Table 1. Demographic and clinical characteristics of included studies.
Study | Country | Cases | Controls | Analytical Method | Mutation Gene | Mutation Site | NOS |
---|---|---|---|---|---|---|---|
Burmer 1991 | UK | UC-CRC | S-CRC | PCR | KRAS | Codon 12 | 7 |
Bell 1991 | USA | UC-CRC or dysplasia | S-CRC | PCR | KRAS | Codon 12 | 9 |
Taylor 1993 | UK | IBD-CRC | S-CRC | IHC positive | TP53 | NA | 9 |
Rashid 1997 | USA | CD associated adenocarcinomas | S-CRC | ≥50% IHC positive/PCR | TP53/KRAS | NA/codon 12, 13 | 7 |
Lashner 1999 | USA | UC-CRC | UC | ≥5% IHC positive | TP53 | NA | 7 |
Walsh 1999 | USA | UC-CRC or dysplasia | S-CRC | IHC positive | TP53 | NA | 9 |
Reeves 2004 | UK | IBD-CRC | S-CRC | PCR | TP53/KRAS | NA/codon 12 | 7 |
Maia 2005 | Portugal | IBD-CRC or dysplasia | IBD | PCR-SSCP | TP53 | Exon 6, 7 | 7 |
Bossard 2007 | France | IBD-CRC | IBD | PCR | KRAS | Codon 12, 13 | 7 |
Nathanson 2008 | USA | CD dysplasia | CD | Dark-brown IHC stain | TP53 | NA | 7 |
Laurent 2011 | France | IBD-CRC | S-CRC, IBD | ≥10% IHC positive | TP53 | NA | 7 |
Sanchez 2011 | USA | UC-CRC | S-CRC | PCR | TP53/KRAS | Exon 4, 8/ codon 12, 13 |
9 |
Olaru 2012 | USA | IBD-CRC | S-CRC | PCR | KRAS | NA | 7 |
Shivakumar 2012 | India | IBD-CRC | S-CRC, UC | PCR | TP53/KRAS | Exon 4-8/ codon 12, 13 | 7 |
Kisiel 2013 | USA | IBD-CRC | IBD | PCR | TP53/KRAS | NA | 9 |
Ottessen 2015 | Norway | UC-CRC | UC | ≥5% IHC positive | TP53 | NA | 7 |
Johnson 2016* | USA | IBD-CRC | IBD | PCR | KRAS | NA | 9 |
Lennerz 2016 | USA | CD-CRC | S-CRC | PCR | KRAS | NA | 7 |
Yaeger 2016 | USA | IBD-CRC | S-CRC | PCR | TP53/KRAS | NA | 7 |
IBD: inflammatory bowel disease; UC: ulcerative colitis; CD: Crohn’s disease; CRC: colorectal cancer; PCR: polymerase chain reaction; SSCP: single-strand conformation polymorphism; S-CRC: sporadic colorectal cancer; NOS: Newcastle-Ottawa Scale.
*The study by Johnson et al 2016 contained two independent phases, and the data of one cohort phase was first presented in 2014