Professional Documents
Culture Documents
BY
NOVEMBER, 2023.
i
INFLUENCE OF LONG TERM EXPOSURE TO SCHISTOSOMIASIS ON
COGNITIVE AND REPRODUCTIVE FUNCTIONS AMONG THE MIDDLE AGE
WOMEN IN EBUTTE IGBOORO, YEWA NORTH LOCAL GOVERNMENT, OGUN
STATE.
BY
NOVEMBER, 2023.
ii
CERTIFICATION
This is to certify that the research work titled “Influence of long-term exposure to
Schistosomiasis on cognitive and reproductive functions among the middle age women in
Ebute Igbooro Yewa North, Ogun State” was carried out by AKANBI, MORENIKEJI
OLUWAFOLAKEMI, matric number; H/ST/21/2083 under the supervision of Mr. A
Adewole and Mrs. Popoola in the Department of Science Laboratory Technology.
__________________________
Mr. A. Adewole
__________________________
Mrs. Popoola
__________________________
iii
DEDICATION
I dedicate this work to the Abba father who is faithful in all things and in whom all
achievement in life are made possible, and my parents who gave me the support to achieve
my dream at their expense. Without them, this project would not have been possible.
iv
ACKNOWLEDGEMENTS
It is my pleasure to register my profound appreciation and gratitude for the moral, financial
support, advice and cooperation received from various people at different stages of this
research work and eventual completion of my course of study in this great citadel of learning.
Firstly, I express my sincere gratitude to my supervisor, Mr. Adewole Adekanmi and co-
supervisor Mrs. Popoola for their patience, enthusiasm, insightful comments and parental
advice in the course of carrying out the research work. Their knowledge and professional
expertise in research work has enabled me to complete this research work successfully.
I also express my sincere thanks to my parents Mr. and Mrs. Festus Akanbi, for their prayers,
love, care, and financial support throughout my academic pursuit; you will live long in good
health and wealth eat the fruits of your labor in Jesus name (Amen).
I would also be ungrateful if I did not acknowledge Dr Oyedeji, Mr. F.T Faparusi, Mrs. F.O
Abdulsalam, and all the lecturers for their impartation of knowledge.
I am also grateful to my friends; Yakub, Micheal, Ayobami, Esther, Aishat, Akorede,
Oreoluwa, John, to mention but a few, for their supports, love and care towards me.
Finally, I am extremely grateful to all Flakkie shiners and my siblings for their financial
support towards the success of this project. Thanks for all you do.
To God be the glory great things he has done.
Thank you all for everything!
v
ABSTRACT
This research work is aimed at the assessment of the influence of long term exposure
to Schistosoma on cognitive and Reproductive functions among the middle age
woman in Ebute Igbooro, Yewa North, Ogun State. The study was descriptive and data
were collected from 50 participant using a purpose designed, and structured questionnaire to
assess their knowledge, perceptions, and practices, in relation to the disease on cognitive and
reproductive functions. Urine analysis was used to determine urinary schistosomiasis
infection. The association test carried out revealed a p-value higher than 0.05 between
how long and symptoms (x2=2.014, ₚ=0.156), thinking and symptoms (x 2=1.891,
ₚ=0.595), forget names and symptoms (x2=1.866, ₚ=0.760), how long and inflammation
(x2=1.043, ₚ=0.594), age and RDT test (x2=1.295, ₚ=0.730), age and microscopy
examination (x2=1.295, ₚ=0.730), blood urine and RDT test (x2=0.378, ₚ=0.539), (table
4.3-4.9). It was concluded that schistosomiasis is a serious public health problem that
has a negative impact on the cognitive and reproductive functions among humans and
must not be taken for granted. It was recommended that mass drug administration
(PRAZIQUANTEL), community mobilization and health education regarding the cause,
transmission and prevention of schistosomiasis and education about good personal and
sanitary hygiene practices should be considered in order to significantly reduce the
exposure and morbidity of infection within these communities.
vi
TABLE OF CONTENTS
Title Page i - ii
Certification iii
Dedication iv
Acknowledgements v
Abstract vi
List of Tables ix
1.0 Introduction 1
CHAPTER TWO
CHAPTER THREE
3.2 Materials 14
3.3 Methods 14
3.5.2 Treatment 16
CHAPTER FOUR
4.1 Results 17
4.2 Discussion 34
viii
CHAPTER FIVE
5.1 Conclusion 37
5.2 Recommendation 37
REFERENCES 38
APPENDIX 44
ix
LIST OF TABLES
x
CHAPTER ONE
1.0 INTRODUCTION
Schistosoma primarily infecting man. (Webbe, 1981). There are five (5) main species that
schistosome species are parasites of animals and birds some of which occasionally hybridize
with human schistosomes (Webbe, 1981). The different species exhibits distinct difference
pertaining to size, the intermediate host and final location in the definitive host and the
number and morphological features of the eggs laid by the adult worms (Webbe, 1981).
Adult males and females of S. heamatobium reside in the venules of the pelvic plexus while
the other species S. mansoni, S. japonicum, S. intercalatum, S. mekongi are found in the
mesenteric veins.
Schistosoma trematode worms, which lives in the blood stream of human (Steinmann
et al., 2006). The World Health Organization (WHO) regards the disease as a neglected
tropical disease, with an estimated 732 million persons being vulnerable to infection
world – wide (WHO, 2004). Steinmann and co-workers documented that over 200
million individual from Africa, Asia and South – America are infected with this
disease (Steinmann et al., 2013). The World Health Organization (WHO) further
estimated that schistosome infections and geo-helminths account for over 40% of the
world tropical disease burden with the exclusive of malaria (Olve Du et al., 2013).
Human get infected with disease when they make contact with water contaminated
1
with the skin – penetrating cercariae (WHO, 2014). Approximately 120 million
individual in sub – Saharan Africa have Schistosomiasis – related symptoms while about
al., 2009). Morocco and some Caribbean Islands countries have made significant
progress on controlling the disease while Brazil, China and Egypt are taking steps
rampant in poor rural communities especially place where fishing and agricultural
activities are dominant. Domestic activities such as washing clothes and fetching in
the infected water exposes woman and children to infection. Recreational activities
like swimming and poor hygiene also make children vulnerable to Schistosomiasis
(WHO, 2014).
The intermediate freshwater snail inhabit calm and slowly moving freshwater lakes,
rivers, ponds or steam. The rate of infection in human increases Subsequently, the
parasites eggs are released into the feaces or urine where they remain alive for about
seven (7) days. When get into fresh water, miracidium is released from the egg with
the aid of chemical stimuli and light, the miracidium seeks the fresh water snails
which is its intermediate host. On locating the snail, the miracidium penetrate it and
al., 2006). After 4-6 weeks of infecting the snail, the cercariae leave the snail and
gyrate around for about 72 hours looking for the skin of a prospective host. Once
released from the snail the cercariae are investigated by light mainly during the day
2
time. On locating the human host skin, the cercariae burrow into it, migrate into the
blood through the liver and lungs and undergo transformation into Schistosomula also
(Aray et al., 2006). Microscopic examination of urine is the gold standard for
detection (diagnosis) of Schistosoma infection. The schistosome eggs are easily seen
and identified on microscope due to its peculiar size and shape, and possession of a
Saharan Africa (WHO, 2009). Adult S. haematobium worms inhabits blood vessels
surrounding the urinary bladder and female genital tract and lay eggs that migrate
commonly in the urinary bladder cervix and vagina, vagina bleeding, pain during
sexual intercourse and modules in the vulva (WHO, 2009). There may be long-term
irreversible consequence, including infertility (WHO, 1998; 1999). Previous policy has
excluded pregnant and lactating women from the control of Schistosomiasis using
Praziquantel treatment (WHO, 1998; 1999) but this policy was rescinded following a
3
1.1.2 Schistosomiasis infection on the cognitive functions of preschool age
children.
affected by the disease for decade, as they account for 123 million of total global
burden of over 250 million people infected (Nelwan, 2019). Schistosomiasis affects
multiple body systems such as the Urogenital, gastrointestinal, respiratory and nervous
systems (Antiwi et al., 2014; de Cleve et al., 2004). The impact of the infection within
the nervous system has been linked to learning difficulties, poor school performance,
growth retardation and cognitive deficits (Development pfc, 2002; Ezeamama et al.,
particularly in region that have poor water supply and sanitation facilities (Hotezp et
al., 2006).
first five years of early childhood development is crucial as it has an impact on the
future success of the child in school, workspace as an adult, and many aspect of a
healthy fulfilling life. The first five years of childhood is characterized by rapid
growth and development of brain (Learning CCO, 2009-2010; Plos Negi, 2018). A
Domestic activities such as washing clothes and fetching in the inflected water
exposes woman and children to infection. Recreation activities like swimming and
4
time exposure to this infection has been known to have impacts on the cognitive functions in
endemic environment.
Ebute Igbooro is endemic for the disease; therefore a study of this nature could provide a
This research work is aimed at the assessment of the influence of long term exposure
to Schistosoma on cognitive and Reproductive functions among the middle age woman
in Ebutte Igbooro.
2) To determine the effects of this on cognitive and reproductive function among the
5
CHAPTER TWO
early adulthood. Survival of the mature worms normally ranges from 2.5 – 12years,
but there have been reported of woman living for up to 30years (Vermund, 1983).
body including the Urinary System. (Smith andSmith Christineand Christine, 1986).
Noted that hydroureter usually precedes hydronephrosis and that Schistosoma hydro
nephrosis pases from progressive renal pelvic dilation to medullary atrophy and finally
Shortly after penetration of the cercariae (within a few hours). A pruritic popular rash
can occur at the site of penetration. The skin manifestation mainly occurs in migrants
and tourists coming into contact with schistosomes for the first time.
6
Two to 10weeks after the initial infection, the katayama syndrome can develop
mainly in non – immune visitors to endemic areas and more severe after S.mansoni
illness. The most common clinical findings are fever, anorexia, headache, abdominal
infection, the pathological changes observed in the bladder wall is duding among others
granulomas consisting of eggs and different type of inflammatory cell, sandy patches
as a result of dead and calcified eggs and polypoid lesions, the extent of which
depends on the intensity and duration of infection. This is more common in children
and young adults (Garba, et al., 2006). In highly endemic areas, bladder lesions can
be detected in up 89% of the population and major bladder lesion in 44% (Hatz et
al., 2001). The lesion produce the early symptoms (terminal) hematuria, dysuria,
urinary frequency and supra public pain. It has been suggested that loss of blood
causes Anemia (Farid et al., 1968). Hematuria is the most common signs of urinary
Schistosomiasis and it has been estimated that infected individual loose between 2.6
and 12.6 millimeters of blood per day. (Tarid et al., 1968). In a well-designed cross
decreased hemoglobin and decreased iron in adults, after adjusting for measure of
7
socio economic status, malaria and hook worm (Tatala et al., 1998). In school
children (aged 5 - 14years), adolescents and adult (aged > 15years) and the presence
1999).
Eggs deposited in the tissue of the ureters can obstructive uropathy, thus hydroureter
that presence of lesion was related to the intensity of infection both on individual and
infection can lead to bladder cancer and kidney failure whereas chronic S.mansoni
infection can lead to hematemesis, and heavy S.japonicum infection to liver cirrhosis,
which is a risk factor for colon and liver cancer (Utzinger, et al., 2011).
the educational, learning and memory domain (Ezeamama et al., 2018). However, to
date there is paucity of research that shows the direct and indirect health development
treatment in the age group. Although the mechanisms of how schistosomiasis cause
cognitive deficits is unknown, it has been suggested that inflammatory mediators could
Vitkoviz et al., 2000; Miller, 2009; Monje, Toda & Palmer, 2003).
8
Studies of S.haematobium epidemiology and denical manifestation have focused
attention, although, histopathogical studies have demonstrated that the female and male
internal genitals are sites of egg – induce granulomatous inflammation (Gelfand, 1971;
Wright, 1982). In a number of clinical studies of the woman living in the area where
with characteristic sandy patch lesson in the cervix and in the virginal (Poggensee, 2000;
Poggensee, 2001; Kjetland, 2006). Egg have also been detected in ejaculated from
most area of endemicity, infection prevalence and intensity normally peak during the
second decade of life (Serieye, 1996; Kwriba, 2005). On the community level infected
S.haematobium to the community through passage of egg in urine to the local water
bodies (Cohan, 1997; Chan, 2007). Chronic female genital – tract inflammation caused
by S.haematobium has been associated with Virginal itching and discharge, (Poggensce
et al., 2006, Kjetland, 2008) post – coital bleeding, (Poggensee, 2000) Genito pelvic
30years of age (Jennifer et al., 2011). These young woman who also have the highest
risk of incident HIV infection and in whom genital lesions may be reversible if
treated early, should be the focus of public health interventions aimed to reduced the
9
The health status of a woman before pregnancy is a crucial determinant of gestational
morbidity and pregnancy outcome. Poor nutritional status, deprived living environment
and higher rates of infection diseases contribute to maternal mortality, infant mortality
and low Birth Weight (WBW) (Kramer, 1987; Hasin et al., 1996; Kramer & Victoria,
2001) in Lesser – Developed Countries (LDCs). Woman who are under weight or
shout and those with anemia or infection are at increased risk of delivering
underweight infants (Steketee, 2003; Kramer, 2003) since, Schistosomiasis causes both
anemia (MC – garvey et al., 1996; Friedman et al., 2005; Leenstra, 2006) and under
Giese et al., 1996). Treatment of high risk group would be beneficial to both the
can cause growth retardation, fatigue, weakness, impairment of memory and cognitive
al., 2011). A study among Zimbabwean women showed that women with
S.haematobium egg in their pap smear had a risk three times higher of having HIV
(Friedman et al., 2007). Another study in Tanzania linked the delivery of Low Birth
10
Weight (LBW) babies to infection with parasitic disease including Schistosomiasis
to various environmental and socio – economic factors such as; Climatic changes
whose local infection and geographical expansion is influenced by climatic change and
global warming (Mas–coma et al., 2009). Rainfall patterns also have an effect on the
responsible for S.mansoni transmission during the raining season, while during the dry
Sellin ; 1999).
The schistosome parasite required an avenue where in there is direct contact between
the molluscan intermediate snail and the final human host for transmission of
population live close to various open water bodies which are infested with the
intermediate snail host necessary for the disease (Steinmann et al., 2006).
dams for agricultural purposes and electricity generation also are responsible for
11
(Fenwick et al., 2009). Construction of dams led to remarkable increase in cases of
Senegal, Cote dIvoire, Ghana, Mali, Namibia, and Cameroon (Olveda et al., 2013).
Steinmann and co-workers estimated that 13.6% (106 million) of people vulnerable
A study carried out in Yewa North Local Government of Ogun State, Nigeria
buttressed the fact that schistosomiasis exists among pregnant women. The study
20.8% of S. haematobium infection was observed, with the younger pregnant women
at greater risk of the infection, which is in consonance with a previous report from
Tanzania. It was also observed that the prevalence recorded within pregnant mothers
in Yewa North was obviously lower compared with earlier reports from similar
population groups due to a taboo in that part of the country restricting pregnant
women from visiting natural water bodies (Salawu and Odaibo; 2013).
Praziquantel (P2Q) was made available in 1997 and has been the minister of
Schistosomiasis control program for decades (Davis et al., 1981). Praziquantel has not
been studies in pregnant or lactating women (middle age women) and was therefore,
studies but lack safety data from studies in pregnant woman. In practice, this has led
12
– endemic countries. This is important in that woman aged 18-25years who live in
schistosomiasis – endemic region might spend almost 25% of their reproductive life
pregnant and 60% of their reproductive time lactating – delay in treatment of more
than one year results in significant morbidity among non-pregnant women (Coutinho,
2006; been Stra, 2006) and such morbidity could be further exacerbated in pregnant
indicated that all Schistosome – infected pregnant and lactating (middle aged) women
should be considered a high – risk group and Allen, 2002 suggested treatment be
the cost of withholding treatment on the expected morbidity that would be suffered
during long periods of pregnancy and lactating. In the cost benefit analysis, an
emphasis was placed in examining the morbidity that woman would be expected to
experience, specially Schistosomiasis induced organ damaged, which can progress over
relatively short periods of time, anemia and pathologies that are largely reversible
when treated early, such as hepatomegaly and urinary tract pathology. Despite this
not adopted this policy because of a lack of pregnancy safety data that had been
13
CHAPTER THREE
The study was conducted in Ebute Igbooro village which is located in Yewa North,
Ogun State, its geographical coordinates are 6 54 ‘0’ East and its Original name
The case control study was conducted among the middle aged women who are
women. A case was determined as a middle aged women who had at least one egg in
their Urine sample following screening with the Urine filtration techniques and
microscopy (Mott’k et al., 1982) and the sampling method was purposive making use
of 50 respondent.
Hand gloves, Hand sanitizer, Sterile urine bottle, Urine samples, Nose cover,
The anthropometric measurements were carried out according to Weiner and Laurice
(Weiner & Laurice, 1969). The respondents measurements were measured with scales
14
3.4.1 ADMINISTRATION OF QUESTIONNAIRES
Structured questionnaires were administered to the respondent middle age women before
collecting their urine samples. The women were interviewed and the questionnaires were
filled on behalf of the respondent for proper record of the data. Demographic data
obtained were sex, age, occupation, house number, community, weight, their place of
birth, stay outside the community sometimes, how long they have been in the
Transparent, capped, sterile, plastic, universal containers also known as urine bottles,
were labeled and was given to the middle age women to collect their urine samples.
2.00pmto 2.00pm. The urine collected was taken immediately to the laboratory for
analysis and the ones that were not allowed to be taken away were tested
immediately with the hematocrit urine test strip to check for the presence of blood,
A reagent strip (Urine- 10 parameters, Cypress Diagnostic (DUS 10 and Uro dip 10)
was carefully dipped into the universal sterile bottle containing the urine for 5
seconds. The resulting change in color of the strip were compared with the
manufacturers color chat to estimate the amount of blood in the urine and also to
15
3.5.1 MICROSCOPIC EXAMINATION FOR SCHISTOSOMIASIS
HAEMATOBIUMSCHISTOSOMIASIS HAEMATOBIUM
10ml of the urine samples were spined with the centrifuge machine at 500rpm for 5
minutes. The supernatant was then discarded to leave the sediment which was then
transferred to the center of a sterile, clean microscope slide to which cover slip were
added. It was then placed or mounted on a light microscope which was examined at
terminal spine. The eggs in infected urine will show a cylindrical shaped with two
3.5.2 TREATMENT
Treatment of all infected member will follow the baseline survey and all infected
middle age women will receive a single dose of 40mg/kg of praziquantel drugs.
Provincial Permission was granted by the Medical Research Council of the Federal
Polytechnic Ilaro, and District Medical Directors and the king of the Ebutte Igbooro
where the participants( middle age women) resides. The study goals and methodology
were explained in the local language( Yoruba) to the king and the participants. The
king instructed his town crier to make an awareness to the community on our behalf
for the recruitment of the middle age women to participate during the study.
basis.
16
CHAPTER FOUR
A total number of 50 middle aged women were enrolled using purposive sampling.
Questionaires wereQuestionnaires usedwere toused obtainto obtain data fromdata
allfrom respondentsall respondents.
TABLE 4.1: Showing the Influence of long term to Schistosomiasis in relation to socio
demographics of middle age women exposure
AGE
25-30 31 62
31-35 8 16
36-40 10 20
41-50 1 2
OCCUPATION
Farming 21 42
Fishing 6 12
Trading 15 30
Others 8 16
TABLE 4.1: Shows the demography variable of the respondent, where the female is the only
sex who responded while (62%) of the age group 25-30 years has the highest and the lowest
is (2%) of 41-50 year.
17
18
Table 2: shows the respondents associationrespondents association of AGE and
SYMPTOM
symptoms Total
yes no
31-35 Count 3 5 8
40-45 Count 2 8 10
46-50 Count 0 1 1
Total Count 12 38 50
This table shows a non-significant, that means no effect was observed between age and
symptoms.
19
A bar chart showing the relationship between AGE AND SYMPTOMS
20
Table 4.3: showing the Influence of long-term exposure to Schistosomiasis in relation to
reproductive functions among the middle age women respondents using their
relationship between HOW LONG and SYMPTOMS
How
long
YES 18.9% 81.1% x2=2.014
This table shows a non-significant, that means no effect was observed between how long and
symptoms.
21
A bar chart showing the relationship between HOWLONG AND SYMPTOMS
22
Table 4.4: showing the Influence of long-term exposure to Schistosomiasis in relation to
cognitive functions among the middle age women respondents using their relationship
between THINKING and SYMPTOMS
yes no
thinki Never 0 2
ng
Occasi 0 3 x2=1.891
onally
Quite 1 4 ₚ=0.595
often
Very 11 29
often
Total 12 38 50
This table shows a non-significant, that means no effect was observed between thinking and
symptoms
23
A bar chart showing the relationship between THINKING AND SYMPTOMS
24
Table 4.5: showing the Influence of long term exposure to Schistosomiasis in relation to
cognitive functions among the middle age women respondents using their relationship
between FORGET NAMES and SYMPTOMS
Yes No
Never 1 3 x2=1.866
Occasionally 2 8
Quite often 0 4
Very often 8 19
Total 12 38 50
This table shows that at p value of 0.05, there is a non-significant, that means no effect was
observed between forget name and symptoms.
25
A bar chart showing the relationship between FORGET NAME AND SYMPTOMS
26
Table 6: showing the Influence of long term exposure to Schistosomiasis in relation to
cognitive functions among the middle age women respondents using their relationship
between HOWLONG and INFLAMMATION
How
long
YES 2.7% 64.9% 32.4% x2=1.043
This table shows a non-significant, that means no effect was observed between how long and
inflammation.
27
A bar chart showing the relationship between HOWLONG AND INFLAMMATION
28
Table 4.7: showing the Influence of long term exposure to Schistosomiasis in relation to
cognitive and reproductive functions among the middle age women respondents using
their relationship between AGE and RDT TEST
RDT Test of
Variable +VE -VE significant
age 25-30 3 28 x2=1.295
31-35 1 7 ₚ=0.730
36-40 0 10
41-45 0 1
Total 4 46
Table 7 shows a non-significant association between AGE and RDT TEST
29
A bar chart showing the relationship between AGE and RDT test
30
Table 4.8: showing the Influence of long term exposure to Schistosomiasis in relation to
cognitive and reproductive functions among the middle age women respondents using
their relationship between AGE and MICROSCOPY EXAMINATION.
MICROSCOPY Test of
Variable +VE -VE significant
age 25-30 3 28 x2=1.295
31-35 1 7 ₚ=0.730
36-40 0 10
41-45 0 1
Total 4 46
Table 8 shows a non-significant between AGE and MICROSCOPY EXAMINATION
31
A bar chart showing the relationship between AGE and MICROSCOPY
EXAMINATION.
32
Table 4.9: showing the Influence of long-term exposure to Schistosomiasis in relation to
cognitive and reproductive functions among the middle age women respondents using
their relationship between BLOOD URINE and RDT test
RDT Test of
Variable +VE -VE significant
bloodu
4 x2=0.378
rine yes 0
no 4 42 ₚ=0.539
Total 4 46
Table 9 shows a non-significant between BLOOD URINE and RDT test
33
A bar chart showing the relationship between BLOOD URINE and RDT test
4.2 Discussion
34
Schistosomiasis is more rampant in poor rural communities especially place where
fishing and agricultural activities are dominant. Domestic activities such as washing
clothes and fetching in the infected water exposes woman and children to infection.
Recreational activities like swimming and poor hygiene also make children vulnerable
to Schistosomiasis (WHO, 2014). Human get infected with disease when they make
contact with water contaminated with the skin – penetrating cercariae (WHO, 2014).
presentation of the disease (Chitsulo et al., 2013). This research work is aimed at the
showed 25-30 years were 31(62%), 31-35 years were 8 (16%), 36-40 years were 10
(20%), while 41-50 was the least year in the study with 1(2%). The demography
variable of the respondent, where the female is the only sex who responded while (62%) of
the age group 25-30 years has the highest and the lowest is (2%) of 41-50 year is similar to
Jennifer, et al., (2011). All of them the were female 50 (100%). The influence of long
exposure among the middle age women on reproductive functions is in line with the
study of WHO, (1994). The respondents occupation showed farming 21(42%), fishing
6(12%), trading 15(30%), while others were 8(16%). Table 4.2 shows respondents
association of age and symptoms where age 25-30years 7(22.6%) can describe the
35
symptoms while 24(77.4%) can not describe the symptoms, 31-35years 3(37.5%) can
described the symptoms while 5(62.5%) cannot describe the symptoms, 40-45years
2(20.0%) can described the symptoms while 8(80.0%) cannot described the symptoms,
46-50years 0(0.0%) can described the symptoms while 1(100.0%) cannot described
the symptoms. Table 4.3 shows respondents association to how long and symptoms
where 24.0% can described the symptoms while 76.0% cannot described the
where 12(24%) do read something and find they have not been thinking about it
and must read it again, while 38(76%) do read something and find they have been
thinking about it and must not read it again. Table 4.5 shows respondent’s
association to forget names and symptoms where 12(24%) do forget people’s names
while 38(76%) do not forget people’s names. Table 4.6 shows respondent’s
18(36.0%) have never experience inflammation of the genital. Table 4.7 reveals
respondent’s association to Age and RDT test where 25-30years has 3(+ve) and 28(-
ve), 31-35years has 1(+ve) and 7(-ve), 36-40years has 0(+ve) with 10(-ve), while age
41-45years has the least RDT test significant of 0(+ve) with 1(-ve). Table 4.8 reveals
3(+ve) and 28(-ve), 31-35years has 1(+ve) and 7(-ve), 36-40years has 0(+ve) with
10(-ve), while age 41-45years has the least microscopy examination of 0(+ve) with 1(-
ve). Table 4.9 reveals the respondent’s association to blood urine and RDT test where
4(+ve) are present and 46(-ve) to the test. A recent intervention program and drug
administration for the infection was active at the time of the study and such influence
as the one gotten in this study is expected to reduce drastically as the intervention
36
program persists. The major problem in this study is attributed to the living pattern
and mentality of the respondents in this study that majorly exposed themselves to
predisposing factors that expose them to the disease. The various study of Betson, et
al., have reported on the prevalence of schistosome infections on primary school age
children, yet the impact on early childhood development has not yet been realized
and quantified. The association test carried out revealed a p-value higher than 0.05
between how long and symptoms (x 2=2.014, ₚ=0.156), thinking and symptoms
(x2=1.891, ₚ=0.595), forget names and symptoms (x2=1.866, ₚ=0.760), how long and
inflammation (x2=1.043, ₚ=0.594), age and RDT test (x2=1.295, ₚ=0.730), age and
microscopy examination (x2=1.295, ₚ=0.730), blood urine and RDT test (x2=0.378,
37
CHAPTER FIVE
5.1 Conclusion
reproductive and cognitive functions among the middle age women of Ebutte Igbooro
community of Nigeria and the participants knowledge about the disease is poor. This
study reveals that knowledge about the cause, transmission, symptoms, and prevention
of schistosomiasis among the rural population in Ebutte was inadequate and that this
communities.
It is also concluded that schistosomiasis is a serious public health problem that has a
negative impact on the cognitive and reproductive functions among humans and must
5.2 Recommendation
and education about good personal and sanitary hygiene practices should be
38
Also, portable water should be provided in the community with other basic amenities
to promote the level of good living in the rural communities, therefore avoiding the
39
REFERENCES
Allen, H. E., Crompton D.W., de Silva N., LoVerde P.T., Olds G.R. (2002). New policies for
using anthelmintics in high risk groups. Trends Parasitology, 18:381-382.
Antwi S, Aboah K, Saprong C. The unacknowledged impact of urinary schistosomiasis in
children: 5 cases from Kumasi, Ghana. Ghana Med J. 2014;48(4):228–33.
Beasley, N. M., Tomkins, A. M., Hall, A., Kihamia, C. M. and Lorri ,W. (1999). The impact
of population level deworming on the haemoglobin levels of schoolchildren in
Tanga, Tanzania. Tropical Medicine International Health 4: 744– 750.
Betson M, Sousa-Figueiredo JC, Rowell C, Kabatereine NB, Stothard JR. Intestinal
schistosomiasis in mothers and young children in Uganda: investigation of field-
applicable markers of bowel morbidity. Am J Trop Med Hyg. 2010;83(5):1048
Brooker S. Spatial epidemiology of human schistosomiasis in Africa: risk models,
transmission dynamics and control. Trans R Soc Trop Med Hyg. 2007;101:1–8.
Bundy D. School health and nutrition: policy and programs. Food Nutr. Bull.
2005;26(2_suppl2):186-S92.
Chen, L., Jha, P., Stirling B., et al. (2007). for the International Studies of HIV/ AIDS (ISHA)
Investigators. Sexual risk factors for HIV infection in early and advanced
epidemics in sub-Saharan Africa: systematic overview of 68 epidemiological
studies. PLoS ONE 2:e1001.
Chitsulo L, Engels D, Montresor A, Savioli L. The global status of schistosomiasis and its
control. Acta Trop. 2000;77:41–51.
Cohen, M.S., Hoffman, I. F., Royce, R.A., et al. (1997). Reduction of concentration of HIV-1
in semen after treatment of urethritis: implications of HIV1. AIDSCAP Malawi
Research Group. Lancet 349:18.
Coutinho, H.M. et al. (2005). Nutritional status and serum cytokine profiles in children,
adolescents, and young adults with Schistosoma japonicum-associated hepatic
fibrosis, in Leyte, Philippines. Journal of Infectious Diseases. 192: 528– 536.
Coutinho, H.M. et al. (2006). Nutritional status improves after treatment of Schistosoma
japonicum-infected children and adolescents. Journal of Nutrition 136: 183–188.
Davis, A., Biles, J. E., Urich, A. M and Dixon, H. (1981). Tolerance and efficacy of
praziquantel in phase IIA and IIB therapeutic trials. Arzneimittel Forschung Res
33:56.
De Cleva R, Herman P, Pugliese V, Zilberstein B, Saad WA, Gama-Rodrigues JJ. Fathal
pulmonary hypertension after distal splenorenal shunt in schistosomal portal
hypertension. World J Gastroenterology: WJG. 2004;10(12):1836.
40
Development PfC. Heavy schistosomiasis associated with poor short-term memory and
slower reaction times in Tanzanian schoolchildren. Tropical Med Int Health.
2002;7(2):104–17.
Doherty, J. F., Moody. A. H. and Wright, S. G. (1996). Katayama fever: an acute
manifestation of schistosomiasis. British Medical Journal 313: 1071 – 1072.
Dreyfuss ML, Msamanga GI, Spiegelman D, et al. Determinants of low birth weight among
HIV-infected pregnant women in Tanzania. Am J Clin Nutr. 2001;74:814–26.
Durand, F., Brion, J. P, Terrier, N., Pinel, C. and Pelloux, H. (2004). Funiculitis due to
Schistosoma haematobium: uncommon diagnosis using parasitologic analysis of
semen. American Journal of Tropical Medicine and Hygine 70: 46–7.
Ernould JC, Ba K, Sellin B. The impact of the local water development programme on the
abundance of the intermediate hosts of schistosomiasis in three villages of the
Senegal River delta. Ann Trop Med Parasit. 1999;93:135–45.
Ezeamama AE, Bustinduy AL, Nkwata AK, Martinez L, Pabalan N, Boivin MJ, et al.
Cognitive deficits and educational loss in children with schistosome infection-a
systematic review and meta-analysis. PLoS Negl Trop Dis. 2018;12(1):e0005524.
Farid, Z., Bassily, S., Schulert, R., Zeind, S., McConnell, E and Abdel Wahab, M. F. (1968).
Urinary blood loses in S. haematobium infection in Egyptian females.
Transactions of the Royal Society of Tropical Medicine and Hygiene 61: 496 –
500.
Fenwick A, Webster JP, Bosque-Oliva E, et al. The schistosomiasis control initiative (SCI):
rationale, development and implementation from 2002 to 2008. Parasitology.
2009;136:1719–30.
Friedman, J.F. et al. (2005). Human schistosomiasis and anemia: the relationship and
potential mechanisms. Trends in Parasitology 21: 386–392.
Friedman JF, Mital P, Kanzaria HK, Olds OR, Kurtis JD. Schistosomiasis and pregnancy.
Trends Parasitol. 2007;23:159–64.
Garba, A., Toure, S., Dembele, R., Bosque-Oliva, E. and Fenwick, A. (2006).
Implementation of national schistosomiasis control programmes in West Africa.
Trends in Parasitology 22: 322–326.
Gelfand, M., Ross, M. D, Blair, D. M, Weber, M. C. (1971). Distribution and extent of
schistosomiasis in female pelvic organs, with special reference to the genital tract,
as determined at autopsy. American Journal of Tropical Medicine Hygine. 20:
846–9. Geneva: WHO; 2003:49.
Gray DJ, Ross AG, Li Y, McManus DP. Diagnosis and management of schistosomiasis. Br
Med J. 2011;342:d2651.
Gryseels B, Polman K, Clerinx J, Kestens L. Human schistosomiasis. Lancet.
2006;368:1106–18.
41
Hatz, C.F.R. (2001). The use of ultrasound in schistosomiasis. Advances in Parasitology, 48,
225-284.
Hasin, A., Begum, R., Khan, M.R. and Ahmed, F. (1996). Relationship between birth weight
and biochemical measures of maternal nutritional status at delivery in a
Bangladeshi urban poor. International Journal of Food Science and Nutrition. 47:
(3) 273-9.
Helling-Giese, G., Kjetland, E. F., Gundersen, S. G, et al. (1996). Schistosomiasis in women:
manifestations in the upper reproductive tract. Acta Tropica. 62: 225-238.
Hennessy E, Gormley S, Lopez-Rodriguez AB, Murray C, Murray C, Cunningham C.
Systemic TNF-α produces acute cognitive dysfunction and exaggerated sickness
behavior when superimposed upon progressive neurodegeneration. Brain Behav
Immun. 2017;
Hotez P, Ottesen E, Fenwick A, Molyneux D. The neglected tropical diseases: the ancient
afflictions of stigma and poverty and the prospects for their control and
elimination. Hot topics in infection and immunity in children III. 2006:23–33.
Jennifer, A. D.,Charles M., Godfrey M. K., Katrina B. M., Heejung B., Harusha S., Samuel
E. K., John M. C., Warren D. J. and Daniel W. F. (2011). Urogenital
Schistosomiasis in Women of Reproductive Age in Tanzania’s Lake Victoria
Region. American Journal of Tropical Medicine and Hygine. 84: (3) 364 – 369.
Kanwai S, Ndams IS, Kogi E, Abdulkadir JS, Gyam ZG, Bechemagbor A. Cofactors
influencing prevalence and intensity of Schistosoma haematobium infection in
sedentary Fulani settlements of Dumbi, Igabi LGA, Kaduna State, Nigeria. Sci
World J. 2011;6:15–9.
Kjetland, E. F., Poggensee, G., Helling-Giese, G., et al. (1996). Female genital
schistosomiasis due to Schistosoma haematobium: clinical and parasitological
findings in women in rural Malawi. Acta Tropica, 62:239–55.
Kjetland EF, Ndhlovu PD, Gomo E, et al. Association between genital schistosomiasis and
HIV in rural Zimbabwean women. AIDS. 2006;20:593–600.
Kjetland, E. F., Kurewa, E. N., Ndhlovu, P. D., Midzi, N., Gwanzura , L., Mason, P. R.,
Gomo, E., Sandvik, L., Mduluza, T., Friis, H. and Gundersen, S. G. ( 2008).
Female genital schistosomiasis—a differential diagnosis to sexually transmitted
disease: genital itch and vaginal discharge as indicators of genital Schistosoma
haematobium morbidity in a cross-sectional study in endemic rural Zimbabwe .
Tropical Medicine and International Health. 13: 1509 – 1517.
Kouriba, B., Traore, H. A, Dabo, A. et al. (2005). Urinary disease in 2 Dogon populations
with different exposure to Schistosoma haematobium infection: progression of
bladder and kidney diseases in children and adults. Journal Infectious Diseases.
192: 2152–9.
Kramer, M. S. (1987). Determinants of low birth weight: methodological assessment and
meta-analysis. Bulletin of World Health Organization. 65: 663– 737.
42
Kramer, M. S and Victora, C. (2001). Low birth weight and perinatal mortality. In: Semba
RD, Bloem MW, eds. Nutrition and health in developing countries. Humana
Press.
Kramer, M.S. (2003). The epidemiology of adverse pregnancy outcomes: an overview.
Journal of Nutrition. 133: 1592S–1596S.
Learning CCo. State of Learning in Canada: A Year in Review, 2009–2010. Executive
Summary. (2010, January 1). The Free library (2010) Retrieved June 04, 2022
from
https://wwwthefreelibrarycom/StateofLearninginCanada:AYearinReview,2009-
2010Executive-a0276752739.
Leenstra, T. et al. (2006). Schistosoma japonicum reinfection after praziquantel treatment
causes anemia associated with inflammation. Infectious. Immunology. 74: 6398–
6407.
Leutscher, P., Ramarokoto, C. E, Reimert, C., Feldmeier, H., Esterre, P., Vennervald, B. J.
(2000). Community-based study of genital schistosomiasis in men from
Madagascar. Lancet 355: 117–8.
Leutscher, P. D. C., Ramarokoto, C. E., Hoffmann, S., Jensen, J. S., Ramaniraka, V.,
Randrianasolo, B., Raharisolo, C., Migliani, R. and Christensen, N. (2008).
Coexistence of urogenital schistosomiasis and sexually transmitted infection in
women and men living in an area where Schistosoma haematobium is endemic.
Clinical Infectious Disease 47: 775 – 782.
Li Y, Ross AG, Hou X, Lou Z, McManus DP. Oriental schistosomiasis with neurological
complications: case report. Ann Clin Microbiol Antimicrob. 2011;10(1):1–5.
Mas-Coma S, Valero MA, Bargues MD. Climate change effects on trematodiases, with
emphasis on zoonotic fascioliasis and schistosomiasis. Vet Parasitol.
2009;163:264–80.
McGarvey, S.T. et al. (1996). Schistosomiasis japonica and childhood nutritional status in
northeastern Leyte, the Philippines: a randomized trial of praziquantel versus
placebo. America Journal of tropical Medicine and Hygiene. 54: 498–502.
McKenna, G., Schousboe, M., Paltridge, G. (1997). Subjective change in ejaculate as
symptom of infection with Schistosoma haematobium in travellers. BMJ journals.
315:1000–1.
Miller AH. Mechanisms of cytokine-induced behavioral changes: Psychoneuroimmunology
at the translational interface. Brain Behav Immun. 2009;23(2):149–58.
Mott K, Baltes R, Bambagha J, Baldassini B. Field studies of a reusable polyamide filter for
detection of Schistosoma haematobium eggs by urine filtration. Tropenmedizin
und Parasitologie. 1982;33(4):227–8.
Monje ML, Toda H, Palmer TD. Inflammatory blockade restores adult hippocampal
neurogenesis. S.
43
Nelwan ML. Schistosomiasis: life cycle, diagnosis, and control. Curr Therapeutic Res.
Olveda DU, Li Y, Olveda RM, et al. Bilharzia: pathology, diagnosis, management and
control. Trop Med Surg. 2013;1:135.
Poggensee, G., Kiwelu, , Weger, V ., Goppner ,D. , Diedrich, T. , Krantz, I and Feldmeier, H.
(2000). Female genital schistosomiasis of the lower genital tract: prevalence and
disease-associated morbidity in northern Tanzania . Journal of Infectious Diseases
181: 1210 – 1213.
Poggensee, G. and Feldmeier, H. (2001). Female genital schistosomiasis: facts and
hypotheses. Acta Tropica 79: 193 – 210.
Poggensee, G., Mtweve, S and Krantz, I. (2006). Female genital schistosomiasis as an
evidence of a neglected cause for reproductive ill-health: a retrospective
histopathological study. BMC Infectious Disease. 6: 134.
Rujeni N, Nausch N, Midzi N, Cowan GJ, Burchmore R, Cavanagh DR, et al. Immunological
consequences of antihelminthic treatment in preschool children exposed to
urogenital schistosome infection. Journal of Tropical Medicine. 2013;2013.
Salawu OT, Odaibo AB. Schistosomiasis among pregnant women in rural communities in
Nigeria. Int J Gynaecol Obstet. 2013;122:1–4.
Schafer TW, Hale BR. Gastrointestinal complications of schistosomiasis. Curr Gastroenterol
Rep. 2001;3(4):293–303.
Serieye, J., Boisier, P., Ravaolimalala, V.E., Ramarokot, C.E. and Leutscher, P.P. (1996).
Schistosoma haematobium infection in western Madagascar: morbidity
determined by ultrasonography. Transaction of the Royal Society of Tropical
Medicine and Hygiene. 90:398–401.
Smith, J. H., and Christie, J. D. (1986). The patho biology of Schistosoma haematobium in
humans. Human Pathology. 17: 383-385.
Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J. Schistosomiasis and water resources
development: systematic review, meta-analysis, and estimates of people at risk.
Lancet Infect Dis. 2006;6:411–25.
Steketee, R.W. (2003). Pregnancy, nutrition and parasitic diseases. Journal of Nutrition. 133,
1661S–1667Sm.
Stephenson, L.S. et al. (1989). Single dose metrifonate or praziquantel treatment in Kenyan
children. II. Effects on growth in relation to Schistosoma haematobium and
hookworm egg counts. American Journal of Tropical Medicine and Hygiene. 41:
445–453.
Stuiver, P. C. (1984). Acute scistosomiasis (Katayama fever). British Medical Journal, 288:
221 – 222.
Tatala, S. et al. (1998). Low dietary iron availability is a major cause of anemia: a nutrition
survey in the Lindi District of Tanzania. American Journal of Clinical Nutrition.
68, 171–178.
44
Utzinger J, Raso G, Brooker S, et al. Schistosomiasis and neglected tropical diseases:
towards integrated and sustainable control and a word of caution. Parasitology.
2009;136:1859–74.
Utzinger, J., Raso, G., Steinmann, P., Zhou, Xn., Vounatsou, P., Brooker, S. and N’Goran, E.
K. (2011). Schistosomiasis. Elsevier. 10-191.
Vermund, S. H., Brandley, D. J. and Ruiz-Tiben, E. (1983). Survival of Schistosoma mansoni
in the human host: estimates from a community-based prospective study in Puerto
Rico. American Journal of Tropical Medicine and Hygiene. 32: 1040 – 1048.
Vitkovic L, Konsman J, Bockaert J, Dantzer R, Homburger V, Jacque C. Cytokine signals
propagate through the brain. Mol Psychiatry. 2000;5(6):604–15.
Wami WM, Nausch N, Midzi N, Gwisai R, Mduluza T, Woolhouse ME, et al. Comparative
assessment of health benefits of praziquantel treatment of urogenital
schistosomiasis in preschool and primary school-aged children. BioMed research
international. 2016;2016.
Webbe, G. (1981). Schistosomiasis: some advances. British Medical Journal, 238: 1104 –
1106.
WHO, (1998). Report of the WHO informal consultation on monitoring drug efficacy in the
control of schistosomiasis and intestinal nematodes. Book Report of the WHO
informal meeting. Geneva.
WHO, (1999). Report of the WHO informal consultation on monitoring drug efficacy in the
control of schistosomiasis and intestinal nematodes; 8–10 July 1998. Geneva.
WHO, (2002). Report of the WHO Informal Consultation on the Use of Praziquantel during
Pregnancy/Lactation and Albendazole/Mebendazole in Children under 24
Months, 8–9 April, 2002. Geneva, Switzerland: WHO.
WHO, (2009). WHO Working Group on Urogenital Schistosomiasis and HIV Transmission.
World Health Organization Neglected Tropical Diseases
http://www.who.int/neglected_diseases/integrated_media_urogenital_schistosomi
asis/en/index.html.
World Health Organization. WHO schistosomiasis fact sheet; 2014. Available from:
http://www.who.int/mediacentre/factsheets/fs115/en[accessed10.04.14].
Wright ED, Chiphangwi, J and Hutt, M. S. (1982). Schistosomiasis of the female genital
tract: a histopathological study of 176 cases from Malawi. Transactions of the
Royal Society of Tropical Medicine and Hygiene 76:822–9.
Zuidema, P. J. (1981). The Katayama syndrome; an outbreak in Dutch tourist to the Omo
National park, Ethiopia. Tropical and geographical medicine 33: 30 - 35.
45
APPENDIX
Dear sir/ma,
I solemnly assure you that every piece of information supplied will be treated
confidentially for academic purpose only.
QUESTIONNAIRE
SOCIO-DEMOGRAPHY
1. Sex: M [ ] F[ ]
2. Age: 25-30years ( ) 31-35years ( ) 36-40years ( ) 41-50years ( ) 50&above ( )
3. Occupation: (a) Farming (b) Fishing (c) Trading (d) Others
4. House Number: …………………………..
5. Community: ……………….………..
6. Weight: …………………….
46
SECTION B: QUESTIONNAIRE ON SCHISTOSOMIASIS
The following questions are about minor mistakes, which everyone makes from time
to time, but some of which happen more often than others. We want to know how
often these things have happened to you in the past 6 months. Please selectPlease
theselect appropriatethe answerappropriate fromanswer thefrom the option below:
QUESTIONS 4 3 2 1 0
11 Do you read something and find you have
not been thinking about it and must it read it
again?
again?
12 Do you fail to notice sign posts on the
road?
47
13 Do you find you confuse right and left
when giving directions?
giving directions?
14 Do you bump into people?
15 Do you find you forget whether you have
turned off light or a fire or locked the door?
door?
16 Do fail to hear people speaking to you
when you are doing something else?
48
INFLUENCE OF LONGTERM EXPOSURE TO SCHISTOSOMIASIS ON COGNITIVE
AND REPRODUCTIVE FUNCTIONS AMONG THE MIDDLE AGE WOMEN IN
EBUTTE IGBOORO, YEWA NORTH LOCAL GOVERNMENT, OGUN STATE.
BY
49
AKANBI, MORENIKEJI OLUWAFOLAKEMI
NOVEMBER, 2023.
50
INFLUENCE OF LONGTERM EXPOSURE TO SCHISTOSOMIASIS ON COGNITIVE
AND REPRODUCTIVE FUNCTIONS AMONG THE MIDDLE AGE WOMEN IN
EBUTTE IGBOORO, YEWA NORTH LOCAL GOVERNMENT. OGUN STATE.
BY
NOVEMBER, 2023.
51
52
CERTIFICATION
This is to certify that the research work titled “Influence of long-term exposure to
Schistosomiasis on cognitive and reproductive functions among the middle age women in
Ebute Igbooro Yewa North, Ogun State” was carried out by AKANBI, MORENIKEJI
OLUWAFOLAKEMI, matric number; H/ST/21/2083 under the supervision of Mr. A
Adewole and Mrs Popoola in the Department of Science Laboratory Technology.
Mr A Adewole
Mrs Popoola
53
DEDICATION
I dedicate this work to the Abba father who is faithful in all things and in whom all
achievement in life are made possible, and my parents who gave me the support to achieve
my dream at their expense. Without them, this project would not have been possible.
54
ACKNOWLEDGEMENTS
It is my pleasure to register my profound appreciation and gratitude for the moral, financial
support, advice and cooperation received from various people at different stages of this
research work and eventual completion of my course of study in this great citadel of learning.
I also express my sincere thanks to my parents Mr and Mrs Festus Akanbi, for their prayers,
love, care, and financial support throughout my academic pursuit; you will live long in good
health and wealth eat the fruits of your labor in Jesus name (Amen).
I would also be ungrateful if I did not acknowledge Dr Oyedeji, Mr F.T Faparusi, Mrs F.O
Abdulsalam, and all the lecturers for their impartation of knowledge.
Finally, I am extremely grateful to all Flakkie shiners and my siblings for their financial
support toward the success of this project. Thanks for all you do.
55
ABSTRACT
56
TABLE OF CONTENTS
Title Page i
Certification ii
Dedication iii
Acknowledgements iv
Abstract v
Table of Contents vi
2.0[1.0] Introduction 1
1.5 Objectives 5
CHAPTER TWO
in sub-saharan of Africa 10
57
2.3.3 Praziquantel treatment and pregnancy 11
CHAPTER THREE
3.2 Materials 13
3.3 Methods 13
3.5.2 Treatment 15
CHAPTER FOUR
4.1 Results 16
58
59