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Even chained acylcarnitines predict long-term cardiovascular prognosis in patients with chest pain and non-obstructive coronary artery disease.
Storesund, Silje Kjellevold; Karaji, Iman; Strand, Elin; Svardal, Asbjørn; Lønnebakken, Mai Tone; Berge, Rolf Kristian; Tveitevåg Svingen, Gard Frodahl; Nygård, Ottar Kjell; Pedersen, Eva Ringdal.
Affiliation
  • Storesund SK; Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
  • Karaji I; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Strand E; Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
  • Svardal A; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Lønnebakken MT; Department of Immunology and Transfusion Medicine, Haukeland University Hospital, Bergen, Norway.
  • Berge RK; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Tveitevåg Svingen GF; Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
  • Nygård OK; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Pedersen ER; Department of Clinical Science, University of Bergen, Bergen, Norway.
Int J Cardiol Cardiovasc Risk Prev ; 14: 200134, 2022 Sep.
Article in En | MEDLINE | ID: mdl-35647612
ABSTRACT

Background:

Acylcarnitines are essential for mitochondrial fatty acid oxidation. Earlier studies suggest that impaired energy metabolism may be implicated in the pathogenesis of microvascular angina. We explored metabolites from the carnitine pathway as predictors of cardiovascular disease (CVD) - and all-cause mortality among patients with non-obstructive coronary artery disease (NOCAD).

Methods:

A total of 1046 patients with suspected stable coronary syndrome underwent coronary angiography during 2000-2004, with findings of NOCAD. Serum levels of 8 selected carnitine metabolites were analyzed through liquid chromatography tandem mass spectrometry. Associations with CVD- and all-cause mortality were assessed by multivariable Cox regression models.

Results:

Median age at inclusion was 57 years. 51.5% were men. During median (25th- 75th percentiles), 14.1 (13.2-15.4) years of follow-up, 5.7% of the participants died from CVD and the incidence of all-cause mortality was 17.3%. Serum acetyl, octanoyl- and palmitoylcarnitine predicted CVD mortality with multivariable HR and 95% CI (per SD increment log transformed) of 1.36 (1.01-1.83), 1.49 (1.15-1.93) and 2.07 (1.49-2.85), p ≤ 0.04, respectively. Higher serum acetyl- and palmitoylcarnitines were also associated with increased risk of all-cause mortality (HR (95% CI) 1.27 (1.01-1.50), and 1.51 (1.26-1.81), p ≤ 0.007. Baseline levels of the precursors trimethyllysine and Æ´-butyrobetaine, carnitine or the odd chained propionylcarnitine and (iso)valerylcarnitine were not associated with adverse outcomes.

Conclusion:

Elevated serum even-chained acylcarnitines predicted adverse long-term prognosis in NOCAD. The strongest risk estimates were observed for palmitoylcarnitine, which predicted both CVD- and all-cause mortality after extensive multivariable adjustments. Underlying pathomechanisms should be further elucidated.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Int J Cardiol Cardiovasc Risk Prev Year: 2022 Type: Article Affiliation country: Norway

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Int J Cardiol Cardiovasc Risk Prev Year: 2022 Type: Article Affiliation country: Norway