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. 2018 Jul 23;41(3):570–577. doi: 10.1590/1678-4685-GMB-2016-0287

Table 2. Paraoxonase-1 allele, genotype, and haplotype distributions of L55M and Q192R polymorphisms in patients and healthy individuals of the hypercholesterolemia family.

Characteristics (Allele/Genotypes) Patients (n = 10) Controls (n = 24) p
Alleles L55 2 (10%) 2 (4.2%) 0.336
M55 18 (90%) 46 (95.8%) 0.927
Q192 19 (95%) 33 (68.7%) 0.0164
R192 1 (5%) 15 (62%) 0.998
Genotypes L55L55 0 (0%) 0 (0%) 1
L55M55 2 (20%) 2 (8.3%) 0.334
M55M55 8 (80%) 22 (91.7%) 0.933
Q192Q192 9 (90%) 10 (41.7%) 0.0113
Q192R192 1 (10%) 13 (54.2%) 0.999
R192R192 0 (0%) 1 (4.2%) 1
Haplotypes M55M55/Q192Q192 8 (80%) 8 (33.3%) 0.017
L55M55/Q192Q192 1 (10%) 2 (8.3%) 0.661
L55M55/Q192R192 1 (10%) 0 (0%) 0.294
M55M55/Q192R192 0 (0%) 13 (54.2%) 1
M55M55/R192R192 0 (0%) 1 (4.2%) 1

p < 0.05 was considered statistically significant; data were analyzed using Fisher’s Exact Test.