Article

AACE/ACE Lipid Guidelines Define Extreme CVD Risk

The AACE/ACE 2017 recommendations on lipid management prescribe LDL-C targets, and go far lower than any group has ventured to date.

The lipid management guidelines issued by the American Association of Clinical Endocrinologists (AACE) and the American College of Endocrinology (ACE) in April 2017 take a step back in time and re-affirm the use of LDL-C targets to help minimize cardiovascular risk in all patients, and especially those with T2DM. The shift away from the 2013 recommendations by cardiology societies, which focus on primary and secondary treatment categories and medications, includes a first-ever "extreme risk" patient category for whom an LDL-C level of < 55 mg/dL is advised. More discussion around targets vs no targets is ensured.

In this short slide show, we summarize the "extreme risk" category and treatment targets as well as other updates to the 2017 AACE/ACE statement.

 

 

AACE/ACE 2017 T2DM guideline emphasizes early intensive management of dyslipidemia to decrease significant risk of ASCVD in T2D and highlights new algorithm for controlling dyslipidemia to decrease ASCVD risk in T2D.

 

AACE/ACE 2017 T2DM guideline defines new major independent risk factors for ASCVD in patients with T2DM: Polycystic ovary syndrome, CKD stage 3-4, signs of coronary artery calcification.

 

 

AACE/ACE 2017 T2DM guideline sets cutoffs for very high risk (T2D + ≥ 1 risk factor) and high risk (T2D, no other risk factors and/or age < 40y) for LDL-C, non-HDL-C, triglycerides, and apo B.

 

 

 

 

 

 

 

 

 

 

 

 

AACE/ACE 2017 T2DM guideline establishes new “extreme” ASCVD risk category: T2D plus prior ASCVD event (“clinical” ASCVD) or CKD stage 3-4; first organization to include recommendation for LDL-C reduction to < 55 mg/dL. 

 

 

AACE/ACE 2017 T2DM guideline notes lipid particle management may be useful but that there is no evidence to establish target goals.

 

AACE/ACE 2017 T2DM guideline recommends statin drugs as first-line therapy with intensification and adjunct medications added as requird to reach targeted therapeutic levels.

Related Videos
Yehuda Handelsman, MD: Insulin Resistance in Cardiometabolic Disease and DCRM 2.0 | Image Credit: TMIOA
Nathan D. Wong, MD, PhD: Growing Role of Lp(a) in Cardiovascular Risk Assessment | Image Credit: UC Irvine
Laurence Sperling, MD: Expanding Cardiologists' Role in Obesity Management  | Image Credit: Emory University
Laurence Sperling, MD: Multidisciplinary Strategies to Combat Obesity Epidemic | Image Credit: Emory University
Matthew J. Budoff, MD: Examining the Interplay of Coronary Calcium and Osteoporosis | Image Credit: Lundquist Institute
Orly Vardeny, PharmD: Finerenone for Heart Failure with EF >40% in FINEARTS-HF | Image Credit: JACC Journals
Matthew J. Budoff, MD: Impact of Obesity on Cardiometabolic Health in T1D | Image Credit: The Lundquist Institute
Matthew Weir, MD: Prioritizing Cardiovascular Risk in Chronic Kidney Disease | Image Credit: University of Maryland
Erin Michos, MD: HFpEF in Women and Sex-Specific Therapeutic Approaches | Image Credit: Johns Hopkins
© 2024 MJH Life Sciences

All rights reserved.