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Evaluation of apolipoprotein b 100 against ldl-cholesterol in profiling cardiovascular disease risk in HIV infected patients

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dc.contributor.author Sado, Belinda
dc.date.accessioned 2014-03-17T10:04:16Z
dc.date.available 2014-03-17T10:04:16Z
dc.date.issued 2014-03-17
dc.identifier.uri http://hdl.handle.net/10646/1207
dc.description.abstract Background This study was carried out to assess the potential clinical utility of measuring apo B 100 in evaluation of CVD risk. The study focused on measurement of the classic parameters of assessing CVD risk. LDL cholesterol and HDL cholesterol have been the cornerstone of stratifying CVD risk. LDL cholesterol is considered to be the major lipid risk factor but it has emerged that apo B 100, as a proxy for all atherogenic lipid particles, is a better marker for CVD risk. Risk of CVD in the HIV infected population appears to be relatively higher than in the general population and thus appropriate screening measures for CVD are needed. There is growing support that addition of apo B 100 measurement to the routine lipid panel would enhance patient management. Methods Sixty ART naive (35 females), 62 HIV positive on ART (47 females) and 64 HIV negative participants (52 females) were recruited from Harare Hospital adult OIC. These participants were aged between 18 and 65 years old and consented to participate in the study and the mean age was 38.4 + 10.4. A questionnaire eliciting socio-demographic and medical history was administered prior to collection of a blood sample for evaluation of lipid status. Total cholesterol, LDL cholesterol, HDL cholesterol, apo B and glucose were determined on the Dimension, Dade Behring analyser (Siemens Healthcare Diagnostics S.A). Ten-year CVD risk scores were calculated using an online calculator formulated by Dr Rupert Payne of the University of Edinburgh in May 2010. iii Results There was an increase in mean total cholesterol, LDL cholesterol and apo B levels from HIV negative people to HIV positive ART naive patients and finally to HIV positive on ART patients which was statistically significantly different (p value< 0.001). There was a decrease in mean HDL cholesterol from 1.6 to1.4 to 1.1 mmol/L across the three groups which was also statistically significantly different (p value<0.001). Generally risk of CVD in the HIV infected population appeared to be relatively higher than the other two groups. Diabetes, age, gender, smoking, and systolic blood pressure had a positive effect on the lipid parameters. There was a weak positive significant correlation between Framingham risk score and apoB (r=0.26, p<0.001).There was no correlation found between Framingham risk score and LDL-c (r=0.144, p=0.11). A moderate positive significant correlation (r=0.44, p<0.001) was found between apo B and LDL-c. Conclusion In this study it was observed that ART increases lipid parameters like total cholesterol, LDL-c and apo B levels thereby increasing risk of CVD. HDL-c levels were decreased in patients on ART. ART therefore seem to affect lipid parameters. The current guidelines should recommend routine monitoring of lipid parameters in HIV patients on ART to actively investigate these changes. Apo B should be included in lipid profiles since there was a weak positive correlation with the Framingham risk score in assessing risk of developing CVD. Apo B also reflects the atherogenic particles not only LDL but also VLDL and IDL. en_UZ
dc.language.iso en_ZW en_UZ
dc.subject CARDIOVASCULAR DISEASE en_UZ
dc.subject CLINICAL BIOCHEMISTRY en_UZ
dc.subject HIV en_UZ
dc.title Evaluation of apolipoprotein b 100 against ldl-cholesterol in profiling cardiovascular disease risk in HIV infected patients en_UZ
dc.contributor.registrationnumber R912042K en_UZ
dc.rights.embargodate 2012-09
thesis.degree.advisor Gomo, Z A R
thesis.degree.advisor Musarurwa, C
thesis.degree.country Zimbabwe en_UZ
thesis.degree.discipline Chemical Pathology en_UZ
thesis.degree.faculty Faculty of Medicine en_UZ
thesis.degree.grantor University of Zimbabwe en_UZ
thesis.degree.grantoremail specialcol@uzlib.uz.ac.zw
thesis.degree.level MSc en_UZ
thesis.degree.name MASTER OF SCIENCE IN CLINICAL BIOCHEMISTRY en_UZ
thesis.degree.thesistype Thesis en_UZ
dc.date.defense 2012-09


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