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. Author manuscript; available in PMC: 2018 Aug 15.
Published in final edited form as: Stat Med. 2017 May 11;36(18):2947–2960. doi: 10.1002/sim.7332

Table 2.

The power (%) of detecting a non-zero GxE interaction or joint exposure effect using different sampling designs and likelihood approaches. Results are based on 1000 replicates, each including a cohort of 1000 subjects from which 250 are selected for retrospective genotyping. Unbalanced longitudinal outcome is considered, with a monotone missing pattern of 10% random dropouts at each follow-up visit and up to 5 measurements for each subject. Genotype assumed to be independent of personal exposure, with a prevalence of 0.2. βE = −1.5 and βGE = −1.5.

Sampling scheme Sampling variable UUL IPWL CCL FCL

βGE βE + βGE βGE βE + βGE βGE βE + βGE βGE βE + βGE
Random - 22 70 - - - - - -
E-enriched Ei 33 89 - - - - 35 94
OLS-based η̂0i 2 80 56 81 25 90 34 92
E + OLS (Ei, η̂0i) 7 42 34 75 29 97 46 98
BLUP-based â0i 18 69 55 84 32 95 33 95
E + BLUP (Ei, â0i) 2 25 36 77 41 95 48 96