Correlation between Loa Loa Infestation Prevalence and Eosinophil Rate among Population of Obout, Centre Region of Cameroon
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Background: Loiasis remains a major public health concern in sub-Saharan Africa (SSA) such as Cameroon. In Cameroon, the prevalence of loiasis varies from one geographical area to another. This study aimed to assess the correlation between Loa loa infestation prevalence and eosinophil rate among population of Obout, centre region of Cameroon.
Methods: A cross-sectional and correlational study was conducted in Obout locality situated in Centre region of Cameroon from June to July 2022. Data were collected using a face-to-face interview questionnaire from participants attending the Christ Roi Medical Centre of Obout (CRMCO). In each participant, a venous blood sample was taken in an EDTA tube after informed consent was obtained. A Full blood count (FBC) and a blood smear were performed on each blood sample. The collected data were recorded in an Excel version 2016 sheet and analysed by statistical package for the social sciences (SPSS) v. 24 software. For any value of p˂0.05, the results were considered statistically significant.
Results: A total of 65 participants were enrolled in this study with a median age of 35 years (Interquartile Range [IQR]: 18-52). The prevalence of Loa loa infestation was 15.38% (95%CI: 7.63%–26.48%) with a high prevalence for males (33.33%) versus (vs.) 2.63% for females (OR= 18.50; 95%IC: 2.17–157.46, p=0.002). Similarly, a high prevalence of Loa loa infestation in participants aged ≥35 years or 27.27% (OR=0.08; 95%IC: 0.01–0.72, p=0.01). Concerning the duration in the locality, the participants with ≥10 years in the locality were more infested with 8.33% for those less than 10 years (p=0.15). Furthermore, the current study shows a positive correlation but weak between eosinophil rate and intensity of Loa loa infestation (r=0.3406; p=0.3).
Conclusion: This study reported a high prevalence of Loa loa microfilaria in Obout locality with statistically significant differences for gender and age. However, no association was found between eosinophil and microfilarial load. Despite the low participation rate, Obout locality remains an area of high endemicity for Loa loa microfilaria.
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References
-
Boussinesq M, Gardon J. Prevalence of Loa loa micofilaraemia throughout the area endemic for the infection. Ann Trop Med Parasitol. 1997; 91:573–89.
DOI |
Google Scholar
1
-
Zoure HG, Wanji S, Noma M, Amazigo UV, Diggle PJ, Tekle AH, et al. The geographic distribution of Loa loa in Africa: results of large-scale implementation of the rapid assessment procedure for Loiasis (RAPLOA). PLoS Negl Trop Dis. 2011;5: e1210
DOI |
Google Scholar
2
-
Boussinesq M. Loiasis external. Annals of tropical medicine and parasitology. 2006; 100: 715–31.
DOI |
Google Scholar
3
-
Boussinesq M, Gardon J, Gardon-Wendel N, Kamgno J, Ngoumou P, Chippaux JP. Three probable cases of Loa loa encephalopathy following Ivermectin treatment for onchocerciasis. Am J Trop Med Hyg. 1998; 58:461–9.
DOI |
Google Scholar
4
-
Gardon J, Gardon-Wendel N, Demanga N, Kamgno J, Chippaux JP, Boussinesq M. Serious reactions after mass treatment of onchocerciasis with Ivermectin in an area endemic for Loa loa infection. Lancet. 1997; 350:18–22.
DOI |
Google Scholar
5
-
Agbolade OM, Akinboye DO, Ogunkolo OF. Loa loa and Mansonella perstans: neglected human infections that need control in Nigeria. Afr J Biotechnol. 2005; 4:1554–8.
Google Scholar
6
-
Boulesteix G, Carme B. Encephalite au cours du traitement de la filariose à Loa loa par la diethylcarbamazine. A propos de six observations. Bull Soc Pathol Exot. 1986; 79:649–54. French.
Google Scholar
7
-
Pinder M. Loa loa: a neglected filaria. Parasitol Today. 1988; 4:279–84.
DOI |
Google Scholar
8
-
CDC. (2019). Loiasis—epidemiology & risk factors. https://www.cdc.gov/parasites/loiasis/epi.html.
Google Scholar
9
-
Mogoung-Wafo, A.E., Nana-Djeunga, H.C., Domche, A. et al. Prevalence and intensity of Loa loa infection over twenty-three years in three communities of the Mbalmayo health district (Central Cameroon). BMC Infect Dis. February 13, 2019; 19:1–146. https://doi.org/10.1186/s12879-019-3776-y.
DOI |
Google Scholar
10
-
Tatuene, J. K., Fotsing, R. G., Nkoa, T., Mbougua, J. T., Djeunga, H. N., Bopda, J., & Kamgno, J. Epidemiology of Loa loa and Mansonella perstans filariasis in the Akonolinga health district, Centre Region, Cameroon. HEALTH SCIENCES AND DISEASE. 2014; 15(1): Article 1. https://www.hsd-fmsb.org/index.php/hsd/article/view/297.
Google Scholar
11
-
Takougang, I., Meli, J., Lamlenn, S., Tatah, P. N., & Ntep, M. Loiasis--a neglected and under-estimated affliction: Endemicity, morbidity and perceptions in eastern Cameroon. Annals of Tropical Medicine and Parasitology. 2007; 101(2): 151–160.
DOI |
Google Scholar
12
-
Mommers EC, Dekker HS, Richard P, Garcia A, Chippaux JP. Prevalence of L. loa and M. perstans in southern Cameroon. Trop Geo Med. 1994; 47:2–5.
Google Scholar
13
-
Garcia A, Abel L, Cot M, Ranque S, Richard P, Boussinesq M, et al. Longitudinal survey of Loa loa filariasis in southern Cameroon: long-term stability and factors influencing individual microfilarial status. Am J Top Med Hyg. 1995; 52:370–5.
DOI |
Google Scholar
14
-
Institut National de la Statistique (INS), 2018. ENQUÊTE DÉMOGRAPHIQUE ET DE SANTÉ, Ministère de la Santé Publique Yaoundé, Cameroun. Février, 2020. French.
Google Scholar
15
-
Beng, A. A., et al. Mapping lymphatic filariasis in Loa loa endemic health districts naïve for ivermectin mass administration and situated in the forested zone of Cameroon. BMC Infectious Diseases. 2020; 20(1): 284. https://doi.org/10.1186/s12879-020-05009-3.
DOI |
Google Scholar
16
-
homson, M. C., et al. Mapping the distribution of Loa loa in Cameroon in support of the African Program for Onchocerciasis Control. Filaria Journal. 2004; 3(1): 7. https://doi.org/10.1186/1475-2883-3-7.
DOI |
Google Scholar
17
-
Boussinesq, M., Gardon, J., Kamgno, J., Pion, S. D. S., Gardon-Wendel, N., & Chippaux, J. P. Relationships between the prevalence and intensity of Loa loa infection in the Central province of Cameroon. Annals of Tropical Medicine & Parasitology. 2001; 95(5): 495–507. https://doi.org/10.1080/00034983.2001.11813662.
DOI |
Google Scholar
18
-
Noireau, F., Carme, B., Apembet, J. D., & Gouteux, J. P. Loa loa and Mansonella perstans filariasis in the Chaillu mountains, Congo: Parasitological prevalence. Transactions of the Royal Society of Tropical Medicine and Hygiene. 1989; 83(4), 529–534. https://doi.org/10.1016/0035-9203(89)90280-0.
DOI |
Google Scholar
19
-
Pion, D. S. S., Gardon, J., Kamgno, J., Gardon-Wendel, N., Chippaux, J. P., & Boussinesq, M. Structure of the microfilarial reservoir of Loa loa in the human host and its implications for monitoring the progr,ammes of Community-Directed Treatment with Ivermectin carried out in Africa. Parasitology. 2004; 129(Pt 5), 613–626. https://doi.org/10.1017/s0031182004005694.
DOI |
Google Scholar
20
-
Pion SDS, Demanou M., Oudin, B., & Boussinesq, M. Loiasis: The individual factors associated with the presence of microfilaraemia. Annals of Tropical Medicine and Parasitology. 2005; 99(5), 491–500. https://doi.org/10.1179/136485905X51300.
DOI |
Google Scholar
21
-
ANOFEL. Parasitologie et mycologie médicales. Guide des analyses et pratiques diagnostiques. Elsevier Masson, 496 pages. 2016. French.
Google Scholar
22