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Copeptin predicts 10-year all-cause mortality in community patients: a 10-year prospective cohort study

  • Jonas Odermatt , Rebekka Bolliger , Lara Hersberger , Manuel Ottiger , Mirjam Christ-Crain , Matthias Briel , Heiner C. Bucher , Beat Mueller and Philipp Schuetz EMAIL logo
Published/Copyright: May 12, 2016

Abstract

Background:

Copeptin, the C-terminal part of the arginine vasopressin (AVP) precursor peptide, is secreted in response to stress and correlates with adverse clinical outcomes in the acute-care hospital setting. There are no comprehensive data regarding its prognostic value in the community. We evaluated associations of copeptin levels with 10-year mortality in patients visiting their general practitioner (GP) for a respiratory infection included in a previous trial.

Methods:

This is a post hoc analysis including data from 359 patients included in the PARTI trial. Copeptin was measured in batch-analysis on admission and after 7 days. We calculated Cox regression models and area under the receiver operating characteristic curve (AUC) to assess an association of copeptin with mortality and adverse outcome. Follow-up data were collected by GP, patient and relative tracing through phone interviews 10 years after trial inclusion.

Results:

After a median follow-up of 10.0 years, mortality was 9.8%. Median admission copeptin levels (pmol/L) were significantly elevated in non-survivors compared to survivors (13.8, IQR 5.9–27.8; vs. 6.3 IQR 4.1–11.5; p<0.001). Admission copeptin levels were associated with 10-year all-cause mortality [age-adjusted hazard ratio 1.7 (95% CI, 1.2–2.5); p<0.001, AUC 0.68]. Results were similar for discharge copeptin levels. Copeptin also predicted adverse outcomes defined as death, pulmonary embolism and major adverse cardiac and cerebrovascular events.

Conclusions:

In a sample of community-dwelling patients visiting their GP for a respiratory infection, copeptin levels were associated with 10-year all-cause mortality. In conjunction with traditional risk factors, this marker may help to better direct preventive measures in this population.

Award Identifier / Grant number: 3300C0-107772

Funding statement: This investigator-initiated PARTI trial was sponsored by a grant from the Swiss National Science Foundation (3300C0-107772) and by the Association for the Promotion of Science and Postgraduate Training of the University Hospital Basel. B.R.A.H.M.S AG provided assay and kit material related to the study. Dr. Schuetz and Dr. Christ-Crain were supported by funds from the Freiwillige Akademische Gesellschaft, the Department of Endocrinology, Diabetology and Clinical Nutrition, and the Department of Clinical Chemistry, all Basel, Switzerland. Drs. Christ-Crain, Mueller, and Schuetz, received support from B.R.A.H.M.S to attend meetings and fulfilled speaking engagements. Drs. Schuetz, Christ-Crain and Mueller received support from bioMérieux to attend meetings and fulfilled speaking engagements. Dr. Mueller has served as a consultant and received research support from B.R.A.H.M.S and bioMérieux. All other authors declare that the answer to the questions on the competing interest form is all “No” and therefore have nothing to declare.

Acknowledgments:

We are grateful to the physicians, their staffs and patients who participated in the PARTI trial and the follow-up data collection. We would also like to thank the staff of the central laboratory of the University Hospital Basel for their assistance and technical support.

  1. Author contributions: Mr. Odermatt and Ms. Bolliger contributed equally to this study. Mr. Odermatt, Ms. Bolliger and Dr. Schuetz had full access to all of the data in the study and take responsibility for the integrity of the data and performed the statistical work, and drafted the manuscript. All authors helped to interpret the findings, read and revised the manuscript critically for important intellectual content, and approved the final version of the manuscript.

  2. Research funding: This investigator-initiated PARTI trial was sponsored by a grant from the Swiss National Science Foundation (3300C0-107772) and by the Association for the Promotion of Science and Postgraduate Training of the University Hospital Basel. B.R.A.H.M.S AG provided assay and kit material related to the study. Dr. Schuetz and Dr. Christ-Crain were supported by funds from the Freiwillige Akademische Gesellschaft, the Department of Endocrinology, Diabetology and Clinical Nutrition, and the Department of Clinical Chemistry, all Basel, Switzerland. Drs. Christ-Crain, Mueller, and Schuetz, received support from B.R.A.H.M.S to attend meetings and fulfilled speaking engagements. Drs. Schuetz, Christ-Crain and Mueller received support from bioMérieux to attend meetings and fulfilled speaking engagements. Dr. Mueller has served as a consultant and received research support from B.R.A.H.M.S and bioMérieux. All other authors declare that the answer to the questions on the competing interest form is all “No” and therefore have nothing to declare.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplemental Material:

The online version of this article (DOI: 10.1515/cclm-2016-0151) offers supplementary material, available to authorized users.


Received: 2016-2-23
Accepted: 2016-4-6
Published Online: 2016-5-12
Published in Print: 2016-10-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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