Research Article, Vector Biol J Vol: 6 Issue: 1

Impact of intestinal parasite/malaria co-infection on haemoglobin in patients of Melong and Denzo health facilities, Littoral region,Cameroon

Ebanga Echi Joan Eyong^*, Makebe Sylvie, Gangue Tiburce, Yana Wenceslas

Department of Biological Sciences, University of Bamenda, Bambili, North West Region, Cameroon

*Corresponding Author:Ebanga Echi Joan Eyong, Department of Biological Sciences, University of Bamenda, Bambili, North West Region, Cameroon, Tel: (+237) 677 67 07 24; E-mail: joan.ebangaechi@gmail.com

Received: September 21, 2020; Accepted: October 5, 2020; Published: January 15, 2021

Citation: Eyong et al. (2020) Impact of intestinal parasite/ malaria co-infection on haemoglobin in patients of Melong and Denzo health facilities, Littoral region, Cameroon. Vector Biol J 5:5.

Abstract

Keywords: Malaria; Intestinal parasites; Co-Infection; Anemia;Melong; Denzo; Littoral Region, Cameroon

Keywords: Malaria; Intestinal parasites; Co-Infection; Anemia; Melong; Denzo; Littoral Region, Cameroon

Background

An intestinal parasitic infection is a condition in which a parasite infects the gastrointestinal tract of humans and animals. Intestinal parasitic infections comprise both helminthes and protozoans which form the most common infections worldwide [1]. According to the London School of Hygiene and Tropical Medicine [2], the most frequent helminths species are Ascaris lumbricoides, Enterobius vermicularis, Hymenolepis spp, Trichuris trichiura, Strongyloides stercolaris, Schistosoma mansoni, Taenia spp and Hookworm. While most frequent protozoans areEntamoeba histolyticaand Giardia intestinalis. These parasites modify gastrointestinal conditions and produce a variety of symptoms in infected persons such as, inflammation of the small and large intestine, diarrhoea/dysentery, abdominal pain and nausea/vomiting [3]. It has also been estimated that about 3.5 billion people in the world are infected with intestinal parasites of which 450 million are ill [4,5]. Malaria is endemic in all the 10 Regions of Cameroon with a percentage prevalence of about 20% [6].

Five species of Plasmodium cause malaria; Plasmodium malariae, P. vivax, P. ovale, P. knowlesi and P. falciparium with the last one being the most virulent accounting for the majority of malaria deaths [7]. Coinfection of malaria and intestinal parasites is common in individuals in developing countries [8] and severe infections can lead to blood loss, tissue damage, spontaneous abortion and death. However, variation in the prevalence of intestinal parasites and malaria can be related to some factors such as, Climate, geographical localization, hygiene as well as a variety of cultural, economic and social variables [9].

Most intestinal parasites cause infection that lead to acute and chronic diarrhoea in healthy individuals and December lead to life threatening illness in patients with immunosuppressive disease like HIV/AIDS. The inhabitants of Melong and Denzo localities are faced with the challenge of the factors that favour the transmission of these parasites which are poor sanitation, poor drainage and poor quality of water. In addition to these factors, Melong is located at a crossroad from Bamenda to other major towns like Nkongssamba, Douala, Buea and Limbe and it is where travelers usually stop to take a break consuming different types of food which might promote propagation of intestinal parasites.

The findings from this study will provide a better understanding of intestinal parasites/malaria co-infection as predictors of anaemia so as to generate baseline data on the parasites as this will add knowledge about malaria transmission and influence policy to improve community health. The aim of this study was to assess the prevalence of intestinal parasites and malaria co-infection as well as to determine its association with anemia in patients of Melong and Denzo, Littoral Region of Cameroon.

Materials and Methods

Description of study site

Melong is a semi-urban area found in the Littoral Region of Cameroon. Located at Latitude 5o 7’18 N; longitude 9o 57’41”E with an of altitude of 760 m a.s.l. It has an average temperature of 19oC and the climate is marked by two seasons, the rainy and dry seasons. It has an estimated population of 102,000 inhabitants [10] and the area is characterized by poor hygienic conditions due to presence of bushes and poor drainage systems. Inhabitants are engaged in various socio-economic activities.

Denzo, also known as New Melong is a rural area, one of the 40 villages found in Melong sub-division. It is divided into two ethnic groups (New Melong A and New Melong B) headed by a chief. It is made up of 5,099 inhabitants [10].

Farming and trading are the main economic activities of the people in these localities.

Ethical considerations

An ethical clearance was obtained from the University of Bamenda review board. Administrative clearances to carry out this study in Melong district hospital and Denzo integrated Health centre were obtained from the Director of the respective medical facilities. Participation in this study was voluntary. Participants had to fill and sign the informed consent form which explained the benefits of the study (that is, those found infected would be treated). Parents/legal guardians had to fill and sign the informed consent form for minors (children below 18 years).

Study design and study population

This study was a cross-sectional examination in which the prevalence of intestinal parasites and malaria were determined. The study population was made of patients of all age groups, both males and females, that presented stool and blood samples for analysis in the Melong District Hospital and Denzo Integrated Health Centre.

Inclusion criteria

Only patients that brought stool samples for analysis and blood for malaria parasite examination in Melong District Hospital and in Denzo Integrated Health Centre and had signed the informed consent form participated in the study.

Exclusion criteria

Patients who did not present stool samples for analysis and blood for malaria parasite examination in Melong District Hospital and Denzo integrated Health Centre were excluded. Patients who did not bring the required quantity of stool sample and those who did not sign the informed consent form were excluded. Those who signed the informed consent form but wanted to withdraw were not forced to participate in this study.

Sample size estimation

The sample size of this study was calculated based on a similar prevalence study by Williams et al. [11] and the Cochran formula [12], were used. The formulation is:

n=Z²pq/e²

Where Z=standard number deviate (1.96 for a 95% confidence value).

n=desired sample size

P=prevalence of intestinal protozoan 42.9% [11].

q=1-p (proportion in the population that does not have the characteristics being measured).

e=desired level of precision 0.05.

n=(1.96)²(0.429)(0.571)/(0.05)²

n=376 participants.

It was calculated that a minimum sample size of 376 participants was required. A total of 400 participants were sampled to minimize bias.

Stool collection and examination

Patients were given clean, dry and air tight bottles labeled with their initials. They were given instructions on how to collect the required stool sample. A macroscopic examination was done to determine the presence of adult worms in the stool, consistency, and the colour. Direct microscopy examination was done using normal saline. The slides were observed under x10 objective and x40 objective lens of the microscope to detect trophozoite and cyst forms especially the motile forms. The Kato-katz concentration technique was used following the Tadesse et al. [13] and WHO [14] methods to determine the presence and intensity of helminth eggs.

Blood collection, preparation and staining of blood smears

Prior to blood sample collection demographic information such as the age, sex, area of residence were recorded. Using sterile disposable lancets, finger pricks were performed. Thick and thin blood films were prepared using the method described by Cheesbrough [15]. The code number of each individual was written on the slide and the blood films were allowed to air dry protected from dust and flies. In the laboratory, the thin films were fixed with 100% methanol for one minute and both thick and thin blood films were stained with 5% Giemsa stain solution for 30 minutes [15].

Detection and estimation of parasitaemia of Plasmodium species

The slides were read under x100 (oil immersion) objective of the microscope for the detection of malaria parasites by an experienced microscopist. A second experienced microscopist, blinded to the first reading, read all thick smears and any discrepancies (positive vs. negative; results that did not match each other; >25% difference in parasite density) were resolved by a third microscopist. Parasite densities were determined from thick blood smears by counting the number of asexual parasites or sexual parasites per 200 WBCs and converted to number of parasites/μ l blood assuming a standard WBC count of 8,000/μ l. A smear was considered negative if no parasites were seen after a review of 100 high-powered fields.

Haemoglobin concentration

Haemoglobin concentration was detected by putting a drop of blood on the mission digital Hb haemoglobin testing machine. The results were recorded after 15 seconds according to methods described by Crawley [16]. Anemia was defined as Hb<11.0 g/dL [17].

Data Analysis

Data collected were recorded in the Microsoft excel. The data was analysed using the Statistical package for social sciences (SPSS) version 23. Proportions were calculated to obtain the prevalences of infection. Chi Square contigency test was used to test for significant differences in proportions. Binary logistic Regression was used to assess the association between intestinal parasites and malaria-intestinal parasites co-infection and anemia. The Pearson’s correlation coefficient (r) was calculated to determine if anemia is linked with co-infection malaria and intestinal infections. The Mann-Whitney test was to check for significant differences in the geometric mean parasite density (GMPD) between localities and also between males and females. The Kruskal-Wallis test was used to test for significant differences in GMPD between age groups. All the tests were performed at the 5% significance level.

Results

Demographic characteristics of the study population

A total of 400 persons were enrolled into the study. In Melong, 274(68.8%) were sampled while 126(31.5%) were sampled in Denzo, (Table 1). More females (248, 62%) were enrolled into the study than men (152, 38%), (Table 1). The highest number of participants 110(27.5%) belonged to the ≤ 5 years age group while the lowest number 48, 12% was in the age group ≥ 51 years, (Table 1).

Table 1: Demographic characteristics of the study population

Prevalence of intestinal parasites in the study

The overall prevalence of intestinal parasites was 28.3% (113). Out of the 113 patients infected with intestinal parasites, 31.8% (87/113) were from Melong and 20.6% (26/113) from Denzo. E. histolytica had a prevalence of 27.7% (76/274) in Melong and Denzo 9.5% (12/126) and the difference in the prevalence of E. histolytica between the 2 localities was highly significant (χ²=16.68, P<0.001), (Table 2). The prevalence of Ascaris lumbricoides was higher in Denzo 10.3% (13/126) than in Melong 0.3% (1/274) and the difference was highly significant (χ²=25.31, P<0.001), (Table 2). The prevalence of the other intestinal parasites observed can be seen in (Table 2).

Table 2: Prevalence of intestinal parasites in the study

With respect to sex, the overall prevalence of intestinal parasites in males was 24.3% (37/152) and females 30.6% (76/248). Females were more infected with E. histolytica than males although the difference was not significant (χ²=0.13, P=0.720), (Table 2). Trichomonas hominis was found only in females 2.4% (6/248) with no significant difference (χ²=3.73, P=0.05). Females were more infected with Ascaris lumbricoides 3.6% (9/248) than males 3.2% (5/152) but the difference was not statistically significant (χ²=0.32, P=0.858). T. hominis, Giardia lamblia, Taenia spp and Trichuris trichiura were not found in males (0%), while females had varied prevalence; T. hominis 2.4% (6/248), G. lamblia 1.2% (3/248), Taenia spp 0.4% (1/248) and T. trichiura 0.4%(1/248) the difference was not significant (χ²=3.73, P=0.053; χ²=1.85, P=0.173; χ²=4.27, P=0.370; χ²=0.61, P=0.433), respectively in Table 2.

The overall prevalence of intestinal parasites was highest 35%, (21/60) in adults aged 31-50 years and the lowest 20.9% (23/110) in participants aged ≥ 51 years. The prevalence of E. histolytica was highest in adults 16-30 years 27.4% (29/106) and the lowest in children ≤ 5 years 14.5% (16/110) although the difference was not significant (χ²=5.72, P=0.221). The prevalence of A. lumbricoides amongst the different age group highest in children ≤ 5 years 4.5% (5/110) and lowest in patients ≥ 51 years 2.0% (1/48). There was no significant difference (χ²=3.63, P=0.458). Trichomonas hominis which was least in age group ≤ 5 years (0%) and ≥ 51 years (0%) while most of the parasites was seen in 31-50 years patients (6.6%, 4/60) and the difference was statistically highly significant (χ²=13.49, P=0.009), (Table 2). Giardia lamblia, Taenia spp, T. trichiura had no significant difference in the prevalence amongst the various age groups (P>0.05), (Table 2).

Intensity of intestinal parasites in the study

Participants in Melong recorded a higher parasite load (range) 38(24- 384) than those in Denzo 38(24-96) although the difference was not significant (Mann Whitney U Test, P=0.466), (Table 3). In relation to sex, females, had a higher parasite load (range) 39(24-384) than males 36(24-144) but the difference was not significant (Mann Whitney U Test, P=0.541), (Table 3). With respect to age, the highest parasite load (range) was recorded in patients aged 16-30 years 41(24-384) and the least in patients 31-50 years 34(24-96) and ≥ 51 years 34(24-96) and the difference was significant (Kruskal Wallis Test, P=0.041), (Table 3).

EPG= Egg per gram, CPG= cyst per gram, SEM=standard error of mean

Table 3: Intensity of intestinal parasites in the study

Prevalence and intensity of malaria in the study

The overall prevalence of malaria was 66.5% (266). With respect to localities, Denzo recorded a higher prevalence 79.3% (100/126) of malaria than Melong 60.5% (166/274) and the difference was highly significant (χ²=13.666 P=0.001), (Table 4). The prevalence of malaria was higher in males 72.3% (110/152) than in females 60.5% (166/248), although the difference was not statistically significant (χ²=3.790, P=0.052), (Table 4). The highest prevalence of malaria, 75.4% (83/110) was recorded in the age group ≤ 5 years while the lowest, 56.6% (34/60) was recorded in patients aged 31-50 years and the difference was significant (χ²=12.249, P=0.016), (Table 4).

GMPD = Geometric mean parasite density, n= Number positive, N= Number examined, SD= standard deviation

Table 4: Prevalence and intensity of malaria in the study

Participants in Melong recorded a higher GMPD, 762 (160-200,000 trophozoites/ μ l of blood) than those in Denzo, 444 (40-10,000 trophozoites/ μ l of blood) and the difference was highly significant p<0.001, (Table 4) Females had a higher 624(40-200,000 trophozoites/ μ l) GMPD than males 620(40-8,000 trophozoites/ μ l), although the difference was not significant (P=0.477), (Table 4). Based on age, the highest GMPD range was found in children ≤ 5 years old 645(40- 200,000 trophozoites/ μ l of blood) and the lowest in adults ≥ 51 years old 425(40-1,600 parasites/ μ l of blood), although there was no significant difference (p=0.161), (Table 4).

Haemoglobin (Hb) profile in the study population

The mean Hb in the study population was 11.38 ± 1.86 (range: 4.8- 17.7 g/dL). A total of 165 (41.3%) participants recorded normal Hb values while 235 (58.8%) were anaemic. Of those anaemic, 12(3.0%) suffered from severe anaemia (<7 g/dL), 142(35.5%) from moderate anaemia (7.0-9.9 g/dL) and 81(20.3%) from mild anaemia (10.0-10.9 g/dL). More persons were anemic in Denzo 53.2% (67/126) than in Melong 41.2% (113/274) and the difference was statistically significant (χ²=4.97, P=0.026), (Table 5). Males recorded a higher prevalence of anaemia 45.4% (69/152) than females 44.8% (111/248) with no significant difference (χ²=0.02, P=0.901), (Table 5). Children ≤ 5 years old were more anaemic 58.2% (64/110) while the least anemic cases were adults 31-50 years old 26.7% (16/60). Prevalence of anemia according to age range had a highly significant difference (χ²=18.32, P=0.001), (Table 5).

Table 5: Prevalence of anaemia in the study population

Prevalence of co-infection Malaria-intestinal parasites

The overall prevalence of malaria-intestinal parasite coinfection was 16.3(65). Out of the 6 intestinal parasites seen in the study population, four species were co-infected with malaria (E. histolytica, A. lumbricoides, G. lamblia and T. hominis). The prevalence of E. histolytica malaria co-infection 12.3% (49/400) was the highest and the lowest was G. lamblia-malaria co-infection 0.3% (1/400), (Figure 1).

Figure 1: Co-infection of malaria and intestinal parasites (M.P= malaria parasite)

There was no significant difference in the prevalence of co-infection according to site, sex and age, but according to anemic status, anemic patients had a higher prevalence 20.6% (37/180) than those nonanemic patient 12.7% (28/220) and the difference was significant difference (χ²=4.46, P=0.035), (Table 6).

Table 6: Prevalence of co-infection of malaria/intestinal parasite with respect to site, sex, age and anaemic status

Association of malaria parasite/intestinal parasites/co-infection with anemia

The prevalence of anemia in malaria positive patients was higher 49.2% (131/226) than in malaria negative patients 36.6% (49/134). The risk of being anemic was reduced in malaria negative patients when compared to malaria positive patients with an odds ratio OR=0.6(0.39-0.91). The association between malaria and anemia was statistically significant, p=0.017. There was no significant association of intestinal parasite and co-infection intestinal parasite with anemia as shown in (Table 7).

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