Abstract
General background: Amoebic dysentery caused by Entamoeba histolytica is a significant public health concern, particularly in regions with poor sanitation. It can lead to various complications, including changes in blood parameters. Specific background: Identifying changes in blood indicators during amoebic infections can aid early diagnosis and improve patient outcomes. Knowledge gap: There is limited research exploring gender-based differences in blood parameters of patients with amoebiasis. Aims: This study aimed to evaluate the effect of E. histolytica infection on specific blood parameters in male and female patients and to assess gender-based variations in these parameters. Results: A total of 45 patients (20 males, 25 females) diagnosed with amoebiasis were included, with samples collected between May 2023 and January 2024. Significant differences (P ≤ 0.05) were observed between male and female patients in RBC, HB, HCT, and MCH, while no significant differences were noted for MCV, MCHC, RDW, PLT, WBC, or LYM. Male patients showed higher mean values of RBC (5.01 ± 0.65) and HB (14.6 ± 1.61) compared to females (RBC: 4.5 ± 0.54; HB: 12.28 ± 1.24). Novelty: This study highlights gender-specific alterations in blood parameters during amoebiasis, providing new insights into how gender affects physiological responses to E. histolytica infection. Implications: Regular monitoring of blood parameters, particularly RBC and HB, in patients with amoebiasis is crucial for early diagnosis and treatment. The findings also underscore the importance of gender considerations in clinical management and suggest the need for larger studies to confirm these results and explore their diagnostic and therapeutic implications.
Highlights:
- Gender impacts blood parameters in amoebiasis patients.
- Males show higher RBC and HB than females.
- Regular monitoring aids early E. histolytica diagnosis.
Keywords: Amoebic dysentery, Entamoeba histolytica, blood parameters, gender differences, early diagnosis
Introduction
Low levels of environmental sanitation, cultural practices, poor socioeconomic status, and frequent exposure to contaminated water facilitate the transmission and widespread distribution of intestinal parasitic infections among parasites(1), intestinal parasites have proven to be highly prevalent and it is estimated that more than three billion people are infected with them in the world today(2). Nearly 450 million people suffer from parasitic infections, and about half of this number are children (3). Intestinal parasites often have no symptoms, however, they can be a cause of dehydration, mucous or watery diarrhea, nausea, abdominal pain, vomiting, fever, vitamin deficiencies, iron deficiency anemia, and physical and mental health disorders(4).
Intestinal parasites that infect humans are considered one of the most widespread health problems, especially in hot, tropical and subtropical regions. It is no less important than other microscopic causes, as it has the ability to infect most of the body’s organs, which leads to pathological complications that sometimes end in death(5).
There is a need to control these parasites and reduce their impact on humans. In addition to its ability to reproduce in huge numbers, this has led to it not being completely eliminated, and there is widespread interest. Protozoa and intestinal helminths constitute a large group of parasites that live in the intestine. The parasite is either It is pathogenic, as it does not cause symptoms of disease, or it is pathogenic that attacks and destroys tissues, and this depends on the type and number of parasite, in addition to the duration of infection, food, and factors(6) . The current study aims to measure some blood indicators for men and female suffering from Entamoeba histolytica (cyst + trophozoite) and compare them.
Methods
Data collection and laboratory processing:
The current study included 45 stool samples taken from visitors to Al-Sadr Teaching Hospital, Al-Hakeem General Hospital, and General Hospital for both sexes and for different numbers of individuals in the family and for different ages.
Stool examination:
Macroscopic examination: The stool is examined with the naked eye, and the texture, color, and smell of the stool are taken into consideration. Note that the liquid stool contains more of the active, nutritious phases, and therefore it must be examined before 30 minutes of taking the sample.
Microscopic examination: A stool sample the size of a pinhead containing the bloody and mucus parts is taken with a wooden stick, divided into two parts and placed on both ends of the glass slide. Then one drop of Normal solution with a concentration of 0.9% is added to one end in order to detect the nutritional and cystic stages, in addition to showing Red blood cells and white cells. To the second end, add a drop of aqueous iodine solution (Logols Iodine). Then the slide cover is placed on it and then examined with an optical microscope to search for the nutrient stages under a powerful optical microscope (40 x)(7) .
Blood collection:
5 ml of venous blood was collected from all patienys to test blood parameters. The samples were placed in sterile EDTA tubes containing an anticoagulant, and the samples were placed in the Hemolyzer Analyticon (Germany) automatic blood analysis device, where the device takes test samples, dilutes them automatically, and corrects errors in a way. Automatically then the results are read.
Determination of blood parameters:
Estimation of blood parameters was used which included(Red Blood Cells count RBC , Hemoglobin levels Hb , Hematocrit Hct , Mean Corpuscular Volume MCV, Mean Corpuscular Hemoglobin MCH, Mean Corpuscular Hemoglobin Concentration MCHC, Red Corpuscular Distribution Width RDW- CV , White Blood Cells count WBC, Lymphocytes Percentage LYM, Platelet PLT ).
Statistical Analysis:
The obtained data, which included 45 cases of male and female patients with Entamoeba histolytica, was statistically analyzed using the SPSS version 23 statistical analysis program to express the results. There were substantial differences between the two groups, as indicated by the mean and standard deviation of P ≤ 0.05.
Result and Discussion
Result
The study included 45 infected people, 25 males and 20 females. We divided it into three age groups. The first age group was less than 30, number 20, 12 females, and 8 males. The second age group was 30-50, number 17, 7 males and 10 females, and the third age group was more than 50, number 8, 5 males and 3 females, as shown in Table 1.
Age (years) | N. male | N. female | Total |
<30 | 8 | 12 | 20 |
30-50 | 7 | 10 | 17 |
>50 | 5 | 3 | 8 |
Total | 20 | 25 | 45 |
Table 2. Showed the highest significant differences in the mean (±SD) of RBC, HB, HCT, and MCH of male patients compared with female patients. While it appears there are no significant differences (p≤0.05) in the mean of MCV, MCHC, RDW-SD, RDW-CV, PLT, WBC and LYM in the male patients compared with female patients.
Gender | Male | Female | P-value |
Mean ± SD RBC (106/L) | 5.01 ± 0.65 | 4.5 ± 0.54 | 0.01 |
Mean ± SD HB (g /dL) | 14.6±1.61 | 12.28±1.24 | 0.00 |
Mean ± SD HCT(%) | 42.40 ±3.78 | 36.82±3.13 | 0.00 |
Mean± SD MCV(fl) | 85.61±8.66 | 81.83±8.49 | 0.15 |
Mean ± SD MCH(pg) | 29.66±3.71 | 27.42±3.54 | 0.04 |
Mean ± SD MCH(pg) | 29.66±3.71 | 27.42±3.54 | 0.04 |
Mean ± SD MCHC (g/dl) | 35.52±4.57 | 33.40±1.85 | 0.06 |
Mean ± SD RDW-SD (fl) | 35.46±13.20 | 31.11±16.27 | 0.32 |
Mean ± SD RDW-CV | 12.71± 1.11 | 12.70± 1.08 | 0.98 |
Mean ± SD PLT (103/μl) | 250.0±72.39 | 277.08±90.14 | 0.27 |
Mean ± SD WBC | 9.03±3.29 | 9.15±3.73 | 0.90 |
Mean ± SD LYM | 13.77± 13.35 | 7.17± 10.20 | 0.07 |
Table 3. shows that the comparison between male and female for under 30 years of age. It was observed that there were significant differences (p≤0.05) in the value of (HB and HCT). As well as there was observed that there were no significant differences in the value of (RBC, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, WBC and LYM).
Gender | Male 8 | Female 12 | P-value |
Mean ± SD RBC (106/L) | 5.11 ± 0.77 | 4.62 ± 0.55 | 0.14 |
Mean ± SD HB (g /dL) | 14.52±2.30 | 12.20±1.04 | 0.02 |
Mean ± SD HCT (%) | 41.45±4.86 | 36.64±2.91 | 0.03 |
Mean± SD MCV(fl) | 82.07±10.47 | 80.02±9.88 | 0.66 |
Mean ± SD MCH(pg) | 28.91±4.95 | 26.67±3.75 | 0.29 |
Mean ± SD MCHC (g/dl) | 34.71±2.22 | 33.31±1.50 | 0.14 |
Mean ± SD RDW-SD (fl) | 31.45±13.56 | 82.21±15.64 | 0.63 |
Mean ± SD RDW-CV | 12.92± 1.59 | 12.39± 0.90 | 0.41 |
Mean ± SD PLT (103/μl) | 10.79±14.93 | 3.35±1.65 | 0.20 |
Mean ± SD WBC (103/μl) | 10.67±4.01 | 10.79±3.87 | 0.94 |
Mean ± SD LYM | 266.0± 73.03 | 283.9±164.67 | 0.58 |
Table 4. shows that the comparison between male and female form age 30 to age 50. It was observed that there were significant differences (p≤0.05) in the value of (RBC, HB, and HCT). As well as there was observed that there were no significant differences in the value of (MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, WBC, and LYM).
Gender | Male 6 | Female 10 | P-value |
Mean ± SD RBC (106/L) | 5.28 ± 0.51 | 4.47 ± 0.60 | 0.01 |
Mean ± SD HB (g /dL) | 15.01±1.22 | 11.95±1.38 | 0.00 |
Mean ± SD HCT(%) | 43.98±2.89 | 36.02±3.21 | 0.00 |
Mean± SD MCV(fl) | 82.07±10.47 | 80.02±9.88 | 0.46 |
Mean ± SD MCH(pg) | 28.91±4.95 | 26.67±3.75 | 0.39 |
Mean ± SD MCHC (g/dl) | 34.71±2.22 | 33.31±1.50 | 0.38 |
Mean ± SD RDW-SD (fl) | 31.45±13.56 | 82.21±15.64 | 0.79 |
Mean ± SD RDW-CV | 12.92± 1.59 | 12.39± 0.90 | 0.58 |
Mean ± SD PLT (103/μl) | 246.85±85.59 | 290.80±118.50 | 0.38 |
Mean ± SD WBC | 7.80±2.72 | 7.57±309 | 0.87 |
Mean ± SD LYM | 19.22± 14.26 | 11.68±14.61 | 0.30 |
Table 5 shows that the comparison between male and female older than 50 years. It was observed that there were no significant differences (p≤0.05) in the value of (RBC, HB, HCT, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, WBC, and LYM).
Gender | Male 5 | Female 3 | P-value |
Mean ± SD RBC (106/L) | 4.47±0.30 | 4.47±0.41 | 0.98 |
Mean ± SD HB (g /dL) | 14.48±0.66 | 13.70±0.55 | 0.13 |
Mean ± SD Hct(%) | 14.72±2.69 | 40.20±1.90 | 0.39 |
Mean± SD MCV(fl) | 94.28±3.54 | 90.06±4.56 | 0.25 |
Mean ± SD MCH(pg) | 32.46±1.28 | 30.73±1.62 | 0.20 |
Mean ± SD MCHC (g/dl) | 38.78±8.38 | 34.10±0.59 | 0.28 |
Mean ± SD RDW-SD (fl) | 45.88±4.34 | 44.83±2.23 | 0.66 |
Mean ± SD RDW-CV | 12. 28± 0.79 | 12.83± 0.23 | 0.20 |
Mean ± SD PLT (103/μl) | 228.80±85.99 | 204.00±45.70 | 0.53 |
Mean ± SD WBC | 45.88±4.34 | 44.83±2.23 | 0.66 |
Mean ± SD LYM | 10.90± 8.45 | 7.40±9.19 | 0.61 |
As for Table 6., the results show that the comparison between males and females infected with both cyst and trophozoite parasites It was observed that there were significant differences (p≤0.05) in the values of RBC, HB, HCT, and LYM, while there were no significant differences in the values of MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT and WBC.
Gender | Male | Female | P-value |
Mean±SD RBC (106/L) | 5.05±0.74 | 4.61±0.37 | 0.06 |
Mean ± SD HB (g /dL) | 14.40 ±1.80 | 12.41± 1.28 | 0.02 |
Mean ± SD Hct(%) | 14.70±4.13 | 37.15±2.99 | 0.02 |
Mean± SD MCV(fl) | 83.88±9.50 | 81.20±7.87 | 0.39 |
Mean ± SD MCH(pg) | 28.87±4.16 | 27.28±3.41 | 0.24 |
Mean ± SD MCHC (g/dl) | 35.89±5.47 | 33.46±1.94 | 0.13 |
Mean ± SD RDW-SD (fl) | 34.33±13.42 | 29.91±16.03 | 0.38 |
Mean ± SD RDW-CV | 12.88± 1.26 | 12.67± 1.14 | 0.62 |
Mean ± SD PLT (103/μl) | 263.21±81.72 | 249.66±66.27 | 0.61 |
Mean ± SD WBC | 8.61±2.97 | 9.28±3.99 | 0.57 |
Mean±SD LYM | 15.42±15.00 | 5.22±7.30 | 0.03 |
Discussion
Infection with the parasite E. histolytica is one of the major health problems in many tropical and subtropical regions, especially in developing countries (8). Environmental factors, age, gender, and health habits play an important and prominent role in the occurrence of infection intestinal bacteria are easily transmitted through water and Food contaminated with infectious cysts, which vary in their ability to resist gastric and intestinal juices (9). As for species that do not form cysts, their transmission is direct. Also, the most widespread intestinal parasite infection in third world countries is amoebiasis, or what is called dysentery. Dysentery amoebic and giardiasis. One of the most important factors that help increase the incidence of these parasites is the deteriorating economic conditions and wrong social habits (10).One of causes of the increases in parasite infections is use the river water ,liquefied water , or other peoples unsterilized tools (11,12).
In Table No. 2, there is a significant difference between the number of red blood cells, hemoglobin and hematocrit between males and females, even though the number of blood cells,HB and HCT are within the normal ranges for the international reference , but there are closer to the lowest range ,the reason may be that this parasite causes disturbance in the digestive system and also secretes a motile feeding stage that attaches to the villi of the intestine and absorbs renin from them(13) . The renin-angiotensin system, especially Ang II , contributes to the regulation of red blood cell mass and plasma volume, and is therefore the ultimate regulator of hemoglobin and hematocrit levels(14) . In addition, infection with the parasite E. histolytica leads to necrosis and damage to the intestinal mucosa, which negatively affects the sites of absorption of necessary substances. In addition to the bleeding caused by necrosis of the membrane, infection with intestinal parasites has a great impact on blood values(15) . In general, intestinal parasite infestation is strongly associated with anemia because it causes malabsorption, nutritional deficiencies, and blood loss in the gastrointestinal tract(16,17) .Changes in values occur of RBC , HB , HCT , MCV , MCH, MCHC, RDW-SD, RDW-CV this indicated anemia due to iron deficiency ,also the parasite can cause diarrhea in the patients(18,19) . Samples of those infected with the cyst and trophzoite phase were studied due to the large number of people infected with these stages. It was noted that there were significant differences (p≤0.05) in hemoglobin, hematocrit and lymphocytes between males and females ,also, in the research, we did not mention the case of cysts only or trophozoites only due to the small number of patients, this is consistent with a study(20). Where it was found that most cases of infection were in the cyst and trophozoite phase. this result because the cyst and trophzoite represents the chronic stage of infection with the disease and causes recurrent diarrhea
Conclusion
The study showed the extent to which intestinal parasite infection affects blood indicators, and that examining the complete blood count is of great importance to help diagnose the infection and may be a guide to further treatment and follow-up. However, it is recommended to conduct more studies with a larger sample to confirm the results of the study and the validity of these indicators. In diagnosing infection with Entamoeba histolytic parasite.
References
- . M. Abdi, E. Nibret, and A. Munshea, "Prevalence of intestinal helminthic infections and malnutrition among schoolchildren of the Zegie Peninsula, northwestern Ethiopia," J. Infect. Public Health, vol. 10, no. 1, pp. 84–92, 2017.
- . S. Fallahi, A. Rostami, M. Mohammadi, F. Ebrahimzadeh, and Y. Pournia, "Practical parasitology courses and infection with intestinal parasites in students," J. Infect. Public Health, vol. 9, no. 5, pp. 654–660, 2016.
- . H. Sadeghi and H. Borji, "A survey of intestinal parasites in a population in Qazvin, north of Iran," Asian Pacific J. Trop. Dis., vol. 5, no. 3, pp. 231–233, 2015. [Online]. Available: https://www.sciencedirect.com/science/article/pii/S2222180814606599
- . M. Shobha, D. Bithika, and S. Bhavesh, "The prevalence of intestinal parasitic infections in the urban slums of a city in Western India," J. Infect. Public Health, vol. 6, no. 2, pp. 142–149, Apr. 2013.
- . M. Ahmed, "Intestinal parasitic infections in 2023," Gastroenterology Research, vol. 16, no. 3, pp. 127, 2023.
- . R. Mrishih, "Prevalence of intestinal parasites among patients at Tishreen University Hospital in Lattakia," Tishreen Univ. J. - Med. Sci. Ser., vol. 45, no. 4, pp. 209–219, 2023. [Online]. Available: https://journal.tishreen.edu.sy/index.php/hlthscnc/article/view/15377
- . Z. Al-Shaheen, A. Kassim Al-Maki, and H. K. Kassim, "A study on prevalence of Entamoeba histolytica & Giardia lamblia infection among patients attending Qurna Hospital in Basrah," BasJ Vet Res., vol. 6, no. 2, pp. 30–36, 2007.
- . L. L. Braga, M. L. Gomes, M. W. Silva, C. Paiva, A. Sales, and B. J. Mann, "Entamoeba histolytica and Entamoeba dispar infections as detected by monoclonal antibody in an urban slum in Fortaleza, Northeastern Brazil," Rev. Soc. Bras. Med. Trop., vol. 34, no. 5, pp. 467–471, 2001.
- . F.-H. Lin, B.-C. Chen, Y.-C. Chou, W.-C. Chien, C.-H. Chung, C.-J. Hsieh, et al., "The epidemiology of Entamoeba histolytica infection and its associated risk factors among domestic and imported patients in Taiwan during the 2011-2020 period," Medicina (Kaunas), vol. 58, no. 6, Jun. 2022.
- . G. Garbossa, M. P. Buyayisqui, L. Geffner, L. López Arias, S. de la Fournière, A. S. Haedo, et al., "Social and environmental health determinants and their relationship with parasitic diseases in asymptomatic children from a shantytown in Buenos Aires, Argentina," Pathog. Glob. Health, vol. 107, no. 3, pp. 141–152, Apr. 2013.
- . Z. G. F. Almojaamaee, A. S. Al-Ezee, and E. M. Al-Hussuny, "Culture of Entamoeba histolytica in vitro and the role of starch on its growth," Acad. Sci. J., vol. 12, no. 1, 2016.
- . N. T. Khan and N. Jahan, "Prevalence of E. histolytica-associated dysentery in children in Satellite Town, Quetta," Epidemiol. Open Access, vol. 7, no. 1, 2017.
- . L. Adday, "Hematological test in patients with intestinal parasites in Al-Hashimiah village," Kufa J. Biol., vol. 1, pp. 2–6, May 2008.
- . A. Nehme, F. A. Zouein, Z. Deris Zayeri, and K. Zibara, "An update on the tissue renin angiotensin system and its role in physiology and pathology," J. Cardiovasc. Dev. Dis., vol. 6, no. 2, 2019. [Online]. Available: https://www.mdpi.com/2308-3425/6/2/14
- . A. H. A. Al-Mosa and H. H. I. Al-Taie, "Effect of infection with intestinal parasites on blood picture," Al-Taqani, vol. 20, no. 1, pp. 1–7, 2007.
- . S. G. Ahmed and J. Uraka, "Impact of intestinal parasites on haematological parameters of sickle-cell anaemia patients in Nigeria," East Mediterr. Health J., vol. 17, no. 9, pp. 710–713, Sep. 2011.
- . U. M. Alkholy, S. M. El Gebaly, W. E. M. A. Morsi, W. E. Elawamy, S. E. Etewa, and A. M. Yousef, "The impact of parasitic infestation on nutritional status and micronutrients among children," J. Parasitol. Res., vol. 2024, pp. 6996968, 2024.
- . Y. T. Daoud, K. M. Dakhil, and D. K. H. Al-Mozan, "Study of infection with intestinal parasites (Entamoeba histolytica) and its effect on the blood nature in children from Thi-Qar province," Al-Qadisiyah Med. J., vol. 10, no. 18, pp. 152–158, 2017.
- . I. Momodu and I. Yahaya, "Changes in packed cell volume and some biochemical parameters of adult females during pregnancy in North-West Nigeria," Int. Blood Res. Rev., vol. 5, no. 2, pp. 1–6, 2016.
- . G. H. Al-Khaysee and A. A. Sultan, "The factors that affect the epidemiology of Entamoeba histolytica and Giardia lamblia among population of Khalis and Baledrose," Diala J., vol. 27, 2008.