| Age groups | ||
| ≤ 10 | 1 (0.6%) | |
| 11 – 24 | 6 (3.9%) | |
| 25 – 49 | 45 (29.2%) | |
| ≥ 50 | 102 (66.2%) | |
| Education | ||
| None | 79 (51.3%) | |
| Primary | 68 (44.2%) | |
| Secondary | 7 (4.5%) | |
| Marital status | ||
| Single | 44 (29.1%) | |
| Married | 71 (47.0%) | |
| Separated/divorced | 26 (17.2%) | |
| Cohabiting | 3 (2.0%) | |
| Widowed | 7 (4.6%) | |
| Tribe | ||
| Munyankole | 3 (1.9%) | |
| Mukiga | 132 (85.7%) | |
| Others | 19 (12.3%) | |
| Religion | ||
| Catholic | 64 (42.1%) | |
| Protestant | 66 (43.4%) | |
| Moslem | 1 (0.7%) | |
| Pentecostal | 11 (7.2%) | |
| Others | 10 (6.6%) | |
| Occupation | ||
| Housewife | 9 (5.9%) | |
| Business | 8 (5.3%) | |
| Peasant farmer/Grazing | 114 (75.0%) | |
| Student | 2 (1.3%) | |
| Civil servant | 1 (0.7%) | |
| Others | 18 (11.8%) | |
| Residence type | ||
| Rural | 137 (91.3%) | |
| Semi-urban/Trading centre | 13 (8.7%) | |
| Limbs affected | ||
| Lower limbs | 149 (96.8%) | |
| Upper limbs | 2 (1.3%) | |
| All limbs | 3 (1.9%) | |
| Discharging wounds | ||
| Yes | 16 (11.3%) | |
| No | 125 (88.7%) |
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsMalaria Research and Control · Mosquito-borne diseases and control · Global Health and Epidemiology
Introduction
Lymphedema, particularly affecting the lower limbs and commonly referred to as “elephantiasis,” is a chronic and debilitating condition resulting from impaired lymphatic drainage, leading to the accumulation of protein-rich interstitial fluid [1,2]. This stagnation of lymph causes progressive swelling, fibrosis, and skin changes such as dermal thickening, papillomatosis, and acanthosis [3]. Although the condition can arise from a variety of causes, it is generally classified as either primary, due to congenital or genetic defects in the lymphatic system, or secondary, resulting from external factors such as infection, surgery, or trauma [4,5].
Globally, lymphatic filariasis (LF), a mosquito-borne parasitic disease, is a leading cause of secondary lymphedema. It is caused by Wuchereria bancrofti, Brugia malayi, and Brugia timori, which can obstruct lymphatic vessels over time [6,7]. Malaria, caused by Plasmodium spp., remains one of the leading causes of morbidity and mortality in Uganda. In 2023, malaria remained a major global health challenge, with an estimated 263 million cases reported, an increase from 252 million in 2022, and approximately 597,000 associated deaths, translating to a mortality rate of 13.7 per 100,000 people at risk [8]. The World Health Organization (WHO) African Region continued to carry the heaviest burden, accounting for 94% of all malaria cases and 95% of malaria-related deaths. In Uganda alone, more than 16 million cases were recorded in 2023, leading to roughly 2,793 deaths, the majority of which occurred in children under the age of five.
Additionally, LF and malaria are endemic in Kamwenge District in Western Uganda [7,9]. The co-infection of these diseases poses unique epidemiological, clinical, diagnostic, and public health challenges that warrant comprehensive investigation. The presence of both malaria and lymphedema in Kamwenge District, Western Uganda, poses a significant public health challenge, as malaria infection in individuals with lymphedema may contribute to more severe disease outcomes and complicate clinical management. A 2018 sero-survey in Busiriba sub-county reported a circulating filarial antigen (CFA) prevalence of approximately 1.0% among 101 participants, confirming the continued presence of LF in the area [7]. Malaria remains highly prevalent nationally, accounting for 30-50% of outpatient visits, 15-20% of hospital admissions, and 9-14% of inpatient deaths, with an estimated incidence of 478 cases per 1,000 population annually. Although local malaria prevalence data for Kamwenge are limited, these national figures suggest a substantial burden. Malaria infection in individuals with lymphedema is particularly concerning, as their compromised immune function may increase susceptibility to more severe forms of the disease. Furthermore, the chronic inflammatory state associated with lymphedema can complicate the clinical presentation of malaria, making diagnosis and timely treatment more difficult [10]. These challenges highlight the importance of integrated surveillance and management approaches in regions where both conditions are prevalent. In regions like Kamwenge District, Uganda, malaria remains a major public health concern and may be underdiagnosed among individuals with lymphedema due to overlapping symptoms and limitations in standard diagnostic methods.
In resource-limited settings, malaria diagnosis through microscopy or rapid diagnostic tests remains the standard approach. Identifying malaria in individuals with lymphedema is particularly important, as coexisting infections may influence disease severity and progression. Understanding the presence of malaria in this population helps inform clinical management and supports efforts to prevent further complications associated with chronic conditions like lymphedema.
Although some research has examined the individual impact of malaria, few studies have investigated its role in individuals already living with lymphedema. In malaria-endemic areas like Kamwenge District, Uganda, infection with Plasmodium falciparum may further complicate the clinical picture and influence the progression of lymphedema [11]. Despite this potential interaction, limited research has explored the burden of malaria among individuals affected by lymphedema. Gaining insight into this relationship is essential for informing targeted interventions and improving health outcomes in the region.
This study assessed the occurrence of malaria among individuals living with lymphedema in Kamwenge District, Western Uganda.
Materials and methods
Study design
This study was a cross-sectional survey.
Study population and setting
Individuals with lymphedema who had resided in Kamwenge District for over three months were selected using purposive sampling.
Inclusion and exclusion criteria
Participants were eligible for inclusion if they showed signs of lymphedema, regardless of age, and were either receiving treatment at Rukunyu Hospital or had been recruited from the broader Kamwenge District community. Informed consent was required from adult participants and emancipated minors, while for children over seven years, both caregiver consent and the child’s assent were necessary. The study excluded individuals who were currently undergoing treatment.
Sample size calculation
The sample size for this study was calculated using the Kish and Leslie formula (1965),
n = Z2 P(1-P)
r2
Where:
Z is the standard normal deviate corresponding to a 95% confidence level (Z = 1.96),
P is the estimated prevalence of lymphedema in Kamwenge district, which was 34.7% (0.347), based on a recent study [7]
r is the desired margin of error, set at 8% (0.08).
By substituting these values into the formula, the calculation was as follows:
n = 1.96² × 0.347 × (1 - 0.347) / 0.08² n = 136 participants
Based on the Kish and Leslie (1965) formula, the initial calculated sample size was 136 participants. To account for potential non-response and incomplete data, a 10% adjustment was applied, increasing the minimum required sample size to 150 individuals with lymphedema. These participants were to be recruited from Rukunyu Hospital. Ultimately, a total of 154 participants were successfully enrolled in the study.
Laboratory procedures
Sample Collection and Processing
A vein was identified and punctured using a sterile vacutainer needle and holder, with blood collected into an ethylenediaminetetraacetic acid (EDTA) vacutainer tube. Following standard venipuncture protocols, about 2 mL of venous blood was drawn from each participant into a clean, labeled collection tube. The median cubital vein was typically used, and the area was disinfected with cotton wool soaked in 70% alcohol, then allowed to air dry. The collected blood samples were transported to the laboratory, where blood smears were examined for malaria parasites.
Malaria Testing
Blood films were prepared, stained, and examined to detect malaria parasites. Both thick and thin smears were made on clean glass slides and allowed to air-dry. The dried smears were then stained with 10% Giemsa solution for 10-15 minutes, followed by rinsing with buffered water at pH 7.2. After drying, the slides were examined under a light microscope using oil immersion at 100x magnification. Thick films were primarily used for parasite detection, while thin films facilitated the identification of Plasmodium species. Thick and thin blood smears are widely regarded as the gold standard for diagnosing malaria, as they allow for both detection and differentiation of Plasmodium species. The sensitivity of thick smear microscopy typically ranges from 75% to 90%, depending on parasite load and the skill of the microscopist, while its specificity is usually above 90%. Although thin smears are less sensitive, they play a crucial role in accurately identifying the Plasmodium species involved.
Data Management and Statistical Analysis
Data were double-entered by the principal investigator into Microsoft Excel (Redmond, USA) and subsequently exported to STATA version 17 for cleaning and statistical analysis. The Shapiro-Wilk test was used to assess the normality of age distribution, which was found to be normally distributed (p = 0.08797). Age was summarized as mean ± standard deviation. Categorical variables were described using frequencies and percentages and analyzed using Fisher’s exact test.
Results
Socio-demographic characteristics of study participants
Out of the 154 participants enrolled in the study, the majority were female (110, 71.4%), while 44 (28.6%) were male. The average age was 54.7 years (±15.6). Age distribution showed that 1 participant (0.6%) was under 10 years, 6 (3.9%) were between 11 and 24 years, 45 (29.2%) were aged 25 to 49 years, and 102 (66.2%) were over 50 years old. Regarding educational background, 79 participants (51.3%) had not completed primary education, 68 (44.2%) had attained primary-level education, and 8 (7.9%) had reached secondary education. Marital status distribution showed 44 (29.1%) were single, 71 (47.0%) married, 26 (17.2%) separated or divorced, three (2.0%) cohabiting, and 7 (4.6%) widowed. Ethnically, the majority were Bakiga (132 participants, 85.7%), followed by Banyankole (3 participants, 1.9%), and 19 (12.3%) from other ethnic groups. Most participants (114, 75.0%) were peasants or farmers involved in agriculture and livestock rearing, with 137 (91.3%) living in rural areas. Lymphedema predominantly affected the lower limbs, with 149 participants (96.8%) presenting with bilateral lower limb involvement. Additionally, 16 participants (11.3%) had discharging wounds (Table 1).
Malaria test results
Among the 154 participants, Plasmodium falciparum was detected in 3.3% (n=5) of the individuals tested.
Discussion
This study explored the presence of malaria among individuals diagnosed with lymphedema in Kamwenge District, Western Uganda. Out of 154 participants, Plasmodium falciparum infection was detected in 3.3% of cases, indicating ongoing malaria transmission within this population. Although the prevalence was relatively low, the presence of malaria among individuals already burdened by chronic lymphedema has important clinical implications [12]. Coexisting malaria can potentially exacerbate inflammation, weaken immunity, or complicate the clinical management of lymphedema [13], especially in low-resource settings where access to prompt diagnosis and treatment may be limited [14]. This finding aligns with broader concerns in co-endemic regions, where overlapping diseases can influence one another’s progression and outcomes [15].
The results suggest that even in areas where malaria control efforts such as insecticide-treated nets (ITNs) and public health campaigns are active, residual transmission remains a challenge [16]. For individuals with lymphedema, already vulnerable to infections and secondary complications, malaria adds an additional layer of health risk that should not be overlooked in disease surveillance or care planning [12].
Moreover, given the broader burden of non-infectious causes of lymphedema in the region, such as podoconiosis, it is essential to recognize malaria not as a primary cause but as a complicating factor that may worsen health outcomes for those living with this chronic condition [17].
These findings emphasize the importance of integrated disease management strategies that take into account the complex interactions between malaria and other chronic conditions like lymphedema. Strengthening diagnostic capacity, increasing community awareness, and promoting comprehensive care, particularly in rural, high-risk populations, are key steps in improving long-term health outcomes.
Limitations
This study relied on microscopy to detect malaria infections, which, while specific, may miss low-density parasitemia or asymptomatic cases. Additionally, because the study focused solely on individuals with clinically confirmed lymphedema, the findings may not represent the broader population. The cross-sectional nature of the study also limits the ability to assess causality or determine seasonal variation in malaria transmission. Further research, including longitudinal studies and the use of more sensitive diagnostic tools, would enhance understanding of the relationship between malaria and chronic lymphedema.
Conclusions
The detection of Plasmodium falciparum in individuals living with lymphedema in Kamwenge District highlights the need to consider malaria as an ongoing public health concern for this population. While prevalence was low, the presence of malaria in people already affected by chronic swelling points to the importance of integrated healthcare approaches that address both infectious diseases and chronic conditions. Continued surveillance, public education, improved access to timely malaria diagnosis, and tailored interventions targeting high-risk groups are essential in reducing the compounded burden of disease in this setting.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Global elimination of lymphatic filariasis: addressing the public health problem P Lo S Negl Trop Dis Addiss DG 04201010.1371/journal.pntd.0000741 PMC 289413020614015 · doi ↗ · pubmed ↗
- 2Lymphatic filariasis (LF) elimination: what is the current situation? Asare KK Adu-Gyamfi CO Afful P 2024
- 3Update June 2023 Lymph Res Bio Blei F 314335212023 https://www.liebertpub.com/doi/10.1089/lrb.2023.29143.fb
- 4Zenodo: MORU tropical health network annual report 2021 MORU Tropical Health Network annual report 10 2025 Day N Dondorp A Limmathurotsakul D 2025 https://zenodo.org/records/7330492
- 5Protecting the neglected from disease: the role of gender, health equity and human rights in the fight against neglected tropical diseasesinfo Lep de Rijk S Klemperer K Depierreux D 2021 https://www.leprosy-information.org/resource/protecting-neglected-disease-role-gender-health-equity-and-human-rights-fight-against
- 6Mapping and modelling the geographical distribution and environmental limits of podoconiosis in Ethiopia P Lo S Negl Trop Dis Deribe K Cano J Newport MJ 09201510.1371/journal.pntd.0003946 PMC 451924626222887 · doi ↗ · pubmed ↗
- 7The global prevalence of and factors associated with parasitic coinfection in people living with viruses: a systematic review and meta-analysis Pathogens Ge Y Liu H Ren N 14202510.3390/pathogens 14060534 PMC 1219584340559542 · doi ↗ · pubmed ↗
- 8Lymphedema: Pathophysiology and clinical manifestations J Am Acad Dermatol Grada AA Phillips TJ 100910207720172913284810.1016/j.jaad.2017.03.022 · doi ↗ · pubmed ↗
