The prevalence of malaria among HIV seropositive individuals and the impact of the co- infection on their hemoglobin levels
© Tay et al.; licensee BioMed Central. 2015
Received: 2 June 2014
Accepted: 12 January 2015
Published: 7 March 2015
Malaria and HIV/AIDS are the two most common infections in sub-Sahara Africa. There are hypotheses and study reports on the possible association between these two infections, hence the prevalence and outcome of their co-infection in an endemic population will be important in defining healthcare strategies. A cross sectional study was carried out at the Holy Family Hospital in Techiman, Ghana, between November 2011 and January 2012, to determine the prevalence of malaria among HIV sero-positive patients and its impact on hemoglobin levels.
A total of 400 HIV sero-positive participants (292 females and 108 males) aged between 1 and 73 years were randomly sampled for the study. A questionnaire was administered and 2 ml of venous blood samples were drawn for malaria parasites detection, CD4 count and haemoglobin level estimations.
Malaria parasites were detected in 47 (11.75%) of the participants. There was no statistically significant difference between the malaria prevalence rate of females (12.1%) and males (10.2%) P = 0.6047. An overall anaemia prevalence of 67% was observed. Among participants with malaria the anaemia prevalence was 93.6%. The CD4 cell count of all the participants ranged between 3 and 1604 cells/μl with a mean of 386.2 (±274.3) cells/μl. Participants with malaria had CD4 cell count ranged 3 and 512 Cells/μl with the mean being 186.33 (±133.49) Cells/μl. Out of 377 participants (all above 15 years) interviewed on knowledge of malaria transmission and prevention, 87.0% had knowledge on transmission but only 8.5% use in bed nets.
It was revealed that almost all the patients with malaria infection were anemic.
KeywordsHIV/AIDS CD4 cells Malaria co-infection Anaemia Anti-retroviral
Malaria and Human immunodeficiency virus (HIV) infections are major public health problems in many parts of the world. Both infections kill millions of people each year with disproportionate heavy burden on Africa, India, Southeast Asia and South America .
Sub-Saharan Africa harbors 90% of the estimated 219 million cases that results in over 600,000 deaths annually [2,3]. Severe anemia as a result of malaria occurs in 1.5 to 6.0 million African children annually with mortality rate of nearly 10%; respiratory distress, hypoglycaemia and other complications result in an additional 1–2 million cases . Malaria is a major cause of maternal anemia, which in turn is a risk factor for maternal mortality resulting in about 35% of preventable cases of low birth weight . In Ghana malaria is still the leading cause of loss of days of healthy life  as it accounts for at least 20% of child deaths and over 45% of out-patient attendances .
Because of the high prevalence of HIV and malaria in sub-Saharan Africa, co-infections are common. Recent estimates put HIV/AIDS prevalence in Ghana at 2.9% . It is known that some 225,478 persons are living with the disease. Further to this, about 12,077 new infections are recorded annually with corresponding 15, 263 deaths [6,7]. By 2011, 59,007 people had access to anti-retroviral treatment; however this represented 57.9% of eligible patients . Implying that an excess of 40% of people living with HIV/AIDS are left to die without getting access to anti-retroviral treatment. Notwithstanding the public huge health burden presented by these two infections, their interaction is still not completely understood .
Because of the high prevalence of HIV and malaria in sub-Saharan Africa, co-infections are common, Because of the geographic overlap between high-prevalence areas for malaria and HIV infection, there is growing evidence that the two infections may synergistically intensify each other, increasing incidence and complicating treatment efforts . In a region of unstable malaria, HIV infection had an unexpectedly large association with the outcome of falciparum malaria where HIV infection was associated with severe/complicated malaria . Recently Gupta and Shah using Sensitivity analysis and simulation has shown that malaria makes people move faster from HIV to AIDS class and reduce their life span. Radad and coworkers reported that an increase of one log in HIV viral load occurs during febrile malaria episodes enhancing susceptibility to malaria in HIV infected patients and this was found to facilitate the geographic expansion of malaria in areas where HIV prevalence was high .
As the number of malaria and HIV co-infection increased, it has become apparent that anti-retroviral drugs interact with the few anti-malaria drugs in use, complicating treatment efforts for both infections . Malaria and HIV co-infection also result in interactions that adversely affect the outcome of both conditions, especially among pregnant women and infants born to HIV infected mothers . Malaria  and HIV  individually are known to cause maternal anemia. Further to this, a number of researchers have reported a negative effect of the combined impact of HIV and malaria on maternal hemoglobin (Hb) concentrations . However, there is a dearth of information on the collective impact of HIV-malaria co-infection on the hemoglobin levels in the general population. Understanding the impact of HIV and malaria co-infection therefore, is important for determining approaches to treatment and prevention.
The study was conducted in the Holy Family Hospital; the only facility that provides ART services to HIV patients in the municipality. It has bed capacity of 167 beds. Patients diagnosed to have HIV/AIDS infection and who sought treatment at ART clinic at the Holy Family Hospital were the source population for the study. The drugs administered for the first line of treatment were Azidovudine (d4T), Lamivudine (3TC) plus Nevirapine or Efavirenz. Nelfinavir, Kaletra and Indinavir were occasionally used in combination with nucleoside based reverse transcriptase inhibitor drugs. The study was cross-sectional serological survey where HIV sero-positive patients attending ART Clinic at the hospital were randomly approached and invited to participate in the study provided they gave their consent. The study took place between November 2011 and January 2012.
In the equation below, n is the sample size, z is the critical value of the standard normal distribution at the 5% level (1.96), p is the estimated malaria prevalence (0.60), q = 1 – p, and d is the precision level. This is used for a small population of up to 3,000. The sample size obtained was 369. A total of 400 HIV sero-positive individuals who sought care at the ART Clinic of the Holy Family Hospital in Techiman and were willing to participate in the study were recruited.
Techiman, is a major commercial town in the Brong Ahafo region linking not only most of Ghana’s major cities, but also the republic of Togo, Burkina Faso and Cote D’Ivoire. It has an estimated total land area of about 669.7 square kilometers. According to the 2000 population and housing census, the population of the municipality was estimated to be 202,409 by December 2005, with an average growth rate of 3.0% per annum. Agriculture and related trades are the major economic activities in the municipality. Over half of the economically active population is engaged in these activities. This makes Techiman market the largest food crop market in Ghana. The municipality has twenty four (24) health care facilities; including two mission hospitals in Techiman, (i.e. Holy Family and Ahamadiya Hospitals), nine government health centers, four private maternity homes and three private clinics.
The study was approved by the Committee on Human Research Publication and Ethics from Kwame Nkrumah University of Science Technology and the management of Holy Family Hospital - Techiman. Consent of participants was also obtained prior to the study. All consenting patients attending the ART clinic were eligible for participation except infants less than 6 months. Refusal of some patients to participate in the study did not interfere with their routine care at the hospital.
A questionnaire, in both English and Twi (the local language) which included the basic socio- demographics of the study subjects as well as their knowledge and prevention of malaria was used. Two independent translators were engaged, one translated the English to Twi, the other was who had no prior copy of the English was tasked to translate the local language back into English. This was done to ensure the consistency of thought. No personal identifiers were included and individuals were given unique codes on the questionnaires and their laboratory specimens.
Laboratory investigation was conducted using the Thin Blood Film method. A drop of blood, 3–5 mm in diameter was put on a slide and spread with the corner of another slide to form a thin blood smear. The smear was thoroughly allowed to dry, fixed with methanol and stained with Giemsa stain for about 15 minutes. The stained smear was washed with running tap water, allowed to dry in air and examined microscopically for the presence of malaria parasites.
HIV test was conducted using First Response HIV Card Test 1–2.0 (Premier Medical Corporation Ltd, Mumbai, India). Reactive blood samples were confirmed with Oraquick Rapid HIV – ½ Antibody Test (OraSure Technologies Inc., Bethlehem, USA). Both test kits are immuno-chromatographic rapid tests for qualitative detection of antibodies specific to HIV in human serum, plasma or whole blood.
CD4 count and Haemoglobin concentration
The CD4 count of the study population was determined using Becton-Dickinson FASCount flow cytometer (BD Biosciences, California, USA) whilst the haemoglobin concentration was estimated with Sysmex XT – 2000i Haematology Analyzer (Sysmex Corporation, Hong Kong, China).
Socio-economic and demographic characteristics
Socio-economic and demographic characteristics of patients (participants)
15 – 24
25 – 34
45 – 60
No formal education
Hemoglobin level of patients (participants)
Hemoglobin levels in different gender
Male frequency (%)
Female frequency (%)
Total frequency (%)
CD4 count of patients
CD4 count of participants stratified according to gender
Male frequency (%)
Female frequency (%)
Total frequency (%)
Malaria parasite prevalence
Malaria co infected participants and hemoglobin levels
Malaria infection and CD4 count
Knowledge of malaria transmission and prevention
Knowledge of malaria transmission and prevention
No. of respondents
Knowledge about malaria
(n = 328)
Means of malaria transmission
Malaria is preventable
(n = 328)
Use of bed nets
(n = 377)
CD4 cell count in participants co-infected with malaria
Accumulating data points to pathological interactions between HIV and malaria in co infected individuals. However, the public health consequences of this interaction have not been completely deciphered. Abu-Radad and coworkers in Kenya observed that a temporary one-log elevation in HIV viral load occurs during febrile malaria episodes; in addition, susceptibility to malaria is enhanced in HIV-infected patients .
In a one-time cross-sectional serological survey, the current study sought to determine malaria prevalence in HIV seropositive individuals; their CD4 count to identify the various stages of immuno-suppression and their hemoglobin levels to possibly associate the impact of the co-infection on the outcome of anemia in the study participants.
Generally malaria transmission in the forest zone of Ghana is intense [6,15] with very high parasite prevalence up to 50% [15,16]. But the overall malaria prevalence in this study was low; this may be due to the fact that the study was conducted during the drought months (November- January) which coincide in Ghana with very low malaria transmission. However in comparison with similar studies in the African region, malaria prevalence in this study appears to be higher. The prevalence of malaria infection among HIV sero-positive patients in South Africa and Mozambique were lower [17,18]. But the observed prevalence is similar with a study done in Southeastern part of Nigeria in which the prevalence of malaria as a co-infection amongst asymptomatic HIV sero positive patients was 11.8% . Malaria is known to cause an increase in transitory viral load while HIV causes more clinical malaria, higher parasitemia and higher rates of treatment failure in co-infected patients .
Females had relatively higher malaria infection compared with their male counterparts. This may be explained by their typical lifestyle in the community, where females tend stay out late during mosquito biting hours carrying out domestic activities. This has variously been reported elsewhere. Also, among the various age groups, it was determined that the age 30–34 years harbored more parasites than the other age groups. This was also confirmed with the high cumulative density index. However, prevalence of malaria infection was high in children within the age group of 0–4 years in which out of 12 patients, four patients representing 33.3% had malaria infection. This is consistent with several studies in malaria endemic Africa  where prevalence of malaria infection in HIV children was high. However some studies have reported lower prevalence of malaria among non HIV children less than five years in the Brong-Ahafo region of Ghana .
The mean (SD) CD4 cell count of the patients was 386.2 (274.3). Males and females had CD4 count mean (SD) of 345.7(270.1) cells/μl and 386.1(276.0) cells/μl respectively. The difference in the mean CD4 count is due to the fact that HIV infection is detected earlier in females than their male counterparts. With the introduction of Prevention of Mother -To- Child Transmission of HIV (PMTCT) programme, women of child bearing age are screened for HIV infection during antenatal care or at obstetrics and gynecology clinics. Those who test positive are then incorporated into ART clinics while there is no similar program for males for the early detection of HIV.
CD4 cell count less than 200 cells/μl (signifying the terminal stage of HIV infection (AIDS) was seen in 34.5% patients. Obviously the major reason for this high proportion of AIDS is because of late presentation, largely due to the fact that we are yet to imbibe the culture of voluntary screening for early detection and treatment. Fear of stigmatization, lack of awareness and inadequate trained counseling personnel are some of the factors militating against voluntary screening. Many patients only seek medical attention and are diagnosed when HIV infection becomes complicated by AIDS defining illnesses. Majority of the patients (66.0%) with malaria infection had CD4 cells count less than 200 cells/μl. This can be attributed to the well establishment that CD4+ T lymphocyte cells <200 cells/μl is associated with a higher risk of opportunistic infection and poor disease progression .
Anemia is a frequent complication of infection with the human immunodeficiency virus, and could be clinically important. Multifactorial origin of anemia complicates determining its original cause and/or its proper treatment . Using hemoglobin level of less than 13.0 g/dl and 12.0 g/dl as the cutoff point for anemia in males and females respectively, the overall prevalence of anemia among the patients was 67%. The prevalence of anemia in this study is comparable with other studies (approximately 70%) [22,23]. The incidence of anemia was strongly and consistently associated with the progression of HIV disease as measured by diagnosis of an AIDS-defining opportunistic illness and measurement of a CD4 count of 200 cells/μl. This association is most likely explained by the increasing viral burden as HIV disease progresses, which could cause anemia by increased cytokine mediated myelosuppression which impair erythropoiesis. Also several opportunistic organisms like Mycobacterium tuberculosis, Histoplasma, Cryptococcus, Coccidiodes, Pneumocystis carinii, and Leishmania have been shown to infiltrate the bone marrow and disrupt erythropoiesis . Alternatively anemia may be a surrogate marker for some aspect of disease progression not captured by controlling for CD4 count and clinical AIDS diagnosis.
Several drugs used to combat HIV and its complications may contribute to the anemia that is seen in HIV infection. The administration of Zidovudine is recognized to cause anemia because of myelo-suppression .
Males and females did not show significant difference in the prevalence of anemia. Different studies have reported increase prevalence of anemia in females than males which were largely attributed to menstrual blood loss and to the drains on iron stores that occur with pregnancy and delivery . However in this study, it was revealed that most males report to the ART clinic late by which HIV infection without antiretroviral therapy in the vast majority of infected males has progressively destroyed the immune system leading to opportunistic diseases and other condition that lead to anemia in HIV infection has advanced.
Majority of the HIV patients with anemia were mild to moderate anemia with few patients (2.75%) with severe anemia. This is in agreement with studies by Meidani and co workers  where mild to moderate anemia was observed in majority of HIV patients with anemia in their studies. It was revealed that almost all the patients with malaria infection were anemic. This may be due to the clearance and or destruction of infected RBCs, the clearance of uninfected RBCs, erythropoietic suppression and dyserythropoiesis as reported as reported by others elsewhere by .
About 87% of the patients who responded to the questionnaire claimed to have some knowledge on malaria transmission in their area. This is an indication that the area selected for the study is malarious and known to have malaria transmission. More than half (65.9%) of the respondents who claimed to know or have heard of malaria, reported malaria to be transmissible. The rest (34.1%) reported that malaria cannot be transmitted from infected person to healthy ones or they have no idea about it at all. Among those who knew that malaria is transmitted, 91.2% reported mosquito bite as a means of transmission. These are encouraging results and show the presence of a better knowledge in the method of malaria transmission however despite good knowledge about malaria transmission, this study also revealed evidence of knowledge gaps about malaria by some respondents misconception that that malaria is transmitted through drinking contaminated water, eating contaminated food, staying in the sun and working in rain.
Over 92.0% of the patients in this study reported that malaria is preventable. Over 75% of the patients who reported malaria are preventable stated taking tablets and use of bednets as methods of malaria prevention however only 8.5% use bednets. Discomfort, primarily due to heat, and perceived (low) mosquito density were the most widely identified reason for non-use of mosquito net. There were concerns by respondents about higher prices of mosquito nets to the extent of not being affordable by some respondents.
Malaria infection was high in HIV positive patients with CD4 count less than 200 cells/μl. Mild to moderate anemia was frequent in HIV positive patients but severe anemia was not prevalent in the study population. Almost all study participants with malaria were found to be anemic. This confirms the association between malaria and anemia. Future studies should compare prevalence of malaria co-infection among HIV/AIDS Sero-positive individuals and non HIV/AIDS individuals with malaria.
We are grateful to the staff of Holy Family Hospital Techiman especially the staff of the Anti-Retroviral Treatment (ART) clinic and to Mr. Christopher Nkrumah (Methodist Hospital – Wenchi) for his help and support.
- Asante PK, Zandoh C, Dery DB, Brown C, Adjei G, Antwi-Dadzie Y, et al. ‘Malaria epidemiology in the Ahafo area of Ghana’. Malar J. 2011;10:211.View ArticlePubMed CentralPubMedGoogle Scholar
- Palella FJ, Delaney KM, Moorman AC, Loveless MO, Fuhrer J, Satten GA, et al. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. N Engl J Med. 1998;338(13):853–60.View ArticlePubMedGoogle Scholar
- Frontiera M, Myers AM. ‘Peripheral blood and bone marrow abnormalities in the acquired immunodeficiency syndrome’. West J Med. 1987;147:157.PubMed CentralPubMedGoogle Scholar
- Huff B. HIV and malaria: Two intertwining epidemics’. Am Found Aids Res. 2000;6:1–5.Google Scholar
- World Health Organization. World Malaria Report. Geneva: WHO; 2012.Google Scholar
- Badu K, Brenya RC, Timmann C, Garms R, Kruppa TF. Malaria transmission intensity and dynamics of clinical malaria incidence in a mountainous forest region of Ghana. MWJ. 2013;4:14.Google Scholar
- Murphy SC, Breman JG. Gaps in the childhood malaria burden in Africa: cerebral malaria, neurological sequelae, anemia, respiratory distress, hypoglycemia, and complications of pregnancy. Am J Trop Med Hyg. 2001;64:57–67.PubMedGoogle Scholar
- Ministry of Health. Annual Report of the Ghana National Malaria Control Programme. Ghana: Ghana Health Service; 2006.Google Scholar
- UNAIDS World AIDS Day report 2012, Regional fact sheets 2012. http://www.unaids.org/enresources/campaigns/20121120_globalreport2012/factsheet/
- Sentinel Survey Report HIV. Republic of Ghana and Ghana Health Service. 2009.Google Scholar
- Abu-Raddad LJ, Patnaik P, Kublin JG. Dual infection with HIV and malaria fuels the spread of both diseases in sub-Saharan Africa. Science. 2006;314(5805):1603–6.View ArticlePubMedGoogle Scholar
- Grimwade K, French N, Mbatha DD, Zunga DD, Dedicoat M, Gilks CF. HIV-infection as a co-factor for severe falciparum malaria in adults living in a region of unstable malaria transmission in South Africa. AIDS. 2004;18:547–54.View ArticlePubMedGoogle Scholar
- Bretlinger PE, Behren CB, Micek MA. Challenges in the concurrent management of malarial and HIV in pregnancy in sub-Saharan Africa’. Lancet Infect Dis. 2006;6(2):100–11.View ArticleGoogle Scholar
- Guyatt HL, Snow RW. 'Malaria in pregnancy as an indirect cause of infant mortality in sub-Saharan Africa’. Trans R Soc Trop Med Hyg. 2001;95(6):569–76.View ArticlePubMedGoogle Scholar
- Owusu-Agyei S, Poku Asante K, Adjuik M, Adjei G, Awini E, Adams M, et al. Epidemiology of malaria in the forest-savanna transitional zone of Ghana. Malar J. 2009;8:220.View ArticlePubMed CentralPubMedGoogle Scholar
- Browne ENL, Frimpong E, Sievertsen J, Hagen J, Hamelmann C, Dietz K, et al. Malariometric update for the rainforest and savannah of Ashanti region, Ghana. Ann Trp Med Parasitol. 2000;94(1):15–22.View ArticleGoogle Scholar
- Guyatt HL, Snow RW. The epidemiology and burden of Plasmodium falciparum-related anemia among pregnant women in sub-Saharan Africa. Am J Trop Med Hyg. 2001;64:36–44.PubMedGoogle Scholar
- Mocroft A, Kirk O, Barton SE, Dietrich M, Proenca R, Colebunders R, et al. Anaemia is an independent predictive marker for clinical prognosis in HIV-infected patients from across Europe. EuroSIDA study group. AIDS. 1999;13:943–50.View ArticlePubMedGoogle Scholar
- FO T k, Parise ME, Verhoeff FH, Udhayakumar V, Newman RD, MA V e, et al. The Burden of Co-infection with human immunodeficiency virus type 1 and malaria in pregnant women in Sub-Saharan Africa. Am J Trop Med Hyg. 2004;71(Suppl):41–54.Google Scholar
- Cohen C, Karstaedt A, Frean J, Thomas J, Govender N, Prentice E, et al. ‘Increased prevalence of severe malaria in HIV-infected adults in South Africa’. Clin Infect Dis. 2005;41:1631–7.View ArticlePubMedGoogle Scholar
- Meidani M, Rezaei F, Maracy MR, Avijgan M, Tayeri K. ‘Prevalence, severity, and related factors of anemia in HIV/AIDS patients’. J Res Med Sci. 2012;17(2):138–42.PubMed CentralPubMedGoogle Scholar
- Aase B, Sam P, Nina L, Bjorn B. ‘Falciparum malaria and HIV-1 in hospitalized adults in Maputo, Mozambique: does HIV-infection obscure the malaria diagnosis?’. Malar J. 2008;7:252.View ArticleGoogle Scholar
- Onyenekwea CC, Ukibea N, Meludub SC, Ilikac A, Abohb N, Ofiaelid N, et al. ‘Prevalence of malaria as co-infection in HIV-infected individuals in a malaria endemic area of southeastern Nigeria’. J Vector Borne Dis. 2007;44:250–4.Google Scholar
- Hambleton J. ‘Hematologic complications of HIV infection. Oncology. 1996;10:671–80.PubMedGoogle Scholar
- Blake M, Sherer R. Management of the Adverse Effects of Antiretroviral Therapy and Medication Adherence. Clin Infect Dis. 2000;30 Suppl 2:S96–116. doi:10.1086/313859.Google Scholar
- Lamikanra AA, Brown D, Potocnik A, Casals-Pascual C, Langhorne J, Roberts DJ. Malarial anaemia: of mice and men. Blood. 2007;110:18–28.View ArticlePubMedGoogle Scholar
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