4.5 Article

The Shrunken pore syndrome is associated with poor prognosis and lower quality of life in heart failure patients: the HARVEST-Malmo study

Journal

ESC HEART FAILURE
Volume 8, Issue 5, Pages 3577-3586

Publisher

WILEY PERIODICALS, INC
DOI: 10.1002/ehf2.13485

Keywords

Cardiorenal syndrome; Creatinine; Cystatin C; Mortality; Quality of life; Shrunken pore

Funding

  1. Medical Faculty of Lund University (Medicinska Fakulteten, Lunds Universitet)
  2. Skane University Hospital (Skanes universitetssjukhus)
  3. Crafoord Foundation (Crafoordska Stiftelsen)
  4. Ernhold Lundstrom's Research Foundation (Ernhold Lundstrom Stiftelse)
  5. Region Skane (HjartLungfonden)
  6. Hulda and Conrad Mossfelt Foundation (Hulda och E Conrad Mossfelts Stiftelse for Vetenskaplig Forskning Inom Hjart-och Karlsjukdomarnas Omrade)
  7. Southwest Skane's Diabetes Foundation (Sydvastra Skanes Diabetesforening)
  8. Kockska Foundation
  9. Research Funds of Region Skane
  10. Swedish Heart and Lung Foundation
  11. Wallenberg Center for Molecular Medicine, Lund University
  12. Medical Faculty of Lund University
  13. Swedish Kidney Foundation (Njurfonden)
  14. Njurstiftelsen
  15. Skane University Hospital Research Fund
  16. Research and Development Council of Region Skane (Skane County Council's Research and Development Foundation), Sweden
  17. Region Skane
  18. Lund University (Lunds Universitet)

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This study found an association between 'Shrunken pore syndrome' (SPS) and increased risk of death, 30 day rehospitalization, as well as impaired health-related quality of life in heart failure patients.
Aims This study aimed to investigate the association between the 'Shrunken pore syndrome' (SPS) and risk of death, 30 day rehospitalization, and health-related quality of life (QoL) in heart failure (HF) patients. SPS is characterized by a difference in renal filtration between cystatin C and creatinine, resulting in a low eGFR(cystatin C)/eGFR(creatinine) ratio. Methods and results A total of 373 patients hospitalized for HF [mean age 74.8 (+/- 12.1) years; 118 (31.6%) women] were retrieved from the HeARt and brain failure inVESTigation trial (HARVEST-Malmo). Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formulas were used for estimation of glomerular filtration rate (eGFR). Presence of SPS was defined as eGFR(cystatin C) <= 60% of eGFR(creatinine). In Cox regression multivariate models, associations between SPS, risk of death (median follow-up time 1.8 years), and risk of 30 day rehospitalization were studied. Associations between SPS and impaired QoL were studied using multivariate logistic regressions. In multivariate models, SPS was associated with all-cause mortality [124 events; hazard ratio (HR) 1.99; 95% confidence interval (95% CI) 1.23-3.21; P = 0.005] and with 30 day rehospitalization (70 events; HR 1.82; CI 95% 1.04-3.18; P = 0.036). Analyses of QoL, based on a Kansas City Cardiomyopathy Questionnaire overall score < 50, revealed that SPS was associated with higher risk of low health-related QoL (odds ratios 2.15; CI 95% 1.03-4.49; P = 0.042). Conclusions The results of this observational study show for the first time an association between SPS and poor prognosis in HF. Further studies are needed to confirm the results in HF cohorts and experimental settings to identify pathophysiological mechanisms.

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