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. 2013 Dec 5;4:271. doi: 10.3389/fgene.2013.00271

Table 4.

Aberrant methylation and clinicopathological features.

Clinical features All Cases (n = 34) Aberrant Methylation(+) (n = 26, Figure 7B) Aberrant Methylation(−) (n = 8, Figure 7B) P-values
SEX
Male/female 11/23 10/16 1/7 0.17 (Fisher)
AGE (YEAR)
Mean ± SE 56.0 ± 2.7 57.2 ± 3.1 52.4 ± 4.9 0.45 (t-test)
TUMOR SIZE (mm)
Mean ± SE 26.2 ± 2.6 28.3 ± 3.3 20.1 ± 2.0 0.06 (t-test)
NUMBER OF LYMPH NODES WITH METASTASIS
Mean ± SE 2.6 ± 0.7 2.2 ± 0.6 3.3 ± 1.6 0.53 (t-test)
DISTANT METASTASIS
(+)/(−) 0/34 0/26 0/8 1 (Fisher)
RECURRENCE
(+)/(−) 5/28 3/22 2/6 0.37 (Fisher)
Unknown 1 1 0
THYROGLOBULIN (ng/ml)
Mean ± SE 104.6 ± 52.1 129.3 ± 68.6 30.5 ± 9.3 0.08 (t-test)
MUTATION OF BRAF/RAS ONCOGENES
(+)/(−) 26/7 22/3 4/4 0.04* (Fisher)
Unknown 1 1 0

SE, standard error. P-values were calculated to compare methylation(+) group and methylation(−) groups and to analyze the correlation of methylation status to clinicopathological features. Fisher, calculated by Fisher's exact test. t-test, calculated by t-test.

*

P < 0.05, which is considered as statistically significant. Mutations of BRAF/RAS oncogenes are thus considered to correlate significantly with methylation(+) groups.