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. 2019 Dec 26;11:198. doi: 10.1186/s13148-019-0792-0

Table 2.

Evolution of CRTC1 methylation sites during the first month of psychotropic treatment

Probe ID β at baseline, median (IQR) β after 1 month, median (IQR) p value FDR p value1
All patients (n = 78) cg21310814 81.7 (78.5–84.3) 83.7 (81.2–84.9) 0.00005 0.004
cg07015183 88.3 (87–89.5) 89.1 (88–90.3) 0.0001 0.004
cg02961385 94.7 (94.2–95.4) 95.2 (94.7–96) 0.0009 0.02
cg17006757 82.8 (80.4–84.2) 83.7 (82–85.3) 0.003 0.048
cg22536770 94.1 (93.3–94.7) 94.5 (93.9–95.1) 0.003 0.048
Controls (n = 39) None
Cases (n = 39) cg07015183 88.3 (87–89.5) 89.1 (88–90.3) 0.0006 0.02
cg12034943 7.4 (6.4–8.4) 7.2 (6.5–8) 0.0007 0.02
cg17006757 82.8 (80.4–84.2) 83.7 (82–85.3) 0.0008 0.02

Only the sites with significant changes during the first month of treatment are shown. Of note, all significant methylation sites presented in this table are localized in the gene body region of CRTC1

β at baseline refers to methylation levels before starting the current psychotropic treatment

β at first month refers to methylation levels after one month of treatment with psychotropic treatment

Controls indicate patients whose weight remained stable during the first month of treatment

Cases indicate patients with important (≥5%) early weight gain during the first month of treatment

p values were calculated using paired t-tests. Probes are sorted by significance

1p values were adjusted using the false discovery rate approach

None: No site with significant change during the first month was observed in control patients