Impact of Simultaneous Pancreas-kidney Transplantation on Cardiovascular Risk in Patients With Diabetes.


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
01 01 2022
Historique:
pubmed: 5 3 2021
medline: 29 3 2022
entrez: 4 3 2021
Statut: ppublish

Résumé

Cardiovascular disease is the major cause of death in patients with type 1 diabetes. Of the available risk predictors for this population, the Steno Type 1 Risk Engine (STENO T1) is the only one that includes kidney function as a risk factor, which is a well-described independent risk factor for cardiovascular disease. We explore how simultaneous pancreas-kidney transplantation (SPKT) modifies the predicted cardiovascular risk by the STENO T1 through a retrospective study including recipients of a first SPKT between 2000 and 2016. Two hundred sixty-eight SPKT recipients with a mean age of 40 y old and a median follow-up of 10 y were included. Before transplantation, the expected incidence of cardiovascular events (CVEs) at 5 and 10 y according to STENO T1 would have been 31% and 50%, respectively, contrasting with an actual incidence of 9.3% and 16% for the same timepoints, respectively (P < 0.05). These differences were attenuated when STENO T1 was recalculated assuming 12th-mo glomerular filtration rate (at 5 and 10 y predicted CVE incidence was 10.5% and 19.4%, respectively). Early pancreas graft failure (hazard ratio [HR] 3.00, 95% confidence interval [CI], 1.14-7.88; P = 0.02) was an independent risk factor for post-SPKT CVE, alongside kidney graft failure (HR 2.90, 95% CI, 1.53-5.48; P = 0.001), and diabetes duration (HR 1.04, 95% CI, 1.00-1.09, P = 0.04). SPKT decreases in more than two-thirds of the predicted cardiovascular risk by the STENO T1. A functioning pancreas graft further reduces CVE risk, independently of kidney graft function.

Sections du résumé

BACKGROUND
Cardiovascular disease is the major cause of death in patients with type 1 diabetes. Of the available risk predictors for this population, the Steno Type 1 Risk Engine (STENO T1) is the only one that includes kidney function as a risk factor, which is a well-described independent risk factor for cardiovascular disease.
METHODS
We explore how simultaneous pancreas-kidney transplantation (SPKT) modifies the predicted cardiovascular risk by the STENO T1 through a retrospective study including recipients of a first SPKT between 2000 and 2016.
RESULTS
Two hundred sixty-eight SPKT recipients with a mean age of 40 y old and a median follow-up of 10 y were included. Before transplantation, the expected incidence of cardiovascular events (CVEs) at 5 and 10 y according to STENO T1 would have been 31% and 50%, respectively, contrasting with an actual incidence of 9.3% and 16% for the same timepoints, respectively (P < 0.05). These differences were attenuated when STENO T1 was recalculated assuming 12th-mo glomerular filtration rate (at 5 and 10 y predicted CVE incidence was 10.5% and 19.4%, respectively). Early pancreas graft failure (hazard ratio [HR] 3.00, 95% confidence interval [CI], 1.14-7.88; P = 0.02) was an independent risk factor for post-SPKT CVE, alongside kidney graft failure (HR 2.90, 95% CI, 1.53-5.48; P = 0.001), and diabetes duration (HR 1.04, 95% CI, 1.00-1.09, P = 0.04).
CONCLUSIONS
SPKT decreases in more than two-thirds of the predicted cardiovascular risk by the STENO T1. A functioning pancreas graft further reduces CVE risk, independently of kidney graft function.

Identifiants

pubmed: 33660656
doi: 10.1097/TP.0000000000003710
pii: 00007890-202201000-00032
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

158-166

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare no funding or conflicts of interest.

Références

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Auteurs

Enrique Montagud-Marrahi (E)

Nephrology and Kidney Transplant Department, Hospital Clínic Barcelona, Spain.
Laboratori Experimental de Nefrologia I Trasplantament (LENIT), Fundació Clínic per a la Recerca Biomèdica (FCRB), Barcelona, Spain.

Alicia Molina-Andújar (A)

Nephrology and Kidney Transplant Department, Hospital Clínic Barcelona, Spain.
Laboratori Experimental de Nefrologia I Trasplantament (LENIT), Fundació Clínic per a la Recerca Biomèdica (FCRB), Barcelona, Spain.

Adriana Pané (A)

Diabetes Unit, Endocrinology and Nutrition Department, Hospital Clínic Barcelona, Spain.

Sabina Ruiz (S)

Diabetes Unit, Endocrinology and Nutrition Department, Hospital Clínic Barcelona, Spain.

Antonio J Amor (AJ)

Diabetes Unit, Endocrinology and Nutrition Department, Hospital Clínic Barcelona, Spain.

Enric Esmatjes (E)

Diabetes Unit, Endocrinology and Nutrition Department, Hospital Clínic Barcelona, Spain.

Joana Ferrer (J)

Hepatobiliopancreatic and Liver Transplant Department, Hospital Clínic Barcelona, Spain.

Elisenda Banon-Maneus (E)

Laboratori Experimental de Nefrologia I Trasplantament (LENIT), Fundació Clínic per a la Recerca Biomèdica (FCRB), Barcelona, Spain.
Red de Investigación Renal (REDinREN), Madrid, Spain.

Evelyn Hermida (E)

Nephrology and Kidney Transplant Department, Hospital Clínic Barcelona, Spain.

Mireia Musquera (M)

Urology Department, Hospital Clinic de Barcelona, Spain.

Constantino Fondevila (C)

Hepatobiliopancreatic and Liver Transplant Department, Hospital Clínic Barcelona, Spain.

Fritz Diekmann (F)

Nephrology and Kidney Transplant Department, Hospital Clínic Barcelona, Spain.
Laboratori Experimental de Nefrologia I Trasplantament (LENIT), Fundació Clínic per a la Recerca Biomèdica (FCRB), Barcelona, Spain.
Red de Investigación Renal (REDinREN), Madrid, Spain.

Pedro Ventura-Aguiar (P)

Nephrology and Kidney Transplant Department, Hospital Clínic Barcelona, Spain.
Laboratori Experimental de Nefrologia I Trasplantament (LENIT), Fundació Clínic per a la Recerca Biomèdica (FCRB), Barcelona, Spain.

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