Apolipoprotein A1 gene polymorphisms as risk factors for hypertension and obesity

Male 0301 basic medicine Polymerase Chain Reaction Body Mass Index Cohort Studies 03 medical and health sciences Glycated hemoglobin Gene Frequency 616 Humans Obesity APOA1 polymorphisms Alleles Aged Aged, 80 and over 2. Zero hunger Polymorphism, Genetic Apolipoprotein A-I Middle Aged 3. Good health Cholesterol Haplotypes Cardiovascular Diseases Hypertension Female Brazil Polymorphism, Restriction Fragment Length
DOI: 10.1007/s10238-009-0051-3 Publication Date: 2009-05-04T18:49:45Z
ABSTRACT
Several polymorphisms in apolipoprotein A1 (APOA1) gene have been associated with metabolic diseases. Increased transcription efficiency was observed in -75A allele carriers compared to -75G allele homozygotes. +83C allele was associated with higher body mass index and waist-to-hip ratio in type II diabetes subjects. -75G/A and +83C/T polymorphisms were analyzed by RFLP-PCR in 334 individuals from a Brazilian elderly cohort. APOA1 polymorphisms were associated with age-related morbidities, as well as with triglycerides, total cholesterol, HDL, VLDL, LDL, creatinine, urea, albumin, glycated hemoglobin and fasting glucose serum levels. Allele frequencies were 0.102 and 0.21, respectively, for -75A and +83T. -75G allele showed significant association with hypertension (P = 0.001). An association between +83C allele and obesity was observed (P = 0.040) and this allele also showed an association with hypertension in the presence of cardiovascular disease (P = 0.047). Moreover, +83T allele was associated with lower glycated hemoglobin values (P = 0.026). To our knowledge, there is no data associating this polymorphism with glycated hemoglobin. Furthermore, individuals carrying AT haplotype have lower risk for developing hypertension (P = 0.0002), while GT haplotype carriers present decreased risk to develop obesity comparing to GC haplotype (P = 0.025). APOA1 polymorphisms analysis may be a useful tool to identify risk factors for subjects and families and clarify the physiopathological role of these polymorphisms in age-related diseases, such as hypertension and obesity.
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