Research Article

Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters

Table 5

Multivariate linear regression models of genetic polymorphisms and confounding variables on laboratory parameters in SCA-HU+ and SCA-HU patients.
(a)

SCA-HU+ patients
Independent variablesDependent variableβ valueR2 value of the model

Model
MPOTotal cholesterol−0.3910.0010.744<0.001a
 MCH−02740.011
 LDL-C0.667<0.001
 Iron serum0.2660.013
 Lactate dehydrogenase−0.2720.019

Model
CYP2E1Alpha-1 antitrypsin−0.3500.0170.596<0.001a
 Uric acid−0.5630.001
 Urea0.2700.047
 Creatinine0.3860.014
 Iron serum−03980.005
 Direct bilirubin0.4400.007

Model
GSTT1Total bilirubin0.4640.0040.2830.005a
 Creatinine−0.3370.033

Model
GSTT1Indirect bilirubin0.4330.0090.2330.014a
 Creatinine−0.2860.077

(b)

SCA-HU patients
Independent variablesDependent variableβ valueR2 value of model

Model
MPOUric acid0.3790.0010.244<0.001a
 Total cholesterol0.2930.010

Model
CYP2E1Urea0.3890.0010.1750.007a
 Globulin−0.1870.124
 Uric acid0.1100.363

LDL-C: low-density lipoprotein cholesterol; MCH: mean corpuscular hemoglobin; MPO: myeloperoxidase; CYP2E1: cytochrome P450 2E1; GSTT1: glutathione S-transferase; SCA-HU+: SCA patient treated with HU; SCA-HU: SCA patient untreated with HU; R2: coefficient of determination; β: coefficient of regression; aANOVA; dominant genetic model.