4.7 Article

Time-dependent lipid profile inversely associates with mortality in hemodialysis patients - independent of inflammation/malnutrition

期刊

JOURNAL OF INTERNAL MEDICINE
卷 290, 期 4, 页码 910-921

出版社

WILEY
DOI: 10.1111/joim.13291

关键词

albumin; cholesterol; chronic kidney disease; haemodialysis; inflammation; lipid profile; mortality

资金

  1. Amgen (Europe) GmbH, Rotkreuz, Switzerland
  2. Strategic Research Program in Diabetes at Karolinska Institutet (Swedish Research Council) [2009-1068]
  3. Heart and Lung Foundation [20160384]
  4. Njurfonden
  5. Westmans Foundation
  6. Novo Nordisk
  7. Karolinska Institutet, Stockholm, Sweden
  8. Karolinska Institutet Research Foundation
  9. Swedish Kidney Foundation (Njurfonden)
  10. EFSD Mentorship Programme by AstraZeneca
  11. German Research Foundation [SFB TRR 219]
  12. National Institute for Health Research (UK) Clinician Scientist Award

向作者/读者索取更多资源

In patients with end-stage kidney disease, there is an inverse relationship between lipid profile and mortality in European haemodialysis patients, which is not affected by inflammation/malnutrition.
Background Patients with end-stage kidney disease have an extremely high cardiovascular mortality rate, but there is a paradoxical relationship between lipid profile and survival in haemodialysis patients. To investigate whether inflammation/malnutrition confounds the associations between lipids and mortality, we studied a full lipid profile comprising of five clinically well-established lipid parameters and its associations with mortality in a large, multinational European cohort with a median follow-up >3 years. Methods The association between quartiles of total, high-density lipoprotein (HDL), non-HDL, low-density lipoprotein (LDL) cholesterol, as well as triglyceride, levels and the end-points of all-cause, cardiovascular and non-cardiovascular mortality was assessed in a cohort of 5,382 incident, adult haemodialysis patients from >250 Fresenius Medical Care dialysis centres out of 14 participating countries using baseline and time-dependent Cox models. Analyses were fully adjusted and stratified for inflammation/malnutrition status and other patient-level variables. Results Time-dependent quartiles of total, HDL, non-HDL and LDL cholesterol were inversely associated with the hazard for all-cause, cardiovascular and non-cardiovascular mortality. Compared with the lowest quartile of the respective lipid parameter, hazard ratios of other quartiles were <0.86. Similar, albeit weaker, associations were found with baseline lipid profile and mortality. Neither time-dependent nor baseline associations between lipid profile and mortality were affected by inflammation/malnutrition, statin use or geography. Conclusions Baseline and time-dependent lipid profile are inversely associated with mortality in a large, multicentre cohort of incident haemodialysis patients. Inflammation/malnutrition is not a confounder nor effect modificator of the associations between lipid profile and mortality in European haemodialysis patients.

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