Status of oxidative stress and characterization of APOB gene mutation in patients with familial hypercholesterolaemia

• Main Author: Nur Suhana Hamzah (Author)
• Format: Thesis Book
• Language: English
• Published: Sungai Buloh, Selangor Universiti Teknologi MARA. Faculty of Medicine 2016
• Subjects: Oxidative Stress > physiology; Hyperlipoproteinemia Type II
• Online Access: Click Here to View Status and Holdings.
• Item Description: UiTM Digitized
• Physical Description: xvi, 153 pages illustrations, charts (some colour) 30 cm 1 computer optical disc (4 ¾ in.)
• Format: System requirements for CD-ROM: Intel Pentium II or faster processor with 450 MHz (or equivalent), browser Internet Explorer 5.5 or higher (6.0 or higher recommended), Firefox 1.0.2 or higher, Acrobat
• Bibliography: Includes bibliographical references (page 98-117)

Familial hypercholesterolaemia (FH) is an autosomal dominant genetic disorder characterized by high cholesterol concentration which increases oxidative stress and leads to coronary artery disease. Mutation in exon 26 and exon 29 of Apolipoprotein B (APOB) gene is one of the causes of FH. Oxidized low-density lipoprotein (ox LDL), F₂-isoprostanes (ISP) and Malondialdehyde (MDA) are established oxidative stress biomarker. The aim of this study is to investigate oxidative stress status and to identify genetic variants in APOB gene among FH patients and normocholesterolaemic (NC) subjects. Ninety-eight FH patients and 100 (age, gender and BMI matched) NC subjects were recruited in series of health screening programmes across the country. Fasting blood samples were analysed for serum ox LDL (ELISA), ISP (LCMS/MS) and MDA. Amplicons of exon 26 and 29 of APOB gene were screened by DNA sequencing. Ox-LDL, ISP and MDA concentrations were significantly higher in FH groups compared to NC (mean+SEM: 63.0+6.5 vs 25.5+1.2 (U/1), p<0.001); 749.7+74.0 vs 354.2+18.1 pg/ml, p<0.0001; 342.4+46.0 vs 162.7 13.5 nmol/g, p<0.0001), Ox-LDL shows significant correlation with glucose (p<0.05), TC (p<0.001), LDL-c (p<0.001) and HDL-c (p<0.01) in all subjects. High LDL-c was associated with high ox-LDL (p<0.001). LDL-c is an independent predictor for ox-LDL concentration (p<0.001). Known mutations were not found in all FH cases except for few insignificant genetic variations which are pThr2515Thr, p.lle2716lle, p.Pro2739Leu, p.Glu4181 Lys, p.Arg4270Thr, p.Arg4297His and p.Ser4338Asn. These findings demonstrate that FH patients have higher oxidative stress concentration which suggests a greater ris hbk of developing atherosclerosis. These results provide additional knowledge regarding FH in Malaysians