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. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: J Psychiatr Res. 2018 May 26;103:182–188. doi: 10.1016/j.jpsychires.2018.05.021

Table 2.

Association between polygenic risk score of shorter telomere length and lifetime risk of depression and anxiety a,b

Depression c Anxiety d

N (yes/no) OR (95% CI) N (yes/no) OR (95% CI)
Quintile 1 1407/1965 1.00 (ref) 960/2150 1.00 (ref)
Quintile 2 1427/1941 1.04 (0.94–1.14) 925/2208 0.94 (0.84–1.05)
Quintile 3 1429/1882 1.06 (0.94–1.19) 971/2115 1.03 (0.92–1.15)
Quintile 4 1396/1971 1.00 (0.91–1.10) 999/2110 1.07 (0.96–1.19)
Quintile 5 1398/2005 0.98 (0.89–1.08) 953/2171 1.00 (0.89–1.11)
Per 1 SD increase 7057/9764 0.99 (0.96–1.02) 4808/10754 1.01 (0.98–1.05)
a

All models adjust for age at baseline, first three genetic principal components-derived eigenvectors, and disease endpoints in original nested case-control studies.

b

Analyses were first conducted within each of the platform-specific genetic datasets and then a combined estimate was obtained using a random-effect meta-analysis. There was no effect heterogeneity between platforms. The estimates and p-values shown in the table were meta-analyzed results.

c

Depression was defined as self-reported doctor-diagnosed depression, regular antidepressant use, or the presence of severe depressive symptoms above clinical cutoff (Mental Health Index-5 ≤52 measured on the 1992Mental Health Index-5 ≤52 measured on the 1996, and 2000 questionnaires, 10-item Center for Epidemiologic Studies Depression ≥ 10 measured on the 2004 questionnaire, and/or 15-item Geriatric Depression Scale ≥ 6 measured on the 2012 questionnaire) anytime between 1992 and 2012 in the NHS cohort follow-up.

d

The presence of severe anxiety symptom was defined by Crown-Crisp Index ≥ 6 measured in 1988 and 2004 and/or Generalized Anxiety Disorder Questionnaire (GAD-7) ≥ 5 measured in 2012