TY - JOUR
T1 - Circulating levels of miR-574-5p are associated with neurological outcome after cardiac arrest in women
T2 - A target temperature management (TTM) trial substudy
AU - Boileau, Adeline
AU - Somoza, Antonio Salgado
AU - Dankiewicz, Josef
AU - Stammet, Pascal
AU - Gilje, Patrik
AU - Erlinge, David
AU - Hassager, Christian
AU - Wise, Matthew P.
AU - Kuiper, Michael
AU - Friberg, Hans
AU - Nielsen, Niklas
AU - Devaux, Yvan
AU - TTM-Trial Investigators on behalf of Cardiolinc
N1 - Funding Information:
A.B. is funded by the National Research Fund of Luxembourg (grant # AFR 8832104). A.S.S. is funded by the National Research Fund of Luxembourg (grants nos. C14/BW1/8225223 and C17/BM/11613033). Y.D. is supported by the National Research Fund and the Ministry of Higher Education and Research of Luxembourg. The TTM trial and the TTM trial biobank were funded by independent research grants from the Swedish Heart Lung Foundation; Arbetsmarknadens Försäkringsaktiebolag (AFA) Insurance Foundation; Swedish Research Council; Regional research support, Region Skåne; government funding of clinical research within the Swedish NHS (National Health Services); Thelma Zoega Foundation; Krapperup Foundation; Thure Carlsson Foundation; Hans-Gabriel and Alice Trolle-Wachtmeister Foundation for Medical Research; Skåne University Hospital, Sweden; TrygFonden, Denmark; European Clinical Research Infrastructures Network; and European Critical Care Research Network. The contribution of TTM trial investigators and Cardiolinc™ network members to this work is greatly acknowledged. There was no commercial funding. We would like to thank all the staff involved in the recruitment sites of TTM trial.
Funding Information:
A.B. is funded by the National Research Fund of Luxembourg (grant # AFR 8832104). A.S.S. is funded by the National Research Fund of Luxembourg (grants nos. C14/BW1/8225223 and C17/BM/11613033). Y.D. is supported by the National Research Fund and the Ministry of Higher Education and Research of Luxembourg. The TTM trial and the TTM trial biobank were funded by independent research grants from the Swedish Heart Lung Foundation; Arbetsmarknadens F?rs?kringsaktiebolag (AFA) Insurance Foundation; Swedish Research Council; Regional research support, Region Sk?ne; government funding of clinical research within the Swedish NHS (National Health Services); Thelma Zoega Foundation; Krapperup Foundation; Thure Carlsson Foundation; Hans-Gabriel and Alice Trolle-Wachtmeister Foundation for Medical Research; Sk?ne University Hospital, Sweden; TrygFonden, Denmark; European Clinical Research Infrastructures Network; and European Critical Care Research Network. The contribution of TTM trial investigators and Cardiolinc? network members to this work is greatly acknowledged. There was no commercial funding. We would like to thank all the staff involved in the recruitment sites of TTM trial.
Publisher Copyright:
© 2019 Adeline Boileau et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2019
Y1 - 2019
N2 - Purpose. Postresuscitation neuroprognostication is guided by neurophysiological tests, biomarker measurement, and clinical examination. Recent investigations suggest that circulating microRNAs (miRNA) may help in outcome prediction after cardiac arrest. We assessed the ability of miR-574-5p to predict neurological outcome after cardiac arrest, in a sex-specific manner. Methods. In this substudy of the Target Temperature Management (TTM) Trial, we enrolled 590 cardiac arrest patients for which blood samples were available. Expression levels of miR-574-5p were measured by quantitative PCR in plasma samples collected 48 h after cardiac arrest. The endpoint of the study was poor neurological outcome at 6 months (cerebral performance category scores 3 to 5). Results. Eighty-one percent of patients were men, and 49% had a poor neurological outcome. Circulating levels of miR-574-5p at 48 h were higher in patients with a poor neurological outcome at 6 months (p < 0 001), both in women and in men. Circulating levels of miR-574-5p were univariate predictors of neurological outcome (odds ratio (OR) [95% confidence interval (CI)]: 1.5 [1.26-1.78]). After adjustment with clinical variables and NSE, circulating levels of miR-574-5p predicted neurological outcome in women (OR [95% CI]: 1.9 [1.09-3.45]), but not in men (OR [95% CI]: 1.0 [0.74-1.28]). Conclusion. miR-574-5p is associated with neurological outcome after cardiac arrest in women.
AB - Purpose. Postresuscitation neuroprognostication is guided by neurophysiological tests, biomarker measurement, and clinical examination. Recent investigations suggest that circulating microRNAs (miRNA) may help in outcome prediction after cardiac arrest. We assessed the ability of miR-574-5p to predict neurological outcome after cardiac arrest, in a sex-specific manner. Methods. In this substudy of the Target Temperature Management (TTM) Trial, we enrolled 590 cardiac arrest patients for which blood samples were available. Expression levels of miR-574-5p were measured by quantitative PCR in plasma samples collected 48 h after cardiac arrest. The endpoint of the study was poor neurological outcome at 6 months (cerebral performance category scores 3 to 5). Results. Eighty-one percent of patients were men, and 49% had a poor neurological outcome. Circulating levels of miR-574-5p at 48 h were higher in patients with a poor neurological outcome at 6 months (p < 0 001), both in women and in men. Circulating levels of miR-574-5p were univariate predictors of neurological outcome (odds ratio (OR) [95% confidence interval (CI)]: 1.5 [1.26-1.78]). After adjustment with clinical variables and NSE, circulating levels of miR-574-5p predicted neurological outcome in women (OR [95% CI]: 1.9 [1.09-3.45]), but not in men (OR [95% CI]: 1.0 [0.74-1.28]). Conclusion. miR-574-5p is associated with neurological outcome after cardiac arrest in women.
UR - http://www.scopus.com/inward/record.url?scp=85069267381&partnerID=8YFLogxK
U2 - 10.1155/2019/1802879
DO - 10.1155/2019/1802879
M3 - Article
C2 - 31275442
AN - SCOPUS:85069267381
SN - 0278-0240
VL - 2019
JO - Disease Markers
JF - Disease Markers
M1 - 1802879
ER -