Age-Dependent Efficacy of Ezetimibe for Low-Density Lipoprotein Cholesterol Reduction in Japanese Patients with or without Type 2 Diabetes Mellitus.

age ezetimibe low-density lipoprotein cholesterol

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
01 Jun 2020
Historique:
received: 03 05 2020
revised: 28 05 2020
accepted: 29 05 2020
entrez: 5 6 2020
pubmed: 5 6 2020
medline: 5 6 2020
Statut: epublish

Résumé

Ezetimibe reduces cardiovascular risk by lowering the levels of low-density lipoprotein cholesterol (LDL-C). However, there is limited information regarding the factors associated with ezetimibe-mediated LDL-C reduction. We investigated the factors associated with LDL-C reduction after ezetimibe administration in Japanese patients with or without type 2 diabetes mellitus (T2DM). This single-center retrospective observational study enrolled a total of 266 consecutive ezetimibe-naïve patients, of which 154 were excluded because of either switching from statin or fenofibrate to ezetimibe (n = 52) or ezetimibe discontinuation (n = 102). Finally, 112 patients were eligible for analysis. To identify the factors influencing LDL-C levels, univariate and multivariate linear regression analyses were performed after 52 weeks of ezetimibe treatment. Overall, advanced age, T2DM, and high baseline LDL-C were significantly associated with a greater decrease in LDL-C levels. In the non-T2DM group, advanced age and high baseline LDL-C were associated with greater decrease in LDL-C levels. In the T2DM group, baseline LDL-C was the only factor that influenced the change in LDL-C levels. Advanced age was significantly associated with higher LDL-C reduction in non-T2DM patients, but not in T2DM patients. Ezetimibe use might be beneficial in older patients without T2DM. The lack of association between age and the LDL-C lowering effect by ezetimibe in patients with T2DM may be due to yet unknown mechanism except low statistical power.

Identifiants

pubmed: 32492927
pii: jcm9061675
doi: 10.3390/jcm9061675
pmc: PMC7356893
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Circulation. 2018 Apr 10;137(15):1571-1582
pubmed: 29263150
Eur Heart J. 2003 Apr;24(8):729-41
pubmed: 12713767
Am J Cardiol. 1997 Jul 1;80(1):106-7
pubmed: 9205036
J Am Coll Cardiol. 2006 Aug 1;48(3):438-45
pubmed: 16875966
Prim Care. 2013 Mar;40(1):195-211
pubmed: 23402469
Atherosclerosis. 2016 Feb;245:161-70
pubmed: 26722833
Arterioscler Thromb Vasc Biol. 2001 May;21(5):832-7
pubmed: 11348882
Circulation. 2014 Jun 24;129(25 Suppl 2):S1-45
pubmed: 24222016
Int J Clin Pract. 2005 Jun;59(6):619-27
pubmed: 15924587
Endocr J. 2010;57(10):903-8
pubmed: 20733267
Eur Heart J. 2020 Jan 1;41(1):111-188
pubmed: 31504418
Vasc Health Risk Manag. 2012;8:415-27
pubmed: 22910633
N Engl J Med. 2015 Jun 18;372(25):2387-97
pubmed: 26039521
Diabetes Care. 2010 May;33(5):1021-4
pubmed: 20150290
Pharmacotherapy. 2003 Nov;23(11):1463-74
pubmed: 14620392
JAMA. 1998 May 27;279(20):1643-50
pubmed: 9613915
Ther Adv Chronic Dis. 2017 Jan;8(1):4-11
pubmed: 28203346
Diabetes Obes Metab. 2011 Jul;13(7):615-28
pubmed: 21332628

Auteurs

Satoshi Yamaguchi (S)

Department of Diabetes, Endocrinology and Metabolism, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1247, Japan.
Department of Cardiology, Nakagami Hospital, 610 Noborikawa, Okinawa 904-2195, Japan.

Kageyuki Oba (K)

Department of Cardiology, Tomishiro Central Hospital, 25 Ueta, Tomishiro, Okinawa 901-0243, Japan.

Moritake Higa (M)

Department of Diabetes and Life-Style Related Disease Center, Tomishiro Central Hospital, 25 Ueta, Tomishiro, Okinawa 901-0243, Japan.

Osamu Arasaki (O)

Department of Cardiology, Tomishiro Central Hospital, 25 Ueta, Tomishiro, Okinawa 901-0243, Japan.

Michio Shimabukuro (M)

Department of Diabetes, Endocrinology and Metabolism, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1247, Japan.

Classifications MeSH