<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(1)</volume><submitter>Fruchart JC</submitter><pubmed_abstract>In the era of precision medicine, treatments that target specific modifiable characteristics of high-risk patients have the potential to lower further the residual risk of atherosclerotic cardiovascular events. Correction of atherogenic dyslipidemia, however, remains a major unmet clinical need. Elevated plasma triglycerides, with or without low levels of high-density lipoprotein cholesterol (HDL-C), offer a key modifiable component of this common dyslipidemia, especially in insulin resistant conditions such as type 2 diabetes mellitus. The development of selective peroxisome proliferator-activated receptor alpha modulators (SPPARMα) offers an approach to address this treatment gap. This Joint Consensus Panel appraised evidence for the first SPPARMα agonist and concluded that this agent re</pubmed_abstract><journal>Cardiovascular diabetology</journal><pagination>71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6549355</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) paradigm: conceptual framework and therapeutic potential : A consensus statement from the International Atherosclerosis Society (IAS) and the Residual Risk Reduction Initiative (R3i) Foundation.</pubmed_title><pmcid>PMC6549355</pmcid><pubmed_authors>Wahli W</pubmed_authors><pubmed_authors>Vrablik M</pubmed_authors><pubmed_authors>Sadikot S</pubmed_authors><pubmed_authors>Ogawa H</pubmed_authors><pubmed_authors>Santos RD</pubmed_authors><pubmed_authors>Hermans MP</pubmed_authors><pubmed_authors>Lorenzatti AJ</pubmed_authors><pubmed_authors>Su TC</pubmed_authors><pubmed_authors>Corsini A</pubmed_authors><pubmed_authors>Eckel RH</pubmed_authors><pubmed_authors>Nordestgaard BG</pubmed_authors><pubmed_authors>Ceska R</pubmed_authors><pubmed_authors>Tartar A</pubmed_authors><pubmed_authors>Ezhov MV</pubmed_authors><pubmed_authors>Aguilar-Salinas C</pubmed_authors><pubmed_authors>Krempf M</pubmed_authors><pubmed_authors>Pradhan A</pubmed_authors><pubmed_authors>Zambon A</pubmed_authors><pubmed_authors>Tenenbaum A</pubmed_authors><pubmed_authors>Aikawa M</pubmed_authors><pubmed_authors>Despres JP</pubmed_authors><pubmed_authors>Ponte-Negretti CI</pubmed_authors><pubmed_authors>Susekov AV</pubmed_authors><pubmed_authors>Taskinen MR</pubmed_authors><pubmed_authors>Kodama T</pubmed_authors><pubmed_authors>Sritara P</pubmed_authors><pubmed_authors>Amarenco P</pubmed_authors><pubmed_authors>Libby P</pubmed_authors><pubmed_authors>Farnier M</pubmed_authors><pubmed_authors>Al Rasadi K</pubmed_authors><pubmed_authors>Barter PJ</pubmed_authors><pubmed_authors>Reiner Z</pubmed_authors><pubmed_authors>Plutzky J</pubmed_authors><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Duriez P</pubmed_authors><pubmed_authors>Tomlinson B</pubmed_authors><pubmed_authors>Ruscica M</pubmed_authors><pubmed_authors>Stock JK</pubmed_authors><pubmed_authors>Ginsberg HN</pubmed_authors><pubmed_authors>Ray KK</pubmed_authors><pubmed_authors>Tybjærg-Hansen A</pubmed_authors><pubmed_authors>Ishibashi S</pubmed_authors><pubmed_authors>McPherson R</pubmed_authors><pubmed_authors>Watts GF</pubmed_authors><pubmed_authors>Ridker PM</pubmed_authors><pubmed_authors>Karpe F</pubmed_authors><pubmed_authors>Fruchart JC</pubmed_authors><pubmed_authors>Koenig W</pubmed_authors><pubmed_authors>Packard CJ</pubmed_authors><pubmed_authors>Tokgozoglu LS</pubmed_authors><pubmed_authors>Shimano H</pubmed_authors><pubmed_authors>Yokote K</pubmed_authors><pubmed_authors>Yamashita S</pubmed_authors><pubmed_authors>Valensi P</pubmed_authors><pubmed_authors>Nunez-Cortes JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>The selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) paradigm: conceptual framework and therapeutic potential : A consensus statement from the International Atherosclerosis Society (IAS) and the Residual Risk Reduction Initiative (R3i) Foundation.</name><description>In the era of precision medicine, treatments that target specific modifiable characteristics of high-risk patients have the potential to lower further the residual risk of atherosclerotic cardiovascular events. Correction of atherogenic dyslipidemia, however, remains a major unmet clinical need. Elevated plasma triglycerides, with or without low levels of high-density lipoprotein cholesterol (HDL-C), offer a key modifiable component of this common dyslipidemia, especially in insulin resistant conditions such as type 2 diabetes mellitus. The development of selective peroxisome proliferator-activated receptor alpha modulators (SPPARMα) offers an approach to address this treatment gap. This Joint Consensus Panel appraised evidence for the first SPPARMα agonist and concluded that this agent re</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-06-19T03:17:25.777Z</modification><creation>2019-07-24T07:10:06Z</creation></dates><accession>S-EPMC6549355</accession><cross_references><pubmed>31164165</pubmed><doi>10.1186/s12933-019-0864-7</doi></cross_references></HashMap>