1. The role of HDL in atherosclerosis Prof. M. John Chapman (Paris, France) in discussion with Dr. Kees Hovingh (Amsterdam, The Netherlands)

2. Genetics (1) What is the relationship between functional mutations in the major genes involved in HDL metabolism and cardiovascular risk?

3. Genetics of HDL metabolism (1) Studying families with carries of mutations Mutations in LCAT, ABCA1, ApoA-1

4. HDL metabolism

5. Genetics of HDL metabolism (2) Relatively small number of subjects Heterozygous carriers: increased IMT Lack of large numbers and relevance of the genes Different groups showing different data ApoA-1, one of the best targets of atherosclerosis

6. ApoA-1

7. Genetics (2) Should we widen our studies of the key genes within a specific family or cohort?

8. Genetics of HDL metabolism (2) Individual with SRB1 mutation, but a low-normal HDL level: counterintuitive Sequencing ApoA-1, LCAT and ABCA1 Neutralizing effects of other monogenetic disorders: HDL level and CAD risk Sequencing a lot of genes all at once Better view of the landscape of genetic disorders underpinning HDL levels

9. Systems biology Is this approach comparable with systems biology?

10. Systems biology (1) Measure enzymatic endpoints Concept: impact of a gene on the phenotype We might have been using the wrong system

11. Systems biology (2) Our field: primarily focused on murine cell lines Also human cell lines: little relation to the profile in in vitro cultured macrophages

12. HDL-mediated cholesterol efflux from cholesterol-rich macrophages apo E apo A-1 Rader DJ. J Clin Invest. 2006;116:3090–3100.

13. Systems biology (3) Effort to define standard culture conditions Complexity of the HDL or ApoA-1 ligand

14. Mechanisms of cellular cholesterol efflux to HDL particles

15. HDL metabolism: impact of CETP inhibition

16. Systems biology (4) CETP: most significant gene (genome studies) Reevaluate our ex vivo/in vitro approaches

17. Controversy Is the controversy mainly associated with the systems that have been used?

18. Controversy Great deal of difference between the expression of these receptors, not only in macrophages from different species, but also in human conditions