Literature DB >> 31487564

Longitudinal low density lipoprotein cholesterol goal achievement and cardiovascular outcomes among adult patients with familial hypercholesterolemia: The CASCADE FH registry.

P Barton Duell1, Samuel S Gidding2, Rolf L Andersen3, Thomas Knickelbine4, Lars Anderson3, Eugenia Gianos5, Peter Shrader6, Iris Kindt7, Emily C O'Brien6, Dervilla McCann8, Linda C Hemphill9, Catherine D Ahmed10, Seth S Martin11, John A Larry12, Zahid S Ahmad13, Iftikhar J Kullo14, James A Underberg15, John Guyton16, Paul Thompson17, Katherine Wilemon10, Matthew T Roe6, Daniel J Rader18, Marina Cuchel19, MacRae F Linton20, Michael D Shapiro1, Patrick M Moriarty21, Joshua W Knowles22.   

Abstract

BACKGROUND AND AIMS: There are limited data from the US on outcomes of patients in specialty care for familial hypercholesterolemia (FH).
METHODS: CASCADE FH Registry data were analyzed to assess longitudinal changes in medication usage, in low density lipoprotein cholesterol (LDL-C) levels, and the rate of major adverse cardiovascular events (MACE (myocardial infarction, coronary revascularization, stroke or transient ischemic attack) in adults with FH followed in US specialty clinics.
RESULTS: The cohort consisted of 1900 individuals (61% women, 87% Caucasian), with mean age of 56 ± 15 years, 37% prevalence of ASCVD at enrollment, mean pretreatment LDL-C 249 ± 68 mg/dl, mean enrollment LDL-C 145 mg/dl and 93% taking lipid lowering therapy. Over follow up of 20 ± 11 months, lipid lowering therapy use increased (mean decrease in LDL-C of 32 mg/dl (p < 0.001)). Only 48% of participants achieved LDL-C < 100 mg/dl and 22% achieved LDL-C < 70 mg/dl; ASCVD at enrollment was associated with greater likelihood of goal achievement. MACE event rates were almost 6 times higher among patients with prior ASCVD compared to those without (4.6 vs 0.8/100 patient years). Also associated with incident MACE were markers of FH severity and conventional ASCVD risk factors.
CONCLUSIONS: With care in FH specialized clinics, LDL-C decreased, but LDL-C persisted >100 mg/dl in 52% of patients. High ASCVD event rates suggest that adults with FH warrant designation as having an ASCVD risk equivalent. Earlier and more aggressive therapy of FH is needed to prevent ASCVD events.
Copyright © 2019 [The Author/The Authors]. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cardiovascular disease; Familial hypercholesterolemia; LDL cholesterol goal achievement; Low density lipoprotein (LDL) cholesterol; PCSK9 inhibitor

Mesh:

Substances:

Year:  2019        PMID: 31487564     DOI: 10.1016/j.atherosclerosis.2019.08.007

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  14 in total

Review 1.  Familial Hypercholesterolemia and Lipoprotein(a): Two Partners in Crime?

Authors:  Rodrigo Alonso; Rosa Argüeso; Pilar Álvarez-Baños; Ovidio Muñiz-Grijalvo; Jose Luis Diaz-Diaz; Pedro Mata
Journal:  Curr Atheroscler Rep       Date:  2022-04-07       Impact factor: 5.113

Review 2.  Familial hypercholesterolaemia: evolving knowledge for designing adaptive models of care.

Authors:  Gerald F Watts; Samuel S Gidding; Pedro Mata; Jing Pang; David R Sullivan; Shizuya Yamashita; Frederick J Raal; Raul D Santos; Kausik K Ray
Journal:  Nat Rev Cardiol       Date:  2020-01-23       Impact factor: 32.419

Review 3.  Women Living with Familial Hypercholesterolemia: Challenges and Considerations Surrounding Their Care.

Authors:  Sujana Balla; Eson P Ekpo; Katherine A Wilemon; Joshua W Knowles; Fatima Rodriguez
Journal:  Curr Atheroscler Rep       Date:  2020-08-20       Impact factor: 5.113

4.  Pediatric Lipid Disorders.

Authors:  Scott Leopold; Justin P Zachariah
Journal:  Pediatr Ann       Date:  2021-03-01       Impact factor: 1.132

5.  Pediatric Obesity, Hypertension, Lipids.

Authors:  Scott Leopold; Justin P Zachariah
Journal:  Curr Treat Options Pediatr       Date:  2020-04-15

6.  Impact of Diet on Plasma Lipids in Individuals with Heterozygous Familial Hypercholesterolemia: A Systematic Review of Randomized Controlled Nutritional Studies.

Authors:  Gabrielle Roy; Anykim Boucher; Patrick Couture; Jean-Philippe Drouin-Chartier
Journal:  Nutrients       Date:  2021-01-15       Impact factor: 5.717

7.  Cardiology clinic visit increases likelihood of evidence-based cholesterol prescribing in severe hypercholesterolemia.

Authors:  Nicole A Groth; Neil J Stone; Catherine P Benziger
Journal:  Clin Cardiol       Date:  2020-12-23       Impact factor: 2.882

8.  Cost-effectiveness of cascade genetic testing for familial hypercholesterolemia in the United States: A simulation analysis.

Authors:  Candace L Jackson; Todd Huschka; Bijan Borah; Katherine Agre; Magdi Zordok; Medhat Farwati; James Moriarty; Iftikhar J Kullo
Journal:  Am J Prev Cardiol       Date:  2021-08-15

Review 9.  Homozygous Familial Hypercholesterolemia.

Authors:  Atsushi Nohara; Hayato Tada; Masatsune Ogura; Sachiko Okazaki; Koh Ono; Hitoshi Shimano; Hiroyuki Daida; Kazushige Dobashi; Toshio Hayashi; Mika Hori; Kota Matsuki; Tetsuo Minamino; Shinji Yokoyama; Mariko Harada-Shiba
Journal:  J Atheroscler Thromb       Date:  2021-04-18       Impact factor: 4.928

Review 10.  Diagnosis and Treatment of Heterozygous Familial Hypercholesterolemia.

Authors:  Mary P McGowan; Seyed Hamed Hosseini Dehkordi; Patrick M Moriarty; P Barton Duell
Journal:  J Am Heart Assoc       Date:  2019-12-16       Impact factor: 5.501

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