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Gut Microbiota‐Dependent Trimethylamine N‐oxide and Cardiovascular Outcomes in Patients With Prior Myocardial Infarction: A Nested Case Control Study From the PEGASUS‐TIMI 54 Trial

Authors: Stanley L. Hazen; Stanley L. Hazen; David A. Morrow; Zeneng Wang; Marc P. Bonaca; Marc S. Sabatine; Marc Cohen; +7 Authors

Gut Microbiota‐Dependent Trimethylamine N‐oxide and Cardiovascular Outcomes in Patients With Prior Myocardial Infarction: A Nested Case Control Study From the PEGASUS‐TIMI 54 Trial

Abstract

Background Trimethylamine N‐oxide ( TMAO ) may have prothrombotic properties. We examined the association of TMAO quartiles with major adverse cardiovascular events ( MACE ) and the effect of TMAO on the efficacy of ticagrelor. Methods and Results PEGASUS ‐ TIMI 54 (Prevention of Cardiovascular Events in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin ‐ Thrombolysis in Myocardial Infarction 54) randomized patients with prior myocardial infarction to ticagrelor or placebo (median follow‐up 33 months). Baseline plasma concentrations of TMAO were measured in a nested case‐control study of 597 cases with cardiovascular death, myocardial infarction, or stroke ( MACE ) and 1206 controls matched for age, sex, and estimated glomerular filtration rate [ eGFR ]. Odds ratios ( OR ) were used for the association between TMAO quartiles and MACE , adjusting for baseline clinical characteristics (age, sex, eGFR , region, body mass index, hypertension, hypercholesterolemia, diabetes mellitus, smoking, peripheral artery disease, index event, aspirin dosage and treatment arm), and cardiovascular biomarkers (hs‐TnT [high‐sensitivity troponin T], hs‐ CRP [high‐sensitivity C‐reactive protein], NT ‐pro BNP [N‐terminal‐pro‐B‐type natriuretic peptide]). Higher TMAO quartiles were associated with risk of MACE ( OR for quartile 4 versus quartile 1, 1.43, 95% CI, 1.06–1.93, P trend=0.015). The association was driven by cardiovascular death ( OR 2.25, 95% CI, 1.28–3.96, P trend=0.003) and stroke ( OR 2.68, 95% CI, 1.39–5.17, P trend<0.001). After adjustment for clinical factors, the association persisted for cardiovascular death ( OR adj 1.89, 95% CI, 1.03–3.45, P trend=0.027) and stroke ( OR adj 2.01, 95% CI, 1.01–4.01, P trend=0.022), but was slightly attenuated after adjustment for cardiovascular biomarkers (cardiovascular death: OR adj 1.74, 95% CI, 0.88–3.45, P trend=0.079; and stroke: OR adj 1.82, 95% CI, 0.88–3.78, P trend=0.056). The reduction in MACE with ticagrelor was consistent across TMAO quartiles ( P interaction=0.92). Conclusions Among patients with prior myocardial infarction, higher TMAO levels were associated with cardiovascular death and stroke but not with recurrent myocardial infarction. The efficacy of ticagrelor was consistent regardless of TMAO levels. Registration URL : https://www.clini​caltr​ials.gov ; Unique identifiers: PEGASUS ‐ TIMI 54, NCT 01225562.

Keywords

Male, Ticagrelor, Time Factors, Myocardial Infarction, Ticagrelor / adverse effects, Aspirin / therapeutic use, antiplatelet therapy, Recurrence, Risk Factors, Myocardial Infarction / microbiology, Secondary Prevention, Methylamines / blood, Original Research, Randomized Controlled Trials as Topic, Trimethylamine N‐oxide, Dual Anti-Platelet Therapy, Middle Aged, Stroke / mortality, stroke, Myocardial Infarction / mortality, Thrombosis / blood, Up-Regulation, Intestines, Stroke, Treatment Outcome, myocardial infarction, Intestines / microbiology, Female, Dual Anti-Platelet Therapy / adverse effects, Stroke / prevention & control, Gut microbiota, Risk Assessment, Ticagrelor / therapeutic use, ticagrelor, Thrombosis / mortality, Methylamines, Diseases of the circulatory (Cardiovascular) system, Humans, Myocardial Infarction / blood, Aged, gut microbiota, Aspirin, Bacteria, Antiplatelet therapy, Thrombosis / prevention & control, Stroke / blood, Platelet Aggregation Inhibitors / adverse effects, Platelet Aggregation Inhibitors / therapeutic use, cardiovascular death, Myocardial Infarction / drug therapy, United States, Gastrointestinal Microbiome, Myocardial infarction, Bacteria / metabolism, RC666-701, Case-Control Studies, Cardiovascular death, Platelet Aggregation Inhibitors

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
34
Top 10%
Average
Top 10%
Green
gold