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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 4.

Association between polygenic risk score of shorter telomere length and the risk of later-life onset of depression and anxiety a,b

Depression c Anxiety d

N (yes/no) OR (95% CI) N (yes/no) OR (95% CI)
Quintile 1 432/1342 1.00 (ref) 356/1583 1.00 (ref)
Quintile 2 440/1356 1.03 (0.88–1.20) 357/1682 0.91 (0.71–1.16)
Quintile 3 466/1308 1.10 (0.94–1.28) 336/1603 0.93 (0.79–1.10)
Quintile 4 455/1375 1.06 (0.91–1.23) 344/1565 0.98 (0.83–1.15)
Quintile 5 461/1353 1.07 (0.91–1.24) 351/1628 0.95 (0.82–1.11)
Per 1 SD increase 2254/6734 1.02 (0.97–1.07) 1744/8061 1.00 (0.95–1.06)
a

All models adjust for age at baseline, first three genetic principal components-derived eigenvectors, and disease status of 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

Only participants with age 60 years or above and with no prior history of depression in 2000 were included. New cases of depression was defined as self-reported doctor diagnosed depression, regular use of antidepressants, or depressive symptoms above the clinical cutoff (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 after 2000 to 2012 in the NHS follow-up.

d

Only participants with age of 50 or above and with Crown-Crisp Index score of 3 points or below in 1988 were included. New cases of severe anxiety symptoms was defined by Crown-Crisp Index ≥ 6 measured in 2004 and/or Generalized Anxiety Disorder Questionnaire (GAD-7) ≥ 5 measured in 2012