H₂S donor does not reduce infarct size after STEMI
ACC 2022 There was no reduction in infarct size after 4 months in STEMI patients treated with sodium thiosulfate compared with patients in the placebo group, in the GIPS-IV trial.
The Groningen Intervention Study For The Preservation Of Cardiac Function With Sodium Thiosulfate After ST-segment Elevation Myocardial Infarction (GIPS-IV)
News - Apr. 12, 2022
Presented at ACC.22 by **Marie-Sophie de Koning, MD (Groningen, The Netherlands)
Introduction and methods
Sodium thiosulfate is a strong antioxidant and H₂S donor, which has an established clinical safety profile. There is preclinical evidence that shows that administration of H₂S or H₂S donating compounds prevent damage after heart attack in animal studies.
The aim of the trial was to investigate whether sodium thiosulfate can reduce damage after a heart attack to ultimately improve prognosis.
Eligible patients who presented with a first STEMI were randomized to sodium thiosulfate (n=186) or matching placebo (n=187). The first dose was given directly at the cath lab and the second dose was administered 6 hours later.
The primary outcome was infarct size measured by cardiac magnetic resonance imaging at 4 months
Results
- There was no difference in infarct size after 4 months between the two groups.
- The secondary outcomes of LVEF, enzymatic infarct size, and NT-proBNP levels were not different between the two groups after 4 months.
- Rate of MACE appeared to be similar between the two treatment arms, and an increase in nausea and vomiting was observed in the sodium thiosulfate group.
Conclusion
In the GIPS-IV trial, administration of sodium thiosulfate did not reduce damage after heart attack. “Future studies should establish the role of H₂S in protecting the heart against damage, as this study does not exclude H₂S in total as a potential new therapy”, concluded De Koning.
Discussion
The discussant,**Prof. Roxane Mehran (New York, NY, USA) said that the infarct sizes in these patients were small; the investigators did a great job in treating these patients quickly, making it difficult to demonstrate benefit with a new compound.
– Our coverage of ACC.22 is based on the information provided during the congress –