Depression and markers of inflammation as predictors of all-cause mortality in heart failure

Paula M. C. Mommersteeg*, Regien G. Schoemaker, Petrus J. W. Naude, Ulrich L. M. Eisel, Ingrid M. Garrelds, Casper G. Schalkwijk, Bert W. J. J. M. Westerhuis, Willem J. Kop, Johan Denollet

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Web of Science)

Abstract

Background: In patients with heart failure (HF) depressive symptoms have been associated with mortality, as well as biological risk factors, including inflammation, nitric oxide (NO) regulation, and oxidative stress. We investigated the joint predictive value of depressive symptoms, inflammation and NO regulation on all-cause mortality in patients with HF, adjusted for covariates. Methods: Serum levels of inflammation (TNF alpha, sTNFr1, sTNFr2, IL-6, hsCRP, NGAL), NO regulation (L-arginine, ADMA, and SDMA), and oxidative stress (isoprostane 8-Epi Prostaglandin F2 Alpha) were measured in 104 patients with HF (mean age 65.7 +/- SD 8.4 years, 28% women). Depressive symptoms (Beck Depression Inventory, BDI) were measured as continuous total, cognitive, and somatic symptoms, as well as categorized presence of mild moderate depression (cut-off BDI >= 10). In Cox proportional hazard models we adjusted for age, sex, poor exercise tolerance and comorbidity. Results: After on average 6.1 years follow-up (SD = 2.9, range 0.4-9.2), 49 patients died. Total and somatic depressive symptoms, mild/moderate depression, higher NGAL, sTNFr2, IL-6, hsCRP and SDMA serum levels were significantly associated with a higher all-cause mortality rate, adjusted for covariates. The findings were most consistent for CRP level and somatic depressive symptoms. When combined, both depressive symptoms and markers of inflammation and NO regulation remained significantly associated with all-cause mortality. These associations were not confounded by age, sex, poor exercise tolerance and comorbidity. Conclusion: Depressive symptoms and markers of inflammation and NO regulation are codominant risk factors for all- cause mortality in heart failure.
Original languageEnglish
Pages (from-to)144-150
JournalBrain Behavior and Immunity
Volume57
DOIs
Publication statusPublished - Oct 2016

Keywords

  • Heart failure
  • Depressive symptoms
  • Inflammation
  • CRP
  • All-cause mortality
  • NGAL
  • NO regulation
  • Methylarginines
  • Prognosis

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