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Table 5 Analysis of association between HPRL and the genetic polymorphisms in patients from risperidone/paliperidone group

From: A pharmacogenetic study of patients with schizophrenia from West Siberia gets insight into dopaminergic mechanisms of antipsychotic-induced hyperprolactinemia

Gene

SNP

OR

95% CI

Lower bound

95% CI

Upper bound

p-value

DRD1

rs4532

0.522

0.216

1.261

0.148

DRD2

rs1076562

0.490

0.192

1.249

0.135

DRD2

rs4245147

1.148

0.519

2.541

0.733

DRD2

rs2283265

0.900

0.301

2.686

0.850

DRD2

rs2734842

0.472

0.187

1.194

0.113

DRD2

rs6277

2.081

0.864

5.011

0.102

DRD2

rs6279

0.434

0.164

1.145

0.092

DRD2

rs1076560

0.969

0.327

2.878

0.955

DRD2/ANKK1

rs2734849

1.833

0.781

4.302

0.164

DRD3

rs11721264

2.042

0.677

6.156

0.205

DRD3

rs2134655

0.659

0.203

2.140

0.488

DRD3

rs963468

0.647

0.251

1.666

0.367

DRD3

rs167771

1.150

0.244

5.414

0.859

DRD3

rs324035

1.719

0.380

7.783

0.482

DRD3

rs167770

1.963

0.622

6.195

0.250

DRD3

rs7633291

2.462

0.640

9.473

0.190

DRD3

rs9817063

1.635

0.626

4.270

0.316

DRD3

rs1587756

2.407

0.489

11.861

0.280

DRD3

rs1800828

2.813

0.739

10.711

0.129

DRD3

rs3773678

1.556

0.326

7.412

0.579

DRD3

rs6280

2.153

0.668

6.947

0.199

DRD4

rs3758653

1.403

0.410

4.806

0.590

DRD4

rs936461

1.500

0.577

3.895

0.405

DRD4

rs11246226

2.421

0.955

6.142

0.063

SLC6A3

rs27048

1.419

0.660

3.054

0.370

SLC6A3

rs3756450

1.373

0.512

3.684

0.529

SLC6A3

rs40184

0.341

0.137

0.852

0.021*

SLC6A3

rs4975646

0.640

0.258

1.589

0.336

SLC6A3

rs2617605

0.880

0.337

2.299

0.794

SLC6A3

rs464049

0.538

0.209

1.384

0.199

SLC6A3

rs1048953

0.823

0.337

2.008

0.668

SLC6A3

rs250686

0.563

0.214

1.482

0.245

SLC6A3

rs3863145

0.362

0.135

0.970

0.043*

  1. Logistic regression analysis was used to test an additive genetic model for association between HPRL and the polymorphisms in adjusting for age, sex and CPZeq. OR – odds ratio; CI – lower and upper bound 95% confidence intervals. ORs are reported for the risk of HPRL attributable to the rare allele vs common allele
  2. *Values are deemed to have significance