Understanding interactions between risk factors, and assessing the utility of the additive and multiplicative models through simulations

被引:15
作者
Diaz-Gallo, Lina-Marcela [1 ]
Brynedal, Boel [2 ]
Westerlind, Helga [3 ]
Sandberg, Rickard [4 ]
Ramskold, Daniel [4 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp, Div Rheumatol, Dept Med Solna,Ctr Mol Med, Stockholm, Sweden
[2] Karolinska Inst, Inst Environm Med, Stockholm, Sweden
[3] Karolinska Inst, Dept Med Solna, Clin Epidemiol Div, Stockholm, Sweden
[4] Karolinska Inst, Dept Cell & Mol Biol, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
GENOME-WIDE ASSOCIATION; MISSING HERITABILITY;
D O I
10.1371/journal.pone.0250282
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the genetic background of complex diseases requires the expansion of studies beyond univariate associations. Therefore, it is important to use interaction assessments of risk factors in order to discover whether, and how genetic risk variants act together on disease development. The principle of interaction analysis is to explore the magnitude of the combined effect of risk factors on disease causation. In this study, we use simulations to investigate different scenarios of causation to show how the magnitude of the effect of two risk factors interact. We mainly focus on the two most commonly used interaction models, the additive and multiplicative risk scales, since there is often confusion regarding their use and interpretation. Our results show that the combined effect is multiplicative when two risk factors are involved in the same chain of events, an interaction called synergism. Synergism is often described as a deviation from additivity, which is a broader term. Our results also confirm that it is often relevant to estimate additive effect relationships, because they correspond to independent risk factors at low disease prevalence. Importantly, we evaluate the threshold of more than two required risk factors for disease causation, called the multifactorial threshold model. We found a simple mathematical relationship (square root) between the threshold and an additive-to-multiplicative linear effect scale (AMLES), where 0 corresponds to an additive effect and 1 to a multiplicative. We propose AMLES as a metric that could be used to test different effects relationships at the same time, given that it can simultaneously reveal additive, multiplicative and intermediate risk effects relationships. Finally, the utility of our simulation study was demonstrated using real data by analyzing and interpreting gene-gene interaction odds ratios from a rheumatoid arthritis case-control cohort.
引用
收藏
页数:17
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