Key result
N-acetylcysteine administration prevented the significant increase in pro-fibrotic TGF-β levels at 72 hours that was observed in the placebo group following ST-segment elevation myocardial infarction.
Why the study?
Does N-acetylcysteine prevent the increase of pro-fibrotic and inflammatory biomarkers (TGF-β and TNF-α) in patients following ST-segment elevation myocardial infarction?
RCT (n=88)
Double-blind
Randomized
No
Does N-acetylcysteine prevent the increase of pro-fibrotic and inflammatory biomarkers (TGF-β and TNF-α) in patients following ST-segment elevation myocardial infarction?
Short-term oral N-acetylcysteine administration following acute myocardial infarction prevents the early rise of the pro-fibrotic biomarker TGF-β, which correlates with ejection fraction.
Answers are grounded in this paper and cite their sources.
NAC prevents early TGF-β rise post-STEMI; supports trials evaluating effects on remodeling and outcomes.
BACKGROUND AND AIMS: Ischemia following acute myocardial infarction (AMI) increases the level of pro-fibrotic and inflammatory cytokines, including transforming growth factor (TGF)-β and tumor necrosis factor (TNF)-α. N-acetylcysteine (NAC) has therapeutic benefits in the management of patients with AMI. To the best of our knowledge, this is the first study that has evaluated the effect of NAC on TNF-α and TGF-β levels in patients with AMI. METHODS: Following confirmation of AMI, 88 patients were randomly administered NAC 600 mg (Fluimucil(®), Zambon, Ticino, Switzerland) or placebo orally twice daily for 3 days. For quantification of TGF-β and TNF-α serum levels after 24 and 72 h of NAC or placebo administration, peripheral venous blood (10 mL) samples were collected at these time points. RESULTS: Comparisons between levels of TGF-β and TNF-α after 24 and 72 h within the NAC or placebo groups revealed that there was not any significant difference except for TGF-β levels in the placebo group, which increased significantly over time (p = 0.042). Significant relationships existed between patients' ejection fraction (p = 0.005) and TGF-β levels. CONCLUSIONS: Receiving NAC could prevent TGF-β levels from increasing after 72 h as compared with not receiving NAC. As TGF-β had strong correlations with the ejection fraction, its antagonism seems to be important in the prevention of remodeling.
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Talasaz et al. (2013) conducted an RCT in ST-Segment Elevation Myocardial Infarction (STEMI) (n=88). N-acetylcysteine vs. Placebo was evaluated on TGF-β serum levels at 72 hours (pg/mL) (p=0.255). N-acetylcysteine administration prevented the significant increase in pro-fibrotic TGF-β levels at 72 hours that was observed in the placebo group following ST-segment elevation myocardial infarction.
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