Characteristics and Outcomes of Atrial Fibrillation in Patients With Thyroid Disease (from the ARISTOTLE Trial).


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 11 2019
Historique:
received: 09 05 2019
revised: 25 07 2019
accepted: 26 07 2019
pubmed: 3 9 2019
medline: 17 3 2020
entrez: 3 9 2019
Statut: ppublish

Résumé

Whether patients with atrial fibrillation (AF) and thyroid disease are clinically distinct from those with AF and no thyroid disease is unknown. Furthermore, the effectiveness of anticoagulation for prevention of AF-related thromboembolic events in patients with thyroid disease has not been adequately studied. Patients enrolled in the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation, which compared apixaban with warfarin in patients with AF (n = 18,201), were categorized by thyroid disease history at randomization (hypothyroidism, hyperthyroidism, and no thyroid disease). Adjusted hazard ratios derived from Cox models were used to compare outcomes by thyroid disease history. Associations between randomized treatment and outcomes by thyroid disease history were examined using Cox models with interaction terms. A total of 18,021/18,201 (99%) patients had available thyroid disease history at randomization: 1,656 (9%) had hypothyroidism, 321 (2%) had hyperthyroidism, and 16,044 (89%) had no thyroid disease. When compared with those without a history of thyroid disease, patients with hypo- or hyperthyroidism were more likely to be female (60.4% vs 32.1%; 52.0% vs 32.1%; both p <0.0001). Patients with hypothyroidism were older (73 vs 70 years, p <0.0001) and more likely to have had previous falls (8.7% vs 4.3%, p <0.0001). There was no difference in clinical outcomes by thyroid disease history. The benefit of apixaban compared with warfarin was similar regardless of thyroid disease history (interaction p >0.10). In conclusion, despite differences in baseline characteristics of patients with and without thyroid disease, their clinical outcomes were similar. The benefit of apixban compared with warfarin was preserved regardless of thyroid disease history.

Identifiants

pubmed: 31474328
pii: S0002-9149(19)30877-X
doi: 10.1016/j.amjcard.2019.07.046
pmc: PMC7194994
mid: NIHMS1580947
pii:
doi:

Substances chimiques

Anticoagulants 0
Pyrazoles 0
Pyridones 0
apixaban 3Z9Y7UWC1J
Warfarin 5Q7ZVV76EI

Banques de données

ClinicalTrials.gov
['NCT00412984']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1406-1412

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL069749
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Références

Thyroid. 2006 Apr;16(4):369-74
pubmed: 16646683
Lancet. 1989 Jan 28;1(8631):175-9
pubmed: 2563096
N Engl J Med. 2001 Feb 15;344(7):501-9
pubmed: 11172193
Case Rep Med. 2014;2014:292468
pubmed: 24991217
N Engl J Med. 2013 Nov 28;369(22):2093-104
pubmed: 24251359
BMJ. 2012 Nov 27;345:e7895
pubmed: 23186910
Circulation. 2014 Feb 25;129(8):837-47
pubmed: 24345399
Q J Med. 1986 Jan;58(225):43-51
pubmed: 3704105
N Engl J Med. 2011 Sep 8;365(10):883-91
pubmed: 21830957
N Engl J Med. 2009 Sep 17;361(12):1139-51
pubmed: 19717844
Am Heart J. 2010 Mar;159(3):331-9
pubmed: 20211292
PLoS One. 2013;8(2):e57893
pubmed: 23469097
South Med J. 1989 Oct;82(10):1292-3
pubmed: 2799447
Am Heart J. 2014 Jan;167(1):123-6
pubmed: 24332151
N Engl J Med. 2011 Sep 15;365(11):981-92
pubmed: 21870978
J Am Coll Cardiol. 2014 Dec 2;64(21):e1-76
pubmed: 24685669
J Thromb Haemost. 2018 Apr;16(4):634-645
pubmed: 29573126

Auteurs

Sarah A Goldstein (SA)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina. Electronic address: sarah.goldstein@duke.edu.

Jennifer Green (J)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Kurt Huber (K)

Wilhelminenspital, 3rd Medical Department, Cardiology, Medical University of Vienna, Vienna, Austria.

Daniel M Wojdyla (DM)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

John H Alexander (JH)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Dragos Vinereanu (D)

University of Medicine and Pharmacy Carol Davila, University and Emergency Hospital, Bucharest, Romania.

Lars Wallentin (L)

Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.

Christopher B Granger (CB)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Sana M Al-Khatib (SM)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH