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. 2016 Sep 22;8(1):1871–1883. doi: 10.18632/oncotarget.12202

Table 5. Pooled results for the association between P16INK4a promoter hypermethylation and CC risk.

Comparisons Studies (N) Sample size (CC/controls) Heterogeneity Model a Effect size
I2(%) PQ-test OR (95% CI) P
Total 18 950/732 58 0.001 R 12.17 (5.86-25.27) < 0.001
Ethnicity
Asian 10 631/385 19 0.272 F 18.94 (9.75-36.81) < 0.001
Caucasian 5 270/200 60 0.039 R 6.83 (1.98-23.55) 0.002
Other ethnicities 3 135/179 88 < 0.001 R 9.87 (4.45-21.90) < 0.001
Source of controls
Healthy 9 322/267 44 0.073 R 13.67 (5.64-33.10) < 0.001
Non-healthy 9 628/465 69 0.001 R 11.32 (3.28-39.05) < 0.001
Quality of studies
High (≥ 12) 11 583/491 0 0.495 F 18.81 (10.84-32.63) < 0.001
Low (< 12) 7 427/311 77 < 0.001 R 8.83 (1.85-42.11) 0.006
a

When significant heterogeneity was found (I2≥ 50% or PQ-test ≤ 0.1), the random-effects model (DerSimonian-Laird method) was used to pool the results; otherwise, the fixed-effects model (Mantel-Haenszel method) was applied.

b

Non-healthy controls included autologous controls (normal tissues adjacent to HSIL specimens), controls with benign gynecological diseases and mixed controls.

Abbreviations: N, number; CC, cervical cancer; R, random-effects model; F, fixed-effects model.