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Screening for genetic mutations in LDLR gene with familial hypercholesterolemia patients in the Saudi population
Author(s) -
Khalid Khalaf Alharbi,
Tarek Kashour,
Wejdan Al-Hussaini,
May Salem Nbaheen,
Rana Hasanato,
Sarar Mohamed,
Waleed Tamimi,
Imran Ali Khan
Publication year - 2015
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2015_1015
Subject(s) - exon , familial hypercholesterolemia , ldl receptor , mutation , genetics , population , gene , biology , medicine , lipoprotein , cholesterol , environmental health
Familial hypercholesterolemia (FH) is caused by genetic defects involving the low density lipoprotein-receptor (LDL-R), predisposing affected people to premature atherosclerotic cardiovascular disease and death. The aim of the present study was to assess certain exons in the LDLR gene mutation detection analysis affecting in the Saudi population with FH. This case-control study was carried out with 200 subjects; 100 were FH cases and 100 were healthy controls. Five mL of venous blood samples were collected from all the subjects and used for biochemical and genetic analysis. DNA was extracted from 2 mL of the EDTA samples, and precise primers were designed for LDL-R gene which includes Exon 3, 4 and 8. PCR was followed by DNA sequencing. In our study, we found 25 mutations in cases in Exon-3 and 2 mutations in controls, however, we have found only 5 mutations in exon 4 and none of the mutations were identified in exon 8. We conclude that screening of FH among Saudi population is very important to identify individuals who are prone to develop the disease.

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