Liver Function Alterations in Armed Forces Infected with Malaria and Intestinal Helminths in Cameroon’s North West and South West Regions

BI STELLA CHE 1, NGUM HELEN NTONIFOR 2*, KATAMSSADAN HAMAN TOFEL 3, VANESSA TITA JUGHA 4, BERTRAND YUWONG WANYU 4, GERMAIN SOTOING TAIWE 4 

1Department of Microbiology and Parasitology, Faculty of Science, The University of Bamenda, P.O. Box 39, Bamenda, Cameroon. 

2Department of Zoology, Faculty of Science, The University of Bamenda, P.O. Box 39, Bamenda, Cameroon. 

3Department of Phytosanitary Protection, Higher Institute of Agriculture, Wood, Water Resources and Environment, The University of Bertoua, P.O. Box 416, Bertoua, Cameroon. 

4Department of Animal Biology and Conservation, Faculty of Science, University of Buea, P.O. Box 63, Buea, Cameroon. 

*Corresponding Author: ngumnto@yahoo.com, +237 675 21 31 56.

Received: 03 Jun 2025, Reviewed: 02 Jul 2025, Revised: 22 Jul 2025, Accepted: 05 Aug 2025, Published: 22 Oct 2025.

https://doi.org/10.63342/cjbbs2025.33.022.fr

DOWNLOAD PDF HERE

ABSTRACT

Cameroon is one of the sub-Saharan countries where malaria and intestinal helminths are endemic. The study evaluated the influence of malaria and intestinal helminths on liver parameters among armed forces in the North West and South West regions of Cameroon. This was a cross-sectional study conducted between May 2022 and April 2023. A total of 812 stool and venous blood samples were collected from males aged 18 to 52 years to identify malaria and intestinal parasites and to evaluate liver parameters. Giemsa staining and Kato-Katz microscopic methods were used for parasite identification, while the enzyme-linked immunosorbent assay (ELISA) was used for liver parameters evaluation. Statistical comparisons were performed using the Statistical Package for Social Sciences (SPSS). Results obtained showed that Plasmodium falciparum (11.9%) and Plasmodium vivax (1.7%) were identified. Five different species of intestinal helminths were identified out of which Ascaris lumbricoides was the most prevalent (4.7%), and the least prevalent species was Schistosoma intercalatum (1.2%). The overall co-infection rate was 3.2%. Plasmodium sp significantly affected the values of all the liver parameters (Aspartate transaminase: p = 0.003; Alanine transaminase: p = 0.002; Alkaline phosphatase: p = 0.000; Total Bilirubin: p = 0.001) while Trichuris trichiura and Schistosoma mansoni infection significantly influenced Alkaline phosphatase (p = 0.000) and (p = 0.007) respectively. Schistosoma mansoni equally significantly affected the value of Aspartate transaminase (p = 0.018). Malaria and intestinal helminths co-infection significantly influenced the values of all liver parameters at p = 0.000. Plasmodium parasite densities positively correlated with liver parameters and were statistically significant at p = 0.0008 with AST and at p = 0.0004 with Alanine transaminase. Ascaris lumbricoide, Hookworms, S. mansoni, and S. intercalatum negatively correlated with liver parameters, while T. trichiura positively correlated with these parameters. To improve management of liver-related complications, we recommend adding hepatic function assessments to routine evaluations of malaria and intestinal helminths in endemic areas.

Keywords: Malaria, Intestinal helminths, Liver parameters, Armed forces.

RÉSUMÉ

Le Cameroun est l’un des pays d’Afrique subsaharienne oĂą le paludisme et les helminthes intestinaux sont endĂ©miques. L’Ă©tude a Ă©valuĂ© l’influence du paludisme et des helminthes intestinaux sur les paramètres hĂ©patiques au sein des forces armĂ©es des rĂ©gions du Nord-Ouest et du Sud-Ouest du Cameroun. Il s’agissait d’une Ă©tude transversale menĂ©e entre mai 2022 et avril 2023. Un total de 812 Ă©chantillons de selles et de sang veineux ont Ă©tĂ© prĂ©levĂ©s chez des hommes âgĂ©s de 18 Ă  52 ans afin d’identifier le paludisme et les parasites intestinaux et d’Ă©valuer les paramètres hĂ©patiques. La coloration au Giemsa et les mĂ©thodes microscopiques de Kato-Katz ont Ă©tĂ© utilisĂ©es pour l’identification des parasites, tandis que le test immuno-enzymatique (ELISA) a Ă©tĂ© utilisĂ© pour l’Ă©valuation des paramètres hĂ©patiques. Les comparaisons statistiques ont Ă©tĂ© effectuĂ©es Ă  l’aide du logiciel SPSS (Statistical Package for Social Sciences). Les rĂ©sultats obtenus ont identifiĂ© Plasmodium falciparum (11,9 %) et Plasmodium vivax (1,7 %). Cinq espèces diffĂ©rentes d’helminthes intestinaux ont Ă©tĂ© identifiĂ©es, parmi lesquelles Ascaris lumbricoides Ă©tait la plus rĂ©pandue (4,7 %) et l’espèce la moins rĂ©pandue Ă©tait Schistosoma intercalatum (1,2 %). Le taux global de co-infection Ă©tait de 3,2 %. Les parasites du paludisme ont affectĂ© de manière significative les valeurs de tous les paramètres hĂ©patiques (aspartate transaminase : p = 0,003 ; alanine transaminase : p = 0,002 ; phosphatase alcaline : p = 0,000 ; bilirubine totale : p = 0,001) ; tandis que l’infection par Trichuris trichiura et Schistosoma mansoni a influencĂ© de manière significative la phosphatase alcaline (p = 0,000) et (p = 0,007) respectivement. Schistosoma mansoni a Ă©galement affectĂ© de manière significative la valeur de l’aspartate transaminase (p = 0,018). La co-infection par le paludisme et les helminthes intestinaux a eu une influence significative sur les valeurs de tous les paramètres hĂ©patiques Ă  p = 0,000. Les densitĂ©s de parasites Plasmodium Ă©taient positivement corrĂ©lĂ©es aux paramètres hĂ©patiques et Ă©taient statistiquement significatives Ă  p = 0,0008 avec l’AST et Ă  p = 0,0004 avec l’ALT. Ascaris lumbricoide, les ankylostomes, S. mansoni et S. intercalatum Ă©taient nĂ©gativement corrĂ©lĂ©s aux paramètres hĂ©patiques tandis que T. trichiura Ă©tait positivement corrĂ©lĂ© Ă  ces paramètres. Pour amĂ©liorer la prise en charge des complications hĂ©patiques, nous recommandons d’ajouter des Ă©valuations de la fonction hĂ©patique aux Ă©valuations de routine du paludisme et des helminthes intestinaux dans les zones d’endĂ©mie.

Mots-clés: Paludisme, Helminthes intestinaux, Paramètres hépatiques, Forces armées.

REFERENCES

Al-Salahy M, Shnawa B, Abed G, Mandour A and Al-Ezzi A (2016). Parasitaemia and Its Relation to Hematological Parameters and Liver Function among Patients Malaria in Abs, Hajjah, Northwest Yemen. Interdisciplinary perspectives on infectious diseases 2016, 5954394. https://doi.org/10.1155/2016/5954394

Bangert M, Molyneux D, Lindsay SW, Fitzpatrick C and Engels D (2017). The cross-cutting contribution of the end of neglected tropical diseases to the Sustainable Development Goals. Infectious Diseases of Poverty 6(1), 73.

Bisetegn H, Feleke DG, Debash H, Erkihun Y and Ebrahim H (2022). Hematological and Biochemical changes in Schistosoma mansoni infected patients at Haik Primary Hospital, North-East Ethiopia: A comparative cross-sectional study. PLoS Neglected Tropical Disease 16(8), e0010728. https://doi.org/10.1371/journal.pntd.0010728

Cheesbrough (2009). District Laboratory Practice in Tropical Countries, 3Rd ed., part 1. United Kingdom: Cambridge University Press, pp 178–215.

Chou YC, Lin YT and Tze-Kiong Er (2025). Unmasking an Incidental Trichuris trichiura Infection in a Patient with Acute Hepatobiliary and Gastrointestinal Illness. Journal of Gastroenterology and Hepatology Open 9(4), e70146. https://doi.org/10.1002/jgh3.70146

Cochran WG (1977) Sampling Techniques. 3rd Edition, John Wiley & Sons, New York

CS4ME (2021). Increase Community Led Monitoring For Malaria Programs and Advocacy for Quality Health Services for All Communities. Annual report. 28p

Dessie N, Wossenseged L and  Mulugeta A (2020). Haematological and Biochemical Profiles of Patients Infected with Schistosoma mansoni in Comparison with Apparently Healthy Individuals at Sanja Town, Northwest Ethiopia: A Cross-Sectional Study. Journal of Tropical Medicine, 2020, 4083252. https://doi.org/10.1155/2020/4083252

Dockrell HM, de Souza JB, Plafair JH (1980). The role of the liver in immunity to blood-stage murine malaria. Immunology 41:421-430.

Ebai CB, Ngoufo FN, Nlinwe ON, Mefoumanyi JA, Yamssi C and Kimbi HN (2023). “Prevalence of Malaria Parasitaemia and Intestinal Protozoan Infections Among Schoolchildren in Ndop, Northwest Cameroon, A Conflict-Hit Locality”. International Journal of Tropical Disease and Health 44 (24):10-21 https://doi.org/10.9734/ijtdh/2023/v44i241505

Gontie GB, Wolde HF and Baraki AG (2020). Prevalence and associated factors of malaria among pregnant women in Sherkole district, Benishangul Gumuz regional state, West Ethiopia. BMC infectious diseases 20(1), 573. https://doi.org/10.1186/s12879-020-05289-9

Imboumy-Limoukou  R K, Maghendji-Nzondo S, Sir-Ondo-Enguier P N, Niemczura De Carvalho J, Tsafack-Tegomo N P, Buekens J, Okouga AP, Mouinga-Ondeme A, Kwedy Nolna S and Lekana-Douki J B (2020). Malaria in children and women of childbearing age: infection prevalence, knowledge and use of malaria prevention tools in the province of Nyanga, Gabon. Malaria journal 19(1), 387. https://doi.org/10.1186/s12936-020-03411-5

Kamgain ML, Assam AJP, Kojom LP and Kamga FHL (2016). Impact of malaria infection on renal and liver functions in patients living with HIV/AIDS on HAART in Douala, Cameroon. Scholars Journal of Applied Medical Sciences. 4(11A):3916-3920. DOI: 10.36347/sjams.2016.v04i11.012

Kaplan A and Glucose K (1984) The CV Mosby Co., St Louis, Toronto, Princeton, Clinical Chemistry 436: 1238-1241.

Karan A, Chapman GB and Galvani A (2012). The influence of poverty and culture on the transmission of parasitic infections in rural Nicaraguan Villages. Journal of Parasitology Research, 2012, 478292. https://doi.org/10.1155/2012/478292

Katz N, Chaves A and Pellegreno J (1972). Simple device for quantitative stool thick-smear technique in Schistosoma mansoni. Revista do Instituto de Medicina Tropical de Sao Paulo 14(6), 397–400.

Kimbi HK, Njoh TD, Ndamukong KJN and Lehman LG (2013). Malaria in HIV/AIDS patients at different CD4 T cell levels in Limbe, Cameroon. Journal of  Bacteriology and Parasitology 4(164). https://doi.org/10.4172/2155-9597.1000164

Kouam AF, Ngoumé NAN, Fepa AGK, Wainfen Z, Ngounou E, Galani BRT, Nembo EN, Chuisseu PDD, Njayou FN and Moundipa PF (2023). Liver injury in malaria-infected patients in Douala-Cameroon and its association with poor medical practice. Egyptian Liver Journal 13, 67. https://doi.org/10.1186/s43066-023-00300-9

Letouzey (1980). Phytogeographic map of Cameron. In: JA, editor. Les Atlas Jeune Afrique : Paris, France ; p20-24.

Lindrose AR, Mitra I, Fraser J, Mitre E, Hickey PW (2021). Helminth infections in the US military: from strongyloidiasis to schistosomiasis. Journal of Travel Medicine 28(6), 004. https://doi.org/10.1093/jtm/taab004

Liu K, Yu Y, Yuan Y, Xu X, Lei W, Niu R, Shen M, Zhou L, Peng R, Wang Q, Yang H, Guo H, Ge Y, Liu G, He M, Wu T and Zhang X (2023). Elevated Levels of Serum Alkaline Phosphatase are Associated with Increased Risk of Cardiovascular Disease: A Prospective Cohort Study. Journal of atherosclerosis and thrombosis 30(7), 795–819. https://doi.org/10.5551/jat.63646

Mekachie SS, Sumbele IUN, Tasah MM and Kimbi HK (2021). Malaria and intestinal parasite co-infection and its association with anaemia among people living with HIV in Buea, Southwest Cameroon: A community-based retrospective cohort study. PLoS One 16(1), e0245743. https://doi.org/10.1371/journal.pone.0245743

Messina JP, Taylor SM, Meshnick SR, Linke AM, Tshefu AK, Atua B, Mwandagalirwa K and Emch KM (2011). Population, behavioural and environmental drivers of malaria prevalence in theDemocratic Republic of Congo. Malaria journal 10, 161. https://doi.org/10.1186/1475-2875-10-161

Minsante (2018).XIième Journée mondiale de lutte contre le paludisme “prêt à vaincre le paludisme” Nous sommes la génération qui peut éliminer le paludisme. Dossier de Presse. Minsante. :1–20.

Mojoko (2011). Urban Development in Fako Division (Unpublished M.Sc. Thesis). Department of Geography, University of Buea, 17p.

Mugob  BB, Ntonifor HN, Boubga FC, Ngwenah E and Oumar M (2024). Analysis of oxidative status, inflammatory cytokines, and Ascaris lumbricoides infection in women at a health district in Bamenda, Northwest, Cameroon. The Egyptian Journal of Internal Medicine 36, 42. https://doi.org/10.1186/s43162-024-00306-8

Ntonifor HN, Chewa JS, Oumar M and Mbouobda HD (2021). Intestinal helminths as predictors of some malaria clinical outcomes and IL-1β levels in outpatients attending two public hospitals in Bamenda, North West Cameroon. PLoS neglected tropical diseases 15(3), e0009174. https://doi.org/10.1371/journal.pntd.0009174

Ntonifor HN, Ngahbort B F, Abongwa EL and Oumar M (2023). Prevalence of malaria and associated clinical manifestations and myeloperoxidase amongst populations living in different altitudes of Mezam division, North West Region, Cameroon. Malaria Journal 22: 20. https://doi.org/10.1186/s12936-022-04438-6

Nyasa RB, Fotabe EL and Ndip RN (2021). Trends in malaria prevalence and risk factors associated with the disease in Nkonghombeng; A typical rural setting in the equatorial rainforest of the South West Region of Cameroon. PloS one, 16(5), e0251380. https://doi.org/10.1371/journal.pone.0251380

Okafor RA, Nyenke C, Okeke CU and Konne F (2022). Malaria Parasitaemia and Effect on Liver Enzymes. Geobiology. 10. 033-039. DOI: 10.5281/zenodo.7032979

Peter V, Damanet B, Maussen C, Esbroeck MV, and Soentjens P (2021). Screening the asymptomatic soldiers after a stay in sub-Saharan Africa. A retrospective observational study. Travel Medicine and Infectious Disease 39:101941. https://doi.org/10.1016/j.tmaid.2020.101941

Pourhoseingholi MA, Mohsen V and Mitra R (2013). Sample size calculation in medical studies. Gastroenterol Hepatol Bed Benchv. Winter 6(1):14-7.

Programme National de Développement Participatif (PNDP), Tiko (2011).  https://www.pndp.org › 21_CDP_TIKO1

TchindeYD, Lem EA, Fotsing D and Ntonifor HN (2021). “The Prevalence, Intensity and Risk Factors of Gastrointestinal Parasitic Infections in Outpatients in Bafoussam II, West Region, Cameroon”. International Journal of Tropical Disease and Health 42 (15):25-36. DOI: 10.9734/ijtdh/2021/v42i1530519

Tchuem-Tchuenté LA , Noumedem  CD, Ngassam P, Kenfack CM, Gipwe NF, DankoniE, TariniA and hang Y(2013). Mapping of schistosomiasis and soil-transmitted helminthiasis in the regions of Littoral, North-West, South and South-West Cameroon and recommendations for treatment. PLoS neglected tropical diseases 6(3), e1553. https://doi.org/10.1371/journal.pntd.0001553

Temesgen and Feysal (2024). Prevalence of Malaria and Associated Factors during the Minor Malaria Season among Febrile Under-Five Children Attending Mohammed Akile Memorial General Hospital, Journal of Parasitology Research, 2024, 6365077. https://doi.org/10.1155/2024/6365077

Vilkman Vilkman K, Pakkanen SH, Lääveri T, Siikamäki H and Kantele A (2016). Travelers’ health problems and behavior: prospective study with post-travel follow-up. BioMed Central Diseases. 16:328. https://doi.org/10.1186/s12879-016-1682-0

WHO (2006). Basic Documents, Forty-fifth edition, Supplement. 20p.

WHO (2010). Basic malaria microscopy – Part I: Learner’s guide. Second edition: World Health Organization 90p.

WHO (2019). Bench aids for the diagnosis of intestinal parasites, second edition. Geneva 32p.

WHO (2020). World Malaria report , 20 years of global progress and challenges. Geneva,300p.

WHO (2020).https://apps.who.int/neglected_diseases/ntddata/sth/sth.html. Accessed 20 July 2020.

WHO (2024). World Malaria report, 316p; ISBN: 978-92-4-010 444-0

Yousefi Y, Haq S, Banskota S, Kwon YH and Khan W (2021). “Trichuris muris Model: Role in Understanding Intestinal Immune Response, Inflammation and Host Defense,” Pathogens (Basel, Switzerland), 10(8), 925. https://doi.org/10.3390/pathogens10080925

Zhang P, Wang CY, Li YX, Pan Y, Niu JQ and He SM (2015). Determination of the upper cut-off values of serum alanine aminotransferase and aspartate aminotransferase in Chinese. World journal of gastroenterology, 21(8), 2419–2424. https://doi.org/10.3748/wjg.v21.i8.2419