Neuropeptide Y predicts cardiovascular events in chronic kidney disease patients: a cohort study.


Journal

Journal of hypertension
ISSN: 1473-5598
Titre abrégé: J Hypertens
Pays: Netherlands
ID NLM: 8306882

Informations de publication

Date de publication:
07 2019
Historique:
pubmed: 12 1 2019
medline: 4 7 2020
entrez: 12 1 2019
Statut: ppublish

Résumé

Neuropeptide Y (NPY) is a multifaceted sympathetic neurotransmitter regulating reflex cardiovascular control, myocardial cell growth, inflammation and innate immunity. Circulating NPY levels predict cardiovascular mortality in patients with end stage kidney disease on dialysis but this relationship has never been tested in predialysis chronic kidney disease (CKD) patients. We investigated the relationship between circulating NPY and the risk for cardiovascular events (Fine & Gray competing risks model) in a cohort of 753 stages 2-5 CKD patients over a median follow-up of 36 months. Independently of other risk factors, plasma NPY was directly related with the glomerular filtration rate (β = -0.19, P < 0.001) but was independent of systemic inflammation as quantified by serum IL6 and C reactive protein. Over follow-up 112 patients had cardiovascular events and 12 died. In analyses fully adjusted for traditional risk factors and a large series of CKD-specific risk factors and considering death as a competing event (Fine and Gray model) a 0.25 μmol/l increase in NPY robustly predicted the incident risk for cardiovascular events (subdistribution hazard ratio: 1.25; 95% confidence interval: 1.09-1.44; P = 0.002). Furthermore, the fully adjusted NPY - cardiovascular outcomes relationship was modified by age (P = 0.012) being quite strong in young patients but weaker in the old ones. NPY is an independent, robust predictor of cardiovascular events in predialysis CKD patients and the risk for such events is age-dependent being maximal in young patients. These findings suggest that NPY may play a role in the high risk of cardiovascular disease in this population.

Sections du résumé

BACKGROUND
Neuropeptide Y (NPY) is a multifaceted sympathetic neurotransmitter regulating reflex cardiovascular control, myocardial cell growth, inflammation and innate immunity. Circulating NPY levels predict cardiovascular mortality in patients with end stage kidney disease on dialysis but this relationship has never been tested in predialysis chronic kidney disease (CKD) patients.
METHODS
We investigated the relationship between circulating NPY and the risk for cardiovascular events (Fine & Gray competing risks model) in a cohort of 753 stages 2-5 CKD patients over a median follow-up of 36 months.
RESULTS
Independently of other risk factors, plasma NPY was directly related with the glomerular filtration rate (β = -0.19, P < 0.001) but was independent of systemic inflammation as quantified by serum IL6 and C reactive protein. Over follow-up 112 patients had cardiovascular events and 12 died. In analyses fully adjusted for traditional risk factors and a large series of CKD-specific risk factors and considering death as a competing event (Fine and Gray model) a 0.25 μmol/l increase in NPY robustly predicted the incident risk for cardiovascular events (subdistribution hazard ratio: 1.25; 95% confidence interval: 1.09-1.44; P = 0.002). Furthermore, the fully adjusted NPY - cardiovascular outcomes relationship was modified by age (P = 0.012) being quite strong in young patients but weaker in the old ones.
CONCLUSION
NPY is an independent, robust predictor of cardiovascular events in predialysis CKD patients and the risk for such events is age-dependent being maximal in young patients. These findings suggest that NPY may play a role in the high risk of cardiovascular disease in this population.

Identifiants

pubmed: 30633126
doi: 10.1097/HJH.0000000000002030
doi:

Substances chimiques

Biomarkers 0
Neuropeptide Y 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1359-1365

Auteurs

Carmine Zoccali (C)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.

Graziella D'Arrigo (G)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.

Daniela Leonardis (D)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.

Patrizia Pizzini (P)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.

Maurizio Postorino (M)

Nephrology and Transplantation Unit, Ospedali Riuniti, Reggio Calabria, Italy.

Giovanni Tripepi (G)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.

Francesca Mallamaci (F)

CNR-IFC, Center of Clinical Physiology, Clinical Epidemiology of Renal Diseases and Hypertension.
Nephrology and Transplantation Unit, Ospedali Riuniti, Reggio Calabria, Italy.

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Classifications MeSH