Yong Hu1, Yong-Ming He2. 1. Division of Cardiology, 903 Hospital, Jiangyou, China. 2. Division of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou, China.
We read with great interest the article by Guo et al. (1). This study has demonstrated that lipoprotein(a) [Lp(a)] is significantly associated with the risk of coronary heart disease in a dose-responding manner. Subgroup analysis has not altered this association. Our prior cross-sectional study has a similar finding with respect to Lp(a)’s role played in incidence of coronary artery disease (2). However, the study method regarding the synergistic effects between Lp(a) and dyslipidemia should be reconsidered. Assume that risk A for a disease is 1.10 and that risk B for the same disease is 1.21, and coexistent risk A and B for the disease may be greater, equal or less than 1.10+1.21. If coexistent risk A and B for the disease is 1.50 (greater than the sum of the separate effect), the synergistic effect (1.50–1.31), measured by Relative excess risk due to interaction (RERI) (3), occures. Our previous studies have demonstrated that the Lp(a) has a synergistic effect with low density lipoprotein cholesterol (LDL-C) or body mass index on the incidence of coronary artery disease (4,5).The article’s supplementary files as
Authors: Tomas Andersson; Lars Alfredsson; Henrik Källberg; Slobodan Zdravkovic; Anders Ahlbom Journal: Eur J Epidemiol Date: 2005 Impact factor: 8.082