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Table 1 Basic characteristics of all eligible studies in the meta-analysis

From: Role of CYP2E1 polymorphisms in breast cancer: a systematic review and meta-analysis

Author, year

Region

Ethnicity

Case/control

BC confirmation

Genotyping method

Source of control

PI

HWE (yes/no)

QS

Khedhaier, 2008

Tunisia

African

304/244

HC

PCR–RFLP

H-B

rs2031920 C>T

Yes

13

Sangrajrang, 2010

Thailand

Asian

570/479

PC

PCR

H-B

rs2031920 C>T

No

9

McCarty, 2012

Thailand

Mix

1041/1070

PC

TaqMan™

P-B

rs2031920 C>T

No

9

Choi, 2003

Korea

Asian

346/377

HC

PCR

H-B

CYP2E1*5 Rsa I/Rst I

Yes

11

Wu, 2006

Taiwan

Asian

262/225

PC

PCR–RFLP

H-B

CYP2E1*5 Rsa I/Rst I

Yes

11

Zgheib, 2013

Lebanese

Arab

227/99

PC

PCR–RFLP

H-B

CYP2E1*5 Rsa I/Rst I

Yes

10

Chong, 2016

Malaysian

Asian

71/260

PC

PCR–RFLP

H-B

CYP2E1*5 Rsa I/Rst I

Yes

11

Shields, 1996

New York, Niagara and Erie

Caucasian

272/334

PC

PCR–RFLP

P-B

CYP2E1*6 Dra I

Yes

14

Anderson, 2012

Canada

Caucasian

920/960

NM

PCR

P-B

CYP2E1*6 Dra I

Yes

12

Zgheib, 2013

Lebanese

Arab

227/99

PC

PCR–RFLP

H-B

CYP2E1*6 Dra I

Yes

10

Chong, 2016

Malaysian

Asian

71/260

PC

PCR–RFLP

H-B

CYP2E1*6 Dra I

Yes

11

  1. BC breast cancer, HC histologically confirmed, PC pathologically confirmed, NM not mentioned, PCR polymerase chain reaction, PCR–RFLP polymerase chain reaction–restriction fragment length polymorphism, HB hospital-based, PB population-based, PI polymorphism(s) investigated, HWE Hardy–Weinberg equilibrium, QS quality score