Table 5. The trends of BRAF mutations prevalence of micro PTCs from individual institutions.
Country | City (State) | Institution (Reference) |
Prevalence of BRAF mutations in micro PTCs | ||||
---|---|---|---|---|---|---|---|
Period 1 | Period 2 | Period 3 | Period 4 | P | |||
US | Pittsburgh (PA) | Univ. of Pittsburgh [14] | 1974-1985 10/31(32.3%) FMCA |
1990-1992 3/16(18.8%) FMCA |
2000 4/17 (23.5%) FMCA |
2009 19/50(38%) FMCA |
NS |
Poland | Kielce | Holycross Cancer Center [21] | 2000-2004 45/90 (50%) Three methods a |
2005-2009 104/147 (70.7) Three methods a |
2010-2013 147/203 (72.4) Three methodsa |
0.001 b | |
Korea | Seoul | Samsung Medical Centre [26, 27] | 2008-2009 253/396(63.9%) DS |
2010-2011 97/128(75.8%) DS |
0.013 | ||
China | Tianjin | Tianjin Medical Univ. Cancer Hospital [24, 25] | 2001-2010 392/977(40.1%) DS |
2013-2014 1244/1984(62.7%) DS |
<0.001 |
Abbreviations: NS, not significant; DS, direct sequencing; FMCA, fluorescent melting curve analysis
a All analyses that were performed prior to 2013 by DS and allele-specific PCR (AS-PCR) were verified by quantitative Real time PCR (qPCR). In total, the authors used qPCR to analyze BRAF mutations in 705/723 PTCs (97.5%). The majority of samples were tested using the three methods (DS, AS-PCR and qPCR).
b P value for trend adjusted for age and sex