4.6 Article

Association Between Plasma Trimethyllysine and Prognosis of Patients With Ischemic Stroke

Journal

JOURNAL OF THE AMERICAN HEART ASSOCIATION
Volume 10, Issue 23, Pages -

Publisher

WILEY
DOI: 10.1161/JAHA.121.020979

Keywords

gut microbiota; ischemic stroke; trimethylamine N-oxide; trimethyllysine

Funding

  1. Ministry of Science and Technology of the People's Republic of China [2017YFC1310901, 2017YFC1307905]
  2. National Key Research and Development Program of China [2020YFA0803700]
  3. Beijing Municipal Administration of Hospitals' Mission Plan [SML20150502]
  4. National Natural Science Foundation of China [81600999, 81701141, 91639108, 81770272, 81970425]
  5. Beijing Municipal Science & Technology Commission [D171100003017002, D151100002015003]
  6. China Postdoctoral Science Foundation [2018M630179]
  7. National Science and Technology Major Project [2017ZX09304018]
  8. Young Scientist Program [YSP201704]

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Elevated levels of trimethyllysine are associated with increased risk of cardiovascular death in patients with ischemic stroke/transient ischemic attack. Mediation analyses suggest that trimethyllysine may contribute to cardiovascular death through inflammation and renal function, indicating a possible pathomechanistic link.
Background Trimethyllysine, a trimethylamine N-oxide precursor, has been identified as an independent cardiovascular risk factor in acute coronary syndrome. However, limited data are available to examine the role of trimethyllysine in the population with stroke. We aimed to examine the relationship between plasma trimethyllysine levels and stroke outcomes in patients presenting with ischemic stroke or transient ischemic attack. Methods and Results Data of 10 027 patients with ischemic stroke/transient ischemic attack from the CNSR-III (Third China National Stroke Registry) and 1-year follow-up data for stroke outcomes were analyzed. Plasma levels of trimethyllysine were measured with mass spectrometry. The association between trimethyllysine and stroke outcomes was analyzed using Cox regression models. Mediation analysis was performed to examine the mediation effects of risk factors on the associations of trimethyllysine and stroke outcomes. Elevated trimethyllysine levels were associated with increased risk of cardiovascular death (quartile 4 versus quartile 1: adjusted hazard ratio [HR], 1.72; 95% CI, 1.03-2.86) and all-cause mortality (quartile 4 versus quartile 1: HR, 1.97; 95% CI, 1.40-2.78) in multivariate Cox regression model. However, no associations were found between trimethyllysine and nonfatal stroke recurrence or nonfatal myocardial infarction. Trimethyllysine was associated with cardiovascular death independent of trimethylamine N-oxide. Both estimated glomerular filtration rate and hs-CRP (high-sensitivity C-reactive protein) had significant mediation effects on the association of trimethyllysine with cardiovascular death, with a mediation effect of 37.8% and 13.4%, respectively. Conclusions Elevated trimethyllysine level is associated with cardiovascular death among patients with ischemic stroke/transient ischemic attack. Mediation analyses propose that trimethyllysine contributes to cardiovascular death through inflammation and renal function, suggesting a possible pathomechanistic link.

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