Table 1

Milestones in HDL science.

  • Epidemiological studies reveal an independent inverse relationship between HDL-C concentrations and CHD (1976)

  • Elucidation of monogenic disorders affecting HDL-C concentrations including CETP deficiency (1989)

  • CETP inhibitors developed as potential antiatherogenic therapies (1990)

  • APOA1 overexpression reduces atherosclerosis in animal models (1991)

  • ABCA1 deficiency elucidated as the cause of Tangier Disease (1999)

  • ABCA1 found to be an LXR target (2000)

  • LXR activators reduce atherosclerosis (2002)

  • The first CETP inhibitor in clinical trials (torcetrapib) increases CHD and overall mortality (2007)

  • Dozens of novel SNPs found to associate with HDL concentrations in human GWAS (2010)

  • Cholesterol efflux capacity of HDL correlates inversely with CHD independent of HDL-C (2011)

  • Mendelian Randomization studies suggest that SNPs that associate with HDL-C concentrations do not associate with CHD (2012)

  • The CETP inhibitor anacetrapib produces a significant but moderate reduction in CHD. The sponsors decline to seek marketing approval (2017)

  • Reconstituted HDL preparations optimized for human phase 3 studies (2018)

  • Epidemiological studies reveal an independent inverse relationship between HDL-C concentrations and CHD (1976)

  • Elucidation of monogenic disorders affecting HDL-C concentrations including CETP deficiency (1989)

  • CETP inhibitors developed as potential antiatherogenic therapies (1990)

  • APOA1 overexpression reduces atherosclerosis in animal models (1991)

  • ABCA1 deficiency elucidated as the cause of Tangier Disease (1999)

  • ABCA1 found to be an LXR target (2000)

  • LXR activators reduce atherosclerosis (2002)

  • The first CETP inhibitor in clinical trials (torcetrapib) increases CHD and overall mortality (2007)

  • Dozens of novel SNPs found to associate with HDL concentrations in human GWAS (2010)

  • Cholesterol efflux capacity of HDL correlates inversely with CHD independent of HDL-C (2011)

  • Mendelian Randomization studies suggest that SNPs that associate with HDL-C concentrations do not associate with CHD (2012)

  • The CETP inhibitor anacetrapib produces a significant but moderate reduction in CHD. The sponsors decline to seek marketing approval (2017)

  • Reconstituted HDL preparations optimized for human phase 3 studies (2018)

Table 1

Milestones in HDL science.

  • Epidemiological studies reveal an independent inverse relationship between HDL-C concentrations and CHD (1976)

  • Elucidation of monogenic disorders affecting HDL-C concentrations including CETP deficiency (1989)

  • CETP inhibitors developed as potential antiatherogenic therapies (1990)

  • APOA1 overexpression reduces atherosclerosis in animal models (1991)

  • ABCA1 deficiency elucidated as the cause of Tangier Disease (1999)

  • ABCA1 found to be an LXR target (2000)

  • LXR activators reduce atherosclerosis (2002)

  • The first CETP inhibitor in clinical trials (torcetrapib) increases CHD and overall mortality (2007)

  • Dozens of novel SNPs found to associate with HDL concentrations in human GWAS (2010)

  • Cholesterol efflux capacity of HDL correlates inversely with CHD independent of HDL-C (2011)

  • Mendelian Randomization studies suggest that SNPs that associate with HDL-C concentrations do not associate with CHD (2012)

  • The CETP inhibitor anacetrapib produces a significant but moderate reduction in CHD. The sponsors decline to seek marketing approval (2017)

  • Reconstituted HDL preparations optimized for human phase 3 studies (2018)

  • Epidemiological studies reveal an independent inverse relationship between HDL-C concentrations and CHD (1976)

  • Elucidation of monogenic disorders affecting HDL-C concentrations including CETP deficiency (1989)

  • CETP inhibitors developed as potential antiatherogenic therapies (1990)

  • APOA1 overexpression reduces atherosclerosis in animal models (1991)

  • ABCA1 deficiency elucidated as the cause of Tangier Disease (1999)

  • ABCA1 found to be an LXR target (2000)

  • LXR activators reduce atherosclerosis (2002)

  • The first CETP inhibitor in clinical trials (torcetrapib) increases CHD and overall mortality (2007)

  • Dozens of novel SNPs found to associate with HDL concentrations in human GWAS (2010)

  • Cholesterol efflux capacity of HDL correlates inversely with CHD independent of HDL-C (2011)

  • Mendelian Randomization studies suggest that SNPs that associate with HDL-C concentrations do not associate with CHD (2012)

  • The CETP inhibitor anacetrapib produces a significant but moderate reduction in CHD. The sponsors decline to seek marketing approval (2017)

  • Reconstituted HDL preparations optimized for human phase 3 studies (2018)

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