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Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria

A thesis submitted in fulfillment of the requirements for the degree of Master of Philosophy in the Department of Clinical Microbiology, School of Medical Sciences, College of Health Sciences.

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Main Author: Lamptey, Theodora
Format: Thesis
Language:English
Published: 2016
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access_status_str Open Access
author Lamptey, Theodora
author_browse Lamptey, Theodora
author_facet Lamptey, Theodora
author_sort Lamptey, Theodora
collection Thesis
description A thesis submitted in fulfillment of the requirements for the degree of Master of Philosophy in the Department of Clinical Microbiology, School of Medical Sciences, College of Health Sciences.
format Thesis
id oai:ir.knust.edu.gh:123456789/8172
institution KNUST (Ghana)
language English
last_indexed 2026-06-10T12:31:23.640Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from KNUSTSpace — Kwame Nkrumah University of Science & Technology (Ghana)
publishDate 2016
publishDateRange 2016
publishDateSort 2016
record_format dspace
source_str KNUSTSpace — Kwame Nkrumah University of Science & Technology (Ghana)
spelling oai:ir.knust.edu.gh:123456789/8172 Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria Lamptey, Theodora A thesis submitted in fulfillment of the requirements for the degree of Master of Philosophy in the Department of Clinical Microbiology, School of Medical Sciences, College of Health Sciences. People living in areas with stable transmission of Plasmodium falciparum parasites acquire protective immunity to malaria following multiple disease episodes. Immunity acquired this way is mediated by IgG with specificity for parasite-encoded, clonally variant surface antigens (VSA) on the surface of infected erythrocytes (IEs). However, women in endemic areas become susceptible to P. falciparum infection during pregnancy, particularly for the first time, regardless of acquired protective immunity. Aggregation of erythrocytes infected by P. falciparum in the intervillous spaces of the placenta using chondroitin sulphate A (CSA) as the dominant placental adhesion receptor has been identified. Chondroitin sulfate A is a sulfated glycosaminoglycan (GAG) composed of a chain of alternating sugars. It is usually found attached to proteins as part of a proteoglycan. This study sought to investigate the role of chondroitin sulphate A in malaria susceptibility in pregnant women. A total of 160 clients attending two selected health facilities, namely Kaneshie Polyclinic and Our Lady of Grace Hospital, were recruited. They were stratified into three groups: Pregnant women with malaria (n=80), non-pregnant women with malaria (n=40) and pregnant women without malaria (n=40). Full blood count (FBC), malaria RDT, thick film for malaria parasites and ELISA for chondroitin sulphate-A concentration were conducted for each volunteer. The mean haemoglobin count in pregnant women with malaria was 9.6 ± 1.4 g/dl and that of non-pregnant women with malaria was 10.3 ± 1.6 g/dL and the pregnant women without malaria was 11.5 ± 1.1 g/dL. The median CSA concentration in non-pregnant women with malaria was 2.24 ng/mL; that of pregnant women with malaria was 50.76 ng/mL, and pregnant women without malaria was 44.94 ng/mL. There were significant differences between non-pregnant women with malaria and pregnant women with malaria (P=0.0001) and also between non-pregnant with malaria and pregnant women with no malaria (P=0.0001) but no difference between pregnant women with malaria and pregnant women without malaria (P=0.084). Haemoglobin and haematocrit concentrations were significantly associated with malaria infection. The parasite count in pregnant women with malaria compared with that in non-pregnant women with malaria was significantly lower (P=0.0001). Malaria infection was associated with reduction in haemoglobin concentration, which worsened when pregnancy was present. In conclusion, CSA was elicited in pregnant women but had inverse correlation with peripheral malaria parasitaemia. KNUST 2016-02-10T13:01:18Z 2023-04-20T19:08:21Z 2016-02-10T13:01:18Z 2023-04-20T19:08:21Z AUGUST, 2015 Thesis https://ir.knust.edu.gh/handle/123456789/8172 en application/pdf
spellingShingle Lamptey, Theodora
Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title_full Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title_fullStr Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title_full_unstemmed Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title_short Clinical utilization of Chondroitin Sulphate-A to determine the susceptibility of pregnant women to malaria
title_sort clinical utilization of chondroitin sulphate a to determine the susceptibility of pregnant women to malaria
url https://ir.knust.edu.gh/handle/123456789/8172
work_keys_str_mv AT lampteytheodora clinicalutilizationofchondroitinsulphateatodeterminethesusceptibilityofpregnantwomentomalaria