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Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure.

Publication ,  Journal Article
Adel, FW; Rikhi, A; Wan, S-H; Iyer, SR; Chakraborty, H; McNulty, S; Tang, WHW; Felker, GM; Givertz, MM; Chen, HH
Published in: J Card Fail
August 2020

OBJECTIVES: This study sought to identify the role of annexin A1 (AnxA1) as a congestion marker in acute heart failure (AHF) and to identify its putative role in predicting clinical outcomes. BACKGROUND: AnxA1 is a protein that inhibits inflammation following ischemia-reperfusion injury in cardiorenal tissues. Because AHF is a state of tissue hypoperfusion, we hypothesized that plasma AnxA1 levels are altered in AHF. METHODS: In the Renal Optimization Strategies Evaluation (ROSE) trial, patients hospitalized for AHF with kidney injury were randomized to receive dopamine, nesiritide, or placebo for 72 hours in addition to diuresis. In a subanalysis, plasma AnxA1 levels were measured at baseline and at 72 hours in 275 patients. Participants were divided into 3 tertiles based on their baseline AnxA1 levels. RESULTS: The prevalence of peripheral edema 2+ increased with increasing AnxA1 levels (P < .007). Cystatin C, blood urea nitrogen, and kidney injury molecule-1 plasma levels were higher among participants in tertile 3 vs tertiles 1 or 2 (P< .05). Patients with a congestion score of 4 had a mean baseline AnxA1 level 8.63 units higher than those with a congestion score of 0 (P = .03). Patients in tertiles 2 and 3 were twice as likely to experience creatinine elevation as patients in tertile 1 (P = .03). Patients in tertiles 2 and 3 were at a higher risk of 60-day all-cause mortality or heart failure hospitalization and 180-day all-cause mortality (P < .05). CONCLUSIONS: Among patients hospitalized for AHF with impaired kidney function, elevated AnxA1 levels are associated with worse congestion, higher risk for further creatinine elevation, and higher rates of 60-day morbidity or all-cause mortality and 180-day all-cause mortality. CLINICAL TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01132846.

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Published In

J Card Fail

DOI

EISSN

1532-8414

Publication Date

August 2020

Volume

26

Issue

8

Start / End Page

727 / 732

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Natriuretic Peptide, Brain
  • Humans
  • Heart Failure
  • Cardiovascular System & Hematology
  • Biomarkers
  • Annexin A1
  • Acute Disease
  • 3202 Clinical sciences
  • 3201 Cardiovascular medicine and haematology
 

Citation

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Adel, F. W., Rikhi, A., Wan, S.-H., Iyer, S. R., Chakraborty, H., McNulty, S., … Chen, H. H. (2020). Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure. J Card Fail, 26(8), 727–732. https://doi.org/10.1016/j.cardfail.2020.05.012
Adel, Fadi W., Aruna Rikhi, Siu-Hin Wan, Seethalakshmi R. Iyer, Hrishikesh Chakraborty, Steven McNulty, WH Wilson Tang, G Michael Felker, Michael M. Givertz, and Horng H. Chen. “Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure.J Card Fail 26, no. 8 (August 2020): 727–32. https://doi.org/10.1016/j.cardfail.2020.05.012.
Adel FW, Rikhi A, Wan S-H, Iyer SR, Chakraborty H, McNulty S, et al. Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure. J Card Fail. 2020 Aug;26(8):727–32.
Adel, Fadi W., et al. “Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure.J Card Fail, vol. 26, no. 8, Aug. 2020, pp. 727–32. Pubmed, doi:10.1016/j.cardfail.2020.05.012.
Adel FW, Rikhi A, Wan S-H, Iyer SR, Chakraborty H, McNulty S, Tang WHW, Felker GM, Givertz MM, Chen HH. Annexin A1 is a Potential Novel Biomarker of Congestion in Acute Heart Failure. J Card Fail. 2020 Aug;26(8):727–732.
Journal cover image

Published In

J Card Fail

DOI

EISSN

1532-8414

Publication Date

August 2020

Volume

26

Issue

8

Start / End Page

727 / 732

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Natriuretic Peptide, Brain
  • Humans
  • Heart Failure
  • Cardiovascular System & Hematology
  • Biomarkers
  • Annexin A1
  • Acute Disease
  • 3202 Clinical sciences
  • 3201 Cardiovascular medicine and haematology